Abstract: A method of preparing an alkoxy-functional organosilicon compound is provided. The method comprises reacting (A) an initial organosilicon compound and (B) an alcohol component in the presence of (C) a catalyst, thereby preparing the alkoxy-functional organosilicon compound. The initial organosilicon compound (A) comprises at least one alkoxysilyl group. The alcohol component (B) comprises an organic alcohol. The catalyst (C) comprises (C1) an ammonium carboxylate compound or (C2) a titanate compound. A reaction product comprising an alkoxy-functional organosilicon compound prepared in accordance with the method, and a composition comprising the reaction product, are also provided. The alkoxy-functional organosilicon compound, and the reaction product and composition comprising the same, are prepared in increased purity under functional group-tolerant conditions.

Abstract: A silicon glycan is provided. The silicon glycan comprises a glycoside moiety, independently selected organosilicon moieties, and beta-amino alcohol moieties joining the organosilicon moieties to the glycoside moiety. The glycoside moiety comprises independently selected saccharide moieties, which may be substituted with hydrocarbyl groups, ether moieties, and/or amine moieties. A method of preparing the silicon glycan is also provided. The method includes reacting (A) an aminoethyl polysaccharide and (B) an epoxide-functional organosilicon compound, to give the silicon glycan. The method may include preparing the aminoethyl polysaccharide (A) by first reacting (At) a hydroxyl-functional polysaccharide and (A2) an aziridinium halide compound to give the aminoethyl polysaccharide (A).

Abstract: A method of preparing an alkoxy-functional organosilicon compound is provided. The method comprises reacting (A) an initial organosilicon compound and (B) an alcohol component in the presence of (C) a catalyst, thereby preparing the alkoxy-functional organosilicon compound. The initial organosilicon compound (A) comprises at least one alkoxysilyl group. The alcohol component (B) comprises an organic alcohol. The catalyst (C) comprises (C1) an ammonium carboxylate compound or (C2) a titanate compound. A reaction product comprising an alkoxy-functional organosilicon compound prepared in accordance with the method, and a composition comprising the reaction product, are also provided. The alkoxy-functional organosilicon compound, and the reaction product and composition comprising the same, are prepared in increased purity under functional group-tolerant conditions.

Abstract: A method of preparing an alkoxy-functional organosiloxane compound is provided. The method comprises reacting (A) an initial organosiloxane compound and (B) an alcohol component in the presence of (C) a catalyst and, optionally, (D) an organosilicon compound, thereby preparing the alkoxy-functional organosiloxane compound. The initial organosiloxane compound (A) comprises at least one silanol group. The alcohol component (B) comprises an organic alcohol. The catalyst (C) comprises an ammonium carboxylate compound. The organosilicon compound (D), when utilized, comprises at least one alkoxysilyl group. A reaction product comprising an alkoxy-functional organosiloxane compound prepared in accordance with the method, and compositions comprising the reaction product and the alkoxy-functional organosiloxane compound are also provided.

Abstract: A silicon glycan is provided. The silicon glycan comprises a glycoside moiety, independently selected organosilicon moieties, and beta-amino alcohol moieties joining the organosilicon moieties to the glycoside moiety. The glycoside moiety comprises independently selected saccharide moieties, which may be substituted with hydrocarbyl groups, ether moieties, and/or amine moieties. A method of preparing the silicon glycan is also provided. The method includes reacting (A) an aminoethyl polysaccharide and (B) an epoxide-functional organosilicon compound, to give the silicon glycan. The method may include preparing the aminoethyl polysaccharide (A) by first reacting (At) a hydroxyl-functional polysaccharide and (A2) an aziridinium halide compound to give the aminoethyl polysaccharide (A).

Abstract: A composition comprising: an organosilane having formula (I) (I) X-A-Z, wherein X is —SiR4nR2(3-n) wherein each R4 is independently OR1 or halogen, wherein each R1 in independently hydrogen or C1-4 hydrocarbyl and each R2 is independently C1-4 hydrocarbyl, and n is from 1 to 3, A is C1-10 hydrocarbylene, wherein the backbone of the hydrocarbylene is substituted with one or more oxygen atoms, one or more nitrogen atoms, or carbonyl, Z is a sugar group, a monoglycerol group, a diglycerol group, a polyglycerol group, or a xylitol group, and wherein the composition is a personal care composition, surface treating composition, an antifog composition, a coating composition, a surface treated powder, a paint composition, or an ink composition.

