CN100361712C - 恶臭味冲消剂组合物,使该组合物分散在空间内的方法,和赋予基质moc效果的方法 - Google Patents
恶臭味冲消剂组合物,使该组合物分散在空间内的方法,和赋予基质moc效果的方法 Download PDFInfo
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- CN100361712C CN100361712C CNB2005100879202A CN200510087920A CN100361712C CN 100361712 C CN100361712 C CN 100361712C CN B2005100879202 A CNB2005100879202 A CN B2005100879202A CN 200510087920 A CN200510087920 A CN 200510087920A CN 100361712 C CN100361712 C CN 100361712C
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- moc
- spice
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- LXCFILQKKLGQFO-UHFFFAOYSA-N methylparaben Chemical compound COC(=O)C1=CC=C(O)C=C1 LXCFILQKKLGQFO-UHFFFAOYSA-N 0.000 description 1
- 229960002216 methylparaben Drugs 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000002808 molecular sieve Substances 0.000 description 1
- QJKBHDRXPAOHSY-UHFFFAOYSA-N morpholine;pyridine Chemical compound C1COCCN1.C1=CC=NC=C1 QJKBHDRXPAOHSY-UHFFFAOYSA-N 0.000 description 1
- DUWWHGPELOTTOE-UHFFFAOYSA-N n-(5-chloro-2,4-dimethoxyphenyl)-3-oxobutanamide Chemical compound COC1=CC(OC)=C(NC(=O)CC(C)=O)C=C1Cl DUWWHGPELOTTOE-UHFFFAOYSA-N 0.000 description 1
- WASNIKZYIWZQIP-AWEZNQCLSA-N nerolidol Natural products CC(=CCCC(=CCC[C@@H](O)C=C)C)C WASNIKZYIWZQIP-AWEZNQCLSA-N 0.000 description 1
- 229960002715 nicotine Drugs 0.000 description 1
- SNICXCGAKADSCV-UHFFFAOYSA-N nicotine Natural products CN1CCCC1C1=CC=CN=C1 SNICXCGAKADSCV-UHFFFAOYSA-N 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- BOPPSUHPZARXTH-UHFFFAOYSA-N ocean propanal Chemical compound O=CC(C)CC1=CC=C2OCOC2=C1 BOPPSUHPZARXTH-UHFFFAOYSA-N 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 150000002923 oximes Chemical class 0.000 description 1
- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 1
- QNGNSVIICDLXHT-UHFFFAOYSA-N para-ethylbenzaldehyde Natural products CCC1=CC=C(C=O)C=C1 QNGNSVIICDLXHT-UHFFFAOYSA-N 0.000 description 1
- RUVINXPYWBROJD-UHFFFAOYSA-N para-methoxyphenyl Natural products COC1=CC=C(C=CC)C=C1 RUVINXPYWBROJD-UHFFFAOYSA-N 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- WVDDGKGOMKODPV-ZQBYOMGUSA-N phenyl(114C)methanol Chemical compound O[14CH2]C1=CC=CC=C1 WVDDGKGOMKODPV-ZQBYOMGUSA-N 0.000 description 1
- 150000003053 piperidines Chemical class 0.000 description 1
- 229950001046 piroctone Drugs 0.000 description 1
- BTSZTGGZJQFALU-UHFFFAOYSA-N piroctone olamine Chemical compound NCCO.CC(C)(C)CC(C)CC1=CC(C)=CC(=O)N1O BTSZTGGZJQFALU-UHFFFAOYSA-N 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- 239000004405 propyl p-hydroxybenzoate Substances 0.000 description 1
- 235000010232 propyl p-hydroxybenzoate Nutrition 0.000 description 1
- QELSKZZBTMNZEB-UHFFFAOYSA-N propylparaben Chemical compound CCCOC(=O)C1=CC=C(O)C=C1 QELSKZZBTMNZEB-UHFFFAOYSA-N 0.000 description 1
- 150000003233 pyrroles Chemical class 0.000 description 1
- 229960004889 salicylic acid Drugs 0.000 description 1
- HFHDHCJBZVLPGP-UHFFFAOYSA-N schardinger α-dextrin Chemical compound O1C(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(O)C2O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC2C(O)C(O)C1OC2CO HFHDHCJBZVLPGP-UHFFFAOYSA-N 0.000 description 1
