CZ304798A3 - Biodegradovatelné látky pro změkčování tkanin a přípravky pro změkčování tkanin obsahující tyto látky - Google Patents
Biodegradovatelné látky pro změkčování tkanin a přípravky pro změkčování tkanin obsahující tyto látky Download PDFInfo
- Publication number
- CZ304798A3 CZ304798A3 CZ983047A CZ304798A CZ304798A3 CZ 304798 A3 CZ304798 A3 CZ 304798A3 CZ 983047 A CZ983047 A CZ 983047A CZ 304798 A CZ304798 A CZ 304798A CZ 304798 A3 CZ304798 A3 CZ 304798A3
- Authority
- CZ
- Czechia
- Prior art keywords
- methyl
- dimethyl
- pentanediol
- hexanediol
- diol
- Prior art date
Links
- 238000002360 preparation method Methods 0.000 title claims abstract description 216
- 239000004744 fabric Substances 0.000 title claims abstract description 95
- 239000000126 substance Substances 0.000 title claims description 144
- 239000002904 solvent Substances 0.000 claims abstract description 230
- 239000000203 mixture Substances 0.000 claims abstract description 181
- 150000002009 diols Chemical class 0.000 claims abstract description 89
- 239000002979 fabric softener Substances 0.000 claims abstract description 54
- 239000007787 solid Substances 0.000 claims abstract description 47
- 238000009472 formulation Methods 0.000 claims abstract description 18
- 239000006185 dispersion Substances 0.000 claims abstract description 6
- -1 2,3-dimethyl-2,4-dimethyl-1, 5-pentanediol Chemical compound 0.000 claims description 287
- VNAWKNVDKFZFSU-UHFFFAOYSA-N 2-ethyl-2-methylpropane-1,3-diol Chemical compound CCC(C)(CO)CO VNAWKNVDKFZFSU-UHFFFAOYSA-N 0.000 claims description 169
- ZSCKAEOFRPCEES-UHFFFAOYSA-N 2-(3-methylbutan-2-yl)propane-1,3-diol Chemical compound CC(C)C(C)C(CO)CO ZSCKAEOFRPCEES-UHFFFAOYSA-N 0.000 claims description 147
- 150000001875 compounds Chemical class 0.000 claims description 106
- PFURGBBHAOXLIO-UHFFFAOYSA-N cyclohexane-1,2-diol Chemical compound OC1CCCCC1O PFURGBBHAOXLIO-UHFFFAOYSA-N 0.000 claims description 100
- 125000000217 alkyl group Chemical group 0.000 claims description 75
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 claims description 72
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 71
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 56
- 239000000194 fatty acid Substances 0.000 claims description 56
- 229930195729 fatty acid Natural products 0.000 claims description 56
- 150000004665 fatty acids Chemical class 0.000 claims description 56
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 55
- BTVWZWFKMIUSGS-UHFFFAOYSA-N 2-methylpropane-1,2-diol Chemical compound CC(C)(O)CO BTVWZWFKMIUSGS-UHFFFAOYSA-N 0.000 claims description 49
- 125000004417 unsaturated alkyl group Chemical group 0.000 claims description 39
- 125000004432 carbon atom Chemical group C* 0.000 claims description 34
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 29
- 239000002304 perfume Substances 0.000 claims description 29
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 claims description 28
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 26
- 229920006395 saturated elastomer Polymers 0.000 claims description 26
- BKKAVOLVYULZEM-UHFFFAOYSA-N 2-(2-methylpropyl)propane-1,3-diol Chemical compound CC(C)CC(CO)CO BKKAVOLVYULZEM-UHFFFAOYSA-N 0.000 claims description 25
- 229960004063 propylene glycol Drugs 0.000 claims description 25
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 claims description 23
- IPUNFZAUNSJGPB-UHFFFAOYSA-N 2,2,3-trimethylbutane-1,4-diol Chemical compound OCC(C)C(C)(C)CO IPUNFZAUNSJGPB-UHFFFAOYSA-N 0.000 claims description 23
- 229940043375 1,5-pentanediol Drugs 0.000 claims description 22
- 239000004480 active ingredient Substances 0.000 claims description 22
- YPFDHNVEDLHUCE-UHFFFAOYSA-N 1,3-propanediol Substances OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 claims description 21
- HIYKOZFIVZIBFO-UHFFFAOYSA-N 3-methylpentane-1,3-diol Chemical compound CCC(C)(O)CCO HIYKOZFIVZIBFO-UHFFFAOYSA-N 0.000 claims description 21
- VLKZOEOYAKHREP-UHFFFAOYSA-N hexane Substances CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 claims description 21
- 229940035437 1,3-propanediol Drugs 0.000 claims description 20
- JCTXKRPTIMZBJT-UHFFFAOYSA-N 2,2,4-trimethylpentane-1,3-diol Chemical compound CC(C)C(O)C(C)(C)CO JCTXKRPTIMZBJT-UHFFFAOYSA-N 0.000 claims description 20
- UNVGBIALRHLALK-UHFFFAOYSA-N 1,5-Hexanediol Chemical compound CC(O)CCCCO UNVGBIALRHLALK-UHFFFAOYSA-N 0.000 claims description 19
- JCYHHICXJAGYEL-UHFFFAOYSA-N 3-butoxypropane-1,2-diol Chemical class CCCCOCC(O)CO JCYHHICXJAGYEL-UHFFFAOYSA-N 0.000 claims description 19
- UQGLNXPQGUMNRU-UHFFFAOYSA-N heptane-1,6-diol Chemical compound CC(O)CCCCCO UQGLNXPQGUMNRU-UHFFFAOYSA-N 0.000 claims description 19
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims description 19
- 229920000166 polytrimethylene carbonate Polymers 0.000 claims description 19
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims description 18
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 18
- 229910052739 hydrogen Inorganic materials 0.000 claims description 17
- MZQZXSHFWDHNOW-UHFFFAOYSA-N 1-phenylpropane-1,2-diol Chemical compound CC(O)C(O)C1=CC=CC=C1 MZQZXSHFWDHNOW-UHFFFAOYSA-N 0.000 claims description 16
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims description 16
- 239000001257 hydrogen Substances 0.000 claims description 16
- IVDFJHOHABJVEH-UHFFFAOYSA-N pinacol Chemical compound CC(C)(O)C(C)(C)O IVDFJHOHABJVEH-UHFFFAOYSA-N 0.000 claims description 16
- RWLALWYNXFYRGW-UHFFFAOYSA-N 2-Ethyl-1,3-hexanediol Chemical compound CCCC(O)C(CC)CO RWLALWYNXFYRGW-UHFFFAOYSA-N 0.000 claims description 15
- GVIOYVUZPOGQQP-UHFFFAOYSA-N 2-methyl-3-propan-2-ylbutane-1,4-diol Chemical compound CC(C)C(CO)C(C)CO GVIOYVUZPOGQQP-UHFFFAOYSA-N 0.000 claims description 15
- JHWQMXKQJVAWKI-UHFFFAOYSA-N 3-phenylpropane-1,2-diol Chemical compound OCC(O)CC1=CC=CC=C1 JHWQMXKQJVAWKI-UHFFFAOYSA-N 0.000 claims description 15
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims description 15
- 150000001298 alcohols Chemical class 0.000 claims description 15
- AUGLSFONVIKZLA-UHFFFAOYSA-N 2-methylheptane-3,5-diol Chemical compound CCC(O)CC(O)C(C)C AUGLSFONVIKZLA-UHFFFAOYSA-N 0.000 claims description 14
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims description 14
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 14
- AVIYEYCFMVPYST-UHFFFAOYSA-N hexane-1,3-diol Chemical compound CCCC(O)CCO AVIYEYCFMVPYST-UHFFFAOYSA-N 0.000 claims description 14
- 229910052740 iodine Inorganic materials 0.000 claims description 14
- 239000011630 iodine Substances 0.000 claims description 14
- SVTBMSDMJJWYQN-UHFFFAOYSA-N 2-methylpentane-2,4-diol Chemical compound CC(O)CC(C)(C)O SVTBMSDMJJWYQN-UHFFFAOYSA-N 0.000 claims description 13
- ZMWAURRHTDCQCX-UHFFFAOYSA-N 3-methylheptane-2,4-diol Chemical compound CCCC(O)C(C)C(C)O ZMWAURRHTDCQCX-UHFFFAOYSA-N 0.000 claims description 13
- MFBMFHMAWZBOEZ-UHFFFAOYSA-N 6-methylheptane-2,5-diol Chemical compound CC(C)C(O)CCC(C)O MFBMFHMAWZBOEZ-UHFFFAOYSA-N 0.000 claims description 13
- GSQFUEPQVUSAPE-UHFFFAOYSA-N 2-methylpentane-2,3-diol Chemical compound CCC(O)C(C)(C)O GSQFUEPQVUSAPE-UHFFFAOYSA-N 0.000 claims description 12
- LPEVSCRXBSHMOZ-UHFFFAOYSA-N 2-propylbutane-1,4-diol Chemical compound CCCC(CO)CCO LPEVSCRXBSHMOZ-UHFFFAOYSA-N 0.000 claims description 12
- AREOBENUACTGHH-UHFFFAOYSA-N 3-methylheptane-3,5-diol Chemical compound CCC(O)CC(C)(O)CC AREOBENUACTGHH-UHFFFAOYSA-N 0.000 claims description 12
- POWFRZFDXPVABI-UHFFFAOYSA-N 6-methylheptane-2,4-diol Chemical compound CC(C)CC(O)CC(C)O POWFRZFDXPVABI-UHFFFAOYSA-N 0.000 claims description 12
- ALQSHHUCVQOPAS-UHFFFAOYSA-N Pentane-1,5-diol Chemical compound OCCCCCO ALQSHHUCVQOPAS-UHFFFAOYSA-N 0.000 claims description 12
- DNIAPMSPPWPWGF-VKHMYHEASA-N (+)-propylene glycol Chemical compound C[C@H](O)CO DNIAPMSPPWPWGF-VKHMYHEASA-N 0.000 claims description 11
- PTCYLOJKSMVJTR-RMKNXTFCSA-N (2e)-3,7-dimethylocta-2,6-diene-1,4-diol Chemical compound CC(C)=CCC(O)C(\C)=C\CO PTCYLOJKSMVJTR-RMKNXTFCSA-N 0.000 claims description 11
- DEPDXIXAMMDTBV-UHFFFAOYSA-N 2-ethylpentane-1,5-diol Chemical compound CCC(CO)CCCO DEPDXIXAMMDTBV-UHFFFAOYSA-N 0.000 claims description 11
- IOMHEFJNPZANMF-UHFFFAOYSA-N 2-methylheptane-2,6-diol Chemical compound CC(O)CCCC(C)(C)O IOMHEFJNPZANMF-UHFFFAOYSA-N 0.000 claims description 11
- XGGVPUCMUQQFJM-UHFFFAOYSA-N 2-methylhexane-1,3-diol Chemical compound CCCC(O)C(C)CO XGGVPUCMUQQFJM-UHFFFAOYSA-N 0.000 claims description 11
- 150000001450 anions Chemical class 0.000 claims description 11
- HTXVEEVTGGCUNC-UHFFFAOYSA-N heptane-1,3-diol Chemical compound CCCCC(O)CCO HTXVEEVTGGCUNC-UHFFFAOYSA-N 0.000 claims description 11
- OZIMXLFSRSPFAS-UHFFFAOYSA-N heptane-2,6-diol Chemical compound CC(O)CCCC(C)O OZIMXLFSRSPFAS-UHFFFAOYSA-N 0.000 claims description 11
- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 claims description 11
- BGQUJDPWPVVEGV-UHFFFAOYSA-N 2,2-dimethylhexane-1,3-diol Chemical compound CCCC(O)C(C)(C)CO BGQUJDPWPVVEGV-UHFFFAOYSA-N 0.000 claims description 10
- RAGADMCTGXFOFR-UHFFFAOYSA-N 2-ethyl-2-methylbutane-1,4-diol Chemical compound CCC(C)(CO)CCO RAGADMCTGXFOFR-UHFFFAOYSA-N 0.000 claims description 10
- DXWLGCKTCQEDOO-UHFFFAOYSA-N 2-methylheptane-2,4-diol Chemical compound CCCC(O)CC(C)(C)O DXWLGCKTCQEDOO-UHFFFAOYSA-N 0.000 claims description 10
- WPIMUZQTFDJTFU-UHFFFAOYSA-N 2-methylheptane-2,5-diol Chemical compound CCC(O)CCC(C)(C)O WPIMUZQTFDJTFU-UHFFFAOYSA-N 0.000 claims description 10
- XERGTCWVYOKNAV-UHFFFAOYSA-N 2-methylpentane-1,2-diol Chemical compound CCCC(C)(O)CO XERGTCWVYOKNAV-UHFFFAOYSA-N 0.000 claims description 10
- MFYZEGVPIKYAGE-UHFFFAOYSA-N 6-methylheptane-1,4-diol Chemical compound CC(C)CC(O)CCCO MFYZEGVPIKYAGE-UHFFFAOYSA-N 0.000 claims description 10
- BTANRVKWQNVYAZ-UHFFFAOYSA-N butan-2-ol Chemical compound CCC(C)O BTANRVKWQNVYAZ-UHFFFAOYSA-N 0.000 claims description 10
- NNYOSLMHXUVJJH-UHFFFAOYSA-N heptane-1,5-diol Chemical compound CCC(O)CCCCO NNYOSLMHXUVJJH-UHFFFAOYSA-N 0.000 claims description 10
- XVEOUOTUJBYHNL-UHFFFAOYSA-N heptane-2,4-diol Chemical compound CCCC(O)CC(C)O XVEOUOTUJBYHNL-UHFFFAOYSA-N 0.000 claims description 10
- QVTWBMUAJHVAIJ-UHFFFAOYSA-N hexane-1,4-diol Chemical compound CCC(O)CCCO QVTWBMUAJHVAIJ-UHFFFAOYSA-N 0.000 claims description 10
- WYNVIVRXHYGNRT-UHFFFAOYSA-N octane-3,5-diol Chemical compound CCCC(O)CC(O)CC WYNVIVRXHYGNRT-UHFFFAOYSA-N 0.000 claims description 10
- 235000013772 propylene glycol Nutrition 0.000 claims description 10
- 239000003021 water soluble solvent Substances 0.000 claims description 10
- QQOJDTOGFYCSAU-UHFFFAOYSA-N 2,2-dimethylpentane-1,5-diol Chemical compound OCC(C)(C)CCCO QQOJDTOGFYCSAU-UHFFFAOYSA-N 0.000 claims description 9
- IDEOPBXRUBNYBN-UHFFFAOYSA-N 2-methylbutane-2,3-diol Chemical compound CC(O)C(C)(C)O IDEOPBXRUBNYBN-UHFFFAOYSA-N 0.000 claims description 9
- DYHGIZFXHVQIEA-UHFFFAOYSA-N 2-methylhexane-1,6-diol Chemical compound OCC(C)CCCCO DYHGIZFXHVQIEA-UHFFFAOYSA-N 0.000 claims description 9
- LNCZPZFNQQFXPT-UHFFFAOYSA-N 2-phenyl-1,2-propanediol Chemical compound OCC(O)(C)C1=CC=CC=C1 LNCZPZFNQQFXPT-UHFFFAOYSA-N 0.000 claims description 9
- OORRBWLVIVLEFE-UHFFFAOYSA-N 3-methylheptane-2,5-diol Chemical compound CCC(O)CC(C)C(C)O OORRBWLVIVLEFE-UHFFFAOYSA-N 0.000 claims description 9
- RLWWHEFTJSHFRN-UHFFFAOYSA-N 3-methylpentane-2,3-diol Chemical compound CCC(C)(O)C(C)O RLWWHEFTJSHFRN-UHFFFAOYSA-N 0.000 claims description 9
- FQJXITFHANYMET-UHFFFAOYSA-N 3-pentoxypropane-1,2-diol Chemical compound CCCCCOCC(O)CO FQJXITFHANYMET-UHFFFAOYSA-N 0.000 claims description 9
- AMOCOBXCNIBDMC-UHFFFAOYSA-N 4-Methyl-1,2-dihydroxypentane Chemical compound CC(C)CC(O)CO AMOCOBXCNIBDMC-UHFFFAOYSA-N 0.000 claims description 9
- FWDSFJJVDRVTJZ-UHFFFAOYSA-N 4-methylheptane-2,4-diol Chemical compound CCCC(C)(O)CC(C)O FWDSFJJVDRVTJZ-UHFFFAOYSA-N 0.000 claims description 9
- INVGCXXCVPGTOA-UHFFFAOYSA-N 4-methylheptane-2,5-diol Chemical compound CCC(O)C(C)CC(C)O INVGCXXCVPGTOA-UHFFFAOYSA-N 0.000 claims description 9
- DCBLTYZAUIEBCX-UHFFFAOYSA-N 4-methylpentane-1,3-diol Chemical compound CC(C)C(O)CCO DCBLTYZAUIEBCX-UHFFFAOYSA-N 0.000 claims description 9
- FNWJZNQLNMUDGE-UHFFFAOYSA-N 5-methylheptane-2,4-diol Chemical compound CCC(C)C(O)CC(C)O FNWJZNQLNMUDGE-UHFFFAOYSA-N 0.000 claims description 9
- NKWKZLRCUPYPSO-UHFFFAOYSA-N 5-methylheptane-2,5-diol Chemical compound CCC(C)(O)CCC(C)O NKWKZLRCUPYPSO-UHFFFAOYSA-N 0.000 claims description 9
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 9
- BMRWNKZVCUKKSR-UHFFFAOYSA-N butane-1,2-diol Chemical compound CCC(O)CO BMRWNKZVCUKKSR-UHFFFAOYSA-N 0.000 claims description 9
- 229910052799 carbon Inorganic materials 0.000 claims description 9
- POFSNPPXJUQANW-UHFFFAOYSA-N hexane-3,4-diol Chemical compound CCC(O)C(O)CC POFSNPPXJUQANW-UHFFFAOYSA-N 0.000 claims description 9
- XRVCFZPJAHWYTB-UHFFFAOYSA-N prenderol Chemical compound CCC(CC)(CO)CO XRVCFZPJAHWYTB-UHFFFAOYSA-N 0.000 claims description 9
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 claims description 9
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 9
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 claims description 8
- UZOYKBBAMVVEMJ-UHFFFAOYSA-N 1-(3-methylphenyl)propane-1,3-diol Chemical compound CC1=CC=CC(C(O)CCO)=C1 UZOYKBBAMVVEMJ-UHFFFAOYSA-N 0.000 claims description 8
- PTXIOWUPCBAQBY-UHFFFAOYSA-N 1-(4-methylphenyl)propane-1,3-diol Chemical compound CC1=CC=C(C(O)CCO)C=C1 PTXIOWUPCBAQBY-UHFFFAOYSA-N 0.000 claims description 8
- UGRRTZQNTWNFSI-UHFFFAOYSA-N 2,2,3-trimethylpentane-1,3-diol Chemical compound CCC(C)(O)C(C)(C)CO UGRRTZQNTWNFSI-UHFFFAOYSA-N 0.000 claims description 8
- HNIDTKCNPXBSLD-UHFFFAOYSA-N 2,3-dimethylpentane-2,3-diol Chemical compound CCC(C)(O)C(C)(C)O HNIDTKCNPXBSLD-UHFFFAOYSA-N 0.000 claims description 8
- ZJWDJIVISLUQQZ-UHFFFAOYSA-N 2,4-dimethylpentane-1,5-diol Chemical compound OCC(C)CC(C)CO ZJWDJIVISLUQQZ-UHFFFAOYSA-N 0.000 claims description 8
- ZWNMRZQYWRLGMM-UHFFFAOYSA-N 2,5-dimethylhexane-2,5-diol Chemical compound CC(C)(O)CCC(C)(C)O ZWNMRZQYWRLGMM-UHFFFAOYSA-N 0.000 claims description 8
- YTCRRFFBEJJVLV-UHFFFAOYSA-N 2-butan-2-ylpropane-1,3-diol Chemical compound CCC(C)C(CO)CO YTCRRFFBEJJVLV-UHFFFAOYSA-N 0.000 claims description 8
- ALVVFCGEWCJMES-UHFFFAOYSA-N 2-ethyl-3-methylpentane-1,3-diol Chemical compound CCC(CO)C(C)(O)CC ALVVFCGEWCJMES-UHFFFAOYSA-N 0.000 claims description 8
- BQVXBKKPUDNXPR-UHFFFAOYSA-N 2-methylheptane-1,3-diol Chemical compound CCCCC(O)C(C)CO BQVXBKKPUDNXPR-UHFFFAOYSA-N 0.000 claims description 8
- SPXWGAHNKXLXAP-UHFFFAOYSA-N 2-methylpentane-1,3-diol Chemical compound CCC(O)C(C)CO SPXWGAHNKXLXAP-UHFFFAOYSA-N 0.000 claims description 8
- PNJNLCNHYSWUPT-UHFFFAOYSA-N 2-methylpentane-1,4-diol Chemical compound CC(O)CC(C)CO PNJNLCNHYSWUPT-UHFFFAOYSA-N 0.000 claims description 8
- FZHZPYGRGQZBCV-UHFFFAOYSA-N 2-propylpropane-1,3-diol Chemical compound CCCC(CO)CO FZHZPYGRGQZBCV-UHFFFAOYSA-N 0.000 claims description 8
- YVHAOWGRHCPODY-UHFFFAOYSA-N 3,3-dimethylbutane-1,2-diol Chemical compound CC(C)(C)C(O)CO YVHAOWGRHCPODY-UHFFFAOYSA-N 0.000 claims description 8
- IYBKMQPSCYKLDV-UHFFFAOYSA-N 3,3-dimethylpentane-1,4-diol Chemical compound CC(O)C(C)(C)CCO IYBKMQPSCYKLDV-UHFFFAOYSA-N 0.000 claims description 8
- CFEPFAMBMGCTQM-UHFFFAOYSA-N 3,3-dimethylpentane-1,5-diol Chemical compound OCCC(C)(C)CCO CFEPFAMBMGCTQM-UHFFFAOYSA-N 0.000 claims description 8
- VWRMHWAYIOHUNG-UHFFFAOYSA-N 3-methylheptane-2,6-diol Chemical compound CC(O)CCC(C)C(C)O VWRMHWAYIOHUNG-UHFFFAOYSA-N 0.000 claims description 8
- OGLLAZUAZSIDFE-UHFFFAOYSA-N 3-methylpentane-1,2-diol Chemical compound CCC(C)C(O)CO OGLLAZUAZSIDFE-UHFFFAOYSA-N 0.000 claims description 8
- WOHXXIWTEHLCQK-UHFFFAOYSA-N 3-methylpentane-1,4-diol Chemical compound CC(O)C(C)CCO WOHXXIWTEHLCQK-UHFFFAOYSA-N 0.000 claims description 8
- HAIVWDGLCRYQMC-UHFFFAOYSA-N 4-methylpentane-1,4-diol Chemical compound CC(C)(O)CCCO HAIVWDGLCRYQMC-UHFFFAOYSA-N 0.000 claims description 8
- RNKURRDNOYXATR-UHFFFAOYSA-N 4-methylpentane-2,3-diol Chemical compound CC(C)C(O)C(C)O RNKURRDNOYXATR-UHFFFAOYSA-N 0.000 claims description 8
- YRDZJWZHGKDMBL-UHFFFAOYSA-N 5-methylhexane-2,4-diol Chemical compound CC(C)C(O)CC(C)O YRDZJWZHGKDMBL-UHFFFAOYSA-N 0.000 claims description 8
- XICLOMYOBVKLTR-UHFFFAOYSA-N 6-methylheptane-1,6-diol Chemical compound CC(C)(O)CCCCCO XICLOMYOBVKLTR-UHFFFAOYSA-N 0.000 claims description 8
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 claims description 8
- 229910002651 NO3 Inorganic materials 0.000 claims description 8
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 claims description 8
