MXPA98001663A - Use of alylic alcohol perfumes as agents of reduction of evil or - Google Patents
Use of alylic alcohol perfumes as agents of reduction of evil orInfo
- Publication number
- MXPA98001663A MXPA98001663A MXPA/A/1998/001663A MX9801663A MXPA98001663A MX PA98001663 A MXPA98001663 A MX PA98001663A MX 9801663 A MX9801663 A MX 9801663A MX PA98001663 A MXPA98001663 A MX PA98001663A
- Authority
- MX
- Mexico
- Prior art keywords
- perfume
- mixtures
- alcohol
- smoke
- agents
- Prior art date
Links
- 239000002304 perfume Substances 0.000 title claims abstract description 46
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 title claims description 29
- 239000003795 chemical substances by application Substances 0.000 title description 12
- 239000000203 mixture Substances 0.000 claims abstract description 81
- 235000019645 odor Nutrition 0.000 claims abstract description 24
- 239000000779 smoke Substances 0.000 claims abstract description 24
- OZAIFHULBGXAKX-UHFFFAOYSA-N precursor Substances N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 claims abstract description 23
- GLZPCOQZEFWAFX-JXMROGBWSA-N β-Geraniol Chemical group CC(C)=CCC\C(C)=C\CO GLZPCOQZEFWAFX-JXMROGBWSA-N 0.000 claims abstract description 23
- -1 cooking Substances 0.000 claims abstract description 15
- 238000010411 cooking Methods 0.000 claims abstract description 11
- XXROGKLTLUQVRX-UHFFFAOYSA-N Allyl alcohol Chemical compound OCC=C XXROGKLTLUQVRX-UHFFFAOYSA-N 0.000 claims abstract 7
- 238000004140 cleaning Methods 0.000 claims description 19
- 239000004744 fabric Substances 0.000 claims description 18
- 239000004902 Softening Agent Substances 0.000 claims description 11
- 241000208152 Geranium Species 0.000 claims description 9
- 229940086735 succinate Drugs 0.000 claims description 5
- 230000001476 alcoholic Effects 0.000 claims description 4
- 125000000129 anionic group Chemical group 0.000 claims description 4
- WCOGJMOUNVGCLA-YHARCJFQSA-N bis[(2E)-3,7-dimethylocta-2,6-dienyl] butanedioate Chemical group CC(C)=CCC\C(C)=C\COC(=O)CCC(=O)OC\C=C(/C)CCC=C(C)C WCOGJMOUNVGCLA-YHARCJFQSA-N 0.000 claims description 4
- KDYFGRWQOYBRFD-UHFFFAOYSA-L succinate(2-) Chemical compound [O-]C(=O)CCC([O-])=O KDYFGRWQOYBRFD-UHFFFAOYSA-L 0.000 claims description 4
- 125000000217 alkyl group Chemical group 0.000 claims description 3
- 125000002947 alkylene group Chemical group 0.000 claims description 3
- 125000002091 cationic group Chemical group 0.000 claims description 3
- 125000004122 cyclic group Chemical group 0.000 claims description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 3
- 241000893864 Nerium Species 0.000 claims description 2
- 125000003545 alkoxy group Chemical group 0.000 claims description 2
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 2
- 229910052736 halogen Inorganic materials 0.000 claims description 2
- 150000002367 halogens Chemical class 0.000 claims description 2
- 125000001424 substituent group Chemical group 0.000 claims description 2
- 125000002877 alkyl aryl group Chemical group 0.000 claims 2
- LSNNMFCWUKXFEE-UHFFFAOYSA-L Sulphite Chemical compound [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 claims 1
- 125000003342 alkenyl group Chemical group 0.000 claims 1
- 125000000304 alkynyl group Chemical group 0.000 claims 1
- 125000005025 alkynylaryl group Chemical group 0.000 claims 1
- 125000005418 aryl aryl group Chemical group 0.000 claims 1
- 125000003118 aryl group Chemical group 0.000 claims 1
- QAOWNCQODCNURD-UHFFFAOYSA-L sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims 1
- 150000002148 esters Chemical class 0.000 abstract description 22
- 239000005792 Geraniol Substances 0.000 abstract description 3
- GLZPCOQZEFWAFX-YFHOEESVSA-N Geraniol Natural products CC(C)=CCC\C(C)=C/CO GLZPCOQZEFWAFX-YFHOEESVSA-N 0.000 abstract description 3
- 229930008393 geraniol Natural products 0.000 abstract description 3
- 229940113087 geraniol Drugs 0.000 abstract description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 23
- 239000000047 product Substances 0.000 description 15
- 150000001875 compounds Chemical class 0.000 description 11
- 239000000463 material Substances 0.000 description 11
- 239000002253 acid Substances 0.000 description 10
- 239000004615 ingredient Substances 0.000 description 10
- 238000000034 method Methods 0.000 description 10
- 239000011780 sodium chloride Substances 0.000 description 10
- 235000014113 dietary fatty acids Nutrition 0.000 description 9
- 239000000194 fatty acid Substances 0.000 description 9
- 235000011187 glycerol Nutrition 0.000 description 9
- 229960005150 glycerol Drugs 0.000 description 9
- 239000007788 liquid Substances 0.000 description 9
- 150000003839 salts Chemical class 0.000 description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
- 102000014961 Protein Precursors Human genes 0.000 description 8
- 108010078762 Protein Precursors Proteins 0.000 description 8
- 150000004665 fatty acids Chemical class 0.000 description 8
- 229920000223 polyglycerol Chemical class 0.000 description 7
- 150000001298 alcohols Chemical class 0.000 description 6
- 150000001412 amines Chemical class 0.000 description 6
- 229940027983 antiseptics and disinfectants Quaternary ammonium compounds Drugs 0.000 description 6
- 125000004432 carbon atoms Chemical group C* 0.000 description 6
- 235000019504 cigarettes Nutrition 0.000 description 6
- 239000003599 detergent Substances 0.000 description 6
- 150000003856 quaternary ammonium compounds Chemical class 0.000 description 6
- 239000004094 surface-active agent Substances 0.000 description 6
- 239000003981 vehicle Substances 0.000 description 6
