BR122020004104B8 - Composições de perfume - Google Patents
Composições de perfumeInfo
- Publication number
- BR122020004104B8 BR122020004104B8 BR122020004104A BR122020004104A BR122020004104B8 BR 122020004104 B8 BR122020004104 B8 BR 122020004104B8 BR 122020004104 A BR122020004104 A BR 122020004104A BR 122020004104 A BR122020004104 A BR 122020004104A BR 122020004104 B8 BR122020004104 B8 BR 122020004104B8
- Authority
- BR
- Brazil
- Prior art keywords
- composition
- aldehyde
- perfume
- methyl
- damascone
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title abstract 8
- 239000002304 perfume Substances 0.000 title abstract 4
- -1 Galbanone (10) Chemical compound 0.000 abstract 4
- PXIKRTCSSLJURC-UHFFFAOYSA-N Dihydroeugenol Chemical compound CCCC1=CC=C(O)C(OC)=C1 PXIKRTCSSLJURC-UHFFFAOYSA-N 0.000 abstract 2
- ZFMSMUAANRJZFM-UHFFFAOYSA-N Estragole Chemical compound COC1=CC=C(CC=C)C=C1 ZFMSMUAANRJZFM-UHFFFAOYSA-N 0.000 abstract 2
- HCRBXQFHJMCTLF-ZCFIWIBFSA-N ethyl (2r)-2-methylbutanoate Chemical compound CCOC(=O)[C@H](C)CC HCRBXQFHJMCTLF-ZCFIWIBFSA-N 0.000 abstract 2
- CBOQJANXLMLOSS-UHFFFAOYSA-N ethyl vanillin Chemical compound CCOC1=CC(C=O)=CC=C1O CBOQJANXLMLOSS-UHFFFAOYSA-N 0.000 abstract 2
- RRAFCDWBNXTKKO-UHFFFAOYSA-N eugenol Chemical compound COC1=CC(CC=C)=CC=C1O RRAFCDWBNXTKKO-UHFFFAOYSA-N 0.000 abstract 2
- JARKCYVAAOWBJS-UHFFFAOYSA-N hexanal Chemical compound CCCCCC=O JARKCYVAAOWBJS-UHFFFAOYSA-N 0.000 abstract 2
- QPJVMBTYPHYUOC-UHFFFAOYSA-N methyl benzoate Chemical compound COC(=O)C1=CC=CC=C1 QPJVMBTYPHYUOC-UHFFFAOYSA-N 0.000 abstract 2
- ZRSNZINYAWTAHE-UHFFFAOYSA-N p-methoxybenzaldehyde Chemical compound COC1=CC=C(C=O)C=C1 ZRSNZINYAWTAHE-UHFFFAOYSA-N 0.000 abstract 2
- PHXATPHONSXBIL-UHFFFAOYSA-N xi-gamma-Undecalactone Chemical compound CCCCCCCC1CCC(=O)O1 PHXATPHONSXBIL-UHFFFAOYSA-N 0.000 abstract 2
- 239000001695 (2E)-1,1-dimethoxy-3,7-dimethylocta-2,6-diene Substances 0.000 abstract 1
- ZSKAJFSSXURRGL-PKNBQFBNSA-N (2e)-1,1-dimethoxy-3,7-dimethylocta-2,6-diene Chemical compound COC(OC)\C=C(/C)CCC=C(C)C ZSKAJFSSXURRGL-PKNBQFBNSA-N 0.000 abstract 1
- KHWTYGFHPHRQMP-UHFFFAOYSA-N (4-propan-2-ylcyclohexyl)methanol Chemical compound CC(C)C1CCC(CO)CC1 KHWTYGFHPHRQMP-UHFFFAOYSA-N 0.000 abstract 1
- 239000001674 (E)-1-(2,6,6-trimethyl-1-cyclohexenyl)but-2-en-1-one Substances 0.000 abstract 1
- KJPRLNWUNMBNBZ-QPJJXVBHSA-N (E)-cinnamaldehyde Chemical compound O=C\C=C\C1=CC=CC=C1 KJPRLNWUNMBNBZ-QPJJXVBHSA-N 0.000 abstract 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 abstract 1
- WUOACPNHFRMFPN-SECBINFHSA-N (S)-(-)-alpha-terpineol Chemical compound CC1=CC[C@@H](C(C)(C)O)CC1 WUOACPNHFRMFPN-SECBINFHSA-N 0.000 abstract 1
- XEJGJTYRUWUFFD-FNORWQNLSA-N (e)-1-(2,6,6-trimethyl-1-cyclohex-3-enyl)but-2-en-1-one Chemical compound C\C=C\C(=O)C1C(C)C=CCC1(C)C XEJGJTYRUWUFFD-FNORWQNLSA-N 0.000 abstract 1
- RNLHVODSMDJCBR-VURMDHGXSA-N (z)-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-VURMDHGXSA-N 0.000 abstract 1