- 239000004902 Softening Agent Substances 0.000 claims description 8
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims description 8
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 claims description 8
- 150000001768 cations Chemical class 0.000 claims description 8
- VSSAZBXXNIABDN-UHFFFAOYSA-N cyclohexylmethanol Chemical compound OCC1CCCCC1 VSSAZBXXNIABDN-UHFFFAOYSA-N 0.000 claims description 8
- OGRCRHSHBFQRKO-UHFFFAOYSA-N heptane-1,4-diol Chemical compound CCCC(O)CCCO OGRCRHSHBFQRKO-UHFFFAOYSA-N 0.000 claims description 8
- BQWORYKVVNTRAW-UHFFFAOYSA-N heptane-3,5-diol Chemical compound CCC(O)CC(O)CC BQWORYKVVNTRAW-UHFFFAOYSA-N 0.000 claims description 8
- QCIYAEYRVFUFAP-UHFFFAOYSA-N hexane-2,3-diol Chemical compound CCCC(O)C(C)O QCIYAEYRVFUFAP-UHFFFAOYSA-N 0.000 claims description 8
- WCVRQHFDJLLWFE-UHFFFAOYSA-N pentane-1,2-diol Chemical compound CCCC(O)CO WCVRQHFDJLLWFE-UHFFFAOYSA-N 0.000 claims description 8
- RUOPINZRYMFPBF-UHFFFAOYSA-N pentane-1,3-diol Chemical compound CCC(O)CCO RUOPINZRYMFPBF-UHFFFAOYSA-N 0.000 claims description 8
- CYVMBANVYOZFIG-ZCFIWIBFSA-N (2r)-2-ethylbutane-1,4-diol Chemical compound CC[C@@H](CO)CCO CYVMBANVYOZFIG-ZCFIWIBFSA-N 0.000 claims description 7
- UPQBAPMBTTWGMM-UHFFFAOYSA-N 2,2,4-trimethylpentane-1,4-diol Chemical compound CC(C)(O)CC(C)(C)CO UPQBAPMBTTWGMM-UHFFFAOYSA-N 0.000 claims description 7
- AKPLTHZVVWBOPT-UHFFFAOYSA-N 2,2-diethylbutane-1,3-diol Chemical compound CCC(CC)(CO)C(C)O AKPLTHZVVWBOPT-UHFFFAOYSA-N 0.000 claims description 7
- PHNDFOOEKCHRTF-UHFFFAOYSA-N 2,2-dimethylpentane-1,4-diol Chemical compound CC(O)CC(C)(C)CO PHNDFOOEKCHRTF-UHFFFAOYSA-N 0.000 claims description 7
- SQLSBTNINKQQPG-UHFFFAOYSA-N 2,3-dimethylbutane-1,2-diol Chemical compound CC(C)C(C)(O)CO SQLSBTNINKQQPG-UHFFFAOYSA-N 0.000 claims description 7
- YBOUZGKOQSXVHS-UHFFFAOYSA-N 2,3-dimethylpentane-1,4-diol Chemical compound CC(O)C(C)C(C)CO YBOUZGKOQSXVHS-UHFFFAOYSA-N 0.000 claims description 7
- JANSZBDMCKVQEK-UHFFFAOYSA-N 2,5-dimethylhexane-2,4-diol Chemical compound CC(C)C(O)CC(C)(C)O JANSZBDMCKVQEK-UHFFFAOYSA-N 0.000 claims description 7
- NSMIMJYEKVSYMT-UHFFFAOYSA-N 2,6-dimethylocta-2,7-diene-1,6-diol Chemical compound OCC(C)=CCCC(C)(O)C=C NSMIMJYEKVSYMT-UHFFFAOYSA-N 0.000 claims description 7
- OXFPHRVNCNWTJZ-UHFFFAOYSA-N 2-ethyl-2-methylbutane-1,3-diol Chemical compound CCC(C)(CO)C(C)O OXFPHRVNCNWTJZ-UHFFFAOYSA-N 0.000 claims description 7
- IFPWAVCXUHSXDW-UHFFFAOYSA-N 2-ethyl-3-methylbutane-1,4-diol Chemical compound CCC(CO)C(C)CO IFPWAVCXUHSXDW-UHFFFAOYSA-N 0.000 claims description 7
- IZUABMDVMAFWOP-UHFFFAOYSA-N 2-ethyl-4-methylpentane-1,3-diol Chemical compound CCC(CO)C(O)C(C)C IZUABMDVMAFWOP-UHFFFAOYSA-N 0.000 claims description 7
- HYFFNAVAMIJUIP-UHFFFAOYSA-N 2-ethylpropane-1,3-diol Chemical compound CCC(CO)CO HYFFNAVAMIJUIP-UHFFFAOYSA-N 0.000 claims description 7
- MWCBGWLCXSUTHK-UHFFFAOYSA-N 2-methylbutane-1,4-diol Chemical compound OCC(C)CCO MWCBGWLCXSUTHK-UHFFFAOYSA-N 0.000 claims description 7
- AAAWJUMVTPNRDT-UHFFFAOYSA-N 2-methylpentane-1,5-diol Chemical compound OCC(C)CCCO AAAWJUMVTPNRDT-UHFFFAOYSA-N 0.000 claims description 7
- KWMHZRGWEGBCTJ-UHFFFAOYSA-N 2-propan-2-ylbutane-1,3-diol Chemical compound CC(C)C(CO)C(C)O KWMHZRGWEGBCTJ-UHFFFAOYSA-N 0.000 claims description 7
- XWFCJSXTVSOIDN-UHFFFAOYSA-N 2-propan-2-ylbutane-1,4-diol Chemical compound CC(C)C(CO)CCO XWFCJSXTVSOIDN-UHFFFAOYSA-N 0.000 claims description 7
- XPFCZYUVICHKDS-UHFFFAOYSA-N 3-methylbutane-1,3-diol Chemical compound CC(C)(O)CCO XPFCZYUVICHKDS-UHFFFAOYSA-N 0.000 claims description 7
- CQWIPNBVYUKTRO-UHFFFAOYSA-N 3-methylheptane-1,4-diol Chemical compound CCCC(O)C(C)CCO CQWIPNBVYUKTRO-UHFFFAOYSA-N 0.000 claims description 7
- SKIKWYMNQLOTQO-UHFFFAOYSA-N 3-methylhexane-1,5-diol Chemical compound CC(O)CC(C)CCO SKIKWYMNQLOTQO-UHFFFAOYSA-N 0.000 claims description 7
- HSFITJPGVVSHAQ-UHFFFAOYSA-N 3-methylhexane-2,4-diol Chemical compound CCC(O)C(C)C(C)O HSFITJPGVVSHAQ-UHFFFAOYSA-N 0.000 claims description 7
- GAASGTOOMWIDNB-UHFFFAOYSA-N 4-methylcyclohexane-1,2-diol Chemical compound CC1CCC(O)C(O)C1 GAASGTOOMWIDNB-UHFFFAOYSA-N 0.000 claims description 7
- LFWYBPFYLUEUIJ-UHFFFAOYSA-N 4-methylheptane-2,6-diol Chemical compound CC(O)CC(C)CC(C)O LFWYBPFYLUEUIJ-UHFFFAOYSA-N 0.000 claims description 7
- ZRCYHJNCCBSTSZ-UHFFFAOYSA-N 4-methylhexane-1,4-diol Chemical compound CCC(C)(O)CCCO ZRCYHJNCCBSTSZ-UHFFFAOYSA-N 0.000 claims description 7
- MAFZESLKUFXGHA-UHFFFAOYSA-N 5-methylheptane-1,4-diol Chemical compound CCC(C)C(O)CCCO MAFZESLKUFXGHA-UHFFFAOYSA-N 0.000 claims description 7
- LNFDWQCEHXSMLT-UHFFFAOYSA-N 5-methylhexane-1,5-diol Chemical compound CC(C)(O)CCCCO LNFDWQCEHXSMLT-UHFFFAOYSA-N 0.000 claims description 7
- GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 claims description 7
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 7
- KIWBPDUYBMNFTB-UHFFFAOYSA-N Ethyl hydrogen sulfate Chemical compound CCOS(O)(=O)=O KIWBPDUYBMNFTB-UHFFFAOYSA-N 0.000 claims description 7
- OWBTYPJTUOEWEK-UHFFFAOYSA-N butane-2,3-diol Chemical compound CC(O)C(C)O OWBTYPJTUOEWEK-UHFFFAOYSA-N 0.000 claims description 7
- GPLRAVKSCUXZTP-UHFFFAOYSA-N diglycerol Chemical class OCC(O)COCC(O)CO GPLRAVKSCUXZTP-UHFFFAOYSA-N 0.000 claims description 7
- 150000002170 ethers Chemical class 0.000 claims description 7
- OHMBHFSEKCCCBW-UHFFFAOYSA-N hexane-2,5-diol Chemical compound CC(O)CCC(C)O OHMBHFSEKCCCBW-UHFFFAOYSA-N 0.000 claims description 7
- 229960004592 isopropanol Drugs 0.000 claims description 7
- JZMJDSHXVKJFKW-UHFFFAOYSA-M methyl sulfate(1-) Chemical compound COS([O-])(=O)=O JZMJDSHXVKJFKW-UHFFFAOYSA-M 0.000 claims description 7
- 229950006800 prenderol Drugs 0.000 claims description 7
- MZQZXSHFWDHNOW-IONNQARKSA-N (1S,2S)-1-phenyl-1,2-dihydroxypropane Natural products C[C@H](O)[C@@H](O)C1=CC=CC=C1 MZQZXSHFWDHNOW-IONNQARKSA-N 0.000 claims description 6
- OKWLUBCSBVYYTC-UHFFFAOYSA-N 1-phenylbutane-1,4-diol Chemical compound OCCCC(O)C1=CC=CC=C1 OKWLUBCSBVYYTC-UHFFFAOYSA-N 0.000 claims description 6
- LHOBKFFUEUQRQX-UHFFFAOYSA-N 2,2,4-trimethylpentane-1,5-diol Chemical compound OCC(C)CC(C)(C)CO LHOBKFFUEUQRQX-UHFFFAOYSA-N 0.000 claims description 6
- GQSZUUPRBBBHRI-UHFFFAOYSA-N 2,2-dimethylbutane-1,4-diol Chemical compound OCC(C)(C)CCO GQSZUUPRBBBHRI-UHFFFAOYSA-N 0.000 claims description 6
- PKJRYBRCZGCXPB-UHFFFAOYSA-N 2,3,4-trimethylpentane-1,4-diol Chemical compound OCC(C)C(C)C(C)(C)O PKJRYBRCZGCXPB-UHFFFAOYSA-N 0.000 claims description 6
- RBNLKEZJTWJUAY-UHFFFAOYSA-N 2,3-dimethylpentane-1,3-diol Chemical compound CCC(C)(O)C(C)CO RBNLKEZJTWJUAY-UHFFFAOYSA-N 0.000 claims description 6
- MJGXPIYXMGYKTR-UHFFFAOYSA-N 2,3-dimethylpentane-1,5-diol Chemical compound OCC(C)C(C)CCO MJGXPIYXMGYKTR-UHFFFAOYSA-N 0.000 claims description 6
- LDKQSAYLQSMHQP-UHFFFAOYSA-N 2,4,4-trimethylpentane-1,3-diol Chemical compound OCC(C)C(O)C(C)(C)C LDKQSAYLQSMHQP-UHFFFAOYSA-N 0.000 claims description 6
- MHNYUMPVQKTSLK-UHFFFAOYSA-N 2,4-dimethylhexane-2,4-diol Chemical compound CCC(C)(O)CC(C)(C)O MHNYUMPVQKTSLK-UHFFFAOYSA-N 0.000 claims description 6
- HXOVAKFPZAHQQZ-UHFFFAOYSA-N 2,4-dimethylpentane-1,4-diol Chemical compound OCC(C)CC(C)(C)O HXOVAKFPZAHQQZ-UHFFFAOYSA-N 0.000 claims description 6
- OTKHZEOSBVSFCJ-UHFFFAOYSA-N 2-butylbutane-1,3-diol Chemical compound CCCCC(CO)C(C)O OTKHZEOSBVSFCJ-UHFFFAOYSA-N 0.000 claims description 6
- SIMYRXPCIUXDGR-UHFFFAOYSA-N 2-butylpropane-1,3-diol Chemical compound CCCCC(CO)CO SIMYRXPCIUXDGR-UHFFFAOYSA-N 0.000 claims description 6
- NKUSBXAXENGEJW-UHFFFAOYSA-N 2-ethylhexane-1,4-diol Chemical compound CCC(O)CC(CC)CO NKUSBXAXENGEJW-UHFFFAOYSA-N 0.000 claims description 6
- CMFPYSAYYUSFQC-UHFFFAOYSA-N 2-ethylpentane-1,3-diol Chemical compound CCC(O)C(CC)CO CMFPYSAYYUSFQC-UHFFFAOYSA-N 0.000 claims description 6
- DOPZLYNWNJHAOS-UHFFFAOYSA-N 2-methyl-1,2-butanediol Chemical compound CCC(C)(O)CO DOPZLYNWNJHAOS-UHFFFAOYSA-N 0.000 claims description 6
- GNBPEYCZELNJMS-UHFFFAOYSA-N 2-methylbutane-1,3-diol Chemical compound CC(O)C(C)CO GNBPEYCZELNJMS-UHFFFAOYSA-N 0.000 claims description 6
- KQZLLXRPZSRICO-UHFFFAOYSA-N 2-methylheptane-1,5-diol Chemical compound CCC(O)CCC(C)CO KQZLLXRPZSRICO-UHFFFAOYSA-N 0.000 claims description 6
- OGXGGTVYUCWRNU-UHFFFAOYSA-N 2-methylheptane-1,6-diol Chemical compound CC(O)CCCC(C)CO OGXGGTVYUCWRNU-UHFFFAOYSA-N 0.000 claims description 6
- DLPUSSBLZXSHCZ-UHFFFAOYSA-N 2-methylhexane-1,5-diol Chemical compound CC(O)CCC(C)CO DLPUSSBLZXSHCZ-UHFFFAOYSA-N 0.000 claims description 6
- XCTVTCALBXLITL-UHFFFAOYSA-N 2-methylhexane-2,4-diol Chemical compound CCC(O)CC(C)(C)O XCTVTCALBXLITL-UHFFFAOYSA-N 0.000 claims description 6
- PMYMNKGSHYYMNT-UHFFFAOYSA-N 2-pentan-3-ylpropane-1,3-diol Chemical compound CCC(CC)C(CO)CO PMYMNKGSHYYMNT-UHFFFAOYSA-N 0.000 claims description 6
- BUEWHVFJJWPDLH-UHFFFAOYSA-N 2-propylbutane-1,3-diol Chemical compound CCCC(CO)C(C)O BUEWHVFJJWPDLH-UHFFFAOYSA-N 0.000 claims description 6
- FNQLMCZQKOBWJQ-UHFFFAOYSA-N 2-propylpentane-1,4-diol Chemical compound CCCC(CO)CC(C)O FNQLMCZQKOBWJQ-UHFFFAOYSA-N 0.000 claims description 6
- XSVKRMZQGLKDGT-UHFFFAOYSA-N 3,3,4-trimethylpentane-1,4-diol Chemical compound CC(C)(O)C(C)(C)CCO XSVKRMZQGLKDGT-UHFFFAOYSA-N 0.000 claims description 6
- DQCNVHDYCALYIF-UHFFFAOYSA-N 3,3-dimethylhexane-2,5-diol Chemical compound CC(O)CC(C)(C)C(C)O DQCNVHDYCALYIF-UHFFFAOYSA-N 0.000 claims description 6
- FVSGQDYLPCUSNF-UHFFFAOYSA-N 3,3-dimethylpentane-2,4-diol Chemical compound CC(O)C(C)(C)C(C)O FVSGQDYLPCUSNF-UHFFFAOYSA-N 0.000 claims description 6
- RMJMOIGSWATFGE-UHFFFAOYSA-N 3,4-dimethylpentane-1,4-diol Chemical compound CC(O)(C)C(C)CCO RMJMOIGSWATFGE-UHFFFAOYSA-N 0.000 claims description 6
- DKAPFPUUXKLAJO-UHFFFAOYSA-N 3,4-dimethylpentane-2,3-diol Chemical compound CC(C)C(C)(O)C(C)O DKAPFPUUXKLAJO-UHFFFAOYSA-N 0.000 claims description 6
- HJJZIMFAIMUSBW-UHFFFAOYSA-N 3-methylbutane-1,2-diol Chemical compound CC(C)C(O)CO HJJZIMFAIMUSBW-UHFFFAOYSA-N 0.000 claims description 6
- RPMYTAWDAZFCBO-UHFFFAOYSA-N 3-methylhexane-1,3-diol Chemical compound CCCC(C)(O)CCO RPMYTAWDAZFCBO-UHFFFAOYSA-N 0.000 claims description 6
- SBEAASQNRARXJX-UHFFFAOYSA-N 3-methylhexane-1,4-diol Chemical compound CCC(O)C(C)CCO SBEAASQNRARXJX-UHFFFAOYSA-N 0.000 claims description 6
- LRBAFUJEQQGGBH-UHFFFAOYSA-N 4-ethylhexane-2,4-diol Chemical compound CCC(O)(CC)CC(C)O LRBAFUJEQQGGBH-UHFFFAOYSA-N 0.000 claims description 6
- JPAIHHDYGSYVPR-UHFFFAOYSA-N 4-methylhexane-1,5-diol Chemical compound CC(O)C(C)CCCO JPAIHHDYGSYVPR-UHFFFAOYSA-N 0.000 claims description 6
- WENTZDHRLQWAEJ-UHFFFAOYSA-N 4-prop-2-enylhept-6-ene-2,4-diol Chemical compound CC(O)CC(O)(CC=C)CC=C WENTZDHRLQWAEJ-UHFFFAOYSA-N 0.000 claims description 6
- IUJRDJJYJQFDFL-UHFFFAOYSA-N 5-methylheptane-1,5-diol Chemical compound CCC(C)(O)CCCCO IUJRDJJYJQFDFL-UHFFFAOYSA-N 0.000 claims description 6
- XTVHTJKQKUOEQA-UHFFFAOYSA-N heptane-2,5-diol Chemical compound CCC(O)CCC(C)O XTVHTJKQKUOEQA-UHFFFAOYSA-N 0.000 claims description 6
- TXGJTWACJNYNOJ-UHFFFAOYSA-N hexane-2,4-diol Chemical compound CCC(O)CC(C)O TXGJTWACJNYNOJ-UHFFFAOYSA-N 0.000 claims description 6
- XLMFDCKSFJWJTP-UHFFFAOYSA-N pentane-2,3-diol Chemical compound CCC(O)C(C)O XLMFDCKSFJWJTP-UHFFFAOYSA-N 0.000 claims description 6
- GTCCGKPBSJZVRZ-UHFFFAOYSA-N pentane-2,4-diol Chemical compound CC(O)CC(C)O GTCCGKPBSJZVRZ-UHFFFAOYSA-N 0.000 claims description 6
- VKWZWOKLRQWMPC-UHFFFAOYSA-N 1-(2-hydroxybutoxy)butan-2-ol Chemical compound CCC(O)COCC(O)CC VKWZWOKLRQWMPC-UHFFFAOYSA-N 0.000 claims description 5
- YHSJEDVJYGRFHX-UHFFFAOYSA-N 1-(2-hydroxyethyl)cyclohexan-1-ol Chemical compound OCCC1(O)CCCCC1 YHSJEDVJYGRFHX-UHFFFAOYSA-N 0.000 claims description 5
- PWMWNFMRSKOCEY-UHFFFAOYSA-N 1-Phenyl-1,2-ethanediol Chemical compound OCC(O)C1=CC=CC=C1 PWMWNFMRSKOCEY-UHFFFAOYSA-N 0.000 claims description 5
- BBWBGVJEDBJKEO-UHFFFAOYSA-N 2,2,3-trimethylpentane-1,4-diol Chemical compound CC(O)C(C)C(C)(C)CO BBWBGVJEDBJKEO-UHFFFAOYSA-N 0.000 claims description 5
- QXKKYNIWAYERHT-UHFFFAOYSA-N 2,2-dimethylbutane-1,3-diol Chemical compound CC(O)C(C)(C)CO QXKKYNIWAYERHT-UHFFFAOYSA-N 0.000 claims description 5
- QHDADHHODABHLK-UHFFFAOYSA-N 2,2-dimethylpentane-1,3-diol Chemical compound CCC(O)C(C)(C)CO QHDADHHODABHLK-UHFFFAOYSA-N 0.000 claims description 5
- GPLLBLPMTRGQIX-UHFFFAOYSA-N 2,3,3-trimethylpentane-1,4-diol Chemical compound CC(O)C(C)(C)C(C)CO GPLLBLPMTRGQIX-UHFFFAOYSA-N 0.000 claims description 5
- MDYZOQGAPOJXPI-UHFFFAOYSA-N 2,3,3-trimethylpentane-1,5-diol Chemical compound OCC(C)C(C)(C)CCO MDYZOQGAPOJXPI-UHFFFAOYSA-N 0.000 claims description 5
- SKQUTIPQJKQFRA-UHFFFAOYSA-N 2,3-dimethylbutane-1,4-diol Chemical compound OCC(C)C(C)CO SKQUTIPQJKQFRA-UHFFFAOYSA-N 0.000 claims description 5
- OQGDYHLGWMRXBL-UHFFFAOYSA-N 2,3-dimethylpentane-2,4-diol Chemical compound CC(O)C(C)C(C)(C)O OQGDYHLGWMRXBL-UHFFFAOYSA-N 0.000 claims description 5
- LHFXJWUNNQVLMQ-UHFFFAOYSA-N 2,4-dimethylhexane-1,3-diol Chemical compound CCC(C)C(O)C(C)CO LHFXJWUNNQVLMQ-UHFFFAOYSA-N 0.000 claims description 5
- KHVMKJQZHRKYEV-UHFFFAOYSA-N 2,4-dimethylpentane-1,3-diol Chemical compound CC(C)C(O)C(C)CO KHVMKJQZHRKYEV-UHFFFAOYSA-N 0.000 claims description 5
- OFRKYCJLCQRYTG-UHFFFAOYSA-N 2,5-dimethylhexane-1,3-diol Chemical compound CC(C)CC(O)C(C)CO OFRKYCJLCQRYTG-UHFFFAOYSA-N 0.000 claims description 5
- ZBTGPMOUTUVXJH-UHFFFAOYSA-N 2,7-dimethylocta-3,7-diene-2,5-diol Chemical compound CC(=C)CC(O)C=CC(C)(C)O ZBTGPMOUTUVXJH-UHFFFAOYSA-N 0.000 claims description 5
- ZZQJAFZLFCRYEH-UHFFFAOYSA-N 2-(2-hydroxycyclopentyl)oxycyclopentan-1-ol Chemical compound OC1CCCC1OC1C(O)CCC1 ZZQJAFZLFCRYEH-UHFFFAOYSA-N 0.000 claims description 5
- SGGOHJWIIUDPAE-UHFFFAOYSA-N 2-ethylpentane-1,4-diol Chemical compound CCC(CO)CC(C)O SGGOHJWIIUDPAE-UHFFFAOYSA-N 0.000 claims description 5
- HOZWNKKVYXPKSI-UHFFFAOYSA-N 2-methyl-1-phenylpropane-1,3-diol Chemical compound OCC(C)C(O)C1=CC=CC=C1 HOZWNKKVYXPKSI-UHFFFAOYSA-N 0.000 claims description 5
- REQVMPVOKUHDOZ-UHFFFAOYSA-N 2-methyl-2-(2-methylpropyl)propane-1,3-diol Chemical compound CC(C)CC(C)(CO)CO REQVMPVOKUHDOZ-UHFFFAOYSA-N 0.000 claims description 5
- AHACCVCMRSHWPX-UHFFFAOYSA-N 2-methylheptane-1,4-diol Chemical compound CCCC(O)CC(C)CO AHACCVCMRSHWPX-UHFFFAOYSA-N 0.000 claims description 5
- PIGIJFKGLQGMPY-UHFFFAOYSA-N 2-methylhexane-1,4-diol Chemical compound CCC(O)CC(C)CO PIGIJFKGLQGMPY-UHFFFAOYSA-N 0.000 claims description 5
- KZWQVDXGMOSSNY-UHFFFAOYSA-N 2-methylhexane-2,5-diol Chemical compound CC(O)CCC(C)(C)O KZWQVDXGMOSSNY-UHFFFAOYSA-N 0.000 claims description 5
- GVBPPHRWPUZNJZ-UHFFFAOYSA-N 2-propan-2-ylpentane-1,4-diol Chemical compound CC(C)C(CO)CC(C)O GVBPPHRWPUZNJZ-UHFFFAOYSA-N 0.000 claims description 5
- ULJJXDAGVBDQBJ-UHFFFAOYSA-N 3,3-dimethylhexane-2,4-diol Chemical compound CCC(O)C(C)(C)C(C)O ULJJXDAGVBDQBJ-UHFFFAOYSA-N 0.000 claims description 5
- TWSGDKHAZBKYMM-UHFFFAOYSA-N 3,4-dimethylhexane-2,4-diol Chemical compound CCC(C)(O)C(C)C(C)O TWSGDKHAZBKYMM-UHFFFAOYSA-N 0.000 claims description 5
- JAOPNHYJQGAQTB-UHFFFAOYSA-N 3,4-dimethylpentane-1,3-diol Chemical compound CC(C)C(C)(O)CCO JAOPNHYJQGAQTB-UHFFFAOYSA-N 0.000 claims description 5
- MXBAXTVFBBFNGU-UHFFFAOYSA-N 3,5-dimethylhexane-2,4-diol Chemical compound CC(C)C(O)C(C)C(C)O MXBAXTVFBBFNGU-UHFFFAOYSA-N 0.000 claims description 5
- GIJUUECDGIVMIX-UHFFFAOYSA-N 3-(2-hydroxyethyl)cyclohexan-1-ol Chemical compound OCCC1CCCC(O)C1 GIJUUECDGIVMIX-UHFFFAOYSA-N 0.000 claims description 5
- FLJBNQNPSJCBQL-UHFFFAOYSA-N 3-ethylcyclopentane-1,2-diol Chemical compound CCC1CCC(O)C1O FLJBNQNPSJCBQL-UHFFFAOYSA-N 0.000 claims description 5
- YTJWKNCMSKASQG-UHFFFAOYSA-N 3-methyl-2-propylbutane-1,3-diol Chemical compound CCCC(CO)C(C)(C)O YTJWKNCMSKASQG-UHFFFAOYSA-N 0.000 claims description 5
- MEJJUZUMTCTDCF-UHFFFAOYSA-N 3-methylheptane-1,3-diol Chemical compound CCCCC(C)(O)CCO MEJJUZUMTCTDCF-UHFFFAOYSA-N 0.000 claims description 5
- VNDGADZIZILHQL-UHFFFAOYSA-N 3-methylheptane-1,5-diol Chemical compound CCC(O)CC(C)CCO VNDGADZIZILHQL-UHFFFAOYSA-N 0.000 claims description 5
- NZDAGFSBWSORFP-UHFFFAOYSA-N 3-methylheptane-1,6-diol Chemical compound CC(O)CCC(C)CCO NZDAGFSBWSORFP-UHFFFAOYSA-N 0.000 claims description 5
- LNBXHVBRHXOSGV-UHFFFAOYSA-N 3-methylheptane-3,4-diol Chemical compound CCCC(O)C(C)(O)CC LNBXHVBRHXOSGV-UHFFFAOYSA-N 0.000 claims description 5
- PMORVUNYTOZCSE-UHFFFAOYSA-N 3-methylhexane-2,5-diol Chemical compound CC(O)CC(C)C(C)O PMORVUNYTOZCSE-UHFFFAOYSA-N 0.000 claims description 5
- RBQLGIKHSXQZTB-UHFFFAOYSA-N 3-methylpentane-2,4-diol Chemical compound CC(O)C(C)C(C)O RBQLGIKHSXQZTB-UHFFFAOYSA-N 0.000 claims description 5
