CN111432851B - 挥发性成分限制或消除对恶臭的感知的用途 - Google Patents
挥发性成分限制或消除对恶臭的感知的用途 Download PDFInfo
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- CN111432851B CN111432851B CN201880075477.2A CN201880075477A CN111432851B CN 111432851 B CN111432851 B CN 111432851B CN 201880075477 A CN201880075477 A CN 201880075477A CN 111432851 B CN111432851 B CN 111432851B
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- 150000001875 compounds Chemical class 0.000 claims description 417
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- OEVIJAZJVZDBQL-UHFFFAOYSA-N 1-(5,5-dimethylcyclohexen-1-yl)pent-4-en-1-one Chemical compound CC1(C)CCC=C(C(=O)CCC=C)C1 OEVIJAZJVZDBQL-UHFFFAOYSA-N 0.000 claims description 32
- 238000000034 method Methods 0.000 claims description 30
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- 230000002401 inhibitory effect Effects 0.000 claims description 18
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- XKZRHGWZYDQHSN-UHFFFAOYSA-N undec-2-en-4-one Chemical compound CCCCCCCC(=O)C=CC XKZRHGWZYDQHSN-UHFFFAOYSA-N 0.000 description 1
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- MWOOGOJBHIARFG-UHFFFAOYSA-N vanillin Chemical compound COC1=CC(C=O)=CC=C1O MWOOGOJBHIARFG-UHFFFAOYSA-N 0.000 description 1
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- 239000011746 zinc citrate Substances 0.000 description 1
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- 235000006076 zinc citrate Nutrition 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
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- 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
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- A—HUMAN NECESSITIES
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- 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
- A61K8/34—Alcohols
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- 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
- A61K8/34—Alcohols
- A61K8/347—Phenols
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- 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
- A61K8/35—Ketones, e.g. benzophenone
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- A—HUMAN NECESSITIES
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- 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
- A61K8/49—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
- A61K8/4973—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with oxygen as the only hetero atom
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- A—HUMAN NECESSITIES
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- 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
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- A—HUMAN NECESSITIES
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- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q13/00—Formulations or additives for perfume preparations
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11B—PRODUCING, e.g. BY PRESSING RAW MATERIALS OR BY EXTRACTION FROM WASTE MATERIALS, REFINING OR PRESERVING FATS, FATTY SUBSTANCES, e.g. LANOLIN, FATTY OILS OR WAXES; ESSENTIAL OILS; PERFUMES
- C11B9/00—Essential oils; Perfumes
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- C11B9/0034—Essential oils; Perfumes compounds containing an alicyclic ring not condensed with another ring the ring containing six carbon atoms
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- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11B—PRODUCING, e.g. BY PRESSING RAW MATERIALS OR BY EXTRACTION FROM WASTE MATERIALS, REFINING OR PRESERVING FATS, FATTY SUBSTANCES, e.g. LANOLIN, FATTY OILS OR WAXES; ESSENTIAL OILS; PERFUMES
