| Patent Number |
Title Of Patent |
Date Issued |
| 7202198 |
Substituted phenolic composition and process for using same for inhibiting malodours |
April 10, 2007 |
| Described is a process for reducing a malodour formed as a result of fatty acid derivative degradation and/or organic amine degradation taking place in a fabric care base contained in a fabric article or in a cosmetic or therapeutic base adsorbed on the human epidermis by treating the |
| 7201915 |
Polyamide stick dispensing product and method of use |
April 10, 2007 |
| Described for the purpose of application to an inanimate laminar substantially solid surface is a substantially hydrocarbon-free functional substance-providing stick article having consistently-maintained functional composition integrity comprising a stiff, substantially monophasic, |
| 7172998 |
Fragrance material |
February 6, 2007 |
| Non-aqueous based fragrance compositions containing a siloxane material are disclosed. The fragrance compositions are suitable for many applications including cosmetics, laundry care and personal care items. The fragrance compositions can also be used in air fresheners, particularly |
| 6861031 |
Fragrance material |
March 1, 2005 |
| Non-aqueous based fragrance compositions containing a siloxane material are disclosed. The fragrance compositions are suitable for many applications including cosmetics, laundry care and personal care items. The fragrance compositions can also be used in air fresheners, particularly thos |
| 6844302 |
Encapsulated flavor and fragrance |
January 18, 2005 |
| The present invention provides solid complexes of urea and flavor and fragrance chemicals as well as methods of providing the complexes. The complexes are advantageously incorporated in powdered detergent and bleach products. The urea complexes protect the flavor or fragrance molecules |
| 6808684 |
Fragrance material |
October 26, 2004 |
| Non-aqueous based fragrance compositions containing a siloxane material are disclosed. The fragrance compositions are suitable for many applications including cosmetics, laundry care and personal care items. The fragrance compositions can also be used in air fresheners, particularly thos |
| 6610647 |
Fragrance molecule |
August 26, 2003 |
| The present invention is directed to the use of insoluble acesulfame in creating fragrances and scents in such items as perfumes, colognes, toilet waters, cleaning products and personal care products. |
| 6506723 |
Single phase aqueous surfactant-free nontoxic air freshening composition and wick-containing air |
January 14, 2003 |
| Described is a single phase aqueous surfactant-free nontoxic air freshening composition containing 30-70% water, 5-20% of a fragrance, at least 60% of the components of which has a C log.sub.10 P.ltoreq.2.5 and 30-60 weight percent of a mixture of two glycol ether components: (i) dipr |
| 6468949 |
Cyclohexenyl cyclopropyl ketone |
October 22, 2002 |
| The present invention is directed to cyclopropyl-2,6,6-trimethylcyclohex-3-enyl ketone and is use in creating perfumes and scents in such items as perfumes, colognes, toilet water and personal care products. |
| 6437183 |
Method for making amides |
August 20, 2002 |
| The invention relates to the manufacture of amide compounds provided through the reaction of nitrile compounds and a sulfate compound to form the related amide compound. In a preferred embodiment a diol or a triol is employed as a solvent, thereby increasing the yield of the product. |
| 6371049 |
Animal litter |
April 16, 2002 |
| Odor-inhibiting materials comprising litter containing an odor-inhibiting quantity of western juniper. The litter materials of the present invention are advantageous in that they can be used as animal bedding and the like to mask or prevent the formation of undesirable odors in animal |
| 6303817 |
Method for making amides |
October 16, 2001 |
| The invention relates to the manufacture of amide compounds provided through the reaction of nitrile compounds and a sulfate compound to form the related amide compound. In a preferred embodiment a diol or a triol is employed as a solvent, thereby increasing the yield of the product. |
| 6180595 |
Single phase aqueous surfactant-free nontoxic air freshening composition and wick-containing air |
January 30, 2001 |
| Described is a single phase aqueous surfactant-free nontoxic air freshening composition containing 30-70% water, 5-20% of a fragrance, at least 60% of the components of which has a C log.sub.10 P.ltoreq.2.5 and 30-60 weight percent of a mixture of two glycol ether components:(i) dipropyl |
| 6165452 |
Cyclic trimers of aldehydes, organoletpic uses thereof and process for preparing same |
