JP2002542380A - 芳香剤原料アルデヒドおよび第三級α炭素原子をもつ芳香剤原料前駆体 - Google Patents
芳香剤原料アルデヒドおよび第三級α炭素原子をもつ芳香剤原料前駆体Info
- Publication number
- JP2002542380A JP2002542380A JP2000612409A JP2000612409A JP2002542380A JP 2002542380 A JP2002542380 A JP 2002542380A JP 2000612409 A JP2000612409 A JP 2000612409A JP 2000612409 A JP2000612409 A JP 2000612409A JP 2002542380 A JP2002542380 A JP 2002542380A
- Authority
- JP
- Japan
- Prior art keywords
- substituted
- unsubstituted
- group
- fragrance
- alkyl group
- 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- Withdrawn
Links
- 239000003205 fragrance Substances 0.000 title claims abstract description 285
- 239000002994 raw material Substances 0.000 title claims abstract description 163
- 239000002243 precursor Substances 0.000 title claims abstract description 110
- 229910052799 carbon Inorganic materials 0.000 title claims abstract description 12
- 125000003118 aryl group Chemical group 0.000 title claims description 22
- 125000002485 formyl group Chemical class [H]C(*)=O 0.000 title claims 7
- 125000004432 carbon atom Chemical group C* 0.000 title claims 4
- 239000000203 mixture Substances 0.000 claims abstract description 75
- 239000002304 perfume Substances 0.000 claims abstract description 33
- 125000000217 alkyl group Chemical group 0.000 claims description 63
- 125000003342 alkenyl group Chemical group 0.000 claims description 58
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 45
- 125000004429 atom Chemical group 0.000 claims description 26
- 125000000623 heterocyclic group Chemical group 0.000 claims description 20
- -1 ketals Chemical class 0.000 claims description 20
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 19
- 239000004615 ingredient Substances 0.000 claims description 18
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 17
- 125000005343 heterocyclic alkyl group Chemical group 0.000 claims description 13
- 239000000126 substance Substances 0.000 claims description 13
- 239000007983 Tris buffer Substances 0.000 claims description 12
- 150000002905 orthoesters Chemical class 0.000 claims description 11
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 10
- 239000003795 chemical substances by application Substances 0.000 claims description 10
- 125000005529 alkyleneoxy group Chemical group 0.000 claims description 9
- 125000004122 cyclic group Chemical group 0.000 claims description 9
- 125000000392 cycloalkenyl group Chemical group 0.000 claims description 9
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 9
- 150000002576 ketones Chemical class 0.000 claims description 9
- 150000002148 esters Chemical class 0.000 claims description 8
- 125000006615 aromatic heterocyclic group Chemical group 0.000 claims description 7
- 239000000872 buffer Substances 0.000 claims description 7
- 239000003381 stabilizer Substances 0.000 claims description 7
- 125000005275 alkylenearyl group Chemical group 0.000 claims description 6
- 230000014759 maintenance of location Effects 0.000 claims description 6
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 5
- 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 description 5
- 125000006574 non-aromatic ring group Chemical group 0.000 claims description 5
- 150000001298 alcohols Chemical class 0.000 claims description 4
- 125000002648 azanetriyl group Chemical group *N(*)* 0.000 claims description 4
- 150000004649 carbonic acid derivatives Chemical class 0.000 claims description 4
- 150000003333 secondary alcohols Chemical class 0.000 claims description 4
- 150000003509 tertiary alcohols Chemical class 0.000 claims description 4
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims description 3
- 229930195733 hydrocarbon Natural products 0.000 claims description 3
- 230000007935 neutral effect Effects 0.000 claims description 3
