JP2020521787A5 - - Google Patents
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- Publication number
- JP2020521787A5 JP2020521787A5 JP2019566073A JP2019566073A JP2020521787A5 JP 2020521787 A5 JP2020521787 A5 JP 2020521787A5 JP 2019566073 A JP2019566073 A JP 2019566073A JP 2019566073 A JP2019566073 A JP 2019566073A JP 2020521787 A5 JP2020521787 A5 JP 2020521787A5
- Authority
- JP
- Japan
- Prior art keywords
- microemulsion
- alkyl
- formula
- microemulsion according
- weight
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Withdrawn
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- 239000004530 micro-emulsion Substances 0.000 claims description 29
- 125000000217 alkyl group Chemical group 0.000 claims description 13
- -1 alkyl glucoside Chemical class 0.000 claims description 11
- 125000004432 carbon atom Chemical group C* 0.000 claims description 10
- 239000003945 anionic surfactant Substances 0.000 claims description 8
- 229930182478 glucoside Natural products 0.000 claims description 7
- 125000003118 aryl group Chemical group 0.000 claims description 6
- 230000002209 hydrophobic effect Effects 0.000 claims description 6
- 239000000203 mixture Substances 0.000 claims description 6
- 239000000126 substance Substances 0.000 claims description 6
- 150000002314 glycerols Chemical class 0.000 claims description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 4
- 239000004094 surface-active agent Substances 0.000 claims description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 4
- FBPFZTCFMRRESA-NQAPHZHOSA-N Sorbitol Chemical compound OCC(O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-NQAPHZHOSA-N 0.000 claims description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 3
- 235000010356 sorbitol Nutrition 0.000 claims description 3
- JDRSMPFHFNXQRB-CMTNHCDUSA-N Decyl beta-D-threo-hexopyranoside Chemical compound CCCCCCCCCCO[C@@H]1O[C@H](CO)C(O)[C@H](O)C1O JDRSMPFHFNXQRB-CMTNHCDUSA-N 0.000 claims description 2
- 150000001298 alcohols Chemical class 0.000 claims description 2
- 150000001299 aldehydes Chemical class 0.000 claims description 2
- 150000001336 alkenes Chemical class 0.000 claims description 2
- 230000029936 alkylation Effects 0.000 claims description 2
- 238000005804 alkylation reaction Methods 0.000 claims description 2
- 150000001721 carbon Chemical class 0.000 claims description 2
- 150000001768 cations Chemical class 0.000 claims description 2
- 239000002537 cosmetic Substances 0.000 claims description 2
- 229940073499 decyl glucoside Drugs 0.000 claims description 2
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 2
- BSDORLCHFMTALP-UHFFFAOYSA-N dipropoxy sulfate Chemical compound CCCOOS(=O)(=O)OOCCC BSDORLCHFMTALP-UHFFFAOYSA-N 0.000 claims description 2
- 150000002148 esters Chemical class 0.000 claims description 2
- 150000002170 ethers Chemical class 0.000 claims description 2
- 229930195729 fatty acid Natural products 0.000 claims description 2
- 239000000194 fatty acid Substances 0.000 claims description 2
- 239000003205 fragrance Substances 0.000 claims description 2
- 239000003752 hydrotrope Substances 0.000 claims description 2
- 150000002500 ions Chemical class 0.000 claims description 2
- 150000002576 ketones Chemical class 0.000 claims description 2
- 229930014626 natural product Natural products 0.000 claims description 2
- HEGSGKPQLMEBJL-RKQHYHRCSA-N octyl beta-D-glucopyranoside Chemical compound CCCCCCCCO[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O HEGSGKPQLMEBJL-RKQHYHRCSA-N 0.000 claims description 2
- 150000002989 phenols Chemical class 0.000 claims description 2
- 150000003839 salts Chemical class 0.000 claims description 2
- 229920006395 saturated elastomer Polymers 0.000 claims description 2
- QUCDWLYKDRVKMI-UHFFFAOYSA-M sodium;3,4-dimethylbenzenesulfonate Chemical compound [Na+].CC1=CC=C(S([O-])(=O)=O)C=C1C QUCDWLYKDRVKMI-UHFFFAOYSA-M 0.000 claims description 2
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 claims description 2
- 150000003505 terpenes Chemical class 0.000 claims description 2
- 235000007586 terpenes Nutrition 0.000 claims description 2
- 239000000341 volatile oil Substances 0.000 claims description 2
- 235000002595 Solanum tuberosum Nutrition 0.000 claims 1
- 244000061456 Solanum tuberosum Species 0.000 claims 1
- 125000004429 atom Chemical group 0.000 claims 1
- 229910052799 carbon Inorganic materials 0.000 claims 1
- 150000004665 fatty acids Chemical class 0.000 claims 1
- 150000002761 monoalkylglycerols Chemical class 0.000 claims 1
- 239000011734 sodium Substances 0.000 description 9
