USE OF VOLATILE COMPOSITIONS TO LIMIT OR ELIMINATE PERCEPTION OF FECAL MALODOUR
20190343977 ยท 2019-11-14
Inventors
- Christian Margot (Geneva 8, CH)
- Matthew ROGERS (Plainsboro, NJ, US)
- Gary MARR (Plainsboro, NJ, US)
- Christine Vuilleumier (Geneva 8, CH)
- Ben SMITH (Plainsboro, NJ, US)
- Christian Chappuis (Geneva 8, CH)
- Christian Starkenmann (Geneva 8, CH)
- Charles Jean-Fran?ois Chappuis (Geneva 8, US)
- Nicholas John O'Leary (Plainsboro, NJ, US)
Cpc classification
A61L9/013
HUMAN NECESSITIES
A61L9/042
HUMAN NECESSITIES
A61L9/044
HUMAN NECESSITIES
A61L9/014
HUMAN NECESSITIES
A61L9/14
HUMAN NECESSITIES
International classification
A61L9/04
HUMAN NECESSITIES
A61L9/013
HUMAN NECESSITIES
Abstract
Described herein is a method of using volatile compositions to limit, decrease or eliminate a perception of fecal malodour. Such compositions include a malodour antagonist system associated with perfuming ingredients performing as malodour counteractant, in a combination that significantly reduces the perception of fecal malodour. Such compositions, methods of using the compositions in combination with delivery systems and their applications in consumer products are described herein.
Claims
1. A method of using a composition comprising (i) from about 2 wt % to about 85 wt %, of a malodour receptor antagonist system comprising at least one ingredient selected from the group of Table 1; (ii) from about 15 wt % to 98 wt % of a functional perfume accord comprising at least 2 perfuming ingredient(s) provided that any ingredient listed in Table 1 is excluded, the accord having a tonality selected from floral, citrus and jasmine; and (iii) optionally a non-functional perfume accord; to decrease, limit or eliminate a perception of fecal malodour.
2. The method of use according to claim 1, characterized in that the malodour receptor antagonist system comprises at least 3 ingredients selected from Table 1.
3. The method of use according to claim 1, characterized in that the malodour receptor antagonist system comprises at least 4 ingredients selected from the group of Table 1.
4. The method of use according to claim 1, characterized in that the functional perfume accord comprises ingredient(s) selected from the group of Table 2 and mixtures thereof.
5. The method of use according to claim 1, characterized in that the functional perfume accord comprises ingredients selected from the group consisting of ionones, irones, damascones, citral, methylcinnamic aldehyde, pelargodienal, orivone, derivatives and mixtures thereof.
6. The method of use according to claim 1, characterized in that the composition further comprises encapsulating materials such as polymers to form microcapsules or microparticles, or materials to form liquid delivery system for the composition such as an emulsion, a microemulsion, a miniemulsion, a gel, a microgel, an anhydrous gel or a dispersion.
7. The method of use according to claim 1, characterized in that the composition is absorbed on a porous or non-porous substrate in loose powder or compacted form, the substrate being selected from cellulose (paper/cardboard), vermiculite, other industrial absorbents, perlite, calcium carbonate, pumice, wood, sawdust, ground corn cob, ground rice hull, rice hull ash, biochars, starches, modified starches and mixtures thereof.
8. A malodour receptor antagonist system consisting of at least 3 or at least 4 ingredients selected from the group of Table 1.
9. A malodour counteracting composition comprising a) from 2 to 85 wt % of an active amount a malodour receptor antagonist system comprising at least one or at least 3 ingredients selected from Table 1; b) from 15 to 98 wt % of a functional perfume accord comprising at least two ingredients selected from Table 2 and derivatives and mixtures thereof; and c) optionally a non-functional perfume accord comprising at least two perfuming ingredients.
10. The composition according to claim 9, characterized in that malodour receptor antagonist system comprises (2,5-dimethyl-2,3-dihydro-1H-inden-2-yl)methanol, and the functional perfume accord comprises citral, isoraldeine and ?-ionone.
11. The composition according to claim 10, characterized in that (2,5-dimethyl-2,3-dihydro-1H-inden-2-yl)methanol is present at least at 2% or at 3% of the composition.
12. The malodour counteracting composition according to claim 9, characterized in that it further comprises an encapsulating materials or other materials to form an emulsion, a dispersion, a micro-emulsion, a miniemulsion, a gel, a micro-gel, a microcapsule or a microparticle.
13. A perfumed consumer product comprising an effective amount of a malodour counteracting composition as defined in claim 9.
14. The perfumed consumer product according to claim 13, selected from the group consisting of air care products, home care products and laundry care products.
15. The perfumed consumer product according to claim 13, characterized in that it is in a form of an aerosol and/or water-based air freshener spray, wick/reed air freshener, liquid electrical (plug-in) air freshener, a solid support air freshener, gel-based air freshener, membrane-containing air freshener, bleaching, cleaning, washing detergent powder, liquid all-purpose cleaner, specialty cleaner or liquid detergent.
16. A non-therapeutic method for counteracting fecal malodour, the method comprising treating a surface or dispensing at least partly in air a composition as defined in claim 1.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
[0021]
[0022]
[0023]
[0024]
[0025]
[0026]
[0027]
[0031]
[0032]
[0033]
[0034]
[0035]
[0036]
[0037]
[0038]
[0039]
[0040]
[0041]
[0042]
[0043] The numbers 1, 2, 3 correspond to the three latrines tested. Stars showed significant differences in ratings obtained without and with treatments: ns P>0.05; *P<=0.05; ** P<0.01; ***P<0.001. The black bars denote the fecal character ratings observed for the test formulation. The grey bars denote the fecal character ratings observed in the absence of the test formulation.
[0044]
[0045]
[0046]
[0047]
[0048] dihyd dihydrolinalol; io ?-ionone; iso isoraldeine; jas cis jasmone; lily lyliflore; lina linalyl acetate;ros rosinol; zest zestover. The upper left panel denotes the values observed in latrine no. 2 in Durban. The upper right panel denotes the values observed in latrine no. 3 in Durban. The lower left panel denotes the values observed in latrine no. 1 in Pune. The lower right panel denotes the values observed in latrine no. 2 in Pune.
[0049]
[0050]
[0051]
[0052]
DETAILED DESCRIPTION
Definitions
[0053] Unless otherwise indicated, percentages are meant to designate percentages by weight.
[0054] As used herein, the terms include or comprise are meant to be non-limiting.
[0055] As used herein, the terms malodour receptor antagonist, malodour antagonist system or malodour antagonist ingredient, also referred to as group I is meant to designate one or several compounds that each have the capacity to inhibit at least one olfactory receptor that responds to a malodour target, identified by measuring activity of olfactory neurons or isolated receptors in cultured cell lines whose responses are driven by receptors as described under the examples below.
[0056] As used herein, malodour target is meant to designate a molecular component of fecal malodour characterized in Lin et al, Environ. Sci. Technol., 2013, 47 (14), pp 7876-7882, including indole, butyric acid, p-cresol, skatole, and dimethyl trisulfide.
[0057] As used herein, the term functional perfume accord (referred to as group II) is meant to designate a mixture of at least two perfuming ingredients, referred as functional perfuming ingredients which have been established through e.g. sensory measurement as performing against at least one element of a fecal malodour.
[0058] As used herein, the term non-functional perfume accord (referred to as group III) is meant to be a mixture of at least one, alternatively, at least two perfuming ingredients, referred to as non-functional perfuming ingredients that are not performing as fecal malodour counteractant, i.e. perfuming ingredients that are not part of group I or group II .
[0059] As used herein, the term perfume or perfume oil or perfume accord are used to designate a mixture of perfuming ingredients.
[0060] Moreover, by perfuming ingredient it is meant here a compound, which can be used in a perfuming preparation or a composition to impart at least an hedonic effect. In other words such an ingredient, to be considered as being a perfuming one, must be recognized by a person skilled in the art of perfumery as being able to impart or modify in a positive or pleasant way the odour of a composition, and not just as having an odour.
[0061] The nature and type of the perfuming ingredients do not warrant a more detailed description here, which in any case would not be exhaustive, the skilled person being able to select them on the basis of their general knowledge and according to intended use or application and the desired organoleptic effect. In general terms, these perfuming ingredients belong to chemical classes as varied as alcohols, lactones, aldehydes, ketones, esters, ethers, acetates, nitriles, terpenoids, nitrogenous or sulphurous heterocyclic compounds and essential oils, and the perfuming co-ingredients can be of natural or synthetic origin.
[0062] In particular one may cite perfuming ingredients which are commonly used in perfume formulations, such as: [0063] Aldehydic ingredients: decanal, dodecanal, 2-methyl-undecanal, 10-undecenal, octanal and/or nonenal; [0064] Aromatic-herbal ingredients: eucalyptus oil, camphor, eucalyptol, menthol and/or alpha-pinene; [0065] Balsamic ingredients: coumarine, ethylvanillin and/or vanillin; [0066] Citrus ingredients: dihydromyrcenol, citral, orange oil, linalyl acetate, citronellyl nitrile, orange terpenes, limonene, 1-P-menthen-8-yl acetate and/or 1,4(8)-P-menthadiene; [0067] Floral ingredients: Methyl dihydrojasmonate, linalool, Citronellol, phenylethanol, 3-(4-tert-butylphenyl)-2-methylpropanal, hexyl cinnamic aldehyde, benzyl acetate, benzyl salicylate, tetrahydro-2-isobutyl-4-methyl-4(2H)-pyranol, beta ionone, methyl 2-(methyl amino)benzoate, (E)-3-methyl-4-(2,6,6-trimethyl-2-cyclohexen-1-yl)-3-buten-2-one, hexyl salicylate, 3,7-dimethyl-1,6-nonadien-3-ol, 3-(4-isopropylphenyl)-2-methylpropanal, verdyl acetate, geraniol, P-menth-1-en-8-ol, 4-(1,1-dimethylethyl)-1-cyclohexyle acetate, 1,1-dimethyl-2-phenylethyl acetate, 4-cyclohexyl-2-methyl-2-butanol, amyl salicylate, high cis methyl dihydrojasmonate, 3-methyl-5-phenyl-1-pentanol, verdyl proprionate, geranyl acetate, tetrahydro linalool, cis-7-P-menthanol, Propyl (S)-2-(1,1-dimethylpropoxy)propanoate, 2-methoxynaphthalene, 2,2,2-tri chloro-1-phenylethyl acetate, 4/3-(4-hydroxy-4-methylpentyl)-3-cyclohexene-1-carbaldehyde, amylcinnamic aldehyde, 4-phenyl-2-butanone, isononyle acetate, 4-(1,1-dim?thyl?thyl)-1-cyclohexyl acetate, verdyl isobutyrate and/or mixture of methylionones isomers; [0068] Fruity ingredients: gamma undecalactone, 4-decanolide, ethyl 2-methyl-pentanoate, hexyl acetate, ethyl 2-methylbutanoate, gamma nonalactone, allyl heptanoate, 2-phenoxyethyl isobutyrate, ethyl 2-methyl-1,3-dioxolane-2-acetate and/or diethyl 1,4-cyclohexane dicarboxylate; [0069] Green ingredients: 2,4-Dimethyl-3-cyclohexene-1-carbaldehyde, 2-tert-butyl-1-cyclohexyl acetate, styrallyl acetate, allyl (2-methylbutoxy)acetate, 4-methyl-3-decen-5-ol, diphenyl ether, (Z)-3-hexen-1-ol and/or 1-(5,5-dimethyl-1-cyclohexen-1-yl)-4-penten-1-one; [0070] Musk ingredients: 1,4-dioxa-5,17-cycloheptadecanedione, pentadecenolide, 3-Methyl-5-cyclopentadecen-1-one, 1,3,4,6,7,8-hexahydro-4,6,6,7,8,8-hexamethyl-cyclopenta-g-2-benzopyrane, (1S,1R)-2-[1-(3,3-dimethyl-1-cyclohexyl)ethoxy]-2-methylpropyl propanoate, pentadecanolide and/or (1S,1R)-[1-(3,3-Dimethyl-1-cyclohexyl)ethoxycarbonyl]methyl propanoate; [0071] Woody ingredients: 1-(octahydro-2,3,8,8-tetramethyl-2-naphtalenyl)-1-ethanone, patchouli oil, terpenes fractions of patchouli oil, (1R,E)-2-ethyl-4-(2,2,3-trimethyl-3-cyclopenten-1-yl)-2-buten-1-ol, 2-ethyl-4-(2,2,3-trimethyl-3-cyclopenten-1-yl)-2-buten-1-ol, Methyl cedryl ketone, 5-(2,2,3-trimethyl-3-cyclopentenyl)-3-methylpentan-2-ol, 1-(2,3,8,8-tetramethyl-1,2,3,4,6,7,8,8a-octahydronaphthalen-2-yl)ethan-1-one and/or isobornyl acetate; [0072] Other ingredients (e.g. amber, powdery spicy or watery): dodecahydro-3a,6,6,9a-tetramethyl-naphtho[2,1-b]furan and any of its stereoisomers, heliotropin, anisic aldehyde, eugenol, cinnamic aldehyde, clove oil, 3-(1,3-benzodioxol-5-yl)-2-methylpropanal and/or 3-(3-isopropyl-1-phenyl)butanal.
[0073] Perfuming ingredients may not be limited to the above mentioned, and many other of these ingredients are in any case listed in reference texts such as the book by S. Arctander, Perfume and Flavor Chemicals, 1969, Montclair, N.J., USA, or its more recent versions, or in other works of a similar nature, as well as in the patent literature in the field of perfumery. It is also understood that co-ingredients may also be compounds known to release in a controlled manner various types of perfuming compounds.
[0074] It has now been surprisingly established that the association of a malodour receptor antagonist system comprising at least one ingredient selected from the group of Table 1 with a functional perfume accord consisting of perfuming ingredients performing against fecal malodour, improves the effect of the functional perfume accord in limiting, decreasing or eliminating the perception of fecal malodour.
[0075] A first object according to the present disclosure is therefore the use of a composition comprising: [0076] (i) from about 2 wt % to about 85 wt %, of a malodour receptor antagonist system comprising at least one ingredient selected from the group of Table 1; [0077] (ii) from about 15 wt % to 98 wt % of a functional perfume accord comprising at least 2 perfuming ingredient(s) provided that any ingredient listed in Table 1 is excluded, alternatively selected from Table 2, the accord having a tonality selected from floral, citrus and jasmine; and [0078] (iii) optionally a non-functional perfume accord; to decrease, limit or eliminate the perception of fecal malodour.
