BR112013014612B1 - composições moc - Google Patents
composições moc Download PDFInfo
- Publication number
- BR112013014612B1 BR112013014612B1 BR112013014612-5A BR112013014612A BR112013014612B1 BR 112013014612 B1 BR112013014612 B1 BR 112013014612B1 BR 112013014612 A BR112013014612 A BR 112013014612A BR 112013014612 B1 BR112013014612 B1 BR 112013014612B1
- Authority
- BR
- Brazil
- Prior art keywords
- methyl
- moc
- dec
- fact
- composition
- Prior art date
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- 239000000203 mixture Substances 0.000 title claims abstract description 85
- 150000001875 compounds Chemical class 0.000 claims abstract description 46
- 239000002781 deodorant agent Substances 0.000 claims abstract description 41
- -1 2-ethoxy-4-formylphenyl Chemical group 0.000 claims abstract description 32
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims abstract description 15
- ZHOOOLQOWQVYOE-UHFFFAOYSA-N 2-cyclohexylidene-2-phenylacetonitrile Chemical compound C=1C=CC=CC=1C(C#N)=C1CCCCC1 ZHOOOLQOWQVYOE-UHFFFAOYSA-N 0.000 claims abstract description 7
- 239000003085 diluting agent Substances 0.000 claims abstract description 6
- 230000003472 neutralizing effect Effects 0.000 claims abstract description 6
- NUEJKVHPFVKGKP-UHFFFAOYSA-N 1-(2,3,4-trimethylcyclododeca-1,3,5-trien-1-yl)ethanone Chemical compound CC(=O)C1=C(C)C(C)=C(C)C=CCCCCCC1 NUEJKVHPFVKGKP-UHFFFAOYSA-N 0.000 claims abstract description 5
- WPFFGMCNILGTEA-UHFFFAOYSA-N 1-spiro[4.5]dec-8-en-9-ylpent-4-en-1-one Chemical compound C1C(C(=O)CCC=C)=CCCC11CCCC1 WPFFGMCNILGTEA-UHFFFAOYSA-N 0.000 claims abstract description 5
- FUNYLZYOEJSMTO-UHFFFAOYSA-N 2-(2,4-dimethylcyclohexyl)pyridine Chemical compound CC1CC(C)CCC1C1=CC=CC=N1 FUNYLZYOEJSMTO-UHFFFAOYSA-N 0.000 claims abstract description 5
- KNHGOYVXAHUDHP-UHFFFAOYSA-N 2-[2-(4-methylcyclohex-3-en-1-yl)propyl]cyclopentan-1-one Chemical compound C1CC(C)=CCC1C(C)CC1CCCC1=O KNHGOYVXAHUDHP-UHFFFAOYSA-N 0.000 claims abstract description 5
- VLFBSPUPYFTTNF-UHFFFAOYSA-N 3-(4-methoxyphenyl)-2-methylpropanal Chemical compound COC1=CC=C(CC(C)C=O)C=C1 VLFBSPUPYFTTNF-UHFFFAOYSA-N 0.000 claims abstract description 5
- ATYBXHSAIOKLMG-UHFFFAOYSA-N oxepin Chemical compound O1C=CC=CC=C1 ATYBXHSAIOKLMG-UHFFFAOYSA-N 0.000 claims abstract description 5
- KHQDWCKZXLWDNM-GHXNOFRVSA-N (z)-2-ethyl-4-(2,2,3-trimethylcyclopent-3-en-1-yl)but-2-en-1-ol Chemical compound CC\C(CO)=C\CC1CC=C(C)C1(C)C KHQDWCKZXLWDNM-GHXNOFRVSA-N 0.000 claims abstract 3
- 230000001166 anti-perspirative effect Effects 0.000 claims description 21
- 239000003213 antiperspirant Substances 0.000 claims description 21
- 238000000034 method Methods 0.000 claims description 9
- YQYKESUTYHZAGG-UHFFFAOYSA-N 1-(1,2,8,8-tetramethyl-1,3,4,5,6,7-hexahydronaphthalen-2-yl)ethanone Chemical compound C1CC(C(C)=O)(C)C(C)C2=C1CCCC2(C)C YQYKESUTYHZAGG-UHFFFAOYSA-N 0.000 claims description 6