- 150000004666 short chain fatty acids Chemical class 0.000 description 1
- 229910052814 silicon oxide Inorganic materials 0.000 description 1
- ZFRKQXVRDFCRJG-UHFFFAOYSA-N skatole Natural products C1=CC=C2C(C)=CNC2=C1 ZFRKQXVRDFCRJG-UHFFFAOYSA-N 0.000 description 1
- 239000002893 slag Substances 0.000 description 1
- URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000004334 sorbic acid Substances 0.000 description 1
- 235000010199 sorbic acid Nutrition 0.000 description 1
- 229940075582 sorbic acid Drugs 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 229960000790 thymol Drugs 0.000 description 1
- CRDAMVZIKSXKFV-UHFFFAOYSA-N trans-Farnesol Natural products CC(C)=CCCC(C)=CCCC(C)=CCO CRDAMVZIKSXKFV-UHFFFAOYSA-N 0.000 description 1
- RBNWAMSGVWEHFP-UHFFFAOYSA-N trans-p-Menthane-1,8-diol Chemical compound CC(C)(O)C1CCC(C)(O)CC1 RBNWAMSGVWEHFP-UHFFFAOYSA-N 0.000 description 1
- WGIWBXUNRXCYRA-UHFFFAOYSA-H trizinc;2-hydroxypropane-1,2,3-tricarboxylate Chemical compound [Zn+2].[Zn+2].[Zn+2].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O.[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O WGIWBXUNRXCYRA-UHFFFAOYSA-H 0.000 description 1
- MWOOGOJBHIARFG-UHFFFAOYSA-N vanillin Chemical compound COC1=CC(C=O)=CC=C1O MWOOGOJBHIARFG-UHFFFAOYSA-N 0.000 description 1
- FGQOOHJZONJGDT-UHFFFAOYSA-N vanillin Natural products COC1=CC(O)=CC(C=O)=C1 FGQOOHJZONJGDT-UHFFFAOYSA-N 0.000 description 1
- 235000012141 vanillin Nutrition 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 239000010457 zeolite Substances 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011746 zinc citrate Substances 0.000 description 1
- 229940068475 zinc citrate Drugs 0.000 description 1
- 235000006076 zinc citrate Nutrition 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/612—Esters of carboxylic acids having a carboxyl group bound to an acyclic carbon atom and having a six-membered aromatic ring in the acid moiety
- C07C69/618—Esters of carboxylic acids having a carboxyl group bound to an acyclic carbon atom and having a six-membered aromatic ring in the acid moiety having unsaturation outside the six-membered aromatic ring
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/37—Esters of carboxylic acids
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L9/00—Disinfection, sterilisation or deodorisation of air
- A61L9/01—Deodorant compositions
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q15/00—Anti-perspirants or body deodorants
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/66—Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety
- C07C69/73—Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety of unsaturated acids
- C07C69/732—Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety of unsaturated acids of unsaturated hydroxy carboxylic acids
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/66—Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety
- C07C69/73—Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety of unsaturated acids