- 238000005406 washing Methods 0.000 description 6
- UKMSUNONTOPOIO-UHFFFAOYSA-N Behenic acid Chemical compound CCCCCCCCCCCCCCCCCCCCCC(O)=O UKMSUNONTOPOIO-UHFFFAOYSA-N 0.000 description 5
- TUNFSRHWOTWDNC-UHFFFAOYSA-N Myristic acid Chemical compound CCCCCCCCCCCCCC(O)=O TUNFSRHWOTWDNC-UHFFFAOYSA-N 0.000 description 5
- 150000007513 acids Chemical class 0.000 description 5
- LYCAIKOWRPUZTN-UHFFFAOYSA-N glycol Chemical group OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 5
- 238000006460 hydrolysis reaction Methods 0.000 description 5
- 230000001953 sensory Effects 0.000 description 5
- 210000002445 Nipples Anatomy 0.000 description 4
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N Oleic acid Natural products CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 4
- IPCSVZSSVZVIGE-UHFFFAOYSA-N Palmitic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 4
- JNYAEWCLZODPBN-CTQIIAAMSA-N Sorbitan Chemical compound OCC(O)C1OCC(O)[C@@H]1O JNYAEWCLZODPBN-CTQIIAAMSA-N 0.000 description 4
- 238000004458 analytical method Methods 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-M chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 4
- 230000000875 corresponding Effects 0.000 description 4
- 229920005862 polyol Polymers 0.000 description 4
- 150000003077 polyols Chemical class 0.000 description 4
- 239000003760 tallow Substances 0.000 description 4
- 229920000742 Cotton Polymers 0.000 description 3
- 210000002374 Sebum Anatomy 0.000 description 3
- 150000001450 anions Chemical class 0.000 description 3
- 239000007844 bleaching agent Substances 0.000 description 3
- 239000000975 dye Substances 0.000 description 3
- 239000011888 foil Substances 0.000 description 3
- 238000009472 formulation Methods 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- WSEBKJRVPMLGFV-UHFFFAOYSA-M (3-chloro-2-hydroxypropyl)-(2-hydroxyethyl)-dimethylazanium;chloride Chemical compound [Cl-].OCC[N+](C)(C)CC(O)CCl WSEBKJRVPMLGFV-UHFFFAOYSA-M 0.000 description 2
- YPFDHNVEDLHUCE-UHFFFAOYSA-N 1,3-Propanediol Chemical compound OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 description 2
- GPLRAVKSCUXZTP-UHFFFAOYSA-N 3-(2,3-dihydroxypropoxy)propane-1,2-diol Chemical compound OCC(O)COCC(O)CO GPLRAVKSCUXZTP-UHFFFAOYSA-N 0.000 description 2
- 235000021357 Behenic acid Nutrition 0.000 description 2
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 2
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 2
- 102000004190 Enzymes Human genes 0.000 description 2
- 108090000790 Enzymes Proteins 0.000 description 2
- KWGKDLIKAYFUFQ-UHFFFAOYSA-M Lithium chloride Chemical compound [Li+].[Cl-] KWGKDLIKAYFUFQ-UHFFFAOYSA-M 0.000 description 2
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L MgCl2 Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 2
- 235000021360 Myristic acid Nutrition 0.000 description 2
- IOLCXVTUBQKXJR-UHFFFAOYSA-M Potassium bromide Chemical compound [K+].[Br-] IOLCXVTUBQKXJR-UHFFFAOYSA-M 0.000 description 2
- 229940100515 SORBITAN Drugs 0.000 description 2
- QIQXTHQIDYTFRH-UHFFFAOYSA-N Stearic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 2
- 239000004480 active ingredient Substances 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminum Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 150000008064 anhydrides Chemical class 0.000 description 2
- 150000001735 carboxylic acids Chemical class 0.000 description 2
- 239000000969 carrier Substances 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000012467 final product Substances 0.000 description 2
- 150000002314 glycerols Chemical class 0.000 description 2
- 239000008187 granular material Substances 0.000 description 2
- 150000002500 ions Chemical class 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N iso-propanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- OKKJLVBELUTLKV-UHFFFAOYSA-N methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 2
- JZMJDSHXVKJFKW-UHFFFAOYSA-M methyl sulfate(1-) Chemical compound COS([O-])(=O)=O JZMJDSHXVKJFKW-UHFFFAOYSA-M 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N n-butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- 239000004669 nonionic softener Substances 0.000 description 2
- 239000002736 nonionic surfactant Substances 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 230000003287 optical Effects 0.000 description 2
- BDERNNFJNOPAEC-UHFFFAOYSA-N propanol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 239000000600 sorbitol Substances 0.000 description 2
- 229960002920 sorbitol Drugs 0.000 description 2
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (-)-propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 description 1
- 229940035437 1,3-propanediol Drugs 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N 2,2-bis(hydroxymethyl)propane-1,3-diol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- AGNTUZCMJBTHOG-UHFFFAOYSA-N 3-[3-(2,3-dihydroxypropoxy)-2-hydroxypropoxy]propane-1,2-diol Chemical compound OCC(O)COCC(O)COCC(O)CO AGNTUZCMJBTHOG-UHFFFAOYSA-N 0.000 description 1
- WPYMKLBDIGXBTP-UHFFFAOYSA-N Benzoic acid Natural products OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 1
- 239000007848 Bronsted acid Substances 0.000 description 1
- UNXHWFMMPAWVPI-QWWZWVQMSA-N D-Threitol Natural products OC[C@@H](O)[C@H](O)CO UNXHWFMMPAWVPI-QWWZWVQMSA-N 0.000 description 1
- CZMRCDWAGMRECN-UGDNZRGBSA-N D-sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 1
- XLMALTXPSGQGBX-GCJKJVERSA-N Dextropropoxyphene Chemical class C([C@](OC(=O)CC)([C@H](C)CN(C)C)C=1C=CC=CC=1)C1=CC=CC=C1 XLMALTXPSGQGBX-GCJKJVERSA-N 0.000 description 1