TABLE-US-00001 TABLE 1 Malodour receptor antagonists - Group I Common Name Chemical name ACETAROLLE (1RS,6RS,11RS)-2,2,9,11- tetramethylspiro[5.5]undec-8-en-1-yl acetate BENZYL ACETATE Benzyl Acetate PHENYLETHYL ACETATE 2-PHENYLETHYL ACETATE ISOBORNYL ACETATE (1R,2R)-1,7,7-TRIMETHYL-BICYCLO[2.2.1]HEPT-2- YL ACETATE ACROPAL 3-(4-METHYL-3-PENTENYL)-3-CYCLOHEXENE-1- CARBALDEHYDE (A) + 4-(4-METHYL-3-PENTENYL)- 3-CYCLOHEXENE-1-CARBALDEHYDE ALDOLONE 7-PROPYL-2H,4H-1,5-BENZODIOXEPIN-3-ONE ALLYL AMYL GLYCOLATE ALLYL (3-METHYLBUTOXY)ACETATE (A) + (+?)- ALLYL (2-METHYLBUTOXY)ACETATE (B) AMBERWOOD (ETHOXYMETHOXY)CYCLODODECANE AMIONE (+?)-(1E)-1-(2,6,6-trimethyl-2-cyclohexen-1-yl)-1,6- heptadien-3-one (A) + (1E)-1-(2,6,6-trimethyl-1- cyclohexen-1-yl)-1,6-heptadien-3-one (B) TETRAMETHYL ETHYL CYCLOHEXENONE 3,5-DIETHYL-5,6-DIMETHYL-2-CYCLOHEXEN-1-ONE (A) + 3,5-DIETHYL-2,5-DIMETHYL-2-CYCLOHEXEN- 1-ONE (B) BOURGEONAL 3-(4-TERT-BUTYLPHENYL)PROPANAL CACHALOX 3aRS,5aSR,9aSR,9bSR)-3a,6,6,9a- tetramethyldodecahydronaphtho[2,1-b]furan CASCALONE? 7-ISOPROPYL-2H,4H-1,5-BENZODIOXEPIN-3-ONE CASMIRONE (4E,8E)-4,8-cyclododecadien-1-one (A) + (4E,8Z)- 4,8-cyclododecadien-1-one (B) + (4Z,8E)-4,8- cyclododecadien-1-one (C) CITRONELLAL CP (+)-(R)-3,7-DIMETHYL-6-OCTENAL VETIKOLACETATE (+?)-1,3-DIMETHYL-3-PHENYLBUTYL ACETATE CYCLEMONE A 1,2,3,4,5,6,7,8-OCTAHYDRO-8,8-DIMETHYL-2- NAPHTHALENECARBALDEHYDE (A) + (B,C,D) + OCTAHYDRO-5,5-DIMETHYL-2- NAPHTHALENECARBALDEHYDE CYCLOPENTOL HC (+?)-CIS-2-PENTYL-1-CYCLOPENTANOL CYCLOSAL (+?)-3-(4-isopropylphenyl)-2-methylpropanal ETHYL DAMASCENATE ETHYL 2,6,6-TRIMETHYL-1,3-CYCLOHEXADIENE-1- CARBOXYLATE DELPHONE (+?)-2-pentylcyclopentanone DIHYDROLINALOL (+?)-3,7-DIMETHYL-1-OCTEN-3-OL DYNASCONE 1-(5,5-dimethyl-1-cyclohexen-1-yl)-4-penten-1- one BENZYL FORMATE BENZYL FORMATE PHENYLETHYL FORMATE 2-PHENYLETHYL FORMATE FRUCTALATE DIETHYL 1,4-CYCLOHEXANEDICARBOXYLATE FRUCTOPYRIDINE 3-(2,2-DIMETHYLPROPYL)PYRIDINE GLYCOLIERRAL (1RS,2SR,8RS)-2-(8-ISOPROPYL-6-METHYL- BICYCLO[2.2.2]OCT-5-EN-2-YL)-1,3-DIOXOLANE HIVERNAL? NEO 3-(3,3-dimethyl-2,3-dihydro-1H-inden-5- yl)propanal (A) + 3-(1,1-dimethyl-2,3-dihydro-1H- inden-4-yl)propanal (B) + 3-(1,1-dimethyl-2,3- dihydro-1H-inden-5-yl)propanal (C) ISOCYCLOCITRAI 3,5,6-TRIMETHYL-3-CYCLOHEXENE-1- CARBALDEHYDE (A) + 2,4,6-TRIMETHYL-3- CYCLOHEXENE-1-CARBALDEHYDE (B) ISOBUTYLQUINOLEINE 2-ISOBUTYLQUINOLINE ISOPROPYLQUINOLEINE 6(8)-ISOPROPYLQUINOLINE LILYFLORE? (+?)-2,5-DIMETHYL-2-INDANMETHANOL MELONAL (+?)-2,6-DIMETHYL-5-HEPTENAL MENTHONE (2RS,5SR)-5-methyl-2-(2-propanyl)cyclohexanone (A) + (2RS,5RS)-5-methyl-2-(2- propanyl)cyclohexanone (B) MUSCONE LAEVO (?)-(3R)-3-METHYL-1-CYCLOPENTADECANONE OXYCARYOPHYLLENE 4,12,12-TRIMETHYL-9-METHYLENE-5- OXATRICYCLO[8.2.0.0(4,6)]DODECANE ORIVOL 4-(1,1-DIMETHYLPROPYL)CYCLOHEXANOL PHENETHYLOL ORD 2-PHENYLETHANOL PLICATONE (1RS,2SR,5RS,7RS,8SR)-5- methyltricyclo[6.2.1.0~2,7~]undecan-4-one (A) + (1RS,2SR,5SR,7RS,8SR)-5- methyltricyclo[6.2.1.0~2,7~]undecan-4-one (B) ROSINOL CRYST (+?)-2,2,2-TRICHLORO-1-PHENYLETHYL ACETATE ETHYL SAFRASCENATE ETHYL 4,6,6-TRIMETHYL-1,3-CYCLOHEXADIENE-1- CARBOXYLATE SALVIAC (+?)-(6RS,10RS)-2,2,8,10- tetramethylspiro[5.5]undec-8-en-1-one (A) + (+?)- (6RS,10SR)-2,2,8,10-tetramethylspiro[5.5]undec-8- en-1-one (B) + (6RS,7RS)-2,2,7,9- tetramethylspiro[5.5]undec-8-en-1-one (C) + (6RS,7SR)-2,2,7,9-tetramethylspiro[5.5]undec-8- en-1-one (D) SPIRANOL (5RS,6RS)-2,6,10,10-TETRAMETHYL-1- OXASPIRO[4.5]DECAN-6-OL TANGERINAL (4Z)-4-dodecenal TERRANOL 2,2,7,7-tetramethyltricyclo[6.2.1.0~1,6~]undecan- 6-ol TRIMOFIX 1-(2,6,10-TRIMETHYL)-1-(2,5,9- CYCLODODECATRIEN-1-YL)-1-ETHANONE + 1- (2,6,10-TRIMETHYL)-1-(1,5,9- CYCLODODECATRIEN-1-YL)-1-ETHANONE + 1- (6,10-DIMETHYL, 2-METHYLENE)-1-(2,5,9- CYCLODODECATRIEN-1-YL)-1-ETHANONE WOLFWOOD (+)-(1S,2S,3S,5R)-2,6,6- trimethylspiro[bicyclo[3.1.1]heptane-3,1- cyclohexane]-2-en-4-one 3-PHENYL-1-PROPANOL 3-PHENYL-1-PROPANOL MUGUET ALCOHOL 2,2-DIMETHYL-3-PHENYL-1-PROPANOL CEDRENOL (+?)-3,6,8,8-tetramethyloctahydro-1H-3a,7- methanoazulen-6-ol CEDROXYDE (+?)-(4Z,8E)-1,5,8-trimethyl-13- oxabicyclo[10.1.0]trideca-4,8-diene (A) + (+?)- (4Z,8E)-1,4,8-trimethyl-13- oxabicyclo[10.1.0]trideca-4,8-diene (B) GEONOL (+?)-PERHYDRO-4alpha,8Abeta-DIMETHYL-4A- NAPHTHALENOL HYACINTHOLANE (+?)-2,2-dimethyl-4-phenyl-1,3-dioxolane MAGNOLAN (+?)-2,4-dimethyl-4,4a,5,9b-tetrahydroindeno[1,2- d][1,3]dioxine (ISOMER A) + (+?)-2,4-dimethyl- 4,4a,5,9b-tetrahydroindeno[1,2-d][1,3]dioxine (ISOMER B) (A + B) PATCHOULI ALCOHOL (?)-(3R,6S,8S)-2,2,6,8- tetramethyltricyclo[5.3.1.0~3,8~]undecan-3-ol PATCHOULI OIL PATCHOULI OIL PHENYLETHYL SALICYLATE 2-PHENYLETHYL 2-HYDROXYBENZOATE 4-TERT BUTYLPHENOL 4-TERT BUTYLPHENOL CYCLOHEXYL ACETATE (1RS,2RS)-2-(2-methyl-2-propanyl)cyclohexyl acetate (A) + (1RS,2SR)-2-(2-methyl-2- propanyl)cyclohexyl acetate (B) STYRALLYL ACETATE (+?)-1-PHENYLETHYL ACETATE 3,5,5-TRIETHYL-2,4,6-TRIMETHYL-2- (4RS,6SR)-3,5,5-triethyl-2,4,6-trimethyl-2- CYCLOHEXEN-1-ONE cyclohexen-1-one (A) + (4RS,6RS)-3,5,5-triethyl- 2,4,6-trimethyl-2-cyclohexen-1-one (B) CEDRENE EPOXYDE 8,9-epoxycedrane CYCLODODECANONE CYCLODODECANONE EXALTENONE (Z)-4-CYCLOPENTADECEN-1-ONE FLORHYDRAL (+?)-3-(3-ISOPROPYL-1-PHENYL)BUTANAL FLOROL (+?)-TETRAHYDRO-2-ISOBUTYL-4-METHYL-4(2H)- PYRANOL FRESKOMENTHE 2-(1-METHYLPROPYL)-1-CYCLOHEXANONE MARITIMA 4-(4,8-DIMETHYL-3,7-NONADIEN-1-YL)PYRIDINE MAYOL [cis-4-(2-propanyl)cyclohexyl]methanol MUSCENONE DEXTRO (+)-(3R,5Z)-3-methyl-5-cyclopentadecen-1-one MUSCONE (+?)-3-methylcyclopentadecanone NOOTKETONE (+)-(4R,4aS,6R)-4,4a-dimethyl-6-(1-propen-2-yl)- 4,4a,5,6,7,8-hexahydro-2(3H)-naphthalenone PALISANDIN METHOXYCYCLODODECANE PARA TERT BUTYLCYCLOHEXANONE 4-(2-methyl-2-propanyl)cyclohexanone PINOACETALDEHYDE 3-(6,6-DIMETHYL-BICYCLO[3.1.1]HEPT-2-EN-2- YL)PROPANAL PRODUCT AC cedran-8-yl acetate RHUBOFURAN (+?)-2,4-dimethyl-4-phenyltetrahydrofuran SAFRALEINE (+?)-2,3,3-TRIMETHYL-1-INDANONE TERT-BUTYLPHENOL, 2- 2-TERT-BUTYLPHENOL TRANSLUZONE 7-(2-methyl-2-propanyl)-2H-1,5-benzodioxepin- 3(4H)-one TRICYCLONE (+)-(1R,7R)-10,10-DIMETHYL- TRICYCLO[7.1.1.0(2,7)]UNDEC-2-EN-4-ONE VERDONE (+?)-2-TERT-BUTYL-1-CYCLOHEXANONE Z 11 CRUDE DIST (1S,4S,9S,10R,13R)-5,5,9,13-tetramethyl-14,16- dioxatetracyclo[11.2.1.0~1,10~.0-4,9~]hexadecane (A) + (1R,4S,9S,10R,13S)-5,5,9,13-tetramethyl- 14,16- dioxatetracyclo[11.2.1.0~1,10~.0~4,9]hexadecane (B) (+?)-(4E,8E)-13-oxabicyclo[10.1.0]trideca-4,8-diene (A) + (+?)-(4E,8Z)-13-oxabicyclo[10.1.0]trideca-4,8- diene (B) + (+?)-(4Z,8E)-13- oxabicyclo[10.1.0]trideca-4,8-diene (C) MESO-(1R,2S,4R)-4-METHYL- TRICYCLO[5.2.1.0(2,6)]DECANE-4-METHANOL (+?)-3-(3-METHYL-5-INDANYL)PROPANAL (A) + (+?)- 3-(1-METHYL-5-INDANYL)PROPANAL (B) 2-METHYL-2-INDANMETHANOL (+?)-5-ETHYL-2-METHYL-2-INDANMETHANOL (+?)-5-ISOPROPYL-2-METHYL-2-INDANMETHANOL (2-METHYL-2-INDANYL)METHYL ACETATE (+?)-5-METHYL-2-INDANMETHANOL (+?)-(2,5-DIMETHYL-2-INDANYL)METHYL ACETATE 1-(2,5-DIMETHYL-2-INDANYL)-1-ETHANONE 1-(2,5-DIMETHYL-2-INDANYL)-1-ETHANOL 2-(2,5-DIMETHYL-2-INDANYL)-2-PROPANOL 2-METHOXYMETHYL-2,5-DIMETHYLINDAN (+?)-PERHYDRO-2,5-DIMETHYL-CIS-2- INDENEMETHANOL (+?)-2-ETHYL-5-METHYL-2-INDANMETHANOL 2,5,6-TRIMETHYL-2-INDANMETHANOL (+?)-2,4-DIMETHYL-2-INDANMETHANOL (+?)-1,2,5-TRIMETHYL-2-INDANMETHANOL (+?)-1,2,6-TRIMETHYL-2-INDANMETHANOL (+?)-(2,4,5-trimethyl-2,3-dihydro-1H-inden-2- yl)methanol (+?)-2,3,4,5,6,7-HEXAHYDRO-2,5-DIMETHYL-2(1H)- INDENEMETHANOL (+?)-5-TERT-BUTYL-2-METHYL-2-INDANMETHANOL (+?)-(2,7-dimethyl-1,2,3,4-tetrahydro-2- napththalenyl)methanol (+?)-(2,6-dimethyl-1,2,3,4-tetrahydro-2- naphthalenyl)methanol (+?)-(5-METHOXY-2-METHYL-2,3-DIHYDRO-1H- INDEN-2-YL)METHANOL 2,4,6-TRIMETHYL-2-INDANMETHANOL (+?)-3-(3-ETHYL-2,3-DIHYDRO-1H-INDEN-4- YL)PROPANAL (A) AND/OR (+?)-3-(3-ETHYL-2,3- DIHYDRO-1H-INDEN-5-YL)PROPANAL (B) AND/OR (+?)-3-(1-ETHYL-2,3-DIHYDRO-1H-INDEN-5- YL)PROPANAL (C) AND/OR (+?)-3-(1-ETHYL-2,3- DIHYDRO-1H-INDEN-4-YL)PROPANAL (D) (4aRS,9bRS)-4a,8-dimethyl-4,4a,5,9b- tetrahydroindeno[1,2-d][1,3]dioxin (+?)-2-((methoxymethoxy)methyl)-2,5-dimethyl- 2,3-dihydro-1H-indene (?)-(R)-2,5-DIMETHYL-2-INDANMETHANOL (4aRS,8aSR)-5,5,8a-trimethyloctahydro-2(1H)- naphthalenone