- C11B9/00—Essential oils; Perfumes
- C11B9/0042—Essential oils; Perfumes compounds containing condensed hydrocarbon rings
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- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11B—PRODUCING, e.g. BY PRESSING RAW MATERIALS OR BY EXTRACTION FROM WASTE MATERIALS, REFINING OR PRESERVING FATS, FATTY SUBSTANCES, e.g. LANOLIN, FATTY OILS OR WAXES; ESSENTIAL OILS; PERFUMES
- C11B9/00—Essential oils; Perfumes
- C11B9/0042—Essential oils; Perfumes compounds containing condensed hydrocarbon rings
- C11B9/0046—Essential oils; Perfumes compounds containing condensed hydrocarbon rings containing only two condensed rings
- C11B9/0057—Spiro compounds
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- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11C—FATTY ACIDS FROM FATS, OILS OR WAXES; CANDLES; FATS, OILS OR FATTY ACIDS BY CHEMICAL MODIFICATION OF FATS, OILS, OR FATTY ACIDS OBTAINED THEREFROM
- C11C5/00—Candles
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Landscapes
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- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
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- Organic Chemistry (AREA)
- Birds (AREA)
- Emergency Medicine (AREA)
- General Chemical & Material Sciences (AREA)
- Fats And Perfumes (AREA)
- Disinfection, Sterilisation Or Deodorisation Of Air (AREA)
- Cosmetics (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Description
Claims (5)
Priority Applications (1)
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CN202310577174.3A CN116807912A (zh) | 2017-11-22 | 2018-11-21 | 挥发性成分限制或消除对恶臭的感知的用途 |
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EP18153067.6 | 2018-01-23 | ||
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EP18158074.7 | 2018-02-22 | ||
US201862754860P | 2018-11-02 | 2018-11-02 | |
US201862754875P | 2018-11-02 | 2018-11-02 | |
US201862754849P | 2018-11-02 | 2018-11-02 | |
US201862754899P | 2018-11-02 | 2018-11-02 | |
US62/754,875 | 2018-11-02 | ||
US62/754,860 | 2018-11-02 | ||
US62/754,849 | 2018-11-02 | ||
US62/754,899 | 2018-11-02 | ||
PCT/EP2018/082132 WO2019101821A2 (en) | 2017-11-22 | 2018-11-21 | Use of volatile compositions to limit or eliminate the perception of malodor |
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CN (2) | CN111432851B (zh) |
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CN116763963A (zh) * | 2017-11-22 | 2023-09-19 | 弗门尼舍有限公司 | 作为恶臭抵消成分的螺化合物 |
CN113873884B (zh) * | 2019-05-31 | 2024-06-14 | 弗门尼舍有限公司 | 节肢动物防治组合物 |
JP2021027813A (ja) * | 2019-08-09 | 2021-02-25 | 株式会社豊田中央研究所 | 嗅覚受容体の利用 |
JPWO2021085590A1 (zh) * | 2019-11-01 | 2021-05-06 | ||
US20230060897A1 (en) | 2019-12-17 | 2023-03-02 | Firmenich Sa | Compositions to limit or eliminate perception of raw material malodours in soap bases |
CN114096235A (zh) | 2020-02-21 | 2022-02-25 | 弗门尼舍有限公司 | 抗微生物组合物 |
CN117881386A (zh) | 2021-08-17 | 2024-04-12 | 弗门尼舍有限公司 | 抗微生物组合物 |
CN113663463B (zh) * | 2021-08-26 | 2022-08-02 | 日东生物科技(浙江)有限公司 | 一种异味抑制剂 |
WO2023224604A1 (en) * | 2022-05-17 | 2023-11-23 | Symrise Ag | Fragrance compositions and products conveying a positive mood |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2012050781A (ja) * | 2010-09-03 | 2012-03-15 | Kao Corp | 悪臭抑制剤 |
JP2012250958A (ja) * | 2011-06-06 | 2012-12-20 | Kao Corp | 悪臭抑制剤 |