- FNQIYTUXOKTMDM-UHFFFAOYSA-N 3-phenoxypropane-1,2-diol Chemical compound OCC(O)COC1=CC=CC=C1 FNQIYTUXOKTMDM-UHFFFAOYSA-N 0.000 claims description 5
- LWCIBYRXSHRIAP-UHFFFAOYSA-N 3-phenylmethoxypropane-1,2-diol Chemical compound OCC(O)COCC1=CC=CC=C1 LWCIBYRXSHRIAP-UHFFFAOYSA-N 0.000 claims description 5
- QKFHUOVCOSJIGF-UHFFFAOYSA-N 4-ethylcyclohexane-1,3-diol Chemical compound CCC1CCC(O)CC1O QKFHUOVCOSJIGF-UHFFFAOYSA-N 0.000 claims description 5
- HFLQQTIGUYUCCK-UHFFFAOYSA-N 4-ethylcyclopentane-1,2-diol Chemical compound CCC1CC(O)C(O)C1 HFLQQTIGUYUCCK-UHFFFAOYSA-N 0.000 claims description 5
- FYBJBTBOODXDHA-UHFFFAOYSA-N 4-methylheptane-1,3-diol Chemical compound CCCC(C)C(O)CCO FYBJBTBOODXDHA-UHFFFAOYSA-N 0.000 claims description 5
- AJZGLFMCYYLGCC-UHFFFAOYSA-N 4-methylheptane-1,4-diol Chemical compound CCCC(C)(O)CCCO AJZGLFMCYYLGCC-UHFFFAOYSA-N 0.000 claims description 5
- ZJSKEVZMEACMTC-UHFFFAOYSA-N 4-methylheptane-1,5-diol Chemical compound CCC(O)C(C)CCCO ZJSKEVZMEACMTC-UHFFFAOYSA-N 0.000 claims description 5
- JRSGJJIGDIDBAE-UHFFFAOYSA-N 4-methylheptane-1,6-diol Chemical compound CC(O)CC(C)CCCO JRSGJJIGDIDBAE-UHFFFAOYSA-N 0.000 claims description 5
- UFPKCZXPUJSYMN-UHFFFAOYSA-N 4-methylhexane-2,4-diol Chemical compound CCC(C)(O)CC(C)O UFPKCZXPUJSYMN-UHFFFAOYSA-N 0.000 claims description 5
- CVMXOLXLYCAVNU-UHFFFAOYSA-N 5-methylheptane-1,3-diol Chemical compound CCC(C)CC(O)CCO CVMXOLXLYCAVNU-UHFFFAOYSA-N 0.000 claims description 5
- COOUSMCZIBOBRA-UHFFFAOYSA-N 5-methylheptane-1,6-diol Chemical compound CC(O)C(C)CCCCO COOUSMCZIBOBRA-UHFFFAOYSA-N 0.000 claims description 5
- SIQATKFUBJCOSH-UHFFFAOYSA-N 6-methylheptane-1,5-diol Chemical compound CC(C)C(O)CCCCO SIQATKFUBJCOSH-UHFFFAOYSA-N 0.000 claims description 5
- NSMIMJYEKVSYMT-SNVBAGLBSA-N 8-hydroxylinalool Natural products OCC(C)=CCC[C@](C)(O)C=C NSMIMJYEKVSYMT-SNVBAGLBSA-N 0.000 claims description 5
- PTCYLOJKSMVJTR-SNVBAGLBSA-N Rosiridol Natural products CC(=CC[C@@H](O)C(=CCO)C)C PTCYLOJKSMVJTR-SNVBAGLBSA-N 0.000 claims description 5
- 239000011575 calcium Substances 0.000 claims description 5
- 229910052791 calcium Inorganic materials 0.000 claims description 5
- 150000001805 chlorine compounds Chemical group 0.000 claims description 5
- SXCBDZAEHILGLM-UHFFFAOYSA-N heptane-1,7-diol Chemical compound OCCCCCCCO SXCBDZAEHILGLM-UHFFFAOYSA-N 0.000 claims description 5
- OEIJHBUUFURJLI-UHFFFAOYSA-N octane-1,8-diol Chemical compound OCCCCCCCCO OEIJHBUUFURJLI-UHFFFAOYSA-N 0.000 claims description 5
- AZVKGHXATHHFRF-UHFFFAOYSA-N octane-2,5-diol Chemical compound CCCC(O)CCC(C)O AZVKGHXATHHFRF-UHFFFAOYSA-N 0.000 claims description 5
- GLOBUAZSRIOKLN-UHFFFAOYSA-N pentane-1,4-diol Chemical compound CC(O)CCCO GLOBUAZSRIOKLN-UHFFFAOYSA-N 0.000 claims description 5
- IICHVFLQUNQPON-UHFFFAOYSA-N 1,2-dimethylcyclopentane-1,2-diol Chemical compound CC1(O)CCCC1(C)O IICHVFLQUNQPON-UHFFFAOYSA-N 0.000 claims description 4
- ZHOKPKCKZNPBOA-UHFFFAOYSA-N 1,4-dimethylcyclopentane-1,2-diol Chemical compound CC1CC(O)C(C)(O)C1 ZHOKPKCKZNPBOA-UHFFFAOYSA-N 0.000 claims description 4
- FNEWEOQQGPJOHL-UHFFFAOYSA-N 1-ethylcyclopentane-1,2-diol Chemical compound CCC1(O)CCCC1O FNEWEOQQGPJOHL-UHFFFAOYSA-N 0.000 claims description 4
- YMQBYIZMIOBDOD-UHFFFAOYSA-N 1-propan-2-ylcyclobutane-1,2-diol Chemical compound CC(C)C1(O)CCC1O YMQBYIZMIOBDOD-UHFFFAOYSA-N 0.000 claims description 4
- UHVTZHOHAWSDTG-UHFFFAOYSA-N 2,2-dimethylhept-6-ene-1,3-diol Chemical compound OCC(C)(C)C(O)CCC=C UHVTZHOHAWSDTG-UHFFFAOYSA-N 0.000 claims description 4
- QOTAAARUGAIUFT-UHFFFAOYSA-N 2,2-dimethylhexane-1,4-diol Chemical compound CCC(O)CC(C)(C)CO QOTAAARUGAIUFT-UHFFFAOYSA-N 0.000 claims description 4
- SOZFVEBFRCACOE-UHFFFAOYSA-N 2,3,3-trimethylpentane-2,4-diol Chemical compound CC(O)C(C)(C)C(C)(C)O SOZFVEBFRCACOE-UHFFFAOYSA-N 0.000 claims description 4
- MVHBECGZHRZJKG-UHFFFAOYSA-N 2,3,4-trimethylpentane-2,4-diol Chemical compound CC(O)(C)C(C)C(C)(C)O MVHBECGZHRZJKG-UHFFFAOYSA-N 0.000 claims description 4
- VRVIBKGZLDKSSA-UHFFFAOYSA-N 2,3-dimethylhexane-1,3-diol Chemical compound CCCC(C)(O)C(C)CO VRVIBKGZLDKSSA-UHFFFAOYSA-N 0.000 claims description 4
- QBCWFJLMSMULOG-UHFFFAOYSA-N 2,3-dimethylhexane-2,5-diol Chemical compound CC(O)CC(C)C(C)(C)O QBCWFJLMSMULOG-UHFFFAOYSA-N 0.000 claims description 4
- DBTGFWMBFZBBEF-UHFFFAOYSA-N 2,4-dimethylpentane-2,4-diol Chemical compound CC(C)(O)CC(C)(C)O DBTGFWMBFZBBEF-UHFFFAOYSA-N 0.000 claims description 4
- MWYYRAMJPYBQNL-UHFFFAOYSA-N 2,5,5-trimethylhepta-2,6-diene-1,4-diol Chemical compound OCC(C)=CC(O)C(C)(C)C=C MWYYRAMJPYBQNL-UHFFFAOYSA-N 0.000 claims description 4
- ZQCHRLFUCIMOOM-UHFFFAOYSA-N 2,5-dimethylhexane-1,5-diol Chemical compound OCC(C)CCC(C)(C)O ZQCHRLFUCIMOOM-UHFFFAOYSA-N 0.000 claims description 4
- AJKXQBNRHJAAFP-UHFFFAOYSA-N 2-(4-methylphenoxy)propane-1,3-diol Chemical compound CC1=CC=C(OC(CO)CO)C=C1 AJKXQBNRHJAAFP-UHFFFAOYSA-N 0.000 claims description 4
- MSRXHJALEMAKGB-UHFFFAOYSA-N 2-butan-2-yl-2-methylpropane-1,3-diol Chemical compound CCC(C)C(C)(CO)CO MSRXHJALEMAKGB-UHFFFAOYSA-N 0.000 claims description 4
- CKWHVERMCXNJJZ-UHFFFAOYSA-N 2-ethyl-2,3-dimethylbutane-1,3-diol Chemical compound CCC(C)(CO)C(C)(C)O CKWHVERMCXNJJZ-UHFFFAOYSA-N 0.000 claims description 4
- KTUBYIMDBHTUIU-UHFFFAOYSA-N 2-ethyl-3-methylbutane-1,3-diol Chemical compound CCC(CO)C(C)(C)O KTUBYIMDBHTUIU-UHFFFAOYSA-N 0.000 claims description 4
- MYRIHEILDQDOFM-UHFFFAOYSA-N 2-ethyl-3-methylpentane-1,4-diol Chemical compound CCC(CO)C(C)C(C)O MYRIHEILDQDOFM-UHFFFAOYSA-N 0.000 claims description 4
- HIUWFVLFQYSGME-UHFFFAOYSA-N 2-methyl-2-propan-2-ylbutane-1,3-diol Chemical compound CC(C)C(C)(CO)C(C)O HIUWFVLFQYSGME-UHFFFAOYSA-N 0.000 claims description 4
- MITGOIFBRQUQIE-UHFFFAOYSA-N 2-methyl-6-methylideneoct-2-ene-1,7-diol Chemical compound CC(O)C(=C)CCC=C(C)CO MITGOIFBRQUQIE-UHFFFAOYSA-N 0.000 claims description 4
- JSIXLRUBLQCZLS-UHFFFAOYSA-N 2-methyloct-7-ene-3,5-diol Chemical compound CC(C)C(O)CC(O)CC=C JSIXLRUBLQCZLS-UHFFFAOYSA-N 0.000 claims description 4
- NZAUBFJWMIAEBP-UHFFFAOYSA-N 2-methylocta-2,6-diene-1,8-diol Chemical compound OCC(C)=CCCC=CCO NZAUBFJWMIAEBP-UHFFFAOYSA-N 0.000 claims description 4
- KRYPJSCGSNKAAV-UHFFFAOYSA-N 2-propan-2-ylpentane-1,3-diol Chemical compound CCC(O)C(CO)C(C)C KRYPJSCGSNKAAV-UHFFFAOYSA-N 0.000 claims description 4
- KEKSNIGRWOCLBI-UHFFFAOYSA-N 2-tert-butylbutane-1,4-diol Chemical compound CC(C)(C)C(CO)CCO KEKSNIGRWOCLBI-UHFFFAOYSA-N 0.000 claims description 4
- QGFMKANITOYJSA-UHFFFAOYSA-N 3,4,4-trimethylpentane-1,3-diol Chemical compound CC(C)(C)C(C)(O)CCO QGFMKANITOYJSA-UHFFFAOYSA-N 0.000 claims description 4
- GSEBTJXKFWFGPP-UHFFFAOYSA-N 3,4-dimethylhexane-1,3-diol Chemical compound CCC(C)C(C)(O)CCO GSEBTJXKFWFGPP-UHFFFAOYSA-N 0.000 claims description 4
- YOJQPJQDVTVNEA-UHFFFAOYSA-N 3,4-dimethylhexane-1,5-diol Chemical compound CC(O)C(C)C(C)CCO YOJQPJQDVTVNEA-UHFFFAOYSA-N 0.000 claims description 4
- PXNAPGDENOWLRW-UHFFFAOYSA-N 3,4-dimethylhexane-2,5-diol Chemical compound CC(O)C(C)C(C)C(C)O PXNAPGDENOWLRW-UHFFFAOYSA-N 0.000 claims description 4
- MKRVGNGLIGBXRA-UHFFFAOYSA-N 3,5-dimethylhexane-1,3-diol Chemical compound CC(C)CC(C)(O)CCO MKRVGNGLIGBXRA-UHFFFAOYSA-N 0.000 claims description 4
- PFXRPUFYSLHDMF-UHFFFAOYSA-N 3-(hydroxymethyl)cyclohexan-1-ol Chemical compound OCC1CCCC(O)C1 PFXRPUFYSLHDMF-UHFFFAOYSA-N 0.000 claims description 4
- LOCKMOJIUSFTLA-UHFFFAOYSA-N 3-ethyl-2-methylpentane-1,3-diol Chemical compound CCC(O)(CC)C(C)CO LOCKMOJIUSFTLA-UHFFFAOYSA-N 0.000 claims description 4
- KOCRQAWVMQLLPN-UHFFFAOYSA-N 3-ethylhexane-2,5-diol Chemical compound CCC(C(C)O)CC(C)O KOCRQAWVMQLLPN-UHFFFAOYSA-N 0.000 claims description 4
- VFRVYGUCOZPHEQ-UHFFFAOYSA-N 3-methylcyclohexane-1,2-diol Chemical compound CC1CCCC(O)C1O VFRVYGUCOZPHEQ-UHFFFAOYSA-N 0.000 claims description 4
- BQNJVHGCZBNKBG-UHFFFAOYSA-N 3-phenylbutane-1,3-diol Chemical compound OCCC(O)(C)C1=CC=CC=C1 BQNJVHGCZBNKBG-UHFFFAOYSA-N 0.000 claims description 4
- KGUCQDAECKHULR-UHFFFAOYSA-N 4,4-dimethylcyclopentane-1,2-diol Chemical compound CC1(C)CC(O)C(O)C1 KGUCQDAECKHULR-UHFFFAOYSA-N 0.000 claims description 4
- NXRFQMYYYRHGMU-UHFFFAOYSA-N 4,4-dimethylpentane-1,3-diol Chemical compound CC(C)(C)C(O)CCO NXRFQMYYYRHGMU-UHFFFAOYSA-N 0.000 claims description 4
- UPZJPQJUBMOPKQ-UHFFFAOYSA-N 4,5-dimethylhexane-2,4-diol Chemical compound CC(O)CC(C)(O)C(C)C UPZJPQJUBMOPKQ-UHFFFAOYSA-N 0.000 claims description 4
- WGXSWJYIAWIGBQ-UHFFFAOYSA-N 4,6-dimethylcyclohexane-1,3-diol Chemical compound CC1CC(C)C(O)CC1O WGXSWJYIAWIGBQ-UHFFFAOYSA-N 0.000 claims description 4
- PJFREHRLIJVVST-UHFFFAOYSA-N 4-(1-Propenyl)-1,2-cyclopentanediol Natural products CC=CC1CC(O)C(O)C1 PJFREHRLIJVVST-UHFFFAOYSA-N 0.000 claims description 4
- SZIBVWWQOOVXHS-UHFFFAOYSA-N 4-(2-hydroxyethyl)cyclohexan-1-ol Chemical compound OCCC1CCC(O)CC1 SZIBVWWQOOVXHS-UHFFFAOYSA-N 0.000 claims description 4
- XEXSBXKKNKXLTA-UHFFFAOYSA-N 7-Octen-1,6-diol Natural products OCCCCCC(O)C=C XEXSBXKKNKXLTA-UHFFFAOYSA-N 0.000 claims description 4
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims description 4
- ORLQHILJRHBSAY-UHFFFAOYSA-N [1-(hydroxymethyl)cyclohexyl]methanol Chemical compound OCC1(CO)CCCCC1 ORLQHILJRHBSAY-UHFFFAOYSA-N 0.000 claims description 4
- DCYPPXGEIQTVPI-UHFFFAOYSA-N cycloheptane-1,2-diol Chemical compound OC1CCCCCC1O DCYPPXGEIQTVPI-UHFFFAOYSA-N 0.000 claims description 4
- QKCFSEWOROQABD-UHFFFAOYSA-N deca-1,9-diene-4,6-diol Chemical compound C=CCCC(O)CC(O)CC=C QKCFSEWOROQABD-UHFFFAOYSA-N 0.000 claims description 4
- ACCCMOQWYVYDOT-UHFFFAOYSA-N hexane-1,1-diol Chemical compound CCCCCC(O)O ACCCMOQWYVYDOT-UHFFFAOYSA-N 0.000 claims description 4
- 159000000003 magnesium salts Chemical class 0.000 claims description 4
- QVETUMQDECIBBA-UHFFFAOYSA-N non-1-ene-3,5-diol Chemical compound CCCCC(O)CC(O)C=C QVETUMQDECIBBA-UHFFFAOYSA-N 0.000 claims description 4
- CCSFSOQWGVNVRC-UHFFFAOYSA-N non-1-ene-3,7-diol Chemical compound CCC(O)CCCC(O)C=C CCSFSOQWGVNVRC-UHFFFAOYSA-N 0.000 claims description 4
- QKXJNQWQCGULNC-UHFFFAOYSA-N non-3-ene-2,5-diol Chemical compound CCCCC(O)C=CC(C)O QKXJNQWQCGULNC-UHFFFAOYSA-N 0.000 claims description 4
- KUGKHJMOXIEUNO-UHFFFAOYSA-N non-7-ene-2,4-diol Chemical compound CC=CCCC(O)CC(C)O KUGKHJMOXIEUNO-UHFFFAOYSA-N 0.000 claims description 4
- BCYQTARIMBPDNP-UHFFFAOYSA-N non-8-ene-2,4-diol Chemical compound CC(O)CC(O)CCCC=C BCYQTARIMBPDNP-UHFFFAOYSA-N 0.000 claims description 4
- VOPCSIHRGQNUCF-UHFFFAOYSA-N non-8-ene-2,5-diol Chemical compound CC(O)CCC(O)CCC=C VOPCSIHRGQNUCF-UHFFFAOYSA-N 0.000 claims description 4
- PAXWQLGKYISPNH-UHFFFAOYSA-N octane-2,7-diol Chemical compound CC(O)CCCCC(C)O PAXWQLGKYISPNH-UHFFFAOYSA-N 0.000 claims description 4
- BCKOQWWRTRBSGR-UHFFFAOYSA-N octane-3,6-diol Chemical compound CCC(O)CCC(O)CC BCKOQWWRTRBSGR-UHFFFAOYSA-N 0.000 claims description 4
- KYAWWMLPZVQQTF-XLKYRCCQSA-N (2e,4e,6e)-2,7-dimethylocta-2,4,6-triene-1,8-diol Chemical compound OCC(/C)=C/C=C/C=C(\C)CO KYAWWMLPZVQQTF-XLKYRCCQSA-N 0.000 claims description 3
- ITZWYSUTSDPWAQ-YFKPBYRVSA-N (2s)-2,3-dimethylbutane-1,3-diol Chemical compound OC[C@H](C)C(C)(C)O ITZWYSUTSDPWAQ-YFKPBYRVSA-N 0.000 claims description 3
- ROUNKFJLNCHQLL-UHFFFAOYSA-N 1,2-dimethylcyclohexane-1,3-diol Chemical compound CC1C(O)CCCC1(C)O ROUNKFJLNCHQLL-UHFFFAOYSA-N 0.000 claims description 3
- RYQYTYXVZCAYPW-UHFFFAOYSA-N 1,3-dimethylcyclohexane-1,3-diol Chemical compound CC1(O)CCCC(C)(O)C1 RYQYTYXVZCAYPW-UHFFFAOYSA-N 0.000 claims description 3
- QTYZWFQTOYXFBL-UHFFFAOYSA-N 1-phenylbutane-1,3-diol Chemical compound CC(O)CC(O)C1=CC=CC=C1 QTYZWFQTOYXFBL-UHFFFAOYSA-N 0.000 claims description 3
- FWRDQCHWQGNXNZ-UHFFFAOYSA-N 2,2,3-trimethylbutane-1,3-diol Chemical compound CC(C)(O)C(C)(C)CO FWRDQCHWQGNXNZ-UHFFFAOYSA-N 0.000 claims description 3
- MOCGNGXMQZVBFM-UHFFFAOYSA-N 2,2,3-trimethylpentane-1,5-diol Chemical compound OCCC(C)C(C)(C)CO MOCGNGXMQZVBFM-UHFFFAOYSA-N 0.000 claims description 3
- VXLUKYMRBUQHAY-UHFFFAOYSA-N 2,2-diethylbutane-1,4-diol Chemical compound CCC(CC)(CO)CCO VXLUKYMRBUQHAY-UHFFFAOYSA-N 0.000 claims description 3
- LNUMFJGWIUVKNE-UHFFFAOYSA-N 2,2-dimethylhexane-1,5-diol Chemical compound CC(O)CCC(C)(C)CO LNUMFJGWIUVKNE-UHFFFAOYSA-N 0.000 claims description 3
- NOBUYVZUAMYLSQ-UHFFFAOYSA-N 2,3,4-trimethylpentane-1,3-diol Chemical compound CC(C)C(C)(O)C(C)CO NOBUYVZUAMYLSQ-UHFFFAOYSA-N 0.000 claims description 3
- KOHSZBUMEHKSDK-UHFFFAOYSA-N 2,3-dimethylhexane-2,4-diol Chemical compound CCC(O)C(C)C(C)(C)O KOHSZBUMEHKSDK-UHFFFAOYSA-N 0.000 claims description 3
- JGYCFGUKGWGETF-UHFFFAOYSA-N 2,4,5-trimethylcyclopentane-1,3-diol Chemical compound CC1C(C)C(O)C(C)C1O JGYCFGUKGWGETF-UHFFFAOYSA-N 0.000 claims description 3
- KRZCRLNCQRTCKK-UHFFFAOYSA-N 2,4-dimethylhept-5-ene-1,3-diol Chemical compound CC=CC(C)C(O)C(C)CO KRZCRLNCQRTCKK-UHFFFAOYSA-N 0.000 claims description 3
- QLMODHWUCVHXOD-UHFFFAOYSA-N 2,4-dimethylhexane-1,4-diol Chemical compound CCC(C)(O)CC(C)CO QLMODHWUCVHXOD-UHFFFAOYSA-N 0.000 claims description 3
- BBOMJCSSXWZKGW-UHFFFAOYSA-N 2,4-dimethylhexane-2,5-diol Chemical compound CC(O)C(C)CC(C)(C)O BBOMJCSSXWZKGW-UHFFFAOYSA-N 0.000 claims description 3
- AGUZZWOHVLWNJF-UHFFFAOYSA-N 2,5-dimethylcyclohexane-1,3-diol Chemical compound CC1CC(O)C(C)C(O)C1 AGUZZWOHVLWNJF-UHFFFAOYSA-N 0.000 claims description 3
- ICLPTTARVKZAKL-UHFFFAOYSA-N 2,5-dimethylhepta-1,5-diene-3,4-diol Chemical compound CC=C(C)C(O)C(O)C(C)=C ICLPTTARVKZAKL-UHFFFAOYSA-N 0.000 claims description 3
- OQYKKQQLTKPGSG-UHFFFAOYSA-N 2,5-dimethylhexane-1,6-diol Chemical compound OCC(C)CCC(C)CO OQYKKQQLTKPGSG-UHFFFAOYSA-N 0.000 claims description 3
- KJOUODJIQYVKMG-UHFFFAOYSA-N 2,6-dimethylideneheptane-1,7-diol Chemical compound OCC(=C)CCCC(=C)CO KJOUODJIQYVKMG-UHFFFAOYSA-N 0.000 claims description 3
- HZHJGFRDKJPQPV-UHFFFAOYSA-N 2,6-dimethylocta-1,7-diene-3,6-diol Chemical compound CC(=C)C(O)CCC(C)(O)C=C HZHJGFRDKJPQPV-UHFFFAOYSA-N 0.000 claims description 3
- JFNPIHORQHWCBL-UHFFFAOYSA-N 2,6-dimethylocta-3,7-diene-1,6-diol Chemical compound OCC(C)C=CCC(C)(O)C=C JFNPIHORQHWCBL-UHFFFAOYSA-N 0.000 claims description 3
- TWWHGHSCTCMSRB-UHFFFAOYSA-N 2-(2-methylbutan-2-yl)propane-1,3-diol Chemical compound CCC(C)(C)C(CO)CO TWWHGHSCTCMSRB-UHFFFAOYSA-N 0.000 claims description 3
- SGKWBURAGLWENN-UHFFFAOYSA-N 2-(2-methylbutoxy)propane-1,3-diol Chemical compound CCC(C)COC(CO)CO SGKWBURAGLWENN-UHFFFAOYSA-N 0.000 claims description 3
- RVLQZFNNWUZTNG-UHFFFAOYSA-N 2-(2-methylpropyl)butane-1,3-diol Chemical compound CC(C)CC(CO)C(C)O RVLQZFNNWUZTNG-UHFFFAOYSA-N 0.000 claims description 3
- BSRGFMRXSVKKFV-UHFFFAOYSA-N 2-(3-methylbutoxy)propane-1,3-diol Chemical compound CC(C)CCOC(CO)CO BSRGFMRXSVKKFV-UHFFFAOYSA-N 0.000 claims description 3
- LKANJGRPAVHLIC-UHFFFAOYSA-N 2-(3-methylphenoxy)propane-1,3-diol Chemical compound CC1=CC=CC(OC(CO)CO)=C1 LKANJGRPAVHLIC-UHFFFAOYSA-N 0.000 claims description 3
- SXWAHMJCEARPFM-UHFFFAOYSA-N 2-butan-2-ylbutane-1,3-diol Chemical compound CCC(C)C(CO)C(C)O SXWAHMJCEARPFM-UHFFFAOYSA-N 0.000 claims description 3
- VOISNYJJJSUKMD-UHFFFAOYSA-N 2-cyclohexyloxypropane-1,3-diol Chemical compound OCC(CO)OC1CCCCC1 VOISNYJJJSUKMD-UHFFFAOYSA-N 0.000 claims description 3
- PRYKBHZDAJYRHY-UHFFFAOYSA-N 2-ethenyl-3-ethylpentane-1,3-diol Chemical compound CCC(O)(CC)C(CO)C=C PRYKBHZDAJYRHY-UHFFFAOYSA-N 0.000 claims description 3
- LVGRTOIUMQNQFB-UHFFFAOYSA-N 2-ethenyl-4,4-dimethylpentane-1,3-diol Chemical compound CC(C)(C)C(O)C(CO)C=C LVGRTOIUMQNQFB-UHFFFAOYSA-N 0.000 claims description 3
- RVZMZNBGFUOKJW-UHFFFAOYSA-N 2-ethyl-2-methylpentane-1,3-diol Chemical compound CCC(O)C(C)(CC)CO RVZMZNBGFUOKJW-UHFFFAOYSA-N 0.000 claims description 3
- YFEIEWLHNDHHJU-UHFFFAOYSA-N 2-ethyl-2-prop-2-enylbutane-1,3-diol Chemical compound CCC(CO)(C(C)O)CC=C YFEIEWLHNDHHJU-UHFFFAOYSA-N 0.000 claims description 3
- QZMSJXAOPCOVMI-UHFFFAOYSA-N 2-ethyl-2-prop-2-enylpropane-1,3-diol Chemical compound CCC(CO)(CO)CC=C QZMSJXAOPCOVMI-UHFFFAOYSA-N 0.000 claims description 3
- NCTPQXCGJHWDQF-UHFFFAOYSA-N 2-ethyl-2-propan-2-ylpropane-1,3-diol Chemical compound CCC(CO)(CO)C(C)C NCTPQXCGJHWDQF-UHFFFAOYSA-N 0.000 claims description 3
- DNJLCVGAPQZKST-UHFFFAOYSA-N 2-ethyl-4-methylpentane-1,4-diol Chemical compound CCC(CO)CC(C)(C)O DNJLCVGAPQZKST-UHFFFAOYSA-N 0.000 claims description 3
- RYABSMSKGIFXRC-UHFFFAOYSA-N 2-ethylidene-6-methylhept-6-ene-1,5-diol Chemical compound CC=C(CO)CCC(O)C(C)=C RYABSMSKGIFXRC-UHFFFAOYSA-N 0.000 claims description 3
- YJLDMKCKDOVGCP-UHFFFAOYSA-N 2-methylcycloheptane-1,3-diol Chemical compound CC1C(O)CCCCC1O YJLDMKCKDOVGCP-UHFFFAOYSA-N 0.000 claims description 3
