Alcohol free, low viscosity, and high water content air freshener compositions

Abstract

An alcohol free, low viscosity, and high-water content air freshener composition is provided. The transparent microemulsion system is stable at a broad range of temperatures. The main ingredient of the composition is water. The composition is free of conventionally-used amphiphilic surfactants including ionic and non-ionic surfactants. The composition contains an oil phase, an aqueous phase and at least one glycol ether solvent. The system is compatible for a wide scope of water-immiscible ingredients that are used in fragrances and flavors.

Claims

1. An air freshener system consisting of: water in a portion by weight of between 40% and 60%; water-immiscible oil in a portion by weight of between 0.01% and 40%; and glycol ether in a portion by weight of between 10% and 70%, where the glycol ether has a lipophilic aliphatic chain comprising between 1 to 6 carbons and a hydrophilic chain comprising between 1 and 3 glycol units.

2. The system of system of claim 1, where: the glycol units are ethylene glycol units.

3. The system of system of claim 1, where: the glycol units are propylene glycol units.

4. The system of system of claim 1, where: the glycol ether is diethylene glycol mono butyl ether.

5. The system of system of claim 1, where: the glycol ether comprises a phenyl ring.

6. The system of system of claim 1, where: the glycol ether comprises a polyaromatic ring.

7. The system of claim 1, where: the water-immiscible oil is present in a portion by weight of between 0.01% and 20%.

8. The system of claim 1, Where: the water is present in a portion by weight of between 50% and 50%.

9. The system of claim 1, where: the water comprises at least one of tap water, deionized water, and distilled water.

10. The system of claim 1, where: the glycol ether has a calculated HLB value between 12 and 16.

11. An air freshener base consisting of: water in a portion by weight of between 40% and 60%; glycol ether in a portion by weight of between 40% and 60%; and a preservative in a portion by weight of between 0.1% and 2.0%, where the glycol ether has a lipophilic aliphatic chain comprising between 1 to 6 carbons and a hydrophilic chain comprising between 1 and 3 glycol units.

12. The air freshener base of claim 1, where: the glycol ether is diethylene glycol mono butyl ether.

13. The air freshener base of claim 1, where: the glycol ether is dipropylene glycol mono n-hexyl ether.

14. An air freshener system consisting of: water in a portion by weight of between 40% and 60%; water-immiscible oil in a portion by weight ot between 0.01% and 40%; and glycol ether in a portion by weight of between 10% and 70%, where the glycol ether has hydrophilic-lipophilic balance between 12 and 16.

15. The system of system of claim 14, where: the glycol ether is diethylene glycol mono butyl ether.

16. The system of system of claim 14, where: the glycol ether is dipropylene glycol mono n-hexyl ether.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

(1) FIG. 1 shows the hydrophilic and lipophilic ends of diethylene glycol mono n-butyl ether.

(2) FIG. 2 shows the hydrophilic and lipophilic ends of dipropylene glycol mono n-hexyl ether.

(3) FIG. 3 shows an oil-in-water microemulsion in which a micelle is stabilized by an interfacial glycol ether.

DETAILED DESCRIPTION OF THE INVENTION

(4) It has been surprisingly found that a stable, optically clear microemulsion can be prepared by a glycol ether solvent without using any short chain alcohols or traditional amphiphilic surfactants. While glycol ethers have been used as co-solvents or solubilizing aids, glycol ethers have never been used as the only ingredients to solubilize water-immiscible oils. This unexpected discovery can be explained by the amphiphilic properties of glycol ethers. Glycol ethers comprises of two parts for each molecule. The poly-ol chain represents the hydrophilic part of the molecule. The linear or branched alkyl chain or phenyl group represents the lipophilic part of the molecule. For example, FIG. 1 shows a molecule of diethylene glycol mono n-butyl ether 100 having a lipophilic end 101 and a hydrophilic end 102. Similarly, FIG. 2 shows a molecule of dipropylene glycol mono n-hexyl ether 200 having a lipophilic end 201 and a hydrophilic end 202. FIG. 3 shows a swollen micelle 300 having an oil phase 301 inside micelle 300, a water phase 302 outside micelle 300, and an interfacial layer 303 that is composed of glycol ethers which stabilize micelle 300. Without this interfacial layer 303, oil droplets will coalesce and eventually separate out from the water phase. In a mixture comprising a plurality of micelle 300 structures, if each micelle 300 has a size of less than 100 nm, the whole mixture is a transparent microemulsion.