December 26, 2000 |
| Described are novel aldehyde cyclic trimers which are useful for controllably releasing fragrance composition components into the environment surrounding the location of said trimers. The trimers are particularly useful in effecting malodor elimination from solid or semisolid surface |
| 6051548 |
Trimethylcyclohexenylcyclopropyl ketones perfume composition |
April 18, 2000 |
| Described are trimethylcyclohexenylcyclopropyl ketones having the structure: ##STR1## wherein one of the dashed lines is a carbon--carbon double bond and the other of the dashed lines is a carbon--carbon single bond, uses thereof in augmenting, enhancing or imparting aromas in or |
| 6025527 |
Trimethylcyclohexenylcyclopropyl ketones, process for producing same, and uses thereof in perfum |
February 15, 2000 |
| Described are trimethylcyclohexenylcyclopropyl ketones having the structure: ##STR1## wherein one of the dashed lines is a carbon--carbon double bond and the other of the dashed lines is a carbon--carbon single bond, uses thereof in augmenting, enhancing or imparting aromas in or |
| 5711952 |
Use of 7-isopropyl - -8, 8-dimethyl-6, 10-dioxaspiro-C.sub.10 and C.sub.11 alkane derivatives fo |
January 27, 1998 |
| Described is the use of 7-isopropyl-8,8-dimethyl-6,10-dioxaspiro-C.sub.10 and C.sub.11 alkane derivatives defined according to the structure: ##STR1## wherein N is 1 or 2 for their organoleptic properties, particularly for use in imparting, augmenting or enhancing the aroma of a perf |
| 5665697 |
Use of 1 (3H)-isobenzofuranone in perfumery |
September 9, 1997 |
| Described is the use of 1(3H)-isobenzofuranone having the structure: ##STR1## in augmenting, enhancing or imparting aromas in or to perfume compositions, colognes and perfumed articles. |
| 5633236 |
Insect repellent compositions and methods for using same |
May 27, 1997 |
| Described is a method of repelling Musca domestica L.(Diptera:Muscidae), Aedes aegypti, Culex nigripalpus, Aedes atlanticus, Culex salinarius, Aedes vexans, Culex spp., Simulium spp., Psoroferia ferox, Aedes infirmatus, Drosophila melanogaster, Coccinellidae, Anopheles crucians, Psor |
| 5599960 |
3,5-dimethyl-pentenyl-dihydro-2(3H)-furanone isomer mixtures, organoleptic uses thereof, process |
February 4, 1997 |
| Described are 3,5-dimethyl-pentenyl-dihydro-2(3H)-furanone isomer mixtures defined according to the structure: ##STR1## wherein structure represents mixtures wherein in the mixture in each of the compounds, one of the dashed lines represents a carbon-carbon double bond and the ot |
| 5583237 |
3,5-dimethyl-pentenyl-dihydro-2(3H)-furanone isomer mixtures, organoleptic uses thereof, process |
December 10, 1996 |
| Described are 3,5-dimethyl-pentenyl-dihydro-2(3H)-furanone isomer mixtures defined according to the structure: ##STR1## wherein structure represents mixtures wherein in the mixture in each of the compounds, one of the dashed lines represents a carbon-carbon double bond and the ot |
| 5521165 |
Insect repellent compositions and methods for using same |
May 28, 1996 |
| Described is a method of repelling Musca domestica L. (Diptera:Muscidae), Aedes aegypti, Culex nigripalpus, Aedes atlanticus, Culex salinarius, Aedes vexans, Culex spp., Simulium spp., Psoroferia ferox, Aedes infirmatus, Drosophila melanogaster, Coccinellidae, Anopheles crucians, Pso |
| 5478803 |
3,5-dimethyl-pentenyl-dihydro-2(3H)-furanone isomer mixtures, organoleptic uses thereof, process |
December 26, 1995 |
| Described are 3,5-dimethyl-pentenyl-dihydro-2(3H)-furanone isomer mixtures defined according to the structure: ##STR1## wherein structure represents mixtures wherein in the mixture in each of the compounds, one of the dashed lines represents a carbon-carbon double bond and the ot |
| 5366959 |
Mixtures of 2-(2-bornyloxy)-ethyl-1-ethanols and perfumery uses thereof |
November 22, 1994 |
| Described are mixtures of 2-(2-bornyloxy)-ethyl-1-ethanols defined according to the structure: ##STR1## which represents a mixture wherein in the mixture one of R.sub.1 or R.sub.2 is ethyl and the other of R.sub.1 or R.sub.2 is hydrogen, and organoleptic uses thereof in augmentin |
| 5358930 |
2-ethoxy-4-formyl phenyl ester of propionic acid and use in augmenting or enhancing the aroma of |
October 25, 1994 |
| Described is 2-ethoxy-4-formyl phenyl ester of propionic acid of our invention defined according to the structure: ##STR1## and uses thereof in augmenting or enhancing the aroma of perfume compositions, perfumed articles and colognes. |
| 5321164 |
Use in perfumery of 2(1-vinyl-5-hexenyl) cyclopentanone, a process for preparing same, and proce |
June 14, 1994 |