- C07C69/734—Ethers
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Epidemiology (AREA)
- Birds (AREA)
- Emergency Medicine (AREA)
- Fats And Perfumes (AREA)
- Disinfection, Sterilisation Or Deodorisation Of Air (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Cosmetics (AREA)
- Anti-Oxidant Or Stabilizer Compositions (AREA)
Abstract
Description
化合物编码 | A类化合物+恶臭味 | 单独的恶臭味 |
4 | 3.4 | 3.9 |
3 | 2.9 | 3.9 |
8 | 2.8 | 3.9 |
6 | 3.5 | 3.9 |
10 | 2.7 | 3.7 |
9 | 3.3 | 3.7 |
5 | 2.9 | 3.9 |
7 | 3.0 | 3.9 |
2 | 2.9 | 3.9 |
1 | 2.8 | 3.9 |
OMC | 2.6 | 4.0 |
BC | 2.3 | 4.1 |
PC | 2.2 | 4.3 |
A类化合物 | 50%DHF/50%A类化合物 | 单独的恶臭味 |
4 | 3.0 | 3.9 |
3 | 3.1 | 3.9 |
8 | 3.3 | 3.9 |
6 | 2.9 | 3.9 |
10 | 3.1 | 3.7 |
9 | 2.8 | 3.7 |
5 | 2.4 | 3.9 |
7 | 3.3 | 3.9 |
2 | 2.5 | 3.9 |
1 | 3.0 | 3.9 |
OMC | 2.3 | 4.0 |
样品编号 | DHF/MOC | DHF | MOC |
C | 溶液3 | ||
D | 溶液2 | ||
E | 溶液1 |
样品C | 样品D | 样品E | |
30分钟 | 2.6 | 3.4 | 3.3 |
3小时 | 2.6 | 3.0 | 3.3 |
材料 | 分数 |
肉桂醛 | 5(气味值=12000) |
苯甲酸己酯 | 3(气味值=1000) |
己基肉桂醛 | 2(气味值=384) |
二丙二醇 | 1(0V=40 ) |
化合物1 | 1 |
2 | 1 |
3 | 4 |
4 | 3 |
5 | 3 |
6 | 1 |
7 | 2 |
8 | 2 |
9 | 2 |
10 | 2 |
OMC | 1 |
3小时后腋臭味 | |||
小组成员 | 对照 | 香料 | 香料+OMC |
1 | 3 | 3 | 1 |
2 | 4 | 3 | 2 |
3 | 3 | 1 | 1 |
4 | 4 | 2 | 2 |
5 | 4 | 2 | 3 |
6 | 3 | 2 | 3 |
7 | 3 | 3 | 1 |
8 | 4 | 2 | 2 |
9 | 5 | 3 | 2 |
10 | 3 | 3 | 2 |
11 | 4 | 3 | 1 |
12 | 4 | 2 | 3 |
平均 | 3.6 | 2.3 | 1.8 |
STDEV | 0.651 | 0.669 | 0.793 |
RSD | 18.02 | 28.92 | 45.14 |
降低% | 36.0 | 51.4 |
3小时 在头发上的烟草烟 | |||
小组成员 | 对照 | 1%香料 | 香料+MOC |
1 | 4 | 3 | 1 |
2 | 3 | 3 | 3 |
3 | 4 | 2 | 3 |
4 | 4 | 2 | 2 |
5 | 3 | 3 | 3 |
6 | 5 | 3 | 2 |
7 | 4 | 2 | 2 |
8 | 4 | 2 | 2 |
9 | 4 | 3 | 2 |
10 | 3 | 2 | 2 |
11 | 4 | 3 | 2 |
12 | 5 | 3 | 2 |
平均 | 3.9 | 2.5 | 2.1 |
STDEV | 0.669 | 0.515 | 0.577 |
RSD | 17.30 | 20.32 | 27.64 |
% | 34.4 | 45.9 |
恶臭味 | OMC | 对照 |
烟尘 | 1.8 | 4.5 |
洋葱 | 2.7 | 4.0 |
大蒜 | 2.6 | 4.8 |
Claims (13)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US09/745,790 US6610648B2 (en) | 2000-12-22 | 2000-12-22 | Malodor counteractant compositions |
US09/745,790 | 2000-12-22 |
Related Parent Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN01821078.3A Division CN1227209C (zh) | 2000-12-22 | 2001-12-18 | 恶臭味冲消剂组合物 |
Publications (2)
Publication Number | Publication Date |
---|---|
CN1721001A CN1721001A (zh) | 2006-01-18 |
CN100361712C true CN100361712C (zh) | 2008-01-16 |
Family
ID=24998269
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN01821078.3A Expired - Lifetime CN1227209C (zh) | 2000-12-22 | 2001-12-18 | 恶臭味冲消剂组合物 |
CNB2005100879202A Expired - Lifetime CN100361712C (zh) | 2000-12-22 | 2001-12-18 | 恶臭味冲消剂组合物,使该组合物分散在空间内的方法,和赋予基质moc效果的方法 |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN01821078.3A Expired - Lifetime CN1227209C (zh) | 2000-12-22 | 2001-12-18 | 恶臭味冲消剂组合物 |
Country Status (10)
Country | Link |
---|---|
US (1) | US6610648B2 (zh) |
EP (1) | EP1345883B1 (zh) |
CN (2) | CN1227209C (zh) |
AT (1) | ATE457970T1 (zh) |
BR (1) | BR0116345B1 (zh) |
CA (1) | CA2428903C (zh) |
DE (1) | DE60141347D1 (zh) |