- 239000004386 Erythritol Substances 0.000 description 1
- UNXHWFMMPAWVPI-ZXZARUISSA-N Erythritol Chemical compound OC[C@H](O)[C@H](O)CO UNXHWFMMPAWVPI-ZXZARUISSA-N 0.000 description 1
- 229940009714 Erythritol Drugs 0.000 description 1
- QUPDWYMUPZLYJZ-UHFFFAOYSA-N Ethyl radical Chemical class C[CH2] QUPDWYMUPZLYJZ-UHFFFAOYSA-N 0.000 description 1
- 229940015001 Glycerin Drugs 0.000 description 1
- BVHLGVCQOALMSV-JEDNCBNOSA-N L-lysine hydrochloride Chemical compound Cl.NCCCC[C@H](N)C(O)=O BVHLGVCQOALMSV-JEDNCBNOSA-N 0.000 description 1
- 229950004297 Lauril Drugs 0.000 description 1
- 239000006057 Non-nutritive feed additive Substances 0.000 description 1
- 235000021314 Palmitic acid Nutrition 0.000 description 1
- 229960004063 Propylene glycol Drugs 0.000 description 1
- HVUMOYIDDBPOLL-XWVZOOPGSA-N Sorbitan monostearate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O HVUMOYIDDBPOLL-XWVZOOPGSA-N 0.000 description 1
- 229950003429 Sorbitan palmitate Drugs 0.000 description 1
- 229950011392 Sorbitan stearate Drugs 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Chemical compound OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
- 229960004793 Sucrose Drugs 0.000 description 1
- CZMRCDWAGMRECN-GDQSFJPYSA-N Sucrose Natural products O([C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@H](CO)O1)[C@@]1(CO)[C@H](O)[C@@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-GDQSFJPYSA-N 0.000 description 1
- BGRJTUBHPOOWDU-UHFFFAOYSA-N Sulpiride Chemical compound CCN1CCCC1CNC(=O)C1=CC(S(N)(=O)=O)=CC=C1OC BGRJTUBHPOOWDU-UHFFFAOYSA-N 0.000 description 1
- XOAAWQZATWQOTB-UHFFFAOYSA-N Taurine Chemical compound NCCS(O)(=O)=O XOAAWQZATWQOTB-UHFFFAOYSA-N 0.000 description 1
- 241000120020 Tela Species 0.000 description 1
- HEBKCHPVOIAQTA-SCDXWVJYSA-N Xylitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)CO HEBKCHPVOIAQTA-SCDXWVJYSA-N 0.000 description 1
- 229960002675 Xylitol Drugs 0.000 description 1
- IYFATESGLOUGBX-CBOZIWPYSA-N [2-[(2R,3S,4R)-3,4-dihydroxyoxolan-2-yl]-2-hydroxyethyl] hexadecanoate Chemical compound CCCCCCCCCCCCCCCC(=O)OCC(O)[C@H]1OC[C@@H](O)[C@@H]1O IYFATESGLOUGBX-CBOZIWPYSA-N 0.000 description 1
- HVUMOYIDDBPOLL-IIZJTUPISA-N [2-[(2R,3S,4R)-3,4-dihydroxyoxolan-2-yl]-2-hydroxyethyl] octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)[C@H]1OC[C@@H](O)[C@@H]1O HVUMOYIDDBPOLL-IIZJTUPISA-N 0.000 description 1
- 239000012190 activator Substances 0.000 description 1
- 125000002252 acyl group Chemical group 0.000 description 1
- 238000007792 addition Methods 0.000 description 1
- 238000005054 agglomeration Methods 0.000 description 1
- 230000002776 aggregation Effects 0.000 description 1
- 125000003158 alcohol group Chemical group 0.000 description 1
- 125000000746 allylic group Chemical group 0.000 description 1
- 230000000844 anti-bacterial Effects 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- JXLHNMVSKXFWAO-UHFFFAOYSA-N azane;7-fluoro-2,1,3-benzoxadiazole-4-sulfonic acid Chemical compound N.OS(=O)(=O)C1=CC=C(F)C2=NON=C12 JXLHNMVSKXFWAO-UHFFFAOYSA-N 0.000 description 1
- 239000003899 bactericide agent Substances 0.000 description 1
- 229940116226 behenic acid Drugs 0.000 description 1
- 235000010233 benzoic acid Nutrition 0.000 description 1
- 150000001559 benzoic acids Chemical class 0.000 description 1
- 238000005282 brightening Methods 0.000 description 1
- CPELXLSAUQHCOX-UHFFFAOYSA-M bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 1
- 229920005549 butyl rubber Polymers 0.000 description 1
- UXVMQQNJUSDDNG-UHFFFAOYSA-L cacl2 Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 1
- 239000001110 calcium chloride Substances 0.000 description 1
- 229910001628 calcium chloride Inorganic materials 0.000 description 1
- ODINCKMPIJJUCX-UHFFFAOYSA-N calcium oxide Inorganic materials [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 description 1
- 239000003093 cationic surfactant Substances 0.000 description 1
- 239000002738 chelating agent Substances 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 229910052570 clay Inorganic materials 0.000 description 1
- 230000003749 cleanliness Effects 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 230000000295 complement Effects 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 230000001276 controlling effect Effects 0.000 description 1
- 238000006297 dehydration reaction Methods 0.000 description 1
- 230000003111 delayed Effects 0.000 description 1
- 230000000249 desinfective Effects 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 229950008690 docosanoic acid Drugs 0.000 description 1
- 235000013399 edible fruits Nutrition 0.000 description 1
- 239000003792 electrolyte Substances 0.000 description 1
- BRLQWZUYTZBJKN-UHFFFAOYSA-N epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 1
- 235000019414 erythritol Nutrition 0.000 description 1
- CCIVGXIOQKPBKL-UHFFFAOYSA-N ethanesulfonic acid Chemical class CCS(O)(=O)=O CCIVGXIOQKPBKL-UHFFFAOYSA-N 0.000 description 1
- 229940093476 ethylene glycol Drugs 0.000 description 1
- 239000002979 fabric softener Substances 0.000 description 1
- 125000005313 fatty acid group Chemical group 0.000 description 1
- 125000001924 fatty-acyl group Chemical group 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 125000002485 formyl group Chemical class [H]C(*)=O 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- 125000005908 glyceryl ester group Chemical group 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 230000003301 hydrolyzing Effects 0.000 description 1
- 239000003752 hydrotrope Substances 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 230000000670 limiting Effects 0.000 description 1