TABLE-US-00002 TABLE 2 Functional perfuming ingredients - Group II Common Name Chemical Name METHYLCINNAMIC ALDEHYDE (2E)-2-methyl-3-phenyl-2-propenal CITRAL (E)-3,7-DIMETHYL-2,6-OCTADIENAL (A) + (Z)-3,7- DIMETHYL-2,6-OCTADIENAL (B) DAMASCONE ALPHA (+?)-(2E)-1-(2,6,6-trimethyl-2-cyclohexen-1-yl)-2- buten-1-one DAMASCONE BETA (2E)-1-(2,6,6-trimethyl-1-cyclohexen-1-yl)-2- buten-1-one DELTA DAMASCONE (2E)-1-[(1RS,2SR)-2,6,6-trimethyl-3-cyclohexen-1- yl]-2-buten-1-one GALIONE (+?)-(E)-3-METHYL-4-(2,6,6-TRIMETHYL-2- CYCLOHEXEN-1-YL)-3-BUTEN-2-ONE (A) + (E)-1- (2,6,6-TRIMETHYL-2-CYCLOHEXEN-1-YL)-1- PENTEN-3-ONE (B) + (+?)-(E)-1-(2,2-DIMETHYL-6- METHYLENE-1-CYCLOHEXYL)-1-PENTEN-3-ONE (C) + (E)-1-(2,6,6-TRIMETHYL-1-CYCLOHEXEN-1-YL)-1- PENTEN-3-ONE (D) GAMMA DAMASCONE (+?)-(E)-1-(2,2-DIMETHYL-6-METHYLENE-1- CYCLOHEXYL)-2-BUTEN-1-ONE IRONE ALPHA (+?)-(E)-TRANS-alpha-IRONE (A) + (+?)-(E)-CIS- alpha-IRONE (B) + (+?)-(E)-beta-IRONE (C) IRONE BETA (+?)-(E)-4-(2,5,6,6-TETRAMETHYL-1-CYCLOHEXEN- 1-YL)-3-BUTEN-2-ONE ISORALDEINE 70 P (+?)-(3E)-3-methyl-4-(2,6,6-trimethyl-2- cyclohexen-1-yl)-3-buten-2-one (A) + (+?)-(1E)-1- (2,6,6-trimethyl-2-cyclohexen-1-yl)-1-penten-3- one (B) METHYLIONONE BETA (1E)-1-(2,6,6-trimethyl-1-cyclohexen-1-yl)-1- penten-3-one METHYLIONONE GAMMA (+?)-(E)-3-METHYL-4-(2,6,6-TRIMETHYL-2- CYCLOHEXEN-1-YL)-3-BUTEN-2-ONE ORIVONE 4-(1,1-DIMETHYLPROPYL)-1-CYCLOHEXANONE PELARGODIENAL (2E,6Z)-2,6-NONADIENAL VIOLETTE AT (+?)-(3E)-4-(2,6,6-trimethyl-2-cyclohexen-1-yl)-3- buten-2-one (A) + (3E)-4-(2,6,6-trimethyl-1- cyclohexen-1-yl)-3-buten-2-one (B); VIOLETTE AI (+?)-(3E)-4-(2,6,6-trimethyl-2-cyclohexen-1-yl)-3- buten-2-one VIOLETTE BC (3E)-4-(2,6,6-trimethyl-1-cyclohexen-1-yl)-3- buten-2-one ALDEHYDE C11 UNDECYLIC undecanal CINNAMIC ALDEHYDE (E)-3-PHENYL-2-PROPENAL ALDEHYDE SUPRA ALPINOLIDE (1S,1R)-2-[1-(3,3-DIMETHYL-1- CYCLOHEXYL)ETHOXY]-2-METHYLPROPYL 2- PROPENOATE ETHYL BUTYRATE ETHYL BUTANOATE CALONE 7-methyl-2H-1,5-benzodioxepin-3(4H)-one CARYOPHYLLENE (?)-(1R,9S)-4,11,11-trimethyl-8- methylenebicyclo[7.2.0]undec-4-ene CEDARWOOD OIL VIRGINIA CEDARWOOD OIL VIRGINIA CETOCEDRENE 4,7,11,11-TETRAMETHYL- TRICYCLO[5.4.0.0(1,3)]UNDECAN-5-ONE (A) + 2,6,6,8-TETRAMETHYL- TRICYCLO[5.3.1.0(1,5)]UNDECAN-9-ONE (B) CITRONELLOL BJ (+?)-3,7-DIMETHYL-6-OCTEN-1-OL CITRONELLYL NITRILE (?)-(R)-3,7-DIMETHYL-6-OCTENENITRILE COUMARINE 2-CHROMENONE DODECENAL (2E)-2-dodecenal FIRASCONE methyl (1RS,2SR)-2,6,6-trimethyl-3-cyclohexene- 1-carboxylate (A) + methyl (1RS,2RS)-2,6,6- trimethyl-3-cyclohexene-1-carboxylate (B) LEMONILE 3,7-DIMETHYL-2,6-NONADIENENITRILE (A) + 3,7- DIMETHYL-3,6-NONADIENENITRILE (B) LILIAL (+?)-2-methyl-3-[4-(2-methyl-2- propanyl)phenyl]propanal LIMBANOL (+?)-1-(2,2,3,6-TETRAMETHYL-CYCLOHEXYL)-3- HEXANOL LIMINAL (+)-(3S)-3-[(1R)-4-methyl-3-cyclohexen-1- yl]butanal (A) + (+)-(3R)-3-[(1R)-4-methyl-3- cyclohexen-1-yl]butanal METHYLCITRAL 3,6,7-TRIMETHYL-2,6-OCTADIENAL PAMPLEWOOD (+?)-3ENDO-METHOXY-7,7-DIMETHYL-10- METHYLENE-BICYCLO[4.3.1]DECANE (A) + (+?)- 3EXO-METHOXY-7,7-DIMETHYL-10-METHYLENE- BICYCLO[4.3.1]DECANE (B) TILLENAL 3-(4,4-dimethyl-1-cyclohexen-1-yl)propanal UNIPINE 85 Alpha.-Terpineol + .Gamma.-Terpineol Mixture with other terpenes VERTOXIME 2-METHYL-3-HEXANONE OXIME VIONIL 10 DIPG (2Z,6Z)-2,6-nonadienenitrile (A) + (2E,6Z)-2,6- nonadienenitrile (B) ZESTOVER (1RS,2RS)-2,4-dimethyl-3-cyclohexene-1- carbaldehyde (A) + (1RS,2SR)-2,4-dimethyl-3- cyclohexene-1-carbaldehyde (B) ALDEHYDE C10 DECANAL ALDEHYDE C12 DODECANAL ALDEHYDE C8 OCTANAL ALDEHYDE C9 NONANAL HEXYLCINNAMIC ALDEHYDE (2E)-2-benzylideneoctanal BASE XI (+?)-5-heptyldihydro-2(3H)-furanone BERGAMOT BERGAMOT ABERGAPT BERGAMOT FUROCOUMARIN-FREE FIRWOOD (+?)-(1-ethoxyethoxy)cyclododecane LAVANDIN GROSSO ARR LAVANDIN GROSSO SYNTH METHYLOCTYNE CARBONATE (OCM) METHYL 2-NONYNOATE METHYLPARACRESOL 1-METHOXY-4-METHYLBENZENE TERPINOLENE 1-methyl-4-(2-propanylidene)cyclohexene UNDECAVERTOL (+?)-(E)-4-METHYL-3-DECEN-5-OL VIOLETTYNE 10 MIP 1,3-UNDECADIEN-5-YNE YLANG YLANG EXTRA
Group I:
[0079] Ingredient(s) from Table 1 are comprised between 2 and 85 wt % of the composition used according to the present disclosure. According to one aspect, the composition used according to the present disclosure comprises a malodour antagonist system as defined above in an amount comprised between 6 and 70 wt %. According to another aspect, the composition used according to the present disclosure comprises a malodour antagonist system as defined above in an amount comprised between 8 and 60 wt %. According to another aspect, the composition used according to the present disclosure comprises a malodour antagonist system as defined above in an amount comprised between 8 and 46 wt %.
[0080] According to a particular aspect of the present disclosure the malodour receptor antagonist system (group I) from the composition used according to the present disclosure comprises at least 3 ingredients selected from Table 1. According to another aspect, at least 4, alternatively, at least 5, alternatively, at least 6, or alternatively, at least 8 ingredients selected from Table 1 are part of the malodour receptor antagonist system.
Group II:
[0081] Group II in the present disclosure is a functional perfume accord as defined above. It is present in amounts ranging from 15 to 98 wt % of the composition used according to the present disclosure. According to one aspect, it is present in amounts ranging from 30-94 wt %. According to another aspect, it is present in amounts ranging from 40-92 wt % of the composition. According to another aspect, it is present in amounts ranging from 29-92 wt % of the composition.
[0082] According to a particular aspect, group II consists of ingredients selected from the group consisting of ionones, irones, damascones, citral, citronellol BJ, citronellyl nitrile, lemonile, methylcitral, cinnamic aldehyde, methylcinnamic aldehyde, hexylcinnamic aldehyde, pelargodienal, aldehyde C11 undecylic, aldehyde supra, dodecanal, aldehyde C8, aldehyde C9, aldehyde C12, orivone and mixtures thereof.
[0083] According to a particular aspect, group II consists of ingredients from the group of Table 2.
[0084] According to a particular aspect, group II consists of selected from the group consisting of ionones, irones, damascones, citral, methylcinnamic aldehyde, pelargodienal, orivone, derivatives and mixtures thereof.
[0085] In some aspects, ionones, irones, damascones include damascone alpha, damascone beta, delta damascone, firascone, galione, gamma damascone, irone alpha, irone beta, isoraldeine 70 P, methyionone beta, methylionone gamma Coeur IFF, violet AI, violet AT, and violet BC.
[0086] In some aspects, methylcinnamic aldehyde includes alkyl derivatives, including cinnamic aldehyde, methylcinnamic aldehyde, hexythylcinnamic aldehyde. In some aspects, methylcinnamic aldehyde includes alkyl derivatrives, including cinnamic aldehyde, methylcinnamic aldehyde, hexythylcinnamic aldehyde.
Group III:
[0087] According to a particular aspect, the composition used according to the present disclosure comprise a nonfunctional perfume accord as defined above. The nonfunctional perfume accord consists of perfuming ingredients as defined above which are neither part of group II nor part of group I. If present in the composition according to the present disclosure, a non-functional perfume accord can typically be comprised in amounts ranging from 0.5 to 70 wt %, alternatively, from 0.5 to 50 wt % of the composition as defined in any of the above aspects.
Group IV: delivery system
[0088] According to a particular aspect, compositions as defined above can be used in combination with a delivery system. The use of a delivery system allows achieving optimal gas-phase concentrations of active ingredients in the composition. Suitable delivery systems for the purpose of the present disclosure include but are not limited to: [0089] Passive plating supports comprising one or more of the following porous or non-porous substrates in loose powder or compacted form chosen from the following non-limiting examples: cellulose (paper/cardboard), vermiculite, other industrial absorbents, perlite, calcium carbonate, pumice, other minerals, wood, sawdust, ground corn cob, ground rice hull, rice hull ash, other agricultural by-products, biochars, starches, modified starches; [0090] Spray-dried moisture-activated encapsulation systems wherein compositions according to the present disclosure are encapsulated by a spray drying process within a matrix containing but not limited to one or more of the following: maltodextrin, octenyl succinated starch (modified starch); [0091] Core-shell encapsulation systems, such as mechanically activated microcapsules with an impermeable shell (for example, polyurea, polyurethane, and others) and composition according to the present disclosure in the core; [0092] Liquid mixtures containing surfactants; [0093] Polymeric materials.
[0094] Use of a composition as defined in any of the above aspects, wherein the composition further comprises encapsulating materials such as polymers to form microcapsules or microparticles, or materials to form liquid delivery system for the composition such as an emulsion, a microemulsion, a miniemulsion, a gel, a microgel, an anhydrous gel or a dispersion is therefore also an object of the present disclosure.
[0095] According to a particular aspect, the composition as defined in any of the above aspects is absorbed on a porous or non-porous substrate in loose powder or compacted form, the substrate being selected from cellulose (paper/cardboard), vermiculite, other industrial absorbents, perlite, calcium carbonate, pumice, wood, sawdust, ground corn cob, ground rice hull, rice hull ash, biochars, starches, modified starches and mixtures thereof.
[0096] A second object of the present disclosure consists of a malodour receptor antagonist system consisting of at least 3, alternatively, at least 4 ingredients selected from the group of Table 1.
