RU2006110633A - Отбеливающая композиция - Google Patents
Отбеливающая композиция Download PDFInfo
- Publication number
- RU2006110633A RU2006110633A RU2006110633/04A RU2006110633A RU2006110633A RU 2006110633 A RU2006110633 A RU 2006110633A RU 2006110633/04 A RU2006110633/04 A RU 2006110633/04A RU 2006110633 A RU2006110633 A RU 2006110633A RU 2006110633 A RU2006110633 A RU 2006110633A
- Authority
- RU
- Russia
- Prior art keywords
- alkyl
- whitening
- whitening composition
- hydrogen
- transition metal
- Prior art date
Links
- 230000002087 whitening effect Effects 0.000 title claims 14
- 239000000203 mixture Substances 0.000 title claims 11
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims 5
- 229910052739 hydrogen Inorganic materials 0.000 claims 5
- 239000001257 hydrogen Substances 0.000 claims 5
- -1 hydrogen acid Chemical class 0.000 claims 5
- 229910052723 transition metal Inorganic materials 0.000 claims 5
- 150000003624 transition metals Chemical class 0.000 claims 5
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 4
- GLZPCOQZEFWAFX-UHFFFAOYSA-N Geraniol Chemical compound CC(C)=CCCC(C)=CCO GLZPCOQZEFWAFX-UHFFFAOYSA-N 0.000 claims 4
- 239000003054 catalyst Substances 0.000 claims 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 4
- 239000007788 liquid Substances 0.000 claims 3
- 239000000758 substrate Substances 0.000 claims 3
- 125000000041 C6-C10 aryl group Chemical group 0.000 claims 2
- 238000004061 bleaching Methods 0.000 claims 2
- NEHNMFOYXAPHSD-UHFFFAOYSA-N citronellal Chemical compound O=CCC(C)CCC=C(C)C NEHNMFOYXAPHSD-UHFFFAOYSA-N 0.000 claims 2
- QMVPMAAFGQKVCJ-UHFFFAOYSA-N citronellol Chemical compound OCCC(C)CCC=C(C)C QMVPMAAFGQKVCJ-UHFFFAOYSA-N 0.000 claims 2
- 239000003205 fragrance Substances 0.000 claims 2
- 125000005842 heteroatom Chemical group 0.000 claims 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 2
- XMGQYMWWDOXHJM-UHFFFAOYSA-N limonene Chemical compound CC(=C)C1CCC(C)=CC1 XMGQYMWWDOXHJM-UHFFFAOYSA-N 0.000 claims 2
- CDOSHBSSFJOMGT-UHFFFAOYSA-N linalool Chemical compound CC(C)=CCCC(C)(O)C=C CDOSHBSSFJOMGT-UHFFFAOYSA-N 0.000 claims 2
- UWKAYLJWKGQEPM-LBPRGKRZSA-N linalyl acetate Chemical compound CC(C)=CCC[C@](C)(C=C)OC(C)=O UWKAYLJWKGQEPM-LBPRGKRZSA-N 0.000 claims 2
- VAMXMNNIEUEQDV-UHFFFAOYSA-N methyl anthranilate Chemical compound COC(=O)C1=CC=CC=C1N VAMXMNNIEUEQDV-UHFFFAOYSA-N 0.000 claims 2
- 239000002304 perfume Substances 0.000 claims 2
- XOKSLPVRUOBDEW-UHFFFAOYSA-N pinane Chemical compound CC1CCC2C(C)(C)C1C2 XOKSLPVRUOBDEW-UHFFFAOYSA-N 0.000 claims 2
- CZCBTSFUTPZVKJ-UHFFFAOYSA-N rose oxide Chemical compound CC1CCOC(C=C(C)C)C1 CZCBTSFUTPZVKJ-UHFFFAOYSA-N 0.000 claims 2