- LCRAQVLYPVUBKY-UHFFFAOYSA-N 2-methylcycloheptane-1,4-diol Chemical compound CC1CC(O)CCCC1O LCRAQVLYPVUBKY-UHFFFAOYSA-N 0.000 claims description 3
- LYXVKANYTQUNOS-UHFFFAOYSA-N 2-pent-2-en-3-ylbutane-1,3-diol Chemical compound CCC(=CC)C(CO)C(C)O LYXVKANYTQUNOS-UHFFFAOYSA-N 0.000 claims description 3
- DVRJCMLOAVLPPD-UHFFFAOYSA-N 2-pent-4-enylpropane-1,3-diol Chemical compound OCC(CO)CCCC=C DVRJCMLOAVLPPD-UHFFFAOYSA-N 0.000 claims description 3
- BLKZCZCGTIUOAF-UHFFFAOYSA-N 2-pentan-2-yloxypropane-1,3-diol Chemical compound CCCC(C)OC(CO)CO BLKZCZCGTIUOAF-UHFFFAOYSA-N 0.000 claims description 3
- LLVUKDVGWSAQIE-UHFFFAOYSA-N 2-pentan-3-yloxypropane-1,3-diol Chemical compound CCC(CC)OC(CO)CO LLVUKDVGWSAQIE-UHFFFAOYSA-N 0.000 claims description 3
- GTZDHQWPMJPPHS-UHFFFAOYSA-N 2-prop-1-en-2-ylhexane-1,5-diol Chemical compound CC(O)CCC(CO)C(C)=C GTZDHQWPMJPPHS-UHFFFAOYSA-N 0.000 claims description 3
- AJZZKVGVIWBSLJ-UHFFFAOYSA-N 3,3-dimethylhexane-1,4-diol Chemical compound CCC(O)C(C)(C)CCO AJZZKVGVIWBSLJ-UHFFFAOYSA-N 0.000 claims description 3
- QJECFNQNOWKSQU-UHFFFAOYSA-N 3,4-dimethylhexane-1,4-diol Chemical compound CCC(C)(O)C(C)CCO QJECFNQNOWKSQU-UHFFFAOYSA-N 0.000 claims description 3
- HRFAQTLGZYUGEP-UHFFFAOYSA-N 3,5-dimethylcyclopentane-1,2-diol Chemical compound CC1CC(C)C(O)C1O HRFAQTLGZYUGEP-UHFFFAOYSA-N 0.000 claims description 3
- PTCYLOJKSMVJTR-MBACFSSFSA-N 3,7-Dimethyl-2,6-octadiene-1,4-diol Natural products O[C@H](/C(=C\CO)/C)C/C=C(\C)/C PTCYLOJKSMVJTR-MBACFSSFSA-N 0.000 claims description 3
- XCUXNHVHTMFMLJ-UHFFFAOYSA-N 3-(2-phenylethoxy)propane-1,2-diol Chemical compound OCC(O)COCCC1=CC=CC=C1 XCUXNHVHTMFMLJ-UHFFFAOYSA-N 0.000 claims description 3
- AIOHBDYXYKMBIF-UHFFFAOYSA-N 3-(3-methylbutoxy)propane-1,2-diol Chemical compound CC(C)CCOCC(O)CO AIOHBDYXYKMBIF-UHFFFAOYSA-N 0.000 claims description 3
- OWTXHZITCDRRTI-UHFFFAOYSA-N 3-cyclohexyloxypropane-1,2-diol Chemical compound OCC(O)COC1CCCCC1 OWTXHZITCDRRTI-UHFFFAOYSA-N 0.000 claims description 3
- AARVDYXRQGKRTO-UHFFFAOYSA-N 3-ethenyl-5-methylhept-1-ene-3,5-diol Chemical compound CCC(C)(O)CC(O)(C=C)C=C AARVDYXRQGKRTO-UHFFFAOYSA-N 0.000 claims description 3
- IEKLVSPQBKHGBQ-UHFFFAOYSA-N 3-ethenyloct-1-ene-3,6-diol Chemical compound CCC(O)CCC(O)(C=C)C=C IEKLVSPQBKHGBQ-UHFFFAOYSA-N 0.000 claims description 3
- JWNUWWGHRVMYCY-UHFFFAOYSA-N 3-ethyl-2,2-dimethylbutane-1,4-diol Chemical compound CCC(CO)C(C)(C)CO JWNUWWGHRVMYCY-UHFFFAOYSA-N 0.000 claims description 3
- VAERVOGGUYQEBS-UHFFFAOYSA-N 3-ethyl-3-methylpentane-1,5-diol Chemical compound OCCC(C)(CC)CCO VAERVOGGUYQEBS-UHFFFAOYSA-N 0.000 claims description 3
- LVNKGPOCWWAWOA-UHFFFAOYSA-N 3-ethylhexane-2,4-diol Chemical compound CCC(O)C(CC)C(C)O LVNKGPOCWWAWOA-UHFFFAOYSA-N 0.000 claims description 3
- HWABDWFWKVAHTH-UHFFFAOYSA-N 3-methyl-2-propan-2-ylbutane-1,3-diol Chemical compound CC(C)C(CO)C(C)(C)O HWABDWFWKVAHTH-UHFFFAOYSA-N 0.000 claims description 3
- HBIDQESLANDBPJ-UHFFFAOYSA-N 3-pentan-2-yloxypropane-1,2-diol Chemical compound CCCC(C)OCC(O)CO HBIDQESLANDBPJ-UHFFFAOYSA-N 0.000 claims description 3
- ZHYNWTRHGRBVIM-UHFFFAOYSA-N 3-propylcyclobutane-1,2-diol Chemical compound CCCC1CC(O)C1O ZHYNWTRHGRBVIM-UHFFFAOYSA-N 0.000 claims description 3
- CNDPNCDBQDTLGU-UHFFFAOYSA-N 4,4-dimethylcyclohexane-1,3-diol Chemical compound CC1(C)CCC(O)CC1O CNDPNCDBQDTLGU-UHFFFAOYSA-N 0.000 claims description 3
- XIRSHWKLORMCKB-UHFFFAOYSA-N 4,5-dimethylcyclohexane-1,3-diol Chemical compound CC1CC(O)CC(O)C1C XIRSHWKLORMCKB-UHFFFAOYSA-N 0.000 claims description 3
- QBXNMEDPFCPAKP-UHFFFAOYSA-N 4,5-dimethylhexane-1,4-diol Chemical compound CC(C)C(C)(O)CCCO QBXNMEDPFCPAKP-UHFFFAOYSA-N 0.000 claims description 3
- IBMZJAQJXADOBG-UHFFFAOYSA-N 4-ethyl-2-methylidenehexane-1,4-diol Chemical compound CCC(O)(CC)CC(=C)CO IBMZJAQJXADOBG-UHFFFAOYSA-N 0.000 claims description 3
- SOCPMADZMUNIPS-UHFFFAOYSA-N 4-ethylhexane-1,4-diol Chemical compound CCC(O)(CC)CCCO SOCPMADZMUNIPS-UHFFFAOYSA-N 0.000 claims description 3
- UMJUHGFIVJJRAE-UHFFFAOYSA-N 4-methylcycloheptane-1,3-diol Chemical compound CC1CCCC(O)CC1O UMJUHGFIVJJRAE-UHFFFAOYSA-N 0.000 claims description 3
- OCXHYXBMBDHYQJ-UHFFFAOYSA-N 4-methylhexane-2,3-diol Chemical compound CCC(C)C(O)C(C)O OCXHYXBMBDHYQJ-UHFFFAOYSA-N 0.000 claims description 3
- CYDATYWYXFODRO-UHFFFAOYSA-N 4-methyloct-6-ene-3,5-diol Chemical compound CCC(O)C(C)C(O)C=CC CYDATYWYXFODRO-UHFFFAOYSA-N 0.000 claims description 3
- NJXUEMXZEWDLBJ-UHFFFAOYSA-N 4-prop-2-enylhept-6-ene-1,4-diol Chemical compound OCCCC(O)(CC=C)CC=C NJXUEMXZEWDLBJ-UHFFFAOYSA-N 0.000 claims description 3
- MTPUFPIZVDRORX-UHFFFAOYSA-N 5,5-dimethylhexane-2,4-diol Chemical compound CC(O)CC(O)C(C)(C)C MTPUFPIZVDRORX-UHFFFAOYSA-N 0.000 claims description 3
- WSCOOJKGWPEQIU-UHFFFAOYSA-N 5-ethylcyclohexane-1,3-diol Chemical compound CCC1CC(O)CC(O)C1 WSCOOJKGWPEQIU-UHFFFAOYSA-N 0.000 claims description 3
- NQLXXGALEYREGL-UHFFFAOYSA-N 6,6-dimethylhept-1-ene-3,5-diol Chemical compound CC(C)(C)C(O)CC(O)C=C NQLXXGALEYREGL-UHFFFAOYSA-N 0.000 claims description 3
- UYYMSQUXTDNENC-UHFFFAOYSA-N 6-methyl-5-methylideneheptane-1,4-diol Chemical compound CC(C)C(=C)C(O)CCCO UYYMSQUXTDNENC-UHFFFAOYSA-N 0.000 claims description 3
- 239000011203 carbon fibre reinforced carbon Substances 0.000 claims description 3
- BDNXUVOJBGHQFD-UHFFFAOYSA-N cyclooctane-1,5-diol Chemical compound OC1CCCC(O)CCC1 BDNXUVOJBGHQFD-UHFFFAOYSA-N 0.000 claims description 3
- XUHNSDFQZQVOGL-UHFFFAOYSA-N deca-1,9-diene-3,8-diol Chemical compound C=CC(O)CCCCC(O)C=C XUHNSDFQZQVOGL-UHFFFAOYSA-N 0.000 claims description 3
- 229960004756 ethanol Drugs 0.000 claims description 3
- FBZFJKZTEPYJSN-UHFFFAOYSA-N non-4-ene-2,8-diol Chemical compound CC(O)CCC=CCC(C)O FBZFJKZTEPYJSN-UHFFFAOYSA-N 0.000 claims description 3
- XBDHZLPXXFXIHQ-UHFFFAOYSA-N nona-6,8-diene-1,5-diol Chemical compound OCCCCC(O)C=CC=C XBDHZLPXXFXIHQ-UHFFFAOYSA-N 0.000 claims description 3
- DQZRAEOPSNPXSQ-UHFFFAOYSA-N oct-2-ene-1,4-diol Chemical compound CCCCC(O)C=CCO DQZRAEOPSNPXSQ-UHFFFAOYSA-N 0.000 claims description 3
- ONGUKKAIGDNAGC-UHFFFAOYSA-N octane-2,6-diol Chemical compound CCC(O)CCCC(C)O ONGUKKAIGDNAGC-UHFFFAOYSA-N 0.000 claims description 3
- RUOJZAUFBMNUDX-UHFFFAOYSA-N propylene carbonate Chemical compound CC1COC(=O)O1 RUOJZAUFBMNUDX-UHFFFAOYSA-N 0.000 claims description 3
- NSMIMJYEKVSYMT-RMKNXTFCSA-N (2E)-2,6-dimethylocta-2,7-diene-1,6-diol Chemical compound OCC(/C)=C/CCC(C)(O)C=C NSMIMJYEKVSYMT-RMKNXTFCSA-N 0.000 claims description 2
- RULZVSSELRBGIK-UHFFFAOYSA-N 1,6-dimethylcyclohexane-1,3-diol Chemical compound CC1CCC(O)CC1(C)O RULZVSSELRBGIK-UHFFFAOYSA-N 0.000 claims description 2
- KNUGAYCUAPXLQK-UHFFFAOYSA-N 2,2-bis(prop-2-enyl)propane-1,3-diol Chemical compound C=CCC(CO)(CO)CC=C KNUGAYCUAPXLQK-UHFFFAOYSA-N 0.000 claims description 2
- VMYFNOZUIREUKA-UHFFFAOYSA-N 2,2-dimethylocta-4,6-diene-1,3-diol Chemical compound CC=CC=CC(O)C(C)(C)CO VMYFNOZUIREUKA-UHFFFAOYSA-N 0.000 claims description 2
- DKFCMHMIUZWEOJ-UHFFFAOYSA-N 2,3,5-trimethylhexa-1,5-diene-3,4-diol Chemical compound CC(=C)C(O)C(C)(O)C(C)=C DKFCMHMIUZWEOJ-UHFFFAOYSA-N 0.000 claims description 2
- KKPFRIAITUWOAQ-UHFFFAOYSA-N 2,3-di(propan-2-ylidene)butane-1,4-diol Chemical compound CC(C)=C(CO)C(CO)=C(C)C KKPFRIAITUWOAQ-UHFFFAOYSA-N 0.000 claims description 2
- ABACYJCCWHMUFL-UHFFFAOYSA-N 2,3-dimethylcyclohexane-1,4-diol Chemical compound CC1C(C)C(O)CCC1O ABACYJCCWHMUFL-UHFFFAOYSA-N 0.000 claims description 2
- TYYJZMXHCABLCL-UHFFFAOYSA-N 2,3-dimethylhept-5-ene-2,4-diol Chemical compound CC=CC(O)C(C)C(C)(C)O TYYJZMXHCABLCL-UHFFFAOYSA-N 0.000 claims description 2
- BKGOBDHAVYQNAH-UHFFFAOYSA-N 2,3-dimethylhexane-1,6-diol Chemical compound OCC(C)C(C)CCCO BKGOBDHAVYQNAH-UHFFFAOYSA-N 0.000 claims description 2
- ZLVQJEHUXKCVLN-UHFFFAOYSA-N 2,4-dimethylcyclohexane-1,3-diol Chemical compound CC1CCC(O)C(C)C1O ZLVQJEHUXKCVLN-UHFFFAOYSA-N 0.000 claims description 2
- XDHSSENSQITPGI-UHFFFAOYSA-N 2,4-dimethylhept-6-ene-1,5-diol Chemical compound OCC(C)CC(C)C(O)C=C XDHSSENSQITPGI-UHFFFAOYSA-N 0.000 claims description 2
- CMYVGRYIVRMDBW-UHFFFAOYSA-N 2,5,5-trimethylhexane-2,4-diol Chemical compound CC(C)(C)C(O)CC(C)(C)O CMYVGRYIVRMDBW-UHFFFAOYSA-N 0.000 claims description 2
- MJVCRHAMYHFDNV-UHFFFAOYSA-N 2,5-dimethylhept-3-ene-2,5-diol Chemical compound CCC(C)(O)C=CC(C)(C)O MJVCRHAMYHFDNV-UHFFFAOYSA-N 0.000 claims description 2
- QEOHJVNDENHRCH-VOTSOKGWSA-N 2,6-Dimethyl-3,7-octadiene-2,6-diol Chemical compound CC(C)(O)\C=C\CC(C)(O)C=C QEOHJVNDENHRCH-VOTSOKGWSA-N 0.000 claims description 2
- QEOHJVNDENHRCH-SNVBAGLBSA-N 2,6-dimethyl-3,7-octadiene-2,6-diol Natural products CC(C)(O)C=CC[C@](C)(O)C=C QEOHJVNDENHRCH-SNVBAGLBSA-N 0.000 claims description 2
- PLGMVQJXPQHEGV-UHFFFAOYSA-N 2,6-dimethylhept-5-ene-1,4-diol Chemical compound OCC(C)CC(O)C=C(C)C PLGMVQJXPQHEGV-UHFFFAOYSA-N 0.000 claims description 2
- IMFBTIFWPGDPDM-UHFFFAOYSA-N 2,6-dimethylocta-2,5-diene-1,7-diol Chemical compound CC(O)C(C)=CCC=C(C)CO IMFBTIFWPGDPDM-UHFFFAOYSA-N 0.000 claims description 2
- LIALMGLAKIIADU-UHFFFAOYSA-N 2,6-dimethylocta-2,7-diene-1,5-diol Chemical compound C=CC(C)C(O)CC=C(C)CO LIALMGLAKIIADU-UHFFFAOYSA-N 0.000 claims description 2
- OPTPXJNTFWGGHM-UHFFFAOYSA-N 2,6-dimethylocta-4,7-diene-2,3-diol Chemical compound C=CC(C)C=CC(O)C(C)(C)O OPTPXJNTFWGGHM-UHFFFAOYSA-N 0.000 claims description 2
- IZZWTAFSKCSXSB-UHFFFAOYSA-N 2,6-dimethylocta-4,7-diene-2,6-diol Chemical compound CC(C)(O)CC=CC(C)(O)C=C IZZWTAFSKCSXSB-UHFFFAOYSA-N 0.000 claims description 2
- XKRHFOBMXMMLGH-UHFFFAOYSA-N 2,7-dimethylocta-2,7-diene-1,6-diol Chemical compound CC(=C)C(O)CCC=C(C)CO XKRHFOBMXMMLGH-UHFFFAOYSA-N 0.000 claims description 2
- RDGOOKINPYLSSK-UHFFFAOYSA-N 2-(1-phenylethoxy)propane-1,3-diol Chemical compound OCC(CO)OC(C)C1=CC=CC=C1 RDGOOKINPYLSSK-UHFFFAOYSA-N 0.000 claims description 2
- KELMAQQLJLWUAY-UHFFFAOYSA-N 2-(2-hydroxyethyl)cyclohexan-1-ol Chemical compound OCCC1CCCCC1O KELMAQQLJLWUAY-UHFFFAOYSA-N 0.000 claims description 2
- PZNXWWSNYDVGBG-UHFFFAOYSA-N 2-(2-methylbutan-2-yl)but-2-ene-1,4-diol Chemical compound CCC(C)(C)C(CO)=CCO PZNXWWSNYDVGBG-UHFFFAOYSA-N 0.000 claims description 2
- DOQOORRFKPURFW-UHFFFAOYSA-N 2-(2-methylbutyl)propane-1,3-diol Chemical compound CCC(C)CC(CO)CO DOQOORRFKPURFW-UHFFFAOYSA-N 0.000 claims description 2
- VZIZXHUWMDIHIG-UHFFFAOYSA-N 2-(2-methylprop-2-enyl)-2-prop-2-enylpropane-1,3-diol Chemical compound CC(=C)CC(CO)(CO)CC=C VZIZXHUWMDIHIG-UHFFFAOYSA-N 0.000 claims description 2
- WTJXKNVEYKZJET-UHFFFAOYSA-N 2-(2-phenylethoxy)propane-1,3-diol Chemical compound OCC(CO)OCCC1=CC=CC=C1 WTJXKNVEYKZJET-UHFFFAOYSA-N 0.000 claims description 2
- WTGHMMCCVVEKNV-UHFFFAOYSA-N 2-(3-methylbut-1-enyl)propane-1,3-diol Chemical compound CC(C)C=CC(CO)CO WTGHMMCCVVEKNV-UHFFFAOYSA-N 0.000 claims description 2
- ANRUNQAJXRKLSE-UHFFFAOYSA-N 2-(3-methylbut-2-enyl)-3-methylidenebutane-1,4-diol Chemical compound CC(C)=CCC(CO)C(=C)CO ANRUNQAJXRKLSE-UHFFFAOYSA-N 0.000 claims description 2
- ZUGPTLWEXPUNSH-UHFFFAOYSA-N 2-(cyclohexen-1-yloxy)propane-1,3-diol Chemical compound OCC(CO)OC1=CCCCC1 ZUGPTLWEXPUNSH-UHFFFAOYSA-N 0.000 claims description 2
- FKRFWRMGCSEJQS-UHFFFAOYSA-N 2-ethenylhexane-1,6-diol Chemical compound OCCCCC(CO)C=C FKRFWRMGCSEJQS-UHFFFAOYSA-N 0.000 claims description 2
- KQXFCBBJCHWOAT-UHFFFAOYSA-N 2-ethyl-2,3-dimethylpent-4-ene-1,3-diol Chemical compound CCC(C)(CO)C(C)(O)C=C KQXFCBBJCHWOAT-UHFFFAOYSA-N 0.000 claims description 2
- BCRSWYZITXCYDH-UHFFFAOYSA-N 2-ethyl-2-(2-methylprop-2-enyl)propane-1,3-diol Chemical compound CCC(CO)(CO)CC(C)=C BCRSWYZITXCYDH-UHFFFAOYSA-N 0.000 claims description 2
- QPIAAQDLOJNQMP-UHFFFAOYSA-N 2-ethyl-2-propylpropane-1,3-diol Chemical compound CCCC(CC)(CO)CO QPIAAQDLOJNQMP-UHFFFAOYSA-N 0.000 claims description 2
- ATABKUAXRIBAHM-UHFFFAOYSA-N 2-ethyl-3-methylpentane-1,5-diol Chemical compound CCC(CO)C(C)CCO ATABKUAXRIBAHM-UHFFFAOYSA-N 0.000 claims description 2
- UEQSTOOLOFRXQP-UHFFFAOYSA-N 2-ethyl-4-methylpentane-1,5-diol Chemical compound CCC(CO)CC(C)CO UEQSTOOLOFRXQP-UHFFFAOYSA-N 0.000 claims description 2
- ULEZJXNOBWDMON-UHFFFAOYSA-N 2-ethylcyclohexane-1,3-diol Chemical compound CCC1C(O)CCCC1O ULEZJXNOBWDMON-UHFFFAOYSA-N 0.000 claims description 2
- FJFVJKVFGPDPPT-UHFFFAOYSA-N 2-ethylhex-3-ene-1,6-diol Chemical compound CCC(CO)C=CCCO FJFVJKVFGPDPPT-UHFFFAOYSA-N 0.000 claims description 2
- QHQHLZGWLIABDT-UHFFFAOYSA-N 2-ethylidene-3-methylpentane-1,5-diol Chemical compound CC=C(CO)C(C)CCO QHQHLZGWLIABDT-UHFFFAOYSA-N 0.000 claims description 2
- RQVDEHHNJPAHTK-UHFFFAOYSA-N 2-methyl-2-(3-methylbut-3-enyl)propane-1,3-diol Chemical compound CC(=C)CCC(C)(CO)CO RQVDEHHNJPAHTK-UHFFFAOYSA-N 0.000 claims description 2
- VKYYRXODWWYJHR-UHFFFAOYSA-N 2-methyl-3-propylbutane-1,4-diol Chemical compound CCCC(CO)C(C)CO VKYYRXODWWYJHR-UHFFFAOYSA-N 0.000 claims description 2
- CGYHLYIJXNGAPC-UHFFFAOYSA-N 2-methyl-6-methylideneoct-7-ene-2,4-diol Chemical compound CC(C)(O)CC(O)CC(=C)C=C CGYHLYIJXNGAPC-UHFFFAOYSA-N 0.000 claims description 2
- RJRAWHJCVFSUBF-UHFFFAOYSA-N 2-methylhept-2-ene-1,7-diol Chemical compound OCC(C)=CCCCCO RJRAWHJCVFSUBF-UHFFFAOYSA-N 0.000 claims description 2
- YUSJUDCEATVNFA-UHFFFAOYSA-N 2-methylhexane-2,3-diol Chemical compound CCCC(O)C(C)(C)O YUSJUDCEATVNFA-UHFFFAOYSA-N 0.000 claims description 2
- QISRZWMZOKNHFP-UHFFFAOYSA-N 2-methyloct-7-ene-1,3-diol Chemical compound OCC(C)C(O)CCCC=C QISRZWMZOKNHFP-UHFFFAOYSA-N 0.000 claims description 2
- IMZFWBUCFOWCSW-UHFFFAOYSA-N 2-pent-1-enylpropane-1,3-diol Chemical compound CCCC=CC(CO)CO IMZFWBUCFOWCSW-UHFFFAOYSA-N 0.000 claims description 2
- DIAKBGLNNAQLNA-UHFFFAOYSA-N 2-pentan-2-ylpropane-1,3-diol Chemical compound CCCC(C)C(CO)CO DIAKBGLNNAQLNA-UHFFFAOYSA-N 0.000 claims description 2
- ZQZTVETVPBHROI-UHFFFAOYSA-N 2-pentoxypropane-1,3-diol Chemical compound CCCCCOC(CO)CO ZQZTVETVPBHROI-UHFFFAOYSA-N 0.000 claims description 2
- VYXUCIGUSHNVAY-UHFFFAOYSA-N 2-propylidenepentane-1,5-diol Chemical compound CCC=C(CO)CCCO VYXUCIGUSHNVAY-UHFFFAOYSA-N 0.000 claims description 2
- IYDAOFZZRIDUTE-UHFFFAOYSA-N 3,5-dimethylhepta-1,5-diene-3,4-diol Chemical compound CC=C(C)C(O)C(C)(O)C=C IYDAOFZZRIDUTE-UHFFFAOYSA-N 0.000 claims description 2
- OIKMSSUOKAEXAS-UHFFFAOYSA-N 3,6-dimethylhept-5-ene-1,3-diol Chemical compound CC(C)=CCC(C)(O)CCO OIKMSSUOKAEXAS-UHFFFAOYSA-N 0.000 claims description 2
- GWDWEDCUCJEAJX-UHFFFAOYSA-N 3,6-dimethylhept-5-ene-1,4-diol Chemical compound OCCC(C)C(O)C=C(C)C GWDWEDCUCJEAJX-UHFFFAOYSA-N 0.000 claims description 2
- QHPOKHQEHXNNFX-UHFFFAOYSA-N 3,7-dimethylocta-1,6-diene-3,5-diol Chemical compound CC(C)=CC(O)CC(C)(O)C=C QHPOKHQEHXNNFX-UHFFFAOYSA-N 0.000 claims description 2
- RIEVYMMWQZWVIF-UHFFFAOYSA-N 3,7-dimethylocta-2,5-diene-1,7-diol Chemical compound OCC=C(C)CC=CC(C)(C)O RIEVYMMWQZWVIF-UHFFFAOYSA-N 0.000 claims description 2
- YMWYBTHTHCAXIF-UHFFFAOYSA-N 3,7-dimethylocta-2,7-diene-1,4-diol Chemical compound CC(=C)CCC(O)C(C)=CCO YMWYBTHTHCAXIF-UHFFFAOYSA-N 0.000 claims description 2
- KASLFMQMPVSXKQ-UHFFFAOYSA-N 3,7-dimethylocta-3,5-diene-1,7-diol Chemical compound OCCC(C)=CC=CC(C)(C)O KASLFMQMPVSXKQ-UHFFFAOYSA-N 0.000 claims description 2
- IWKCFOCVPJRTHT-UHFFFAOYSA-N 3-(3-methylbutan-2-yloxy)propane-1,2-diol Chemical compound CC(C)C(C)OCC(O)CO IWKCFOCVPJRTHT-UHFFFAOYSA-N 0.000 claims description 2
- HYJQDYQOBRWHTR-UHFFFAOYSA-N 3-butylcyclobut-3-ene-1,2-diol Chemical compound CCCCC1=CC(O)C1O HYJQDYQOBRWHTR-UHFFFAOYSA-N 0.000 claims description 2
- MNNUMABXOYEVSY-UHFFFAOYSA-N 3-ethenyl-2,5-dimethylhex-5-ene-2,4-diol Chemical compound CC(=C)C(O)C(C=C)C(C)(C)O MNNUMABXOYEVSY-UHFFFAOYSA-N 0.000 claims description 2
- HSJBKLJJHJCSLR-UHFFFAOYSA-N 3-ethyl-3-methylpentane-2,4-diol Chemical compound CCC(C)(C(C)O)C(C)O HSJBKLJJHJCSLR-UHFFFAOYSA-N 0.000 claims description 2
- CLKQOXKWPNWUOI-UHFFFAOYSA-N 3-ethylidene-2,4-dimethylpentane-2,4-diol Chemical compound CC=C(C(C)(C)O)C(C)(C)O CLKQOXKWPNWUOI-UHFFFAOYSA-N 0.000 claims description 2
- JQLFINSIOWZVCZ-UHFFFAOYSA-N 3-methyl-2-prop-2-enylpentane-1,4-diol Chemical compound CC(O)C(C)C(CO)CC=C JQLFINSIOWZVCZ-UHFFFAOYSA-N 0.000 claims description 2
- AOXQXQBDWSYBKV-UHFFFAOYSA-N 3-methyl-6-methylidenehept-3-ene-1,7-diol Chemical compound OCCC(C)=CCC(=C)CO AOXQXQBDWSYBKV-UHFFFAOYSA-N 0.000 claims description 2
- PJCFOSBWMFNMHT-UHFFFAOYSA-N 3-methylhexane-2,3-diol Chemical compound CCCC(C)(O)C(C)O PJCFOSBWMFNMHT-UHFFFAOYSA-N 0.000 claims description 2
- BMMOTZVPJMIVRL-UHFFFAOYSA-N 3-pentan-3-yloxypropane-1,2-diol Chemical compound CCC(CC)OCC(O)CO BMMOTZVPJMIVRL-UHFFFAOYSA-N 0.000 claims description 2
- QTVDRJYISJWBFJ-UHFFFAOYSA-N 3-prop-2-enylhex-5-ene-1,3-diol Chemical compound OCCC(O)(CC=C)CC=C QTVDRJYISJWBFJ-UHFFFAOYSA-N 0.000 claims description 2