- UFRXZBSLNJCLJM-YILJOUTGSA-N (2e)-1-[bis[(2e)-3,7-dimethylocta-2,6-dienoxy]methoxy]-3,7-dimethylocta-2,6-diene Chemical group CC(C)=CCC\C(C)=C\COC(OC\C=C(/C)CCC=C(C)C)OC\C=C(/C)CCC=C(C)C UFRXZBSLNJCLJM-YILJOUTGSA-N 0.000 claims description 2
- SSXQYJPANSDSBP-LRRVACHLSA-N (Z)-1-[1,1-bis[(Z)-hex-3-enoxy]ethoxy]hex-3-ene Chemical compound CC\C=C/CCOC(C)(OCC\C=C/CC)OCC\C=C/CC SSXQYJPANSDSBP-LRRVACHLSA-N 0.000 claims description 2
- NPJXLXXYLFEXAA-MDBXUZFLSA-N (z)-1-[bis[(z)-hex-3-enoxy]methoxy]hex-3-ene Chemical compound CC\C=C/CCOC(OCC\C=C/CC)OCC\C=C/CC NPJXLXXYLFEXAA-MDBXUZFLSA-N 0.000 claims description 2
- NXEZWKZWRKAFKW-MDBXUZFLSA-N (z)-9-[bis[(z)-non-6-enoxy]methoxy]non-3-ene Chemical compound CC\C=C/CCCCCOC(OCCCCC\C=C/CC)OCCCCC\C=C/CC NXEZWKZWRKAFKW-MDBXUZFLSA-N 0.000 claims description 2
- NDQXKKFRNOPRDW-UHFFFAOYSA-N 1,1,1-triethoxyethane Chemical compound CCOC(C)(OCC)OCC NDQXKKFRNOPRDW-UHFFFAOYSA-N 0.000 claims description 2
- OPEWOMFEHGAUNI-UHFFFAOYSA-N 1,1-bis(phenylmethoxy)ethoxymethylbenzene Chemical compound C=1C=CC=CC=1COC(OCC=1C=CC=CC=1)(C)OCC1=CC=CC=C1 OPEWOMFEHGAUNI-UHFFFAOYSA-N 0.000 claims description 2
- YFNGVMLFPLXMSF-UHFFFAOYSA-N 1-[1,1-bis[(4-propan-2-ylcyclohexyl)methoxy]ethoxymethyl]-4-propan-2-ylcyclohexane Chemical compound C1CC(C(C)C)CCC1COC(C)(OCC1CCC(CC1)C(C)C)OCC1CCC(C(C)C)CC1 YFNGVMLFPLXMSF-UHFFFAOYSA-N 0.000 claims description 2
- YNAAEYUIHHOXDE-UHFFFAOYSA-N 10-[bis(dec-9-enoxy)methoxy]dec-1-ene Chemical compound C=CCCCCCCCCOC(OCCCCCCCCC=C)OCCCCCCCCC=C YNAAEYUIHHOXDE-UHFFFAOYSA-N 0.000 claims description 2
- DWTTYHDKQIPJEL-UHFFFAOYSA-N 2-[1,1-bis(2-phenylethoxy)ethoxy]ethylbenzene Chemical compound C=1C=CC=CC=1CCOC(OCCC=1C=CC=CC=1)(C)OCCC1=CC=CC=C1 DWTTYHDKQIPJEL-UHFFFAOYSA-N 0.000 claims description 2
- CPBDRNSJHVLPNM-UHFFFAOYSA-N 2-[bis(2-phenoxyethoxy)methoxy]ethoxybenzene Chemical compound C=1C=CC=CC=1OCCOC(OCCOC=1C=CC=CC=1)OCCOC1=CC=CC=C1 CPBDRNSJHVLPNM-UHFFFAOYSA-N 0.000 claims description 2
- QELVJBZOCOAMTA-UHFFFAOYSA-N 2-[bis(2-phenylethoxy)methoxy]ethylbenzene Chemical compound C=1C=CC=CC=1CCOC(OCCC=1C=CC=CC=1)OCCC1=CC=CC=C1 QELVJBZOCOAMTA-UHFFFAOYSA-N 0.000 claims description 2
- LYAPIWFCHVDKGU-UHFFFAOYSA-N 4-[4-[bis[[3-methyl-5-(2,2,3-trimethylcyclopent-3-en-1-yl)pent-4-en-2-yl]oxy]methoxy]-3-methylpent-1-enyl]-1,5,5-trimethylcyclopentene Chemical compound C1C=C(C)C(C)(C)C1C=CC(C)C(C)OC(OC(C)C(C)C=CC1C(C(C)=CC1)(C)C)OC(C)C(C)C=CC1CC=C(C)C1(C)C LYAPIWFCHVDKGU-UHFFFAOYSA-N 0.000 claims description 2
- PBJMYBITWKUWDM-UHFFFAOYSA-N 7-[1,1-bis(2,6-dimethylhept-5-enoxy)ethoxy]-2,6-dimethylhept-2-ene Chemical compound CC(C)=CCCC(C)COC(C)(OCC(C)CCC=C(C)C)OCC(C)CCC=C(C)C PBJMYBITWKUWDM-UHFFFAOYSA-N 0.000 claims description 2
- MGFIWLDAVRLOKZ-UHFFFAOYSA-N 8-[bis(6,8-dimethylnonan-2-yloxy)methoxy]-2,4-dimethylnonane Chemical compound CC(C)CC(C)CCCC(C)OC(OC(C)CCCC(C)CC(C)C)OC(C)CCCC(C)CC(C)C MGFIWLDAVRLOKZ-UHFFFAOYSA-N 0.000 claims description 2
- QFHKNBKFNXAKQK-VCNVVWDHSA-N CC(C)=CCC/C(\C)=C/COC(CCC1=CC=CC=C1)(O)OC/C=C(\C)/CCC=C(C)C Chemical compound CC(C)=CCC/C(\C)=C/COC(CCC1=CC=CC=C1)(O)OC/C=C(\C)/CCC=C(C)C QFHKNBKFNXAKQK-VCNVVWDHSA-N 0.000 claims description 2
- NBEHNIVJBNFNHV-QAHSQZNUSA-N CCCCCCC(O)(OCC/C=C\CC)OCC/C=C\CC Chemical compound CCCCCCC(O)(OCC/C=C\CC)OCC/C=C\CC NBEHNIVJBNFNHV-QAHSQZNUSA-N 0.000 claims description 2
- 239000004215 Carbon black (E152) Substances 0.000 claims description 2
- 238000006243 chemical reaction Methods 0.000 claims description 2
- 125000001316 cycloalkyl alkyl group Chemical group 0.000 claims description 2
- 125000000075 primary alcohol group Chemical group 0.000 claims description 2
- 150000003138 primary alcohols Chemical class 0.000 claims description 2
- 150000001241 acetals Chemical class 0.000 claims 2
- 125000002560 nitrile group Chemical group 0.000 claims 2
- 125000005649 substituted arylene group Chemical group 0.000 claims 2