[0097] Another object of the present disclosure is a malodour counteracting composition comprising:
[0098] a) from about 2 to about 85 wt % of an active amount a malodour receptor antagonist system comprising at least one, alternatively, at least 3 ingredients selected from Table 1; [0099] b) from about 15 to about 98 wt % of a functional perfume accord comprising at least two ingredients selected from the group consisting of ingredients selected from Table 2; and [0100] c) optionally a non-functional perfume accord comprising at least two perfuming ingredients.
[0101] According to a particular aspect, the composition comprises from about 6 to about 70 wt % of group I. According to another aspect, the composition comprises from about 8 to about 60 wt % of group I.
[0102] According to a particular aspect, the malodour receptor antagonist system comprises (2,5-dimethyl-2,3-dihydro-1H-inden-2-yl)methanol (LILYFLORE?), in an amount of at least 2 wt %, alternatively, at least 3 wt % of the composition.
[0103] Without intending to be limited to any particular theory, combinations of ingredients within the malodour receptor antagonist system may exhibit a synergistic reduction or elimination of the perception of fecal malodour. Examples of such malodour counteracting compositions are shown in Example 16 below. Accordingly, in some aspects, the malodour receptor antagonist system comprises (2,5-dimethyl-2,3-dihydro-1H-inden-2-yl)methanol (LILYFLORE?), and the functional perfume accord comprises isoraldeine (alpha-methylionone and isomethyl-alpha-ionone) and ?-ionone (also referred to as Violet AT). Alternatively, the functional perfume accord further comprises citral.
[0104] Alternatively, in some aspects, the malodour receptor antagonist system comprises (2,5-dimethyl-2,3-dihydro-1H-inden-2-yl)methanol (LILYFLORE?) and (+?)-3,7-dimethyl-1-octen-3-ol (dihydrolinalol), and the functional perfume accord comprises isoraldeine (alpha-methylionone and isomethyl-alpha-ionone), and ?-ionone (also referred to as Violet AT).
[0105] The present disclosure's composition may be used in any consumer product for which it may be useful to have an MOC activity at least. Consequently, another object of the present disclosure is represented by a MOC consumer product comprising, as an active ingredient, at least one composition according to the present disclosure, as defined above.
[0106] The composition can be added as such or as part of a MOC composition (including a delivery system) according to the aspects presented herein.
[0107] It is understood that the MOC consumer product, by its nature can also be a perfuming one.
[0108] For the sake of clarity, it has to be mentioned that, by MOC, and optionally perfuming, consumer product or the similar, it is meant a consumer product which is expected to deliver at least a MOC effect, and optionally also a pleasant perfuming effect, to the surface to which it is applied (e.g. skin, hair, textile, or home surface, but also air). In other words, a consumer product according to the present disclosure is a perfumed consumer product which comprises the functional formulation, as well as optionally additional benefit agents, corresponding to the desired consumer product, e.g. a detergent or an air freshener, and an effective amount of at least one compound or composition from the present disclosure. For the sake of clarity, the consumer product is a non-edible product.
[0109] The nature and type of the constituents of the MOC consumer product do not warrant a more detailed description here, which in any case would not be exhaustive, the skilled person being able to select them on the basis of his general knowledge and according to the nature and the desired effect of the product.
[0110] Non-limiting examples of suitable perfuming consumer product can be: [0111] a fabric care product, such as a liquid detergent, a powder detergent, detergent tablets, a detergent bar, a detergent paste, a liquid fabric softener, fabric softener sheets, a fabric scent booster, a laundry pre-treatment, a fabric refresher, an ironing water, a laundry bleach, a carpet powder or a carpet cleaner; the uses for this type of product would be particularly beneficial in the cases where standard water available to the consumers could be associated with malodour as described (e.g. putrid waters); [0112] a toilet paper or napkin; [0113] an air freshening product, such as an air freshener spray, a gel air freshener, a liquid-wick air freshener, a solid air freshener comprising a porous substrate (such as a paper or card blotter, a porous ceramic, or a porous plastic), a liquid or gel air freshener comprising a permeable membrane, an electrically operated air freshener, and a dual purpose air freshener/disinfectant spray; and/or [0114] a surface care product, such as an all-purpose cleaner, a furniture polish, a wood floor cleaner, a toilet care product (such as a toilet bowl cleaning liquid, an in-cistern toilet cleaner, a toilet rim block, or a toilet rim liquid); a pet-litter. Some of the above-mentioned MOC consumer products may represent an aggressive medium for the a compound according to some aspects of the present disclosure, so that it may be necessary to protect the latter from premature decomposition, for example by encapsulation or by chemically bounding it to another chemical which is suitable to release the ingredient upon a suitable external stimulus, such as an enzyme, light, heat or a change of pH.
[0115] It should be appreciated by those skilled in the art that the conception and the specific aspects disclosed might be readily utilized as a basis for modifying or formulating other formulations for carrying the same purposes of the present disclosure. It should also be realized by those skilled in the art that such equivalent formulations do not depart from the spirit and scope of the disclosure as set forth in the appended claims.
[0116] The proportions in which the compound according to the present disclosure can be incorporated into the various aforementioned products or compositions vary within a wide range of values. These values are dependent on the nature of MOC consume product and on the desired organoleptic effect as well as the nature of the co-ingredients in a given composition when the compounds according to the present disclosure are mixed with other ingredients, solvents or additives commonly used in the art.
[0117] For example, in the case of perfuming compositions, typical concentrations are in the order of 0.01% to 60%, or even 1% to 10%, by weight, or even more, of the composition of the present disclosure based on the weight of the composition into which they are incorporated. Concentrations lower than these, such as in the order of 0.01% to 2% by weight, can be used when these compounds are incorporated into MOC consumer products, percentage being relative to the weight of the consumer product.
[0118] In particular, the concentration of MOC compound according to the present disclosure used in the various aforementioned consumer products varies within a various wide range of values depending on the nature of the consumer product.
[0119] A non-therapeutic method for counteracting fecal malodour, the method comprising treating a surface or dispensing at least partly in the air a composition as defined in any of the above-aspects is also an object of the present disclosure.
EXAMPLES
[0120] The present disclosure will now be described in further detail by way of the following examples, wherein the abbreviations have the usual meaning in the art and the temperatures are indicated in degrees centigrade (? C.).
Example 1
Antagonist IdentificationIdentification of Malodour Receptor Antagonists Through an Ex Vivo Live Neuron Assay
[0121] In the ex vivo live neuron assay, olfactory sensory neurons (OSNs) are extracted from the olfactory epithelium of mice and can be tested for responses to sequentially delivered stimuli, where responses are detected through live-cell calcium-imaging microscopy. At least 1000 and approximately 5000-10000 OSNs were tested for every compound listed in table 1. It has been established through prior research in the field that the vast majority of extracted OSNs express 1 out of the approximately 1200 odourant receptors (ORs) present in the genome of a mouse, such that in our samples of extracted OSNs, the majority of the 1200 ORs should have been represented in at least one OSN. Since the responses of the OSNs to the delivered stimuli are entirely driven by the expressed OR, the OSNs selectively detect and collectively encode the identity and intensity of odourants. By stimulating the OSNs with MO molecules and measuring the response of each OSN, the subset in which a response is induced is those that detect and therefore presumably encode the MO. By subsequently delivering a mixture of MO and a candidate antagonist to the same cells, the degree of suppression of signal in each MO-responsive OSN can be determined (level of inhibition). The degree of inhibition in each cell was binned into one of three groups: low inhibition (10-25%), medium inhibition (25-75%) and strong inhibition (75-100%). In addition, the proportion of MO-responsive OSNs displaying low, medium and high inhibition was calculated. Examples of these data are shown in figures la-d. Compounds that inhibited greater than a minimum proportion of OSNs at a minimum strength were considered antagonist hits and putative malodour suppressing compounds. The minimum levels were, respectively, 10% of the population showing strong inhibition and/or 25% of the population showing medium inhibition and/or 40% of the population showing weak inhibition.
[0122] The genetic similarity between mouse and human receptors, due to their shared evolutionary history and presumably similar natural odour environments over evolutionary time-scales leads us to suppose that overall observations on MO-responsive populations of mouse ORs should positively correlate with what would be obtained from human ORs, even if individual orthologous receptors (i.e. those believed to share a common ancestor and typically the most similar in genetic sequence) may show varying levels of functional similarity to those from mouse.
[0123]
Example 2
Sensory Measurement of Residual Fecal Odour Score for Individual Malodour Receptor Antagonist System, Individual Functional Perfuming Ingredients and for Compositions According to the Present Disclosure.
[0124] Malodour receptor antagonist system and compositions were submitted at a unique gas phase concentration of 3.4 ?g/l air.
[0125] The sensory method to evaluate compositions requires the use of Firmenich designed air dilution olfactometers to achieve well controlled and stable gas phase concentrations of the compositions and of the malodour to a group of subjects.
[0126] The 30 subjects had to evaluate first the fecal reconstitution* alone and then rate the 3 attributes Freshness, Pleasantness and Fecal (the malodour character) on a 0 to 10 scale. The next evaluation occurred 30 seconds later to avoid odour adaptation; the fecal malodour reconstitution was injected together with the tested composition in an olfactometer. Ratings for the same descriptors were recorded. *The model malodour is a fecal reconstitution made of indole, methyl mercaptan, p-cresol and butyric acid. The gas phase concentration of the fecal malodour reconstitution and of its ingredients corresponds to the headspace analytical results from a toilet gas phase sampling (Charles J F Chappuis, Yvan Niclass, Christine Vuilleumier, and Christian Starkenmann Quantitative Headspace Analysis of Selected Odourants from Latrines in Africa and India Environ. Sci. Technol. 2015, 49, 6134-6140)
[0127] The results are expressed as the averaged rates for the three descriptors for the fecal reconstitution alone and the fecal reconstitution combined to the tested composition.
[0128]
[0129] It can be seen that a valuable depression of the perception of the fecal reconstitution (residual fecal odour <50%) can be obtained when submitting at the same concentration: [0130] Independently a malodour antagonist system, in particular (2,5-dimethyl-2,3-dihydro-1H-inden-2-yl)methanol (LILYFLORE?), and single ingredients of a functional perfume accord (Violet AT or isoraldeine), OR [0131] Combining the malodour antagonist system consisting of 2,5-dimethyl-2,3-dihydro-1H-inden-2-yl)methanol (LILYFLORE?) with the functional perfume accord (under mixture) OR [0132] Adding a malodour antagonist system with increasing numbers of antagonists from Table 1 to a composition comprising a functional and non-functional perfume accords.
[0133] Alias is a floral composition designed without including antagonists from Table 1 and including perfumery ingredients well known to those skilled in the art; however, it has a limited effect on the fecal reconstitution. The fecal score left when combining this composition to the fecal reconstitution is >50%. This demonstrates that the malodour reduction effects are due to the antagonists are specific and not due to simple masking by perfumery ingredients.
Example 3
Sensory Performance of Compositions According to the Present Disclosure.
[0134] The capability of a mixture of a composition according to the present disclosure consisting of [0135] LILYFLORE? ((2,5-dimethyl-2,3-dihydro-1H-inden-2-yl)methanol) as malodour antagonist system [0136] Isoraldeine and Violet AT (?-ionone) as functional perfume accord to suppress a fecal model malodour* is significantly increased (70%) compared to the capability of each ingredient alone (max 58%) at its dosage in the mixture.
Illustration:
[0137]
[0138] Blind sensory evaluations were organized; no information was disclosed to the 31 participants on the randomized submitted odourous stimuli. The test was duplicated and the observations accumulated.
Example 4
Compositions According to the Present Disclosure
[0139] Following tables represent compositions according to the present disclosure.