- JWQDBZRAEVKBEN-UHFFFAOYSA-N 3-propan-2-ylcyclobutane-1,2-diol Chemical compound CC(C)C1CC(O)C1O JWQDBZRAEVKBEN-UHFFFAOYSA-N 0.000 claims description 2
- RHVLGLNSTLOFRF-UHFFFAOYSA-N 3-tert-butylcyclobut-3-ene-1,2-diol Chemical compound CC(C)(C)C1=CC(O)C1O RHVLGLNSTLOFRF-UHFFFAOYSA-N 0.000 claims description 2
- BHESEAOMOWWEQI-UHFFFAOYSA-N 4,6-dimethylhept-3-ene-1,5-diol Chemical compound CC(C)C(O)C(C)=CCCO BHESEAOMOWWEQI-UHFFFAOYSA-N 0.000 claims description 2
- RGTTZMFLYSSMAN-UHFFFAOYSA-N 4,6-dimethylhepta-2,4-diene-2,6-diol Chemical compound CC(O)=CC(C)=CC(C)(C)O RGTTZMFLYSSMAN-UHFFFAOYSA-N 0.000 claims description 2
- QZDOSIWYLNXBBG-UHFFFAOYSA-N 4-ethenyl-2,5-dimethylhex-2-ene-1,5-diol Chemical compound OCC(C)=CC(C=C)C(C)(C)O QZDOSIWYLNXBBG-UHFFFAOYSA-N 0.000 claims description 2
- XFRSHJSIVZJQDL-UHFFFAOYSA-N 4-ethylhexane-1,5-diol Chemical compound CCC(C(C)O)CCCO XFRSHJSIVZJQDL-UHFFFAOYSA-N 0.000 claims description 2
- BNCOGIRKUKWZKO-UHFFFAOYSA-N 4-methylideneheptane-1,7-diol Chemical compound OCCCC(=C)CCCO BNCOGIRKUKWZKO-UHFFFAOYSA-N 0.000 claims description 2
- NDDPUZGPXMHONS-UHFFFAOYSA-N 4-methyloct-3-ene-1,5-diol Chemical compound CCCC(O)C(C)=CCCO NDDPUZGPXMHONS-UHFFFAOYSA-N 0.000 claims description 2
- GEAOMDITONJGQF-UHFFFAOYSA-N 4-methyloct-7-ene-1,3-diol Chemical compound C=CCCC(C)C(O)CCO GEAOMDITONJGQF-UHFFFAOYSA-N 0.000 claims description 2
- DPKMKMKZYFEXNH-UHFFFAOYSA-N 5,6-dimethylhept-6-ene-1,4-diol Chemical compound CC(=C)C(C)C(O)CCCO DPKMKMKZYFEXNH-UHFFFAOYSA-N 0.000 claims description 2
- IWJRRQXHYLGYOA-UHFFFAOYSA-N 5-ethenyl-4-methylhept-6-ene-2,5-diol Chemical compound CC(O)CC(C)C(O)(C=C)C=C IWJRRQXHYLGYOA-UHFFFAOYSA-N 0.000 claims description 2
- BSCQGWZKVHGOCG-UHFFFAOYSA-N 5-ethylhept-2-ene-1,5-diol Chemical compound CCC(O)(CC)CC=CCO BSCQGWZKVHGOCG-UHFFFAOYSA-N 0.000 claims description 2
- TZTVPRXOBDHAMM-UHFFFAOYSA-N 5-methylhexane-2,3-diol Chemical compound CC(C)CC(O)C(C)O TZTVPRXOBDHAMM-UHFFFAOYSA-N 0.000 claims description 2
- PQACTIYJDNAXRU-UHFFFAOYSA-N 5-methyloct-3-ene-1,5-diol Chemical compound CCCC(C)(O)C=CCCO PQACTIYJDNAXRU-UHFFFAOYSA-N 0.000 claims description 2
- FZYLIFHYHSPCQT-UHFFFAOYSA-N 7-methyloct-4-ene-1,6-diol Chemical compound CC(C)C(O)C=CCCCO FZYLIFHYHSPCQT-UHFFFAOYSA-N 0.000 claims description 2
- IJKWYGLUJSTESM-UHFFFAOYSA-N 7-methyloct-6-ene-1,3-diol Chemical compound CC(C)=CCCC(O)CCO IJKWYGLUJSTESM-UHFFFAOYSA-N 0.000 claims description 2
- CRMDGFDUNAQAAY-UHFFFAOYSA-N 7-methyloct-6-ene-1,4-diol Chemical compound CC(C)=CCC(O)CCCO CRMDGFDUNAQAAY-UHFFFAOYSA-N 0.000 claims description 2
- PAYRFJZGKDBVDX-UHFFFAOYSA-N 7-methyloct-6-ene-1,5-diol Chemical compound CC(C)=CC(O)CCCCO PAYRFJZGKDBVDX-UHFFFAOYSA-N 0.000 claims description 2
- NZHKEQXFUCZCRV-UHFFFAOYSA-N 7-methyloct-7-ene-1,3-diol Chemical compound CC(=C)CCCC(O)CCO NZHKEQXFUCZCRV-UHFFFAOYSA-N 0.000 claims description 2
- DBJKKFUUEVARRO-UHFFFAOYSA-N 7-methylocta-5,7-diene-1,4-diol Chemical compound CC(=C)C=CC(O)CCCO DBJKKFUUEVARRO-UHFFFAOYSA-N 0.000 claims description 2
- JEPDYGVBIPZQKF-UHFFFAOYSA-N C=CC(O)C(C)CCCCO Chemical compound C=CC(O)C(C)CCCCO JEPDYGVBIPZQKF-UHFFFAOYSA-N 0.000 claims description 2
- HKJVQJZRSBGPRA-UHFFFAOYSA-N CC=C(C)C(C)(O)C(C)O Chemical compound CC=C(C)C(C)(O)C(C)O HKJVQJZRSBGPRA-UHFFFAOYSA-N 0.000 claims description 2
- YOMIDPIBJDBFOE-UHFFFAOYSA-N OCC(O)COC1=CCCCC1 Chemical compound OCC(O)COC1=CCCCC1 YOMIDPIBJDBFOE-UHFFFAOYSA-N 0.000 claims description 2
- XDODWINGEHBYRT-UHFFFAOYSA-N [2-(hydroxymethyl)cyclohexyl]methanol Chemical compound OCC1CCCCC1CO XDODWINGEHBYRT-UHFFFAOYSA-N 0.000 claims description 2
- LUSFFPXRDZKBMF-UHFFFAOYSA-N [3-(hydroxymethyl)cyclohexyl]methanol Chemical compound OCC1CCCC(CO)C1 LUSFFPXRDZKBMF-UHFFFAOYSA-N 0.000 claims description 2
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 claims description 2
- 238000004519 manufacturing process Methods 0.000 claims description 2
- DZTXWUVWSFDEKI-UHFFFAOYSA-N oct-2-ene-1,7-diol Chemical compound CC(O)CCCC=CCO DZTXWUVWSFDEKI-UHFFFAOYSA-N 0.000 claims description 2
- MTNZKIPFTFNUDB-UHFFFAOYSA-N oct-6-ene-1,5-diol Chemical compound CC=CC(O)CCCCO MTNZKIPFTFNUDB-UHFFFAOYSA-N 0.000 claims description 2
- 229940032159 propylene carbonate Drugs 0.000 claims description 2
- 229940083957 1,2-butanediol Drugs 0.000 claims 6
- CTAPFRYPJLPFDF-UHFFFAOYSA-N isoxazole Chemical compound C=1C=NOC=1 CTAPFRYPJLPFDF-UHFFFAOYSA-N 0.000 claims 4
- BEQGRRJLJLVQAQ-GQCTYLIASA-N (e)-3-methylpent-2-ene Chemical compound CC\C(C)=C\C BEQGRRJLJLVQAQ-GQCTYLIASA-N 0.000 claims 2
- WHYBHJWYBIXOPS-UHFFFAOYSA-N 1-phenylbutane-2,3-diol Chemical compound CC(O)C(O)CC1=CC=CC=C1 WHYBHJWYBIXOPS-UHFFFAOYSA-N 0.000 claims 2
- HPJKGEUAOBMJFM-UHFFFAOYSA-N 3-ethyl-2-methylpentane-1,4-diol Chemical compound CCC(C(C)O)C(C)CO HPJKGEUAOBMJFM-UHFFFAOYSA-N 0.000 claims 2
- SMQSHSFPVVAMBY-UHFFFAOYSA-N 5,5-dimethylhex-1-ene-3,4-diol Chemical compound CC(C)(C)C(O)C(O)C=C SMQSHSFPVVAMBY-UHFFFAOYSA-N 0.000 claims 2
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 claims 2
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 claims 2
- HITROERJXNWVOI-SOFGYWHQSA-N (5e)-octa-1,5-diene Chemical compound CC\C=C\CCC=C HITROERJXNWVOI-SOFGYWHQSA-N 0.000 claims 1
- JWEYNDRAHPIRPI-UPHRSURJSA-N (5z)-cyclooct-5-ene-1,2-diol Chemical compound OC1CC\C=C/CCC1O JWEYNDRAHPIRPI-UPHRSURJSA-N 0.000 claims 1
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 1
- KVEFSHKXYDKBDT-UHFFFAOYSA-N 1,2,2-trimethylcyclohexane-1,3-diol Chemical compound CC1(C)C(O)CCCC1(C)O KVEFSHKXYDKBDT-UHFFFAOYSA-N 0.000 claims 1
- XERUSAIHHJJPEU-UHFFFAOYSA-N 1,2,3,4-tetramethylcyclobut-3-ene-1,2-diol Chemical compound CC1=C(C)C(C)(O)C1(C)O XERUSAIHHJJPEU-UHFFFAOYSA-N 0.000 claims 1
- YXNHNTGBUZSERC-UHFFFAOYSA-N 1,2-dimethyl-4-methylidenecyclopentane-1,2-diol Chemical compound CC1(O)CC(=C)CC1(C)O YXNHNTGBUZSERC-UHFFFAOYSA-N 0.000 claims 1
- ZMZCAWLBJYOJCA-UHFFFAOYSA-N 1-ethyl-3-methylidenecyclopentane-1,2-diol Chemical compound CCC1(O)CCC(=C)C1O ZMZCAWLBJYOJCA-UHFFFAOYSA-N 0.000 claims 1
- 125000006021 1-methyl-2-propenyl group Chemical group 0.000 claims 1
- VJBHQLSYLSQKPV-UHFFFAOYSA-N 1-methyl-4-methylidenecyclohexane-1,2-diol Chemical compound CC1(O)CCC(=C)CC1O VJBHQLSYLSQKPV-UHFFFAOYSA-N 0.000 claims 1
- KCESCYYRIVTSNC-UHFFFAOYSA-N 1-phenylmethoxypropane-1,3-diol Chemical compound OCCC(O)OCC1=CC=CC=C1 KCESCYYRIVTSNC-UHFFFAOYSA-N 0.000 claims 1
- BWLMKPFFGYWBTQ-UHFFFAOYSA-N 2,3,3,4-tetramethylpentane-2,4-diol Chemical compound CC(C)(O)C(C)(C)C(C)(C)O BWLMKPFFGYWBTQ-UHFFFAOYSA-N 0.000 claims 1
- OZXFPRKPVJGAAN-UHFFFAOYSA-N 2,3-dimethylhepta-1,5-diene-3,4-diol Chemical compound CC=CC(O)C(C)(O)C(C)=C OZXFPRKPVJGAAN-UHFFFAOYSA-N 0.000 claims 1
- SNJAKWDPQBWXFM-UHFFFAOYSA-N 2,3-dimethylhex-5-ene-2,3-diol Chemical compound CC(C)(O)C(C)(O)CC=C SNJAKWDPQBWXFM-UHFFFAOYSA-N 0.000 claims 1
- GFISWRSQINPFOR-UHFFFAOYSA-N 2,4,4-trimethylhexane-2,5-diol Chemical compound CC(O)C(C)(C)CC(C)(C)O GFISWRSQINPFOR-UHFFFAOYSA-N 0.000 claims 1
- VEIKBKUFYVHZMQ-UHFFFAOYSA-N 2,4-dimethylhept-1-ene-3,5-diol Chemical compound CCC(O)C(C)C(O)C(C)=C VEIKBKUFYVHZMQ-UHFFFAOYSA-N 0.000 claims 1
- SOIMUGCEWXVOAG-UHFFFAOYSA-N 2,4-dimethylhept-3-ene-2,5-diol Chemical compound CCC(O)C(C)=CC(C)(C)O SOIMUGCEWXVOAG-UHFFFAOYSA-N 0.000 claims 1
- STIDYKNBYLYCLV-UHFFFAOYSA-N 2,5-dimethylhex-4-ene-2,3-diol Chemical compound CC(C)=CC(O)C(C)(C)O STIDYKNBYLYCLV-UHFFFAOYSA-N 0.000 claims 1
- RWBIPLGQWHLICN-UHFFFAOYSA-N 2,6-dimethylcyclohex-3-ene-1,2-diol Chemical compound CC1CC=CC(C)(O)C1O RWBIPLGQWHLICN-UHFFFAOYSA-N 0.000 claims 1
- ZEEFXBANXKVKTL-UHFFFAOYSA-N 2,6-dimethylhept-1-ene-3,5-diol Chemical compound CC(C)C(O)CC(O)C(C)=C ZEEFXBANXKVKTL-UHFFFAOYSA-N 0.000 claims 1
- YWPJDAROESEAOW-UHFFFAOYSA-N 2,6-dimethylhept-3-ene-2,6-diol Chemical compound CC(C)(O)CC=CC(C)(C)O YWPJDAROESEAOW-UHFFFAOYSA-N 0.000 claims 1
- NIPSREKNTNQZQR-UHFFFAOYSA-N 2,6-dimethylocta-1,6-diene-3,5-diol Chemical compound CC=C(C)C(O)CC(O)C(C)=C NIPSREKNTNQZQR-UHFFFAOYSA-N 0.000 claims 1
- WHADXGQXPFQETJ-UHFFFAOYSA-N 2,7-dimethylocta-1,7-diene-3,6-diol Chemical compound CC(=C)C(O)CCC(O)C(C)=C WHADXGQXPFQETJ-UHFFFAOYSA-N 0.000 claims 1
- DBPRVJUHXUGENI-UHFFFAOYSA-N 2-butan-2-ylbut-2-ene-1,4-diol Chemical compound CCC(C)C(CO)=CCO DBPRVJUHXUGENI-UHFFFAOYSA-N 0.000 claims 1
- QISKUFYBVVZTBL-UHFFFAOYSA-N 2-ethenyl-2,5-dimethylhex-3-ene-1,6-diol Chemical compound OCC(C)C=CC(C)(CO)C=C QISKUFYBVVZTBL-UHFFFAOYSA-N 0.000 claims 1
- UHHZVZMVISQDSP-UHFFFAOYSA-N 2-ethyl-2-methylpentane-1,5-diol Chemical compound CCC(C)(CO)CCCO UHHZVZMVISQDSP-UHFFFAOYSA-N 0.000 claims 1
- BLCPFLMQECTMOA-UHFFFAOYSA-N 2-methyl-2-propylbutane-1,4-diol Chemical compound CCCC(C)(CO)CCO BLCPFLMQECTMOA-UHFFFAOYSA-N 0.000 claims 1
- PUDBJRBLKIPCLF-UHFFFAOYSA-N 2-methylideneoctane-1,3-diol Chemical compound CCCCCC(O)C(=C)CO PUDBJRBLKIPCLF-UHFFFAOYSA-N 0.000 claims 1
- CCQIRDXXPRMICU-UHFFFAOYSA-N 2-methyloct-6-ene-3,5-diol Chemical compound CC=CC(O)CC(O)C(C)C CCQIRDXXPRMICU-UHFFFAOYSA-N 0.000 claims 1
- IEAGXQUAKGSSHK-UHFFFAOYSA-N 2-phenoxypropane-1,3-diol Chemical compound OCC(CO)OC1=CC=CC=C1 IEAGXQUAKGSSHK-UHFFFAOYSA-N 0.000 claims 1
- BVDKYMGISZDCIY-UHFFFAOYSA-N 2-phenylbutane-1,4-diol Chemical compound OCCC(CO)C1=CC=CC=C1 BVDKYMGISZDCIY-UHFFFAOYSA-N 0.000 claims 1
- DCGUEWMCEXFJFA-UHFFFAOYSA-N 2-prop-1-enylpentane-1,5-diol Chemical compound CC=CC(CO)CCCO DCGUEWMCEXFJFA-UHFFFAOYSA-N 0.000 claims 1
- GOMRSIIJSVKXAA-UHFFFAOYSA-N 2-prop-2-enylpentane-1,5-diol Chemical compound OCCCC(CO)CC=C GOMRSIIJSVKXAA-UHFFFAOYSA-N 0.000 claims 1
- SVDQILCKOOAUCM-UHFFFAOYSA-N 2-tert-butylbutane-1,3-diol Chemical compound CC(O)C(CO)C(C)(C)C SVDQILCKOOAUCM-UHFFFAOYSA-N 0.000 claims 1
- PVZIYUMDUJXVFU-UHFFFAOYSA-N 2-tert-butylpent-4-ene-1,3-diol Chemical compound CC(C)(C)C(CO)C(O)C=C PVZIYUMDUJXVFU-UHFFFAOYSA-N 0.000 claims 1
- GGSZAVAHZQDNSI-UHFFFAOYSA-N 3,3,4-trimethylhexane-2,4-diol Chemical compound CCC(C)(O)C(C)(C)C(C)O GGSZAVAHZQDNSI-UHFFFAOYSA-N 0.000 claims 1
- MEBICWCOCUEFSB-UHFFFAOYSA-N 3,3,4-trimethylhexane-2,5-diol Chemical compound CC(O)C(C)C(C)(C)C(C)O MEBICWCOCUEFSB-UHFFFAOYSA-N 0.000 claims 1
- FGIKETQPRLOEDV-UHFFFAOYSA-N 3,3,5-trimethylhexane-2,4-diol Chemical compound CC(C)C(O)C(C)(C)C(C)O FGIKETQPRLOEDV-UHFFFAOYSA-N 0.000 claims 1
- UHNLMOPHXKRLJG-UHFFFAOYSA-N 3,4-diethylcyclobut-3-ene-1,2-diol Chemical compound CCC1=C(CC)C(O)C1O UHNLMOPHXKRLJG-UHFFFAOYSA-N 0.000 claims 1
- DROBWWQYMGRZKW-UHFFFAOYSA-N 3,4-dimethylhex-3-ene-1,6-diol Chemical compound OCCC(C)=C(C)CCO DROBWWQYMGRZKW-UHFFFAOYSA-N 0.000 claims 1
- DRAYZQVMADCPOS-UHFFFAOYSA-N 3,4-dimethylhex-5-ene-2,3-diol Chemical compound CC(O)C(C)(O)C(C)C=C DRAYZQVMADCPOS-UHFFFAOYSA-N 0.000 claims 1
- WIHYIAQKNVOZQU-UHFFFAOYSA-N 3,5,5-trimethylhexane-2,4-diol Chemical compound CC(O)C(C)C(O)C(C)(C)C WIHYIAQKNVOZQU-UHFFFAOYSA-N 0.000 claims 1
- AABXGMAUGVUPTG-UHFFFAOYSA-N 3,5-dimethylhex-5-ene-2,3-diol Chemical compound CC(O)C(C)(O)CC(C)=C AABXGMAUGVUPTG-UHFFFAOYSA-N 0.000 claims 1
- COJIBPSALNCNJV-UHFFFAOYSA-N 3,6-dimethylcyclohex-4-ene-1,2-diol Chemical compound CC1C=CC(C)C(O)C1O COJIBPSALNCNJV-UHFFFAOYSA-N 0.000 claims 1
- HJDDHIRXSIYKMX-UHFFFAOYSA-N 3,6-dimethylocta-1,7-diene-3,6-diol Chemical compound C=CC(O)(C)CCC(C)(O)C=C HJDDHIRXSIYKMX-UHFFFAOYSA-N 0.000 claims 1
- VRYMDLHZMKZLNA-UHFFFAOYSA-N 3,7-dimethylocta-2,4-diene-1,7-diol Chemical compound OCC=C(C)C=CCC(C)(C)O VRYMDLHZMKZLNA-UHFFFAOYSA-N 0.000 claims 1
- DHKOTFKWYDDGLJ-UHFFFAOYSA-N 3-(1-phenylpropan-2-yloxy)propane-1,2-diol Chemical compound OCC(O)COC(C)CC1=CC=CC=C1 DHKOTFKWYDDGLJ-UHFFFAOYSA-N 0.000 claims 1
- YRUKRRMDLVHSDS-UHFFFAOYSA-N 3-ethenylcyclohexane-1,2-diol Chemical compound OC1CCCC(C=C)C1O YRUKRRMDLVHSDS-UHFFFAOYSA-N 0.000 claims 1
- CCKTVTGTWWNRHX-UHFFFAOYSA-N 3-ethylheptane-1,3-diol Chemical compound CCCCC(O)(CC)CCO CCKTVTGTWWNRHX-UHFFFAOYSA-N 0.000 claims 1
- ZGTHJSMNBWHFNG-UHFFFAOYSA-N 3-methyl-5-methylidenehept-1-ene-3,4-diol Chemical compound CCC(=C)C(O)C(C)(O)C=C ZGTHJSMNBWHFNG-UHFFFAOYSA-N 0.000 claims 1
- TUAGLJNGSSWWJF-UHFFFAOYSA-N 3-propan-2-ylpentane-1,5-diol Chemical compound OCCC(C(C)C)CCO TUAGLJNGSSWWJF-UHFFFAOYSA-N 0.000 claims 1
- HVTDFVFZDYCYJI-UHFFFAOYSA-N 3-propylhexane-1,3-diol Chemical compound CCCC(O)(CCC)CCO HVTDFVFZDYCYJI-UHFFFAOYSA-N 0.000 claims 1
- JIFDTGUUYALSLI-UHFFFAOYSA-N 3-tert-butylpentane-2,4-diol Chemical compound CC(O)C(C(C)O)C(C)(C)C JIFDTGUUYALSLI-UHFFFAOYSA-N 0.000 claims 1
- ITIXQCNEKAFDJN-UHFFFAOYSA-N 4,4-dimethylhepta-2,5-diene-1,7-diol Chemical compound OCC=CC(C)(C)C=CCO ITIXQCNEKAFDJN-UHFFFAOYSA-N 0.000 claims 1
- SRPWOVBZOUYCFO-UHFFFAOYSA-N 4,5,5-trimethylhexane-2,4-diol Chemical compound CC(O)CC(C)(O)C(C)(C)C SRPWOVBZOUYCFO-UHFFFAOYSA-N 0.000 claims 1
- NYLIWYGIONCENF-UHFFFAOYSA-N 4,6-dimethylhept-3-ene-2,6-diol Chemical compound CC(O)C=C(C)CC(C)(C)O NYLIWYGIONCENF-UHFFFAOYSA-N 0.000 claims 1
- JMWBJNQNXQPAFO-UHFFFAOYSA-N 4,6-dimethylhept-6-ene-2,5-diol Chemical compound CC(O)CC(C)C(O)C(C)=C JMWBJNQNXQPAFO-UHFFFAOYSA-N 0.000 claims 1
- ZZLCFHIKESPLTH-UHFFFAOYSA-N 4-Methylbiphenyl Chemical compound C1=CC(C)=CC=C1C1=CC=CC=C1 ZZLCFHIKESPLTH-UHFFFAOYSA-N 0.000 claims 1
- XLEGLCSIQAGSCJ-UHFFFAOYSA-N 4-ethenylcyclohex-3-ene-1,2-diol Chemical compound OC1CCC(C=C)=CC1O XLEGLCSIQAGSCJ-UHFFFAOYSA-N 0.000 claims 1
- DUECGFDNFCEUFG-UHFFFAOYSA-N 5,5-dimethylhept-6-ene-2,4-diol Chemical compound CC(O)CC(O)C(C)(C)C=C DUECGFDNFCEUFG-UHFFFAOYSA-N 0.000 claims 1
- JIBUNHUPNHOGAN-UHFFFAOYSA-N 5,6-dimethylhept-2-ene-1,4-diol Chemical compound CC(C)C(C)C(O)C=CCO JIBUNHUPNHOGAN-UHFFFAOYSA-N 0.000 claims 1
- OMSBTDBINXRBHF-UHFFFAOYSA-N 8-methylnona-4,6-diene-1,3-diol Chemical compound CC(C)C=CC=CC(O)CCO OMSBTDBINXRBHF-UHFFFAOYSA-N 0.000 claims 1
- JJMASYVPLWOTOK-UHFFFAOYSA-N CC(O)C(C)(C)CCCO Chemical compound CC(O)C(C)(C)CCCO JJMASYVPLWOTOK-UHFFFAOYSA-N 0.000 claims 1
- FPVDSADXCLSDQF-UHFFFAOYSA-N CC1(C)C=CCC(O)C1O Chemical compound CC1(C)C=CCC(O)C1O FPVDSADXCLSDQF-UHFFFAOYSA-N 0.000 claims 1
- PNVJTEVEZJCCFV-UHFFFAOYSA-N cyclooct-4-ene-1,2-diol Chemical compound OC1CCCC=CCC1O PNVJTEVEZJCCFV-UHFFFAOYSA-N 0.000 claims 1
- BIYRBPAUTLBNTB-UHFFFAOYSA-N cyclooctane-1,4-diol Chemical compound OC1CCCCC(O)CC1 BIYRBPAUTLBNTB-UHFFFAOYSA-N 0.000 claims 1
- VQWAZBMRMSMLPG-UHFFFAOYSA-N cyclopent-3-ene-1,2-diol Chemical compound OC1CC=CC1O VQWAZBMRMSMLPG-UHFFFAOYSA-N 0.000 claims 1
- KIWBPDUYBMNFTB-UHFFFAOYSA-M ethyl sulfate Chemical compound CCOS([O-])(=O)=O KIWBPDUYBMNFTB-UHFFFAOYSA-M 0.000 claims 1
- MHIBEGOZTWERHF-UHFFFAOYSA-N heptane-1,1-diol Chemical compound CCCCCCC(O)O MHIBEGOZTWERHF-UHFFFAOYSA-N 0.000 claims 1
- PHWDEIOWXOIEMQ-UHFFFAOYSA-N hexane-2,3-diol;hexane-3,4-diol Chemical compound CCCC(O)C(C)O.CCC(O)C(O)CC PHWDEIOWXOIEMQ-UHFFFAOYSA-N 0.000 claims 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims 1
- 125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 claims 1
- QFGOVAXBSPZRSN-UHFFFAOYSA-N oct-7-ene-2,5-diol Chemical compound CC(O)CCC(O)CC=C QFGOVAXBSPZRSN-UHFFFAOYSA-N 0.000 claims 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 1
- 229910021653 sulphate ion Inorganic materials 0.000 claims 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims 1
- 238000010438 heat treatment Methods 0.000 abstract description 15
- 230000002209 hydrophobic effect Effects 0.000 abstract description 11
- 150000002148 esters Chemical class 0.000 abstract description 10
- 150000001408 amides Chemical class 0.000 abstract description 4
- 125000001165 hydrophobic group Chemical group 0.000 abstract description 4
- 238000012545 processing Methods 0.000 abstract description 4
- 230000000670 limiting effect Effects 0.000 abstract description 2
- 238000000034 method Methods 0.000 description 243
- NJHQOQAEEYIWOB-UHFFFAOYSA-N 2-methyl-2-propan-2-ylpropane-1,3-diol Chemical compound CC(C)C(C)(CO)CO NJHQOQAEEYIWOB-UHFFFAOYSA-N 0.000 description 194
- 239000013543 active substance Substances 0.000 description 76
- 239000000047 product Substances 0.000 description 56
- 239000002253 acid Substances 0.000 description 47
- ZTQSAGDEMFDKMZ-UHFFFAOYSA-N Butyraldehyde Chemical compound CCCC=O ZTQSAGDEMFDKMZ-UHFFFAOYSA-N 0.000 description 40
- 238000006243 chemical reaction Methods 0.000 description 40
- 239000011541 reaction mixture Substances 0.000 description 34
- 239000000243 solution Substances 0.000 description 33
- 239000007788 liquid Substances 0.000 description 31
- 125000003545 alkoxy group Chemical group 0.000 description 28
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 24
- 229940015975 1,2-hexanediol Drugs 0.000 description 23
- 239000000654 additive Substances 0.000 description 23