- GFBCBQNBXRPRQD-JLHYYAGUSA-N (2e)-2-benzylidenehexanal Chemical compound CCCC\C(C=O)=C/C1=CC=CC=C1 GFBCBQNBXRPRQD-JLHYYAGUSA-N 0.000 claims 1
- 239000001490 (3R)-3,7-dimethylocta-1,6-dien-3-ol Substances 0.000 claims 1
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims 1
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 claims 1
- 239000001244 (E)-1-(2,6,6-trimethyl-1-cyclohex-2-enyl)pent-1-en-3-one Substances 0.000 claims 1
- KJPRLNWUNMBNBZ-QPJJXVBHSA-N (E)-cinnamaldehyde Chemical compound O=C\C=C\C1=CC=CC=C1 KJPRLNWUNMBNBZ-QPJJXVBHSA-N 0.000 claims 1
- QMVPMAAFGQKVCJ-SNVBAGLBSA-N (R)-(+)-citronellol Natural products OCC[C@H](C)CCC=C(C)C QMVPMAAFGQKVCJ-SNVBAGLBSA-N 0.000 claims 1
- DSSYKIVIOFKYAU-XCBNKYQSSA-N (R)-camphor Chemical compound C1C[C@@]2(C)C(=O)C[C@@H]1C2(C)C DSSYKIVIOFKYAU-XCBNKYQSSA-N 0.000 claims 1
- CDOSHBSSFJOMGT-JTQLQIEISA-N (R)-linalool Natural products CC(C)=CCC[C@@](C)(O)C=C CDOSHBSSFJOMGT-JTQLQIEISA-N 0.000 claims 1
- VPKMGDRERYMTJX-XEHSLEBBSA-N (e)-1-[(1r)-2,6,6-trimethylcyclohex-2-en-1-yl]pent-1-en-3-one Chemical compound CCC(=O)\C=C\[C@H]1C(C)=CCCC1(C)C VPKMGDRERYMTJX-XEHSLEBBSA-N 0.000 claims 1
- WBYWAXJHAXSJNI-VOTSOKGWSA-M .beta-Phenylacrylic acid Natural products [O-]C(=O)\C=C\C1=CC=CC=C1 WBYWAXJHAXSJNI-VOTSOKGWSA-M 0.000 claims 1
- HMKKIXGYKWDQSV-SDNWHVSQSA-N 2-Pentyl-3-phenyl-2-propenal Chemical compound CCCCC\C(C=O)=C/C1=CC=CC=C1 HMKKIXGYKWDQSV-SDNWHVSQSA-N 0.000 claims 1
- GOLORTLGFDVFDW-UHFFFAOYSA-N 3-(1h-benzimidazol-2-yl)-7-(diethylamino)chromen-2-one Chemical compound C1=CC=C2NC(C3=CC4=CC=C(C=C4OC3=O)N(CC)CC)=NC2=C1 GOLORTLGFDVFDW-UHFFFAOYSA-N 0.000 claims 1
- 241000723346 Cinnamomum camphora Species 0.000 claims 1
- WTEVQBCEXWBHNA-UHFFFAOYSA-N Citral Natural products CC(C)=CCCC(C)=CC=O WTEVQBCEXWBHNA-UHFFFAOYSA-N 0.000 claims 1
- GLZPCOQZEFWAFX-YFHOEESVSA-N Geraniol Natural products CC(C)=CCC\C(C)=C/CO GLZPCOQZEFWAFX-YFHOEESVSA-N 0.000 claims 1
- 239000005792 Geraniol Substances 0.000 claims 1
- GLZPCOQZEFWAFX-JXMROGBWSA-N Nerol Natural products CC(C)=CCC\C(C)=C\CO GLZPCOQZEFWAFX-JXMROGBWSA-N 0.000 claims 1
- 239000002253 acid Substances 0.000 claims 1
- OENHQHLEOONYIE-UKMVMLAPSA-N all-trans beta-carotene Natural products CC=1CCCC(C)(C)C=1/C=C/C(/C)=C/C=C/C(/C)=C/C=C/C=C(C)C=CC=C(C)C=CC1=C(C)CCCC1(C)C OENHQHLEOONYIE-UKMVMLAPSA-N 0.000 claims 1
- GUUHFMWKWLOQMM-NTCAYCPXSA-N alpha-hexylcinnamaldehyde Chemical compound CCCCCC\C(C=O)=C/C1=CC=CC=C1 GUUHFMWKWLOQMM-NTCAYCPXSA-N 0.000 claims 1
- GUUHFMWKWLOQMM-UHFFFAOYSA-N alpha-n-hexylcinnamic aldehyde Natural products CCCCCCC(C=O)=CC1=CC=CC=C1 GUUHFMWKWLOQMM-UHFFFAOYSA-N 0.000 claims 1
- RWZYAGGXGHYGMB-UHFFFAOYSA-N anthranilic acid Chemical compound NC1=CC=CC=C1C(O)=O RWZYAGGXGHYGMB-UHFFFAOYSA-N 0.000 claims 1
- 239000012736 aqueous medium Substances 0.000 claims 1