ES (1) | ES2340360T3 (zh) |
MX (1) | MXPA03005658A (zh) |
WO (1) | WO2002051788A1 (zh) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN107510858A (zh) * | 2011-10-20 | 2017-12-26 | 国际香料和香精公司 | 低挥发的活性恶臭消除剂及其用法 |
Families Citing this family (75)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20070276053A1 (en) * | 1999-09-17 | 2007-11-29 | Aproa Asesores S.C. | Soap Product with Absorbent Composition of Matter for Controlled Release of an Active Ingredient |
US20050044819A1 (en) | 2003-09-02 | 2005-03-03 | Chomik Richard S. | Waste storage device |
US7958704B2 (en) | 2001-05-02 | 2011-06-14 | Playtex Products, Inc. | Waste disposal device including a mechanism for scoring a flexible tubing dispensed from a cartridge |
US7503152B2 (en) | 2001-05-02 | 2009-03-17 | Playtex Products, Inc. | Waste disposal device including rotating cartridge coupled to lid |
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US8091325B2 (en) | 2001-05-02 | 2012-01-10 | Playtex Products, Inc. | Waste disposal device including a diaphragm for twisting a flexible tubing dispensed from a cartridge |
US7503159B2 (en) | 2001-05-02 | 2009-03-17 | Playtex Products, Inc. | Waste disposal device including an external actuation mechanism to operate a cartridge |
US7316100B2 (en) | 2001-05-02 | 2008-01-08 | Playtex Products, Inc. | Waste disposal device including a film cutting and sealing device |
US7434377B2 (en) | 2001-05-02 | 2008-10-14 | Playtex Products, Inc. | Waste disposal device including a rotatable geared rim to operate a cartridge |
WO2003089312A2 (en) * | 2002-04-17 | 2003-10-30 | Playtex Products, Inc. | Disposable cassette for incremental withdrawal of tubular plastic with malodor-counteractant capacity |
US7204976B2 (en) * | 2003-05-30 | 2007-04-17 | Colgate-Palmolive Company | High efficacy gel with low glycol content |
US20040248762A1 (en) * | 2003-06-09 | 2004-12-09 | Mcgee Thomas | Malodor counteractant compositions |
GB0320441D0 (en) | 2003-09-02 | 2003-10-01 | Givaudan Sa | Organic compounds |
AR045608A1 (es) * | 2003-09-08 | 2005-11-02 | Colgate Palmolive Co | Gel transparente antitranspirante con bajo contenido de glicol |
US6925781B1 (en) | 2004-02-03 | 2005-08-09 | Playtex Products, Inc. | Integrated cutting tool for waste disposal method and apparatus |
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US7015179B1 (en) | 2004-12-22 | 2006-03-21 | Unilever Home & Personal Care Usa | Reduced odor toilet bar composition |
ES2392177T3 (es) * | 2005-02-15 | 2012-12-05 | Colgate-Palmolive Company | Composiciones de fragancia que reducen o eliminan el mal olor, métodos relacionados y composiciones de limpieza relacionadas |
JPWO2007043172A1 (ja) * | 2005-10-12 | 2009-04-16 | 日生バイオ株式会社 | タバコ用フィルタ |
GB0526279D0 (en) * | 2005-12-23 | 2006-02-01 | Givaudan Sa | Improvements in or related to organic compounds |
EP2059265B1 (en) * | 2006-08-28 | 2018-10-17 | Firmenich S.A. | Malodor counteracting compositions and method for their use |
EP2079487A1 (en) * | 2006-10-24 | 2009-07-22 | Givaudan SA | Malodor counteracting compositions |
