Abstract: Described is a genus of compounds defined according to the structure: ##STR1## wherein Z represents carbinol having the structure: ##STR2## or carboxaldehyde having the structure: ##STR3## and wherein R represents 3-heptanyl or phenyl produced by (i) reacting a carboxylic acid with 2,2-dimethyl-1,3-propanediol to form the compound wherein Z represents carbinol; (ii) and then, if, desired, subsequently reacting the resulting alcohol to form an aldehyde; and organoleptic uses of such compounds in the field of perfumery, colognes and perfumed articles (e.g. perfumed polymers, or solid or liquid anionic, cationic, nonionic or zwitterionic detergents, fabric softener compositions, drier-added fabric softener articles, hair preparations, hair sprays, bath preparations and the like).

Abstract: Described is cyclic carbonate, 4-isopropyl-5,5-dimethyl-m-dioxan-2-one and organoleptic uses thereof in augmenting or enhancing the aroma or taste of consumable materials, foodstuffs, chewing gums, toothpastes, medicinal products, smoking tobaccos, perfume compositions, colognes, perfumed articles (e.g., solid or liquid anionic, cationic, nonionic or zwitterionic detergents, fabric softeners, perfumed polymers and cosmetic powders) smoking tobaccos and smoking tobacco articles.

Abstract: Described is a genus of compounds defined according to the structure: ##STR1## wherein Z represents carbinol having the structure: ##STR2## or carboxaldehyde having the structure: ##STR3## and wherein R represents 3-heptanyl or phenyl produced by (i) reacting a carboxylic acid with 2,2-dimethyl-1,3-propanediol to form the compound wherein Z represents carbinol; (ii) and then, if, desired, subsequently reacting the resulting alcohol to form an aldehyde; and organoleptic uses of such compounds in the field of perfumery, colognes and perfumed articles (e.g. perfumed polymers, or solid or liquid anionic, cationic, nonionic or zwitterionic detergents, fabric softener compositions, drier-added fabric softener articles, hair preparations, hair sprays, bath preparations and the like).

Abstract: Described are the 4-cyclooctenyl lower alkyl carbonates reaction products including a major proportion of said 4-cyclooctenyl alkyl carbonates and a minor proportion of bicyclooctanyl carbonates having the structure: ##STR1## wherein R.sub.5 is methyl or ethyl, said mixture being produced by: first reacting 1,5-cyclooctadiene with formic acid to form a mixture of 4-cyclooctenyl formate in a major proportion and bicyclooctanyl formate in a minor proportion and then reacting the resulting mixture with an alkyl carbonate in the presence of an alkali metal alkoxide to form a mixture of compounds defined above and uses thereof in augmenting or enhancing the aroma of perfume compositions, colognes and perfumed articles such as solid or liquid anionic, cationic, nonionic or zwitterionic detergents, fabric softeners, fabric softener articles, hair sprays, shampoos, bath oils and perfumed polymers.

Abstract: Described is a genus of compounds defined according to the structure: ##STR1## wherein Z represents carbinol having the structure: ##STR2## or carboxaldehyde having the structure: ##STR3## and wherein R represents 3-heptanyl or phenyl produced by (i) reacting a carboxylic acid with 2,2-dimethyl-1,3-propanediol to form the compound wherein Z represents carbinol; (ii) and then, if desired, subsequently reacting the resulting alcohol to form an aldehyde; and organoleptic uses of such compounds in the field of perfumery, colognes and perfumed articles (e.g. perfumed polymers, or solid or liquid anionic, cationic, nonionic or switterionic detergents, fabric softener compositions, drier-added fabric softener articles, hair preparations, hair sprays, bath preparations and the like).

Abstract: Described are branched chain alkenyl methyl carbonates and branched chain alkenyl formates defined according to the structure: ##STR1## wherein R.sub.3 represents hydrogen or methoxy and wherein in each of the molecules described by the structure, one of the dashed lines is a carbon-carbon double bond and each of the other of the dashed lines is a carbon-carbon single bond; and uses of the compounds wherein R.sub.3 is methoxy in augmenting or enhancing the aroma of perfume compositions, colognes and perfumed articles such as solid or liquid anionic, cationic, nonionic or zwitterionic detergents, fabric softener compositions, fabric softener articles, hair sprays, shampoos, bath oils and plastic fragrances.

Abstract: Described is a genus of compounds defined according to the structure: ##STR1## wherein Z represents carbinol having the structure: ##STR2## or carboxaldehyde having the structure: ##STR3## and wherein R represents 3-heptanyl or phenyl produced by (i) reacting a carboxylic acid with 2,2-dimethyl-1,3-propanediol to form the compound wherein Z represents carbinol; (ii) and then, if, desired, subsequently reacting the resulting alcohol to form an aldehyde; and organoleptic uses of such compounds in the field of perfumery, colognes and perfumed articles (e.g. perfumed polymers, or solid or liquid anionic, cationic, nonionic or zwitterionic detergents, fabric softener compositions, drier-added fabric softener articles, hair preparations, hair sprays, bath preparations and the like).

Abstract: Described are the alkyl, aralkyl, alkadienyl and bicycloalkyl methyl carbonates defined according to the structure: ##STR1## wherein R represents 2-ethyl hexyl, having the structure: ##STR2## linalyl having the structure: ##STR3## isobornyl having the structure: ##STR4## or 1-phenylethyl having the structure: ##STR5## and uses thereof in augmenting or enhancing the aroma of perfume compositions, colognes and perfumed articles such as solid or liquid anionic, cationic, nonionic or zwitterionic detergents, fabric softeners, fabric softener articles as well as hair sprays, shampoos, bath oils and perfumed plastics.

Abstract: Described is a process for producing a stable single phase aqueous alkali metal hypochlorite solution having good surface tension properties and optionally having a relatively high viscosity (5-25 centipoises at 20.degree.-40.degree. C.) and having a stable fragrance consisting, in sequential order, of the steps of (a) adjusting the pH of an aqueous alkali metal hypochlorite solution to the range of 11-14.0; (b) admixing a composition of matter selected from the group consisting of: (i) a chemical compound having the structure: ##STR1## wherein at least one of R.sub.1 and R.sub.2 is C.sub.10 -C.sub.12 straight chain or branched chain alkyl and M.sub..alpha. and M.sub..beta. are the same or different and each represents alkali metal selected from the group consisting of lithium, potassium and sodium; and (ii) a mixture of at least one compound having the structure: ##STR2## and a compound having the structure: ##STR3## wherein R.sub.3 "' is straight chain alkyl; wherein more than 55% of the R.sub.

Abstract: Described is a genus of compounds defined according to the structure: ##STR1## wherein Z represents carbinol having the structure: ##STR2## or carboxaldehyde having the structure: ##STR3## and wherein R represents 3-heptanyl or phenyl produced by (i) reacting a carboxylic acid with 2,2-dimethyl-1,3--propanediol to form the compound wherein Z represents carbinol; (ii) and then, if, desired, subsequently reacting the resulting alcohol to form an aldehyde; and organoleptic uses of such compounds in the field of perfumery, colognes and perfumed articles (e.g. perfumed polymers, or solid or liquid anionic, cationic, nonionic or zwitterionic detergents, fabric softener compositions, drier-added fabric softener articles, hair preparations, hair sprays, bath preparations and the like).