- LVWCAKMZEKPMNK-CDULXAATSA-N CC(C)=CCC\C(C)=C\COC(C)(OC\C=C(/C)CCC=C(C)C)OC\C=C(/C)CCC=C(C)C Chemical compound CC(C)=CCC\C(C)=C\COC(C)(OC\C=C(/C)CCC=C(C)C)OC\C=C(/C)CCC=C(C)C LVWCAKMZEKPMNK-CDULXAATSA-N 0.000 claims 1
- 150000002170 ethers Chemical class 0.000 claims 1
- 150000002828 nitro derivatives Chemical class 0.000 claims 1
- 229930195735 unsaturated hydrocarbon Natural products 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 abstract description 6
- 230000001953 sensory effect Effects 0.000 abstract description 3
- 230000000694 effects Effects 0.000 abstract description 2
- 230000002045 lasting effect Effects 0.000 abstract 1
- 150000001299 aldehydes Chemical class 0.000 description 34
- 238000001514 detection method Methods 0.000 description 11
- 239000000243 solution Substances 0.000 description 11
- DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 description 10
- 230000001276 controlling effect Effects 0.000 description 9
- 125000002777 acetyl group Chemical class [H]C([H])([H])C(*)=O 0.000 description 8
- 239000000463 material Substances 0.000 description 8
- 238000003756 stirring Methods 0.000 description 8
- 238000004817 gas chromatography Methods 0.000 description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 239000007789 gas Substances 0.000 description 6
- 238000000034 method Methods 0.000 description 6
- WYNCHZVNFNFDNH-UHFFFAOYSA-N Oxazolidine Chemical compound C1COCN1 WYNCHZVNFNFDNH-UHFFFAOYSA-N 0.000 description 5
- 239000000969 carrier Substances 0.000 description 5
- 239000000839 emulsion Substances 0.000 description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- 230000007062 hydrolysis Effects 0.000 description 4
- 238000006460 hydrolysis reaction Methods 0.000 description 4
- 238000002347 injection Methods 0.000 description 4
- 239000007924 injection Substances 0.000 description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- 239000000341 volatile oil Substances 0.000 description 4
- PSQYTAPXSHCGMF-BQYQJAHWSA-N β-ionone Chemical compound CC(=O)\C=C\C1=C(C)CCCC1(C)C PSQYTAPXSHCGMF-BQYQJAHWSA-N 0.000 description 4
- MBVFRSJFKMJRHA-UHFFFAOYSA-N 4-fluoro-1-benzofuran-7-carbaldehyde Chemical compound FC1=CC=C(C=O)C2=C1C=CO2 MBVFRSJFKMJRHA-UHFFFAOYSA-N 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 150000001721 carbon Chemical group 0.000 description 3
- 239000002781 deodorant agent Substances 0.000 description 3
- 229920005989 resin Polymers 0.000 description 3
- 239000011347 resin Substances 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- SFEOKXHPFMOVRM-UHFFFAOYSA-N (+)-(S)-gamma-ionone Natural products CC(=O)C=CC1C(=C)CCCC1(C)C SFEOKXHPFMOVRM-UHFFFAOYSA-N 0.000 description 2
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 2
- SZBYDPJFDSBHLM-UHFFFAOYSA-N 2-(4-methoxybenzoyl)-3,3,7-trimethylnon-8-enoic acid Chemical compound COC1=CC=C(C(=O)C(C(O)=O)C(C)(C)CCCC(C)C=C)C=C1 SZBYDPJFDSBHLM-UHFFFAOYSA-N 0.000 description 2
- ALPILNOHTMEGAY-UHFFFAOYSA-N 2-ethyl-7-hydroxy-2,3,7-trimethyloctanal Chemical compound CCC(C)(C=O)C(C)CCCC(C)(C)O ALPILNOHTMEGAY-UHFFFAOYSA-N 0.000 description 2
- 241000196324 Embryophyta Species 0.000 description 2
- 238000005033 Fourier transform infrared spectroscopy Methods 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- 229910019142 PO4 Inorganic materials 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 239000002202 Polyethylene glycol Substances 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 125000000732 arylene group Chemical group 0.000 description 2
- YWDBHFZUBPOPRQ-UHFFFAOYSA-N bicyclo[2.1.1]hex-2-ene Chemical compound C1C2CC1C=C2 YWDBHFZUBPOPRQ-UHFFFAOYSA-N 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 238000004587 chromatography analysis Methods 0.000 description 2
- 230000001143 conditioned effect Effects 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 238000004128 high performance liquid chromatography Methods 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- 230000002209 hydrophobic effect Effects 0.000 description 2