- YGFGZTXGYTUXBA-UHFFFAOYSA-N (±)-2,6-dimethyl-5-heptenal Chemical compound O=CC(C)CCC=C(C)C YGFGZTXGYTUXBA-UHFFFAOYSA-N 0.000 abstract 1
- FVUGZKDGWGKCFE-UHFFFAOYSA-N 1-(2,3,8,8-tetramethyl-1,3,4,5,6,7-hexahydronaphthalen-2-yl)ethanone Chemical compound CC1(C)CCCC2=C1CC(C(C)=O)(C)C(C)C2 FVUGZKDGWGKCFE-UHFFFAOYSA-N 0.000 abstract 1
- BGTBFNDXYDYBEY-UHFFFAOYSA-N 1-(2,6,6-trimethylcyclohexen-1-yl)but-2-en-1-one Chemical compound CC=CC(=O)C1=C(C)CCCC1(C)C BGTBFNDXYDYBEY-UHFFFAOYSA-N 0.000 abstract 1
- YBUIAJZFOGJGLJ-SWRJLBSHSA-N 1-cedr-8-en-9-ylethanone Chemical compound C1[C@]23[C@H](C)CC[C@H]3C(C)(C)[C@@H]1C(C)=C(C(C)=O)C2 YBUIAJZFOGJGLJ-SWRJLBSHSA-N 0.000 abstract 1
- RCSBILYQLVXLJG-UHFFFAOYSA-N 2-Propenyl hexanoate Chemical compound CCCCCC(=O)OCC=C RCSBILYQLVXLJG-UHFFFAOYSA-N 0.000 abstract 1
- ZHDQGHCZWWDMRS-UHFFFAOYSA-N 3,5-dimethylcyclohex-3-ene-1-carbaldehyde Chemical compound CC1CC(C=O)CC(C)=C1 ZHDQGHCZWWDMRS-UHFFFAOYSA-N 0.000 abstract 1
- JRJBVWJSTHECJK-PKNBQFBNSA-N 3-Methyl-4-(2,6,6-trimethyl-2-cyclohexen-1-yl)-3-buten-2-one Chemical compound CC(=O)C(\C)=C\C1C(C)=CCCC1(C)C JRJBVWJSTHECJK-PKNBQFBNSA-N 0.000 abstract 1
- ZFGBKXBPHOUSJX-UHFFFAOYSA-N 3-methylcyclotetradec-5-en-1-one Chemical compound CC1CC=CCCCCCCCCC(=O)C1 ZFGBKXBPHOUSJX-UHFFFAOYSA-N 0.000 abstract 1
- AZUVBPVDRHGGEP-UHFFFAOYSA-N 6a,9a-dimethyl-4,5,7,8,9,9a-hexahydro-6aH-dipyrrolo(2,3-b;3',2',1'-hi)indole Natural products CC(=C)C1CCC(C)=CCCC(C)=CCCC(C)=CC1O AZUVBPVDRHGGEP-UHFFFAOYSA-N 0.000 abstract 1
- NPBVQXIMTZKSBA-UHFFFAOYSA-N Chavibetol Natural products COC1=CC=C(CC=C)C=C1O NPBVQXIMTZKSBA-UHFFFAOYSA-N 0.000 abstract 1
- 240000008772 Cistus ladanifer Species 0.000 abstract 1
- WEEGYLXZBRQIMU-UHFFFAOYSA-N Eucalyptol Chemical compound C1CC2CCC1(C)OC2(C)C WEEGYLXZBRQIMU-UHFFFAOYSA-N 0.000 abstract 1
- 239000005770 Eugenol Substances 0.000 abstract 1
- MEJYWDUBOCZFFS-FENWIEIGSA-N Labienoxime Chemical compound CC(C)C(=N\O)\C(C)(C)C\C=C(/C)C=C MEJYWDUBOCZFFS-FENWIEIGSA-N 0.000 abstract 1
- WSTYNZDAOAEEKG-UHFFFAOYSA-N Mayol Natural products CC1=C(O)C(=O)C=C2C(CCC3(C4CC(C(CC4(CCC33C)C)=O)C)C)(C)C3=CC=C21 WSTYNZDAOAEEKG-UHFFFAOYSA-N 0.000 abstract 1
- UVMRYBDEERADNV-UHFFFAOYSA-N Pseudoeugenol Natural products COC1=CC(C(C)=C)=CC=C1O UVMRYBDEERADNV-UHFFFAOYSA-N 0.000 abstract 1
- AXMVYSVVTMKQSL-UHFFFAOYSA-N UNPD142122 Natural products OC1=CC=C(C=CC=O)C=C1O AXMVYSVVTMKQSL-UHFFFAOYSA-N 0.000 abstract 1
- 125000005233 alkylalcohol group Chemical group 0.000 abstract 1
- OVKDFILSBMEKLT-UHFFFAOYSA-N alpha-Terpineol Natural products CC(=C)C1(O)CCC(C)=CC1 OVKDFILSBMEKLT-UHFFFAOYSA-N 0.000 abstract 1
- 229940088601 alpha-terpineol Drugs 0.000 abstract 1
- POIARNZEYGURDG-UHFFFAOYSA-N beta-damascenone Natural products CC=CC(=O)C1=C(C)C=CCC1(C)C POIARNZEYGURDG-UHFFFAOYSA-N 0.000 abstract 1
- 239000010627 cedar oil Substances 0.000 abstract 1
- 229960005233 cineole Drugs 0.000 abstract 1
- RFFOTVCVTJUTAD-UHFFFAOYSA-N cineole Natural products C1CC2(C)CCC1(C(C)C)O2 RFFOTVCVTJUTAD-UHFFFAOYSA-N 0.000 abstract 1