- TUPZEYHYWIEDIH-WAIFQNFQSA-N beta-carotene Natural products CC(=C/C=C/C=C(C)/C=C/C=C(C)/C=C/C1=C(C)CCCC1(C)C)C=CC=C(/C)C=CC2=CCCCC2(C)C TUPZEYHYWIEDIH-WAIFQNFQSA-N 0.000 claims 1
- 235000013734 beta-carotene Nutrition 0.000 claims 1
- 239000011648 beta-carotene Substances 0.000 claims 1
- JGQFVRIQXUFPAH-UHFFFAOYSA-N beta-citronellol Natural products OCCC(C)CCCC(C)=C JGQFVRIQXUFPAH-UHFFFAOYSA-N 0.000 claims 1
- 229960002747 betacarotene Drugs 0.000 claims 1
- 229930008380 camphor Natural products 0.000 claims 1
- 229960000846 camphor Drugs 0.000 claims 1
- 239000000969 carrier Substances 0.000 claims 1
- 229930016911 cinnamic acid Natural products 0.000 claims 1
- 235000013985 cinnamic acid Nutrition 0.000 claims 1
- KJPRLNWUNMBNBZ-UHFFFAOYSA-N cinnamic aldehyde Natural products O=CC=CC1=CC=CC=C1 KJPRLNWUNMBNBZ-UHFFFAOYSA-N 0.000 claims 1
- 229940117916 cinnamic aldehyde Drugs 0.000 claims 1
- 229940043350 citral Drugs 0.000 claims 1
- 229930003633 citronellal Natural products 0.000 claims 1
- 235000000983 citronellal Nutrition 0.000 claims 1
- 235000000484 citronellol Nutrition 0.000 claims 1
- 239000000356 contaminant Substances 0.000 claims 1
- 239000013078 crystal Substances 0.000 claims 1
- 150000002009 diols Chemical class 0.000 claims 1
- USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical compound C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 claims 1
- WSALIDVQXCHFEG-UHFFFAOYSA-L disodium;4,8-diamino-1,5-dihydroxy-9,10-dioxoanthracene-2,6-disulfonate Chemical compound [Na+].[Na+].O=C1C2=C(N)C=C(S([O-])(=O)=O)C(O)=C2C(=O)C2=C1C(O)=C(S([O-])(=O)=O)C=C2N WSALIDVQXCHFEG-UHFFFAOYSA-L 0.000 claims 1
- 238000001035 drying Methods 0.000 claims 1
- WTEVQBCEXWBHNA-JXMROGBWSA-N geranial Chemical compound CC(C)=CCC\C(C)=C\C=O WTEVQBCEXWBHNA-JXMROGBWSA-N 0.000 claims 1
- 229940113087 geraniol Drugs 0.000 claims 1
- 125000002350 geranyl group Chemical group [H]C([*])([H])/C([H])=C(C([H])([H])[H])/C([H])([H])C([H])([H])C([H])=C(C([H])([H])[H])C([H])([H])[H] 0.000 claims 1
- 239000004615 ingredient Substances 0.000 claims 1
- 235000001510 limonene Nutrition 0.000 claims 1
- 229940087305 limonene Drugs 0.000 claims 1
- 229930007744 linalool Natural products 0.000 claims 1
- UWKAYLJWKGQEPM-UHFFFAOYSA-N linalool acetate Natural products CC(C)=CCCC(C)(C=C)OC(C)=O UWKAYLJWKGQEPM-UHFFFAOYSA-N 0.000 claims 1
- 238000000034 method Methods 0.000 claims 1
- 229940102398 methyl anthranilate Drugs 0.000 claims 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 1
- WBYWAXJHAXSJNI-UHFFFAOYSA-N methyl p-hydroxycinnamate Natural products OC(=O)C=CC1=CC=CC=C1 WBYWAXJHAXSJNI-UHFFFAOYSA-N 0.000 claims 1
- 239000000178 monomer Substances 0.000 claims 1
- ZRSNZINYAWTAHE-UHFFFAOYSA-N p-methoxybenzaldehyde Chemical compound COC1=CC=C(C=O)C=C1 ZRSNZINYAWTAHE-UHFFFAOYSA-N 0.000 claims 1