- 229910001629 magnesium chloride Inorganic materials 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- BDAGIHXWWSANSR-UHFFFAOYSA-M methanoate Chemical compound [O-]C=O BDAGIHXWWSANSR-UHFFFAOYSA-M 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- NHNBFGGVMKEFGY-UHFFFAOYSA-N nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 1
- 239000003608 nonionic fabric softener Substances 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- IPCSVZSSVZVIGE-UHFFFAOYSA-M palmitate Chemical compound CCCCCCCCCCCCCCCC([O-])=O IPCSVZSSVZVIGE-UHFFFAOYSA-M 0.000 description 1
- 230000036961 partial Effects 0.000 description 1
- 229960001735 pentaerythritol Drugs 0.000 description 1
- 230000000737 periodic Effects 0.000 description 1
- 230000002085 persistent Effects 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- WLJVXDMOQOGPHL-UHFFFAOYSA-M phenylacetate Chemical compound [O-]C(=O)CC1=CC=CC=C1 WLJVXDMOQOGPHL-UHFFFAOYSA-M 0.000 description 1
- 229940049953 phenylacetate Drugs 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229920000166 polytrimethylene carbonate Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000002335 preservative Effects 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 230000002035 prolonged Effects 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 235000013772 propylene glycol Nutrition 0.000 description 1
- 125000001453 quaternary ammonium group Chemical group 0.000 description 1
- 239000003638 reducing agent Substances 0.000 description 1
- 230000001105 regulatory Effects 0.000 description 1
- 150000003335 secondary amines Chemical class 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 230000035943 smell Effects 0.000 description 1
- 230000000391 smoking Effects 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 230000003381 solubilizing Effects 0.000 description 1
- 239000001587 sorbitan monostearate Substances 0.000 description 1
- 235000011076 sorbitan monostearate Nutrition 0.000 description 1
- 229940035048 sorbitan monostearate Drugs 0.000 description 1
- 238000001694 spray drying Methods 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-M stearate Chemical compound CCCCCCCCCCCCCCCCCC([O-])=O QIQXTHQIDYTFRH-UHFFFAOYSA-M 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 238000004659 sterilization and disinfection Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- 230000001629 suppression Effects 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- 210000001519 tissues Anatomy 0.000 description 1
- 230000001256 tonic Effects 0.000 description 1
- 239000000811 xylitol Substances 0.000 description 1
- 235000010447 xylitol Nutrition 0.000 description 1
Abstract
The use is provided of an allyl alcohol perfume precursor, preferably an ester, in which the allyl alcohol perfume is selected from geraniol, nerol, and mixtures thereof, to reduce malodors selected from perspiration odors, of smoke, cooking, and mixtures thereof, also provided herein is the use of a perfume of allylic alcohol selected from geraniol, nerol and mixtures thereof, to reduce odors selected from smoke odors, kitchen, and mixtures of the same
Description
USE OF RLILIC ALCOHOL PERFUMES AS REDUCTION AGENTS OF ODOR ODOR
FIELD OF THE INVENTION
The present invention relates to perfumes of ALOYAL ALCOHOL as reducing agents of the MLLOR. More particularly, it relates to the use of said components to reduce the large amount of smoke coming from the smoke and / or the cooking odors; and / or its precursors to reduce the large amount that comes from perspiration, smoke, and / or kitchen odors.
BACKGROUND OF THE INVENTION
Acceptance of Cleaning Products and
Laundry for the consumer, is determined not only by the performance achieved by these products, but also by the aesthetics associated with them. Therefore, perfume systems are an important aspect of the successful formulation of such a commercial product. They guarantee the provision of a character of freshness and cleanliness to the cleaned surface or to the washing. In WO 95/04809; A method is described that provides delayed release of an odoriferous alcohol, aldehyde or ketone by hydrolysis of an ester compound. It is guaranteed that said method provides a clean and fresh character to the washed tits. In EP 0,404,470, perfume fragrances are described which reduce the large amount arising from perspiration. US pending application No. 08 / 277,558, describes cleaning and laundry compositions containing a nonionic or anionic ester of a perfume of aLolic acid, to provide perfume release for a longer period than through the use of perfume by itself in the Laundry / Cleaning compositions. THE SOLICITOR HAS NOW FOUND THAT ANOTHER IMPORTANT ASPECT OF THE SUCCESSFUL FORMULATION OF THE COMMERCIAL PRODUCT IS DETERMINED BY THE MAXIMUM RESULTING SURFACE OF THE SURFACE.
Clean and / or La teLa Lavada; SPECIALLY AFTER HIS EXPOSURE TO STRONG HEADS, SUCH AS THE OILS OF PERSPIRATION, THE SMOKE, AND / OR THE KITCHEN. THESE OILS are among the most persistent odors on tits and / or clean and dry surfaces. THE SOLICITOR HAS NOW FOUND THAT THE USE OF ALLOYAL ALCOHOL FRUIT PREDICTERS, WHOSE ALCOHOL IS SELECTED FROM GEAR, NEREL AND MIXED THEM, EXCEEDS THE PROBLEM. Therefore, it is an object of the invention to provide the use of said perfume precursors of aLolic aLcohol to reduce the greater odors that come from perspiration, smoke and / or cooking. Another object of the invention is to provide the use of a perfume of aLiCal alcohol selected from geranium, neroL and mixtures thereof, in order to reduce the selected values of the smoke, cooking, and mixtures thereof.