TABLE-US-00003 TABLE 3 Composition Floral E Ingredients Parts 1000 ALDEHYDE C11 15 FPI(functional Perfume Ing) UNDECYLIC CITRONELLOL BJ 200 FPI(functional Perfume Ing) HEXYLCINNAMIC 150 FPI(functional Perfume Ing) ALDEHYDE ISORALDEINE 70 P 70 FPI(functional Perfume Ing) LILIAL 120 FPI(functional Perfume Ing) LILYFLORE? 100 Antagonist System PHENYLETHYL ACETATE 240 Antagonist System VIOLET AT 80 FPI(functional Perfume Ing) ZESTOVER 25 FPI(functional Perfume Ing)
TABLE-US-00004 TABLE 4 Composition Floral P Ingredients Parts 1000 Composition ALDEHYDE C11 15 FPI(functional Perfume Ing) UNDECYLIC CITRONELLOL BJ 180 FPI(functional Perfume Ing) DAMASCONE ALPHA 20 FPI(functional Perfume Ing) DELPHONE 20 Antagonist System HEXYLCINNAMIC 120 FPI(functional Perfume Ing) ALDEHYDE ISORALDEINE 70 P 70 FPI(functional Perfume Ing) LILIAL 120 FPI(functional Perfume Ing) LILYFLORE? 100 Antagonist System PHENYLETHYL ACETATE 200 Antagonist System ROSINOL CRYST 50 Antagonist System VIOLET AT 80 FPI(functional Perfume Ing) ZESTOVER 25 FPI(functional Perfume Ing)
TABLE-US-00005 TABLE 5 Composition Floral RD Ingredients Parts 1000 Composition ALDEHYDE C11 15 FPI(functional Perfume Ing) UNDECYLIC CITRONELLOL BJ 180 FPI(functional Perfume Ing) DAMASCONE ALPHA 20 FPI(functional Perfume Ing) DELPHONE 20 Antagonist System DIHYDROLINALOL 130 Antagonist System HEXYLCINNAMIC 120 FPI(functional Perfume Ing) ALDEHYDE ISORALDEINE 70 P 90 FPI(functional Perfume Ing) LILYFLORE? 40 Antagonist System PHENYLETHYL ALCOHOL 220 Antagonist System ROSINOL CRYST 50 Antagonist System VIOLET AT 90 FPI(functional Perfume Ing) ZESTOVER 25 FPI(functional Perfume Ing)
TABLE-US-00006 TABLE 6 Composition Citrus B Parts Ingredients 1000 ALDEHYDE C8 30 FPI(functional Perfume Ing) ALDEHYDE C9 30 FPI(functional Perfume Ing) ALDEHYDE C10 50 FPI(functional Perfume Ing) ALDEHYDE C11 UNDECYLIC 10 FPI(functional Perfume Ing) CITRAL 170 FPI(functional Perfume Ing) CITRONELLOL BJ 80 FPI(functional Perfume Ing) CITRONELLYL NITRILE 120 FPI(functional Perfume Ing) ISORALDEINE 100 FPI(functional Perfume Ing) LILYFLORE? 80 Antagonist System TERPINOLENE 190 FPI(functional Perfume Ing VIOLET AT 100 FPI(functional Perfume Ing ZESTOVER 40 FPI(functional Perfume Ing
TABLE-US-00007 TABLE 7 Composition Citrus H Parts Ingredients 1000 ALDEHYDE C8 35 FPI(functional Perfume Ing) ALDEHYDE C9 30 FPI(functional Perfume Ing) ALDEHYDE C10 55 FPI(functional Perfume Ing) ALLYL AMYL GLYCOLATE 3 Antagonist System BHT (IONOL) 40 NFPI (non functional perfume I) CACHALOX? 2 Antagonist System CITRAL 170 FPI(functional Perfume Ing) CITRONELLAL CP 90 Antagonist System CITRONELLYL NITRILE 100 FPI(functional Perfume Ing) CYCLOSAL 90 Antagonist System DELTA DAMASCONE 15 FPI(functional Perfume Ing) DIHYDROLINALOL 100 Antagonist System ISORALDEINE 45 FPI(functional Perfume Ing) LILYFLORE? 40 Antagonist System TERPINOLENE 100 FPI(functional Perfume Ing) VIOLET AT 45 FPI(functional Perfume Ing) ZESTOVER 40 FPI(functional Perfume Ing)
TABLE-US-00008 TABLE 8 Composition Citrus 259389 B Parts Ingredients 1000 ALDEHYDE C8 35 FPI(functional Perfume Ing) ALDEHYDE C9 30 FPI(functional Perfume Ing) ALDEHYDE C10 55 FPI(functional Perfume Ing) ALLYL AMYL GLYCOLATE 3 Antagonist System BHT (IONOL) 40 NFPI (non functional perfume I) CACHALOX? 2 Antagonist System CITRAL 180 FPI(functional Perfume Ing) CITRONELLAL CP 100 Antagonist System CITRONELLYL NITRILE 100 FPI(functional Perfume Ing) CYCLOSAL 100 Antagonist System DELTA DAMASCONE 15 FPI(functional Perfume Ing) DIHYDROLINALOL 120 Antagonist System ISORALDEINE 45 FPI(functional Perfume Ing) LILYFLORE? 40 Antagonist System TERPINOLENE 100 FPI(functional Perfume Ing) VIOLET AT 45 FPI(functional Perfume Ing) ZESTOVER 40 FPI(functional Perfume Ing)
TABLE-US-00009 TABLE 9 Composition Jasmin E Parts Ingredients 1000 AMYL CINNAMIC 75 NFPI (non functional perfume I) ALDEHYDE BENZYL ACETATE 250 Antagonist System BENZYL PHENYLACETATE 60 NFPI (non functional perfume I) CIS JASMONE 30 NFPI (non functional perfume I) DECALACTONE CP 25 FPI(functional Perfume Ing) DIHYDROLINALOL 90 Antagonist System ETHYL 2 2 NFPI (non functional perfume I) METHYLBUTYRATE @ 10% DIPG ETHYL PRALINE 7 NFPI (non functional perfume I) EUGENOL 20 NFPI (non functional perfume I) ISOEUGENOL EXTRA 4 NFPI (non functional perfume I) NAT US ISORALDEINE 70P 100 FPI(functional Perfume Ing) LILYFLORE? 50 Antagonist System LINALYL ACETATE AR 55 NFPI (non functional perfume I) METHYL ANTHRANILATE 2 NFPI (non functional perfume I) DIST METHYL BENZOATE 3 FPI(functional Perfume Ing) PARATOLYL ALDEHYDE 8 NFPI (non functional perfume I) PHENYLACETALDEHYDE 4 NFPI (non functional perfume I) ROSINOL CRIST 50 Antagonist System VIOLET AT 150 FPI(functional Perfume Ing) ZESTOVER 15 FPI(functional Perfume Ing)
Example 5
Sensory Evaluation of Compositions According to the Present Disclosure.
[0140] The sensory method to evaluate compositions described under example 4 required the use of Firmenich designed air dilution olfactometers to achieve well controlled and stable gas phase concentrations of the compositions and of the malodour to a group of subjects.
[0141] The 30 subjects had to evaluate first the fecal reconstitution alone and then rate the same descriptors as expressed previously on a line scale. The next evaluation occurred 30 seconds later to avoid odour adaptation; the fecal malodour reconstitution was injected together with the tested composition in an olfactometer. Ratings for the same descriptors were recorded.
[0142] The results are expressed as the averaged rates for the three descriptors for the fecal reconstitution alone and the fecal reconstitution combined to the tested composition.
Illustration: The graphs (
[0147] The number and the % in weight of ingredients from Classes I (antagonist system), II (Functional perfume accord) and III (nonfunctional perfume accord) are indicated.
[0148] All these compositions are tested at 3 decreasing concentrations C1, C2 and C3.
[0149] The lower the fecal score, the more performing the antagonizing composition.
[0150] The dotted lines on the 3 graphs give the scores for the 3 attributes when evaluating the Floral RD, the Citrus H or the Jasmin E alone at C1 concentration (not combined to the fecal reconstitution). The three graphs indicate the minimum that may be expected for the Fecal score and the maximum scores for Freshness and Pleasantness.
[0151] The fecal score for Floral RD, Citrus H or Jasmin E evaluated alone at C1 concentration is not statistically different from the Fecal score of these compositions also tested at C1 concentration and combined to the fecal reconstitution (attested by Student's test, 99% confidence). [0152] The performance of the Floral and Citrus compositions improves when an antagonist system is added. From Floral E to Floral RD, the perception of the fecal malodour is increasingly reduced. A similar observation can be done for Citrus compositions with an increased performance of Citrus H versus Citrus B. [0153] The iterations gradually contain more ingredients in the antagonist system. [0154] The Jasmin composition also attests the interest in involving antagonist systems. [0155] The Floral RD, the Citrus H and the Jasmin E eliminate the fecal malodour perception.
Example 6
[0156]
TABLE-US-00010 TABLE 10 Floral V is a floral-type fragrance composition according to the present disclosure, as follows: Parts Ingredients 1000 Composition ALDEHYDE C 11 17 FPI(functional Perfume Ing) UNDECYLIC BHT (IONOL) 20 NFPI (non functional perfume I) CITRONELLOL BJ 190 FPI(functional Perfume Ing) DAMASCONE ALPHA 21 FPI(functional Perfume Ing) DELPHONE 21 Antagonist System DIYDROLINALOL 110 Antagonist System HEXYLCINNAMIC 100 FPI(functional Perfume Ing) ALDEHYDE ISORALDEINE 70 P 95 FPI(functional Perfume Ing) LILYFLORE? 40 Antagonist System PHENYLETHYL ALCOHOL 232 Antagonist System ROSINOL CRYST 52 Antagonist System VIOLET AT 94 FPI(functional Perfume Ing) ZESTOVER 8 FPI(functional Perfume Ing)
TABLE-US-00011 TABLE 11 Citrus B2 is a citrus-like fragrance composition according to the present disclosure, as follows: Parts Ingredients 1000 CITRAL 180 FPI(functional Perfume Ing) DIHYDROLINALOL 120 FPI(functional Perfume Ing) CITRONELLAL CP 100 FPI(functional Perfume Ing) CITRONELLYL NITRILE 100 Antagonist System CYCLOSAL 100 NFPI (non functional perfume I) ALDEHYDE C 10 55 Antagonist System TERPINOLENE 50 FPI(functional Perfume Ing) ISORALDEINE 70 P 45 Antagonist System VIOLET AT 45 FPI(functional Perfume Ing) BHT (IONOL) 40 Antagonist System LILYFLORE? 40 FPI(functional Perfume Ing) ZESTOVER 40 FPI(functional Perfume Ing) ALDEHYDE C 8 35 Antagonist System ALDEHYDE C 9 30 Antagonist System DELTA DAMASCONE 15 FPI(functional Perfume Ing) ALLYL AMYL 3 FPI(functional Perfume Ing) GLYCOLATE ? CACHALOX? 2 FPI(functional Perfume Ing)
TABLE-US-00012 TABLE 12 Jasmine E is a jasmine-like fragrance composition according to the present disclosure, as follows: Amount Ingredient (parts by weight) BENZYL ACETATE ? 1250 VIOLET AT ? 750 ISORALDEINE 70 P ? 500 DIHYDROLINALOL ? 450 AMYLCINNAMIC ALDEHYDE R 375 BENZYL PHENYLACETATE ? 300 LINALYL ACETATE AR 275 LILYFLORE? ? 250 ROSINOL CRYST ? 250 CIS JASMONE 150 DECALACTONE CP 125 EUGENOL F 100 ZESTOVER 75 PARATOLYL ALDEHYDE 40 ETHYL PRALINE 35 PHENYLACETALDEHYDE 20 ISOEUGENOL EXTRA NAT US 20 METHYL BENZOATE 15 METHYL ANTHRANILATE DIST 10 DIPROPYLENE GLYCOL 9 ETHYL 2 METHYLBUTYRATE 1
Example 7
Latrine Malodour Reduction Efficacy Test of A Cellulose-Based Air Freshener Comprising Fragrance Compositions According to the Present Disclosure.
[0157] The air freshener device used in this example was a cellulose air freshener-type. These air fresheners comprise of an absorbent material infused with a specified amount of fragrance. This material is then placed in a container to control the delivery of the fragrance composition. For this example, a cellulose pad is used as the absorbent material placed in an aluminum tin.
[0158] Test samples were prepared by applying 3 grams of fragrance compositions onto cellulose pads (2.5 in..sup.2) that were placed in round aluminum tins (3 in. diameter). The fragrance compositions used for this test were Floral V (Example 6), two samples of Citrus B2 (Example 6) and Jasmine E (Example 6).
[0159] A synthetic latrine malodour formulation was prepared as follows:
TABLE-US-00013 Ingredient w/w % Triacetin 99.755 Indole 0.1 Butyric Acid 0.009 P-Cresol 0.13 DMTS 0.006
[0160] A 70% by weight latrine malodour loaded vermiculite was prepared by admixing 350 g of the latrine malodour with 150 g of vermiculite (Fine grade, Specialty Vermiculite Corp, Enoree, S.C.).
[0161] The efficacy of the cellulose-based air fresheners comprising fragrance formulations according to the present disclosure was assessed following the practices described in ASTM E 1593-06 Method for Assessing the Efficacy of Air Care Products in Reducing Sensorialy Perceived Indoor Air Malodour Intensity. Six 72 ft.sup.3 evaluation cabins with smelling windows within their doors were used for the sensory evaluation of samples. Five cabins contained a 3 inch diameter aluminum tin with 9 grams of the latrine malodour loaded vermiculite; one cabin contained a 3 inch diameter aluminum tin with 9 grams of vermiculite (without malodour).
[0162] One of the cabins containing the malodour only (no test product) was identified as a reference; the other five cabins were labeled with randomly generated 3 digit codes. The cabins set-up was as follows:
TABLE-US-00014 Cabin Label Cabin Contents Reference Latrine malodour only 196 Latrine malodour + Jasmine E 274 Latrine malodour + Citrus B2 326 Latrine malodour only 487 Citrus B2 only 571 Latrine malodour + Floral V
[0163] The cabins were assessed by 21 untrained but experienced assessors. By untrained but experienced assessors we mean individuals who have not received formal olfactive training but who are used to participating in fragrances assessments and have experience in rating the odour attributes.
[0164] The environmental conditions in the cabins during the test were 72? F., 35% RH with 5 air changes per hour. A portable desk fan, set on low, was placed at the floor of the cabin to circulate the air within. All assessors were first instructed to smell the odour in the reference cabin, in order to familiarize themselves with the malodour. They were then instructed to smell the odour in the test cabins and rate the intensity of the malodour using a 1 to 7 category scale, where 1 indicates no perceivable malodour and 7 indicates very strong malodour. Presentation of the test cabins was blind, balanced, randomized, and sequential monadic. Assessors were directed to open the smelling window to evaluate each sample and wait for 60 seconds before proceeding to the next.
[0165] Data was analyzed using one-way analysis of variance (ANOVA), followed by Fisher's least significant difference (LSD) method for multiple comparisons (?=0.05). The number of assessors (N) and the LSD were as follows: N=21, LSD=0.60. Mean malodour intensity of the cabins is shown in on
[0166] The perceived malodour intensity of the Citrus B2 Only cabin (no malodour) is significantly lower than that of all other cabins. The perceived malodour intensity of the cabins containing malodour and fragrance compositions according to the present disclosure is significantly lower than that of the malodour only cabin; thus, cellulose air fresheners comprising fragrance compositions according to the present disclosure are useful in reducing the perception of latrine malodour.
[0167] Example 8
Latrine Malodour Reduction Efficacy Test of a Candle Comprising Fragrance Compositions According to the Present Disclosure.
[0168] The air freshener device used in this example was a candle; such devices deliver fragrance by two means. First, fragranced incorporated into the candle will evaporate slowly as it migrates through the wax and onto the surface of the candle. The second means, by far greater, is through the melt pool. The melt pool is generated while the candle is lit and the flame melts portions of the candle forming a pool at the top. The warm mixture delivers fragrance at a greater rate.
[0169] The fragrance compositions used for this test were Floral RD (Example 4), two samples of Citrus H (Example 4) and Jasmine E (Example 6). The fragranced candles were prepared by mixing the aforementioned fragrance compositions with the candle formula indicated in the table below. 100 grams of the wax mixture was then placed in a 3 in. tall, round, glass container with a 3 in. diameter and a wax-coated, felt wick (CD# 6, clipped to a 0.5 in. height). For the test sample containing malodour only, a candle without fragrance was prepared (Candle wax 4625A IGI at 88%).
