JP2000053613A - 保護されたヒドロキシ基を有する化合物 - Google Patents
保護されたヒドロキシ基を有する化合物Info
- Publication number
- JP2000053613A JP2000053613A JP11111199A JP11119999A JP2000053613A JP 2000053613 A JP2000053613 A JP 2000053613A JP 11111199 A JP11111199 A JP 11111199A JP 11119999 A JP11119999 A JP 11119999A JP 2000053613 A JP2000053613 A JP 2000053613A
- Authority
- JP
- Japan
- Prior art keywords
- compound
- ester
- dimethyl
- acid
- substituted
- 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.)
- Pending
Links
- 150000001875 compounds Chemical class 0.000 title claims abstract description 59
- 125000002887 hydroxy group Chemical group [H]O* 0.000 title abstract description 3
- 239000002243 precursor Substances 0.000 claims abstract description 22
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims abstract description 17
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 8
- 125000003342 alkenyl group Chemical group 0.000 claims abstract description 7
- 125000000753 cycloalkyl group Chemical group 0.000 claims abstract description 7
- 125000000304 alkynyl group Chemical group 0.000 claims abstract description 3
- 125000000392 cycloalkenyl group Chemical group 0.000 claims abstract description 3
- 239000000203 mixture Substances 0.000 claims description 46
- 238000000034 method Methods 0.000 claims description 42
- 150000002148 esters Chemical class 0.000 claims description 41
- 150000001299 aldehydes Chemical class 0.000 claims description 23
- 125000005842 heteroatom Chemical group 0.000 claims description 15
- 150000002576 ketones Chemical class 0.000 claims description 14
- 239000002253 acid Substances 0.000 claims description 8
- 230000003213 activating effect Effects 0.000 claims description 7
- 238000003776 cleavage reaction Methods 0.000 claims description 7
- 230000007017 scission Effects 0.000 claims description 7
- 229910052739 hydrogen Inorganic materials 0.000 claims description 6
- 239000001257 hydrogen Substances 0.000 claims description 6
- 230000009965 odorless effect Effects 0.000 claims description 6
- 125000003118 aryl group Chemical group 0.000 claims description 4
- ZYGHJZDHTFUPRJ-UHFFFAOYSA-N coumarin Chemical compound C1=CC=C2OC(=O)C=CC2=C1 ZYGHJZDHTFUPRJ-UHFFFAOYSA-N 0.000 claims description 4
- 235000001671 coumarin Nutrition 0.000 claims description 3
- 150000001408 amides Chemical class 0.000 claims description 2
- 150000004718 beta keto acids Chemical class 0.000 claims description 2
- 150000004775 coumarins Chemical class 0.000 claims description 2
- 150000004985 diamines Chemical class 0.000 claims description 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 2
- 125000000467 secondary amino group Chemical group [H]N([*:1])[*:2] 0.000 claims description 2
- 125000000547 substituted alkyl group Chemical group 0.000 claims description 2
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims 3
- 125000002587 enol group Chemical group 0.000 claims 2
- 101100386054 Saccharomyces cerevisiae (strain ATCC 204508 / S288c) CYS3 gene Proteins 0.000 claims 1
- 229960000956 coumarin Drugs 0.000 claims 1
- 101150035983 str1 gene Proteins 0.000 claims 1
- 238000003756 stirring Methods 0.000 abstract description 10
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 abstract description 9
- 230000000845 anti-microbial effect Effects 0.000 abstract description 8
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 abstract description 6
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 abstract description 3
- 238000001816 cooling Methods 0.000 abstract description 3
- 238000010438 heat treatment Methods 0.000 abstract description 3
- 239000001632 sodium acetate Substances 0.000 abstract description 3
- 235000017281 sodium acetate Nutrition 0.000 abstract description 3
- 230000004936 stimulating effect Effects 0.000 abstract description 3
- DFFGXGLKNGYGOY-UHFFFAOYSA-N [3-(4-tert-butylphenyl)-2-methylprop-1-enyl] acetate Chemical compound CC(=O)OC=C(C)CC1=CC=C(C(C)(C)C)C=C1 DFFGXGLKNGYGOY-UHFFFAOYSA-N 0.000 abstract 1
- SDQFDHOLCGWZPU-UHFFFAOYSA-N lilial Chemical compound O=CC(C)CC1=CC=C(C(C)(C)C)C=C1 SDQFDHOLCGWZPU-UHFFFAOYSA-N 0.000 abstract 1
- 210000000056 organ Anatomy 0.000 abstract 1
- -1 aromatic radicals Chemical class 0.000 description 67
- 239000003205 fragrance Substances 0.000 description 57
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 48
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 38
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 32
- 239000000243 solution Substances 0.000 description 32
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 24
- WYURNTSHIVDZCO-UHFFFAOYSA-N tetrahydrofuran Substances C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 23
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 21
- 239000000047 product Substances 0.000 description 20
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 17
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 12
- 230000003111 delayed effect Effects 0.000 description 11
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 11
- KBWRWCSRYCKEOR-UHFFFAOYSA-N 3-capryl propionic acid Chemical compound CCCCCCCC(=O)CCC(O)=O KBWRWCSRYCKEOR-UHFFFAOYSA-N 0.000 description 10
- 239000003599 detergent Substances 0.000 description 10
- 239000007788 liquid Substances 0.000 description 10
- OKKJLVBELUTLKV-UHFFFAOYSA-N methanol Substances OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 10
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 9
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 9
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 9
- 150000002596 lactones Chemical class 0.000 description 9
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 9
- XEXIVNNTJNBUGV-UHFFFAOYSA-N 4-hydroxy-undecanoic acid Chemical compound CCCCCCCC(O)CCC(O)=O XEXIVNNTJNBUGV-UHFFFAOYSA-N 0.000 description 8
- SPUWOYCLMKSXKU-UHFFFAOYSA-N 4-oxo capric acid Chemical compound CCCCCCC(=O)CCC(O)=O SPUWOYCLMKSXKU-UHFFFAOYSA-N 0.000 description 8
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 8
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 8
- 239000004744 fabric Substances 0.000 description 8
- 239000002979 fabric softener Substances 0.000 description 8
- PSHKMPUSSFXUIA-UHFFFAOYSA-N n,n-dimethylpyridin-2-amine Chemical compound CN(C)C1=CC=CC=N1 PSHKMPUSSFXUIA-UHFFFAOYSA-N 0.000 description 8
- 239000003921 oil Substances 0.000 description 8
- 239000012044 organic layer Substances 0.000 description 8
- 239000012074 organic phase Substances 0.000 description 8
- 239000012071 phase Substances 0.000 description 8
- 239000011541 reaction mixture Substances 0.000 description 8
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 8
- 239000004367 Lipase Substances 0.000 description 7
- 102000004882 Lipase Human genes 0.000 description 7
- 108090001060 Lipase Proteins 0.000 description 7
- 235000019421 lipase Nutrition 0.000 description 7
- 235000019645 odor Nutrition 0.000 description 7
- 239000012279 sodium borohydride Substances 0.000 description 7
- 229910000033 sodium borohydride Inorganic materials 0.000 description 7
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 6
- UIIMBOGNXHQVGW-DEQYMQKBSA-M Sodium bicarbonate-14C Chemical class [Na+].O[14C]([O-])=O UIIMBOGNXHQVGW-DEQYMQKBSA-M 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 239000012267 brine Substances 0.000 description 6
- 239000002781 deodorant agent Substances 0.000 description 6
- 230000000694 effects Effects 0.000 description 6
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 6
- 235000019341 magnesium sulphate Nutrition 0.000 description 6
- 230000000873 masking effect Effects 0.000 description 6
- 239000000741 silica gel Substances 0.000 description 6
- 229910002027 silica gel Inorganic materials 0.000 description 6
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 6
- XEFQLINVKFYRCS-UHFFFAOYSA-N Triclosan Chemical compound OC1=CC(Cl)=CC=C1OC1=CC=C(Cl)C=C1Cl XEFQLINVKFYRCS-UHFFFAOYSA-N 0.000 description 5
- 150000001298 alcohols Chemical class 0.000 description 5
- 230000001166 anti-perspirative effect Effects 0.000 description 5
- 239000003213 antiperspirant Substances 0.000 description 5
- 230000015572 biosynthetic process Effects 0.000 description 5
- ULDHMXUKGWMISQ-UHFFFAOYSA-N carvone Chemical compound CC(=C)C1CC=C(C)C(=O)C1 ULDHMXUKGWMISQ-UHFFFAOYSA-N 0.000 description 5
- 238000004587 chromatography analysis Methods 0.000 description 5
- 239000013078 crystal Substances 0.000 description 5
- 238000003786 synthesis reaction Methods 0.000 description 5
- UFLHIIWVXFIJGU-ARJAWSKDSA-N (Z)-hex-3-en-1-ol Chemical compound CC\C=C/CCO UFLHIIWVXFIJGU-ARJAWSKDSA-N 0.000 description 4
- PRDIIROHTWNJDB-UHFFFAOYSA-N 3-caproyl propionic acid Chemical compound CCCCCC(=O)CCC(O)=O PRDIIROHTWNJDB-UHFFFAOYSA-N 0.000 description 4
- GLZPCOQZEFWAFX-UHFFFAOYSA-N Geraniol Chemical compound CC(C)=CCCC(C)=CCO GLZPCOQZEFWAFX-UHFFFAOYSA-N 0.000 description 4
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical class [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 4
- 229910052782 aluminium Inorganic materials 0.000 description 4
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- QMVPMAAFGQKVCJ-UHFFFAOYSA-N citronellol Chemical compound OCCC(C)CCC=C(C)C QMVPMAAFGQKVCJ-UHFFFAOYSA-N 0.000 description 4
- 239000012230 colorless oil Substances 0.000 description 4
- NQGIJDNPUZEBRU-UHFFFAOYSA-N dodecanoyl chloride Chemical compound CCCCCCCCCCCC(Cl)=O NQGIJDNPUZEBRU-UHFFFAOYSA-N 0.000 description 4
- RBBLRYOHDSHTKL-UHFFFAOYSA-N hex-3-enyl 4-hydroxydecanoate Chemical compound CCCCCCC(O)CCC(=O)OCCC=CCC RBBLRYOHDSHTKL-UHFFFAOYSA-N 0.000 description 4
- 239000004615 ingredient Substances 0.000 description 4
- CDOSHBSSFJOMGT-UHFFFAOYSA-N linalool Chemical compound CC(C)=CCCC(C)(O)C=C CDOSHBSSFJOMGT-UHFFFAOYSA-N 0.000 description 4