BRIEF DESCRIPTION OF THE INVENTION
The present invention relates to the use of perfume precursors of aLicoL alcohol, whose perfume of aLicoL alcohol is selected from geranium, neroL and mixtures thereof, in order to reduce the selected values of the perspiration, smoke and cooking temperature. , and mix them. Preferably, said precursors are nonionic or anionic esters of said perfumes of aLolic aLcohol. The present invention also relates to the use of a perfume of aLiCoL aLiCiOl selected from geranium, neroL and mixtures thereof, in order to reduce the selected oLLes of the smoke, cooking and mixture oLLs. In another preferred embodiment of the invention, the aforementioned precursor / perfume is incorporated into a cleaning or laundry composition.
DETAILED DESCRIPTION OF THE INVENTION
The present invention is directed to the use of a perfume precursor of aLicoL aLcohol, whose perfume of aLicoL aLcoL is selected from geranium, neroL and mixtures thereof, to reduce the selected oLLes oF the perspiration, smoke, cooking odors , and mix them, preferably smoke such as cigarette smoke and fire smoke, on clean and dry surfaces and / or tits, washed and dried, which are then exposed to these types of smoke. The present invention is also directed to the use of aLiCoL aLcohol perfumes to reduce the selected loWs oF smoke oLores, cooking, and mix them. Perfume of aLiCal alcohol An essence component for the purpose of the invention, is a perfume of aLiCal alcohol selected from geranium, neroL and mixtures thereof. Geranium and neroL are trans / cis structural isomers (in position 2.3 of the double layer) of the molecules that have the form: H0-CH5a-CH = C (CH3 >); -CH? A-CH1 «! - CH = C (CH3) a. Another essential component of the invention is the precursor of said perfume of aLolic aLcohol. The precursor is preferably a non-ionic or anionic ester of said perfume of aLolic aLcohol. Non-unique ester of perfume from the perfume of aLolIcAl alcohol. The non-ionic or anionic ester of said aLic acid perfume for use in the present is an ester of formula: 0 R - [C-0-CHa-CH - == C (CHa> -CHaCHaCH = - - = C (CHa,) a!] R, in which n is an integer of 1 or greater, and in which the R is selected from an alLquiLo, aLqueniLo, aLquiniLo, alLquiLariLo or ariLo group, nonionic or anionic, substituted or unsubstituted, straight chain, branched or cyclic, of d.-CaO, and represents the group attached to the carboxylic acid carboxylic acid function used to make the perfume ester.The product or products, and the hydrolysis rate of the ester. can be controlled by the selection of R. More specifically, although it is not limited by theory, it is believed that when R is an electron donor group (such as nickel), the hydrolysis product will tend to be the redistributed aLcoholic aLcohol. , whereas the electron-attracting groups (such as phenol) will tend to liberate the perfume alcohol not redistributed by hydrolysis. Also included are acid esters that have more than one acid entity per molecule (eg, diesters, triesters) within the alcoholic acid esters. Preferably, R is selected from an alkylic group of C2-C2 or C3-C2, C3-C2, C3-C2, C3-C2, C3-C2, C3-C3, C3-C2, C3-C2, C3-C2, C3-C2, C3-C2 or cyclicals. As mentioned above, the R entity may be unsubstituted or substituted with one or more nonionic and / or anionic substituents. These substituents may include, for example, halogens, nitro, carboxyl, carbonyl, suLp, suLphonate, hydroxy, and alkoxy, and mixtures thereof. Preferred esters for use in the present are:
referred to herein as "digeranyl succinate" and
referred to herein as "geraniLo phenylacetate" and
referred to in the present as "Laurato de geraniLo", as well as neriLo esters corresponding to these geraniLo esters, including the mixed ester of geraniLo succinate and neriLo, and especially mixtures of the corresponding geraniLo and neriLo esters. Preferred esters for use in the present are selected from digeranyl succinate, dinerol succinate, geranium succinate and nerium, and mixtures thereof. Also provided herein is the use in accordance with the invention of said esters in products of
Cleaning or Laundry, which are typically used to wash tits and clean hard surfaces such as vase and other surfaces in need of cleaning and / or disinfection. Laundry compositions that elicit the contact of the ester perfume of aLicoL aLicoL with Theta are preferred, as described above. It is understood that this includes, not only detergent compositions that provide benefits of cleansing, but also laundry compositions such as blender softening compositions added in the rinse, and aggregate dryers compositions (eg, foils) that provide benefits of softness and / or antistatic. The allylic perfume ester or esters typically comprise from about 0.01% to about 10%, preferably from about 0.05% to about 5%, and from about 0.1% to about 2% by weight of the composition is most preferred. The optional ingredients to formulate such laundry and cleaning compositions include one or more of the following. Tissue softening agents. The blister softening agents suitable for use herein are selected from cationic, nonionic, and mixed blended teat softening agents. The preferred fabric softening agents for use in the present compositions are quaternary ammonium compounds or amine precursors having the following formula (I) or (II):
(I)
(II)
Q is selected from -0-C (0) -, -C (0) -0-, -0-C (0) -0-,
NR ^ -CÍO) -, -C < 0) -NR;