- CFSRLACKBAWQFO-UHFFFAOYSA-N 1-spiro[4.5]dec-9-en-9-ylpent-4-en-1-one Chemical compound C1CCC(C(=O)CCC=C)=CC11CCCC1 CFSRLACKBAWQFO-UHFFFAOYSA-N 0.000 claims description 4
- BDIZOKISHHUZPI-UHFFFAOYSA-N 2-cyclohexylidene-2-(2-methylphenyl)acetonitrile Chemical compound CC1=CC=CC=C1C(C#N)=C1CCCCC1 BDIZOKISHHUZPI-UHFFFAOYSA-N 0.000 claims description 4
- OHRBQTOZYGEWCJ-UHFFFAOYSA-N 3-(3-propan-2-ylphenyl)butanal Chemical compound CC(C)C1=CC=CC(C(C)CC=O)=C1 OHRBQTOZYGEWCJ-UHFFFAOYSA-N 0.000 claims description 4
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 3
- RNLHVODSMDJCBR-SOFGYWHQSA-N (e)-3-methyl-5-(2,2,3-trimethylcyclopent-3-en-1-yl)pent-4-en-2-ol Chemical compound CC(O)C(C)\C=C\C1CC=C(C)C1(C)C RNLHVODSMDJCBR-SOFGYWHQSA-N 0.000 claims 2
- QILMAYXCYBTEDM-IWQZZHSRSA-N Isoambrettolide Chemical compound O=C1CCCCCCC\C=C/CCCCCCO1 QILMAYXCYBTEDM-IWQZZHSRSA-N 0.000 claims 2
- YMGUBTXCNDTFJI-UHFFFAOYSA-M cyclopropanecarboxylate Chemical compound [O-]C(=O)C1CC1 YMGUBTXCNDTFJI-UHFFFAOYSA-M 0.000 claims 1
- YMGUBTXCNDTFJI-UHFFFAOYSA-N cyclopropanecarboxylic acid Chemical compound OC(=O)C1CC1 YMGUBTXCNDTFJI-UHFFFAOYSA-N 0.000 claims 1
- 238000006386 neutralization reaction Methods 0.000 abstract description 4
- NVIPUOMWGQAOIT-UHFFFAOYSA-N (E)-7-Hexadecen-16-olide Natural products O=C1CCCCCC=CCCCCCCCCO1 NVIPUOMWGQAOIT-UHFFFAOYSA-N 0.000 abstract description 3
- QILMAYXCYBTEDM-UHFFFAOYSA-N 1-oxacycloheptadec-10-en-2-one Chemical compound O=C1CCCCCCCC=CCCCCCCO1 QILMAYXCYBTEDM-UHFFFAOYSA-N 0.000 abstract description 3
- WJWBVJLPGOYBGM-UHFFFAOYSA-N 2-cyclohexylhepta-1,6-dien-3-one Chemical compound C=CCCC(=O)C(=C)C1CCCCC1 WJWBVJLPGOYBGM-UHFFFAOYSA-N 0.000 abstract description 3
- RNLHVODSMDJCBR-UHFFFAOYSA-N 3-methyl-5-(2,2,3-trimethylcyclopent-3-en-1-yl)pent-4-en-2-ol Chemical compound CC(O)C(C)C=CC1CC=C(C)C1(C)C RNLHVODSMDJCBR-UHFFFAOYSA-N 0.000 abstract description 3
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 abstract description 3
- WMGVPDQNPUQRND-UHFFFAOYSA-N (2-methylphenyl)acetonitrile Chemical compound CC1=CC=CC=C1CC#N WMGVPDQNPUQRND-UHFFFAOYSA-N 0.000 abstract 1
- MOMFXATYAINJML-UHFFFAOYSA-N 2-Acetylthiazole Chemical group CC(=O)C1=NC=CS1 MOMFXATYAINJML-UHFFFAOYSA-N 0.000 abstract 1
- AEFIZZUZXWBUHO-UHFFFAOYSA-N 3-(3-propan-2-ylphenyl)butan-1-ol Chemical compound CC(C)C1=CC=CC(C(C)CCO)=C1 AEFIZZUZXWBUHO-UHFFFAOYSA-N 0.000 abstract 1
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- WRMNZCZEMHIOCP-UHFFFAOYSA-N 2-phenylethanol Chemical compound OCCC1=CC=CC=C1 WRMNZCZEMHIOCP-UHFFFAOYSA-N 0.000 description 2
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- QFOHBWFCKVYLES-UHFFFAOYSA-N Butylparaben Chemical compound CCCCOC(=O)C1=CC=C(O)C=C1 QFOHBWFCKVYLES-UHFFFAOYSA-N 0.000 description 2
- 229920000858 Cyclodextrin Polymers 0.000 description 2