| Described is the 2(1-vinyl-5-hexenyl)cyclopentanone having the structure: ##STR1## a process for preparing same by reacting the compound having the structure: ##STR2## with the compound having the structure: ##STR3## and then heating the resulting intermediate, and organo |
| 5300489 |
Fragrance use of dihydromethyl jasmonic acid |
April 5, 1994 |
| Described in the use of dihydromethyl jasmonic acid having the structure: ##STR1## in augmenting, enhancing or imparting fragrances in or to perfume compositions, perfumed articles and colognes. |
| 5283237 |
Use in perfumery of 2(1-vinyl-5-hexenyl) cyclopentanone, a process for preparing same, and proce |
February 1, 1994 |
| Described is the 2(1-vinyl-5-hexenyl)cyclopentanone having the structure: ##STR1## a process for preparing same by reacting the compound having the structure: ##STR2## with the compound having the structure: ##STR3## and then heating the resulting intermediate, and organo |
| 5227367 |
Oxypentamethylindane carboxaldehydes, methods for preparing same, organoleptic uses thereof and |
July 13, 1993 |
| Described are oxypentamethylindane carboxaldehydes defined according to the generic structure: ##STR1## wherein R' represents a hydrogen or methyl, methods for preparing same, organoleptic uses thereof and cosmetic and pharmaceutical compositions containing them. The oxypentameth |
| 5091200 |
Process for microwave browning uncooked baked goods foodstuffs |
February 25, 1992 |
| Described is a process for producing cooked browned baked goods including the steps of:(a) providing a particulate flowable flavoring powder which contains individually discretly encapsulated Maillard reaction reagents with the reaction reagents being at least one encapsulated amino acid |
| 5077275 |
Acylated bicycloalkadiene-compound-containing compositions of matter process for preparing same |
December 31, 1991 |
| Described are acylated bicycloalkadiene-compound-containing compositions of matter, mixtures of compounds containing predominantly compounds having the structures: ##STR1## with the compositions of matter containing from 50 up to 100% of the compound having the structure: prepar |
| 5075528 |
Apparatus for carrying out microwave browning process |
December 24, 1991 |
| Described is a process for producing a cooked edibly browned storage-stable fibrous proteinaceous muscle tissue foodstuff including the steps of:(a) providing a particulate flowable flavoring powder which contains individually discretly encapsulated Maillard reaction reagents with the re |
| 5059434 |
Microwave browning composition and process for producing the same |
October 22, 1991 |
| Described is a process for producing a cooked edibly browned storage-stable fibrous proteinaceous muscle tissue foodstuff including the steps of:(a) providing a particulate flowable flavoring powder which contains individually discretly encapsulated Maillard reaction reagents with the re |
| 5021184 |
Adamantane derivatives, compositions of matter containing same, processes for preparing said ada |
June 4, 1991 |
| Described are adamantane derivatives defined according to the generic structure: ##STR1## wherein R.sub.1 ' is hydrogen or acetyl; R.sub.2 ' is hydrogen or lower alkyl and the dashed line is a carbon-carbon single bond or a carbon-carbon double bond as well as uses thereof for au |
| 4985261 |
Process for microwave browning proteinaceous fibrous meat products |
January 15, 1991 |
| Described is a process for producing a cooked edibly browned storage-stable fibrous proteinaceous muscle tissue foodstuff including the steps of:(a) providing a particulate flowable flavoring powder which contains individually discretely encapsulated Maillard reaction reagents with the r |
| 4983579 |
Cyano-substituted sulfur containing compounds, compositions containing same, processes for prepa |
January 8, 1991 |
| Described are cyano-substituted sulfur-containing compounds having the structures: ##STR1## as well as organoleptic uses thereof. |
| 4962089 |
Cyano-substituted sulfur-containing compounds, and compositions containing same and organoleptic |
October 9, 1990 |
| Described are cyano-substituted sulfur-containing compounds defined according to a structure selected from the group consisting of: ##STR1## wherein M is an alkali metal as well as uses of the nonionic structures of said group for their organoleptic properties. |
| 4956481 |
Adamantane derivatives, compositions of matter containing same, processes for preparing said ada |
September 11, 1990 |
| Described are hydroxy adamantane compounds and derivatives thereof and a process for preparing same. |
| 4950495 |
Tetrahydro-5-isopropyl-2-methyl-2-thiophene acetonitrile, organoleptic uses thereof and process |