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 22
- 239000002245 particle Substances 0.000 description 22
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 21
- 238000009833 condensation Methods 0.000 description 21
- 230000005494 condensation Effects 0.000 description 21
- 239000007858 starting material Substances 0.000 description 21
- 101100298295 Drosophila melanogaster flfl gene Proteins 0.000 description 20
- AMIMRNSIRUDHCM-UHFFFAOYSA-N Isopropylaldehyde Chemical compound CC(C)C=O AMIMRNSIRUDHCM-UHFFFAOYSA-N 0.000 description 20
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 20
- QTBSBXVTEAMEQO-UHFFFAOYSA-N acetic acid Substances CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 20
- 239000002738 chelating agent Substances 0.000 description 20
- 230000002829 reductive effect Effects 0.000 description 20
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 19
- 239000003795 chemical substances by application Substances 0.000 description 19
- HGBOYTHUEUWSSQ-UHFFFAOYSA-N valeric aldehyde Natural products CCCCC=O HGBOYTHUEUWSSQ-UHFFFAOYSA-N 0.000 description 19
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 18
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 18
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 18
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 18
- 150000005690 diesters Chemical class 0.000 description 17
- 239000002270 dispersing agent Substances 0.000 description 17
- 239000012535 impurity Substances 0.000 description 16
- 238000010992 reflux Methods 0.000 description 16
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 15
- 238000004821 distillation Methods 0.000 description 15
- 230000000694 effects Effects 0.000 description 15
- FHKSXSQHXQEMOK-UHFFFAOYSA-N hexane-1,2-diol Chemical compound CCCCC(O)CO FHKSXSQHXQEMOK-UHFFFAOYSA-N 0.000 description 15
- 150000000185 1,3-diols Chemical class 0.000 description 14
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 14
- 150000001299 aldehydes Chemical class 0.000 description 14
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 14
- 230000008569 process Effects 0.000 description 14
- 238000003756 stirring Methods 0.000 description 14
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 13
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 13
- AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 description 12
- 125000002252 acyl group Chemical group 0.000 description 12
- 150000001412 amines Chemical class 0.000 description 12
- 239000000463 material Substances 0.000 description 12
- 150000003839 salts Chemical class 0.000 description 12
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 11
- 150000007513 acids Chemical class 0.000 description 11
- 239000008187 granular material Substances 0.000 description 11
- 125000001140 1,4-phenylene group Chemical group [H]C1=C([H])C([*:2])=C([H])C([H])=C1[*:1] 0.000 description 10
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical group C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 10
- 239000010410 layer Substances 0.000 description 10
- 239000004014 plasticizer Substances 0.000 description 10
- XDOFQFKRPWOURC-UHFFFAOYSA-N 16-methylheptadecanoic acid Chemical compound CC(C)CCCCCCCCCCCCCCC(O)=O XDOFQFKRPWOURC-UHFFFAOYSA-N 0.000 description 9
- 150000002081 enamines Chemical class 0.000 description 9
- 238000001914 filtration Methods 0.000 description 9
- 239000004615 ingredient Substances 0.000 description 9
- 229910052757 nitrogen Inorganic materials 0.000 description 9
- 230000009467 reduction Effects 0.000 description 9
- RMEZNLDVMHNLHR-UHFFFAOYSA-N 2-ethylbutane-1,2-diol Chemical compound CCC(O)(CC)CO RMEZNLDVMHNLHR-UHFFFAOYSA-N 0.000 description 8
- SQAJRDHPLTWZQT-UHFFFAOYSA-N 3-methylhexane-1,6-diol Chemical compound OCCC(C)CCCO SQAJRDHPLTWZQT-UHFFFAOYSA-N 0.000 description 8
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 8
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 8
- 230000015572 biosynthetic process Effects 0.000 description 8
- KSMVZQYAVGTKIV-UHFFFAOYSA-N decanal Chemical compound CCCCCCCCCC=O KSMVZQYAVGTKIV-UHFFFAOYSA-N 0.000 description 8
- 238000002156 mixing Methods 0.000 description 8
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 8
- 235000021313 oleic acid Nutrition 0.000 description 8
- 239000011734 sodium Substances 0.000 description 8
- 125000001424 substituent group Chemical group 0.000 description 8
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 7
- 150000000190 1,4-diols Chemical class 0.000 description 7
- JVZZUPJFERSVRN-UHFFFAOYSA-N 2-methyl-2-propylpropane-1,3-diol Chemical compound CCCC(C)(CO)CO JVZZUPJFERSVRN-UHFFFAOYSA-N 0.000 description 7
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 7
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 7
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 7
- 239000005642 Oleic acid Substances 0.000 description 7
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 7
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 7
- SEQDDYPDSLOBDC-UHFFFAOYSA-N Temazepam Chemical compound N=1C(O)C(=O)N(C)C2=CC=C(Cl)C=C2C=1C1=CC=CC=C1 SEQDDYPDSLOBDC-UHFFFAOYSA-N 0.000 description 7
- 230000000996 additive effect Effects 0.000 description 7
- 125000003342 alkenyl group Chemical group 0.000 description 7
- 229910052786 argon Inorganic materials 0.000 description 7
- 125000003118 aryl group Chemical group 0.000 description 7
- 239000003054 catalyst Substances 0.000 description 7
- 239000003599 detergent Substances 0.000 description 7
- 230000007062 hydrolysis Effects 0.000 description 7
- 238000006460 hydrolysis reaction Methods 0.000 description 7
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 7
- 230000008018 melting Effects 0.000 description 7
- 238000002844 melting Methods 0.000 description 7
- 239000002736 nonionic surfactant Substances 0.000 description 7
- 229920000642 polymer Polymers 0.000 description 7
- 239000003381 stabilizer Substances 0.000 description 7
- 239000000758 substrate Substances 0.000 description 7
- 238000012546 transfer Methods 0.000 description 7
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 7
- KBPLFHHGFOOTCA-UHFFFAOYSA-N 1-Octanol Chemical compound CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 description 6
- JULNEFHJBRHDSM-UHFFFAOYSA-N 2-ethylbutane-1,3-diol Chemical compound CCC(CO)C(C)O JULNEFHJBRHDSM-UHFFFAOYSA-N 0.000 description 6
- VVOISBSEMFDYNE-UHFFFAOYSA-N 2-propan-2-ylpropane-1,3-diol Chemical compound CC(C)C(CO)CO VVOISBSEMFDYNE-UHFFFAOYSA-N 0.000 description 6
- VGRZISGVNOKTQU-UHFFFAOYSA-N 4-(hydroxymethyl)cyclohexan-1-ol Chemical compound OCC1CCC(O)CC1 VGRZISGVNOKTQU-UHFFFAOYSA-N 0.000 description 6
- LNKQKVILEYEGNG-UHFFFAOYSA-N 6-methylheptane-1,3-diol Chemical compound CC(C)CCC(O)CCO LNKQKVILEYEGNG-UHFFFAOYSA-N 0.000 description 6
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 6
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 6
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 6
- RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 description 6
- 239000003963 antioxidant agent Substances 0.000 description 6
- 235000006708 antioxidants Nutrition 0.000 description 6
- 235000015278 beef Nutrition 0.000 description 6
- 150000001728 carbonyl compounds Chemical class 0.000 description 6
- 235000015165 citric acid Nutrition 0.000 description 6
- 150000002576 ketones Chemical class 0.000 description 6
- 229940098779 methanesulfonic acid Drugs 0.000 description 6
- VAMXMNNIEUEQDV-UHFFFAOYSA-N methyl anthranilate Chemical compound COC(=O)C1=CC=CC=C1N VAMXMNNIEUEQDV-UHFFFAOYSA-N 0.000 description 6
- 150000007524 organic acids Chemical class 0.000 description 6
- DTUQWGWMVIHBKE-UHFFFAOYSA-N phenylacetaldehyde Chemical compound O=CCC1=CC=CC=C1 DTUQWGWMVIHBKE-UHFFFAOYSA-N 0.000 description 6
- 229920001451 polypropylene glycol Polymers 0.000 description 6
- 238000000746 purification Methods 0.000 description 6
- 239000000376 reactant Substances 0.000 description 6
- 229910052708 sodium Inorganic materials 0.000 description 6
- 238000003786 synthesis reaction Methods 0.000 description 6
- 238000010189 synthetic method Methods 0.000 description 6
- 239000003760 tallow Substances 0.000 description 6
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 6
- 238000005292 vacuum distillation Methods 0.000 description 6
- IOZFUGDROBQPNP-UHFFFAOYSA-N 1-methylcyclohexane-1,2-diol Chemical compound CC1(O)CCCCC1O IOZFUGDROBQPNP-UHFFFAOYSA-N 0.000 description 5
- GCQIRPJZONARRR-UHFFFAOYSA-N 2,4-dimethylpentane-2,3-diol Chemical compound CC(C)C(O)C(C)(C)O GCQIRPJZONARRR-UHFFFAOYSA-N 0.000 description 5
- QWGRWMMWNDWRQN-UHFFFAOYSA-N 2-methylpropane-1,3-diol Chemical compound OCC(C)CO QWGRWMMWNDWRQN-UHFFFAOYSA-N 0.000 description 5
- SXFJDZNJHVPHPH-UHFFFAOYSA-N 3-methylpentane-1,5-diol Chemical compound OCCC(C)CCO SXFJDZNJHVPHPH-UHFFFAOYSA-N 0.000 description 5
- GUNIIZNPUZBGEZ-UHFFFAOYSA-N 4-methylheptane-3,5-diol Chemical compound CCC(O)C(C)C(O)CC GUNIIZNPUZBGEZ-UHFFFAOYSA-N 0.000 description 5
- PESGUTZAXXQWJP-UHFFFAOYSA-N 4-methylhexane-1,3-diol Chemical compound CCC(C)C(O)CCO PESGUTZAXXQWJP-UHFFFAOYSA-N 0.000 description 5
- CXIXEMXKCTZXTQ-UHFFFAOYSA-N 5-methylhexane-1,3-diol Chemical compound CC(C)CC(O)CCO CXIXEMXKCTZXTQ-UHFFFAOYSA-N 0.000 description 5
- ARBBSOILKXUDJE-UHFFFAOYSA-N 5-methylhexane-1,4-diol Chemical compound CC(C)C(O)CCCO ARBBSOILKXUDJE-UHFFFAOYSA-N 0.000 description 5
- 238000005804 alkylation reaction Methods 0.000 description 5
- 238000009835 boiling Methods 0.000 description 5
- 230000015556 catabolic process Effects 0.000 description 5
- 230000003197 catalytic effect Effects 0.000 description 5
- 239000003093 cationic surfactant Substances 0.000 description 5
- 238000006731 degradation reaction Methods 0.000 description 5
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 5
- 150000002190 fatty acyls Chemical class 0.000 description 5
- 150000002191 fatty alcohols Chemical class 0.000 description 5
- 238000007429 general method Methods 0.000 description 5
- 229940093915 gynecological organic acid Drugs 0.000 description 5
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 5
- 230000003287 optical effect Effects 0.000 description 5
- 235000005985 organic acids Nutrition 0.000 description 5
- 230000003647 oxidation Effects 0.000 description 5
- 238000007254 oxidation reaction Methods 0.000 description 5
- 239000003002 pH adjusting agent Substances 0.000 description 5
- 229920001223 polyethylene glycol Polymers 0.000 description 5
- 150000003856 quaternary ammonium compounds Chemical class 0.000 description 5
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 5
- 239000000341 volatile oil Substances 0.000 description 5
- 238000005406 washing Methods 0.000 description 5
- DGASMILFPABBSL-UHFFFAOYSA-N 2,3-dimethylhexane-1,5-diol Chemical compound CC(O)CC(C)C(C)CO DGASMILFPABBSL-UHFFFAOYSA-N 0.000 description 4
- QJZNFTWNCBRRRA-UHFFFAOYSA-N 2-ethylhexane-1,5-diol Chemical compound CCC(CO)CCC(C)O QJZNFTWNCBRRRA-UHFFFAOYSA-N 0.000 description 4
- YLZIMEJTDZWVJG-UHFFFAOYSA-N 2-heptylundecanoic acid Chemical compound CCCCCCCCCC(C(O)=O)CCCCCCC YLZIMEJTDZWVJG-UHFFFAOYSA-N 0.000 description 4
- KDLLLWNHOHIBKV-UHFFFAOYSA-N 2-methyl-2-propylbutane-1,3-diol Chemical compound CCCC(C)(CO)C(C)O KDLLLWNHOHIBKV-UHFFFAOYSA-N 0.000 description 4
- LTKOHFVYDMREPG-UHFFFAOYSA-N 2-phenoxyoctadecanoic acid Chemical compound CCCCCCCCCCCCCCCCC(C(O)=O)OC1=CC=CC=C1 LTKOHFVYDMREPG-UHFFFAOYSA-N 0.000 description 4
- SGEQQFLWQSODRK-UHFFFAOYSA-N 2-propylpentane-1,3-diol Chemical compound CCCC(CO)C(O)CC SGEQQFLWQSODRK-UHFFFAOYSA-N 0.000 description 4
- UMBQWJHNUSDWMU-UHFFFAOYSA-N 2-tert-butyl-2-methylpropane-1,3-diol Chemical compound CC(C)(C)C(C)(CO)CO UMBQWJHNUSDWMU-UHFFFAOYSA-N 0.000 description 4
- WZWLILKCFOVQQK-UHFFFAOYSA-N 3,5-dimethylhexane-1,4-diol Chemical compound CC(C)C(O)C(C)CCO WZWLILKCFOVQQK-UHFFFAOYSA-N 0.000 description 4
- UXLJPCSSECQHKN-UHFFFAOYSA-N 3-propan-2-ylpentane-1,4-diol Chemical compound CC(C)C(C(C)O)CCO UXLJPCSSECQHKN-UHFFFAOYSA-N 0.000 description 4
- KRWAMCIJJYNDDV-UHFFFAOYSA-N 3-propylpentane-2,4-diol Chemical compound CCCC(C(C)O)C(C)O KRWAMCIJJYNDDV-UHFFFAOYSA-N 0.000 description 4
- IKHGUXGNUITLKF-UHFFFAOYSA-N Acetaldehyde Chemical compound CC=O IKHGUXGNUITLKF-UHFFFAOYSA-N 0.000 description 4
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical group O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 4
- RGHNJXZEOKUKBD-SQOUGZDYSA-N D-gluconic acid Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C(O)=O RGHNJXZEOKUKBD-SQOUGZDYSA-N 0.000 description 4
- 241000402754 Erythranthe moschata Species 0.000 description 4
- GLZPCOQZEFWAFX-UHFFFAOYSA-N Geraniol Chemical compound CC(C)=CCCC(C)=CCO GLZPCOQZEFWAFX-UHFFFAOYSA-N 0.000 description 4
- AEMRFAOFKBGASW-UHFFFAOYSA-N Glycolic acid Chemical compound OCC(O)=O AEMRFAOFKBGASW-UHFFFAOYSA-N 0.000 description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 4
- SIKJAQJRHWYJAI-UHFFFAOYSA-N Indole Chemical compound C1=CC=C2NC=CC2=C1 SIKJAQJRHWYJAI-UHFFFAOYSA-N 0.000 description 4
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 4
- 239000002202 Polyethylene glycol Substances 0.000 description 4
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 4
- 239000007868 Raney catalyst Substances 0.000 description 4
- 229910000564 Raney nickel Inorganic materials 0.000 description 4
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical group OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 4
- 230000029936 alkylation Effects 0.000 description 4
- 150000008064 anhydrides Chemical class 0.000 description 4
- HSMPSHPWCOOUJH-UHFFFAOYSA-N anilinyl Chemical group [NH]C1=CC=CC=C1 HSMPSHPWCOOUJH-UHFFFAOYSA-N 0.000 description 4
- 239000002518 antifoaming agent Substances 0.000 description 4
- 230000008901 benefit Effects 0.000 description 4
- UORVGPXVDQYIDP-UHFFFAOYSA-N borane Chemical compound B UORVGPXVDQYIDP-UHFFFAOYSA-N 0.000 description 4
- 229910010277 boron hydride Inorganic materials 0.000 description 4
- UWTDFICHZKXYAC-UHFFFAOYSA-N boron;oxolane Chemical compound [B].C1CCOC1 UWTDFICHZKXYAC-UHFFFAOYSA-N 0.000 description 4
- 239000007795 chemical reaction product Substances 0.000 description 4
- 239000003638 chemical reducing agent Substances 0.000 description 4
- 239000000460 chlorine Substances 0.000 description 4
- QMVPMAAFGQKVCJ-UHFFFAOYSA-N citronellol Chemical compound OCCC(C)CCC=C(C)C QMVPMAAFGQKVCJ-UHFFFAOYSA-N 0.000 description 4
- HFJRKMMYBMWEAD-UHFFFAOYSA-N dodecanal Chemical compound CCCCCCCCCCCC=O HFJRKMMYBMWEAD-UHFFFAOYSA-N 0.000 description 4
- 238000001035 drying Methods 0.000 description 4
- 239000000975 dye Substances 0.000 description 4
- 125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 description 4
- LNTHITQWFMADLM-UHFFFAOYSA-N gallic acid Chemical compound OC(=O)C1=CC(O)=C(O)C(O)=C1 LNTHITQWFMADLM-UHFFFAOYSA-N 0.000 description 4
- 150000004678 hydrides Chemical class 0.000 description 4
- 238000005984 hydrogenation reaction Methods 0.000 description 4
- WPFVBOQKRVRMJB-UHFFFAOYSA-N hydroxycitronellal Chemical compound O=CCC(C)CCCC(C)(C)O WPFVBOQKRVRMJB-UHFFFAOYSA-N 0.000 description 4
- 150000002596 lactones Chemical class 0.000 description 4
- SYSQUGFVNFXIIT-UHFFFAOYSA-N n-[4-(1,3-benzoxazol-2-yl)phenyl]-4-nitrobenzenesulfonamide Chemical class C1=CC([N+](=O)[O-])=CC=C1S(=O)(=O)NC1=CC=C(C=2OC3=CC=CC=C3N=2)C=C1 SYSQUGFVNFXIIT-UHFFFAOYSA-N 0.000 description 4
- NUJGJRNETVAIRJ-UHFFFAOYSA-N octanal Chemical compound CCCCCCCC=O NUJGJRNETVAIRJ-UHFFFAOYSA-N 0.000 description 4
- 239000003921 oil Substances 0.000 description 4
- 235000019198 oils Nutrition 0.000 description 4
- 230000036961 partial effect Effects 0.000 description 4
- 229920001748 polybutylene Polymers 0.000 description 4
- 159000000000 sodium salts Chemical class 0.000 description 4
- 230000000087 stabilizing effect Effects 0.000 description 4
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 4
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 description 4
- 239000010457 zeolite Substances 0.000 description 4
- BQNJVHGCZBNKBG-SNVBAGLBSA-N (3r)-3-phenylbutane-1,3-diol Chemical compound OCC[C@](O)(C)C1=CC=CC=C1 BQNJVHGCZBNKBG-SNVBAGLBSA-N 0.000 description 3
- 150000000180 1,2-diols Chemical class 0.000 description 3
- ZTYXIZHVBQAHBQ-UHFFFAOYSA-N 10-propan-2-yloxyoctadecanoic acid Chemical class CCCCCCCCC(OC(C)C)CCCCCCCCC(O)=O ZTYXIZHVBQAHBQ-UHFFFAOYSA-N 0.000 description 3
- FCTDGGNCLZXZAX-UHFFFAOYSA-N 2,5-dimethylhexane-1,4-diol Chemical compound CC(C)C(O)CC(C)CO FCTDGGNCLZXZAX-UHFFFAOYSA-N 0.000 description 3