Abstract: The present disclosure relates to cosmetic compositions comprising an organosilane (A) having the formula: (R1)n(R2O)(3-n)SiR3O(CH2CH2O)a(C3H6O)bR4 where n is 1, 2, or 3, a?1, b may vary from 0 to 30, with the proviso a?b, R1 is a hydrocarbon group containing 1 to 12 carbon atoms, R2 is hydrogen or an alkyl group containing 1 to 6 carbon atoms, R3 is a divalent hydrocarbon group containing 2 to 12 carbon atoms, R4 is hydrogen, R1, or an acetyl group; and a cosmetic ingredient (B), and optionally in a cosmetically acceptable medium.

Abstract: An organosilane having formula (I) X-A-Z, wherein X is —SiR4nR2(3-n), where each R4 is independently OR1 or halogen, wherein each R1 is independently hydrogen or C1-10 hydrocarbyl and each R2 is independently C1-10 hydrocarbyl, and n is from 1 to 3, A is C1-10 hydrocarbylene, wherein the backbone of the hydrocarbylene is substituted and the substitution comprises one or more oxygen atoms, one or more nitrogen atoms, or carbonyl, Z is a sugar group, a diglycerol group, a polyglycerol group, or a xylitol group, methods of making the organosilane of formula (I), and applications of the organosilane of formula (I).

Abstract: A copolymer of polyalkylphenyl siloxane and alkylfluoroalkyl siloxane obtainable by reacting a dispersion of ingredient (i) an alkylfluoroalkyl siloxane and ingredient (ii) one or more polyalkylphenyl siloxane(s) in the presence of ingredient (iii) a basic catalyst at a temperature of between 40° C. to 300° C.

Abstract: An aminosiloxane polymer includes at least one Si-bonded functional group. This functional group has the chemical formula: —(R—NH)aR1—N(R2)—CH(—COOH)(—R3—C(?O)—NR42) (I). In Formula (I), R is a C1-C10 hydrocarbon group. R1 is a C1-C10 hydrocarbon group. R2 is a hydrogen atom, a C1-C12 hydrocarbon group, or a phenyl group. R3 is a C1-C4 hydrocarbon group. Each R4 is independently a hydrogen atom, a C1-C12 hydrocarbon group, a C1-C12 hydroxyl-hydrocarbon group, or a phenyl group. Moreover, “a” is 0 or 1, such that (R—NH) is optional. The aminosiloxane polymer can be formed using the method of this disclosure and can be formed in, and/or included in, the emulsion of this disclosure.

Abstract: A copolymer of polyalkylphenyl siloxane and alkylfluoroalkyl siloxane obtainable by reacting a dispersion of ingredient (i) an alkylfluoroalkyl siloxane and ingredient (ii) one or more polyalkylphenyl siloxane(s) in the presence of ingredient (iii) a basic catalyst at a temperature of between 40° C. to 300° C.

Abstract: An aminosiloxane polymer includes at least one Si-bonded functional group. This functional group has the chemical formula: —(R—NH)aR1—N(R2)—CH(—COOH)(—R3—C(?O)—NR42) (I). In Formula (I), R is a C1-C10 hydrocarbon group. R1 is a C1-C10 hydrocarbon group. R2 is a hydrogen atom, a C1-C12 hydrocarbon group, or a phenyl group. R3 is a C1-C4 hydrocarbon group. Each R4 is independently a hydrogen atom, a C1-C12 hydrocarbon group, a C1-C12 hydroxyl-hydrocarbon group, or a phenyl group. Moreover, “a” is 0 or 1, such that (R—NH) is optional. The aminosiloxane polymer can be formed using the method of this disclosure and can be formed in, and/or included in, the emulsion of this disclosure.

Abstract: An aminosiloxane polymer includes at least one Si-bonded functional group. This functional group has the chemical formula: —(R—NH)aR1—N(R2)—CH(—COOH)(—R3—C(?O)—NR42) (I). In Formula (I), R is a C1-C10 hydrocarbon group. R1 is a C1-C10 hydrocarbon group. R2 is a hydrogen atom, a C1-C12 hydrocarbon group, or a phenyl group. R3 is a C1-C4 hydrocarbon group. Each R4 is independently a hydrogen atom, a C1-C12 hydrocarbon group, a C1-C12 hydroxyl-hydrocarbon group, or a phenyl group. Moreover, “a” is 0 or 1, such that (R—NH) is optional. The aminosiloxane polymer can be formed using the method of this disclosure and can be formed in, and/or included in, the emulsion of this disclosure.