- CCRCUPLGCSFEDV-UHFFFAOYSA-N cinnamic acid methyl ester Natural products COC(=O)C=CC1=CC=CC=C1 CCRCUPLGCSFEDV-UHFFFAOYSA-N 0.000 abstract 1
- 229940117916 cinnamic aldehyde Drugs 0.000 abstract 1
- KJPRLNWUNMBNBZ-UHFFFAOYSA-N cinnamic aldehyde Natural products O=CC=CC1=CC=CC=C1 KJPRLNWUNMBNBZ-UHFFFAOYSA-N 0.000 abstract 1
- 239000001813 ethyl (2R)-2-methylbutanoate Substances 0.000 abstract 1
- 229940090910 ethyl 2-methylbutyrate Drugs 0.000 abstract 1
- 229940073505 ethyl vanillin Drugs 0.000 abstract 1
- 229960002217 eugenol Drugs 0.000 abstract 1
- PHXATPHONSXBIL-JTQLQIEISA-N gamma-Undecalactone Natural products CCCCCCC[C@H]1CCC(=O)O1 PHXATPHONSXBIL-JTQLQIEISA-N 0.000 abstract 1
- 229940020436 gamma-undecalactone Drugs 0.000 abstract 1
- 229930195733 hydrocarbon Natural products 0.000 abstract 1
- 229940095102 methyl benzoate Drugs 0.000 abstract 1
- CCRCUPLGCSFEDV-BQYQJAHWSA-N methyl trans-cinnamate Chemical compound COC(=O)\C=C\C1=CC=CC=C1 CCRCUPLGCSFEDV-BQYQJAHWSA-N 0.000 abstract 1
- VWMVAQHMFFZQGD-UHFFFAOYSA-N p-Hydroxybenzyl acetone Natural products CC(=O)CC1=CC=C(O)C=C1 VWMVAQHMFFZQGD-UHFFFAOYSA-N 0.000 abstract 1
- 239000001631 piper nigrum l. fruit oil black Substances 0.000 abstract 1
- SATCULPHIDQDRE-UHFFFAOYSA-N piperonal Chemical compound O=CC1=CC=C2OCOC2=C1 SATCULPHIDQDRE-UHFFFAOYSA-N 0.000 abstract 1
- 239000000843 powder Substances 0.000 abstract 1
- NJGBTKGETPDVIK-UHFFFAOYSA-N raspberry ketone Chemical compound CC(=O)CCC1=CC=C(O)C=C1 NJGBTKGETPDVIK-UHFFFAOYSA-N 0.000 abstract 1
- 230000001953 sensory effect Effects 0.000 abstract 1
- 230000002195 synergetic effect Effects 0.000 abstract 1
- 229940085790 synthetic camphor Drugs 0.000 abstract 1
- 235000007586 terpenes Nutrition 0.000 abstract 1
Classifications
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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
-
- 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
- C11B9/0003—Compounds of unspecified constitution defined by the chemical reaction for their preparation
-
- 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
- C11B9/0007—Aliphatic compounds
- C11B9/0015—Aliphatic compounds containing oxygen as the only heteroatom
-
- 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
- C11B9/0007—Aliphatic compounds
- C11B9/0015—Aliphatic compounds containing oxygen as the only heteroatom
- C11B9/0019—Aliphatic compounds containing oxygen as the only heteroatom carbocylic acids; Salts or esters thereof
-
- 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
- C11B9/0026—Essential oils; Perfumes compounds containing an alicyclic ring not condensed with another ring
- C11B9/003—Essential oils; Perfumes compounds containing an alicyclic ring not condensed with another ring the ring containing less than six carbon atoms
-
- 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
- C11B9/0026—Essential oils; Perfumes compounds containing an alicyclic ring not condensed with another ring
- C11B9/0034—Essential oils; Perfumes compounds containing an alicyclic ring not condensed with another ring the ring containing six carbon atoms