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 description 4
- 229960003500 triclosan Drugs 0.000 description 4
- PHXATPHONSXBIL-UHFFFAOYSA-N xi-gamma-Undecalactone Chemical compound CCCCCCCC1CCC(=O)O1 PHXATPHONSXBIL-UHFFFAOYSA-N 0.000 description 4
- BUIQYRMXTZBRTB-UHFFFAOYSA-N 2,6-dimethylheptan-2-yl 4-oxodecanoate Chemical compound CCCCCCC(=O)CCC(=O)OC(C)(C)CCCC(C)C BUIQYRMXTZBRTB-UHFFFAOYSA-N 0.000 description 3
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- DKULSTMKCYRQCP-UHFFFAOYSA-N 2-phenylethyl carbonochloridate Chemical compound ClC(=O)OCCC1=CC=CC=C1 DKULSTMKCYRQCP-UHFFFAOYSA-N 0.000 description 3
- SWXKLOXBUBQJQN-UHFFFAOYSA-N 3,7-dimethylocta-2,6-dienyl 4-hydroxynonanoate Chemical compound CCCCCC(O)CCC(=O)OCC=C(C)CCC=C(C)C SWXKLOXBUBQJQN-UHFFFAOYSA-N 0.000 description 3
- RJDHDCLWRJEPEJ-UHFFFAOYSA-N 3,7-dimethylocta-2,6-dienyl 4-hydroxyundecanoate Chemical compound CCCCCCCC(O)CCC(=O)OCC=C(C)CCC=C(C)C RJDHDCLWRJEPEJ-UHFFFAOYSA-N 0.000 description 3
- QQAVZEYXLCYOKO-UHFFFAOYSA-N 4-Hydroxycapric acid Chemical compound CCCCCCC(O)CCC(O)=O QQAVZEYXLCYOKO-UHFFFAOYSA-N 0.000 description 3
- KRGVTRNRRGDYON-UHFFFAOYSA-N 4-oxoundecanoyl chloride Chemical compound CCCCCCCC(=O)CCC(Cl)=O KRGVTRNRRGDYON-UHFFFAOYSA-N 0.000 description 3
- XVMSFILGAMDHEY-UHFFFAOYSA-N 6-(4-aminophenyl)sulfonylpyridin-3-amine Chemical compound C1=CC(N)=CC=C1S(=O)(=O)C1=CC=C(N)C=N1 XVMSFILGAMDHEY-UHFFFAOYSA-N 0.000 description 3
- WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 3
- QOSSAOTZNIDXMA-UHFFFAOYSA-N Dicylcohexylcarbodiimide Chemical compound C1CCCCC1N=C=NC1CCCCC1 QOSSAOTZNIDXMA-UHFFFAOYSA-N 0.000 description 3
- 102000004190 Enzymes Human genes 0.000 description 3
- 108090000790 Enzymes Proteins 0.000 description 3
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- JGNPMRZXWSYRPI-UHFFFAOYSA-N [1-(3,7-dimethylocta-2,6-dienoxy)-1-oxoundecan-4-yl] benzoate Chemical compound CC(C)=CCCC(C)=CCOC(=O)CCC(CCCCCCC)OC(=O)C1=CC=CC=C1 JGNPMRZXWSYRPI-UHFFFAOYSA-N 0.000 description 3
- 238000004458 analytical method Methods 0.000 description 3
- 244000309464 bull Species 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 229940008099 dimethicone Drugs 0.000 description 3
- 239000004205 dimethyl polysiloxane Substances 0.000 description 3
- 235000013870 dimethyl polysiloxane Nutrition 0.000 description 3
- 238000004821 distillation Methods 0.000 description 3
- UFLHIIWVXFIJGU-UHFFFAOYSA-N hex-3-en-1-ol Natural products CCC=CCCO UFLHIIWVXFIJGU-UHFFFAOYSA-N 0.000 description 3
- GJFQZYHSFMMUOK-UHFFFAOYSA-N hex-3-enyl 4-hydroxynonanoate Chemical compound CCCCCC(O)CCC(=O)OCCC=CCC GJFQZYHSFMMUOK-UHFFFAOYSA-N 0.000 description 3
- JOVQDKYEUSPVHU-UHFFFAOYSA-N hex-3-enyl 4-oxodecanoate Chemical compound CCCCCCC(=O)CCC(=O)OCCC=CCC JOVQDKYEUSPVHU-UHFFFAOYSA-N 0.000 description 3
- BEJDQQMKQCEZFV-UHFFFAOYSA-N hex-3-enyl 4-oxononanoate Chemical compound CCCCCC(=O)CCC(=O)OCCC=CCC BEJDQQMKQCEZFV-UHFFFAOYSA-N 0.000 description 3
- SLGWLOYQWMFQBC-UHFFFAOYSA-N hex-3-enyl 4-oxoundecanoate Chemical compound CCCCCCCC(=O)CCC(=O)OCCC=CCC SLGWLOYQWMFQBC-UHFFFAOYSA-N 0.000 description 3
- 150000002431 hydrogen Chemical class 0.000 description 3
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 3
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 3
- 239000006210 lotion Substances 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 239000002304 perfume Substances 0.000 description 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 3
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 3
- 238000010992 reflux Methods 0.000 description 3
- 229920006395 saturated elastomer Polymers 0.000 description 3
- BEOOHQFXGBMRKU-UHFFFAOYSA-N sodium cyanoborohydride Chemical compound [Na+].[B-]C#N BEOOHQFXGBMRKU-UHFFFAOYSA-N 0.000 description 3
- 238000003860 storage Methods 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- TUNFSRHWOTWDNC-UHFFFAOYSA-N tetradecanoic acid Chemical compound CCCCCCCCCCCCCC(O)=O TUNFSRHWOTWDNC-UHFFFAOYSA-N 0.000 description 3
- CRDAMVZIKSXKFV-YFVJMOTDSA-N (2-trans,6-trans)-farnesol Chemical compound CC(C)=CCC\C(C)=C\CC\C(C)=C\CO CRDAMVZIKSXKFV-YFVJMOTDSA-N 0.000 description 2
- 239000001490 (3R)-3,7-dimethylocta-1,6-dien-3-ol Substances 0.000 description 2
- MEJYDZQQVZJMPP-ULAWRXDQSA-N (3s,3ar,6r,6ar)-3,6-dimethoxy-2,3,3a,5,6,6a-hexahydrofuro[3,2-b]furan Chemical compound CO[C@H]1CO[C@@H]2[C@H](OC)CO[C@@H]21 MEJYDZQQVZJMPP-ULAWRXDQSA-N 0.000 description 2
- QMVPMAAFGQKVCJ-SNVBAGLBSA-N (R)-(+)-citronellol Natural products OCC[C@H](C)CCC=C(C)C QMVPMAAFGQKVCJ-SNVBAGLBSA-N 0.000 description 2
- JHEPBQHNVNUAFL-AATRIKPKSA-N (e)-hex-1-en-1-ol Chemical compound CCCC\C=C\O JHEPBQHNVNUAFL-AATRIKPKSA-N 0.000 description 2
- QLAJNZSPVITUCQ-UHFFFAOYSA-N 1,3,2-dioxathietane 2,2-dioxide Chemical compound O=S1(=O)OCO1 QLAJNZSPVITUCQ-UHFFFAOYSA-N 0.000 description 2
- BBMCTIGTTCKYKF-UHFFFAOYSA-N 1-heptanol Chemical compound CCCCCCCO BBMCTIGTTCKYKF-UHFFFAOYSA-N 0.000 description 2
- AYJXHIDNNLJQDT-UHFFFAOYSA-N 2,6,6-Trimethyl-2-cyclohexene-1,4-dione Chemical compound CC1=CC(=O)CC(C)(C)C1=O AYJXHIDNNLJQDT-UHFFFAOYSA-N 0.000 description 2
- HGDVHRITTGWMJK-UHFFFAOYSA-N 2,6-dimethylheptan-2-ol Chemical compound CC(C)CCCC(C)(C)O HGDVHRITTGWMJK-UHFFFAOYSA-N 0.000 description 2
- GMTKKOJWCRJLFA-UHFFFAOYSA-N 2,6-dimethylheptan-2-yl 4-hydroxydecanoate Chemical compound CCCCCCC(O)CCC(=O)OC(C)(C)CCCC(C)C GMTKKOJWCRJLFA-UHFFFAOYSA-N 0.000 description 2
- DBZAKQWXICEWNW-UHFFFAOYSA-N 2-acetylpyrazine Chemical compound CC(=O)C1=CN=CC=N1 DBZAKQWXICEWNW-UHFFFAOYSA-N 0.000 description 2
- VGECIEOJXLMWGO-UHFFFAOYSA-N 2-hexylcyclopent-2-en-1-one Chemical compound CCCCCCC1=CCCC1=O VGECIEOJXLMWGO-UHFFFAOYSA-N 0.000 description 2
- WRMNZCZEMHIOCP-UHFFFAOYSA-N 2-phenylethanol Chemical compound OCCC1=CC=CC=C1 WRMNZCZEMHIOCP-UHFFFAOYSA-N 0.000 description 2
- RRSAEHIIUDIBBP-UHFFFAOYSA-N 3,7-dimethyloct-6-enyl 4-hydroxydecanoate Chemical compound CCCCCCC(O)CCC(=O)OCCC(C)CCC=C(C)C RRSAEHIIUDIBBP-UHFFFAOYSA-N 0.000 description 2
- MXQLKIWCJNLACB-UHFFFAOYSA-N 3,7-dimethylocta-2,6-dienyl 4-(2-phenylethoxycarbonyloxy)undecanoate Chemical compound CC(C)=CCCC(C)=CCOC(=O)CCC(CCCCCCC)OC(=O)OCCC1=CC=CC=C1 MXQLKIWCJNLACB-UHFFFAOYSA-N 0.000 description 2
- BDSYJWYMYJLOGP-UHFFFAOYSA-N 3,7-dimethylocta-2,6-dienyl 4-hex-3-enoxycarbonyloxyundecanoate Chemical compound CCC=CCCOC(=O)OC(CCCCCCC)CCC(=O)OCC=C(C)CCC=C(C)C BDSYJWYMYJLOGP-UHFFFAOYSA-N 0.000 description 2
- PRNCMAKCNVRZFX-UHFFFAOYSA-N 3,7-dimethyloctan-1-ol Chemical compound CC(C)CCCC(C)CCO PRNCMAKCNVRZFX-UHFFFAOYSA-N 0.000 description 2
- UNSAJINGUOTTRA-UHFFFAOYSA-N 3-(3-bromophenyl)prop-2-yn-1-ol Chemical compound OCC#CC1=CC=CC(Br)=C1 UNSAJINGUOTTRA-UHFFFAOYSA-N 0.000 description 2
- MKZHVQSYPRGNAH-UHFFFAOYSA-N 3-(3-propan-2-ylphenyl)but-1-enyl 4-hydroxyundecanoate Chemical compound CCCCCCCC(O)CCC(=O)OC=CC(C)C1=CC=CC(C(C)C)=C1 MKZHVQSYPRGNAH-UHFFFAOYSA-N 0.000 description 2
- GMFMSOANCBJHLV-UHFFFAOYSA-N 3-(3-propan-2-ylphenyl)but-1-enyl 4-oxoundecanoate Chemical compound CCCCCCCC(=O)CCC(=O)OC=CC(C)C1=CC=CC(C(C)C)=C1 GMFMSOANCBJHLV-UHFFFAOYSA-N 0.000 description 2
- OHRBQTOZYGEWCJ-UHFFFAOYSA-N 3-(3-propan-2-ylphenyl)butanal Chemical compound CC(C)C1=CC=CC(C(C)CC=O)=C1 OHRBQTOZYGEWCJ-UHFFFAOYSA-N 0.000 description 2
- VAJVDSVGBWFCLW-UHFFFAOYSA-N 3-Phenyl-1-propanol Chemical compound OCCCC1=CC=CC=C1 VAJVDSVGBWFCLW-UHFFFAOYSA-N 0.000 description 2
- IWTBVKIGCDZRPL-UHFFFAOYSA-N 3-methylpentanol Chemical compound CCC(C)CCO IWTBVKIGCDZRPL-UHFFFAOYSA-N 0.000 description 2
- OSDLLIBGSJNGJE-UHFFFAOYSA-N 4-chloro-3,5-dimethylphenol Chemical compound CC1=CC(O)=CC(C)=C1Cl OSDLLIBGSJNGJE-UHFFFAOYSA-N 0.000 description 2
- YFXHYHIJRNUIGB-UHFFFAOYSA-N 4-hex-3-enoxy-4-oxobutanoic acid Chemical compound CCC=CCCOC(=O)CCC(O)=O YFXHYHIJRNUIGB-UHFFFAOYSA-N 0.000 description 2
- KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Chemical compound CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 description 2
- 239000005973 Carvone Substances 0.000 description 2
- 229920000858 Cyclodextrin Polymers 0.000 description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- 239000005792 Geraniol Substances 0.000 description 2
- GLZPCOQZEFWAFX-YFHOEESVSA-N Geraniol Natural products CC(C)=CCC\C(C)=C/CO GLZPCOQZEFWAFX-YFHOEESVSA-N 0.000 description 2
- NFLGAXVYCFJBMK-UHFFFAOYSA-N Menthone Chemical compound CC(C)C1CCC(C)CC1=O NFLGAXVYCFJBMK-UHFFFAOYSA-N 0.000 description 2
- OPKOKAMJFNKNAS-UHFFFAOYSA-N N-methylethanolamine Chemical compound CNCCO OPKOKAMJFNKNAS-UHFFFAOYSA-N 0.000 description 2
- IYTXKIXETAELAV-UHFFFAOYSA-N Nonan-3-one Chemical compound CCCCCCC(=O)CC IYTXKIXETAELAV-UHFFFAOYSA-N 0.000 description 2
- YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 description 2
- QMUOCAUEELOMAI-UHFFFAOYSA-N [3-oxo-3-phenylmethoxy-2-(phenylmethoxycarbonylamino)propyl] 4-hydroxyundecanoate Chemical compound C=1C=CC=CC=1COC(=O)C(COC(=O)CCC(O)CCCCCCC)NC(=O)OCC1=CC=CC=C1 QMUOCAUEELOMAI-UHFFFAOYSA-N 0.000 description 2
- 230000002378 acidificating effect Effects 0.000 description 2
- 239000002386 air freshener Substances 0.000 description 2
- 239000004411 aluminium Substances 0.000 description 2
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 2
- 239000004599 antimicrobial Substances 0.000 description 2
- DMSMPAJRVJJAGA-UHFFFAOYSA-N benzo[d]isothiazol-3-one Chemical compound C1=CC=C2C(=O)NSC2=C1 DMSMPAJRVJJAGA-UHFFFAOYSA-N 0.000 description 2
- AKGGYBADQZYZPD-UHFFFAOYSA-N benzylacetone Chemical compound CC(=O)CCC1=CC=CC=C1 AKGGYBADQZYZPD-UHFFFAOYSA-N 0.000 description 2
- JGQFVRIQXUFPAH-UHFFFAOYSA-N beta-citronellol Natural products OCCC(C)CCCC(C)=C JGQFVRIQXUFPAH-UHFFFAOYSA-N 0.000 description 2
- IJOOHPMOJXWVHK-UHFFFAOYSA-N chlorotrimethylsilane Chemical compound C[Si](C)(C)Cl IJOOHPMOJXWVHK-UHFFFAOYSA-N 0.000 description 2