- 230000007774 longterm Effects 0.000 description 2
- 239000006210 lotion Substances 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 2
- 239000010452 phosphate Substances 0.000 description 2
- 229920001223 polyethylene glycol Polymers 0.000 description 2
- 230000001105 regulatory effect Effects 0.000 description 2
- MTCFGRXMJLQNBG-REOHCLBHSA-N (2S)-2-Amino-3-hydroxypropansäure Chemical compound OC[C@H](N)C(O)=O MTCFGRXMJLQNBG-REOHCLBHSA-N 0.000 description 1
- JCKZVZPLEZEUIC-GJHDBBOXSA-N (2e)-1-[[(2e)-3,7-dimethylocta-2,6-dienoxy]-diethoxymethoxy]-3,7-dimethylocta-2,6-diene Chemical compound CC(C)=CCCC(/C)=C/COC(OCC)(OCC)OC\C=C(/C)CCC=C(C)C JCKZVZPLEZEUIC-GJHDBBOXSA-N 0.000 description 1
- PANBRUWVURLWGY-MDZDMXLPSA-N (E)-2-undecenal Chemical compound CCCCCCCC\C=C\C=O PANBRUWVURLWGY-MDZDMXLPSA-N 0.000 description 1
- JOVSIYGSCKFQPQ-HWAYABPNSA-N (z)-1-[diethoxy-[(z)-hex-3-enoxy]methoxy]hex-3-ene Chemical compound CC\C=C/CCOC(OCC)(OCC)OCC\C=C/CC JOVSIYGSCKFQPQ-HWAYABPNSA-N 0.000 description 1
- YGFGZTXGYTUXBA-UHFFFAOYSA-N (±)-2,6-dimethyl-5-heptenal Chemical compound O=CC(C)CCC=C(C)C YGFGZTXGYTUXBA-UHFFFAOYSA-N 0.000 description 1
- YJOSRDWPQRSPIW-UHFFFAOYSA-N 1,2,4,6-tetramethylcyclohex-3-ene-1-carbaldehyde Chemical compound CC1CC(C)=CC(C)C1(C)C=O YJOSRDWPQRSPIW-UHFFFAOYSA-N 0.000 description 1
- YMUKLYKGWJPUDZ-UHFFFAOYSA-N 1,3,5,6-tetramethylcyclohex-3-ene-1-carbaldehyde Chemical compound CC1C=C(C)CC(C)(C=O)C1C YMUKLYKGWJPUDZ-UHFFFAOYSA-N 0.000 description 1
- LQPOOAJESJYDLS-UHFFFAOYSA-N 1,3-oxazinane Chemical compound C1CNCOC1 LQPOOAJESJYDLS-UHFFFAOYSA-N 0.000 description 1
- HOQOADCYROWGQA-UHFFFAOYSA-N 1,3-thiazinane Chemical compound C1CNCSC1 HOQOADCYROWGQA-UHFFFAOYSA-N 0.000 description 1
- OGYGFUAIIOPWQD-UHFFFAOYSA-N 1,3-thiazolidine Chemical compound C1CSCN1 OGYGFUAIIOPWQD-UHFFFAOYSA-N 0.000 description 1
- OCFYTOIAJLLHDS-UHFFFAOYSA-N 1-ethoxybutane-1,1-diol Chemical compound CCCC(O)(O)OCC OCFYTOIAJLLHDS-UHFFFAOYSA-N 0.000 description 1
- JEFVINNUVBGSKK-UHFFFAOYSA-N 1-ethyl-3-(4-hydroxy-4-methylpentyl)cyclohex-3-ene-1-carbaldehyde Chemical compound CCC1(C=O)CCC=C(CCCC(C)(C)O)C1 JEFVINNUVBGSKK-UHFFFAOYSA-N 0.000 description 1
- GPHMZKGSVFJRBK-UHFFFAOYSA-N 1-ethyl-4-(4-hydroxy-4-methylpentyl)cyclohex-3-ene-1-carbaldehyde Chemical compound CCC1(C=O)CCC(CCCC(C)(C)O)=CC1 GPHMZKGSVFJRBK-UHFFFAOYSA-N 0.000 description 1
- PBWKVGVYEICDAU-UHFFFAOYSA-N 2,2,3,5,5-pentamethylhexanal Chemical compound CC(C)(C)CC(C)C(C)(C)C=O PBWKVGVYEICDAU-UHFFFAOYSA-N 0.000 description 1
- CSRAGHUCJRIZAS-UHFFFAOYSA-N 2,2,3,7-tetramethyloctanal Chemical compound CC(C)CCCC(C)C(C)(C)C=O CSRAGHUCJRIZAS-UHFFFAOYSA-N 0.000 description 1
- GNHGZHHOTMCLKX-UHFFFAOYSA-N 2,2,6,10-tetramethylundec-9-enal Chemical compound CC(C)=CCCC(C)CCCC(C)(C)C=O GNHGZHHOTMCLKX-UHFFFAOYSA-N 0.000 description 1
- GTCMGPLNPCXOFB-UHFFFAOYSA-N 2,2,6,10-tetramethylundeca-5,9-dienal Chemical compound CC(C)=CCCC(C)=CCCC(C)(C)C=O GTCMGPLNPCXOFB-UHFFFAOYSA-N 0.000 description 1
- WYXYNKRNJIGUOT-UHFFFAOYSA-N 2,2-dimethyldec-8-enal Chemical compound CC=CCCCCCC(C)(C)C=O WYXYNKRNJIGUOT-UHFFFAOYSA-N 0.000 description 1
- OSZZNCOFBUIXGB-UHFFFAOYSA-N 2,2-dimethylnon-6-enal Chemical compound CCC=CCCCC(C)(C)C=O OSZZNCOFBUIXGB-UHFFFAOYSA-N 0.000 description 1
- MBPLRQXATZSHBD-UHFFFAOYSA-N 2,2-dimethylundec-10-enal Chemical compound O=CC(C)(C)CCCCCCCC=C MBPLRQXATZSHBD-UHFFFAOYSA-N 0.000 description 1
- KRPQFIFJUHWITM-UHFFFAOYSA-N 2,2-dimethylundecanal Chemical compound CCCCCCCCCC(C)(C)C=O KRPQFIFJUHWITM-UHFFFAOYSA-N 0.000 description 1
- MMVJPADAJYOOBB-UHFFFAOYSA-N 2,3,3,7-tetramethyl-2-(naphthalene-2-carbonyl)non-8-enoic acid Chemical compound CC(CCCC(C)(C)C(C)(C(=O)C1=CC2=CC=CC=C2C=C1)C(=O)O)C=C MMVJPADAJYOOBB-UHFFFAOYSA-N 0.000 description 1
- GPWNWKWQOLEVEQ-UHFFFAOYSA-N 2,4-diaminopyrimidine-5-carbaldehyde Chemical compound NC1=NC=C(C=O)C(N)=N1 GPWNWKWQOLEVEQ-UHFFFAOYSA-N 0.000 description 1