(5) The hydrophilic-lipophilic balance (HLB) metric measures the hydrophilicity versus the lipophilicity of a surfactant according to equation 1:

(6) $\begin{array}{cc}HLB=20\times \frac{M_H}{M}& \left(\mathrm{eq}.1\right)\end{array}$
where M.sub.H is the molecular mass of the hydrophilic part of the molecule and M is the molecular mass of the whole molecule. An HLB value less than 10 generally means that the molecule will be more lipid-soluble/water-insoluble while an HLB value more than 10 generally means that the molecule will be more water-soluble/lipid-insoluble. Traditional surfactants used to solubilize fragrance oils typically have HLB values ranging from 12 to 16.

(7) The inventors have found that certain glycol ethers may have similar HLB values, and as such, may be used to solubilize fragrance oils. The following lists a number of commercially-available glycol ethers and their calculated HLBs using equation 1:

(8) TABLE-US-00001 Chemical Nomenclature Calculated HLB ethylene glycol propyl ether 11.7 ethylene glycol n-butyl ether 10.3 ethylene glycol hexyl ether 8.4 ethylene glycol phenyl ether 8.8 diethylene glycol ethyl ether 15.7 diethylene glycol n-butyl ether 13.0 diethylene glycol hexyl ether 11.1 diethylene glycol phenyl ether 11.5 propylene glycol methyl ether 16.7 propylene glycol n-propyl ether 12.7 propylene glycol n-butyl ether 11.4 propylene glycol phenyl ether 9.9 dipropylene glycol methyl ether 18.0 dipropylene glycol n-propyl ether 15.1 dipropylene glycol n-butyl ether 14.0 dipropylene glycol phenyl ether 12.7

(9) In addition to having HLB values similar to those of traditional surfactants, certain glycol ethers have molecular structures that enhance their use as solubilizing agents. More preferably, mono-, di- or polyethylene glycol chains are linear structure and are easy to pack together in a microenvironment such as micelles. Less preferably, mono-, di- or polypropylene glycols have branched chains, making them more difficult to pack together in a microenvironment.

(10) Further, in addition to having favorable HLB values and molecular structures, the size of the hydrophilic and lipophilic portions of the molecule play a role in the usefulness of glycol ethers as solubilizing agents. By way of example and not limitation, the hydrophilic part of the molecule may have 1 to 3 ethylene glycol or propylene units and the lipophilic part may be a linear or branched alkyl group with 1 to 6 carbons and may include a substituted or unsubstituted aromatic group.

(11) Without limiting the solubilizing effect to a particular mechanism, the inventors believe that this combination of the balance of the hydrophilic to lipophilic portions, the shape of the molecule, and the size of the molecule gives certain glycol ethers solubilizing characteristics that are comparable to traditional surfactants agents without the unfavorable characteristics such as low diffusibility, high viscosity, and/or high foaming.

(12) The inventors have identified the following glycol ethers as having the right combination of HLB, shape, and size to be suitable for use as solubilizing agents in fragrance systems: ethylene glycol propyl ether, ethylene glycol n-butyl ether, ethylene glycol hexyl ether, ethylene glycol phenyl ether, diethylene glycol ethyl ether, diethylene glycol n-propyl ether, diethylene glycol n-butyl ether, diethylene glycol n-pentyl ether, diethylene glycol hexyl ether, diethylene glycol phenyl ether, propylene glycol methyl ether, propylene glycol n-propyl ether, propylene glycol n-butyl ether, propylene glycol phenyl ether, dipropylene glycol methyl ether, dipropylene glycol n-propyl ether, dipropylene glycol n-butyl ether, dipropylene glycol phenyl ether, tripropylene glycol methyl ether and tripropylene glycol methyl ether. These glycol ethers are commercially available by Dow Chemicals under the names of Cellosolve™, Carbitol™ and Dowanol™. This list is exemplary only, and one of ordinary skill in the art could, without undue experimentation, find additional glycol ethers that are suitable for use in solubilizing fragrance oils.