-
- 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
-
- 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
-
- 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
- C11B9/0061—Essential oils; Perfumes compounds containing a six-membered aromatic ring not condensed with another ring
-
- 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
- C11B9/0069—Heterocyclic compounds
- C11B9/0073—Heterocyclic compounds containing only O or S as heteroatoms
- C11B9/0076—Heterocyclic compounds containing only O or S as heteroatoms the hetero rings containing less than six atoms
-
- 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
- C11B9/0069—Heterocyclic compounds
- C11B9/0073—Heterocyclic compounds containing only O or S as heteroatoms
- C11B9/0084—Heterocyclic compounds containing only O or S as heteroatoms the hetero rings containing more than six atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Fats And Perfumes (AREA)
- Cosmetics (AREA)
Abstract
A presente invenção refere-se a uma composição de perfume que inclui grupos de componentes de perfume que produzem desempenho sensorial aprimorado. A composição inclui componentes que têm propriedades odoríferas sinérgicas. Uma composição de perfume compreende ao menos quatro membros selecionados do grupo (1A) que consiste em: acetil-cedreno, pó de cânfora sintética, óleo de madeira de cedro, cineol, aldeído cinâmico (10), cistus labdanum, citral dimetil acetal, Cosmone, Ciclal C, beta-damascone (10), delta-damascone (10), Ebanol (10), Etil vanilina (10), eugenol, Galbanona (10), gama-undecalactona, heliotropina, aldeído hexil cinâmico, iso E super, alfa-isometil ionona, Mayol, metil-chavicol, cinamato de metila, 2-metilbutirato de etila, Silvanone, Silvial, alfa-terpineol, hexanoato de alila, Labienoxima (10), aldeído anísico (10), óleo de pimenta preta, Polisantol (10), Habanolida, di-hidroeugenol, Melonal, Violetina (10), benzoato de metila, cetona de framboesa, e misturas dos mesmos, sendo que a quantidade total desses membros é de 40% a cerca de 80% em peso da composição; e ao menos um membro selecionado do grupo (1b) que consiste em álcoois alquílicos, álcoois fenilalquílicos, hidrocarbonetos de terpeno e misturas dos mesmos em quantidades de cerca de 5% a cerca de 50% em peso da composição.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201562110747P | 2015-02-02 | 2015-02-02 | |
| US62/110,747 | 2015-02-02 | ||
| PCT/US2016/015286 WO2016126510A1 (en) | 2015-02-02 | 2016-01-28 | Perfume compositions |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| BR122020004104B1 BR122020004104B1 (pt) | 2021-11-23 |
| BR122020004104B8 true BR122020004104B8 (pt) | 2022-08-09 |
Family
ID=55359739
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BR122020004104A BR122020004104B8 (pt) | 2015-02-02 | 2016-01-28 | Composições de perfume |