- ZXGMEZJVBHJYEQ-UHFFFAOYSA-N 2,6,10-trimethylundeca-5,9-dienal Chemical compound O=CC(C)CCC=C(C)CCC=C(C)C ZXGMEZJVBHJYEQ-UHFFFAOYSA-N 0.000 description 1
- UAEHSOYZLMXHSR-UHFFFAOYSA-N 2,6-dimethyloct-7-en-2-yl 3-oxododecanoate Chemical compound CCCCCCCCCC(=O)CC(=O)OC(C)(C)CCCC(C)C=C UAEHSOYZLMXHSR-UHFFFAOYSA-N 0.000 description 1
- UDLJBMAKEKQMGK-UHFFFAOYSA-N 2-(2,6-dimethylhept-5-enoxy)-2-methylbutanal Chemical compound CCC(C)(C=O)OCC(C)CCC=C(C)C UDLJBMAKEKQMGK-UHFFFAOYSA-N 0.000 description 1
- LQGCUXOONJSZKF-UHFFFAOYSA-N 2-(2,6-dimethylhept-5-enoxy)-2-methylpropanal Chemical compound CC(C)=CCCC(C)COC(C)(C)C=O LQGCUXOONJSZKF-UHFFFAOYSA-N 0.000 description 1
- FTSQVJBIYDAGBQ-UHFFFAOYSA-N 2-[(4-methoxyphenyl)methyl]-2-methylbutanal Chemical compound CCC(C)(C=O)CC1=CC=C(OC)C=C1 FTSQVJBIYDAGBQ-UHFFFAOYSA-N 0.000 description 1
- OYWGJTQCPPTAHF-UHFFFAOYSA-N 2-[(4-tert-butylphenyl)methyl]-2-methylbutanal Chemical compound CCC(C)(C=O)CC1=CC=C(C(C)(C)C)C=C1 OYWGJTQCPPTAHF-UHFFFAOYSA-N 0.000 description 1
- GCTIQCSIYAQSSZ-UHFFFAOYSA-N 2-[bis(6-methylheptan-2-yloxy)methoxy]-6-methylheptane Chemical compound CC(C)CCCC(C)OC(OC(C)CCCC(C)C)OC(C)CCCC(C)C GCTIQCSIYAQSSZ-UHFFFAOYSA-N 0.000 description 1
- NJARCAGXIVSBNM-UHFFFAOYSA-N 2-[diethoxy(2-phenylethoxy)methoxy]ethylbenzene Chemical compound C=1C=CC=CC=1CCOC(OCC)(OCC)OCCC1=CC=CC=C1 NJARCAGXIVSBNM-UHFFFAOYSA-N 0.000 description 1
- KZMBBUYBMUAZSB-UHFFFAOYSA-N 2-[diethoxy-(5-methyl-2-propan-2-ylcyclohexyl)oxymethoxy]-4-methyl-1-propan-2-ylcyclohexane Chemical compound C1C(C)CCC(C(C)C)C1OC(OCC)(OCC)OC1CC(C)CCC1C(C)C KZMBBUYBMUAZSB-UHFFFAOYSA-N 0.000 description 1
- WBNRWBWUXLQXPG-UHFFFAOYSA-N 2-acetyl-3,3,7-trimethylnon-8-enoic acid Chemical compound C=CC(C)CCCC(C)(C)C(C(C)=O)C(O)=O WBNRWBWUXLQXPG-UHFFFAOYSA-N 0.000 description 1
- DTYUNOXUGYBBLZ-UHFFFAOYSA-N 2-benzyl-2-methylbutanal Chemical compound CCC(C)(C=O)CC1=CC=CC=C1 DTYUNOXUGYBBLZ-UHFFFAOYSA-N 0.000 description 1
- MNVSZMFPSDFUHP-UHFFFAOYSA-N 2-benzyl-2-methyloctanal Chemical compound CCCCCCC(C)(C=O)CC1=CC=CC=C1 MNVSZMFPSDFUHP-UHFFFAOYSA-N 0.000 description 1
- PLFLLPQQOUGTJW-UHFFFAOYSA-N 2-ethyl-2,3,5,5-tetramethylhexanal Chemical compound CCC(C)(C=O)C(C)CC(C)(C)C PLFLLPQQOUGTJW-UHFFFAOYSA-N 0.000 description 1
- XJAIABDTQDBIQS-UHFFFAOYSA-N 2-ethyl-2,3,7-trimethyloct-6-enal Chemical compound CCC(C)(C=O)C(C)CCC=C(C)C XJAIABDTQDBIQS-UHFFFAOYSA-N 0.000 description 1
- RNPPMTWGWASZDX-UHFFFAOYSA-N 2-ethyl-2,3,7-trimethyloctanal Chemical compound CCC(C)(C=O)C(C)CCCC(C)C RNPPMTWGWASZDX-UHFFFAOYSA-N 0.000 description 1
- ZWDPOJWNWFYIEM-UHFFFAOYSA-N 2-ethyl-2,6-dimethylhept-5-enal Chemical compound CCC(C)(C=O)CCC=C(C)C ZWDPOJWNWFYIEM-UHFFFAOYSA-N 0.000 description 1
- FGNQRMHYRUJXHA-UHFFFAOYSA-N 2-ethyl-2-methyldec-4-enal Chemical compound CCCCCC=CCC(C)(CC)C=O FGNQRMHYRUJXHA-UHFFFAOYSA-N 0.000 description 1
- MCJYZKFIJVTMMY-UHFFFAOYSA-N 2-ethyl-2-methyldec-8-enal Chemical compound CCC(C)(C=O)CCCCCC=CC MCJYZKFIJVTMMY-UHFFFAOYSA-N 0.000 description 1
- XTSHSKGNWNPYTA-UHFFFAOYSA-N 2-ethyl-2-methyldecanal Chemical compound CCCCCCCCC(C)(CC)C=O XTSHSKGNWNPYTA-UHFFFAOYSA-N 0.000 description 1
- QGEVGWGDYVQQFR-UHFFFAOYSA-N 2-ethyl-2-methyldodec-3-enal Chemical compound CCCCCCCCC=CC(C)(CC)C=O QGEVGWGDYVQQFR-UHFFFAOYSA-N 0.000 description 1
- LVUVEELWRJZUEX-UHFFFAOYSA-N 2-ethyl-2-methyldodecanal Chemical compound CCCCCCCCCCC(C)(CC)C=O LVUVEELWRJZUEX-UHFFFAOYSA-N 0.000 description 1
- MNIDGQHIIHQRNT-UHFFFAOYSA-N 2-ethyl-2-methylnon-6-enal Chemical compound CCC=CCCCC(C)(CC)C=O MNIDGQHIIHQRNT-UHFFFAOYSA-N 0.000 description 1
- AAZMJSWVLCAZBI-UHFFFAOYSA-N 2-ethyl-2-methylnonanal Chemical compound CCCCCCCC(C)(CC)C=O AAZMJSWVLCAZBI-UHFFFAOYSA-N 0.000 description 1
- QRIUKUAPENANEZ-UHFFFAOYSA-N 2-ethyl-2-methyloctanal Chemical compound CCCCCCC(C)(CC)C=O QRIUKUAPENANEZ-UHFFFAOYSA-N 0.000 description 1