(13) The following exemplar compositions demonstrate embodiments of the present invention using various glycol ethers and fragrance oils, in combination with water and, in some cases, other ingredients common to fragrance systems.

(14) Example 1 uses the fragrance BAC1342 formulated according to the following:

(15) TABLE-US-00002 CAS Percentage Ingredients number by weight Ambroxan 6790-58-5 0.0500 Cedrol crystals 77-53-2 0.6000 Aldehyde C06 10% BB MIXTURE 0.1000 Aldehyde C18 104-61-0 1.5000 Allyl cyclohexyl propionate 2705-87-5 1.0500 Amber core 139504-68-0 0.8000 Benzylaldehyde 100-52-7 0.0700 Benzyl acetate 140-11-4 2.4000 Boisamrene forte 58567-11-6 3.1000 Cardamon W.I. Oil 8000-66-6 0.0600 Beta caryophellene 87-44-5 0.8500 Cashmeran 33704-61-9 1.2500 Cedramber 19870-74-7 0.7500 Cis jasmone 488-10-8 0.0500 Dihydro myrcenol 18479-58-8 2.3500 Ebanol 67801-20-1 2.1600 Ethyl linanool 10339-55-6 6.2000 Eugenol 97-53-0 0.2100 Floralozone 67634-15-5 0.4000 Gamma octalactone 104-50-7 1.9300 Gurjon balsam oil 8030-55-5 0.2000 Hedione 24851-98-7 9.1500 Hexyl cinnamic aldehyde 101-86-0 4.3500 Kephalis 36306-87-3 0.7300 Koumalactone 10% IN TEC MIXTURE 0.9700 Methyl ionone gamma 70~ 127-51-5 6.2000 Methyl laitone 10% DPG MIXTURE 0.6800 Methyl pample mousse 67674-46-8 1.2100 Styrallyl acetate 93-92-5 0.1800 Timbersilk 54464-57-2 9.6500 DPG—Dipropylene glycol 110-98-5 40.8000

(16) To demonstrate the efficacy of the use of glycol ethers as the solubilizing agent for the freshener oil, three freshener compositions were prepared using BAC1342 at 20% by weight. Two of the compositions used traditional used surfactants (polysorbate 20 and octylphenol oxylate), and the third used a glycol ether (diethylene glycol mono butyl ether). The appearances of the compositions were recorded and their viscosities were measured using a Brookfield Rotational Viscometer with Spindle #1 and Rotational Speed at 12 RPM:

(17) TABLE-US-00003 Air Freshener Compositions Viscosity Ingredients % by weight Appearance (cps) Sample # 1 BAC1342 20 transparent, 10.0 Diethylene glycol mono 35 macroscopically butyl ether* one phase Distilled water 45 Sample # 2 BAC1342 20 translucent, 169.0 Polysorbate 20** 35 separated into Distilled water 45 two phases Sample # 3 BAC1342 20 cloudy 186.0 Octylphenol ethyoxylate*** 35 Distilled water 45 *Commercially available as Butyl Carbitol from Dow Chemical Company **Commercially available as Tween 20 from Croda ***Commercially available as Triton X-100 from Dow

(18) Both of the prior art surfactants fail to form transparent microemulsion with 20% BAC1342 in distilled water. Additionally, both compositions demonstrate high viscosities preventing their applications in air freshener formats such as room sprays. Unexpectedly, the diethylene glycol mono butyl ether forms clear microemulsion with such high level of fragrance oil without any other surfactants. The viscosity is low enough to be applied in various formats such as room sprays and plug-ins.

(19) Example 2 combines the following:

(20) TABLE-US-00004 Percentage Ingredients by weight Hydroxycitronellol 25 Diethylene glycol mono butyl ether 25 Distilled water 50

(21) Hydroxycitronellol has a clogP of 1.55 and its water solubility is 393 mg/L at 25° C. The procedure to prepare the clear microemulsion is independent on the order of addition. In this case, diethylene glycol mono butyl ether is premixed with distilled water. Then hydroxycitronellol is added. The formation of microemulsion seems spontaneous. Using a shaker or rocker, the mixture turns perfectly clear after 5-30 minutes of agitation.