| BR112017016484A BR112017016484B8 (pt) | 2015-02-02 | 2016-01-28 | Método para preparar uma composição de perfume |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BR112017016484A BR112017016484B8 (pt) | 2015-02-02 | 2016-01-28 | Método para preparar uma composição de perfume |
Country Status (10)
| Country | Link |
|---|---|
| US (2) | US9796945B2 (pt) |
| EP (2) | EP3253855A1 (pt) |
| KR (1) | KR102618841B1 (pt) |
| CN (1) | CN107250333A (pt) |
| AU (2) | AU2016215698A1 (pt) |
| BR (2) | BR122020004104B8 (pt) |
| CA (3) | CA3197626A1 (pt) |
| MX (1) | MX2017009943A (pt) |
| RU (1) | RU2719142C2 (pt) |
| WO (1) | WO2016126510A1 (pt) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR102598026B1 (ko) * | 2018-01-05 | 2023-11-06 | 주식회사 엘지생활건강 | 피나무 꿀 향취를 재현한 향료 조성물 |
| KR102104269B1 (ko) * | 2018-02-26 | 2020-05-29 | 주식회사 엘지생활건강 | 심비디움 아로마핑크 향취를 재현한 향료 조성물 |
| CN118415168A (zh) * | 2018-03-20 | 2024-08-02 | 弗门尼舍有限公司 | 抗微生物组合物 |
| CN108761002A (zh) * | 2018-04-25 | 2018-11-06 | 上海应用技术大学 | 一种基于s曲线法分析菊花精油中醇类与萜烯类物质香气协同作用的方法 |
| CN108982755A (zh) * | 2018-04-26 | 2018-12-11 | 上海应用技术大学 | 一种基于s曲线法分析樱桃酒酯类物质香气协同作用的方法 |
| CN108918791A (zh) * | 2018-04-26 | 2018-11-30 | 上海应用技术大学 | 一种基于s曲线法分析苹果汁酯类物质香气协同作用的方法 |
| CN110672787B (zh) * | 2019-08-27 | 2021-11-09 | 上海应用技术大学 | 一种研究玫瑰花中香气物质相互作用的方法 |
| CN115475268A (zh) * | 2021-05-30 | 2022-12-16 | 宝洁公司 | 清新组合物 |
Family Cites Families (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| SU412240A1 (pt) * | 1972-05-26 | 1974-01-25 | ||
| US4281204A (en) * | 1979-10-05 | 1981-07-28 | Fritzsche Dodge & Olcott Inc. | Substituted spirocyclic derivatives |
| DE3208203C1 (de) * | 1982-03-06 | 1983-07-28 | Dragoco Gerberding & Co Gmbh, 3450 Holzminden | Gemisch von Dimethyl-tricyclo [5.2.1.0?] decyl-methyl-ethern und Gemisch von Dimethyl-tricyclo [5.2.1.0?] decenyl-methyl-ethern,Verfahren zu ihrer Herstellung und ihre verwendung als Riech- bzw. Aromastoffe |
| US5482635A (en) * | 1989-06-19 | 1996-01-09 | Lever Brothers Company | Fabric conditioner with deodorant perfume composition |
| US5162588A (en) | 1989-06-30 | 1992-11-10 | Firmenich S.A. | Aromatic compounds, a process for preparation thereof and use of same as perfuming ingredients |
| RU2022001C1 (ru) * | 1991-09-19 | 1994-10-30 | Акционерное общество "Дзинтарс" | Композиция душистых веществ |
| DE69812256T2 (de) | 1997-09-09 | 2004-01-29 | Firmenich & Cie | 7-Propylbenzodioxepin-3-one und seine Verwendung in der Parfümerie |
| GB9814650D0 (en) | 1998-07-07 | 1998-09-02 | Quest Int | Perfume compositions |
| US20020055452A1 (en) * | 2000-07-07 | 2002-05-09 | Givaudan Sa | Process for imparting a fragrance to a product and fragrance and conditioning to a dry fabric |
| GB0031047D0 (en) | 2000-12-20 | 2001-01-31 | Quest Int | Perfume compositions |
| US6872697B2 (en) * | 2001-09-07 | 2005-03-29 | Firmenich Sa | Oxime as perfuming ingredient |
| US6858574B2 (en) * | 2002-02-28 | 2005-02-22 | Unilever Home & Personal Care Usa, Division Of Conopco, Inc. | Process for making perfume containing surfactant compositions having perfume burst when diluted |
| US20050245407A1 (en) * | 2002-08-09 | 2005-11-03 | Kao Corporation | Fragrance composition |