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US7976828B2 (en) | 2007-02-02 | 2011-07-12 | Colgate-Palmolive Company | Antiperspirant/deodorant composition |
WO2008155683A1 (en) | 2007-06-18 | 2008-12-24 | Firmenich Sa | Malodor counteracting compositions and method for their use |
US20090000562A1 (en) | 2007-06-26 | 2009-01-01 | The Clorox Company | Waste encapsulating animal litter |
US20090053268A1 (en) * | 2007-08-22 | 2009-02-26 | Depablo Juan J | Nanoparticle modified lubricants and waxes with enhanced properties |
US8012554B2 (en) * | 2007-09-12 | 2011-09-06 | Pactiv Corporation | Bags having odor management capabilities |
GB0725266D0 (en) * | 2007-12-28 | 2008-02-06 | Innospec Ltd | Novel esters and compositions and uses thereof |
CA2772709C (en) * | 2009-09-30 | 2015-07-21 | Colgate-Palmolive Company | Antiperspirant/deodorant composition |
CA2773164C (en) * | 2009-09-30 | 2014-09-16 | Colgate-Palmolive Company | Antiperspirant/deodorant composition comprising fatty acid and plant oil |
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US10343842B2 (en) | 2009-10-30 | 2019-07-09 | Munchkin, Inc. | System and method for disposing waste packages such as diapers |
US8833592B2 (en) | 2009-10-30 | 2014-09-16 | Munchkin, Inc. | System and method for disposing waste packages such as diapers |
US8739501B2 (en) | 2009-10-30 | 2014-06-03 | Munchkin, Inc. | System for disposing waste packages such as diapers |
US8635838B2 (en) | 2009-10-30 | 2014-01-28 | Munchkin, Inc. | System for disposing waste packages such as diapers |
US8567157B2 (en) | 2009-10-30 | 2013-10-29 | Munchkin, Inc. | System for disposing waste packages such as diapers |
CA2802652A1 (en) | 2010-07-06 | 2012-01-12 | Colgate-Palmolive Company | Personal care product and manufacture thereof |
GB201104766D0 (en) | 2011-03-22 | 2011-05-04 | Givaudan Sa | Compositions |
US20120294821A1 (en) * | 2011-05-20 | 2012-11-22 | International Flavors & Fragrances Inc. | Low Volatile Reactive Malodor Counteractives and Methods of Use Thereof |
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US20130210775A1 (en) | 2012-02-09 | 2013-08-15 | Kao Corporation | Agent for inhibiting odor of pyrazine derivatives |
US20130336914A1 (en) * | 2012-06-15 | 2013-12-19 | Steven Anthony Horenziak | Malodor control compositions having activated alkenes and methods thereof |
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EP2862597B1 (en) | 2013-10-18 | 2018-01-03 | International Flavors & Fragrances Inc. | Stable, flowable silica capsule formulation |
WO2015082380A1 (en) * | 2013-12-03 | 2015-06-11 | Unilever Plc | Deodorant compositions comprising hydrophilic cinnamic acid derivatives |
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CA2970656C (en) | 2014-12-11 | 2024-01-09 | Munchkin, Inc. | Container for receving multiple flexible bag assemblies |
WO2016172699A1 (en) | 2015-04-24 | 2016-10-27 | International Flavors & Fragrances Inc. | Delivery systems and methods of preparing the same |