R * is < CHA! > P1-Q-T »or T3; Ra is (CHa!) M-Q-Tv * or Ts OR R3 Ra is aCLOSuite of C ..- C- * or hydroxysLL of C.t.-Ct + or H; Rw is H or aLQUER of d.-C. + or hydroxylLquiLo of d-Ci *; T1, T '? , T: a, T, TB are (The same or different) aLquiLo or aLqueniLo of Cn-Ca-a .; n and m are integers from 1 to 4; and X ~ is a compatible anion with the softener, such as chloride, methylsulphate, etc. The chain T *, T58, T3, T1 *, Tß of aLquiLo or aLqueniLo, must contain at least 11 carbon atoms, preferably at least 16 carbon atoms. The chain can be straight or branched. Sebum is a convenient and inexpensive source of long-chain material and long-chain products. Particularly preferred are the compounds in which Tx, T '?, Ta, T' *, TB represent the mixture of long chain materials typical of tallow. Specific examples of quaternary ammonium compounds suitable for use in the present invention are the following: 1) N, N-di (seboyl-L-oxyethyl) -N, N-dimethyl-ammonium chloride; 2) N, N-di (seboiLoxietiL) -N-methyl-N- (2-hydroxyethyl) ammonium chloride; 3) N, N-di (2-seboiLoxi-2-oxoetiL) -N, N-dimethylammonium chloride; 4) N, N-di (2-seboiLoxietiLcarboniL-oxietiL) -N, N-dimetiLamonium chloride, 5) N- (seboiLoxi-2-etiL) -N- (2-seboiLoxi-2-oxo-etiD-N, N-dimethylammonium; 6) N, N, N, -tri (seboiLoxietiL) -N-methyl-ammonium chloride; 7) N- (2-seboxy-Oxo-2-oxoetiL> -N- (seboyl) -N jN-Dimeti-Lamonium chloride; 8) 1,2-Disodioxy-3-trimethyl-propane-L-propane; and mix of any of the previous materials. Of these, Compounds 1-7 are examples of compounds of Formula (I); Compound 8 is a compound of Formula (II). Particular preference is given to N, N-di (2-seboiLoxi-etiL) -N, N-dimetiLamonium, where Sebum chains are at least partially unsaturated. The level of unsaturation of the tallow chain can be measured by means of the iodine value (IY) of the corresponding fatty acid, which in this case should preferably be in the range of 5 to 100, distinguishing two categories of compounds, those having a IY below 25, and Those who have it above 25. In reality, for the Formula (I) compounds made from tallow fatty acids having an IY of 5 to 25, preferably 15 to 20, has been found that a weight ratio of the cis / trans isomer greater than about 30/70, preferably greater than about 50/50 and preferably greater than about 70/30, provides optimum concentration ability. For Formula (I) compounds made from tallow fatty acids having an IY above 25, it has been found that the ratio of cis to trans isomers is less critical, unless very high concentrations are required. Other examples of quaternary ammoniums of Formula (I) and (II) are obtained, for example: - replacing the "sebum" in the above compounds with, for example, coco, pamma, LauriL, oLeiL, ricinoLeiL, steariL, paLmitiLo, or Similar; said acyl chains are either fully saturated or preferably at least partially unsaturated; REPLACING THE "METHOD" IN THE PREVIOUS COMPOUNDS WITH ETHYL, ETOXY, PROPYLO, PROPOXY, ISOPROTIL, BUTYLO, ISOLUTYL OR T-BUTYL; - Replacing the "chloride" in the above compounds with bromide, methylsulphate, formate, sulate, nitrate, and simiLares. In fact, the anion is present only as a counter ion of positively charged quaternary ammonium compounds. The nature of the contraction is not in abso- lute criticism for the practice of the present invention. The scope of this invention is not considered to be limited to any particular anion. By "amine precursors of the same" means
The secondary or tertiary amines corresponding to the quaternary ammonium compounds, said amines are substantially protonated in the compositions present due to the claimed pH values. The quaternary ammonium compounds or amine precursors of the present are at levels of 1% to 80% of the compositions present, depending on the embodiment of the composition which may be digested with a preferred level of active agent of 5% to 15%. %, or concentrate, with a preferred level of active agent from 15% to 50%, preferably 15% at
% For the preceding tea-softening agents, the pH of the compositions present is an essential parameter.
In fact, it influences the stability of quaternary ammonium compounds or amine precursors, especially under conditions of prolonged storage. The pH, as defined in the present context, is measured in pure compositions at 20 ° C. For optimum hydrolytic stability of these compositions, the pH in pure form, measured under the conditions mentioned above, should be in the range of 2.0 to 4.5, preferably 2.0 to 3.5. The pH of these compositions can be regulated by the addition of a Bronsted acid.
Examples of suitable acids include inorganic mineral acids, carboxylic acids, in particular low molecular weight carboxylic acids (C __-C3), and alkylsulfonic acids. Suitable inorganic acids include HCL, HaSOf, HN03 and H3P0f. Suitable organic acids include formic, acetic, citric, methylsulphonic and ethyl sulphonic acids. Preferred acids are citric, hydrochloric, phosphoric, formic, ethylsulphonic, and benzoic acids. The useful softening agents are also non-ionic tonic softening materials, preferably in combination with cationic softening agents. Typically, said nonionic fabric softener materials have an HLB of 2 to 9, typically 3 to 7. Such nonionic fabric softening materials tend to disperse easily, either on their own or when combined with other materials, such as a Long single chain alkyl cationic surfactant described in detail below. The dispersion capacity can be improved by using more Long single chain cationic alkyl surfactant, mixing with other materials as indicated below, use of warmer water, and / or further stirring. In general, the selected materials should be relatively crystalline, high melting point, (e.g.,> 40 ° C) and relatively insoluble in water. The optional non-ionic softener level in the present compositions typically is from about 0.1% to about 10%, preferably about 1% to about 5%. Preferred nonionic softeners are partial fatty acid esters of polyhydric alcohols, or anhydrides thereof, in which the alcohol, or anhydride, contains from 2 to 18, preferably from 2 to 8 carbon atoms, and each portion of fatty acid contains from 12 to 30, preferably from 16 to 20 carbon atoms. Typically, these softeners contain from 1 to 3, preferably 2 fatty acid groups per molecule. The polyhydric alcohol moiety of the ester can be ethylene glycol, glycerol, poly (eg, di-, tri-, tetra-, penta-, and / or hexa-) glycerol, xylitol, sucrose, erythritol, pentaerythritol, sorbitol or sorbitan. . Particularly preferred are sorbitan esters and poLigLiceroL monostearate. The fatty acid portion of the ester is usually derived from fatty acids having from 12 to 30, preferably from 16 to 20, carbon atoms; Typical examples of said fatty acids are tauric acid, myristic acid, palmitic acid, stearic acid, oleic and behenic acid. The highly preferred optional nonionic softening agents for use in the present are the sorbitan esters, which are esterified dehydration products of sorbitol, and the glycerol esters.