(22) Example 3 combines the following:

(23) TABLE-US-00005 Percentage Ingredients by weight Methyl dihydrojasmonate* 15 Diethylene glycol mono butyl ether 35 Distilled water 50 *Commercially available as Hedione ® from Firmenich

(24) Methyl dihydrojasmonate is a widely used fragrance ingredient. It has a clogP of 2.65 and its water solubility is 91.7 mg/L at 25° C. Methyl dihydrojasmonate is premixed with diethylene glycol mono butyl ether, followed by addition of distilled water. The mixture turns perfectly clear after 5-30 minutes of agitation.

(25) Example 4 combines the following:

(26) TABLE-US-00006 Percentage Ingredients by weight 3-(4-tert-butylphenyl)butanal* 10 Diethylene glycol mono butyl ether 40 Distilled water 50 *Commercially available as Lilial ® from IFF

(27) 3-(4-tert-butylphenyl)butanal has a clogP of 4.22 and its water solubility is 38 mg/L at 25° C. 3-(4-tert-butylphenyl)butanal is premixed with diethylene glycol mono butyl ether, followed by addition of distilled water. The mixture turns perfectly clear after 5-30 minutes of agitation.

(28) Example 5 combines the following:

(29) TABLE-US-00007 Percentage Ingredients by weight Beta-caryophyllene 2 Diethylene glycol mono butyl ether 49 Distilled water 49

(30) Beta-caryophyllene is among the mostly hydrophobic fragrance ingredients. It is composed entirely of hydrocarbons and has a clogP of 6.3. It has no functional groups to form hydrogen bonds with water molecules. Its water solubility is merely 0.05 mg/L at 25° C. The beta-caryophyllene is premixed with diethylene glycol mono butyl ether, followed by addition of distilled water. The mixture turns perfectly clear after 5-30 minutes of agitation.

(31) Example 6 combines the following:

(32) TABLE-US-00008 Percentage Ingredients by weight BAC1342 20 Diethylene glycol mono butyl ether 35 Imidazolidinyl urea* 0.3 Distilled water 44.7 *Commercially available as Iscarguard DU from ISCA

(33) BAC1342 is premixed with the diethylene glycol mono butyl ether, the imidazolidinyl urea is added to distilled water, and the oil phase and the water phase are mixed. The mixture turns perfectly clear after 5-30 minutes of agitation, and the imidazolidinyl urea acts as a preservative to control microbial growth.

(34) Example 7 combines the following:

(35) TABLE-US-00009 Percentage Ingredients by weight BAC1342 20 Diethylene glycol mono butyl ether 35 Imidazolidinyl urea 0.3 Yellow water-soluble dye 0.1 Distilled water 44.6

(36) The imidazolidinyl urea and the yellow dye are added to distilled water and mixed well, the BAC1342 is added to the diethylene glycol mono butyl ether, and the oil phase and the water phase are mixed. The mixture turns perfectly clear after 5-30 minutes of agitation, and the imidazolidinyl urea and the yellow dye provide microbial control and color respectively.

(37) Example 8 combines the following:

(38) TABLE-US-00010 Percentage Ingredients by weight BAC1342 20 Diethylene glycol mono butyl ether 35 Imidazolidinyl urea 0.3 Yellow water-soluble dye 0.1 Rose essential water* 44.6 *Commercially available from Carrubba Inc.

(39) The imidazolidinyl urea and the yellow dye are added to the Rose Essential Water and mixed well, the BAC1342 is added to the diethylene glycol mono butyl ether, and the oil phase and the water phase are mixed. The mixture turns perfectly clear after 5-30 minutes of agitation.

(40) The foregoing embodiments provide a sampling of embodiments of the present invention. Based on the present disclosure, one of ordinary skill in the art could readily develop other fragrance systems by substituting glycol ethers, modifying the percentages of the components, adding or substituting other dyes, microbial control agents, and other ingredients typically found in fragrance systems, and so on, provided that such fragrance systems are free of (or substantially free of) alcohols or other volatile materials and have high diffusibility, low viscosity, and low foaming characteristics.