- GLZPCOQZEFWAFX-UHFFFAOYSA-N Geraniol Chemical compound CC(C)=CCCC(C)=CCO GLZPCOQZEFWAFX-UHFFFAOYSA-N 0.000 description 2
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- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 239000004599 antimicrobial Substances 0.000 description 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
- SESFRYSPDFLNCH-UHFFFAOYSA-N benzyl benzoate Chemical compound C=1C=CC=CC=1C(=O)OCC1=CC=CC=C1 SESFRYSPDFLNCH-UHFFFAOYSA-N 0.000 description 2
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- FLKPEMZONWLCSK-UHFFFAOYSA-N diethyl phthalate Chemical compound CCOC(=O)C1=CC=CC=C1C(=O)OCC FLKPEMZONWLCSK-UHFFFAOYSA-N 0.000 description 2
- FPAFDBFIGPHWGO-UHFFFAOYSA-N dioxosilane;oxomagnesium;hydrate Chemical compound O.[Mg]=O.[Mg]=O.[Mg]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O FPAFDBFIGPHWGO-UHFFFAOYSA-N 0.000 description 2
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- FQTLCLSUCSAZDY-UHFFFAOYSA-N (+) E(S) nerolidol Natural products CC(C)=CCCC(C)=CCCC(C)(O)C=C FQTLCLSUCSAZDY-UHFFFAOYSA-N 0.000 description 1
- NOOLISFMXDJSKH-UTLUCORTSA-N (+)-Neomenthol Chemical compound CC(C)[C@@H]1CC[C@@H](C)C[C@@H]1O NOOLISFMXDJSKH-UTLUCORTSA-N 0.000 description 1
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| GB1021050.8 | 2010-12-13 | ||
| GB201021050A GB201021050D0 (en) | 2010-12-13 | 2010-12-13 | Moc compositions |
| PCT/EP2011/072590 WO2012080235A1 (en) | 2010-12-13 | 2011-12-13 | Moc compositions |
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| BR112013014612A2 BR112013014612A2 (pt) | 2016-09-20 |
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| JP6202679B2 (ja) * | 2013-02-21 | 2017-09-27 | 花王株式会社 | ４，８−ジメチル−４，９−デカジエンニトリル |
| MX376252B (es) | 2014-10-14 | 2025-03-07 | Givaudan Sa | Composiciones de reduccion del mal olor. |
| JP6869190B2 (ja) * | 2015-05-13 | 2021-05-12 | ジボダン エス エー | 有機化合物における改善または有機化合物に関する改善 |
| CN107847624A (zh) * | 2015-07-07 | 2018-03-27 | 弗门尼舍有限公司 | 用于恶臭抵消的茚满衍生物 |
| JP6741458B2 (ja) * | 2016-03-31 | 2020-08-19 | ライオン株式会社 | 繊維製品用処理剤組成物 |
| KR20180062813A (ko) | 2016-12-01 | 2018-06-11 | 박금히 | 액취증의 예방 또는 개선용 조성물 |
| WO2018197549A1 (en) * | 2017-04-27 | 2018-11-01 | Firmenich Sa | Odor neutralizer for ammonia and primary or secondary amines |
| JP7460981B2 (ja) * | 2017-11-29 | 2024-04-03 | 山本香料株式会社 | アスファルト、汚泥、汚水、銀杏、堆肥、海獣、野菜、生ゴミ又は塗料の臭いの変調用臭気変調剤、及びアスファルト、汚泥、汚水、銀杏、堆肥、海獣、野菜、生ゴミ又は塗料の臭いの臭気変調方法 |
| US20220296495A1 (en) * | 2019-06-11 | 2022-09-22 | Marisa Ann Plescia | Deodorant compositions |
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| US5538719A (en) | 1993-05-26 | 1996-07-23 | Monell Chemical Senses Center | Method for reducing perception of human underarm odor by a pleasant smelling compound |
| EP0858498B1 (de) * | 1995-11-01 | 2001-09-12 | Givaudan SA | Nitril |