Commercial sorbitan monostearate is a suitable material. Also useful are mixtures of sorbitan stearate and sorbitan palmitate having weight ratios of stearate / palmitate ranging from about 10: 1 to about 1:10, and 1,5-sorbitan esters. Preferred in the present are glycerol and polyglycerol esters, especially mono- and / or di-esters of glycerol, diglycerol, triglycerol, and polyglycerol (eg, polyglycerol monostearate) under a trade name of Radiasurf 7248). Useful glycerol and polyglycerol esters include monoesters with stearic, oleic, palmitic, tauric, isostearic, myristic, and / or behenic acids, and diesters of stearic, oleic, palmitic, tauric, isostearic, behenic, and / or myristic acid. It is understood that the typical monoester contains some di- and tri-ester, etc. The "glyceryl esters" also include the polyglycerol esters, for example diglycerol to octaglycerol. The polyglycerol polyols are formed by condensation of glycerin or epichlorohydrin together to bind the glycerol entities by ether linkages. The mono- and / or di-esters of the polyglycerol polyols are preferred, the fatty acyl groups typically being those described hereinabove for the sorbitan and glycerol esters. Additional fabric softening agents useful in the present are described in U.S. 4,661,269; 4,439,335; U.S. 3,862,870; 4,308,151; 3,886,075; 4, 233, 64; 4, 401, 578; 3,974,076; 4,237,016; and EP 472,178. Fully formulated fabric softening compositions preferably contain, in addition to the components described above, one or more of the following ingredients. Concentrated compositions may require organic and / or inorganic concentrating aids, to reach even higher concentrations and / or to satisfy a higher standard of stability, depending on the other ingredients. The surfactant concentration aids are typically selected from the group consisting of long single chain cationic alkyl surfactants; nonionic surfactants; amine oxides; fatty acids; or mixtures thereof, typically used at a level of 0 to about 15% of the composition. Inorganic viscosity control agents that can also act in a similar manner or increase the effect of the surfactant concentration aids, include water soluble ionizable salts which can also be optionally incorporated in the compositions herein. A large variety of ionizing salts can be used. Examples of suitable salts are the halides of the metals of group IR and IIR of the Periodic Table of the Elements, for example, calcium chloride, magnesium chloride, sodium chloride, potassium bromide, and lithium chloride. Ionizable salts are particularly useful during the process of mixing the ingredients to make the compositions present, and then to obtain the desired viscosity. The amount of ionizable salts used depends on the amount of active ingredients used in the compositions, and can be adjusted according to the conveniences of the formulator. Typical levels of salts used to control the viscosity of the composition are from about 20 to about 20,000 parts per million (ppm), preferably about 20 to about 11,000 ppm, by weight of the composition. Alkylene polyammonium salts may be incorporated into the composition to provide viscosity control in addition to, or in place of, the above water-soluble ionizable salts. In addition, these agents can act as scavengers, forming ion pairs with the anionic detergent carried in the main wash, in the rinse, and on the tits, and can improve the performance of softness. These agents can stabilize the viscosity on a wider scale of temperature, especially at low temperatures, compared to inorganic electrolytes. Specific examples of alkylene polyammonium salts include l-lysine monohydrochloride and 1,5-diammonium-2-methylpentane dihydrochloride. Another optional, but preferred, ingredient is a Liquid vehicle. The liquid vehicle used in the present compositions is preferably the least water mainly, due to its low cost, relative availability, safety and compatibility with the environment. The water level in the liquid vehicle is preferably at least about 50%, preferably at least about 60% by weight of the vehicle. Mixtures of water and organic solvents of low molecular weight, for example, less than about 200, for example, lower alcohols such as ethanol, propanol, isopropanol or butanol, are useful as the liquid carrier. Low molecular weight alcohols include dihydric (glycol, etc.), trihydric (glycerol, etc.), and higher polyhydric alcohols (polyols). Other optional ingredients are soil-removing polymers, bactericides, colorants, perfumes, preservatives, optical brighteners, anti-ionization agents, anti-foaming agents, and the like. Fully formulated cleaning or laundry compositions, such as detergent compositions, preferably contain, in addition to the components described above, one or more of the following ingredients selected from: builders, bleaching agents with or without bleach activators, enzymes, enzyme stabilizers, detersive surfactants, chelating agents and mixtures thereof. An exemplary description of said components can be found in IO 94/03572 and WO 94/03552. Other preferred optional ingredients include polymeric soil release agents, materials effective to inhibit the transfer of dyes from one teat to another during the cleaning process (i.e., dye transfer inhibiting agents), polymeric dispersing agents, suds suppressors, brighteners. optical or other brightening agents or bleaching agents, quetatadores agents, fabric softening clay, anti-static agents, other active ingredients, vehicles, hydrotropes, processing aids, dyes or pigments, solvents for liquid formulations, solid fillers for bar compositions, etc. The liquid detergent compositions may contain water and other solvents as carrier. Suitable are low molecular weight alcohols, primary or secondary, exemplified by methanol, ethanol, propanol and isopropanol. Monohydric alcohols are preferred for solubilizing the surfactant, but polyols such as those containing from 2 to about 6 carbon atoms, and from 2 to about 8 hydroxy groups (for example, 1,3-propanediol, ethylene glycol, glycerin and 1,2-propanediol). The compositions may contain from 5% to 90%, typically from 10% to 50%, of said vehicles. Granular detergents can be prepared, for example, by spray drying (density of the final product approximately 520 g / L) or agglomeration (density of the final product above approximately 600 g / t) of the base granule. The rest of the dry ingredients can then be mixed in granular or powder form with the base granule, for example, in a rotating mixing drum, and the liquid ingredients can be applied by spraying (for example, non-ionic surfactant and perfume) . The detergent compositions herein will preferably be formulated so that during use in aqueous cleaning operations, the Wash water has a pH of between about 6.5 and about 11, preferably between about 7.5 and 10.5. The laundry products are typically at a pH of 9 to 11. The techniques for controlling the pH at the recommended use levels include the use of pH regulators., alkalis, acids, etc., and are well known to the person skilled in the art. The invention will be illustrated in the following non-limiting example, in which all percentages are based on weight, unless otherwise indicated.