| CA2587666C (en) * | 2004-11-12 | 2012-09-25 | Takasago International Corporation | Optically active muscone composition and fragrances or cosmetics containing the same |
| ATE466925T1 (de) * | 2005-09-06 | 2010-05-15 | Procter & Gamble | Duftverfahren und produkt |
| DE102005054565A1 (de) * | 2005-11-14 | 2007-05-16 | Henkel Kgaa | Oxidationsmittel enthaltende,wohlriechende Verbrauchsprodukte |
| US8877139B2 (en) * | 2010-08-13 | 2014-11-04 | The Procter & Gamble Company | Compositions comprising a functional perfume component mixture |
| DE102011082464A1 (de) | 2011-09-09 | 2011-12-01 | Symrise Ag | Riechstoffmischungen enthaltend bestimmte Isolongifolenylmethylether |
| EP2594626B1 (de) * | 2011-11-18 | 2014-06-25 | Symrise AG | Verwendung von Oxyacetaldehyden als Maiglöckchen-Riechstoffe |
| CA2895089C (en) * | 2012-12-14 | 2019-02-26 | The Procter & Gamble Company | Fragrance materials |
-
2016
- 2016-01-28 MX MX2017009943A patent/MX2017009943A/es unknown
- 2016-01-28 BR BR122020004104A patent/BR122020004104B8/pt active IP Right Grant
- 2016-01-28 CA CA3197626A patent/CA3197626A1/en not_active Withdrawn
- 2016-01-28 US US15/008,981 patent/US9796945B2/en active Active
- 2016-01-28 AU AU2016215698A patent/AU2016215698A1/en not_active Abandoned
- 2016-01-28 BR BR112017016484A patent/BR112017016484B8/pt active IP Right Grant
- 2016-01-28 WO PCT/US2016/015286 patent/WO2016126510A1/en active Application Filing
- 2016-01-28 CN CN201680008252.6A patent/CN107250333A/zh active Pending
- 2016-01-28 CA CA2974825A patent/CA2974825C/en active Active
- 2016-01-28 EP EP16704752.1A patent/EP3253855A1/en not_active Withdrawn
- 2016-01-28 EP EP22169254.4A patent/EP4086329A1/en active Pending
- 2016-01-28 CA CA3199267A patent/CA3199267A1/en active Pending
- 2016-01-28 RU RU2017130921A patent/RU2719142C2/ru active
- 2016-01-28 KR KR1020177024147A patent/KR102618841B1/ko active IP Right Grant
-
2017
- 2017-09-13 US US15/703,083 patent/US20180010065A1/en active Pending
-
2020
- 2020-05-22 AU AU2020203341A patent/AU2020203341A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| CN107250333A (zh) | 2017-10-13 |
| AU2016215698A1 (en) | 2017-08-03 |
| WO2016126510A1 (en) | 2016-08-11 |
| CA3197626A1 (en) | 2016-08-11 |
| US9796945B2 (en) | 2017-10-24 |
| CA2974825A1 (en) | 2016-08-11 |
| BR122020004104B1 (pt) | 2021-11-23 |
| BR112017016484B1 (pt) | 2021-11-16 |
| KR102618841B1 (ko) | 2023-12-29 |
| MX2017009943A (es) | 2017-12-07 |
| AU2020203341A1 (en) | 2020-06-11 |
| US20160222316A1 (en) | 2016-08-04 |
| KR20170109632A (ko) | 2017-09-29 |
| CA3199267A1 (en) | 2016-08-11 |
| EP3253855A1 (en) | 2017-12-13 |
| BR112017016484B8 (pt) | 2022-08-09 |
| CA2974825C (en) | 2023-08-01 |
| RU2017130921A (ru) | 2019-03-04 |
| BR112017016484A2 (pt) | 2018-04-10 |
| RU2017130921A3 (pt) | 2019-07-17 |
| EP4086329A1 (en) | 2022-11-09 |
| US20180010065A1 (en) | 2018-01-11 |
| RU2719142C2 (ru) | 2020-04-17 |
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