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 6
- 229910052708 sodium Inorganic materials 0.000 description 6
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 3
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 3
- BTBJBAZGXNKLQC-UHFFFAOYSA-N ammonium lauryl sulfate Chemical compound [NH4+].CCCCCCCCCCCCOS([O-])(=O)=O BTBJBAZGXNKLQC-UHFFFAOYSA-N 0.000 description 2
- 229940063953 ammonium lauryl sulfate Drugs 0.000 description 2
- NIDYWHLDTIVRJT-UJPOAAIJSA-N heptyl-β-d-glucopyranoside Chemical compound CCCCCCCO[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O NIDYWHLDTIVRJT-UJPOAAIJSA-N 0.000 description 2
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 2
- CMCBDXRRFKYBDG-UHFFFAOYSA-N 1-dodecoxydodecane Chemical compound CCCCCCCCCCCCOCCCCCCCCCCCC CMCBDXRRFKYBDG-UHFFFAOYSA-N 0.000 description 1
- YUGDYIWBYHTUFR-UHFFFAOYSA-N 10-methylundecyl benzenesulfonate Chemical compound CC(C)CCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 YUGDYIWBYHTUFR-UHFFFAOYSA-N 0.000 description 1
- WCCZCWAWAQBIQU-UHFFFAOYSA-N C(CCCCCC(C)C)OS(=O)(=O)C1=CC=CC=C1 Chemical compound C(CCCCCC(C)C)OS(=O)(=O)C1=CC=CC=C1 WCCZCWAWAQBIQU-UHFFFAOYSA-N 0.000 description 1
- 150000005215 alkyl ethers Chemical class 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- MOTZDAYCYVMXPC-UHFFFAOYSA-N dodecyl hydrogen sulfate Chemical compound CCCCCCCCCCCCOS(O)(=O)=O MOTZDAYCYVMXPC-UHFFFAOYSA-N 0.000 description 1
- 229940043264 dodecyl sulfate Drugs 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- SFNALCNOMXIBKG-UHFFFAOYSA-N ethylene glycol monododecyl ether Chemical compound CCCCCCCCCCCCOCCO SFNALCNOMXIBKG-UHFFFAOYSA-N 0.000 description 1
- 229940049964 oleate Drugs 0.000 description 1
- IWPBANVNTNWEBT-UHFFFAOYSA-M sodium;2-(6-methylheptyl)benzenesulfonate Chemical compound [Na+].CC(C)CCCCCC1=CC=CC=C1S([O-])(=O)=O IWPBANVNTNWEBT-UHFFFAOYSA-M 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR1754850 | 2017-06-01 | ||
| FR1754850A FR3066913B1 (fr) | 2017-06-01 | 2017-06-01 | Parfums sous forme de microemulsions aqueuses |
| PCT/EP2018/064389 WO2018220147A1 (fr) | 2017-06-01 | 2018-05-31 | Parfums sous forme de microémulsions aqueuses |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2020521787A JP2020521787A (ja) | 2020-07-27 |
| JP2020521787A5 true JP2020521787A5 (https=) | 2021-05-06 |
Family
ID=59859199
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2019566073A Withdrawn JP2020521787A (ja) | 2017-06-01 | 2018-05-31 | 水性マイクロエマルジョンの形態の香水 |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US20200179247A1 (https=) |
| EP (1) | EP3630057B1 (https=) |
| JP (1) | JP2020521787A (https=) |
| KR (1) | KR20200031565A (https=) |
| FR (1) | FR3066913B1 (https=) |
| WO (1) | WO2018220147A1 (https=) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP3669859B1 (en) * | 2018-12-20 | 2021-08-18 | Chanel Inc | Aqueous perfumes |
| CN113354804B (zh) * | 2020-12-31 | 2022-06-28 | 山东金智瑞新材料发展有限公司 | 一种脂肪醇聚氧丙烯醚含氧酸及其盐 |
| WO2022245837A1 (en) * | 2021-05-17 | 2022-11-24 | P2S Science, Inc. | Terpene ester surfactants |
| US12209069B2 (en) | 2021-05-17 | 2025-01-28 | P2 Science, Inc. | Fatty acid terpene alcohol esters |
| US12215120B1 (en) | 2021-05-17 | 2025-02-04 | P2 Science, Inc. | Terpene O-glycosides |
| US12528991B2 (en) | 2021-07-15 | 2026-01-20 | P2 Science, Inc. | Citronellol alkoxylate surfactants |
| WO2026008596A1 (en) * | 2024-07-03 | 2026-01-08 | Firmenich Sa | Ethanol-free emulsions and uses thereof |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2414201A2 (fr) | 1978-01-10 | 1979-08-03 | Commissariat Energie Atomique | Olfactometre differentiel |
| EP2340804A1 (en) * | 2009-12-31 | 2011-07-06 | Takasago International Corporation | Fragrance microemulsion compositions |
| FR2998476A1 (fr) * | 2012-11-26 | 2014-05-30 | Univ Lille 1 Sciences & Technologies | Microemulsions aqueuses volatiles de parfums et d huiles essentielles basees sur l utilisation de solvo- surfactifs |
| WO2014090959A1 (en) * | 2012-12-13 | 2014-06-19 | Firmenich Sa | Ethanol-free microemulsion perfuming compositions |
-
2017
- 2017-06-01 FR FR1754850A patent/FR3066913B1/fr not_active Expired - Fee Related
-
2018
- 2018-05-31 JP JP2019566073A patent/JP2020521787A/ja not_active Withdrawn
- 2018-05-31 WO PCT/EP2018/064389 patent/WO2018220147A1/fr not_active Ceased
- 2018-05-31 KR KR1020197036592A patent/KR20200031565A/ko not_active Ceased
- 2018-05-31 EP EP18730991.9A patent/EP3630057B1/fr active Active
- 2018-05-31 US US16/618,195 patent/US20200179247A1/en not_active Abandoned
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