WO2014191047A1 (en) * | 2013-05-31 | 2014-12-04 | Chemcom S.A. | Olfactory receptors involved in the perception of sweat carboxylic acids and the use thereof |
JP2017176134A (ja) * | 2016-03-31 | 2017-10-05 | 株式会社豊田中央研究所 | 嗅覚受容体を用いた評価方法 |
Family Cites Families (19)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE69203575T2 (de) * | 1991-11-25 | 1996-01-18 | Firmenich & Cie | Tertiäre cyclische Alkohole und ihre Anwendung als Riechstoffbestandteile. |
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 |
EP1411110B1 (en) | 2002-10-14 | 2007-08-22 | Firmenich Sa | Spiro compounds as perfuming ingredients |
JP2004263102A (ja) | 2003-03-03 | 2004-09-24 | Takasago Internatl Corp | 擬似体臭組成物 |
EP2806031B1 (en) | 2010-09-03 | 2016-11-02 | Kao Corporation | Method for searching for malodor control agent |
JP5692844B2 (ja) | 2010-09-24 | 2015-04-01 | 高砂香料工業株式会社 | スルフィド類用消臭剤組成物 |
JP5593271B2 (ja) * | 2011-06-06 | 2014-09-17 | 花王株式会社 | 悪臭抑制剤の探索方法 |
KR20140067074A (ko) | 2011-08-31 | 2014-06-03 | 코닝 인코포레이티드 | 허니콤 구조를 갖는 세라믹 성형 장치 및 방법 |
CN104203913B (zh) | 2012-03-20 | 2016-10-19 | 弗门尼舍有限公司 | 用于控释活性加香分子的化合物 |
JP6104058B2 (ja) | 2013-06-03 | 2017-03-29 | 花王株式会社 | カビ臭抑制剤の探索方法 |
US9914760B2 (en) | 2013-06-29 | 2018-03-13 | Firmenich Sa | Methods of identifying, isolating and using odorant and aroma receptors |
JP6422665B2 (ja) | 2014-04-14 | 2018-11-14 | 花王株式会社 | 腋臭抑制剤の探索方法 |
JP6588715B2 (ja) | 2014-04-14 | 2019-10-09 | 花王株式会社 | 尿臭抑制剤の探索方法 |
US20160089464A1 (en) * | 2014-09-26 | 2016-03-31 | The Procter & Gamble Company | Malodor reduction compositions |
BR112017006180B1 (pt) | 2014-10-14 | 2020-11-17 | Givaudan Sa | composição de redução de mau odor, produto para o consumidor, e composição de coloração para os cabelos |
US10918924B2 (en) * | 2015-02-02 | 2021-02-16 | RLT IP Ltd. | Frameworks, devices and methodologies configured to enable delivery of interactive skills training content, including content with multiple selectable expert knowledge variations |
EP3726218B1 (en) | 2015-06-10 | 2023-08-09 | Firmenich Sa | Cell lines for screening odorant and aroma receptors |
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 |
US9714401B2 (en) | 2015-10-19 | 2017-07-25 | The Procter & Gamble Company | Particles for malodor reduction |
-
2018
- 2018-11-21 WO PCT/EP2018/082132 patent/WO2019101821A2/en active Application Filing
- 2018-11-21 JP JP2020522956A patent/JP7231625B2/ja active Active
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- 2018-11-21 BR BR112020008255-4A patent/BR112020008255A2/pt not_active Application Discontinuation
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Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2012050781A (ja) * | 2010-09-03 | 2012-03-15 | Kao Corp | 悪臭抑制剤 |
JP2012250958A (ja) * | 2011-06-06 | 2012-12-20 | Kao Corp | 悪臭抑制剤 |
WO2014191047A1 (en) * | 2013-05-31 | 2014-12-04 | Chemcom S.A. | Olfactory receptors involved in the perception of sweat carboxylic acids and the use thereof |
JP2017176134A (ja) * | 2016-03-31 | 2017-10-05 | 株式会社豊田中央研究所 | 嗅覚受容体を用いた評価方法 |
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US20200345601A1 (en) | 2020-11-05 |
WO2019101821A3 (en) | 2019-10-17 |
JP2023062084A (ja) | 2023-05-02 |
JP2021503975A (ja) | 2021-02-15 |
BR112020008255A2 (pt) | 2020-10-20 |
JP7231625B2 (ja) | 2023-03-01 |
CN116807912A (zh) | 2023-09-29 |
EP3713610A2 (en) | 2020-09-30 |
US11744785B2 (en) | 2023-09-05 |
US20230233425A1 (en) | 2023-07-27 |
WO2019101821A2 (en) | 2019-05-31 |
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