TABLE-US-00015 Candle formulation Ingredient Level Candle wax 4625A IGI 82.5% Microwax 5715A IGI 2.0% Triple press Stearic acid 10.0% Fragrance 5.5% 100.0%
TABLE-US-00016 Control formulation Ingredient Level Candle wax 4625A IGI 88.5% Microwax 5715A IGI 2.0% Triple press Stearic acid 10.0% 100.0%
[0170] The malodour preparation and test procedure was the same as outlined in Example 6. The cabins were assessed by 15 untrained but experienced assessors. Data was analyzed using one-way analysis of variance (ANOVA), followed by Fisher's least significant difference (LSD) method for multiple comparisons (?=0.05). The number of assessors (N) and the LSD were as follows: N=15, LSD=0.70. Mean malodour intensity of the cabins is shown in
[0171] The perceived malodour intensity of the Jasmine E Only cabin (no malodour) is significantly lower than that of all other cabins. The perceived malodour intensity of the cabins containing malodour and fragrance compositions according to the present disclosure is significantly lower than that of the malodour only cabin; thus, candles comprising fragrance compositions according to the present disclosure are useful in reducing the perception of latrine malodour.
Example 9
Latrine Malodour Reduction Efficacy Test of Aerosol Air Fresheners Comprising Fragrance Compositions According to the Present Disclosure.
[0172] The air freshener device used in this example was an aerosol; such devices deliver fragrance into an environment by means of a pressurized aqueous fragranced solution.
[0173] The fragrance compositions used for this test were Floral V (Example 6), two samples of Citrus B2 (Example 6) and Jasmine E (Example 6). The fragranced aerosols were prepared by mixing fragrance compositions with the aerosol formula indicated in the table below.
TABLE-US-00017 Aerosol Formulation Ingredient Level Deionized Water 69.25% Sodium Borate 0.07% Sodium Molybdate 0.34% Span 80 0.25% Dipropylene Glycol 0.09% Fragrance 0.3% A-60 Propellant 29.7% 100.0%
[0174] The malodour preparation and test procedure was the same as outlined in Example 6. The cabins were assessed by 19 untrained but experienced assessors. Data was analyzed using one-way analysis of variance (ANOVA), followed by Fisher's least significant difference (LSD) method for multiple comparisons (?=0.05). The number of assessors (N) and the LSD were as follows: N=19, LSD=0.70. Mean malodour intensity of the cabins is shown in
[0175] The perceived malodour intensity of the Jasmine E Only cabin (no malodour) is significantly lower than that of all other cabins. The perceived malodour intensity of the cabins containing malodour and fragrance compositions according to the present disclosure is significantly lower than that of the malodour only cabin; thus, aerosol air fresheners comprising fragrance compositions according to the present disclosure are useful in reducing the perception of latrine malodour.
Example 10
Latrine Malodour Reduction Efficacy Test of Sachet-Type Air Fresheners Comprising Fragrance Compositions According to the Present Disclosure.
[0176] The air freshener device used in this example was a sachet-type air freshener; such devices utilize a particulate substrate, infused with fragrance contained in a permeable pouch, the pouch being formed from paper, woven fabric or non-woven material.
[0177] The fragrance compositions used for this test were Floral V (Example 6), two samples of Citrus B2 (Example 6) and Jasmine E (Example 6). The fragranced sachets were prepared by mixing the fragrance compositions with ground corn-cob particles (NatureZorb?-100, origin: Aproa) at 20% loading by weight. 12 grams of the resulting mixtures were then placed in a 2.5 inch?2.5 inch paper pouch. A sample comprising un-fragranced corn-cob was prepared for the malodour only cabin.
[0178] The malodour preparation and test procedure was the same as outlined in Example 8. The cabins were assessed by 21 untrained but experienced assessors. Data was analyzed using one-way analysis of variance (ANOVA), followed by Fisher's least significant difference (LSD) method for multiple comparisons (?=0.05). The number of assessors (N) and the LSD were as follows: N=21, LSD=0.62. Mean malodour intensity of the cabins is shown in
[0179] The perceived malodour intensity of the Jasmine E Only cabin (no malodour) is significantly lower than that of the malodour only cabin and Floral V+malodour cabin. The Jasmin E+Malodour cabin and Citrus B2+Malodour cabins were not perceived to be significantly stronger in malodour intensity than the cabin with no malodour, demonstrating how effective these two compositions are reducing the perception of latrine malodour. The perceived malodour intensity of the cabins containing malodour and fragrance compositions according to the present disclosure is significantly lower than that of the malodour only cabin; thus, sachet-type 1 air fresheners comprising fragrance compositions according to the present disclosure are useful in reducing the perception of latrine malodour.
Example 11
Latrine Malodour Reduction Efficacy Test of Liquid Electrical-Type Air Fresheners Comprising Fragrance Compositions According to the Present Disclosure.
[0180] The air freshener device used in this example was an electric-wick air freshener; such devices utilize a heating element to drive fragrance composition from a wick inserted into a reservoir with the fragrance.
[0181] The fragrance compositions used for this test were Floral RD (Example 4), two samples of Citrus H (Example 4) and Jasmine E (Example 6). The fragrance compositions were mixed with equal parts by weight Augeo Clean Multi (Solvay). 20 grams of the resulting mixtures were then placed in reservoirs with wicks (sintered plastic). The heater units used were designed to heat the wick to 70? C.
[0182] The malodour preparation and test procedure was similar to that outlined in Example 8. However, in this example the test cabins comprised a volume of 812 ft.sup.3 and assessors assessed the odour by entering each cabin. Other details were as previously described. The cabins were assessed by 23 untrained but experienced assessors. Data was analyzed using one-way analysis of variance (ANOVA), followed by Fisher's least significant difference (LSD) method for multiple comparisons (?=0.05). The number of assessors (N) and the LSD were as follows: N=23, LSD=0.56. Mean malodour intensity of the cabins is shown in
[0183] The perceived malodour intensity of the Jasmine E Only cabin (no malodour) is significantly lower than that of the malodour only cabin and Floral RD+malodour cabin. The Jasmin E+Malodour cabin and Citrus H+Malodour cabins were not perceived to be significantly stronger in malodour intensity than the cabin with no malodour, demonstrating how effective these two compositions are reducing the perception of latrine malodour. The perceived malodour intensity of the cabins containing malodour and fragrance compositions according to the present disclosure is significantly lower than that of the malodour only cabin; thus, liquid electrical-type air fresheners comprising fragrance compositions according to the present disclosure are useful in reducing the perception of latrine malodour.
Example 12
[0184] The malodour reduction of fragrance composition described by the present disclosure was measured in a bleach cleaning powder.
[0185] The bleach cleaning powder is a bleach powder combined with spray-dried fragrance. Standard usage of this product is to apply the powder to the area to be treated and dissolved with water, followed by scrubbing to loosen all particles and then rinsed.
[0186] Fragranced bleach samples were prepared by adding 0.15 grams of spray-dryed powder (comprised of 50% w/w perfume, 50% w/w octenyl succinated modified starch) to 9.85 grams of Stable Bleaching Powder (Grade I, Gujarat Alkalies and Chemicals Limited, Gujarat, India).
[0187] The malodour composition detailed in Table 1 was applied onto fine vermiculite (Specialty Vermiculite Corp, Enoree, S.C.) with a 70% loading by weight. 9 grams of the composition was then presented to assessors in round aluminum tins. The aluminum tins have a 3 in. diameter with a 1 in. height. For the test sample with fragrance only, a tin with untreated vermiculite is used.
TABLE-US-00018 TABLE 13 Ingredient w/w % Triacetin 99.8775 Indole 0.0500 Butyric Acid 0.0045 P-Cresol 0.0650 DMTS 0.0030
[0188] A 70% by weight latrine malodour loaded vermiculite was prepared by admixing 350 g of the latrine malodour with 150 g of vermiculite (Fine grade, Specialty Vermiculite Corp, Enoree, S.C.). The efficacy of the cellulose-based air fresheners comprising fragrance formulations according to the present disclosure was assessed following the practices described in ASTM E 1593-06 Method for Assessing the Efficacy of Air Care Products in Reducing Sensorialy Perceived Indoor Air Malodour Intensity. A booth labeled Reference containing only a malodour tin was presented to assessors first to familiarize them with the malodour. Using a scale of 1 to 7 (1 signifying no odour, 4 moderate odour and 7 extremely strong malodour), assessors were then asked to evaluate each sample in specified order and rate malodour intensity and total odour intensity.
[0189] The samples were assessed by 19 untrained assessors. By untrained assessors we mean users of air fresheners who have not received formal olfactive training but who are used to participating in fragrances assessments and have experience in rating the odour attributes.
[0190] Using 60 ft.sup.3 evaluation rooms, the floors of the cabins were wet with water and samples were scrubbed onto the floors until dissolved. The malodours were then added. The environmental conditions during the test were 72 F, 40% RH with 5 air changes per hour. A portable desk fan, set on low, is placed at the floor of the cabin to circulate the air within. Booths were labeled with a randomly generated 3 digit code. Sample presentation was blind, balanced, randomized and sequential monadic. After 5 minutes from activation, assessors were directed to open the smelling window to evaluate each sample and wait for 60 seconds before proceeding to answer a series of questions relating to the odour they perceived in the room. The assessors were asked to rate the malodour strength and total odour intensity. Data was analyzed using Analysis of Variance (ANOVA) and the difference between two means determined using the least significant difference (?=0.05). Mean malodour intensity of the cabins is shown below; the least significant difference between means was 0.61.
[0191] Results are shown in
[0192] The perceived malodour intensity of the Floral RD+Bleach Only cabin (no malodour) is significantly lower than that of the malodour only cabin. The Floral RD+Bleach+Malodour cabin was not perceived to be significantly stronger in malodour intensity than the cabin with no malodour, demonstrating how effective this composition is at reducing the perception of latrine malodour. The perceived malodour intensity of the cabin containing malodour and Floral RD composition according to the present disclosure is significantly lower than that of the malodour only cabin; thus, bleach cleaning powders comprising fragrance compositions according to the present disclosure are useful in reducing the perception of latrine malodour.
Example 13
Latrine Malodour Reduction Efficacy Test of Fragrance Compositions According to the Present Disclosure in a Model Latrine
[0193] In this example, in order to evaluate performance of compositions according to according to the present disclosure, a model latrine was constructed. The model latrines were equipped with an odour generator that injected hydrogen sulfide, methyl mercaptan, butyric acid, para-cresol, and indole, allowing the accurate and reliable reconstitution of a toilet malodour headspace. The malodourant concentrations in the model latrines matched the quantitative headspace analysis made in African and Indian toilets. The toilet malodour headspace performances were validated by chemical and sensory analysis. Olfactory stimuli were presented to participants in different climates to assess the effect of climate on the perception of odours. The sensory data showed that increasing temperature and humidity decreased the intensity ratings of malodours but not their quality. Perfume formulations can be delivered in these model latrines by forced evaporation to control the headspace concentration or by delivery systems such as cellulosic pads, liquids, and powders. Our experimental setup provided dose-response curves to assess the performance of perfume formulations in reducing toilet malodour and increasing pleasantness.
Material and Methods
Chemicals
[0194] The compounds triethylamine, N-ethylmaleimide (NEM), and methyl octanoate were purchased from Sigma-Aldrich (Buchs, Switzerland), and butyric acid, p-cresol, indole, and L-cysteine were in-house products. The solvents diethyl ether, methanol, ethyl acetate, and acetone were purchased from Carlo Erba (Val de Reuil, France). For methyl mercaptan and hydrogen sulfide, nitrogen mixtures at 15 ppm (v/v) were used, in pressurized cylinders purchased from Carbagas (Carouge, Switzerland). Oasis HLB 1-g cartridges were purchased from Waters (Montreux-Chailly, Switzerland). The perfume formulation used in this example is described below.
TABLE-US-00019 TABLE 14 Floral D Perfume Formulation Molecule Name Parts UNDECANAL 15 (E)-2-PENTYL-3-PHENYL-2-PROPENAL 150 (+?)-3,7-DIMETHYL-6-OCTEN-1-OL 200 (+?)-(3E)-3-methyl-4-(2,6,6-trimethyl- 70 2-cyclohexen-1-yl)-3-buten-2-one (A) + (+?)-(1E)-1-(2,6,6-trimethyl-2- cyclohexen-1-yl)-1-penten-3-one (B) (+?)-2-methyl-3-[4-(2-methyl-2- 120 propanyl)phenyl]propanal (+?)-2,5-DIMETHYL-2-INDANMETHANOL 100 2-PHENYLETHANOL 240 (+?)-(3E)-4-(2,6,6-trimethyl-2- 80 cyclohexen-1-yl)-3-buten-2-one (A) + (3E)- 4-(2,6,6-trimethyl-1-cyclohexen-1-yl)-3- buten-2-one (B); (1RS,2RS)-2,4-dimethyl-3-cyclohexene-1- 25 carbaldehyde (A) + (1RS,2SR)-2,4- dimethyl-3-cyclohexene-1-carbaldehyde (B)
Model Latrines
[0195] Three 1.7 m.sup.3 model latrines (1.95 m?0.985 m?0.89 m) made of 8-mm transparent polyethylene terephthalate were placed in a climate chamber, and each latrine was equipped with a 29 cm?39 cm rotating door to allow evaluation of odours (
Odour Generator
[0196] To force the evaporation of liquids, we modified the lower chamber of a publically available olfactometer. A 150 L/h nitrogen flow flushed a 500-ml round-bottom flask, where liquids were introduced via a polytetrafluorethylene (PTFE) capillary linked to a 1-ml polypropylene syringe (
Climate Chamber
[0197] The climate chamber dimensions were 3.42 m?2.95 m?2.5 m, resulting in a volume of 25 m.sup.3. The temperature and humidity of the climate chamber was controlled in a closed cycle of 540 m.sup.3/h. Fresh air entered the chamber at a rate of 51 m.sup.3/h and air left the chamber at the same rate. The working range for temperature and relative humidity (RH) was 12? C. to 45? C. and 30% RH to 90% RH, respectively. The climate chamber was equipped with temperature and RH probes placed at the entrance and outlet of the temperature and humidity controlling cycle. The data from the probes at the entrance were recorded every 5 min, allowing the measurement of temperature and RH of the air inside the climate chamber during the experiments. Moreover, a proble was placed (Traceable? hygrometer, VWR International, Radnor, Pa., USA) inside the latrine to punctually measure the RH and temperature to ensure that the differences in temperature and RH between the air inside the climate chamber and the air inside the latrines was minimal. A temperature difference below 1.5? C. and a RH difference below 5% was mainteind.