- PLWQDACNHXVVLS-UHFFFAOYSA-N 3-ethyl-2-methylpentane-2,4-diol Chemical compound CCC(C(C)O)C(C)(C)O PLWQDACNHXVVLS-UHFFFAOYSA-N 0.000 description 3
- YNHJRRTYFZNWGC-UHFFFAOYSA-N 4,4-dimethylhexane-1,3-diol Chemical compound CCC(C)(C)C(O)CCO YNHJRRTYFZNWGC-UHFFFAOYSA-N 0.000 description 3
- RJLNJAFYQUXNPP-UHFFFAOYSA-N 4,5-dimethylhexane-1,3-diol Chemical compound CC(C)C(C)C(O)CCO RJLNJAFYQUXNPP-UHFFFAOYSA-N 0.000 description 3
- LLLVZDVNHNWSDS-UHFFFAOYSA-N 4-methylidene-3,5-dioxabicyclo[5.2.2]undeca-1(9),7,10-triene-2,6-dione Chemical compound C1(C2=CC=C(C(=O)OC(=C)O1)C=C2)=O LLLVZDVNHNWSDS-UHFFFAOYSA-N 0.000 description 3
- LDJFUTSVFHJIAC-UHFFFAOYSA-N 5,5-dimethylcyclohexane-1,3-diol Chemical compound CC1(C)CC(O)CC(O)C1 LDJFUTSVFHJIAC-UHFFFAOYSA-N 0.000 description 3
- YZMQAPHVUWXTLY-UHFFFAOYSA-N 5,5-dimethylhexane-1,4-diol Chemical compound CC(C)(C)C(O)CCCO YZMQAPHVUWXTLY-UHFFFAOYSA-N 0.000 description 3
- CSEOAAUANZHLIA-UHFFFAOYSA-N 7-methyloct-7-ene-2,5-diol Chemical compound CC(O)CCC(O)CC(C)=C CSEOAAUANZHLIA-UHFFFAOYSA-N 0.000 description 3
- KXDHJXZQYSOELW-UHFFFAOYSA-N Carbamic acid Chemical class NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 description 3
- ZNZYKNKBJPZETN-WELNAUFTSA-N Dialdehyde 11678 Chemical compound N1C2=CC=CC=C2C2=C1[C@H](C[C@H](/C(=C/O)C(=O)OC)[C@@H](C=C)C=O)NCC2 ZNZYKNKBJPZETN-WELNAUFTSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- DBVJJBKOTRCVKF-UHFFFAOYSA-N Etidronic acid Chemical compound OP(=O)(O)C(O)(C)P(O)(O)=O DBVJJBKOTRCVKF-UHFFFAOYSA-N 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- FKNQFGJONOIPTF-UHFFFAOYSA-N Sodium cation Chemical compound [Na+] FKNQFGJONOIPTF-UHFFFAOYSA-N 0.000 description 3
- 235000021355 Stearic acid Nutrition 0.000 description 3
- BGNXCDMCOKJUMV-UHFFFAOYSA-N Tert-Butylhydroquinone Chemical compound CC(C)(C)C1=CC(O)=CC=C1O BGNXCDMCOKJUMV-UHFFFAOYSA-N 0.000 description 3
- 238000005054 agglomeration Methods 0.000 description 3
- 230000002776 aggregation Effects 0.000 description 3
- 238000005882 aldol condensation reaction Methods 0.000 description 3
- 150000001336 alkenes Chemical class 0.000 description 3
- 125000002947 alkylene group Chemical group 0.000 description 3
- 239000012298 atmosphere Substances 0.000 description 3
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 3
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
- 239000000828 canola oil Substances 0.000 description 3
- 235000019519 canola oil Nutrition 0.000 description 3
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 3
- 239000000969 carrier Substances 0.000 description 3
- 125000002091 cationic group Chemical group 0.000 description 3
- 239000007859 condensation product Substances 0.000 description 3
- 239000012043 crude product Substances 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical class CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 3
- 150000002118 epoxides Chemical class 0.000 description 3
- 125000001924 fatty-acyl group Chemical group 0.000 description 3
- 238000004508 fractional distillation Methods 0.000 description 3
- JMOLZNNXZPAGBH-UHFFFAOYSA-N hexyldecanoic acid Chemical compound CCCCCCCCC(C(O)=O)CCCCCC JMOLZNNXZPAGBH-UHFFFAOYSA-N 0.000 description 3
- 150000002430 hydrocarbons Chemical class 0.000 description 3
- 239000000155 melt Substances 0.000 description 3
- 229940102398 methyl anthranilate Drugs 0.000 description 3
- KVWWIYGFBYDJQC-UHFFFAOYSA-N methyl dihydrojasmonate Chemical compound CCCCCC1C(CC(=O)OC)CCC1=O KVWWIYGFBYDJQC-UHFFFAOYSA-N 0.000 description 3
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 3
- 239000003607 modifier Substances 0.000 description 3
- SFDZETWZUCDYMD-UHFFFAOYSA-N monosodium acetylide Chemical class [Na+].[C-]#C SFDZETWZUCDYMD-UHFFFAOYSA-N 0.000 description 3
- 239000012299 nitrogen atmosphere Substances 0.000 description 3
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical class CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 3
- HOWLAKMIIWUJEJ-UHFFFAOYSA-N octane-2,4-diol Chemical compound CCCCC(O)CC(C)O HOWLAKMIIWUJEJ-UHFFFAOYSA-N 0.000 description 3
- 239000012044 organic layer Substances 0.000 description 3
- 125000006353 oxyethylene group Chemical group 0.000 description 3
- 230000020477 pH reduction Effects 0.000 description 3
- 238000005192 partition Methods 0.000 description 3
- 229940044654 phenolsulfonic acid Drugs 0.000 description 3
- 229940100595 phenylacetaldehyde Drugs 0.000 description 3
- 229920000728 polyester Polymers 0.000 description 3
- 239000002243 precursor Substances 0.000 description 3
- 239000011164 primary particle Substances 0.000 description 3
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 3
- 239000011780 sodium chloride Substances 0.000 description 3
- FVAUCKIRQBBSSJ-UHFFFAOYSA-M sodium iodide Chemical compound [Na+].[I-] FVAUCKIRQBBSSJ-UHFFFAOYSA-M 0.000 description 3
- 238000003860 storage Methods 0.000 description 3
- 238000006467 substitution reaction Methods 0.000 description 3
- KKEYFWRCBNTPAC-UHFFFAOYSA-L terephthalate(2-) Chemical compound [O-]C(=O)C1=CC=C(C([O-])=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-L 0.000 description 3
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 3
- 238000004809 thin layer chromatography Methods 0.000 description 3
- DCTMXCOHGKSXIZ-UHFFFAOYSA-N (R)-1,3-Octanediol Chemical compound CCCCCC(O)CCO DCTMXCOHGKSXIZ-UHFFFAOYSA-N 0.000 description 2
- BJEPYKJPYRNKOW-REOHCLBHSA-N (S)-malic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O BJEPYKJPYRNKOW-REOHCLBHSA-N 0.000 description 2
- SPEUIVXLLWOEMJ-UHFFFAOYSA-N 1,1-dimethoxyethane Chemical compound COC(C)OC SPEUIVXLLWOEMJ-UHFFFAOYSA-N 0.000 description 2
- RBACIKXCRWGCBB-UHFFFAOYSA-N 1,2-Epoxybutane Chemical compound CCC1CO1 RBACIKXCRWGCBB-UHFFFAOYSA-N 0.000 description 2
- BGZGQDDKQNYZID-UHFFFAOYSA-N 1-(hydroxymethyl)cyclohexan-1-ol Chemical compound OCC1(O)CCCCC1 BGZGQDDKQNYZID-UHFFFAOYSA-N 0.000 description 2
- NPZGQIIAVOOHNM-UHFFFAOYSA-N 1-cyclohex-3-en-1-ylethane-1,2-diol Chemical compound OCC(O)C1CCC=CC1 NPZGQIIAVOOHNM-UHFFFAOYSA-N 0.000 description 2
- FNELHTCOGDXUFU-UHFFFAOYSA-N 10-methoxy-octadecanoic acid Chemical class CCCCCCCCC(OC)CCCCCCCCC(O)=O FNELHTCOGDXUFU-UHFFFAOYSA-N 0.000 description 2
- 238000001644 13C nuclear magnetic resonance spectroscopy Methods 0.000 description 2
- FVNFTAQJARARPD-UHFFFAOYSA-N 18-phenyloctadecanoic acid Chemical compound OC(=O)CCCCCCCCCCCCCCCCCC1=CC=CC=C1 FVNFTAQJARARPD-UHFFFAOYSA-N 0.000 description 2
- 238000005160 1H NMR spectroscopy Methods 0.000 description 2
- MAYREUPTYJOUHK-UHFFFAOYSA-N 2,3-dimethylhexane-1,4-diol Chemical compound CCC(O)C(C)C(C)CO MAYREUPTYJOUHK-UHFFFAOYSA-N 0.000 description 2
- FDGBSYKWQLUSRA-UHFFFAOYSA-N 2,4,5-trimethylhexane-2,4-diol Chemical compound CC(C)C(C)(O)CC(C)(C)O FDGBSYKWQLUSRA-UHFFFAOYSA-N 0.000 description 2
- CVCPRQBVFCVAQA-UHFFFAOYSA-N 2,4-dimethylhex-5-ene-2,4-diol Chemical class CC(C)(O)CC(C)(O)C=C CVCPRQBVFCVAQA-UHFFFAOYSA-N 0.000 description 2
- XTYRJOKNCLJXJF-UHFFFAOYSA-N 2,4-dimethylhexane-1,5-diol Chemical compound OCC(C)CC(C)C(C)O XTYRJOKNCLJXJF-UHFFFAOYSA-N 0.000 description 2
- WRFXXJKURVTLSY-UHFFFAOYSA-N 2,6-dimethyloctan-2-ol Chemical compound CCC(C)CCCC(C)(C)O WRFXXJKURVTLSY-UHFFFAOYSA-N 0.000 description 2
- KIVZOYUIGURFOK-UHFFFAOYSA-N 2-(3-methylbutan-2-yloxy)propane-1,3-diol Chemical compound CC(C)C(C)OC(CO)CO KIVZOYUIGURFOK-UHFFFAOYSA-N 0.000 description 2
- SZZINZURZKQZLG-UHFFFAOYSA-N 2-(4-chlorobutoxy)oxane Chemical compound ClCCCCOC1CCCCO1 SZZINZURZKQZLG-UHFFFAOYSA-N 0.000 description 2
- IQCASZIDTNHBIW-UHFFFAOYSA-N 2-(pentoxymethyl)oxirane Chemical compound CCCCCOCC1CO1 IQCASZIDTNHBIW-UHFFFAOYSA-N 0.000 description 2
- NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 description 2
- CEEWUMDNMIAOEE-UHFFFAOYSA-N 2-but-3-en-2-yl-2-methylbutane-1,3-diol Chemical compound CC(O)C(C)(CO)C(C)C=C CEEWUMDNMIAOEE-UHFFFAOYSA-N 0.000 description 2
- XMVBHZBLHNOQON-UHFFFAOYSA-N 2-butyl-1-octanol Chemical compound CCCCCCC(CO)CCCC XMVBHZBLHNOQON-UHFFFAOYSA-N 0.000 description 2
- DSKYSDCYIODJPC-UHFFFAOYSA-N 2-butyl-2-ethylpropane-1,3-diol Chemical compound CCCCC(CC)(CO)CO DSKYSDCYIODJPC-UHFFFAOYSA-N 0.000 description 2
- OARDBPIZDHVTCK-UHFFFAOYSA-N 2-butyloctanoic acid Chemical compound CCCCCCC(C(O)=O)CCCC OARDBPIZDHVTCK-UHFFFAOYSA-N 0.000 description 2
- YRNNTRRZQYKYGB-UHFFFAOYSA-N 2-chloro-1,1,1-triethoxy-2-methoxyethane Chemical compound CCOC(OCC)(OCC)C(Cl)OC YRNNTRRZQYKYGB-UHFFFAOYSA-N 0.000 description 2
- UPFQUOWXDNUBNS-UHFFFAOYSA-N 2-ethyl-2,3-dimethylbutane-1,4-diol Chemical compound CCC(C)(CO)C(C)CO UPFQUOWXDNUBNS-UHFFFAOYSA-N 0.000 description 2
- IQCDIRVZHUDSHF-UHFFFAOYSA-N 2-ethyl-2-methylpentane-1,4-diol Chemical compound CCC(C)(CO)CC(C)O IQCDIRVZHUDSHF-UHFFFAOYSA-N 0.000 description 2
- SNHWVZAWIAOEPS-UHFFFAOYSA-N 2-hydroxy-2-phenyloctadecanoic acid Chemical compound CCCCCCCCCCCCCCCCC(O)(C(O)=O)C1=CC=CC=C1 SNHWVZAWIAOEPS-UHFFFAOYSA-N 0.000 description 2
- RLHGFJMGWQXPBW-UHFFFAOYSA-N 2-hydroxy-3-(1h-imidazol-5-ylmethyl)benzamide Chemical compound NC(=O)C1=CC=CC(CC=2NC=NC=2)=C1O RLHGFJMGWQXPBW-UHFFFAOYSA-N 0.000 description 2
- UBNIJVDFUWZODL-UHFFFAOYSA-N 2-methylheptane-1,2-diol Chemical compound CCCCCC(C)(O)CO UBNIJVDFUWZODL-UHFFFAOYSA-N 0.000 description 2
- WRMNZCZEMHIOCP-UHFFFAOYSA-N 2-phenylethanol Chemical compound OCCC1=CC=CC=C1 WRMNZCZEMHIOCP-UHFFFAOYSA-N 0.000 description 2
- UDIPIOHLDFSMLR-UHFFFAOYSA-N 2-phenylmethoxypropane-1,3-diol Chemical compound OCC(CO)OCC1=CC=CC=C1 UDIPIOHLDFSMLR-UHFFFAOYSA-N 0.000 description 2
- QLXSWIFREIGVAB-UHFFFAOYSA-N 3,3-dimethylhexane-1,5-diol Chemical compound CC(O)CC(C)(C)CCO QLXSWIFREIGVAB-UHFFFAOYSA-N 0.000 description 2
- LTIMVARCDQKGLB-UHFFFAOYSA-N 3,4-dimethylcyclopentane-1,2-diol Chemical compound CC1CC(O)C(O)C1C LTIMVARCDQKGLB-UHFFFAOYSA-N 0.000 description 2
- MDVHFDLZNABHTQ-UHFFFAOYSA-N 3,5-dimethylhexane-1,5-diol Chemical compound OCCC(C)CC(C)(C)O MDVHFDLZNABHTQ-UHFFFAOYSA-N 0.000 description 2
- MMINFSMURORWKH-UHFFFAOYSA-N 3,6-dioxabicyclo[6.2.2]dodeca-1(10),8,11-triene-2,7-dione Chemical group O=C1OCCOC(=O)C2=CC=C1C=C2 MMINFSMURORWKH-UHFFFAOYSA-N 0.000 description 2
- DLHQZZUEERVIGQ-UHFFFAOYSA-N 3,7-dimethyl-3-octanol Chemical compound CCC(C)(O)CCCC(C)C DLHQZZUEERVIGQ-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
- HYBDKQBWJNPOJR-UHFFFAOYSA-N 3-(2-methylbutoxy)propane-1,2-diol Chemical compound CCC(C)COCC(O)CO HYBDKQBWJNPOJR-UHFFFAOYSA-N 0.000 description 2
- DLRLJRUDHDJCSW-UHFFFAOYSA-N 3-ethyl-4-methylcyclobutane-1,2-diol Chemical compound CCC1C(C)C(O)C1O DLRLJRUDHDJCSW-UHFFFAOYSA-N 0.000 description 2
- FKPLZJCSXGKJNK-UHFFFAOYSA-N 4,4-dimethylpentane-2,3-diol Chemical compound CC(O)C(O)C(C)(C)C FKPLZJCSXGKJNK-UHFFFAOYSA-N 0.000 description 2
- PJZGKZGHIBCAIV-UHFFFAOYSA-N 4,5-dimethylhexane-1,5-diol Chemical compound CC(O)(C)C(C)CCCO PJZGKZGHIBCAIV-UHFFFAOYSA-N 0.000 description 2
- ORMHZBNNECIKOH-UHFFFAOYSA-N 4-(4-hydroxy-4-methylpentyl)cyclohex-3-ene-1-carbaldehyde Chemical compound CC(C)(O)CCCC1=CCC(C=O)CC1 ORMHZBNNECIKOH-UHFFFAOYSA-N 0.000 description 2
- PFDFWGVYIJZTCJ-UHFFFAOYSA-N 4-ethylhexane-1,3-diol Chemical compound CCC(CC)C(O)CCO PFDFWGVYIJZTCJ-UHFFFAOYSA-N 0.000 description 2
- NTPLXRHDUXRPNE-UHFFFAOYSA-N 4-methoxyacetophenone Chemical compound COC1=CC=C(C(C)=O)C=C1 NTPLXRHDUXRPNE-UHFFFAOYSA-N 0.000 description 2
- BUTCMXUVVHPZEP-UHFFFAOYSA-N 4-methylideneoctane-3,5-diol Chemical compound CCCC(O)C(=C)C(O)CC BUTCMXUVVHPZEP-UHFFFAOYSA-N 0.000 description 2
- DCDISHARGWMOMM-UHFFFAOYSA-N 4-phenylbutane-1,3-diol Chemical compound OCCC(O)CC1=CC=CC=C1 DCDISHARGWMOMM-UHFFFAOYSA-N 0.000 description 2
- MBZRJSQZCBXRGK-UHFFFAOYSA-N 4-tert-Butylcyclohexyl acetate Chemical compound CC(=O)OC1CCC(C(C)(C)C)CC1 MBZRJSQZCBXRGK-UHFFFAOYSA-N 0.000 description 2
- SDXDTTKJHSDBHF-UHFFFAOYSA-N 5,7-dimethyldecanoic acid Chemical compound CCCC(C)CC(C)CCCC(O)=O SDXDTTKJHSDBHF-UHFFFAOYSA-N 0.000 description 2
- CNGYZEMWVAWWOB-VAWYXSNFSA-N 5-[[4-anilino-6-[bis(2-hydroxyethyl)amino]-1,3,5-triazin-2-yl]amino]-2-[(e)-2-[4-[[4-anilino-6-[bis(2-hydroxyethyl)amino]-1,3,5-triazin-2-yl]amino]-2-sulfophenyl]ethenyl]benzenesulfonic acid Chemical compound N=1C(NC=2C=C(C(\C=C\C=3C(=CC(NC=4N=C(N=C(NC=5C=CC=CC=5)N=4)N(CCO)CCO)=CC=3)S(O)(=O)=O)=CC=2)S(O)(=O)=O)=NC(N(CCO)CCO)=NC=1NC1=CC=CC=C1 CNGYZEMWVAWWOB-VAWYXSNFSA-N 0.000 description 2
- 229940100484 5-chloro-2-methyl-4-isothiazolin-3-one Drugs 0.000 description 2
- MWOXKHJWGMCHOA-UHFFFAOYSA-N 5-methylcycloheptane-1,3-diol Chemical compound CC1CCC(O)CC(O)C1 MWOXKHJWGMCHOA-UHFFFAOYSA-N 0.000 description 2
- YOXJGPGAEKHOFF-UHFFFAOYSA-N 5-methylcycloheptane-1,4-diol Chemical compound CC1CCC(O)CCC1O YOXJGPGAEKHOFF-UHFFFAOYSA-N 0.000 description 2
- ZNYRFEPBTVGZDN-UHFFFAOYSA-N 5S,6S-epoxy-15R-hydroxy-ETE Chemical compound COCCOCCOCCOCCO ZNYRFEPBTVGZDN-UHFFFAOYSA-N 0.000 description 2
- HFFAMNTYCKXUMP-UHFFFAOYSA-N 6-methylcycloheptane-1,4-diol Chemical compound CC1CC(O)CCC(O)C1 HFFAMNTYCKXUMP-UHFFFAOYSA-N 0.000 description 2
- GSOCFGPQNAFJLB-UHFFFAOYSA-N 6-methylheptane-1,2-diol Chemical compound CC(C)CCCC(O)CO GSOCFGPQNAFJLB-UHFFFAOYSA-N 0.000 description 2
- GJEZBVHHZQAEDB-UHFFFAOYSA-N 6-oxabicyclo[3.1.0]hexane Chemical compound C1CCC2OC21 GJEZBVHHZQAEDB-UHFFFAOYSA-N 0.000 description 2
- 244000283070 Abies balsamea Species 0.000 description 2
- 235000007173 Abies balsamea Nutrition 0.000 description 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 2
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 2
- ZCTQGTTXIYCGGC-UHFFFAOYSA-N Benzyl salicylate Chemical compound OC1=CC=CC=C1C(=O)OCC1=CC=CC=C1 ZCTQGTTXIYCGGC-UHFFFAOYSA-N 0.000 description 2
- LVDKZNITIUWNER-UHFFFAOYSA-N Bronopol Chemical compound OCC(Br)(CO)[N+]([O-])=O LVDKZNITIUWNER-UHFFFAOYSA-N 0.000 description 2
- 229910014033 C-OH Inorganic materials 0.000 description 2
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 2
- FKUPPRZPSYCDRS-UHFFFAOYSA-N Cyclopentadecanolide Chemical compound O=C1CCCCCCCCCCCCCCO1 FKUPPRZPSYCDRS-UHFFFAOYSA-N 0.000 description 2
- 229910014570 C—OH Inorganic materials 0.000 description 2
- RGHNJXZEOKUKBD-UHFFFAOYSA-N D-gluconic acid Natural products OCC(O)C(O)C(O)C(O)C(O)=O RGHNJXZEOKUKBD-UHFFFAOYSA-N 0.000 description 2
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 2
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 2
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
- GLZPCOQZEFWAFX-YFHOEESVSA-N Geraniol Natural products CC(C)=CCC\C(C)=C/CO GLZPCOQZEFWAFX-YFHOEESVSA-N 0.000 description 2
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 2
- QPCDCPDFJACHGM-UHFFFAOYSA-N N,N-bis{2-[bis(carboxymethyl)amino]ethyl}glycine Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(=O)O)CCN(CC(O)=O)CC(O)=O QPCDCPDFJACHGM-UHFFFAOYSA-N 0.000 description 2
- AMQJEAYHLZJPGS-UHFFFAOYSA-N N-Pentanol Chemical compound CCCCCO AMQJEAYHLZJPGS-UHFFFAOYSA-N 0.000 description 2
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 2
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 2
- 235000019483 Peanut oil Nutrition 0.000 description 2
- KFSLWBXXFJQRDL-UHFFFAOYSA-N Peracetic acid Chemical compound CC(=O)OO KFSLWBXXFJQRDL-UHFFFAOYSA-N 0.000 description 2
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 2
- 239000004721 Polyphenylene oxide Substances 0.000 description 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
- QOSMNYMQXIVWKY-UHFFFAOYSA-N Propyl levulinate Chemical compound CCCOC(=O)CCC(C)=O QOSMNYMQXIVWKY-UHFFFAOYSA-N 0.000 description 2
- 235000019774 Rice Bran oil Nutrition 0.000 description 2
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 2
- WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 description 2
- 235000019486 Sunflower oil Nutrition 0.000 description 2
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 2
- 229910021536 Zeolite Inorganic materials 0.000 description 2
- LUSFFPXRDZKBMF-YUMQZZPRSA-N [(1s,3s)-3-(hydroxymethyl)cyclohexyl]methanol Chemical compound OC[C@H]1CCC[C@H](CO)C1 LUSFFPXRDZKBMF-YUMQZZPRSA-N 0.000 description 2
- YSMAMMWBEBTNEH-UHFFFAOYSA-N [2-[2-[bis(phosphonomethyl)amino]ethoxy]ethyl-(phosphonomethyl)amino]methylphosphonic acid Chemical compound OP(O)(=O)CN(CP(O)(O)=O)CCOCCN(CP(O)(O)=O)CP(O)(O)=O YSMAMMWBEBTNEH-UHFFFAOYSA-N 0.000 description 2
- 239000006096 absorbing agent Substances 0.000 description 2
- 229940022663 acetate Drugs 0.000 description 2
- 230000010933 acylation Effects 0.000 description 2
- 238000005917 acylation reaction Methods 0.000 description 2
- IGODOXYLBBXFDW-UHFFFAOYSA-N alpha-Terpinyl acetate Chemical compound CC(=O)OC(C)(C)C1CCC(C)=CC1 IGODOXYLBBXFDW-UHFFFAOYSA-N 0.000 description 2