- NEHNMFOYXAPHSD-UHFFFAOYSA-N citronellal Chemical compound O=CCC(C)CCC=C(C)C NEHNMFOYXAPHSD-UHFFFAOYSA-N 0.000 description 2
- 235000000484 citronellol Nutrition 0.000 description 2
- 239000012141 concentrate Substances 0.000 description 2
- WCASXYBKJHWFMY-UHFFFAOYSA-N crotyl alcohol Chemical compound CC=CCO WCASXYBKJHWFMY-UHFFFAOYSA-N 0.000 description 2
- OSOIQJGOYGSIMF-UHFFFAOYSA-N cyclopentadecanone Chemical compound O=C1CCCCCCCCCCCCCC1 OSOIQJGOYGSIMF-UHFFFAOYSA-N 0.000 description 2
- MWKFXSUHUHTGQN-UHFFFAOYSA-N decan-1-ol Chemical compound CCCCCCCCCCO MWKFXSUHUHTGQN-UHFFFAOYSA-N 0.000 description 2
- KSMVZQYAVGTKIV-UHFFFAOYSA-N decanal Chemical compound CCCCCCCCCC=O KSMVZQYAVGTKIV-UHFFFAOYSA-N 0.000 description 2
- 239000008367 deionised water Substances 0.000 description 2
- 229910021641 deionized water Inorganic materials 0.000 description 2
- HFJRKMMYBMWEAD-UHFFFAOYSA-N dodecanal Chemical compound CCCCCCCCCCCC=O HFJRKMMYBMWEAD-UHFFFAOYSA-N 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 150000002085 enols Chemical group 0.000 description 2
- CBOQJANXLMLOSS-UHFFFAOYSA-N ethyl vanillin Chemical compound CCOC1=CC(C=O)=CC=C1O CBOQJANXLMLOSS-UHFFFAOYSA-N 0.000 description 2
- RRAFCDWBNXTKKO-UHFFFAOYSA-N eugenol Chemical compound COC1=CC(CC=C)=CC=C1O RRAFCDWBNXTKKO-UHFFFAOYSA-N 0.000 description 2
- 230000001815 facial effect Effects 0.000 description 2
- 150000002191 fatty alcohols Chemical class 0.000 description 2
- 239000010408 film Substances 0.000 description 2
- 239000000706 filtrate Substances 0.000 description 2
- 239000012467 final product Substances 0.000 description 2
- PHXATPHONSXBIL-JTQLQIEISA-N gamma-Undecalactone Natural products CCCCCCC[C@H]1CCC(=O)O1 PHXATPHONSXBIL-JTQLQIEISA-N 0.000 description 2
- 229940020436 gamma-undecalactone Drugs 0.000 description 2
- 229940113087 geraniol Drugs 0.000 description 2
- KWLMIXQRALPRBC-UHFFFAOYSA-L hectorite Chemical compound [Li+].[OH-].[OH-].[Na+].[Mg+2].O1[Si]2([O-])O[Si]1([O-])O[Si]([O-])(O1)O[Si]1([O-])O2 KWLMIXQRALPRBC-UHFFFAOYSA-L 0.000 description 2
- 229910000271 hectorite Inorganic materials 0.000 description 2
- CATSNJVOTSVZJV-UHFFFAOYSA-N heptan-2-one Chemical compound CCCCCC(C)=O CATSNJVOTSVZJV-UHFFFAOYSA-N 0.000 description 2
- QCKBSOUVQDCAJW-UHFFFAOYSA-N hex-3-enyl 4-(2-phenylethoxycarbonyloxy)decanoate Chemical compound CCC=CCCOC(=O)CCC(CCCCCC)OC(=O)OCCC1=CC=CC=C1 QCKBSOUVQDCAJW-UHFFFAOYSA-N 0.000 description 2
- OIZBXHBSGZMPCU-UHFFFAOYSA-N hex-3-enyl 4-hydroxyundecanoate Chemical compound CCCCCCCC(O)CCC(=O)OCCC=CCC OIZBXHBSGZMPCU-UHFFFAOYSA-N 0.000 description 2
- BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 2
- ZSIAUFGUXNUGDI-UHFFFAOYSA-N hexan-1-ol Chemical compound CCCCCCO ZSIAUFGUXNUGDI-UHFFFAOYSA-N 0.000 description 2
- WPFVBOQKRVRMJB-UHFFFAOYSA-N hydroxycitronellal Chemical compound O=CCC(C)CCCC(C)(C)O WPFVBOQKRVRMJB-UHFFFAOYSA-N 0.000 description 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- ZWRUINPWMLAQRD-UHFFFAOYSA-N nonan-1-ol Chemical compound CCCCCCCCCO ZWRUINPWMLAQRD-UHFFFAOYSA-N 0.000 description 2
- VKCYHJWLYTUGCC-UHFFFAOYSA-N nonan-2-one Chemical compound CCCCCCCC(C)=O VKCYHJWLYTUGCC-UHFFFAOYSA-N 0.000 description 2
- GYHFUZHODSMOHU-UHFFFAOYSA-N nonanal Chemical compound CCCCCCCCC=O GYHFUZHODSMOHU-UHFFFAOYSA-N 0.000 description 2
- BOPPSUHPZARXTH-UHFFFAOYSA-N ocean propanal Chemical compound O=CC(C)CC1=CC=C2OCOC2=C1 BOPPSUHPZARXTH-UHFFFAOYSA-N 0.000 description 2
- GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 2
- CTSLXHKWHWQRSH-UHFFFAOYSA-N oxalyl chloride Chemical compound ClC(=O)C(Cl)=O CTSLXHKWHWQRSH-UHFFFAOYSA-N 0.000 description 2
- QJJDNZGPQDGNDX-UHFFFAOYSA-N oxidized Latia luciferin Chemical compound CC(=O)CCC1=C(C)CCCC1(C)C QJJDNZGPQDGNDX-UHFFFAOYSA-N 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- ASUAYTHWZCLXAN-UHFFFAOYSA-N prenol Chemical compound CC(C)=CCO ASUAYTHWZCLXAN-UHFFFAOYSA-N 0.000 description 2
- 125000006239 protecting group Chemical group 0.000 description 2
- 150000003254 radicals Chemical class 0.000 description 2
- 210000000697 sensory organ Anatomy 0.000 description 2
- 244000005714 skin microbiome Species 0.000 description 2
- RYYKJJJTJZKILX-UHFFFAOYSA-M sodium octadecanoate Chemical compound [Na+].CCCCCCCCCCCCCCCCCC([O-])=O RYYKJJJTJZKILX-UHFFFAOYSA-M 0.000 description 2
- VQTLGLGPQXZERV-UHFFFAOYSA-M sodium;4-hydroxyundecanoate Chemical compound [Na+].CCCCCCCC(O)CCC([O-])=O VQTLGLGPQXZERV-UHFFFAOYSA-M 0.000 description 2
- KDYFGRWQOYBRFD-UHFFFAOYSA-L succinate(2-) Chemical compound [O-]C(=O)CCC([O-])=O KDYFGRWQOYBRFD-UHFFFAOYSA-L 0.000 description 2
- UHEPJGULSIKKTP-UHFFFAOYSA-N sulcatone Chemical compound CC(C)=CCCC(C)=O UHEPJGULSIKKTP-UHFFFAOYSA-N 0.000 description 2
- 238000013268 sustained release Methods 0.000 description 2
- 239000012730 sustained-release form Substances 0.000 description 2
- 239000003760 tallow Substances 0.000 description 2
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 2
- FPGGTKZVZWFYPV-UHFFFAOYSA-M tetrabutylammonium fluoride Chemical compound [F-].CCCC[N+](CCCC)(CCCC)CCCC FPGGTKZVZWFYPV-UHFFFAOYSA-M 0.000 description 2
- HLZKNKRTKFSKGZ-UHFFFAOYSA-N tetradecan-1-ol Chemical compound CCCCCCCCCCCCCCO HLZKNKRTKFSKGZ-UHFFFAOYSA-N 0.000 description 2
- MGSRCZKZVOBKFT-UHFFFAOYSA-N thymol Chemical compound CC(C)C1=CC=C(C)C=C1O MGSRCZKZVOBKFT-UHFFFAOYSA-N 0.000 description 2
- CRDAMVZIKSXKFV-UHFFFAOYSA-N trans-Farnesol Natural products CC(C)=CCCC(C)=CCCC(C)=CCO CRDAMVZIKSXKFV-UHFFFAOYSA-N 0.000 description 2
- RUVINXPYWBROJD-ONEGZZNKSA-N trans-anethole Chemical compound COC1=CC=C(\C=C\C)C=C1 RUVINXPYWBROJD-ONEGZZNKSA-N 0.000 description 2
- KMPQYAYAQWNLME-UHFFFAOYSA-N undecanal Chemical compound CCCCCCCCCCC=O KMPQYAYAQWNLME-UHFFFAOYSA-N 0.000 description 2
- KJIOQYGWTQBHNH-UHFFFAOYSA-N undecanol Chemical compound CCCCCCCCCCCO KJIOQYGWTQBHNH-UHFFFAOYSA-N 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- NOOLISFMXDJSKH-UTLUCORTSA-N (+)-Neomenthol Chemical compound CC(C)[C@@H]1CC[C@@H](C)C[C@@H]1O NOOLISFMXDJSKH-UTLUCORTSA-N 0.000 description 1
- DTGKSKDOIYIVQL-WEDXCCLWSA-N (+)-borneol Chemical compound C1C[C@@]2(C)[C@@H](O)C[C@@H]1C2(C)C DTGKSKDOIYIVQL-WEDXCCLWSA-N 0.000 description 1
- REPVLJRCJUVQFA-UHFFFAOYSA-N (-)-isopinocampheol Natural products C1C(O)C(C)C2C(C)(C)C1C2 REPVLJRCJUVQFA-UHFFFAOYSA-N 0.000 description 1
- DVSUACUEHYSEMY-UHFFFAOYSA-N (1-hex-3-enoxy-1-oxodecan-4-yl) tetradecanoate Chemical compound CCCCCCCCCCCCCC(=O)OC(CCCCCC)CCC(=O)OCCC=CCC DVSUACUEHYSEMY-UHFFFAOYSA-N 0.000 description 1
- FMZUHGYZWYNSOA-VVBFYGJXSA-N (1r)-1-[(4r,4ar,8as)-2,6-diphenyl-4,4a,8,8a-tetrahydro-[1,3]dioxino[5,4-d][1,3]dioxin-4-yl]ethane-1,2-diol Chemical compound C([C@@H]1OC(O[C@@H]([C@@H]1O1)[C@H](O)CO)C=2C=CC=CC=2)OC1C1=CC=CC=C1 FMZUHGYZWYNSOA-VVBFYGJXSA-N 0.000 description 1
- MBDOYVRWFFCFHM-SNAWJCMRSA-N (2E)-hexenal Chemical compound CCC\C=C\C=O MBDOYVRWFFCFHM-SNAWJCMRSA-N 0.000 description 1
- 239000000260 (2E,6E)-3,7,11-trimethyldodeca-2,6,10-trien-1-ol Substances 0.000 description 1
- 239000001304 (2R)-2,6-dimethylhept-5-enal Substances 0.000 description 1
- WBNJCBPWAMSDMR-YFVJMOTDSA-N (2e,6e)-3,7,11-trimethyldodeca-2,6-dienal Chemical compound CC(C)CCC\C(C)=C\CC\C(C)=C\C=O WBNJCBPWAMSDMR-YFVJMOTDSA-N 0.000 description 1
- UPMAOXLCTXPPAG-BBBLOLIVSA-N (2s,4ar,8ar)-1,2,3,4,4a,5,6,7,8,8a-decahydronaphthalen-2-ol Chemical compound C1CCC[C@@H]2C[C@@H](O)CC[C@H]21 UPMAOXLCTXPPAG-BBBLOLIVSA-N 0.000 description 1
- 239000001618 (3R)-3-methylpentan-1-ol Substances 0.000 description 1
- CIXAYNMKFFQEFU-UHFFFAOYSA-N (4-Methylphenyl)acetaldehyde Chemical compound CC1=CC=C(CC=O)C=C1 CIXAYNMKFFQEFU-UHFFFAOYSA-N 0.000 description 1
- MSBGPEACXKBQSX-UHFFFAOYSA-N (4-fluorophenyl) carbonochloridate Chemical compound FC1=CC=C(OC(Cl)=O)C=C1 MSBGPEACXKBQSX-UHFFFAOYSA-N 0.000 description 1
- KFGBSCFOJPHENY-OWOJBTEDSA-N (9e)-1-oxacycloheptadec-9-en-2-one Chemical compound O=C1CCCCCC\C=C\CCCCCCCO1 KFGBSCFOJPHENY-OWOJBTEDSA-N 0.000 description 1
- 239000001178 (E)-dec-3-en-2-one Substances 0.000 description 1
- SSNZFFBDIMUILS-ZHACJKMWSA-N (E)-dodec-2-enal Chemical compound CCCCCCCCC\C=C\C=O SSNZFFBDIMUILS-ZHACJKMWSA-N 0.000 description 1
- 239000001179 (E)-hex-2-enal Substances 0.000 description 1
- CDOSHBSSFJOMGT-JTQLQIEISA-N (R)-linalool Natural products CC(C)=CCC[C@@](C)(O)C=C CDOSHBSSFJOMGT-JTQLQIEISA-N 0.000 description 1
- IXIYWQIFBRZMNR-CMDGGOBGSA-N (e)-3,4,5,6,6-pentamethylhept-3-en-2-one Chemical group CC(C)(C)C(C)\C(C)=C(/C)C(C)=O IXIYWQIFBRZMNR-CMDGGOBGSA-N 0.000 description 1
- VTIODUHBZHNXFP-IHWYPQMZSA-N (e)-4-hexen-1-ol Chemical compound C\C=C/CCCO VTIODUHBZHNXFP-IHWYPQMZSA-N 0.000 description 1
- JRPDANVNRUIUAB-CMDGGOBGSA-N (e)-dec-3-en-2-one Chemical compound CCCCCC\C=C\C(C)=O JRPDANVNRUIUAB-CMDGGOBGSA-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
- 150000000185 1,3-diols Chemical class 0.000 description 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 description 1
- NELDPSDYTZADSA-UHFFFAOYSA-N 1-(2,4,4-trimethylcyclohex-2-en-1-yl)but-2-en-1-one Chemical compound CC=CC(=O)C1CCC(C)(C)C=C1C NELDPSDYTZADSA-UHFFFAOYSA-N 0.000 description 1
- GQBVHGLNSHPKPG-UHFFFAOYSA-N 1-(2-tert-butylcyclohexyl)oxybutan-2-ol Chemical compound CCC(O)COC1CCCCC1C(C)(C)C GQBVHGLNSHPKPG-UHFFFAOYSA-N 0.000 description 1
- JIYZCVGAWRMUDR-UHFFFAOYSA-N 1-(3,3-dimethylcyclohexen-1-yl)ethanone Chemical compound CC(=O)C1=CC(C)(C)CCC1 JIYZCVGAWRMUDR-UHFFFAOYSA-N 0.000 description 1
- YPDFQGCFDQLIFL-UHFFFAOYSA-N 1-(4,4,5,5-tetramethylcyclopenten-1-yl)propan-1-one Chemical compound CCC(=O)C1=CCC(C)(C)C1(C)C YPDFQGCFDQLIFL-UHFFFAOYSA-N 0.000 description 1
- NEHPIUGJDUWSRR-UHFFFAOYSA-N 1-(4-propan-2-ylcyclohexyl)ethanol Chemical compound CC(C)C1CCC(C(C)O)CC1 NEHPIUGJDUWSRR-UHFFFAOYSA-N 0.000 description 1