- BSZPOBDLOMCMJB-UHFFFAOYSA-N 2-ethyl-2-methylundec-10-enal Chemical compound CCC(C)(C=O)CCCCCCCC=C BSZPOBDLOMCMJB-UHFFFAOYSA-N 0.000 description 1
- QGQBWPNVWZNCBM-UHFFFAOYSA-N 2-ethyl-5,5-dimethyl-1,3,4,6,7,8-hexahydronaphthalene-2-carbaldehyde Chemical compound C1C(CC)(C=O)CCC2=C1CCCC2(C)C QGQBWPNVWZNCBM-UHFFFAOYSA-N 0.000 description 1
- AQBXGSQMTSOAIE-UHFFFAOYSA-N 2-ethyl-7-methoxy-2,3,7-trimethyloctanal Chemical compound CCC(C)(C=O)C(C)CCCC(C)(C)OC AQBXGSQMTSOAIE-UHFFFAOYSA-N 0.000 description 1
- PDFNJSAIJWEXKD-UHFFFAOYSA-N 2-ethyl-8,8-dimethyl-1,3,4,5,6,7-hexahydronaphthalene-2-carbaldehyde Chemical compound CC1(C)CCCC2=C1CC(CC)(C=O)CC2 PDFNJSAIJWEXKD-UHFFFAOYSA-N 0.000 description 1
- UTMJWHAVPAOCJF-UHFFFAOYSA-N 2-methyl-2-(4-propan-2-ylphenyl)butanal Chemical compound CCC(C)(C=O)C1=CC=C(C(C)C)C=C1 UTMJWHAVPAOCJF-UHFFFAOYSA-N 0.000 description 1
- SKHUPTUYEMALRL-UHFFFAOYSA-N 2-methyl-2-[(4-propan-2-ylphenyl)methyl]butanal Chemical compound CCC(C)(C=O)CC1=CC=C(C(C)C)C=C1 SKHUPTUYEMALRL-UHFFFAOYSA-N 0.000 description 1
- 125000000094 2-phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 description 1
- QLXFSJDVOCHENG-UHFFFAOYSA-N 3,7-dimethylocta-1,6-dien-3-yl 2-methyl-3-naphthalen-2-yl-3-oxopropanoate Chemical compound C1=CC=CC2=CC(C(=O)C(C(=O)OC(C)(CCC=C(C)C)C=C)C)=CC=C21 QLXFSJDVOCHENG-UHFFFAOYSA-N 0.000 description 1
- XXMIJRJVDPXOLN-UHFFFAOYSA-N 3,7-dimethylocta-1,6-dien-3-yl 3-naphthalen-1-yl-3-oxopropanoate Chemical compound C1=CC=C2C(C(=O)CC(=O)OC(C)(CCC=C(C)C)C=C)=CC=CC2=C1 XXMIJRJVDPXOLN-UHFFFAOYSA-N 0.000 description 1
- ZANSWOBXLYAUHS-UHFFFAOYSA-N 3,7-dimethylocta-1,6-dien-3-yl 3-oxobutanoate Chemical compound CC(C)=CCCC(C)(C=C)OC(=O)CC(C)=O ZANSWOBXLYAUHS-UHFFFAOYSA-N 0.000 description 1
- QLEXBOIOJCMDRO-UHFFFAOYSA-N 3-[3,7-dimethylocta-1,6-dien-3-yloxy(diethoxy)methoxy]-3,7-dimethylocta-1,6-diene Chemical compound CC(C)=CCCC(C)(C=C)OC(OCC)(OCC)OC(C)(CCC=C(C)C)C=C QLEXBOIOJCMDRO-UHFFFAOYSA-N 0.000 description 1
- KRESMFMUTRXHHN-UHFFFAOYSA-N 3-ethyl-2-propylbicyclo[2.2.1]hept-5-ene-3-carbaldehyde Chemical compound C1C2C=CC1C(CCC)C2(CC)C=O KRESMFMUTRXHHN-UHFFFAOYSA-N 0.000 description 1
- QOZRLPGWWJUHCT-UHFFFAOYSA-N 3-methyl-2-propylbicyclo[2.2.1]hept-5-ene-3-carbaldehyde Chemical compound C1C2C=CC1C(CCC)C2(C)C=O QOZRLPGWWJUHCT-UHFFFAOYSA-N 0.000 description 1
- FHFZALNHPZPAPU-UHFFFAOYSA-N 4-(4-propan-2-ylcyclohexyl)-1,3-dioxolan-2-ol Chemical compound CC(C)C1CCC(CC1)C2COC(O2)O FHFZALNHPZPAPU-UHFFFAOYSA-N 0.000 description 1
- LYLGCNKHSTVUJP-UHFFFAOYSA-N 4-ethenyl-2,4,8-trimethyl-2-(naphthalene-2-carbonyl)non-7-enoic acid Chemical compound CC(=CCCC(C)(CC(C)(C(=O)C1=CC2=CC=CC=C2C=C1)C(=O)O)C=C)C LYLGCNKHSTVUJP-UHFFFAOYSA-N 0.000 description 1
- UFTHEDBYLPFRDP-UHFFFAOYSA-N 5,6-dihydro-2h-oxazine Chemical compound C1CC=CNO1 UFTHEDBYLPFRDP-UHFFFAOYSA-N 0.000 description 1
- ITULLLOAEUGEOF-UHFFFAOYSA-N 5,9-dimethyl-2-(naphthalene-2-carbonyl)deca-4,8-dienoic acid Chemical compound CC(=CCCC(=CCC(C(=O)C1=CC2=CC=CC=C2C=C1)C(=O)O)C)C ITULLLOAEUGEOF-UHFFFAOYSA-N 0.000 description 1
- LTQNXGWGFHXEJA-UHFFFAOYSA-N 5,9-dimethyl-2-octanoyldeca-4,8-dienoic acid Chemical compound CCCCCCCC(=O)C(CC=C(C)CCC=C(C)C)C(=O)O LTQNXGWGFHXEJA-UHFFFAOYSA-N 0.000 description 1
- NPBYXVUJZOJMLZ-UHFFFAOYSA-N 7-hydroxy-2,2,3,7-tetramethyloctanal Chemical compound O=CC(C)(C)C(C)CCCC(C)(C)O NPBYXVUJZOJMLZ-UHFFFAOYSA-N 0.000 description 1
- XUHIARSTMOMEQT-UHFFFAOYSA-N 7-methoxy-2,2,3,7-tetramethyloctanal Chemical compound COC(C)(C)CCCC(C)C(C)(C)C=O XUHIARSTMOMEQT-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N Acrylic acid Chemical compound OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- ZRSNZINYAWTAHE-UHFFFAOYSA-N Anisaldehyde Natural products COC1=CC=C(C=O)C=C1 ZRSNZINYAWTAHE-UHFFFAOYSA-N 0.000 description 1
- YGNTXLJZYRVIJS-UHFFFAOYSA-N CC(C)=CCCC(C)=CCOC(C)(C)C=O Chemical compound CC(C)=CCCC(C)=CCOC(C)(C)C=O YGNTXLJZYRVIJS-UHFFFAOYSA-N 0.000 description 1