- 229930006728 pinane Natural products 0.000 claims 1
- 229930007790 rose oxide Natural products 0.000 claims 1
- OENHQHLEOONYIE-JLTXGRSLSA-N β-Carotene Chemical compound CC=1CCCC(C)(C)C=1\C=C\C(\C)=C\C=C\C(\C)=C\C=C\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C OENHQHLEOONYIE-JLTXGRSLSA-N 0.000 claims 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/39—Organic or inorganic per-compounds
- C11D3/3902—Organic or inorganic per-compounds combined with specific additives
- C11D3/3905—Bleach activators or bleach catalysts
- C11D3/3932—Inorganic compounds or complexes
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/168—Organometallic compounds or orgometallic complexes
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/50—Perfumes
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Inorganic Chemistry (AREA)
- Detergent Compositions (AREA)
- Fats And Perfumes (AREA)
Claims (5)
1. Жидкая отбеливающая композиция с рН 10 или ниже, содержащая
(а) катализатор отбеливания на воздухе на основе переходного металла, причем отбеливающая композиция содержит менее 1 мас./мас.% общей концентрации надкислоты или пероксида водорода или его источника;
(b) от 0,001 до 3 мас./мас.% отдушки, причем отдушку выбирают из группы, включающей: альфа-демаскон, дельта-демаскон, Iso Е super, коричный альдегид, гексилкоричный альдегид, бутилкоричный альдегид, анисовый альдегид, линалоол, тетрагидролиналоол, ундекавертол, гераниол, нерол, цитронеллол, цитраль, Роза-оксид, геранилацетат, цитронеллилацетат, кумарин, линалилацетат, геранилнитрат, цитронеллилнитрил, нитрил коричной кислоты и цитронитрил, амилкоричный альдегид, метилантранилат, диэтилантранилат, метил-н-ацетилантранилат, дифенилоксид, вердокс, бензилацетат, диола, оранжевые кристаллы, пеонил, клональ, лимонен, камфора, антранилат, диизобутилантранилат, вердилацетат, пинан, велоутон, альфа-метилионон и дамасценон; и
(с) остальные носители и дополнительные ингредиенты до 100 мас./мас.% от всей отбеливающей композиции,
причем отбеливающая активность жидкой отбеливающей композиции по меньшей мере в 10 раз выше по сравнению с отбеливающей композицией, в которой в качестве отдушки присутствует мольный эквивалент цитронеллаля, после хранения при 37°С в течение 14 сут, как показала отбеливающая активность катализатора на основе переходного металла по отношению к Кислому Голубому 45 в присутствии пероксида водорода или отбеливающая активность катализатора на основе переходного металла по отношению к бета-каротину в отсутствие пероксильных форм.
2. Отбеливающая композиция по п.1, содержащая 0,05-2 мас./мас.% отдушки.
3. Жидкая отбеливающая композиция по п.1 или 2, которая имеет рН в интервале 6-9.