| EP0936211B1 (en) | 1998-02-13 | 2010-07-07 | Givaudan SA | Aryl-acrylic acid esters useful as precursors for organoleptic compounds |
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| EP1340741A1 (en) * | 2002-02-28 | 2003-09-03 | Givaudan SA | Indane derivatives and their use in perfumery |
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| US20040248762A1 (en) * | 2003-06-09 | 2004-12-09 | Mcgee Thomas | Malodor counteractant compositions |
| JP2005060477A (ja) * | 2003-08-08 | 2005-03-10 | Kao Corp | 香料組成物 |
| ES2343738T3 (es) * | 2004-12-08 | 2010-08-09 | Givaudan Sa | Compuestos organicos. |
| GB0512284D0 (en) | 2005-06-16 | 2005-07-27 | Givaudan Sa | Organic compounds |
| GB0518558D0 (en) * | 2005-09-12 | 2005-10-19 | Givaudan Sa | Improvements in or related to organic compounds |
| EP1884555A2 (de) | 2006-08-01 | 2008-02-06 | Symrise GmbH & Co. KG | Maskierung von Mineralölgeruch und Beduftung von Mineralölen |
| EP2086594A1 (en) | 2006-11-07 | 2009-08-12 | Givaudan SA | Malodor counteracting compositions |
| GB0703679D0 (en) | 2007-02-26 | 2007-04-04 | Quest Int Serv Bv | Perfume compositions |
| GB0720851D0 (en) | 2007-10-24 | 2007-12-05 | Givaudan Sa | Perfume compositions |
| GB0812006D0 (en) * | 2008-07-01 | 2008-08-06 | Givaudan Sa | Organic compounds |
-
2010
- 2010-12-13 GB GB201021050A patent/GB201021050D0/en not_active Ceased
-
2011
- 2011-12-13 ES ES11804991.5T patent/ES2607280T3/es active Active
- 2011-12-13 CN CN201180059447.0A patent/CN103249822B/zh not_active Expired - Fee Related
- 2011-12-13 US US13/988,247 patent/US9125828B2/en not_active Expired - Fee Related
- 2011-12-13 KR KR1020137014950A patent/KR102001260B1/ko not_active Expired - Fee Related
- 2011-12-13 WO PCT/EP2011/072590 patent/WO2012080235A1/en not_active Ceased
- 2011-12-13 BR BR112013014612-5A patent/BR112013014612B1/pt not_active IP Right Cessation
- 2011-12-13 JP JP2013543709A patent/JP5937614B2/ja not_active Expired - Fee Related
- 2011-12-13 EP EP11804991.5A patent/EP2652102B1/en not_active Not-in-force
- 2011-12-13 MX MX2013006036A patent/MX355214B/es active IP Right Grant
-
2013
- 2013-05-27 ZA ZA2013/03844A patent/ZA201303844B/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| ZA201303844B (en) | 2014-02-26 |
| JP2014501233A (ja) | 2014-01-20 |
| CN103249822B (zh) | 2015-02-11 |
| KR20130132848A (ko) | 2013-12-05 |
| ES2607280T3 (es) | 2017-03-29 |
| US9125828B2 (en) | 2015-09-08 |
| WO2012080235A1 (en) | 2012-06-21 |
| US20130336911A1 (en) | 2013-12-19 |
| EP2652102B1 (en) | 2016-09-14 |
| KR102001260B1 (ko) | 2019-07-17 |
| MX355214B (es) | 2018-04-10 |
| JP5937614B2 (ja) | 2016-06-22 |
| EP2652102A1 (en) | 2013-10-23 |
| CN103249822A (zh) | 2013-08-14 |
| MX2013006036A (es) | 2013-08-01 |
| GB201021050D0 (en) | 2011-01-26 |
| BR112013014612A2 (pt) | 2016-09-20 |
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