- KBPLFHHGFOOTCA-UHFFFAOYSA-N 1-Octanol Chemical compound CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 description 1
- GYSCBCSGKXNZRH-UHFFFAOYSA-N 1-benzothiophene-2-carboxamide Chemical compound C1=CC=C2SC(C(=O)N)=CC2=C1 GYSCBCSGKXNZRH-UHFFFAOYSA-N 0.000 description 1
- RMSGQZDGSZOJMU-UHFFFAOYSA-N 1-butyl-2-phenylbenzene Chemical group CCCCC1=CC=CC=C1C1=CC=CC=C1 RMSGQZDGSZOJMU-UHFFFAOYSA-N 0.000 description 1
- WLAUCMCTKPXDIY-UHFFFAOYSA-N 1-chloro-3,7-dimethylocta-2,6-diene Chemical compound CC(C)=CCCC(C)=CCCl WLAUCMCTKPXDIY-UHFFFAOYSA-N 0.000 description 1
- HANWHVWXFQSQGJ-UHFFFAOYSA-N 1-tetradecoxytetradecane Chemical compound CCCCCCCCCCCCCCOCCCCCCCCCCCCCC HANWHVWXFQSQGJ-UHFFFAOYSA-N 0.000 description 1
- OFHHDSQXFXLTKC-UHFFFAOYSA-N 10-undecenal Chemical compound C=CCCCCCCCCC=O OFHHDSQXFXLTKC-UHFFFAOYSA-N 0.000 description 1
- COJYJCJUBHUSDJ-UHFFFAOYSA-N 2,3,5,5-tetramethylhexanal Chemical compound CC(C)(C)CC(C)C(C)C=O COJYJCJUBHUSDJ-UHFFFAOYSA-N 0.000 description 1
- WCOXQTXVACYMLM-UHFFFAOYSA-N 2,3-bis(12-hydroxyoctadecanoyloxy)propyl 12-hydroxyoctadecanoate Chemical compound CCCCCCC(O)CCCCCCCCCCC(=O)OCC(OC(=O)CCCCCCCCCCC(O)CCCCCC)COC(=O)CCCCCCCCCCC(O)CCCCCC WCOXQTXVACYMLM-UHFFFAOYSA-N 0.000 description 1
- DBHODFSFBXJZNY-UHFFFAOYSA-N 2,4-dichlorobenzyl alcohol Chemical compound OCC1=CC=C(Cl)C=C1Cl DBHODFSFBXJZNY-UHFFFAOYSA-N 0.000 description 1
- JJADZVVRVJVFEQ-UHFFFAOYSA-N 2,6-dimethylheptan-2-yl 4-[1-(2,6-dimethylheptan-2-yloxy)-1-oxodecan-4-yl]oxycarbonyloxyundecanoate Chemical compound CC(C)CCCC(C)(C)OC(=O)CCC(CCCCCCC)OC(=O)OC(CCCCCC)CCC(=O)OC(C)(C)CCCC(C)C JJADZVVRVJVFEQ-UHFFFAOYSA-N 0.000 description 1
- AOVQFTRJKDXUDV-UHFFFAOYSA-N 2,6-dimethyloct-5-enal 2-(4-propan-2-ylphenyl)acetaldehyde Chemical compound CC(C)C1=CC=C(C=C1)CC=O.CC(C=O)CCC=C(CC)C AOVQFTRJKDXUDV-UHFFFAOYSA-N 0.000 description 1
- JVEKVVQIAUWKAP-UHFFFAOYSA-N 2,6-dimethyloct-7-en-2-ol 4-(4-hydroxyphenyl)butan-2-one Chemical compound CC(C)(CCCC(C=C)C)O.OC1=CC=C(C=C1)CCC(C)=O JVEKVVQIAUWKAP-UHFFFAOYSA-N 0.000 description 1
- RUGISKODRCWQNE-UHFFFAOYSA-N 2-(2-methylphenyl)ethanol Chemical compound CC1=CC=CC=C1CCO RUGISKODRCWQNE-UHFFFAOYSA-N 0.000 description 1
- IZQUWQPXCQLTJY-UHFFFAOYSA-N 2-(4-propan-2-ylphenyl)propanal Chemical compound CC(C)C1=CC=C(C(C)C=O)C=C1 IZQUWQPXCQLTJY-UHFFFAOYSA-N 0.000 description 1
- FALRKNHUBBKYCC-UHFFFAOYSA-N 2-(chloromethyl)pyridine-3-carbonitrile Chemical compound ClCC1=NC=CC=C1C#N FALRKNHUBBKYCC-UHFFFAOYSA-N 0.000 description 1
- BSAIUMLZVGUGKX-UHFFFAOYSA-N 2-Nonenal Natural products CCCCCCC=CC=O BSAIUMLZVGUGKX-UHFFFAOYSA-N 0.000 description 1
- RNDNSYIPLPAXAZ-UHFFFAOYSA-N 2-Phenyl-1-propanol Chemical compound OCC(C)C1=CC=CC=C1 RNDNSYIPLPAXAZ-UHFFFAOYSA-N 0.000 description 1
- XSAYZAUNJMRRIR-UHFFFAOYSA-N 2-acetylnaphthalene Chemical compound C1=CC=CC2=CC(C(=O)C)=CC=C21 XSAYZAUNJMRRIR-UHFFFAOYSA-N 0.000 description 1
- PUAQLLVFLMYYJJ-UHFFFAOYSA-N 2-aminopropiophenone Chemical compound CC(N)C(=O)C1=CC=CC=C1 PUAQLLVFLMYYJJ-UHFFFAOYSA-N 0.000 description 1
- OADSZWXMXIWZSQ-UHFFFAOYSA-N 2-bromo-2-nitropropane Chemical compound CC(C)(Br)[N+]([O-])=O OADSZWXMXIWZSQ-UHFFFAOYSA-N 0.000 description 1
- RQXTZKGDMNIWJF-UHFFFAOYSA-N 2-butan-2-ylcyclohexan-1-one Chemical compound CCC(C)C1CCCCC1=O RQXTZKGDMNIWJF-UHFFFAOYSA-N 0.000 description 1
- IRIVQXLOJHCXIE-UHFFFAOYSA-N 2-cyclohexylpropan-1-ol Chemical compound OCC(C)C1CCCCC1 IRIVQXLOJHCXIE-UHFFFAOYSA-N 0.000 description 1
- PJXHBTZLHITWFX-UHFFFAOYSA-N 2-heptylcyclopentan-1-one Chemical compound CCCCCCCC1CCCC1=O PJXHBTZLHITWFX-UHFFFAOYSA-N 0.000 description 1
- RFVNOJDQRGSOEL-UHFFFAOYSA-N 2-hydroxyethyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCCO RFVNOJDQRGSOEL-UHFFFAOYSA-N 0.000 description 1
- WBIDFZWBPVKNPD-UHFFFAOYSA-N 2-methoxy-4-methylphenol;4-methylphenol;2-methyl-5-propan-2-ylphenol Chemical compound CC1=CC=C(O)C=C1.COC1=CC(C)=CC=C1O.CC(C)C1=CC=C(C)C(O)=C1 WBIDFZWBPVKNPD-UHFFFAOYSA-N 0.000 description 1
- SXGYZCMGVZKIPJ-UHFFFAOYSA-N 2-methyl-4-phenylpentan-1-ol Chemical compound OCC(C)CC(C)C1=CC=CC=C1 SXGYZCMGVZKIPJ-UHFFFAOYSA-N 0.000 description 1
- IJLREUXUKNGCEW-UHFFFAOYSA-N 2-methyl-5-phenylpentan-1-ol 4-phenylbutan-2-ol Chemical compound CC(CO)CCCC1=CC=CC=C1.C1(=CC=CC=C1)CCC(C)O IJLREUXUKNGCEW-UHFFFAOYSA-N 0.000 description 1
- LBICMZLDYMBIGA-UHFFFAOYSA-N 2-methyldecanal Chemical compound CCCCCCCCC(C)C=O LBICMZLDYMBIGA-UHFFFAOYSA-N 0.000 description 1
- NFAVNWJJYQAGNB-UHFFFAOYSA-N 2-methylundecanal Chemical compound CCCCCCCCCC(C)C=O NFAVNWJJYQAGNB-UHFFFAOYSA-N 0.000 description 1
- BSAIUMLZVGUGKX-FPLPWBNLSA-N 2-nonenal Chemical compound CCCCCC\C=C/C=O BSAIUMLZVGUGKX-FPLPWBNLSA-N 0.000 description 1
- ZPVFWPFBNIEHGJ-UHFFFAOYSA-N 2-octanone Chemical compound CCCCCCC(C)=O ZPVFWPFBNIEHGJ-UHFFFAOYSA-N 0.000 description 1
- QCDWFXQBSFUVSP-UHFFFAOYSA-N 2-phenoxyethanol Chemical compound OCCOC1=CC=CC=C1 QCDWFXQBSFUVSP-UHFFFAOYSA-N 0.000 description 1
- IQVAERDLDAZARL-UHFFFAOYSA-N 2-phenylpropanal Chemical compound O=CC(C)C1=CC=CC=C1 IQVAERDLDAZARL-UHFFFAOYSA-N 0.000 description 1
- OOPHUQPRWUXYDI-UHFFFAOYSA-N 2-tert-butyl-4-methylcyclohexan-1-ol Chemical compound CC1CCC(O)C(C(C)(C)C)C1 OOPHUQPRWUXYDI-UHFFFAOYSA-N 0.000 description 1
- DLTWBMHADAJAAZ-UHFFFAOYSA-N 2-tert-butylcyclohexan-1-ol Chemical compound CC(C)(C)C1CCCCC1O DLTWBMHADAJAAZ-UHFFFAOYSA-N 0.000 description 1
- VMUNAKQXJLHODT-VAWYXSNFSA-N 2-tridecenal Chemical compound CCCCCCCCCC\C=C\C=O VMUNAKQXJLHODT-VAWYXSNFSA-N 0.000 description 1
- YXRXDZOBKUTUQZ-UHFFFAOYSA-N 3,4-dimethyloct-3-en-2-one Chemical compound CCCCC(C)=C(C)C(C)=O YXRXDZOBKUTUQZ-UHFFFAOYSA-N 0.000 description 1
- VIACWLHBLCGTAY-UHFFFAOYSA-N 3,5,5-trimethylhexanal undec-9-enal Chemical compound C(CCCCCCCC=CC)=O.CC(CC=O)CC(C)(C)C VIACWLHBLCGTAY-UHFFFAOYSA-N 0.000 description 1
- ZXZACZWNOLBMBI-UHFFFAOYSA-N 3,7-dimethyloct-6-enyl 4-(2-phenylethoxycarbonyloxy)decanoate Chemical compound CC(C)=CCCC(C)CCOC(=O)CCC(CCCCCC)OC(=O)OCCC1=CC=CC=C1 ZXZACZWNOLBMBI-UHFFFAOYSA-N 0.000 description 1
- GCCXEHNHZXPSAP-UHFFFAOYSA-N 3,7-dimethyloct-6-enyl 4-oxodecanoate Chemical compound CCCCCCC(=O)CCC(=O)OCCC(C)CCC=C(C)C GCCXEHNHZXPSAP-UHFFFAOYSA-N 0.000 description 1
- DYKOVUKKCCKNPX-UHFFFAOYSA-N 3,7-dimethylocta-1,6-dien-3-yl 4-hydroxydecanoate Chemical compound CCCCCCC(O)CCC(=O)OC(C)(C=C)CCC=C(C)C DYKOVUKKCCKNPX-UHFFFAOYSA-N 0.000 description 1
- OHRHGRQFCQDNKD-UHFFFAOYSA-N 3,7-dimethylocta-1,6-dien-3-yl 4-oxodecanoate Chemical compound CCCCCCC(=O)CCC(=O)OC(C)(C=C)CCC=C(C)C OHRHGRQFCQDNKD-UHFFFAOYSA-N 0.000 description 1
- ICAWXCQTUNYABR-UHFFFAOYSA-N 3,7-dimethylocta-2,6-dienyl decanoate Chemical compound CCCCCCCCCC(=O)OCC=C(C)CCC=C(C)C ICAWXCQTUNYABR-UHFFFAOYSA-N 0.000 description 1
- UCSIFMPORANABL-UHFFFAOYSA-N 3,7-dimethyloctanal Chemical compound CC(C)CCCC(C)CC=O UCSIFMPORANABL-UHFFFAOYSA-N 0.000 description 1
- RBSXKAMXVFPTNM-UHFFFAOYSA-N 3-(3-propan-2-ylphenyl)but-1-enyl acetate Chemical compound CC(C)C1=CC=CC(C(C)C=COC(C)=O)=C1 RBSXKAMXVFPTNM-UHFFFAOYSA-N 0.000 description 1
- FJYWKCJZUPIDQA-UHFFFAOYSA-N 3-(4-tert-butylphenyl)-2-methylpropanal 2-methyl-4-(2,6,6-trimethylcyclohex-2-en-1-yl)butanal Chemical compound O=CC(C)CCC1C(C)=CCCC1(C)C.O=CC(C)CC1=CC=C(C(C)(C)C)C=C1 FJYWKCJZUPIDQA-UHFFFAOYSA-N 0.000 description 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 description 1
- URQMEZRQHLCJKR-UHFFFAOYSA-N 3-Methyl-5-propyl-2-cyclohexen-1-one Chemical compound CCCC1CC(C)=CC(=O)C1 URQMEZRQHLCJKR-UHFFFAOYSA-N 0.000 description 1
- TYEQOKUTSWWBCR-UHFFFAOYSA-N 3-chloro-2-methyl-3-oxopropanoic acid Chemical compound OC(=O)C(C)C(Cl)=O TYEQOKUTSWWBCR-UHFFFAOYSA-N 0.000 description 1
- CLYICGOQOVMKBS-UHFFFAOYSA-N 3-methyl-2-(3-methylbut-2-enyl)cyclopent-2-en-1-one Chemical compound CC(C)=CCC1=C(C)CCC1=O CLYICGOQOVMKBS-UHFFFAOYSA-N 0.000 description 1
- QQUWZMIGSXXJFV-UHFFFAOYSA-N 3-methyl-5-(2,2,3-trimethylcyclopent-3-en-1-yl)pent-3-en-2-one Chemical compound CC(=O)C(C)=CCC1CC=C(C)C1(C)C QQUWZMIGSXXJFV-UHFFFAOYSA-N 0.000 description 1
- NGYMOTOXXHCHOC-UHFFFAOYSA-N 3-methyl-5-(2,2,3-trimethylcyclopent-3-en-1-yl)pentan-2-ol Chemical compound CC(O)C(C)CCC1CC=C(C)C1(C)C NGYMOTOXXHCHOC-UHFFFAOYSA-N 0.000 description 1
- OXYRENDGHPGWKV-UHFFFAOYSA-N 3-methyl-5-phenylpentan-1-ol Chemical compound OCCC(C)CCC1=CC=CC=C1 OXYRENDGHPGWKV-UHFFFAOYSA-N 0.000 description 1
- NPURTPKIWWAXOG-UHFFFAOYSA-N 3-tert-butylcyclohexan-1-ol Chemical compound CC(C)(C)C1CCCC(O)C1 NPURTPKIWWAXOG-UHFFFAOYSA-N 0.000 description 1
- XXBAQTDVRLRXEV-UHFFFAOYSA-N 3-tetradecoxypropan-1-ol Chemical compound CCCCCCCCCCCCCCOCCCO XXBAQTDVRLRXEV-UHFFFAOYSA-N 0.000 description 1
- PWDOJWCZWKWKSE-BQYQJAHWSA-N 4,7-Megastigmadien-9-ol Chemical compound CC(O)\C=C\C1C(C)=CCCC1(C)C PWDOJWCZWKWKSE-BQYQJAHWSA-N 0.000 description 1
- WKQWDIFHKYWRTA-UHFFFAOYSA-N 4,7-dimethyloct-6-en-3-one Chemical compound CCC(=O)C(C)CC=C(C)C WKQWDIFHKYWRTA-UHFFFAOYSA-N 0.000 description 1
- PCFHYANYPQEMPU-UHFFFAOYSA-N 4-(2,2,3-trimethyl-5-bicyclo[2.2.1]heptanyl)cyclohexan-1-ol Chemical compound CC1(C)C(C)C2CC1CC2C1CCC(O)CC1 PCFHYANYPQEMPU-UHFFFAOYSA-N 0.000 description 1
- UZWOWEPOVKVMEL-UHFFFAOYSA-N 4-(2,2,6-trimethylcyclohexyl)butan-2-ol Chemical compound CC(O)CCC1C(C)CCCC1(C)C UZWOWEPOVKVMEL-UHFFFAOYSA-N 0.000 description 1
- DCSKAMGZSIRJAQ-UHFFFAOYSA-N 4-(2-methylbutan-2-yl)cyclohexan-1-one Chemical compound CCC(C)(C)C1CCC(=O)CC1 DCSKAMGZSIRJAQ-UHFFFAOYSA-N 0.000 description 1
- AHDIXUCOAOMZIX-UHFFFAOYSA-N 4-(3,7-dimethyloctoxy)-4-oxobutanoic acid Chemical compound CC(C)CCCC(C)CCOC(=O)CCC(O)=O AHDIXUCOAOMZIX-UHFFFAOYSA-N 0.000 description 1
- MSHFRERJPWKJFX-UHFFFAOYSA-N 4-Methoxybenzyl alcohol Chemical compound COC1=CC=C(CO)C=C1 MSHFRERJPWKJFX-UHFFFAOYSA-N 0.000 description 1
- MMZMROHDQCJAJT-UHFFFAOYSA-N 4-chloro-4-oxobutanoic acid Chemical compound OC(=O)CCC(Cl)=O MMZMROHDQCJAJT-UHFFFAOYSA-N 0.000 description 1