August 21, 1990 |
| Described is the tetrahydro-5-isopropyl-2-methyl-2-thiophene acetonitrile of our invention having the structure: ##STR1## and organoleptic uses thereof in augmenting or enhancing the aroma or taste of perfume compositions, colognes, perfumed articles, foodstuffs and chewing gums. |
| 4914082 |
S(4-hydroxy-1-isopropyl-4-methylhexyl) thioacetate, organoleptic uses thereof and process for pr |
April 3, 1990 |
| Described is the S(4-hydroxy-1-isopropyl-4-methylhexyl) thioacetate having the structure: ##STR1## and uses thereof in augmenting or enhancing the aroma of consumable materials including perfume compositions, colognes, perfumed articles and perfumed polymers. |
| 4906610 |
Tetrahydro-5-isopropyl-2-methyl-2-thiophene acetonitrile, organoleptic uses thereof and process |
March 6, 1990 |
| Described is the tetrahydro-5-isopropyl-2-methyl-2-thiophene acetonitrile of our invention having the structure: ##STR1## and organoleptic uses thereof in augmenting or enhancing the aroma or taste of perfume compositions, colognes, perfumed articles, foodstuffs and chewing gums. |
| 4900718 |
3-(2-bornyloxy)-2-methyl-1-propanol and perfumery uses thereof |
February 13, 1990 |
| Described is 3-(2-bornyloxy)-2-methyl-1-propanol defined according to the chemical structure: ##STR1## and organoleptic uses thereof in augmenting or enhancing the aroma of perfume compositions, colognes and perfumed articles including but not limited to solid or liquid anionic, |
| 4886897 |
S(4-hydroxy-1-isopropyl-4-methylhexyl) thioacetate |
December 12, 1989 |
| Described is the S(4-hydroxy-1-isopropyl-4-methylhexyl) thioacetate having the structure: ##STR1## and uses thereof in augmenting or enhancing the aroma of consumable materials including perfume compositions, colognes, perfumed articles and perfumed polymers. |
| 4883884 |
Tetrahydro-5-isopropyl-2-methyl-2-thiophene acetonitrile, organoleptic uses thereof and process |
November 28, 1989 |
| Described is the tetrahydro-5-isopropyl-2-methyl-thiophene acetonitrile of our invention having the structure: ##STR1## and organoleptic uses thereof in augmenting or enhancing the aroma or taste of perfume compositions, colognes, perfumed articles, foodstuffs and chewing gums. |
| 4772583 |
Beta-alkylidene phenethyl alcohol esters and ethers, organoleptic uses thereof and processes for |
September 20, 1988 |
| Described is the novel compound genus the beta-alkylidene phenethyl alcohol esters and ethers of our invention defined according to the generic structure: ##STR1## wherein R.sub.5 represents hydrogen or methyl; wherein R.sub.6 represents one of the moieties: ##STR2## wher |
| 4751933 |
Use of hydroxybornyloxybutanes in augmenting or enhancing the aroma or taste of smoking tobacco |
June 21, 1988 |
| Described are the uses of mixtures of hydroxybornyloxybutanes defined according to the generic structure: ##STR1## wherein in the mixture in each of the compounds one or R.sub.1 or R.sub.2 is methyl and the other of R.sub.1 or R.sub.2 is hydrogen in augmenting or enhancing the ar |
| 4742044 |
Aralkoxy, alkoxy, alkadienyloxy and alkenyloxy-1,3,2-dioxaborinane derivatives and uses thereof |
May 3, 1988 |
| Described are the aralkoxy, alkoxy, alkadienyloxy and alkenyloxy-1,3,2-dioxaborinane derivatives defined according to the genus: ##STR1## (wherein R.sub.1, R.sub.2, R.sub.3 and R.sub.4 are the same or different hydrogen, methyl and ethyl; and wherein R represents C.sub.6 straight |
| 4720481 |
Cyclohexenyl pyridine derivatives, organoleptic uses of same and processes for preparing same |
January 19, 1988 |
| Described are cyclohexenyl pyridine derivatives defined according to the structures: ##STR1## formed in admixture when vinyl pyridine having the structure: ##STR2## is reacted with 2-methyl-1,3-pentadiene having the structure: ##STR3## as well as organoleptic uses thereof |
| 4715981 |
Process for augmenting or enhancing the aroma of detergents using mixtures of hydroxybornyloxybu |
December 29, 1987 |
| Described are mixtures of hydroxybornyloxybutanes defined according to the generic structure: ##STR1## wherein in the mixture in each of the compounds one of R.sub.1 or R.sub.2 is methyl and the other of R.sub.1 or R.sub.2 is hydrogen as well as methods for augmenting or enhancin |
| 4681976 |
Process for preparing alkyl substituted and unsubstituted para-carboalkoxy cyclohexanones |
July 21, 1987 |
| Described are para-carboalkoxy cyclohexanones defined according to the structure: ##STR1## wherein R.sub.1 represents hydrogen or C.sub.1 -C.sub.7 alkyl and R.sub.2 represents methyl or ethyl and uses thereof in augmenting or enhancing the aroma of consumable materials including |