EXAMPLE
Washing Procedure Two groups of fabrics (ie, knitted cotton shirts) were treated with a liquid fabric softener composition in cold water. The first group was treated with a fabric softening composition fl, while the second group was treated with a nipple softening composition B. The washing procedure employing Composition A constitutes one embodiment of the invention, while the Washing procedure which The composition B is from the prior art. The formulation is defined below:
(1) Di- (Seboyl (soft) -oxiethyl) dimethylammonium chloride (2) Silicone DC-110R, sold by Dow-Corning (3) Rzul bright polar (4) Ester 3,7-dimethyl-2,6-octadienyl of 1,4-butanedioic acid.
Exposure procedure to the smoke odor The washed and dried fabrics were then suspended for 1 minute in a 200 liter drum that had previously been saturated with cigarette smoke. The saturation of the drum was obtained with the cigarette smoke by placing a smoking cigarette in the closed drum for 2 minutes. Then, the cigarette was removed to be replaced by the two groups of fabrics. After exposure of the fabrics to the cigarette smoke, the groups were removed from the drum and suspended in the open air for 45 seconds, wrapped in aluminum foil for 24 hours and subsequently subjected to sensory analysis. Sensory analysis After exposure to smoke, the perceived intensity of the residual odor on the teat was evaluated by a panel of 6 expert judges, trained for sensory evaluations. In this case, an expert is defined as a person who has at least 6 months in training and with proven evidence of olfactory sensitivity. The data obtained using the intensity scale of perfumes was averaged to give a consensus value for the perceived intensity of the residual odor. The perfume intensity scale is as follows: 0 - no odor, 25 - light odor, 50 - moderate odor, 75 - very strong odor, and 100 - extremely strong odor
RESULTS
It is noted that the use of geraniol released by hydrolysis of digeranyl succinate (3,7-dimethyl-2,6-octadienyl 1,4-butanoic acid ester) in a liquid fabric softening composition, provides an improved reduction of the smell that arises from the smoke on the clean and dry cloth. Identical results were obtained when the cloth was exposed to cooking odor in accordance with the following test: After undergoing the washing procedure mentioned above, the fabrics (ie, knitted cotton shirts) washed and dried, were exposed to odors of kitchen in accordance with the following procedure: Kitchen staff involved in the cooking operation used four groups of fabrics for 4 hours.
Afterwards, the groups were suspended outdoors for 45 seconds, wrapped in aluminum foil during
24 hours, and subsequently underwent the sensory analysis mentioned above. Similar results were obtained when cotton garments were exposed to perspiration. After having been subjected to the washing procedure mentioned above, the washed and dried garments were cut into two equal halves so that one half treated with the product
A could be placed together with the complementary half treated with product B. Afterwards, this "divided article" was used by a panel of 20 people during 8 hours of normal activity (without effort) or 1 to 2 hours of sports session (with effort). Then, the divided items were evaluated on both halves according to the sensory analysis mentioned above. Similar results were obtained when sheets were treated, also cut into two equal halves, respectively with product A and product B, which were used by a panel of 20 users, based on a 5-night exposure.
Claims (5)
1. - The use of a perfume precursor of alcoholic alcohol, wherein the perfume of alcohol is selected from geranium, neroL and mixtures thereof, to reduce malodors selected from odors of perspiration, smoke, cooking, and mixtures of the same.
2. The use of an allyl alcohol perfume precursor according to claim 1, characterized in that said precursor is a perfume of nonionic or anionic allylic ester of the formula: 0 J | R - [C-0-CH_3-CH = C (CH3) -CHS8CH_aCH = C (CH3) *] "in which R is selected from an alkyl, alkenyl, alkynyl, alkylaryl or aryl group, nonionic or anionic, substituted or unsubstituted, straight, branched or cyclic, of Ct-C30; and n is an integer of 1 or more.
3. The use of an allyl alcohol perfume precursor according to claim 2, characterized in that said R is selected from an alkylene group of Ca-Cao alkyl of Ca.-Cao, alkynyl, aryl, or alkylaryl of Ca. Ca non-ionic or anionic, substituted or unsubstituted, branched, straight or cyclic; and The substituents are selected from halogens, nitro, carboxyl, carbonyl, sulfate, sulfonate, hydroxyl and alkoxy, and mixtures thereof. 4. The use of an allyl alcohol perfume precursor according to any of claims 1 to 3, characterized in that said precursor is selected from digeranyl succinate, dineryl succinate, geranyl succinate and nerium, and mixtures thereof. . 5. The use of an alcoholic perfume precursor according to any of the claims 1-4, characterized in that said precursor is incorporated in a cleaning or laundry composition in an amount of 0.05% a 5% by weight of the composition. 6. The use of an allyl alcohol perfume precursor according to claim 5, characterized in that said cleaning or laundry composition is a fabric softening composition comprising softening agents selected from cationic, non-ionic fabric softening agents, and mixtures of them. 7. The use of an aLilic alcohol perfume precursor according to any of claims 5 or 6, characterized in that said fabric softening composition has a pH in pure form at 20 ° C in the case of 2.0 a
4. 5, preferably 2.0 to 3.
5. 8.- The use of a perfume of alcohol, selected from geranium, neroL and mixtures thereof, to reduce the odors selected from smoke odor, kitchen odor, and mixtures thereof.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP95870100A EP0760243B1 (en) | 1995-08-31 | 1995-08-31 | Use of allylic alcohol perfumes as a malodour reduction agent |
EP95870100 | 1995-08-31 |
Publications (2)
Publication Number | Publication Date |
---|---|
MX9801663A MX9801663A (en) | 1998-08-30 |
MXPA98001663A true MXPA98001663A (en) | 1998-11-12 |
Family
ID=
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