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WO2018053356A1 (en) | 2016-09-16 | 2018-03-22 | International Flavors & Fragrances Inc. | Microcapsule compositions stabilized with viscosity control agents |
WO2017165615A1 (en) | 2016-03-24 | 2017-09-28 | The Procter & Gamble Company | Hair care compositions comprising malodor reduction compositions |
JP7159871B2 (ja) * | 2016-12-12 | 2022-10-25 | 理研香料ホールディングス株式会社 | 消臭剤 |
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US12115290B2 (en) * | 2017-10-11 | 2024-10-15 | Microban Products Company | Odor control composition and carpet having a durable odor control property |
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WO2022120109A1 (en) | 2020-12-04 | 2022-06-09 | The Procter & Gamble Company | Hair care compositions comprising malodor reduction materials |
US11771635B2 (en) | 2021-05-14 | 2023-10-03 | The Procter & Gamble Company | Shampoo composition |
US11986543B2 (en) | 2021-06-01 | 2024-05-21 | The Procter & Gamble Company | Rinse-off compositions with a surfactant system that is substantially free of sulfate-based surfactants |
WO2024173230A1 (en) | 2023-02-16 | 2024-08-22 | International Flavors & Fragrances Inc. | Transparent alcohol-free base for fragrance compositions |
WO2024192221A1 (en) | 2023-03-15 | 2024-09-19 | International Flavors & Fragrances Inc. | High performance fragrance compositions for rinse-off conditioner |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4663315A (en) * | 1984-01-31 | 1987-05-05 | Earth Chemical Company, Limited | Device and method for vaporizing thermally vaporizable composition |
EP0404470A1 (en) * | 1989-06-19 | 1990-12-27 | Quest International B.V. | Fragrance compositions and their use in detergent products |
US5066640A (en) * | 1988-05-13 | 1991-11-19 | Consortium Fur Elektrochemische Industrie Gmbh | Phenylethl o-methylcinnamate, a process for preparation and a fragrance composition containing same |
US5135747A (en) * | 1991-05-17 | 1992-08-04 | Chesebrough-Pond's Usa Co., Division Of Conopco, Inc. | Deodorant/antiperspirant products with fragrance and encapsulated odor counteractant |
Family Cites Families (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3074891A (en) | 1960-03-24 | 1963-01-22 | Fritzsche Brothers Inc | Compositions and methods for the deodorization of spaces |
US3077457A (en) | 1960-04-15 | 1963-02-12 | Fritzsche Brothers Inc | Fumaric acid ester space deodorant and method of using same |
US3074892A (en) | 1960-05-09 | 1963-01-22 | Fritzsche Brothers Inc | Space deodorant composition and method of using same |
US4009253A (en) | 1973-11-05 | 1977-02-22 | Monsanto Company | 4-cyclohexyl-4-methyl-2-pentanone useful as a malodor counteractant |
US4622221A (en) | 1975-11-05 | 1986-11-11 | Bush Boake Allen Inc. | Method, compositions and compounds, useful in room fresheners employing cyclohexyl alcohol and ester derivatives |
US4187251A (en) | 1976-12-16 | 1980-02-05 | Schleppnik Alfred A | Malodor counteractants |
US4310512A (en) | 1977-08-29 | 1982-01-12 | Bush Boake Allen Inc. | Derivatives of acetic and propionic acids, compositions containing same and use as malodor counteractants |