- RSTLRVZJJNSHKQ-UHFFFAOYSA-N 4-hex-3-enoxycarbonyloxyundecanoic acid Chemical compound CCCCCCCC(CCC(O)=O)OC(=O)OCCC=CCC RSTLRVZJJNSHKQ-UHFFFAOYSA-N 0.000 description 1
- NIKDJTTZUYNCMM-SNAWJCMRSA-N 4-hydroxy-4-methyl-7-decenoic acid γ-lactone Chemical compound CC\C=C\CCC1(C)CCC(=O)O1 NIKDJTTZUYNCMM-SNAWJCMRSA-N 0.000 description 1
- NTPLXRHDUXRPNE-UHFFFAOYSA-N 4-methoxyacetophenone Chemical compound COC1=CC=C(C(C)=O)C=C1 NTPLXRHDUXRPNE-UHFFFAOYSA-N 0.000 description 1
- YVSNOTITPICPTB-UHFFFAOYSA-N 4-methyl-2-(2-methylpropyl)oxan-4-ol Chemical compound CC(C)CC1CC(C)(O)CCO1 YVSNOTITPICPTB-UHFFFAOYSA-N 0.000 description 1
- KMTDMTZBNYGUNX-UHFFFAOYSA-N 4-methylbenzyl alcohol Chemical compound CC1=CC=C(CO)C=C1 KMTDMTZBNYGUNX-UHFFFAOYSA-N 0.000 description 1
- WGHFCFPCYURDPA-UHFFFAOYSA-N 4-methyldec-3-en-5-ol nona-2,6-dien-1-ol Chemical compound CC(=CCC)C(CCCCC)O.C(C=CCCC=CCC)O WGHFCFPCYURDPA-UHFFFAOYSA-N 0.000 description 1
- DKKRDMLKVSKFMJ-UHFFFAOYSA-N 4-propan-2-ylcyclohexan-1-ol Chemical compound CC(C)C1CCC(O)CC1 DKKRDMLKVSKFMJ-UHFFFAOYSA-N 0.000 description 1
- RGUKYNXWOWSRET-UHFFFAOYSA-N 4-pyrrolidin-1-ylpyridine Chemical compound C1CCCN1C1=CC=NC=C1 RGUKYNXWOWSRET-UHFFFAOYSA-N 0.000 description 1
- CCOQPGVQAWPUPE-UHFFFAOYSA-N 4-tert-butylcyclohexan-1-ol Chemical compound CC(C)(C)C1CCC(O)CC1 CCOQPGVQAWPUPE-UHFFFAOYSA-N 0.000 description 1
- NCACOBUYDXHHJT-UHFFFAOYSA-N 5-butylidene-2,2,4-trimethylcyclopentan-1-one Chemical compound CCCC=C1C(C)CC(C)(C)C1=O NCACOBUYDXHHJT-UHFFFAOYSA-N 0.000 description 1
- LJUPLVQINLSEHF-UHFFFAOYSA-N 5-butyloxolan-2-one;5-(6-methylhept-5-en-2-yl)oxolan-2-one Chemical compound CCCCC1CCC(=O)O1.CC(C)=CCCC(C)C1CCC(=O)O1 LJUPLVQINLSEHF-UHFFFAOYSA-N 0.000 description 1
- GCMKYGAPKQJXOX-UHFFFAOYSA-N 5-heptyloxolan-2-one;6-methylpyran-2-one Chemical compound CC1=CC=CC(=O)O1.CCCCCCCC1CCC(=O)O1 GCMKYGAPKQJXOX-UHFFFAOYSA-N 0.000 description 1
- NTUYHILVAVUKKB-UHFFFAOYSA-N 5-methyl-2-propylcyclohexan-1-one Chemical compound CCCC1CCC(C)CC1=O NTUYHILVAVUKKB-UHFFFAOYSA-N 0.000 description 1
- JBZCLTCZMKROEI-UHFFFAOYSA-N 5-methyl-2-propylidenecyclohexan-1-one Chemical compound CCC=C1CCC(C)CC1=O JBZCLTCZMKROEI-UHFFFAOYSA-N 0.000 description 1
- OALYTRUKMRCXNH-UHFFFAOYSA-N 5-pentyloxolan-2-one Chemical compound CCCCCC1CCC(=O)O1 OALYTRUKMRCXNH-UHFFFAOYSA-N 0.000 description 1
- HNZUNIKWNYHEJJ-UHFFFAOYSA-N 6,10-dimethylundeca-5,9-dien-2-one Chemical compound CC(C)=CCCC(C)=CCCC(C)=O HNZUNIKWNYHEJJ-UHFFFAOYSA-N 0.000 description 1
- VAWSLJPQBJFZMY-UHFFFAOYSA-N 6,8-dimethylnonan-2-ol;5-ethylnonan-2-ol Chemical compound CCCCC(CC)CCC(C)O.CC(C)CC(C)CCCC(C)O VAWSLJPQBJFZMY-UHFFFAOYSA-N 0.000 description 1
- XPPALVZZCMPTIV-ONEGZZNKSA-N 6-[(z)-pent-2-enyl]oxan-2-one Chemical compound CC\C=C\CC1CCCC(=O)O1 XPPALVZZCMPTIV-ONEGZZNKSA-N 0.000 description 1
- XSFCJNDQFKISFC-UHFFFAOYSA-N 6-ethyl-3-methyloct-5-en-1-ol Chemical compound CCC(CC)=CCC(C)CCO XSFCJNDQFKISFC-UHFFFAOYSA-N 0.000 description 1
- FXEKWZPKHGOHHH-UHFFFAOYSA-N 6-heptyloxan-2-one;6-hexyloxan-2-one Chemical compound CCCCCCC1CCCC(=O)O1.CCCCCCCC1CCCC(=O)O1 FXEKWZPKHGOHHH-UHFFFAOYSA-N 0.000 description 1
- ZJVRYPHKSDHLTC-UHFFFAOYSA-N 7-methoxy-3,7-dimethyloctan-2-ol Chemical compound COC(C)(C)CCCC(C)C(C)O ZJVRYPHKSDHLTC-UHFFFAOYSA-N 0.000 description 1
- HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 description 1
- QGFSQVPRCWJZQK-UHFFFAOYSA-N 9-Decen-1-ol Chemical compound OCCCCCCCCC=C QGFSQVPRCWJZQK-UHFFFAOYSA-N 0.000 description 1
- 241000894006 Bacteria Species 0.000 description 1
- FRPHFZCDPYBUAU-UHFFFAOYSA-N Bromocresolgreen Chemical compound CC1=C(Br)C(O)=C(Br)C=C1C1(C=2C(=C(Br)C(O)=C(Br)C=2)C)C2=CC=CC=C2S(=O)(=O)O1 FRPHFZCDPYBUAU-UHFFFAOYSA-N 0.000 description 1
- FIPWRIJSWJWJAI-UHFFFAOYSA-N Butyl carbitol 6-propylpiperonyl ether Chemical compound C1=C(CCC)C(COCCOCCOCCCC)=CC2=C1OCO2 FIPWRIJSWJWJAI-UHFFFAOYSA-N 0.000 description 1
- UKHZKPVDCATILG-UHFFFAOYSA-N C(C=CCCCCCCC)=O.CC(C=O)=CC(CC=C)C Chemical compound C(C=CCCCCCCC)=O.CC(C=O)=CC(CC=C)C UKHZKPVDCATILG-UHFFFAOYSA-N 0.000 description 1
- GOGRGBJFRWDGJW-UHFFFAOYSA-N C(CCCCCCC)=O.C(CCCCCCCCCCCC)=O Chemical compound C(CCCCCCC)=O.C(CCCCCCCCCCCC)=O GOGRGBJFRWDGJW-UHFFFAOYSA-N 0.000 description 1
- JMRNKBWTZQYAHP-UHFFFAOYSA-N C1(=CC=CC=C1)C(C)O.C(CCCCCCCCC=C)O.CC(CO)CCCCCCCCC Chemical compound C1(=CC=CC=C1)C(C)O.C(CCCCCCCCC=C)O.CC(CO)CCCCCCCCC JMRNKBWTZQYAHP-UHFFFAOYSA-N 0.000 description 1
- VNMHMJMPRYMMCV-UHFFFAOYSA-N C=1C=CC=CC=1COC(=O)C(COC(=O)CCC(CCCCCCC)OC(=O)CCCCCCCCCCC)NC(=O)OCC1=CC=CC=C1 Chemical compound C=1C=CC=CC=1COC(=O)C(COC(=O)CCC(CCCCCCC)OC(=O)CCCCCCCCCCC)NC(=O)OCC1=CC=CC=C1 VNMHMJMPRYMMCV-UHFFFAOYSA-N 0.000 description 1
- FRVINLMUYDLZTG-UHFFFAOYSA-N CC(C(C)O)C(C(C(C)(C)C)C)C.CC(CCO)CC(C)(C)C Chemical compound CC(C(C)O)C(C(C(C)(C)C)C)C.CC(CCO)CC(C)(C)C FRVINLMUYDLZTG-UHFFFAOYSA-N 0.000 description 1
- AOOPOXRUQATNRN-UHFFFAOYSA-N CC(C)=CCCC(C)(C=C)OC(=O)CCC(CCCCCC)OC(=O)CCC(=O)OCCC=CCC Chemical class CC(C)=CCCC(C)(C=C)OC(=O)CCC(CCCCCC)OC(=O)CCC(=O)OCCC=CCC AOOPOXRUQATNRN-UHFFFAOYSA-N 0.000 description 1
- JLQAJTYNGUTPPV-UHFFFAOYSA-N CC(CC)(C)C(CCCC1C(CCCC1)=O)C.CC1CC(CCCCCCCCCCCC1)=O Chemical compound CC(CC)(C)C(CCCC1C(CCCC1)=O)C.CC1CC(CCCCCCCCCCCC1)=O JLQAJTYNGUTPPV-UHFFFAOYSA-N 0.000 description 1
- ODAXIMXRLFRFIF-UHFFFAOYSA-N CC1=C(C(CC1)=O)CCCCC.C(CCCC)C=1C(CCC1)=O Chemical compound CC1=C(C(CC1)=O)CCCCC.C(CCCC)C=1C(CCC1)=O ODAXIMXRLFRFIF-UHFFFAOYSA-N 0.000 description 1
- PNSSYLXALNTKCD-UHFFFAOYSA-N CC1C(C(CC(=C1)C)C)CO.CC1(CC(CC(C1)C)O)C Chemical compound CC1C(C(CC(=C1)C)C)CO.CC1(CC(CC(C1)C)O)C PNSSYLXALNTKCD-UHFFFAOYSA-N 0.000 description 1
- WJWBFFMKXLRFNP-UHFFFAOYSA-N CCCCCCCCCCCC(=O)OC(CCCCCC)CCC(=O)OCCC(C)CCC=C(C)C Chemical compound CCCCCCCCCCCC(=O)OC(CCCCCC)CCC(=O)OCCC(C)CCC=C(C)C WJWBFFMKXLRFNP-UHFFFAOYSA-N 0.000 description 1
- KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- NPBVQXIMTZKSBA-UHFFFAOYSA-N Chavibetol Natural products COC1=CC=C(CC=C)C=C1O NPBVQXIMTZKSBA-UHFFFAOYSA-N 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- FKUPPRZPSYCDRS-UHFFFAOYSA-N Cyclopentadecanolide Chemical compound O=C1CCCCCCCCCCCCCCO1 FKUPPRZPSYCDRS-UHFFFAOYSA-N 0.000 description 1
- NOOLISFMXDJSKH-UHFFFAOYSA-N DL-menthol Natural products CC(C)C1CCC(C)CC1O NOOLISFMXDJSKH-UHFFFAOYSA-N 0.000 description 1
- XMSXQFUHVRWGNA-UHFFFAOYSA-N Decamethylcyclopentasiloxane Chemical compound C[Si]1(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O[Si](C)(C)O1 XMSXQFUHVRWGNA-UHFFFAOYSA-N 0.000 description 1
- GHVNFZFCNZKVNT-UHFFFAOYSA-N Decanoic acid Natural products CCCCCCCCCC(O)=O GHVNFZFCNZKVNT-UHFFFAOYSA-N 0.000 description 1
- 239000005770 Eugenol Substances 0.000 description 1
- OWYWGLHRNBIFJP-UHFFFAOYSA-N Ipazine Chemical compound CCN(CC)C1=NC(Cl)=NC(NC(C)C)=N1 OWYWGLHRNBIFJP-UHFFFAOYSA-N 0.000 description 1
- BJIOGJUNALELMI-ONEGZZNKSA-N Isoeugenol Natural products COC1=CC(\C=C\C)=CC=C1O BJIOGJUNALELMI-ONEGZZNKSA-N 0.000 description 1
- AMQJEAYHLZJPGS-UHFFFAOYSA-N N-Pentanol Chemical compound CCCCCO AMQJEAYHLZJPGS-UHFFFAOYSA-N 0.000 description 1
- BJEMGNVSOLCWEA-UHFFFAOYSA-N OC1=CC=C(C=C1)CCC(C)=O.CC(C)C1=CC=C(C=C1)CO Chemical compound OC1=CC=C(C=C1)CCC(C)=O.CC(C)C1=CC=C(C=C1)CO BJEMGNVSOLCWEA-UHFFFAOYSA-N 0.000 description 1
- 102000035195 Peptidases Human genes 0.000 description 1
- 108091005804 Peptidases Proteins 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 239000004365 Protease Substances 0.000 description 1
- UVMRYBDEERADNV-UHFFFAOYSA-N Pseudoeugenol Natural products COC1=CC(C(C)=C)=CC=C1O UVMRYBDEERADNV-UHFFFAOYSA-N 0.000 description 1
- 239000005844 Thymol Substances 0.000 description 1
- 229920004892 Triton X-102 Polymers 0.000 description 1
- 235000018936 Vitellaria paradoxa Nutrition 0.000 description 1
- 241001135917 Vitellaria paradoxa Species 0.000 description 1
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 description 1
- LMETVDMCIJNNKH-UHFFFAOYSA-N [(3,7-Dimethyl-6-octenyl)oxy]acetaldehyde Chemical compound CC(C)=CCCC(C)CCOCC=O LMETVDMCIJNNKH-UHFFFAOYSA-N 0.000 description 1
- JSGAUBMCJQYLTN-UHFFFAOYSA-N [1-(3,7-dimethylocta-2,6-dienoxy)-1-oxoundecan-4-yl] tetradecanoate Chemical compound CCCCCCCCCCCCCC(=O)OC(CCCCCCC)CCC(=O)OCC=C(C)CCC=C(C)C JSGAUBMCJQYLTN-UHFFFAOYSA-N 0.000 description 1
- FIHYYOWBLXKUCW-UHFFFAOYSA-N [3-oxo-3-phenylmethoxy-2-(phenylmethoxycarbonylamino)propyl] 4-oxoundecanoate Chemical compound C=1C=CC=CC=1COC(=O)C(COC(=O)CCC(=O)CCCCCCC)NC(=O)OCC1=CC=CC=C1 FIHYYOWBLXKUCW-UHFFFAOYSA-N 0.000 description 1
- ZGUQGPFMMTZGBQ-UHFFFAOYSA-N [Al].[Al].[Zr] Chemical compound [Al].[Al].[Zr] ZGUQGPFMMTZGBQ-UHFFFAOYSA-N 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000000443 aerosol Substances 0.000 description 1
- PWDOJWCZWKWKSE-UHFFFAOYSA-N alpha-Ionol Natural products CC(O)C=CC1C(C)=CCCC1(C)C PWDOJWCZWKWKSE-UHFFFAOYSA-N 0.000 description 1
- DNXNYEBMOSARMM-UHFFFAOYSA-N alumane;zirconium Chemical compound [AlH3].[Zr] DNXNYEBMOSARMM-UHFFFAOYSA-N 0.000 description 1
- HAMGNFFXQJOFRZ-UHFFFAOYSA-L aluminum;zirconium(4+);chloride;hydroxide;hydrate Chemical compound O.[OH-].[Al+3].[Cl-].[Zr+4] HAMGNFFXQJOFRZ-UHFFFAOYSA-L 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 229940011037 anethole Drugs 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 239000008346 aqueous phase Substances 0.000 description 1
- 235000019568 aromas Nutrition 0.000 description 1
- 150000003934 aromatic aldehydes Chemical class 0.000 description 1
- 230000001580 bacterial effect Effects 0.000 description 1
- PASDCCFISLVPSO-UHFFFAOYSA-N benzoyl chloride Chemical compound ClC(=O)C1=CC=CC=C1 PASDCCFISLVPSO-UHFFFAOYSA-N 0.000 description 1
- MHHDPGHZHFJLBZ-UHFFFAOYSA-N benzyl 3-hydroxy-2-(phenylmethoxycarbonylamino)propanoate Chemical compound C=1C=CC=CC=1COC(=O)C(CO)NC(=O)OCC1=CC=CC=C1 MHHDPGHZHFJLBZ-UHFFFAOYSA-N 0.000 description 1