Abstract: The present disclosure relates to cosmetic compositions comprising an organosilane (A) having the formula: (R1)n(R2O)(3-n)SiR3O(CH2CH2O)a(C3H6O)bR4 where n is 1, 2, or 3, a?1, b may vary from 0 to 30, with the proviso a?b, R1 is a hydrocarbon group containing 1 to 12 carbon atoms, R2 is hydrogen or an alkyl group containing 1 to 6 carbon atoms, R3 is a divalent hydrocarbon group containing 2 to 12 carbon atoms, R4 is hydrogen, R1, or an acetyl group; and a cosmetic ingredient (B), and optionally in a cosmetically acceptable medium.

Abstract: A cosmetic composition comprises a silicone organic elastomer comprising an amino functional group, and at least one cosmetic ingredient, generally in a cosmetically acceptable medium. The silicone organic elastomer is a reaction product of: (A) a linear, branched or cyclic organohydrogensiloxane comprising at least one (1) silicon-bonded hydrogen atom; and (B) a XZ?n derivative comprising at least two (2) unsaturated aliphatic groups; in the presence of (C) a hydrosilylation catalyst. X is an amine group containing compound, Z? is a ring-opened ethylenically-unsaturated epoxide comprising at least one (1) unsaturated aliphatic group and n=1 or 2. A process of preparing the cosmetic composition and method of using the cosmetic composition are also disclosed.

Abstract: A copolymer of polyalkylphenyl siloxane and alkylfluoroalkyl siloxane obtainable by reacting a dispersion of ingredient (i) an alkylfluoroalkyl siloxane and ingredient (ii) one or more polyalkylphenyl siloxane(s) in the presence of ingredient (iii) a basic catalyst at a temperature of between 40° C. to 300° C.

Abstract: A process for preparing an organosilane composition includes reacting a) an organosilane and b) a polyoxyalkylene in the presence of c) a hydrosilylation catalyst. The organosilane a) is of the formula: (R1)(3-n)(R2O)nSiH. R1 is a hydrocarbon group containing 1 to 12 carbon atoms, R2 is hydrogen or an alkyl group containing 1 to 6 carbon atoms, and “n” is 1, 2 or 3. The polyoxyalkylene b) is of the formula: R5O(CH2CH2O)a(C3H6O)bR4. In this formula, a?0 and b?0 with the proviso (a+b)?1. R4 is hydrogen, R1, or an acetyl group. R5 is a hydrocarbon group including a terminal allylic unsaturated group. A composition comprising an organosilane is also disclosed. The organosilane is of the formula: (R1)(3-n)(R2O)nSiR3O(CH2CH2O)a(C3H6O)bR4. Each of “n”, “a”, “b”, R1, R2 and R4 is as defined above. R3 is a divalent hydrocarbon group containing 2 to 12 carbon atoms.

Abstract: The present disclosure relates to compositions comprising an organosilane having the formula; (R1)n(R2O) (3.n)SiR3O(CH2CH2O)a(C3H6O)b R4 where n is 1 or 2, a?1, b may vary from 0 to 30, with the proviso a?b, R1 is a hydrocarbon group containing 1 to 12 carbon atoms, R2 is hydrogen or an alkyl group containing 1 to 6 carbon atoms, R3 is a divalent hydrocarbon group containing 2 to 12 carbon atoms, R4 is hydrogen, R1, or an acetyl group. The present organosilane compositions are particularly useful to treat various surfaces to render them more hydrophilic.

Abstract: A novel saccharide siloxane copolymer has improved stability in the presence of water as compared to certain previously known saccharide siloxanes. The saccharide siloxane copolymer is useful in personal care compositions.

Abstract: The present disclosure relates to cosmetic compositions comprising an organosilane (A) having the formula: (R1)n(R2O)(3?n)SiR3O(CH2CH2O)a(C3H6O)bR4 where n is 1, 2, or 3, a?1, b may vary from 0 to 30, with the proviso a?b, R1 is a hydrocarbon group containing 1 to 12 carbon atoms, R2 is hydrogen or an alkyl group containing 1 to 6 carbon atoms, R3 is a divalent hydrocarbon group containing 2 to 12 carbon atoms, R4 is hydrogen, R1, or an acetyl group; and a cosmetic ingredient (B), and optionally in a cosmetically acceptable medium.