- TYHLQHBWTFEIGC-UHFFFAOYSA-N CCC(C)(OCC=C(C)CCC=C(C)C)C=O Chemical compound CCC(C)(OCC=C(C)CCC=C(C)C)C=O TYHLQHBWTFEIGC-UHFFFAOYSA-N 0.000 description 1
- RGMBCMBNMQOCJV-LRRVACHLSA-N CC\C=C/CCCCCOC(C)(OCCCCC\C=C/CC)OCCCCC\C=C/CC Chemical compound CC\C=C/CCCCCOC(C)(OCCCCC\C=C/CC)OCCCCC\C=C/CC RGMBCMBNMQOCJV-LRRVACHLSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- WTEVQBCEXWBHNA-UHFFFAOYSA-N Citral Natural products CC(C)=CCCC(C)=CC=O WTEVQBCEXWBHNA-UHFFFAOYSA-N 0.000 description 1
- 241000282412 Homo Species 0.000 description 1
- 101000650817 Homo sapiens Semaphorin-4D Proteins 0.000 description 1
- 241000257303 Hymenoptera Species 0.000 description 1
- 102100027744 Semaphorin-4D Human genes 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- CJWYMHMZSRUCHP-UHFFFAOYSA-N [5-[bis(3-methyl-5-phenylpentoxy)methoxy]-3-methylpentyl]benzene Chemical compound C=1C=CC=CC=1CCC(C)CCOC(OCCC(C)CCC=1C=CC=CC=1)OCCC(C)CCC1=CC=CC=C1 CJWYMHMZSRUCHP-UHFFFAOYSA-N 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 239000007853 buffer solution Substances 0.000 description 1
- 229960001631 carbomer Drugs 0.000 description 1
- MIZGSAALSYARKU-UHFFFAOYSA-N cashmeran Chemical compound CC1(C)C(C)C(C)(C)C2=C1C(=O)CCC2 MIZGSAALSYARKU-UHFFFAOYSA-N 0.000 description 1
- 150000005829 chemical entities Chemical class 0.000 description 1
- 229940117916 cinnamic aldehyde Drugs 0.000 description 1
- KJPRLNWUNMBNBZ-UHFFFAOYSA-N cinnamic aldehyde Natural products O=CC=CC1=CC=CC=C1 KJPRLNWUNMBNBZ-UHFFFAOYSA-N 0.000 description 1
- 229940043350 citral Drugs 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 230000003750 conditioning effect Effects 0.000 description 1
- 238000013270 controlled release Methods 0.000 description 1
- 239000006071 cream Substances 0.000 description 1
- 229940019836 cyclamen aldehyde Drugs 0.000 description 1
- 230000003111 delayed effect Effects 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 235000013399 edible fruits Nutrition 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 125000001072 heteroaryl group Chemical group 0.000 description 1
- 125000005842 heteroatom Chemical group 0.000 description 1
- PANBRUWVURLWGY-UHFFFAOYSA-N intreleven aldehyde Natural products CCCCCCCCC=CC=O PANBRUWVURLWGY-UHFFFAOYSA-N 0.000 description 1
- INQOMBQAUSQDDS-UHFFFAOYSA-N iodomethane Chemical compound IC INQOMBQAUSQDDS-UHFFFAOYSA-N 0.000 description 1
- 229940059904 light mineral oil Drugs 0.000 description 1
- 230000005923 long-lasting effect Effects 0.000 description 1
- 230000000873 masking effect Effects 0.000 description 1
- 238000004949 mass spectrometry Methods 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- ANSUDRATXSJBLY-UHFFFAOYSA-N methyl 2-amino-3-hydroxypropanoate Chemical compound COC(=O)C(N)CO ANSUDRATXSJBLY-UHFFFAOYSA-N 0.000 description 1
- 239000003607 modifier Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 125000004430 oxygen atom Chemical group O* 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 239000008055 phosphate buffer solution Substances 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000012898 sample dilution Substances 0.000 description 1
- 239000002453 shampoo Substances 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- AJPJDKMHJJGVTQ-UHFFFAOYSA-M sodium dihydrogen phosphate Chemical compound [Na+].OP(O)([O-])=O AJPJDKMHJJGVTQ-UHFFFAOYSA-M 0.000 description 1
- 229910052717 sulfur Chemical group 0.000 description 1
- 125000004434 sulfur atom Chemical group 0.000 description 1
- 230000000475 sunscreen effect Effects 0.000 description 1
- 239000000516 sunscreening agent Substances 0.000 description 1
- 230000002459 sustained effect Effects 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical compound OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 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