- 235000019445 benzyl alcohol Nutrition 0.000 description 1
- 229960004217 benzyl alcohol Drugs 0.000 description 1
- WMWLMWRWZQELOS-UHFFFAOYSA-N bismuth(III) oxide Inorganic materials O=[Bi]O[Bi]=O WMWLMWRWZQELOS-UHFFFAOYSA-N 0.000 description 1
- 229940116229 borneol Drugs 0.000 description 1
- CKDOCTFBFTVPSN-UHFFFAOYSA-N borneol Natural products C1CC2(C)C(C)CC1C2(C)C CKDOCTFBFTVPSN-UHFFFAOYSA-N 0.000 description 1
- FZJUFJKVIYFBSY-UHFFFAOYSA-N bourgeonal Chemical compound CC(C)(C)C1=CC=C(CCC=O)C=C1 FZJUFJKVIYFBSY-UHFFFAOYSA-N 0.000 description 1
- 239000000872 buffer Substances 0.000 description 1
- IRXBNHGNHKNOJI-UHFFFAOYSA-N butanedioyl dichloride Chemical compound ClC(=O)CCC(Cl)=O IRXBNHGNHKNOJI-UHFFFAOYSA-N 0.000 description 1
- 150000004657 carbamic acid derivatives Chemical class 0.000 description 1
- 125000005587 carbonate group Chemical group 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- DJYWGTBEZVORGE-CVWWDKSYSA-N cedr-8(15)-en-9-ol Chemical compound C1[C@]23[C@H](C)CC[C@H]3C(C)(C)[C@@H]1C(=C)C(O)C2 DJYWGTBEZVORGE-CVWWDKSYSA-N 0.000 description 1
- 229960000541 cetyl alcohol Drugs 0.000 description 1
- 229940015303 cetyl glycol Drugs 0.000 description 1
- FZFAMSAMCHXGEF-UHFFFAOYSA-N chloro formate Chemical compound ClOC=O FZFAMSAMCHXGEF-UHFFFAOYSA-N 0.000 description 1
- BJIOGJUNALELMI-ARJAWSKDSA-N cis-isoeugenol Chemical compound COC1=CC(\C=C/C)=CC=C1O BJIOGJUNALELMI-ARJAWSKDSA-N 0.000 description 1
- WTEVQBCEXWBHNA-UHFFFAOYSA-N citral Chemical compound CC(C)=CCCC(C)=CC=O WTEVQBCEXWBHNA-UHFFFAOYSA-N 0.000 description 1
- 229930003633 citronellal Natural products 0.000 description 1
- 235000000983 citronellal Nutrition 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 210000001072 colon Anatomy 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 239000002537 cosmetic Substances 0.000 description 1
- 239000006071 cream Substances 0.000 description 1
- 229940097362 cyclodextrins Drugs 0.000 description 1
- HGCIXCUEYOPUTN-UHFFFAOYSA-N cyclohexene Chemical compound C1CCC=CC1 HGCIXCUEYOPUTN-UHFFFAOYSA-N 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 229940087101 dibenzylidene sorbitol Drugs 0.000 description 1
- 229960004698 dichlorobenzyl alcohol Drugs 0.000 description 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 description 1
- DTGKSKDOIYIVQL-UHFFFAOYSA-N dl-isoborneol Natural products C1CC2(C)C(O)CC1C2(C)C DTGKSKDOIYIVQL-UHFFFAOYSA-N 0.000 description 1
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 1
- JRBPAEWTRLWTQC-UHFFFAOYSA-N dodecylamine Chemical compound CCCCCCCCCCCCN JRBPAEWTRLWTQC-UHFFFAOYSA-N 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- CHDFNIZLAAFFPX-UHFFFAOYSA-N ethoxyethane;oxolane Chemical compound CCOCC.C1CCOC1 CHDFNIZLAAFFPX-UHFFFAOYSA-N 0.000 description 1
- RIFGWPKJUGCATF-UHFFFAOYSA-N ethyl chloroformate Chemical compound CCOC(Cl)=O RIFGWPKJUGCATF-UHFFFAOYSA-N 0.000 description 1
- 229940073505 ethyl vanillin Drugs 0.000 description 1
- 229960002217 eugenol Drugs 0.000 description 1
- 229940043259 farnesol Drugs 0.000 description 1
- 229930002886 farnesol Natural products 0.000 description 1
- ARJWAURHQDJJAC-GQCTYLIASA-N filbertone Chemical compound CCC(C)C(=O)\C=C\C ARJWAURHQDJJAC-GQCTYLIASA-N 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- WGPCZPLRVAWXPW-LLVKDONJSA-N gamma-Dodecalactone Natural products CCCCCCCC[C@@H]1CCC(=O)O1 WGPCZPLRVAWXPW-LLVKDONJSA-N 0.000 description 1
- 239000001963 growth medium Substances 0.000 description 1
- 238000003988 headspace gas chromatography Methods 0.000 description 1
- UXVAFPVMOZHZEH-UHFFFAOYSA-N heptanal;3,5,5-trimethylhexanal Chemical compound CCCCCCC=O.O=CCC(C)CC(C)(C)C UXVAFPVMOZHZEH-UHFFFAOYSA-N 0.000 description 1
- NDFKTBCGKNOHPJ-UHFFFAOYSA-N hex-2-enal Natural products CCCCC=CC=O NDFKTBCGKNOHPJ-UHFFFAOYSA-N 0.000 description 1
- GCGNOUIBENITEQ-UHFFFAOYSA-N hex-3-enyl 4-(didecylcarbamoyloxy)undecanoate Chemical compound CCCCCCCCCCN(CCCCCCCCCC)C(=O)OC(CCCCCCC)CCC(=O)OCCC=CCC GCGNOUIBENITEQ-UHFFFAOYSA-N 0.000 description 1
- DFLYYIGQFUGKOM-UHFFFAOYSA-N hex-3-enyl 4-[3-[2-[tert-butyl(dimethyl)silyl]oxyphenyl]prop-2-enoyloxy]nonanoate Chemical compound CCC=CCCOC(=O)CCC(CCCCC)OC(=O)C=CC1=CC=CC=C1O[Si](C)(C)C(C)(C)C DFLYYIGQFUGKOM-UHFFFAOYSA-N 0.000 description 1
- RXRRUZYOMGDHLZ-UHFFFAOYSA-N hex-3-enyl carbonochloridate Chemical compound CCC=CCCOC(Cl)=O RXRRUZYOMGDHLZ-UHFFFAOYSA-N 0.000 description 1
- QNVRIHYSUZMSGM-UHFFFAOYSA-N hexan-2-ol Chemical compound CCCCC(C)O QNVRIHYSUZMSGM-UHFFFAOYSA-N 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 238000011534 incubation Methods 0.000 description 1
- DTHIOPUFUOMHAY-UHFFFAOYSA-N isogeraniol Chemical compound CC(C)=CCC=C(C)CCO DTHIOPUFUOMHAY-UHFFFAOYSA-N 0.000 description 1
- 229930007744 linalool Natural products 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 239000002932 luster Substances 0.000 description 1
- 229940041616 menthol Drugs 0.000 description 1
- KTTGOQBBPRTJCQ-UHFFFAOYSA-N methyl 2-(2-oxo-1-pentylcyclopentyl)acetate Chemical compound CCCCCC1(CC(=O)OC)CCCC1=O KTTGOQBBPRTJCQ-UHFFFAOYSA-N 0.000 description 1
- KVWWIYGFBYDJQC-UHFFFAOYSA-N methyl dihydrojasmonate Chemical compound CCCCCC1C(CC(=O)OC)CCC1=O KVWWIYGFBYDJQC-UHFFFAOYSA-N 0.000 description 1
- JPTOCTSNXXKSSN-UHFFFAOYSA-N methylheptenone Chemical compound CCCC=CC(=O)CC JPTOCTSNXXKSSN-UHFFFAOYSA-N 0.000 description 1
- 229940043348 myristyl alcohol Drugs 0.000 description 1
- GMTCPFCMAHMEMT-UHFFFAOYSA-N n-decyldecan-1-amine Chemical compound CCCCCCCCCCNCCCCCCCCCC GMTCPFCMAHMEMT-UHFFFAOYSA-N 0.000 description 1
- KBBZXUDOYKCRBE-UHFFFAOYSA-N n-dodecyl-4-hydroxyundecanamide Chemical compound CCCCCCCCCCCCNC(=O)CCC(O)CCCCCCC KBBZXUDOYKCRBE-UHFFFAOYSA-N 0.000 description 1
- GOQYKNQRPGWPLP-UHFFFAOYSA-N n-heptadecyl alcohol Natural products CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 description 1
- IFYYFLINQYPWGJ-UHFFFAOYSA-N n-hexyl-gamma-butyrolactone Natural products CCCCCCC1CCC(=O)O1 IFYYFLINQYPWGJ-UHFFFAOYSA-N 0.000 description 1
- CMWTZPSULFXXJA-VIFPVBQESA-N naproxen Chemical group C1=C([C@H](C)C(O)=O)C=CC2=CC(OC)=CC=C21 CMWTZPSULFXXJA-VIFPVBQESA-N 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- JETNPTUJXPNCAS-UHFFFAOYSA-N nona-3,5-dien-2-one Chemical compound CCCC=CC=CC(C)=O JETNPTUJXPNCAS-UHFFFAOYSA-N 0.000 description 1
- VDITXDUGYVEVNM-UHFFFAOYSA-N oct-1-en-3-ol 2,5,7-trimethyloctan-3-ol Chemical compound CC(C)C(CC(CC(C)C)C)O.C=CC(CCCCC)O VDITXDUGYVEVNM-UHFFFAOYSA-N 0.000 description 1
- WWZKQHOCKIZLMA-UHFFFAOYSA-M octanoate Chemical compound CCCCCCCC([O-])=O WWZKQHOCKIZLMA-UHFFFAOYSA-M 0.000 description 1
- 239000002674 ointment Substances 0.000 description 1
- 239000003605 opacifier Substances 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- VWMVAQHMFFZQGD-UHFFFAOYSA-N p-Hydroxybenzyl acetone Natural products CC(=O)CC1=CC=C(O)C=C1 VWMVAQHMFFZQGD-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
- ZHZCYWWNFQUZOR-UHFFFAOYSA-N pent-4-en-2-ol Chemical compound CC(O)CC=C ZHZCYWWNFQUZOR-UHFFFAOYSA-N 0.000 description 1
- 238000010419 pet care Methods 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 229960005323 phenoxyethanol Drugs 0.000 description 1
- 229960005235 piperonyl butoxide Drugs 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- LPNYRYFBWFDTMA-UHFFFAOYSA-N potassium tert-butoxide Chemical compound [K+].CC(C)(C)[O-] LPNYRYFBWFDTMA-UHFFFAOYSA-N 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 229940116987 ppg-3 myristyl ether Drugs 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 150000003138 primary alcohols Chemical class 0.000 description 1
- 239000003380 propellant Substances 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- NJGBTKGETPDVIK-UHFFFAOYSA-N raspberry ketone Chemical compound CC(=O)CCC1=CC=C(O)C=C1 NJGBTKGETPDVIK-UHFFFAOYSA-N 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 230000011514 reflex Effects 0.000 description 1
- 238000007363 ring formation reaction Methods 0.000 description 1
- 239000012047 saturated solution Substances 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
- DCKVNWZUADLDEH-UHFFFAOYSA-N sec-butyl acetate Chemical compound CCC(C)OC(C)=O DCKVNWZUADLDEH-UHFFFAOYSA-N 0.000 description 1
- 150000003333 secondary alcohols Chemical class 0.000 description 1
- 229940057910 shea butter Drugs 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 229940033331 soy sterol Drugs 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 239000001384 succinic acid Substances 0.000 description 1
- 229940014800 succinic anhydride Drugs 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 230000002459 sustained effect Effects 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- BCNZYOJHNLTNEZ-UHFFFAOYSA-N tert-butyldimethylsilyl chloride Chemical compound CC(C)(C)[Si](C)(C)Cl BCNZYOJHNLTNEZ-UHFFFAOYSA-N 0.000 description 1
- 150000003509 tertiary alcohols Chemical class 0.000 description 1
- JRMUNVKIHCOMHV-UHFFFAOYSA-M tetrabutylammonium bromide Chemical compound [Br-].CCCC[N+](CCCC)(CCCC)CCCC JRMUNVKIHCOMHV-UHFFFAOYSA-M 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 229960000790 thymol Drugs 0.000 description 1
- MBDOYVRWFFCFHM-UHFFFAOYSA-N trans-2-hexenal Natural products CCCC=CC=O MBDOYVRWFFCFHM-UHFFFAOYSA-N 0.000 description 1
- LVBXEMGDVWVTGY-UHFFFAOYSA-N trans-2-octenal Natural products CCCCCC=CC=O LVBXEMGDVWVTGY-UHFFFAOYSA-N 0.000 description 1
- VTIODUHBZHNXFP-UHFFFAOYSA-N trans-hex-4-en-1-ol Natural products CC=CCCCO VTIODUHBZHNXFP-UHFFFAOYSA-N 0.000 description 1
- BJIOGJUNALELMI-UHFFFAOYSA-N trans-isoeugenol Natural products COC1=CC(C=CC)=CC=C1O BJIOGJUNALELMI-UHFFFAOYSA-N 0.000 description 1
- LADGBHLMCUINGV-UHFFFAOYSA-N tricaprin Chemical compound CCCCCCCCCC(=O)OCC(OC(=O)CCCCCCCCC)COC(=O)CCCCCCCCC LADGBHLMCUINGV-UHFFFAOYSA-N 0.000 description 1
