The present invention relates to the field of perfumery. More particularly, it concerns polymers derived from siloxane derivatives and comprising at least one β-thio carbonyl moiety capable of liberating an active molecule such as, for example, an α,β-unsaturated ketone or aldehyde. The present invention concerns also the use of polymers in perfumery as part of a perfuming or malodor counteracting composition as well as the perfuming compositions or perfumed articles comprising the invention's compounds.

A compound represented by the formula I

##STR00001##

wherein
is indicating a double bond either at C4 or at C5, or single bonds,
R.sub.1, R.sub.2, R.sub.3, R.sub.4 are independently selected from H or Me, and
R.sub.5, R.sub.6 are independently selected from Me or Et,
and wherein the compound is not 9-hydroxy-5,9-dimethyldec-4-enal or 9-hydroxy-5,9-dimethyldecanal.

Said compounds are useful as perfume ingredients in personal care and household care products.

A compound according to formula IIa, which is (S,Z)-3,7-dimethylnon-6-en-1-ol and its use as fragrance.

##STR00001##

A novel fragrance carrier comprising 1,2,3-triacetoxypropane (triacetin) of formula I:

##STR00001##

A novel fragrance carrier comprising 1,2,3-triacetoxypropane (triacetin) of formula I:

##STR00001##

The microcapsules and process of making describe a novel core shell microcapsule. The microcapsule incorporates a polysaccharide such as chitosan into the microcapsule wall forming the shell. The microcapsule shell is formed by dissolving chitosan into a material of structure ##STR00001##
wherein each R is independently selected from hydrogen, C.sub.1 to C.sub.8 alkyl, or a cyano group; and each y is independently an integer from 1 to 8, and reacting with a multifunctional (meth)acrylate.

The microcapsules and process of making describe a novel core shell microcapsule. The microcapsule incorporates a polysaccharide such as chitosan into the microcapsule wall forming the shell. The microcapsule shell is formed by dissolving chitosan into a material of structure ##STR00001##
wherein each R is independently selected from hydrogen, C.sub.1 to C.sub.8 alkyl, or a cyano group; and each y is independently an integer from 1 to 8, and reacting with a multifunctional (meth)acrylate.

Disclosed is a composition including controlled release particles, wherein each of the controlled release particles includes: (a) a core including at least one hydrophobic active ingredient; and (b) a wall at least partially surrounding the core and including the reaction products of: (i) an organofunctional silane; (ii) an epoxy; (iii) an amine; (iv) an isocyanate; (v) an epoxide curing agent; wherein the controlled release particles are effective to retain the at least one hydrophobic active ingredient upon exposure to water and effective to release the at least one hydrophobic active ingredient in response to friction. A method for preparing the composition is also disclosed.

Disclosed is a composition including controlled release particles, wherein each of the controlled release particles includes: (a) a core including at least one hydrophobic active ingredient; and (b) a wall at least partially surrounding the core and including the reaction products of: (i) an organofunctional silane; (ii) an epoxy; (iii) an amine; (iv) an isocyanate; (v) an epoxide curing agent; wherein the controlled release particles are effective to retain the at least one hydrophobic active ingredient upon exposure to water and effective to release the at least one hydrophobic active ingredient in response to friction. A method for preparing the composition is also disclosed.

An encapsulated perfume composition wherein the shell contains a polyurea resin and the core contains a perfume comprising an aldehyde-containing perfume ingredient or ingredients, a non-aromatic cyclic perfume ingredient, and an alkyl salicylate and/or a 2,2,2-trisubstituted acetal,