Participants
[0198] The participants were employees from the research center at Firmenich SA (Geneva, Switzerland). Ten sessions were organized and the number of participants for each session was as follows: 26, 24, 26, 27, 26, 30, 25, 27, 25, 23. The participants signed a consent form before participating in the study. The consent form and experimental protocol were approved by the internal review board of Firmenich in agreement with the Declaration of Helsinki for medical research involving human subjects.
Stimuli
[0199] The participants were exposed to six odourant mixtures delivered in latrines in four different climates. The odourant mixtures were Mukuru (Nairobi) UDT malodour alone, the perfume (Floral D) alone, and mixtures of the malodour and the perfume released at four different concentrations (0.18, 0.54, 1.62, 4.9 ?g/l).
[0200] The malodour was reconstituted from Mukuru toilets because it contains all of the significant molecules and it came from well-maintained toilets. The Mukuru malodour source was composed of hydrogen sulfide, methanethiol, butyric acid, p-cresol, and indole, whose gas phase concentrations were 0.26, 0.018, 0.004, 0.0027 and 0.00018 ?g/l, respectively. Hydrogen sulfide and methanethiol were released from pressurized cylinders at 20.8 l/h and 9.8 l/h, respectively. The remaining malodour products were released in the latrines by forcing the evaporation of a propylene glycol solution that contained 0.775, 0.526 and 0.035 mg/ml of butyric acid, p-cresol and indole, respectively. The perfume formulation was released in pure form in the forced evaporation chamber, resulting in a gas phase concentration of 4.9 ?g/l. The lower gas phase concentration of the perfume was achieved by diluting it in propylene glycol. The gas phase concentrations of 0.18, 0.54 and 1.62 ?g/l were obtained with 3.62%, 11.13% and 33.31% (w/w) propylene glycol solutions, respectively. To release the malodour and the perfume in the same latrine, two syringes via two PTFE capillaries were connected to the same forced evaporation chamber. One syringe contained the malodour solution and the other syringe contained the perfume formulation, either in pure form or diluted in propylene glycol. Both syringes were mounted on the same syringe pump and their pistons were pushed at 0.088 mm/h, resulting in a release rate of 0.088 ml/h. When the malodour or the perfume was presented alone, pure propylene glycol was injected into the forced evaporation chamber with the second syringe. Each odour was presented in four climates: 22? C. at 30% RH, 22? C. at 80% RH, 35? C. at 30% RH, and 35? C. at 80% RH.
Sensory Protocol
[0201] The participants were randomly exposed to the odour stimuli in the different climates. As only three latrines were available, the six odours were split into two groups, each containing the malodour alone or the perfume alone, the malodour plus a low dose of perfume, and the malodour plus a high dose of perfume. The first and the last sessions were used as controls to assess the reliability of the panel and were composed of the malodour alone, the perfume alone, and a mixture of both. The participants entered the climate chamber and directly evaluated the odour of the three latrines by answering a paper questionnaire made with the software FIZZ (Biosystems, Courtenon, France). They reevaluated the odour of each latrine after a 3-min adaptation to the climate. They were asked to rate, on 0-10 linear scales, the pleasantness from I don't like to I like, the familiarity from not familiar to very familiar, the intensity from no odour to very strong, the fecal/toilet character from not fecal/toilet to very fecal/toilet, and whether they wanted to enter the latrine from not at all to very willingly.
Headspace Analysis
[0202] The Mukuru malodour was released in the model latrines as described above. The climate was set to 25? C. at 50% RH. The compounds released into the air were collected with Oasis cartridges conditioned with 20 ml of deionized water, 20 ml of methanol, 20 ml of acetone, and 20 ml of diethyl ether and dried at 50? C. for 1 h in an oven. Hydrogen sulfide and methyl mercaptan were derivatized with NEM in Oasis cartridges loaded with 2 ml of diethyl ether containing 25 mg NEM and 100 ?1 of triethylamine and dried for 1 h at 50? C.
[0203] The air was pumped at 1 l/ min through the cartridges by using GilAir Plus pumps connected with silicon tubes. The volume of the samples was 100 l. Three cartridges were used to sample the air of one latrine. One cartridge was placed in the center of the model latrines, the second 23 cm from the evaluation door, and the third deep at the top right of the latrine (171 cm from the ground). The cartridges were desorbed with 10 ml of diethyl ether added to 100 ?l of 10 ng/?l methyl octanoate (internal standard [IS]) solution in ethyl acetate. To remove the excess NEM, the eluate was washed with 3 ml of 10 mg/ml of L-cysteine solution in water buffered at pH 8 with 0.1 M potassium phosphate. The water phase was removed and the organic phase dried with sodium sulfate. The water phase was acidified with 100 ?l of a 37% HCl solution in water; butyric acid was extracted with 4 ml of diethyl ether added to 100 ?l of IS. Prior to injection in the GC-MS, both organic phases were gently concentrated to 1 ml under argon flow. The analysis was performed by injecting 1 ?l of the eluate into the GC-MS as described below.
Headspace Analysis Calibration Using an Olfactometer
[0204] Using an olfactometer, a headspace was created with known concentrations of butyric acid, indole, p-cresol, methyl mercaptan, and hydrogen sulfide to calibrate the analytical method. Briefly, air with known amounts of compounds was sampled with Oasis cartridges loaded with the derivatization agent NEM (described above) at the outlet of the olfactometer.
[0205] Methyl mercaptan and hydrogen sulfide were released into the olfactometer from pressurized cylinders containing a mixture of 15 ppm of both sulfur compounds in nitrogen. The flow of both sulfur compounds was controlled with rotameters (Vogtlin TV 100). Butyric acid, indole, and p-cresol were released by forcing the evaporation of propylene glycol solutions from a 1-ml polypropylene syringe mounted on a syringe pump delivering 0.101 ml/h. The solution was introduced into the lower chamber, which was heated to 150? C. by using an oil bath. Nitrogen was introduced into the lower chamber at 60 l/h to collect the products that evaporated and was mixed with the airflow of the upper chamber. The airflow was set at 540 l/h and humidified by bubbling in a water-jacketed wash bottle filled with distilled water. The upper chamber of the olfactometers was water jacketed and its temperature was maintained at 29? C. with a water bath. At the outlet of the olfactometers, the temperature was 30? C. and the RH was 40%. The resulting concentrations of methyl mercaptan and hydrogen sulfide compounds in the olfactometer were 0.1, 0.05, 0.0250 and 0.0125 ?g/l. The resulting concentrations of butyric acid, p- cresol, and indole were 0.0001, 0.001, 0.01 and 0.1 ?g/l.
Gas Chromatography-Mass Spectrometry (GC-MS)
[0206] A GC 6890 N (Agilent, Palo Alto, Calif., USA) was used to identify the compounds. A fused silica SPB-1 capillary column (30 m?0.25 mm i.d., 0.25-?m film thickness, Supelco, Bellefonte, Pa., USA) was mounted in the GC. The carrier gas was He (52 kPa) and the injector temperature was set at 250? C. Injections were made with a Combi-Pal autosampler (Zwingen, Switzerland). To analyze butyric acid, p-cresol, indole, and NEM derivatives of methyl mercaptan and hydrogen sulfide, the initial oven temperature was held at 50? C. for 5 min and then increased at 5? C./min to 250? C., split mode 1/5. The GC was coupled to a MS 5975B Inert XL MSP from Agilent. The mass spectra in the electron impact mode were measured at 70 eV in SIM mode. The ions that were monitored were butyric acid (60), p-cresol (107), indole (117), NEM-S-CH.sub.3 (127), and NEM-S-NEM (127).
Data Analysis
[0207] The questionnaires were scanned and the data stored in FIZZ and analyzed with R (https://cran.r-project.org). The response variablespleasantness, enter the latrine, intensity, familiarity, and fecal characterwere analyzed by using analysis of variance (ANOVA), and any significant effect was confirmed with the non-parametric Kruskal-Wallis test. Pairwise comparison tests were made with the Tukey honest difference test (Tukey HSD function in R). The relationship between the pleasantness of the different odour treatments and the willingness to enter the latrines was investigated with linear models. Moreover, pleasantness ratings from odour treatments and pleasantness ratings from the climates were analyzed with linear models. The level of significance was set at P<0.05. To determine the concentrations of malodour compounds in the gas phase of the model latrines, calibration curves were established by using linear models on the ratio of the peak area of volatiles and IS as a function of the gas phase concentrations in the olfactometer. Using these calibration curves and the inverse prediction function in R (chemCal package), the gas phase concentrations inside the model latrines were predicted from the ratios of peak area of volatiles and IS.
Results
[0208] Three toilet models of 1.7 m.sup.3 were built in a climate chamber of 25 m.sup.3. Each toilet had 10 air changes per hour. Inside the toilets, a scale was installed to monitor weight gain or loss of and hard surfaces to receive liquids or powders. When the subjects stepped into the climate chamber, they were exposed to the temperature and humidity set up for the experiment; therefore, for the present study, they were asked to make a first evaluation of the odour directly after entering the chamber and to make a second evaluation after a few minutes of adaptation to the climate. Adaptation had no significant effect on the criteria used to evaluate the odour. The data with and without adaptation were then averaged.
[0209] A typical Mukuru fecal toilet malodour was created through a controlled release of methanethiol, hydrogen sulfide, butyric acid, p-cresol, and indole by spraying the gas and vaporizing the liquids in a hot chamber flushed with nitrogen (
[0210] Four descriptors were proposed to the subjects: pleasantness, enter the toilet, fecal character and intensity. The panel was reliable, as the results obtained with the panel when we repeated the first and last sessions are not significantly different (
[0211] The climate significantly affected the intensity, but had no significant effect on the other criteria of pleasant, familiarity, fecal character, and willingness to enter the latrines. The increase in temperature significantly decreased the overall intensity (ANOVA, P<0.0001; Kruskal-Wallis, P<0.001) independently of the odour (
[0212] Next, the appropriate control was evaluated. The choices were: the malodour (blue bars,
[0213] As opposed to the direction of the fecal character ratings, the pleasantness ratings increased significantly as a function of increasing concentrations of perfume (
[0214] A similar result was obtained with the ratings of willingness to enter the latrines compared with the pleasantness ratings. Ratings of willingness increased significantly as a function of increasing perfume concentrations. The willingness to enter the latrine was strongly correlated to those of pleasantness (
Temperature Measurements
[0215] The climate chamber was set for four climate conditions: 22? C. at 30% RH, 22? C. at 80% RH, 35? C. at 30% RH, and 35? C. at 80% RH. The temperature and RH conditions were reached by using the temperature controlling system (Table 15). The temperature and the RH inside the climate chamber and inside the model latrines were less than 1.5? C. and 5%, respectively (Table 15).
TABLE-US-00020 TABLE 15 Measurements of temperature and relative humidity inside the climate chamber and inside the latrine Standard deviation Average of Average Standard temperature temperature RH of deviation RH of climate of climate of RH of Temperature set chamber climate chamber climate Temperature RH of set (? C.) (%) [? C.] chamber [%] chamber of latrine latrine 22 30 22.0 0.6 32.6 3.1 23.0 31.3 35 30 35.0 0.2 30.4 0.9 34.4 28 22 80 22.0 0.2 73.0 2.5 22.8 75.5 35 80 35.0 0.2 76.0 2.2 34.8 81
Example 14
Latrine Malodour Reduction Efficacy Test of Fragrance Compositions According to the Present Disclosure in Latrines Using Passive Delivery Systems
[0216] Without intending to be limited to any particular theory, the performance of the compositions may be influenced by factors, such as, for example, the volatility of the compound in the formulation, the temperature, airflow, the depth of the boundary layer, the interactions of the compounds with the substrate of the passive delivery system, the interactions between the compounds, the concentrations of each compound in the delivery system, climate, and the like. Such factors may influence the influence the duration and/or the magnitude of the perceived reduction in fecal malodour, and/or the duration and/or the magnitude of changes in other sensory effects, such as, for example, an increased in perceived pleasantness.
[0217] To explore this further, in this example, the performances of compositions according to some aspects of the present invention were evaluated in latrines, where the compositions were incorporated into passive delivery systems. In a first series of experiments using a model system, the following two formulations were tested: Floral V (as described in Table 10), and Jasmin E (as described in Table 9). A panel of 19 to 32 participants was trained on-site to evaluate the performance of the test compositions over a period of 10 days. The headspace of the model latrines were also sampled and analyzed to determine the gas phase concentration of perfume ingredients in the latrines.
[0218] Panelists were exposed to the odour of the three model latrines. The odour of two latrines were composed of perfumes Jasmin E and Floral V released from cellulosic pads in addition to the malodour Mukuru reconstitution delivered by forced evaporation systems as described in the previous example. The odour of the third model latrine was composed of the malodour alone in addition the blank cellulosic pad. The Cellulosic pads were 10.8 cm?7.3 cm?0.15 cm, and were loaded with 2.2 g of a mixture of 60% perfume oil and 40% isopropyl myristate (IPM). The pads were placed on a scale that equipped each latrine. The scales were connected to a computer to monitor every 5 min the loss of mass of each pad. Time of implementation of the pads was time 0. Sensory analysis and headspace analysis were conducted according to the methods described in the previous example.
[0219] Referring to
[0220] The performance of the formulations tended to decrease as a function of time at 25? C., and clearly decreased at 40? C. For Floral V, the pleasantness dropped under the neutral limit (5) to reach the negative valence (I don't like) after 10 days at 25? C., and after 4 days at 40? C. In fact, an inversion between the pleasantness and the fecal character was observed. The Jasmine E formulation demonstrated a better performance in both climates as the pleasantness remained in the positive valence (I like) during the survey and the fecal character ratings were lower than those observed with the Floral V formulation. Unlike the Floral V formulation, no inversion was observed for the Jasmine E formulation. Fluctuations were not related to the malodour, as the associated ratings were remarkably stable over time.
[0221] Analysis of the headspace of the test latrines revealed the variations of the gas phase concentration for all the compounds of the Floral V formulation and for selected compounds for the Jasmin E formulation.
[0222] Referring to
[0223] Violet AT and Isoraldeine 70P demonstrated similar decreases in headspace concentration. Here, their gas phase concentrations were stable at 25? C. whereas, at 40? C., they started higher and decreased faster.