- 239000005051 trimethylchlorosilane Substances 0.000 description 1
- GPRLSGONYQIRFK-MNYXATJNSA-N triton Chemical compound [3H+] GPRLSGONYQIRFK-MNYXATJNSA-N 0.000 description 1
- 229940057402 undecyl alcohol Drugs 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
- 239000011782 vitamin Substances 0.000 description 1
- 229940088594 vitamin Drugs 0.000 description 1
- 229930003231 vitamin Natural products 0.000 description 1
- 235000013343 vitamin Nutrition 0.000 description 1
- ZFNVDHOSLNRHNN-UHFFFAOYSA-N xi-3-(4-Isopropylphenyl)-2-methylpropanal Chemical compound O=CC(C)CC1=CC=C(C(C)C)C=C1 ZFNVDHOSLNRHNN-UHFFFAOYSA-N 0.000 description 1
- WGPCZPLRVAWXPW-UHFFFAOYSA-N xi-Dihydro-5-octyl-2(3H)-furanone Chemical compound CCCCCCCCC1CCC(=O)O1 WGPCZPLRVAWXPW-UHFFFAOYSA-N 0.000 description 1
- 229910052726 zirconium Inorganic materials 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/50—Perfumes
- C11D3/502—Protected perfumes
- C11D3/507—Compounds releasing perfumes by thermal or chemical activation
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES, NOT OTHERWISE PROVIDED FOR; PREPARATION OR TREATMENT THEREOF
- A23L27/00—Spices; Flavouring agents or condiments; Artificial sweetening agents; Table salts; Dietetic salt substitutes; Preparation or treatment thereof
- A23L27/70—Fixation, conservation, or encapsulation of flavouring agents
- A23L27/75—Fixation, conservation, or encapsulation of flavouring agents the flavouring agents being bound to a host by chemical, electrical or like forces, e.g. use of precursors
-
- 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
- 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
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q17/00—Barrier preparations; Preparations brought into direct contact with the skin for affording protection against external influences, e.g. sunlight, X-rays or other harmful rays, corrosive materials, bacteria or insect stings
- A61Q17/005—Antimicrobial preparations
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/007—Esters of unsaturated alcohols having the esterified hydroxy group bound to an acyclic carbon atom
-
- 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
- C07C69/67—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 saturated acids
- C07C69/675—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 saturated acids of saturated 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
- C07C69/67—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 saturated acids
- C07C69/716—Esters of keto-carboxylic acids or aldehydo-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
- C07C69/96—Esters of carbonic or haloformic acids
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/20—Organic compounds containing oxygen
- C11D3/2093—Esters; Carbonates
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/26—Organic compounds containing nitrogen
- C11D3/32—Amides; Substituted amides
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/48—Medical, disinfecting agents, disinfecting, antibacterial, germicidal or antimicrobial compositions
-
- 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
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Emergency Medicine (AREA)
- Nutrition Science (AREA)
- Food Science & Technology (AREA)
- Polymers & Plastics (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Dermatology (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Fats And Perfumes (AREA)
- Saccharide Compounds (AREA)
- Cosmetics (AREA)
- Detergent Compositions (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP98810337 | 1998-04-20 | ||
| EP98810337.0 | 1998-04-20 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2000053613A true JP2000053613A (ja) | 2000-02-22 |
| JP2000053613A5 JP2000053613A5 (https=) | 2006-05-25 |
Family
ID=8236042
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP11111199A Pending JP2000053613A (ja) | 1998-04-20 | 1999-04-19 | 保護されたヒドロキシ基を有する化合物 |
Country Status (6)
| Country | Link |
|---|---|
| US (2) | US6437150B1 (https=) |
| EP (2) | EP0952142B1 (https=) |
| JP (1) | JP2000053613A (https=) |
| DE (1) | DE69933608T2 (https=) |
| ES (1) | ES2273468T3 (https=) |
| SG (1) | SG75160A1 (https=) |
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2006523244A (ja) * | 2003-04-14 | 2006-10-12 | ジボダン エス エー | フレグランスとして有用なカルバメート類 |
| JP2020510048A (ja) * | 2017-03-29 | 2020-04-02 | クリューバー リュブリケーション ミュンヘン ソシエタス ヨーロピア ウント コンパニー コマンディートゲゼルシャフトＫｌｕｅｂｅｒ Ｌｕｂｒｉｃａｔｉｏｎ Ｍｕｅｎｃｈｅｎ ＳＥ ＆ Ｃｏ．ＫＧ | 新規エステル化合物、それらの製造方法ならびにそれらの使用 |
| JP2023553785A (ja) * | 2021-11-18 | 2023-12-26 | ケーティー アンド ジー コーポレイション | 新規な香味剤を含む喫煙物品｛ｓｍｏｋｉｎｇ ａｒｔｉｃｌｅ ｃｏｍｐｒｉｓｉｎｇ ｎｅｗ ｆｌａｖｏｒｉｎｇ ａｇｅｎｔ｝ |
| JP2023553779A (ja) * | 2021-11-18 | 2023-12-26 | ケーティー アンド ジー コーポレイション | 新規な香味剤を含む喫煙物品｛ｓｍｏｋｉｎｇ ａｒｔｉｃｌｅ ｃｏｍｐｒｉｓｉｎｇ ｎｅｗ ｆｌａｖｏｒｉｎｇ ａｇｅｎｔ｝ |
| JP2023554578A (ja) * | 2021-11-18 | 2023-12-28 | ケーティー アンド ジー コーポレイション | 新規な香味剤、香味剤組成物及びこれを含む製品｛ｎｅｗ ｆｌａｖｏｒｉｎｇ ａｇｅｎｔ，ｃｏｍｐｏｓｉｔｉｏｎ ａｎｄ ａｒｔｉｃｌｅ ｃｏｍｐｒｉｓｉｎｇ ｓａｍｅ｝ |
| JP2023554576A (ja) * | 2021-11-18 | 2023-12-28 | ケーティー アンド ジー コーポレイション | 新規な香味剤、香味剤組成物及びこれを含む製品｛ｎｅｗ ｆｌａｖｏｒｉｎｇ ａｇｅｎｔ，ｃｏｍｐｏｓｉｔｉｏｎ ａｎｄ ａｒｔｉｃｌｅ ｃｏｍｐｒｉｓｉｎｇ ｓａｍｅ｝ |
| JP2024501097A (ja) * | 2021-11-18 | 2024-01-11 | ケーティー アンド ジー コーポレイション | 熱によって香味成分が放出される壁紙組成物及び壁紙｛ｗａｌｌｐａｐｅｒ ｃｏｍｐｏｓｉｔｉｏｎ ａｎｄ ｗａｌｌｐａｐｅｒ ｒｅｌｅａｓｉｎｇ ｆｌａｖｏｒａｎｔ ｃｏｍｐｏｎｅｎｔ ｂｙ ｈｅａｔ｝ |
Families Citing this family (71)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE69933608T2 (de) | 1998-04-20 | 2007-08-23 | Givaudan S.A. | Verbindungen mit geschützten Hydroxylgruppen |
| EP1167362B1 (en) * | 2000-06-19 | 2005-05-25 | Givaudan SA | Fragance precursors |
| US20020094938A1 (en) | 2000-11-08 | 2002-07-18 | The Procter & Gamble Company | Photo-labile pro-fragrance conjugates |
| US20030125220A1 (en) | 2001-09-11 | 2003-07-03 | The Procter & Gamble Company | Compositions comprising photo-labile perfume delivery systems |
| JP2006520828A (ja) * | 2003-03-21 | 2006-09-14 | フォ デルマ インコーポレイテッド | 光応答芳香物 |
| DE10348062A1 (de) * | 2003-10-16 | 2005-05-19 | Symrise Gmbh & Co. Kg | Kurzkettige Enolester als Riechstoff-Prekursoren |
| US7361784B2 (en) | 2004-09-02 | 2008-04-22 | Eastman Chemical Company | Optimized liquid-phase oxidation |
| US7683210B2 (en) | 2004-09-02 | 2010-03-23 | Eastman Chemical Company | Optimized liquid-phase oxidation |
| US7399882B2 (en) | 2004-09-02 | 2008-07-15 | Eastman Chemical Company | Optimized liquid-phase oxidation |
| US7495125B2 (en) | 2004-09-02 | 2009-02-24 | Eastman Chemical Company | Optimized liquid-phase oxidation |
| US7507857B2 (en) | 2004-09-02 | 2009-03-24 | Eastman Chemical Company | Optimized liquid-phase oxidation |
| US7504535B2 (en) | 2004-09-02 | 2009-03-17 | Eastman Chemical Company | Optimized liquid-phase oxidation |
| US7692036B2 (en) | 2004-11-29 | 2010-04-06 | Eastman Chemical Company | Optimized liquid-phase oxidation |
| US7582793B2 (en) | 2004-09-02 | 2009-09-01 | Eastman Chemical Company | Optimized liquid-phase oxidation |
| US7608733B2 (en) | 2004-09-02 | 2009-10-27 | Eastman Chemical Company | Optimized liquid-phase oxidation |
| US7371894B2 (en) | 2004-09-02 | 2008-05-13 | Eastman Chemical Company | Optimized liquid-phase oxidation |
| US7390921B2 (en) | 2004-09-02 | 2008-06-24 | Eastman Chemical Company | Optimized liquid-phase oxidation |
| US7482482B2 (en) | 2004-09-02 | 2009-01-27 | Eastman Chemical Company | Optimized liquid-phase oxidation |
| US7608732B2 (en) | 2005-03-08 | 2009-10-27 | Eastman Chemical Company | Optimized liquid-phase oxidation |
| US7568361B2 (en) | 2004-09-02 | 2009-08-04 | Eastman Chemical Company | Optimized liquid-phase oxidation |
| US7589231B2 (en) | 2004-09-02 | 2009-09-15 | Eastman Chemical Company | Optimized liquid-phase oxidation |
| US7692037B2 (en) | 2004-09-02 | 2010-04-06 | Eastman Chemical Company | Optimized liquid-phase oxidation |
| US7572936B2 (en) | 2004-09-02 | 2009-08-11 | Eastman Chemical Company | Optimized liquid-phase oxidation |
| US7586000B2 (en) | 2004-09-02 | 2009-09-08 | Eastman Chemical Company | Optimized liquid-phase oxidation |
| US7572932B2 (en) | 2004-09-02 | 2009-08-11 | Eastman Chemical Company | Optimized liquid-phase oxidation |
| US7910769B2 (en) | 2004-09-02 | 2011-03-22 | Eastman Chemical Company | Optimized liquid-phase oxidation |
| US7381836B2 (en) | 2004-09-02 | 2008-06-03 | Eastman Chemical Company | Optimized liquid-phase oxidation |
| US7563926B2 (en) | 2004-09-02 | 2009-07-21 | Eastman Chemical Company | Optimized liquid-phase oxidation |
| US7741515B2 (en) * | 2004-09-02 | 2010-06-22 | Eastman Chemical Company | Optimized liquid-phase oxidation |
| US20060116531A1 (en) * | 2004-11-29 | 2006-06-01 | Wonders Alan G | Modeling of liquid-phase oxidation |
| US7884232B2 (en) | 2005-06-16 | 2011-02-08 | Eastman Chemical Company | Optimized liquid-phase oxidation |
| US7358389B2 (en) | 2006-01-04 | 2008-04-15 | Eastman Chemical Company | Oxidation system employing internal structure for enhanced hydrodynamics |
| US7355068B2 (en) | 2006-01-04 | 2008-04-08 | Eastman Chemical Company | Oxidation system with internal secondary reactor |
| US20070275866A1 (en) * | 2006-05-23 | 2007-11-29 | Robert Richard Dykstra | Perfume delivery systems for consumer goods |
| WO2008100411A1 (en) * | 2007-02-09 | 2008-08-21 | The Procter & Gamble Company | Perfume systems |
| US8541401B2 (en) * | 2007-07-25 | 2013-09-24 | Philip Morris Usa Inc. | Flavorant ester salts of polycarboxylic acids and methods for immobilizing and delivering flavorants containing hydroxyl groups |
| BRPI0922770A2 (pt) * | 2008-12-01 | 2019-09-24 | Procter & Gamble | sistemas de perfume |
| US9155772B2 (en) | 2008-12-08 | 2015-10-13 | Philip Morris Usa Inc. | Soft, chewable and orally dissolvable and/or disintegrable products |