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q13/00—Formulations or additives for perfume preparations
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
- C07D263/02—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings
- C07D263/04—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
- C07D263/06—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having no double bonds between ring members or between ring members and non-ring members with hydrocarbon radicals, substituted by oxygen atoms, attached to ring 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
- C11B9/0007—Aliphatic compounds
- C11B9/0015—Aliphatic compounds containing oxygen as the only heteroatom
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
- A61K2800/57—Compounds covalently linked to a(n inert) carrier molecule, e.g. conjugates, pro-fragrances
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Emergency Medicine (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Fats And Perfumes (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US13012799P | 1999-04-20 | 1999-04-20 | |
| US60/130,127 | 1999-04-20 | ||
| PCT/US2000/010211 WO2000063329A1 (fr) | 1999-04-20 | 2000-04-14 | Aldehydes utiles en tant que matieres brutes de parfum et precurseurs de parfum contenant un atome de carbone alpha tertiaire |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JP2002542380A true JP2002542380A (ja) | 2002-12-10 |
Family
ID=22443177
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2000612409A Withdrawn JP2002542380A (ja) | 1999-04-20 | 2000-04-14 | 芳香剤原料アルデヒドおよび第三級α炭素原子をもつ芳香剤原料前駆体 |
Country Status (4)
| Country | Link |
|---|---|
| EP (1) | EP1171556A1 (fr) |
| JP (1) | JP2002542380A (fr) |
| AU (1) | AU4353100A (fr) |
| WO (1) | WO2000063329A1 (fr) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2009509934A (ja) * | 2005-09-16 | 2009-03-12 | ジボダン エス エー | ６−メトキシ−２，６−ジメチルオクタナールおよびフレグランス成分としてのこの使用 |
| JP2015521619A (ja) * | 2012-06-19 | 2015-07-30 | ダウ グローバル テクノロジーズ エルエルシー | 抗微生物化合物 |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1332732A (zh) | 1998-10-23 | 2002-01-23 | 宝洁公司 | 香料谐香剂前体和醛和酮类香料释放体 |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3225102A (en) * | 1960-12-13 | 1965-12-21 | Eastman Kodak Co | Allenic aldehydes |
| US4011233A (en) * | 1973-06-28 | 1977-03-08 | Givaudan Corporation | 2-methyl-2-(4-methyl-3-pentene-1-yl) thiazolidine |
| US4068012A (en) * | 1976-11-11 | 1978-01-10 | International Flavors & Fragrances Inc. | Use of 1-(2-propenyl)-3-(4-methyl-3-pentenyl)-Δ3 -cyclohexene-1-carboxaldehyde and 1-(2-propenyl)-4-(4-methyl-3-pentenyl)-Δ3 -cyclohexene-1-carboxaldehyde |
| US4010207A (en) * | 1976-01-15 | 1977-03-01 | International Flavors & Fragrances Inc. | Process for the alkylation of α, β-unsaturated aldehydes |
| US6013618A (en) * | 1997-04-24 | 2000-01-11 | Procter & Gamble Company | Perfumes having odor longevity benefits |
| WO1999043639A1 (fr) * | 1998-02-24 | 1999-09-02 | The Procter & Gamble Company | Systemes de diffusion de substances brutes de fragrances a base d'alcools tertiaires |
-
2000
- 2000-04-14 WO PCT/US2000/010211 patent/WO2000063329A1/fr not_active Application Discontinuation
- 2000-04-14 AU AU43531/00A patent/AU4353100A/en not_active Abandoned
- 2000-04-14 EP EP00923404A patent/EP1171556A1/fr not_active Withdrawn
- 2000-04-14 JP JP2000612409A patent/JP2002542380A/ja not_active Withdrawn
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2009509934A (ja) * | 2005-09-16 | 2009-03-12 | ジボダン エス エー | ６−メトキシ−２，６−ジメチルオクタナールおよびフレグランス成分としてのこの使用 |
| JP2015521619A (ja) * | 2012-06-19 | 2015-07-30 | ダウ グローバル テクノロジーズ エルエルシー | 抗微生物化合物 |
Also Published As
| Publication number | Publication date |
|---|---|
| EP1171556A1 (fr) | 2002-01-16 |
| AU4353100A (en) | 2000-11-02 |
| WO2000063329A1 (fr) | 2000-10-26 |
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