[0224] LILYFLORE? was stable over the period of experiments but in higher concentration at 40? C. compared to 25? C. Here, these data suggest, an increment of temperature helped to release LILYFLORE?. All the antagonist compounds except Dihydrolinalol were in percievable amount in the air over the period of experiments.
TABLE-US-00021 TABLE 16 The concentration at which certain MOCs reduce the percieved intensity of indol, DMTS, p-cresol and butyric acid. Indole DMTS p-cresol Butyric acid Dyn Dyn Dyn Dyn Conc Conc Conc Conc Reduction (ug/l) Reduction (ug/l) Reduction (ug/l) Reduction (ug/l) LILYFLORE? 81 2.06E?01 64 1.26E?01 76 2.20E?01 58 3.51E?02 Violet AT 72 1.33E?01 81 1.51E?01 85 1.33E?01 55 1.23E?01 Isoraldeine 79 5.42E?01 69 2.16E?01 49 6.74E?02 25 6.74E?02 70P Dihydrolinalol NA NA NA NA NA NA 64 7.60E?01 Aldehyde 57 6.68E?02 62 6.67E?02 NA NA NA NA C11 undecylenic Citronellol 65 2.52E?01 NA NA 61 1.10E?01 55 9.47E?02 BJ Alpha NA NA NA NA 62 4.13E?02 43 4.10E?02 damascone Delphone NA NA 67 4.60E?02 64 4.88E?02 NA NA Hexylcinnamic NA NA NA NA 39 1.34E+00 26 1.34E+00 aldehyde Phenylethyl 46 5.38E?01 55 1.03E+00 49 3.18E?01 NA NA alcohol Rosinol NA NA 38 6.59E?01 NA NA NA NA Cryst Zestover 82 3.48E?01 78 3.80E?01 66 6.07E?02 68 8.09E?02 Benzyl NA NA NA NA NA NA 54 1.31E+00 acetate
[0225] Using the performance Floral V formulation at 40? C. as an example, referring to Table 17 below, at Day 0, when the performance of the formulation was greatest (for both fecal malodor reduction and an increased perception of pleasantness), the headspace concentration of most of the ingredients were at or above the effective antagonist concentration for at least one malodour target. At day 2, the headspace concentration of the ingredients declined, with only one ingredient being at or above the effective antagonist concentration for at least one malodour target. Four ingredients were close to the effective antagonist concentration for at least one malodour target, and seven ingredients were below the effective antagonist concentration for at least one malodour target. A corresponding decline in performance of the formulation was observed (
TABLE-US-00022 TABLE 17 Headspace concentration of MOCs. Headspace Concentration (?g/l) Floral V Floral V Floral V 40? C. Day 0 40? C. Day 2 40? C. Day 6 LILYFLORE? 1.00E?02 1.00E?02 1.00E?02 Violet AT 1.00E?01 6.00E?02 1.00E?02 Isoraldeine 70P 1.00E?01 7.00E?02 2.00E?02 Dihydrolinalol 8.00E?01 5.00E?03 3.00E?04 Aldehyde C11 6.00E?02 2.00E?02 0.00E+00 undecylenic Citronellol BJ 7.00E?01 3.00E?01 1.00E?02 Alpha damascone 4.00E?02 2.00E?02 1.00E?03 Delphone 1.00E?01 4.00E?03 0.00E+00 Hexylcinnamic aldehyde 2.00E?03 3.00E?03 3.00E?03 Phenylethyl alcohol 1.00E+00 9.00E?02 1.00E?02 Rosinol Cryst 2.00E?02 2.00E?02 1.00E?02 Zestover 6.00E?02 2.00E?04 8.00E?05
[0226] In another study using latrines in Durban (South Africa), and Pune (India), the performances of the following two formulations were tested: Floral V Jasmin E and Citrus 259389 B (as described in Table 8). The formulations were incorporated into cellulose pads. The panel of participants were trained on-site to evaluate the performance of the test compositions over a period of 3 days. The headspace of the latrines were also sampled and analyzed to determine the gas phase concentration of perfume ingredients in the latrines.
[0227] Odour evaluation was performed by 11 subjects. The test formulations were diluted in isopropyl myristate (IPM; 60% oil, 40% IPM) and loaded on plain cellulose pads (10.8 cm?7.3cm?0.15 cm) at 42% w/w dry substrate. One to two pads were used per latrine according to the resulting intensity of the perfume when implemented. We used three latrines (three replicates) per formulation in both countries. In Durban, Jasmin E and Floral V were implemented in six private and individual ventilated pit-latrines and Citrus 259389 B (as described in Table 7) was implemented in three ventilated improved pit-latrines of a community ablution block. In Pune, each test formulation was implemented in three toilets of a dedicated ablution block.
[0228] The subjects evaluated the olfactory stimuli with our web-questionnaire developed in house and available on the internet at the following link: http://www.pacchiani.ch/firmenich/. They were asked to rate on a linear scale (from 0 to 100), the pleasantness from I don't like to I like, the intensity from no odour to very strong, the fecal character from not fecal to very fecal. They were able to add comments at the end of the questionnaire.
[0229] The odour of the latrines was evaluated before and after the implementation of the pads. A first evaluation was performed in the afternoon to establish the baseline. The pads were then implemented and a second evaluation was performed 10-30 min after the implementation. A third and a fourth evaluation was performed in the morning the next days after the implementation. For the evaluation, the participants were asked to enter the toilet one by one. The toilets were used as usual.
[0230] Headspace Analysis: The day following the implementation of the test formulations, the air of two toilets treated with the test formulations was sampled. The air was pumped at 1 L/min through OASIS HLB 1 g cartridges that were suspended to the walls of the latrines. One cartridge was placed near the ground at 0.15-0.3 m height and a second one was placed at 1.5-1.7 m height. The total volume pumped was 87 L to 100 L. The analysis and the quantifications were achieved according the standard protocols. To determine whether the test formulations changed significantly the pleasantness and the fecal character ratings, the Wilcox signed-rank test was used on the data of each toilet comparing the ratings before and after the implementation of the test formulations. The data obtained from the evaluations performed after the implementation, were pooled. Data of evaluations coming from toilets where the pad was stolen, displaced or removed were discarded.
[0231] Referring to
[0232] The fecal malodour observed was not constant across all the latrines tested. For example, in Pune, the level of the fecal malodour was very low and more similar among the pool of latrines compared to the fecal malodour observed in the latrines tested in Durban (
[0233] In Pune, the test formulations were implemented in three public ablution blocks composed of about 10 flush toilets. They were well maintained and cleaned several times a day. The ventilation was insured by opened windows in each toilet. In contrast, the latrines in Durban were dirty individual pit-latrines that were poorly maintained. For some latrines the pit was full and the ventilation port was missing. This can explain the variability of the malodour level in the different toilets. Examples are latrine N?2 treated with Jasmin E and in latrine N?1 treated with Floral V, the formulations hardly increased the average pleasantness that was not stable in time (
[0234] Analysis of the headspace of the latrines revealed that the MOC molecules ?-ionone, isoraldeine, LILYFLORE?, dihydrolinalol were found in significant amounts in the air sampled in Pune and in Durban. The gas phase concentrations detected exceeded their respective olfactory detection thresholds (ODT) determined in separately, namely: 5.08?10.sup.?4, 1.92?10.sup.?4, 1.28?10.sup.?4, 1.37?10.sup.?3 ?g/L, respectively (
[0235] The headspace analysis shows a certain degree of homogeneity despite the lack of airflow control. The exception of toilet N? 3 may be explained by the fact that the cartridge at high height was too close from the pad during the sampling. Moreover, the gas phase concentrations were similar across both countries. However, two pads per toilets were used in Pune, suggesting that the ventilation rate was higher in Pune than in Durban.
[0236] The analysis revealed also that the profile of compounds concentrations obtained on the field were similar to that found in the model latrines at a similar temperature (
[0237] Taken together, these data demonstrate a correlation between model latrines and field latrines, validating a step further the use of model latrines to make experiments in controlled conditions. Moreover, The Jasmine E formulation appeared to perform longer than the Floral V formulation in suppressing the toilet malodour reconstitution at 25? C. and 40? C. Headspace analysis revealed that the gas phase concentrations of MOC compounds were similar comparing both perfumes and that top note compounds are not involved in the suppression of the malodour, challenging their presence in those formulations.
[0238] Formulations containing antagonists of fecal malodour (Jasmine E, Floral V, Citrus 259389 B) increased the pleasantness of toilets odour by decreasing the fecal character in different and challenging environments. However, the limit of performance was reached in dirty toilets with no ventilation and pit full, environments that are not targeted in this study. Furthermore, the MOC were in a significant amount even in challenging environment and that the suppression effect of the fecal character was not due to perfume overpowering the malodour.
Example 15
Synergistic Effect of Certain Malodour Receptor Antagonists According to Some Aspects of the Present Invention
[0239] The performance of a test formulation containing LILYFLORE?, Violet AT and Isoraldeine to counteract the fecal malodour perceived from a fecal malodour reconstitution was tested. The amount of each single ingredient in the test formulation was the same as the corresponding concentration of the ingredient that was incorporated into the Floral compositions. Separate control formulations were also included, comprising LILYFLORE?, Violet AT and Isoraldeine separately, at the same concentration as each single ingredient in the test formulation. The sensory evaluation was blind, and performed using olfactometers and a set of more than 30 participants evaluating blind. In parallel, the headspace concentration of the ingredients from the test and three control formulations was determined. The results are shown in Table 18 and
TABLE-US-00023 TABLE 18 Gas phase concentrations and attribute scores for the test and control formulations evaluated in combination with a fecal reconstitution. Fecal Score % Freshness Pleasantness Conc Score CI left Redn Score CI Score CI ?g/l air ANOVA Fecal 8.6 0.3 100 0 1.1 0.3 1.0 0.2 0.021/0.021 A Reconstitution Control 1: 3.8 0.6 44 56 4.4 0.6 4.8 0.5 1.36/1.22 B LILYFLORE? Control 2: 3.6 0.6 42 58 4.7 0.6 5.0 0.6 1.09/0.98 B Violette AT Control 3: 3.6 0.6 42 58 4.8 0.6 5.1 0.5 0.96/0.86 B Isoraldeine Test 2.6 0.6 30 70 5.4 0.6 5.7 0.6 3.41/3.47 C Formulation
[0240] Taken together, these data demonstrate that the test formulation comprising a mixture of LILYFLORE?, Violet AT and Isoraldeine was better at reducing the fecal score, and therefore the perception of fecal malodor, and also increasing the pleasantness and freshness score, compared to control formulations containing the single ingredients tested at their same concentration within the mixture.
[0241] The performance of another test formulation containing LILYFLORE?, Violet AT and dihydrolinalol to counteract the fecal malodour perceived from a fecal malodour reconstitution was tested. Separate control formulations were also included, comprising LILYFLORE?, Violet AT and dihydrolinalol separately, at the same concentration as each single ingredient in the test formulation. The sensory evaluation was blind, and performed using olfactometers and a set of more than 30 participants evaluating blind. In parallel, the headspace concentration of the ingredients from the test and three control formulations was determined. The results are shown in Table 19 and
TABLE-US-00024 TABLE 19 Gas phase concentrations and attribute scores for the test and control formulations evaluated in combination with a fecal reconstitution. Fecal Score % Freshness Pleasantness Conc Score CI left Redn Score CI Score CI ?g/l air ANOVA Fecal 8.6 0.2 100 0 1.1 0.3 1.0 0.3 2.1 ? 10.sup.?2 A reconstitution Control 1: 5.6 0.7 65 35 3.9 0.6 3.5 0.7 1.36 B dihydrolinalol Control 2: 4.7 0.7 55 45 4.0 0.6 4.1 0.8 1.13 C LILYFLORE? Control 3: 4.1 0.7 47 53 4.5 0.6 4.8 0.7 0.96 C Violet AT Test 3.1 0.6 35 65 5.3 0.6 5.5 0.7 3.40 D Formulation
[0242] Taken together, these data demonstrate that the test formulation comprising a mixture of LILYFLORE?, Violet AT and dihydrolinalol was better at reducing the fecal score, and therefore the perception of fecal malodor, and also increasing the pleasantness and freshness score, compared to control formulations containing the single ingredients tested at their same concentration within the mixture.
[0243] The performance of another test formulation containing LILYFLORE?, isoraldeine, Violet AT and dihydrolinalol to counteract the fecal malodour perceived from a fecal malodour reconstitution was tested. Separate control formulations were also included, comprising LILYFLORE?, Violet AT, isoraldeine and dihydrolinalol separately, at the same concentration as each single ingredient in the test formulation. The sensory evaluation was blind, and performed using olfactometers and a set of more than 30 participants evaluating blind. In parallel, the headspace concentration of the ingredients from the test and three control formulations was determined. The results are shown in Table 20 and
TABLE-US-00025 TABLE 20 Gas phase concentrations and attribute scores for the test and control formulations evaluated in combination with a fecal reconstitution. Fecal Score % Freshness Pleasantness Conc Score CI left Redn Score CI Score CI ?g/l air ANOVA Fecal 8.6 0.2 100 0 1.1 0.3 1.0 0.3 2.1 ? 10.sup.?2 A reconstitution Control 1: 6.1 0.7 70 30 3.2 0.7 3.2 0.6 1.12 B dihydrolinalol Control 2: 4.9 0.8 56 44 4.1 0.8 4.2 0.7 7.47 C Violete AT Control 3: 4.8 0.8 55 45 3.9 08 3.8 0.6 9.34 C LILYFLORE? Control 4 : 4.4 0.8 51 49 4.6 0.6 4.5 0.8 6.53 C Isoraldeine Test 3.1 0.7 36 64 5.1 0.7 5.5 0.7 3.45 D Formulation
[0244] Taken together, these data demonstrate that the test formulation comprising a mixture of LILYFLORE?, Violet AT, isoarldeine and dihydrolinalol was better at reducing the fecal score, and therefore the perception of fecal malodor, and also increasing the pleasantness and freshness score, compared to control formulations containing the single ingredients tested at their same concentration within the mixture.
[0245] Publications cited throughout this document are hereby incorporated by reference in their entirety. Although the various aspects of the invention have been illustrated above by reference to examples and preferred aspects, it will be appreciated that the scope of the invention is defined not by the foregoing description but by the following claims properly construed under principles of patent law.