BR9204339A (pt) | 1991-11-08 | 1993-05-18 | Unilever Nv | Composicao de pertume,composicao detergente,composicao de condicionamento de tecido e processo para tratar texteis |
US5658580A (en) * | 1993-09-09 | 1997-08-19 | Chanel, Inc. | Skin cream composition |
JP3485375B2 (ja) | 1995-02-17 | 2004-01-13 | 株式会社資生堂 | 皮膚外用剤 |
JPH0940993A (ja) * | 1995-07-28 | 1997-02-10 | Kanebo Ltd | 調香方法 |
DE19547634A1 (de) * | 1995-12-20 | 1997-08-21 | Sara Lee De Nv | Photostabile, emulgatorfreie, kosmetische Mittel |
US6048517A (en) * | 1996-11-25 | 2000-04-11 | Schering-Plough Healthcare Products, Inc. | High SPF sunscreen formulations |
-
2000
- 2000-12-22 US US09/745,790 patent/US6610648B2/en not_active Expired - Lifetime
-
2001
- 2001-12-18 ES ES01271942T patent/ES2340360T3/es not_active Expired - Lifetime
- 2001-12-18 CA CA2428903A patent/CA2428903C/en not_active Expired - Lifetime
- 2001-12-18 EP EP01271942A patent/EP1345883B1/en not_active Expired - Lifetime
- 2001-12-18 CN CN01821078.3A patent/CN1227209C/zh not_active Expired - Lifetime
- 2001-12-18 MX MXPA03005658A patent/MXPA03005658A/es active IP Right Grant
- 2001-12-18 CN CNB2005100879202A patent/CN100361712C/zh not_active Expired - Lifetime
- 2001-12-18 AT AT01271942T patent/ATE457970T1/de not_active IP Right Cessation
- 2001-12-18 DE DE60141347T patent/DE60141347D1/de not_active Expired - Lifetime
- 2001-12-18 BR BRPI0116345-0A patent/BR0116345B1/pt active IP Right Grant
- 2001-12-18 WO PCT/CH2001/000726 patent/WO2002051788A1/en not_active Application Discontinuation
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4663315A (en) * | 1984-01-31 | 1987-05-05 | Earth Chemical Company, Limited | Device and method for vaporizing thermally vaporizable composition |
US5066640A (en) * | 1988-05-13 | 1991-11-19 | Consortium Fur Elektrochemische Industrie Gmbh | Phenylethl o-methylcinnamate, a process for preparation and a fragrance composition containing same |
EP0404470A1 (en) * | 1989-06-19 | 1990-12-27 | Quest International B.V. | Fragrance compositions and their use in detergent products |
US5135747A (en) * | 1991-05-17 | 1992-08-04 | Chesebrough-Pond's Usa Co., Division Of Conopco, Inc. | Deodorant/antiperspirant products with fragrance and encapsulated odor counteractant |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN107510858A (zh) * | 2011-10-20 | 2017-12-26 | 国际香料和香精公司 | 低挥发的活性恶臭消除剂及其用法 |
Also Published As
Publication number | Publication date |
---|---|
CA2428903C (en) | 2011-02-01 |
BR0116345B1 (pt) | 2014-04-22 |
EP1345883B1 (en) | 2010-02-17 |
US20030008787A1 (en) | 2003-01-09 |
ES2340360T3 (es) | 2010-06-02 |
ATE457970T1 (de) | 2010-03-15 |
EP1345883A1 (en) | 2003-09-24 |
DE60141347D1 (de) | 2010-04-01 |
CN1721001A (zh) | 2006-01-18 |
WO2002051788A1 (en) | 2002-07-04 |
CA2428903A1 (en) | 2002-07-04 |
BR0116345A (pt) | 2004-02-25 |
US6610648B2 (en) | 2003-08-26 |
CN1227209C (zh) | 2005-11-16 |
CN1481351A (zh) | 2004-03-10 |
MXPA03005658A (es) | 2004-12-03 |
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