4. Отбеливающая композиция по п.1, в которой катализатор отбеливания на воздухе представляет собой мономерный комплекс переходного металла Fe(II)-(III)-(IV)-(V), имеющий формулу (I)
в которой каждый R независимо выбирают из
водорода, F, Cl, Br, гидроксила, С1-С4-алкил-О-, -NH-CO-H,
-NH-CO-Cl-C4-алкила, -NH2, -NH-C1-C4-алкила и С1-С4-алкила;
R1 и R2 независимо выбирают из
C1-C4-алкила,
С6-С10-арила и
группы, содержащей гетероатом, способный к координации с переходным металлом, в которой по меньшей мере один из R1 и R2 является группой, содержащей гетероатом;
R3 и R4 независимо выбирают из водорода, С1-С8-алкила, С1-С8-алкил-О-C1-C8-алкила, C1-C8-алкил-O-C6-C10-арила, C6-C10-арила, C1-C8-гидроксиалкила и -(CH2)nC(O)OR5,
где R5 независимо выбирают из водорода, C1-С4-алкила, n равен 0-4, и их смесей;
и
Х выбирают из С=О, -[C(R6)2]y, в которой Y равен 0-3 и каждый R6 независимо выбирают из водорода, гидроксила, С1-С4-алкокси и С1-С4-алкила.
5. Способ отбеливания загрязнений ткани, включающий стадии обработки субстрата отбеливающей композицией, как определено по любому из предшествующих пунктов, в водной среде, ополаскивания субстрата и сушки субстрата.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB0323275.8 | 2003-10-04 | ||
| GBGB0323275.8A GB0323275D0 (en) | 2003-10-04 | 2003-10-04 | Bleaching composition |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| RU2006110633A true RU2006110633A (ru) | 2007-10-10 |
| RU2365619C2 RU2365619C2 (ru) | 2009-08-27 |
Family
ID=29415529
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| RU2006110633/04A RU2365619C2 (ru) | 2003-10-04 | 2004-09-13 | Отбеливающая композиция |
Country Status (17)
| Country | Link |
|---|---|
| US (1) | US20070004614A1 (ru) |
| EP (1) | EP1668106B1 (ru) |
| JP (1) | JP2007533784A (ru) |
| CN (1) | CN100430461C (ru) |
| AR (1) | AR045854A1 (ru) |
| AT (1) | ATE360676T1 (ru) |
| AU (1) | AU2004278466B2 (ru) |
| BR (1) | BRPI0413879A (ru) |
| CA (1) | CA2535014A1 (ru) |
| DE (1) | DE602004006144T2 (ru) |
| ES (1) | ES2286665T3 (ru) |
| GB (1) | GB0323275D0 (ru) |
| MY (1) | MY139097A (ru) |
| PL (1) | PL1668106T3 (ru) |
| RU (1) | RU2365619C2 (ru) |
| WO (1) | WO2005033256A1 (ru) |
| ZA (1) | ZA200601276B (ru) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2013092051A1 (en) | 2011-12-20 | 2013-06-27 | Unilever Plc | Liquid detergents comprising lipase and bleach catalyst |
| EP2912112B1 (en) * | 2012-10-29 | 2019-12-18 | Ashland Licensing and Intellectual Property LLC | Resin compositions |
| AU2017225964A1 (en) | 2016-03-02 | 2018-09-20 | Harris Research, Inc. | Stain and odor treatment |
| CN112574819A (zh) * | 2020-11-18 | 2021-03-30 | 云南中烟工业有限责任公司 | 一种巨峰葡萄香精及其制备方法和用途 |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ATE278761T1 (de) * | 1996-03-19 | 2004-10-15 | Procter & Gamble | Herstellngsverfahren von maschinengeschirrspülreinigern enthaltend blumiges parfüm und builder |
| EP0892844B1 (en) * | 1996-04-10 | 2001-05-30 | Unilever N.V. | Cleaning process |
| US5876625A (en) * | 1996-07-22 | 1999-03-02 | Carnegie Mellon University | Metal ligand containing bleaching compositions |
| AU4061900A (en) * | 1999-04-01 | 2000-10-23 | Procter & Gamble Company, The | Transition metal bleaching agents |
| GB0030673D0 (en) * | 2000-12-15 | 2001-01-31 | Unilever Plc | Ligand and complex for catalytically bleaching a substrate |