| US8754028B2 (en) * | 2008-12-16 | 2014-06-17 | The Procter & Gamble Company | Perfume systems |
| US9167835B2 (en) | 2008-12-30 | 2015-10-27 | Philip Morris Usa Inc. | Dissolvable films impregnated with encapsulated tobacco, tea, coffee, botanicals, and flavors for oral products |
| US9167847B2 (en) | 2009-03-16 | 2015-10-27 | Philip Morris Usa Inc. | Production of coated tobacco particles suitable for usage in a smokeless tobacoo product |
| EP2270124A1 (en) | 2009-06-30 | 2011-01-05 | The Procter & Gamble Company | Bleaching compositions comprising a perfume delivery system |
| MX2012006616A (es) | 2009-12-09 | 2012-06-21 | Procter & Gamble | Productos para el cuidado de las telas y el hogar. |
| KR101463727B1 (ko) | 2009-12-17 | 2014-11-21 | 더 프록터 앤드 갬블 캄파니 | 악취 결합 중합체 및 악취 제어 성분을 포함하는 청향 조성물 |
| JP5744192B2 (ja) | 2010-06-22 | 2015-07-01 | ザ プロクター アンド ギャンブルカンパニー | 香料系 |
| EP3287511A1 (en) | 2010-06-22 | 2018-02-28 | The Procter & Gamble Company | Perfume systems |
| CN103025930B (zh) | 2010-07-02 | 2014-11-12 | 宝洁公司 | 递送活性剂的方法 |
| BR112013000101A2 (pt) | 2010-07-02 | 2016-05-17 | Procter & Gamble | filamentos compreendendo mantas de não tecido com agente ativo e métodos de fabricação dos mesmos |
| MX345025B (es) | 2010-07-02 | 2017-01-12 | Procter & Gamble | Producto detergente. |
| RU2541275C2 (ru) | 2010-07-02 | 2015-02-10 | Дзе Проктер Энд Гэмбл Компани | Филаменты, содержащие неароматизированный активный агент, нетканые полотна и способы их получения |
| CN102971126B (zh) | 2010-07-02 | 2016-03-23 | 宝洁公司 | 由非织造纤维网制备膜的方法 |
| BR112013033049A2 (pt) | 2011-06-23 | 2017-01-31 | Procter & Gamble | sistemas de perfume |
| WO2013002786A1 (en) | 2011-06-29 | 2013-01-03 | Solae | Baked food compositions comprising soy whey proteins that have been isolated from processing streams |
| EP2748353B1 (de) * | 2011-08-24 | 2017-04-26 | Basf Se | Verfahren zur elektrochemischen darstellung von gamma-hydroxycarbonsäureestern und gamma-lactonen |
| EP4592449A3 (en) | 2012-01-04 | 2025-10-22 | The Procter & Gamble Company | Fibrous structures comprising particles and methods for making same |
| CN104039945B (zh) | 2012-01-04 | 2017-03-15 | 宝洁公司 | 具有不同密度的多个区域的含活性物质纤维结构 |
| RU2591704C2 (ru) | 2012-01-04 | 2016-07-20 | Дзе Проктер Энд Гэмбл Компани | Содержащие активные агенты волокнистые структуры с множеством областей |
| EP4253649B1 (en) | 2013-12-09 | 2025-04-23 | The Procter & Gamble Company | Fibrous structures including an active agent and having a graphic printed thereon |
| WO2017143174A1 (en) | 2016-02-18 | 2017-08-24 | International Flavors & Fragrances Inc. | Polyurea capsule compositions |
| ES2950434T3 (es) | 2016-09-16 | 2023-10-10 | Int Flavors & Fragrances Inc | Composiciones de microcápsula estabilizadas con agentes de control de la viscosidad |
| US11697905B2 (en) | 2017-01-27 | 2023-07-11 | The Procter & Gamble Company | Active agent-containing articles that exhibit consumer acceptable article in-use properties |
| JP6886045B2 (ja) | 2017-01-27 | 2021-06-16 | ザ プロクター アンド ギャンブル カンパニーＴｈｅ Ｐｒｏｃｔｅｒ ＆ Ｇａｍｂｌｅ Ｃｏｍｐａｎｙ | 消費者に許容可能な物品使用特性を示す、活性剤含有物品 |
| US11697906B2 (en) | 2017-01-27 | 2023-07-11 | The Procter & Gamble Company | Active agent-containing articles and product-shipping assemblies for containing the same |
| US11697904B2 (en) | 2017-01-27 | 2023-07-11 | The Procter & Gamble Company | Active agent-containing articles that exhibit consumer acceptable article in-use properties |
| EP3823951A1 (en) * | 2018-12-20 | 2021-05-26 | Firmenich SA | Alkyl enol ether properfume |
| EP4069811A1 (en) | 2019-12-05 | 2022-10-12 | The Procter & Gamble Company | Method of making a cleaning composition |
| US12122981B2 (en) | 2019-12-05 | 2024-10-22 | The Procter & Gamble Company | Cleaning composition |
| KR102766839B1 (ko) * | 2021-11-18 | 2025-02-14 | 주식회사 케이티앤지 | 열에 의해 향미 성분이 방출되는 벽지 조성물 및 벽지 |
| US12435471B2 (en) | 2021-11-18 | 2025-10-07 | Kt&G Corporation | Wallpaper composition and wallpaper releasing flavorant component by heat |
| KR102774489B1 (ko) * | 2021-11-18 | 2025-03-06 | 주식회사 케이티앤지 | 신규한 향미제를 포함하는 흡연 물품 |
| KR102774498B1 (ko) * | 2021-11-18 | 2025-03-06 | 주식회사 케이티앤지 | 신규한 향미제를 포함하는 흡연 물품 |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0743320A2 (en) * | 1995-05-18 | 1996-11-20 | Bristol-Myers Squibb Company | Acyl guanidine and amidine prodrugs |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2797217A (en) * | 1957-06-25 | Dihydro oxazine diones | ||
| US2855436A (en) * | 1954-07-26 | 1958-10-07 | Koninklijke Pharma Fab Nv | Production of substituted acrylic acid amides |
| US4218370A (en) | 1979-05-14 | 1980-08-19 | Pennwalt Corporation | Azo monomer useful in polymerization systems |
| DE3568771D1 (en) * | 1984-10-10 | 1989-04-20 | Givaudan & Cie Sa | Hexanoates, process for their preparation and perfumes and/or flavouring agents having a content of such compounds |
| US4830787A (en) | 1987-08-13 | 1989-05-16 | Nabisco Brands, Inc. | Low calorie fat mimetics comprising carboxy/carboxylate esters |
| DE69428978T2 (de) | 1993-08-09 | 2002-07-18 | Firmenich S.A., Genf/Geneve | Parfümierungsverfahren von geweben |
| WO1997030687A2 (en) * | 1996-02-21 | 1997-08-28 | Givaudan-Roure (International) S.A. | Fragrance precursors |
| JPH09249683A (ja) | 1996-03-09 | 1997-09-22 | Noguchi Kenkyusho | Ｎ−アセチル−ｄ−ノイラミン酸エステル誘導体、及びその製造法 |
| NZ328102A (en) * | 1996-06-24 | 1998-04-27 | Givaudan Roure Int | Fragrance precursors and deodorant compositions |
| DE69933608T2 (de) | 1998-04-20 | 2007-08-23 | Givaudan S.A. | Verbindungen mit geschützten Hydroxylgruppen |
-
1999
- 1999-03-22 DE DE69933608T patent/DE69933608T2/de not_active Expired - Fee Related
- 1999-03-22 EP EP99810249A patent/EP0952142B1/en not_active Expired - Lifetime
- 1999-03-22 EP EP06021602A patent/EP1760067A3/en not_active Withdrawn
- 1999-03-22 ES ES99810249T patent/ES2273468T3/es not_active Expired - Lifetime
- 1999-03-24 SG SG1999001233A patent/SG75160A1/en unknown
- 1999-04-19 JP JP11111199A patent/JP2000053613A/ja active Pending
-
2000
- 2000-07-13 US US09/615,649 patent/US6437150B1/en not_active Expired - Fee Related
-
2002
- 2002-06-12 US US10/167,535 patent/US6627763B2/en not_active Expired - Fee Related
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0743320A2 (en) * | 1995-05-18 | 1996-11-20 | Bristol-Myers Squibb Company | Acyl guanidine and amidine prodrugs |
Cited By (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2006523244A (ja) * | 2003-04-14 | 2006-10-12 | ジボダン エス エー | フレグランスとして有用なカルバメート類 |
| JP2020510048A (ja) * | 2017-03-29 | 2020-04-02 | クリューバー リュブリケーション ミュンヘン ソシエタス ヨーロピア ウント コンパニー コマンディートゲゼルシャフトＫｌｕｅｂｅｒ Ｌｕｂｒｉｃａｔｉｏｎ Ｍｕｅｎｃｈｅｎ ＳＥ ＆ Ｃｏ．ＫＧ | 新規エステル化合物、それらの製造方法ならびにそれらの使用 |
| JP2023553785A (ja) * | 2021-11-18 | 2023-12-26 | ケーティー アンド ジー コーポレイション | 新規な香味剤を含む喫煙物品｛ｓｍｏｋｉｎｇ ａｒｔｉｃｌｅ ｃｏｍｐｒｉｓｉｎｇ ｎｅｗ ｆｌａｖｏｒｉｎｇ ａｇｅｎｔ｝ |
| JP2023553779A (ja) * | 2021-11-18 | 2023-12-26 | ケーティー アンド ジー コーポレイション | 新規な香味剤を含む喫煙物品｛ｓｍｏｋｉｎｇ ａｒｔｉｃｌｅ ｃｏｍｐｒｉｓｉｎｇ ｎｅｗ ｆｌａｖｏｒｉｎｇ ａｇｅｎｔ｝ |
| JP2023554578A (ja) * | 2021-11-18 | 2023-12-28 | ケーティー アンド ジー コーポレイション | 新規な香味剤、香味剤組成物及びこれを含む製品｛ｎｅｗ ｆｌａｖｏｒｉｎｇ ａｇｅｎｔ，ｃｏｍｐｏｓｉｔｉｏｎ ａｎｄ ａｒｔｉｃｌｅ ｃｏｍｐｒｉｓｉｎｇ ｓａｍｅ｝ |
| JP2023554576A (ja) * | 2021-11-18 | 2023-12-28 | ケーティー アンド ジー コーポレイション | 新規な香味剤、香味剤組成物及びこれを含む製品｛ｎｅｗ ｆｌａｖｏｒｉｎｇ ａｇｅｎｔ，ｃｏｍｐｏｓｉｔｉｏｎ ａｎｄ ａｒｔｉｃｌｅ ｃｏｍｐｒｉｓｉｎｇ ｓａｍｅ｝ |
| JP2024501097A (ja) * | 2021-11-18 | 2024-01-11 | ケーティー アンド ジー コーポレイション | 熱によって香味成分が放出される壁紙組成物及び壁紙｛ｗａｌｌｐａｐｅｒ ｃｏｍｐｏｓｉｔｉｏｎ ａｎｄ ｗａｌｌｐａｐｅｒ ｒｅｌｅａｓｉｎｇ ｆｌａｖｏｒａｎｔ ｃｏｍｐｏｎｅｎｔ ｂｙ ｈｅａｔ｝ |
| JP7572018B2 (ja) | 2021-11-18 | 2024-10-23 | ケーティー アンド ジー コーポレイション | 熱によって香味成分が放出される壁紙組成物及び壁紙｛ｗａｌｌｐａｐｅｒ ｃｏｍｐｏｓｉｔｉｏｎ ａｎｄ ｗａｌｌｐａｐｅｒ ｒｅｌｅａｓｉｎｇ ｆｌａｖｏｒａｎｔ ｃｏｍｐｏｎｅｎｔ ｂｙ ｈｅａｔ｝ |
| JP7600515B2 (ja) | 2021-11-18 | 2024-12-17 | ケーティー アンド ジー コーポレイション | 新規な香味剤を含む喫煙物品｛ｓｍｏｋｉｎｇ ａｒｔｉｃｌｅ ｃｏｍｐｒｉｓｉｎｇ ｎｅｗ ｆｌａｖｏｒｉｎｇ ａｇｅｎｔ｝ |
| JP7609350B2 (ja) | 2021-11-18 | 2025-01-07 | ケーティー アンド ジー コーポレイション | 新規な香味剤を含む喫煙物品｛ｓｍｏｋｉｎｇ ａｒｔｉｃｌｅ ｃｏｍｐｒｉｓｉｎｇ ｎｅｗ ｆｌａｖｏｒｉｎｇ ａｇｅｎｔ｝ |
| JP7609349B2 (ja) | 2021-11-18 | 2025-01-07 | ケーティー アンド ジー コーポレイション | 新規な香味剤、香味剤組成物及びこれを含む製品｛ｎｅｗ ｆｌａｖｏｒｉｎｇ ａｇｅｎｔ，ｃｏｍｐｏｓｉｔｉｏｎ ａｎｄ ａｒｔｉｃｌｅ ｃｏｍｐｒｉｓｉｎｇ ｓａｍｅ｝ |
Also Published As
| Publication number | Publication date |
|---|---|
| SG75160A1 (en) | 2000-09-19 |
| DE69933608T2 (de) | 2007-08-23 |
| EP0952142A1 (en) | 1999-10-27 |
| DE69933608D1 (de) | 2006-11-30 |
| EP0952142B1 (en) | 2006-10-18 |
| US6437150B1 (en) | 2002-08-20 |
| ES2273468T3 (es) | 2007-05-01 |
| US6627763B2 (en) | 2003-09-30 |
| EP1760067A3 (en) | 2007-05-30 |
| US20020193269A1 (en) | 2002-12-19 |
| EP1760067A2 (en) | 2007-03-07 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| EP0952142B1 (en) | Compounds with protected hydroxy groups | |
| US6479682B1 (en) | Compounds having protected hydroxy groups | |
| US6222062B1 (en) | Beta-ketoester compounds | |
| US6207857B1 (en) | Precursor compounds | |
| US6232487B1 (en) | Carbonate precursors for organoleptic compounds | |
| US6258854B1 (en) | Ketone precursors for organoleptic compounds | |
| JPH10330382A (ja) | 芳香性物質前駆体化合物 | |
| EP0980863A1 (en) | Oxime carboxylic acid derivatives | |
| US6369248B1 (en) | Fragrance precursor compounds | |
| EP0983990A2 (en) | Ketones useful as precursors for organoleptic compounds | |
| US6521797B1 (en) | Oxime carboxylic acid derivative precursors | |
| US20030018055A1 (en) | Serine carbonates | |
| EP0911315B1 (en) | Beta-ketoester | |
| EP0953562A1 (en) | Beta, gamma-unsaturated delta-keto esters | |
| MXPA99007962A (en) | Ketones useful as precursors for organoleptic compounds | |
| JP2000186062A (ja) | β，γ―不飽和デルタ―ケトエステル |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20060404 |
|
| A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20060404 |
|
| A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20100402 |
|
| A02 | Decision of refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A02 Effective date: 20101022 |