| MXPA03007235A (es) * | 2001-02-14 | 2003-12-04 | Procter & Gamble | Composiciones para lavavajillas que comprenden un blanqueador de peroxido de diacilo y liberacion de perfume. |
| US6723687B2 (en) * | 2001-05-01 | 2004-04-20 | The Procter & Gamble Company | Automatic dishwashing compositions comprising diacyl peroxide bleach and blooming perfume |
| GB0104980D0 (en) * | 2001-02-28 | 2001-04-18 | Unilever Plc | Liquid cleaning compositions and their use |
| FR2842753B1 (fr) * | 2002-07-26 | 2005-03-11 | Financ D Etudes Et De Dev Ind | Procede de realisation d'un outil destine au formage d'une matiere et outil susceptible d'etre realise par ce procede |
| JP4163462B2 (ja) * | 2002-07-29 | 2008-10-08 | 旭テック株式会社 | 鋳造用金型 |
| EP1631653B1 (en) * | 2003-06-09 | 2007-04-04 | Unilever Plc | Liquid bleaching composition |
| GB0313249D0 (en) * | 2003-06-09 | 2003-07-16 | Unilever Plc | Bleaching composition |
-
2003
- 2003-10-04 GB GBGB0323275.8A patent/GB0323275D0/en not_active Ceased
-
2004
- 2004-09-13 CA CA002535014A patent/CA2535014A1/en not_active Abandoned
- 2004-09-13 BR BRPI0413879-1A patent/BRPI0413879A/pt not_active Application Discontinuation
- 2004-09-13 JP JP2006529987A patent/JP2007533784A/ja active Pending
- 2004-09-13 ZA ZA200601276A patent/ZA200601276B/en unknown
- 2004-09-13 AT AT04765235T patent/ATE360676T1/de not_active IP Right Cessation
- 2004-09-13 ES ES04765235T patent/ES2286665T3/es not_active Expired - Lifetime
- 2004-09-13 EP EP04765235A patent/EP1668106B1/en not_active Expired - Lifetime
- 2004-09-13 US US10/574,813 patent/US20070004614A1/en not_active Abandoned
- 2004-09-13 RU RU2006110633/04A patent/RU2365619C2/ru not_active IP Right Cessation
- 2004-09-13 DE DE602004006144T patent/DE602004006144T2/de not_active Expired - Lifetime
- 2004-09-13 WO PCT/EP2004/010324 patent/WO2005033256A1/en not_active Ceased
- 2004-09-13 AU AU2004278466A patent/AU2004278466B2/en not_active Ceased
- 2004-09-13 CN CNB200480028887XA patent/CN100430461C/zh not_active Expired - Fee Related
- 2004-09-13 PL PL04765235T patent/PL1668106T3/pl unknown
- 2004-10-01 MY MYPI20044039A patent/MY139097A/en unknown
- 2004-10-01 AR ARP040103568A patent/AR045854A1/es unknown
Also Published As
| Publication number | Publication date |
|---|---|
| ES2286665T3 (es) | 2007-12-01 |
| CN1863898A (zh) | 2006-11-15 |
| AU2004278466A1 (en) | 2005-04-14 |
| MY139097A (en) | 2009-08-28 |
| RU2365619C2 (ru) | 2009-08-27 |
| EP1668106B1 (en) | 2007-04-25 |
| EP1668106A1 (en) | 2006-06-14 |
| US20070004614A1 (en) | 2007-01-04 |
| CN100430461C (zh) | 2008-11-05 |
| JP2007533784A (ja) | 2007-11-22 |
| CA2535014A1 (en) | 2005-04-14 |
| DE602004006144T2 (de) | 2008-01-03 |
| WO2005033256A1 (en) | 2005-04-14 |
| PL1668106T3 (pl) | 2007-08-31 |
| GB0323275D0 (en) | 2003-11-05 |
| ZA200601276B (en) | 2007-05-30 |
| DE602004006144D1 (de) | 2007-06-06 |
| ATE360676T1 (de) | 2007-05-15 |
| BRPI0413879A (pt) | 2006-10-24 |
| AU2004278466B2 (en) | 2007-11-01 |
| AR045854A1 (es) | 2005-11-16 |
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Legal Events
| Date | Code | Title | Description |
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| MM4A | The patent is invalid due to non-payment of fees |
Effective date: 20100914 |