- BJEPYKJPYRNKOW-UHFFFAOYSA-N alpha-hydroxysuccinic acid Natural products OC(=O)C(O)CC(O)=O BJEPYKJPYRNKOW-UHFFFAOYSA-N 0.000 description 2
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 2
- 150000003863 ammonium salts Chemical class 0.000 description 2
- 125000000129 anionic group Chemical group 0.000 description 2
- 239000003945 anionic surfactant Substances 0.000 description 2
- 230000000844 anti-bacterial effect Effects 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 125000000732 arylene group Chemical group 0.000 description 2
- 125000004429 atom Chemical group 0.000 description 2
- 239000003899 bactericide agent Substances 0.000 description 2
- 239000002585 base Substances 0.000 description 2
- HUMNYLRZRPPJDN-UHFFFAOYSA-N benzaldehyde Chemical compound O=CC1=CC=CC=C1 HUMNYLRZRPPJDN-UHFFFAOYSA-N 0.000 description 2
- QUKGYYKBILRGFE-UHFFFAOYSA-N benzyl acetate Chemical compound CC(=O)OCC1=CC=CC=C1 QUKGYYKBILRGFE-UHFFFAOYSA-N 0.000 description 2
- 229960004217 benzyl alcohol Drugs 0.000 description 2
- SESFRYSPDFLNCH-UHFFFAOYSA-N benzyl benzoate Chemical compound C=1C=CC=CC=1C(=O)OCC1=CC=CC=C1 SESFRYSPDFLNCH-UHFFFAOYSA-N 0.000 description 2
- 238000007664 blowing Methods 0.000 description 2
- CDQSJQSWAWPGKG-UHFFFAOYSA-N butane-1,1-diol Chemical compound CCCC(O)O CDQSJQSWAWPGKG-UHFFFAOYSA-N 0.000 description 2
- 150000001721 carbon Chemical group 0.000 description 2
- 239000001569 carbon dioxide Substances 0.000 description 2
- 229910002092 carbon dioxide Inorganic materials 0.000 description 2
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 2
- 238000009903 catalytic hydrogenation reaction Methods 0.000 description 2
- HQKQRXZEXPXXIG-VJOHVRBBSA-N chembl2333940 Chemical compound C1[C@]23[C@H](C)CC[C@H]3C(C)(C)[C@H]1[C@@](OC(C)=O)(C)CC2 HQKQRXZEXPXXIG-VJOHVRBBSA-N 0.000 description 2
- 239000003153 chemical reaction reagent Substances 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
- JOZKFWLRHCDGJA-UHFFFAOYSA-N citronellol acetate Chemical compound CC(=O)OCCC(C)CCC=C(C)C JOZKFWLRHCDGJA-UHFFFAOYSA-N 0.000 description 2
- 239000003240 coconut oil Substances 0.000 description 2
- 235000019864 coconut oil Nutrition 0.000 description 2
- 238000004040 coloring Methods 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 239000012141 concentrate Substances 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 229910052802 copper Inorganic materials 0.000 description 2
- 239000010949 copper Substances 0.000 description 2
- 235000005687 corn oil Nutrition 0.000 description 2
- 239000002285 corn oil Substances 0.000 description 2
- 125000004122 cyclic group Chemical group 0.000 description 2
- HGCIXCUEYOPUTN-UHFFFAOYSA-N cyclohexene Chemical class C1CCC=CC1 HGCIXCUEYOPUTN-UHFFFAOYSA-N 0.000 description 2
- LPIQUOYDBNQMRZ-UHFFFAOYSA-N cyclopentene Chemical class C1CC=CC1 LPIQUOYDBNQMRZ-UHFFFAOYSA-N 0.000 description 2
- 230000008021 deposition Effects 0.000 description 2
- FLKPEMZONWLCSK-UHFFFAOYSA-N diethyl phthalate Chemical compound CCOC(=O)C1=CC=CC=C1C(=O)OCC FLKPEMZONWLCSK-UHFFFAOYSA-N 0.000 description 2
- GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical compound C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 description 2
- 239000003085 diluting agent Substances 0.000 description 2
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 2
- 239000012153 distilled water Substances 0.000 description 2
- 150000002085 enols Chemical group 0.000 description 2
- RRAFCDWBNXTKKO-UHFFFAOYSA-N eugenol Chemical compound COC1=CC(CC=C)=CC=C1O RRAFCDWBNXTKKO-UHFFFAOYSA-N 0.000 description 2
- 239000012467 final product Substances 0.000 description 2
- 239000012634 fragment Substances 0.000 description 2
- 238000013467 fragmentation Methods 0.000 description 2
- 238000006062 fragmentation reaction Methods 0.000 description 2
- 239000003205 fragrance Substances 0.000 description 2
- 229940074391 gallic acid Drugs 0.000 description 2
- 235000004515 gallic acid Nutrition 0.000 description 2
- 239000000174 gluconic acid Substances 0.000 description 2
- 235000012208 gluconic acid Nutrition 0.000 description 2
- 239000008172 hydrogenated vegetable oil Substances 0.000 description 2
- SHFJWMWCIHQNCP-UHFFFAOYSA-M hydron;tetrabutylazanium;sulfate Chemical compound OS([O-])(=O)=O.CCCC[N+](CCCC)(CCCC)CCCC SHFJWMWCIHQNCP-UHFFFAOYSA-M 0.000 description 2
- 230000033444 hydroxylation Effects 0.000 description 2
- 238000005805 hydroxylation reaction Methods 0.000 description 2
- PQNFLJBBNBOBRQ-UHFFFAOYSA-N indane Chemical compound C1=CC=C2CCCC2=C1 PQNFLJBBNBOBRQ-UHFFFAOYSA-N 0.000 description 2
- PZOUSPYUWWUPPK-UHFFFAOYSA-N indole Natural products CC1=CC=CC2=C1C=CN2 PZOUSPYUWWUPPK-UHFFFAOYSA-N 0.000 description 2
- RKJUIXBNRJVNHR-UHFFFAOYSA-N indolenine Natural products C1=CC=C2CC=NC2=C1 RKJUIXBNRJVNHR-UHFFFAOYSA-N 0.000 description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 description 2
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 2
- SDQFDHOLCGWZPU-UHFFFAOYSA-N lilial Chemical compound O=CC(C)CC1=CC=C(C(C)(C)C)C=C1 SDQFDHOLCGWZPU-UHFFFAOYSA-N 0.000 description 2
- CDOSHBSSFJOMGT-UHFFFAOYSA-N linalool Chemical compound CC(C)=CCCC(C)(O)C=C CDOSHBSSFJOMGT-UHFFFAOYSA-N 0.000 description 2
- UWKAYLJWKGQEPM-LBPRGKRZSA-N linalyl acetate Chemical compound CC(C)=CCC[C@](C)(C=C)OC(C)=O UWKAYLJWKGQEPM-LBPRGKRZSA-N 0.000 description 2
- 239000001630 malic acid Substances 0.000 description 2
- 235000011090 malic acid Nutrition 0.000 description 2
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 2
- 229910052753 mercury Inorganic materials 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- 229910052759 nickel Inorganic materials 0.000 description 2
- 229910017604 nitric acid Inorganic materials 0.000 description 2
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 2
- GYHFUZHODSMOHU-UHFFFAOYSA-N nonanal Chemical compound CCCCCCCCC=O GYHFUZHODSMOHU-UHFFFAOYSA-N 0.000 description 2
- ZHZUUUXZIMHEKC-UHFFFAOYSA-N oct-7-ene-1,5-diol Chemical compound OCCCCC(O)CC=C ZHZUUUXZIMHEKC-UHFFFAOYSA-N 0.000 description 2
- AEIJTFQOBWATKX-UHFFFAOYSA-N octane-1,2-diol Chemical compound CCCCCCC(O)CO AEIJTFQOBWATKX-UHFFFAOYSA-N 0.000 description 2
- YDKXPCQXDSHQTE-UHFFFAOYSA-N octane-2,2-diol Chemical class CCCCCCC(C)(O)O YDKXPCQXDSHQTE-UHFFFAOYSA-N 0.000 description 2
- XMTUJCWABCYSIV-UHFFFAOYSA-N octane-2,3-diol Chemical compound CCCCCC(O)C(C)O XMTUJCWABCYSIV-UHFFFAOYSA-N 0.000 description 2
- UJWVPVVMYOBBIY-UHFFFAOYSA-N octane-3,4-diol Chemical compound CCCCC(O)C(O)CC UJWVPVVMYOBBIY-UHFFFAOYSA-N 0.000 description 2
- 229960002969 oleic acid Drugs 0.000 description 2
- 239000012074 organic phase Substances 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 229910000487 osmium oxide Inorganic materials 0.000 description 2
- JIWAALDUIFCBLV-UHFFFAOYSA-N oxoosmium Chemical compound [Os]=O JIWAALDUIFCBLV-UHFFFAOYSA-N 0.000 description 2
- WURFKUQACINBSI-UHFFFAOYSA-M ozonide Chemical compound [O]O[O-] WURFKUQACINBSI-UHFFFAOYSA-M 0.000 description 2
- ZRSNZINYAWTAHE-UHFFFAOYSA-N p-methoxybenzaldehyde Chemical compound COC1=CC=C(C=O)C=C1 ZRSNZINYAWTAHE-UHFFFAOYSA-N 0.000 description 2
- 238000004806 packaging method and process Methods 0.000 description 2
- 239000000312 peanut oil Substances 0.000 description 2
- 239000012071 phase Substances 0.000 description 2
- 239000003444 phase transfer catalyst Substances 0.000 description 2
- LCPDWSOZIOUXRV-UHFFFAOYSA-N phenoxyacetic acid Chemical compound OC(=O)COC1=CC=CC=C1 LCPDWSOZIOUXRV-UHFFFAOYSA-N 0.000 description 2
- PTMHPRAIXMAOOB-UHFFFAOYSA-N phosphoramidic acid Chemical class NP(O)(O)=O PTMHPRAIXMAOOB-UHFFFAOYSA-N 0.000 description 2
- 229910052698 phosphorus Inorganic materials 0.000 description 2
- 239000011574 phosphorus Substances 0.000 description 2
- 229920000570 polyether Polymers 0.000 description 2
- 239000011591 potassium Substances 0.000 description 2
- 229910052700 potassium Inorganic materials 0.000 description 2
- 239000003755 preservative agent Substances 0.000 description 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 2
- 239000010453 quartz Substances 0.000 description 2
- 125000001453 quaternary ammonium group Chemical group 0.000 description 2
- 239000008165 rice bran oil Substances 0.000 description 2
- 235000005713 safflower oil Nutrition 0.000 description 2
- 239000003813 safflower oil Substances 0.000 description 2
- YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 239000012312 sodium hydride Substances 0.000 description 2
- 229910000104 sodium hydride Inorganic materials 0.000 description 2
- 229910052938 sodium sulfate Inorganic materials 0.000 description 2
- 235000011152 sodium sulphate Nutrition 0.000 description 2
- 239000011877 solvent mixture Substances 0.000 description 2
- 239000003549 soybean oil Substances 0.000 description 2
- 235000012424 soybean oil Nutrition 0.000 description 2
- 238000001228 spectrum Methods 0.000 description 2
- 239000002600 sunflower oil Substances 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- 239000011975 tartaric acid Substances 0.000 description 2
- 235000002906 tartaric acid Nutrition 0.000 description 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
- 235000015112 vegetable and seed oil Nutrition 0.000 description 2
- 239000008158 vegetable oil Substances 0.000 description 2
- 239000002699 waste material Substances 0.000 description 2
- 239000003232 water-soluble binding agent Substances 0.000 description 2
- DCYPPXGEIQTVPI-RNFRBKRXSA-N (1r,2r)-cycloheptane-1,2-diol Chemical compound O[C@@H]1CCCCC[C@H]1O DCYPPXGEIQTVPI-RNFRBKRXSA-N 0.000 description 1
- AIWBBAVNOGRJMH-JGVFFNPUSA-N (1r,2s)-cyclooct-3-ene-1,2-diol Chemical compound O[C@@H]1CCCCC=C[C@@H]1O AIWBBAVNOGRJMH-JGVFFNPUSA-N 0.000 description 1
- BIYRBPAUTLBNTB-OCAPTIKFSA-N (1r,4s)-cyclooctane-1,4-diol Chemical compound O[C@H]1CCCC[C@@H](O)CC1 BIYRBPAUTLBNTB-OCAPTIKFSA-N 0.000 description 1
- WHOZNOZYMBRCBL-OUKQBFOZSA-N (2E)-2-Tetradecenal Chemical compound CCCCCCCCCCC\C=C\C=O WHOZNOZYMBRCBL-OUKQBFOZSA-N 0.000 description 1
- HLCSDJLATUNSSI-JXMROGBWSA-N (2e)-3,7-dimethylocta-2,6-dienenitrile Chemical compound CC(C)=CCC\C(C)=C\C#N HLCSDJLATUNSSI-JXMROGBWSA-N 0.000 description 1
- BVDKYMGISZDCIY-JTQLQIEISA-N (2r)-2-phenylbutane-1,4-diol Chemical compound OCC[C@@H](CO)C1=CC=CC=C1 BVDKYMGISZDCIY-JTQLQIEISA-N 0.000 description 1
- SZCWBURCISJFEZ-UHFFFAOYSA-N (3-hydroxy-2,2-dimethylpropyl) 3-hydroxy-2,2-dimethylpropanoate Chemical compound OCC(C)(C)COC(=O)C(C)(C)CO SZCWBURCISJFEZ-UHFFFAOYSA-N 0.000 description 1
- VSRVCSJJKWDZSH-UHFFFAOYSA-N (3-pentyloxan-4-yl) acetate Chemical compound CCCCCC1COCCC1OC(C)=O VSRVCSJJKWDZSH-UHFFFAOYSA-N 0.000 description 1
- 239000001490 (3R)-3,7-dimethylocta-1,6-dien-3-ol Substances 0.000 description 1
- 239000001147 (3aR,5aS,9aS,9bR)-3a,6,6,9a-tetramethyl-2,4,5,5a,7,8,9,9b-octahydro-1H-benzo[e][1]benzofuran Substances 0.000 description 1
- 239000001724 (4,8-dimethyl-2-propan-2-ylidene-3,3a,4,5,6,8a-hexahydro-1H-azulen-6-yl) acetate Substances 0.000 description 1
- QTHIKVMVWXLPKQ-ONEGZZNKSA-N (E)-oct-5-ene-1,3-diol Chemical compound CC\C=C\CC(O)CCO QTHIKVMVWXLPKQ-ONEGZZNKSA-N 0.000 description 1
- QMVPMAAFGQKVCJ-SNVBAGLBSA-N (R)-(+)-citronellol Natural products OCC[C@H](C)CCC=C(C)C QMVPMAAFGQKVCJ-SNVBAGLBSA-N 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
- UFLHIIWVXFIJGU-ARJAWSKDSA-N (Z)-hex-3-en-1-ol Chemical compound CC\C=C/CCO UFLHIIWVXFIJGU-ARJAWSKDSA-N 0.000 description 1
- QTHIKVMVWXLPKQ-TUUFMJSCSA-N (Z,3R)-oct-5-ene-1,3-diol Chemical compound CC\C=C/C[C@@H](O)CCO QTHIKVMVWXLPKQ-TUUFMJSCSA-N 0.000 description 1
- KHQDWCKZXLWDNM-KPKJPENVSA-N (e)-2-ethyl-4-(2,2,3-trimethylcyclopent-3-en-1-yl)but-2-en-1-ol Chemical compound CC\C(CO)=C/CC1CC=C(C)C1(C)C KHQDWCKZXLWDNM-KPKJPENVSA-N 0.000 description 1
- LPJKDVHMUUZHRY-KVVVOXFISA-N (z)-octadec-9-en-1-amine;hydrochloride Chemical compound Cl.CCCCCCCC\C=C/CCCCCCCCN LPJKDVHMUUZHRY-KVVVOXFISA-N 0.000 description 1
- DHKHKXVYLBGOIT-UHFFFAOYSA-N 1,1-Diethoxyethane Chemical compound CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 description 1
- PAAZPARNPHGIKF-UHFFFAOYSA-N 1,2-dibromoethane Chemical compound BrCCBr PAAZPARNPHGIKF-UHFFFAOYSA-N 0.000 description 1
- 229940031723 1,2-octanediol Drugs 0.000 description 1
- VNQNXQYZMPJLQX-UHFFFAOYSA-N 1,3,5-tris[(3,5-ditert-butyl-4-hydroxyphenyl)methyl]-1,3,5-triazinane-2,4,6-trione Chemical compound CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(CN2C(N(CC=3C=C(C(O)=C(C=3)C(C)(C)C)C(C)(C)C)C(=O)N(CC=3C=C(C(O)=C(C=3)C(C)(C)C)C(C)(C)C)C2=O)=O)=C1 VNQNXQYZMPJLQX-UHFFFAOYSA-N 0.000 description 1
- 125000001989 1,3-phenylene group Chemical group [H]C1=C([H])C([*:1])=C([H])C([*:2])=C1[H] 0.000 description 1
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- 125000004955 1,4-cyclohexylene group Chemical group [H]C1([H])C([H])([H])C([H])([*:1])C([H])([H])C([H])([H])C1([H])[*:2] 0.000 description 1
- 125000004958 1,4-naphthylene group Chemical group 0.000 description 1
- VDBHOHJWUDKDRW-UHFFFAOYSA-N 1-(1,1,2,3,3,6-hexamethyl-2h-inden-5-yl)ethanone Chemical compound CC1=C(C(C)=O)C=C2C(C)(C)C(C)C(C)(C)C2=C1 VDBHOHJWUDKDRW-UHFFFAOYSA-N 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
- VPKMGDRERYMTJX-CMDGGOBGSA-N 1-(2,6,6-Trimethyl-2-cyclohexen-1-yl)-1-penten-3-one Chemical compound CCC(=O)\C=C\C1C(C)=CCCC1(C)C VPKMGDRERYMTJX-CMDGGOBGSA-N 0.000 description 1
- CRIGTVCBMUKRSL-FNORWQNLSA-N 1-(2,6,6-trimethylcyclohex-2-en-1-yl)but-2-enone Chemical compound C\C=C\C(=O)C1C(C)=CCCC1(C)C CRIGTVCBMUKRSL-FNORWQNLSA-N 0.000 description 1
- JIQXRLOYKOJECL-UHFFFAOYSA-N 1-(2-chloroethoxy)-2-methoxyethane Chemical compound COCCOCCCl JIQXRLOYKOJECL-UHFFFAOYSA-N 0.000 description 1
- MWYYZQGERICSFY-UHFFFAOYSA-N 1-(2-hydroxypentoxy)pentan-2-ol Chemical compound CCCC(O)COCC(O)CCC MWYYZQGERICSFY-UHFFFAOYSA-N 0.000 description 1
- TUSDEZXZIZRFGC-UHFFFAOYSA-N 1-O-galloyl-3,6-(R)-HHDP-beta-D-glucose Natural products OC1C(O2)COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC1C(O)C2OC(=O)C1=CC(O)=C(O)C(O)=C1 TUSDEZXZIZRFGC-UHFFFAOYSA-N 0.000 description 1
- QUMXDOLUJCHOAY-UHFFFAOYSA-N 1-Phenylethyl acetate Chemical compound CC(=O)OC(C)C1=CC=CC=C1 QUMXDOLUJCHOAY-UHFFFAOYSA-N 0.000 description 1
- IMRYETFJNLKUHK-SJKOYZFVSA-N 1-[(2r,3r)-1,1,2,6-tetramethyl-3-propan-2-yl-2,3-dihydroinden-5-yl]ethanone Chemical compound CC1=C(C(C)=O)C=C2[C@H](C(C)C)[C@@H](C)C(C)(C)C2=C1 IMRYETFJNLKUHK-SJKOYZFVSA-N 0.000 description 1
- LSXKDWGTSHCFPP-UHFFFAOYSA-N 1-bromoheptane Chemical compound CCCCCCCBr LSXKDWGTSHCFPP-UHFFFAOYSA-N 0.000 description 1
- BEKHLAMVNMJKKD-UHFFFAOYSA-N 1-cyclopentylpropane-1,2-diol Chemical compound CC(O)C(O)C1CCCC1 BEKHLAMVNMJKKD-UHFFFAOYSA-N 0.000 description 1
- PWQCJGYCAFMCFT-UHFFFAOYSA-N 1-ethenyl-2-ethylcyclobutane-1,2-diol Chemical compound CCC1(O)CCC1(O)C=C PWQCJGYCAFMCFT-UHFFFAOYSA-N 0.000 description 1
- LOMFGTMAAGBFNZ-UHFFFAOYSA-N 1-ethyl-5,5-dimethylcyclohexane-1,3-diol Chemical compound CCC1(O)CC(O)CC(C)(C)C1 LOMFGTMAAGBFNZ-UHFFFAOYSA-N 0.000 description 1
- JAVLHTSDGLGMMP-UHFFFAOYSA-N 1-ethylcyclohexane-1,3-diol Chemical compound CCC1(O)CCCC(O)C1 JAVLHTSDGLGMMP-UHFFFAOYSA-N 0.000 description 1
- DHBADUTWLRKGCV-UHFFFAOYSA-N 1-methylcyclohept-5-ene-1,3-diol Chemical compound CC1(O)CC=CCC(O)C1 DHBADUTWLRKGCV-UHFFFAOYSA-N 0.000 description 1
- YXZQSMBYXJWRSP-UHFFFAOYSA-N 1-methylcyclohexane-1,4-diol Chemical compound CC1(O)CCC(O)CC1 YXZQSMBYXJWRSP-UHFFFAOYSA-N 0.000 description 1
- CVZBNRSGTBIHPO-UHFFFAOYSA-N 1-methylcyclopentane-1,2-diol Chemical compound CC1(O)CCCC1O CVZBNRSGTBIHPO-UHFFFAOYSA-N 0.000 description 1
- QQLIGMASAVJVON-UHFFFAOYSA-N 1-naphthalen-1-ylethanone Chemical compound C1=CC=C2C(C(=O)C)=CC=CC2=C1 QQLIGMASAVJVON-UHFFFAOYSA-N 0.000 description 1
- JLIDVCMBCGBIEY-UHFFFAOYSA-N 1-penten-3-one Chemical compound CCC(=O)C=C JLIDVCMBCGBIEY-UHFFFAOYSA-N 0.000 description 1
- AOPDRZXCEAKHHW-UHFFFAOYSA-N 1-pentoxypentane Chemical class CCCCCOCCCCC AOPDRZXCEAKHHW-UHFFFAOYSA-N 0.000 description 1
- RIPIXXDNCPWNKK-UHFFFAOYSA-N 1-pentoxypropane-1,3-diol Chemical compound CCCCCOC(O)CCO RIPIXXDNCPWNKK-UHFFFAOYSA-N 0.000 description 1
- 239000001875 1-phenylethyl acetate Substances 0.000 description 1
- RRVFYOSEKOTFOG-UHFFFAOYSA-N 1-phenylpropane-1,3-diol Chemical compound OCCC(O)C1=CC=CC=C1 RRVFYOSEKOTFOG-UHFFFAOYSA-N 0.000 description 1
- OQNBTEMKXZJVPO-UHFFFAOYSA-N 1-prop-1-en-2-ylcyclopentane-1,2-diol Chemical compound CC(=C)C1(O)CCCC1O OQNBTEMKXZJVPO-UHFFFAOYSA-N 0.000 description 1
- OFHHDSQXFXLTKC-UHFFFAOYSA-N 10-undecenal Chemical compound C=CCCCCCCCCC=O OFHHDSQXFXLTKC-UHFFFAOYSA-N 0.000 description 1
- UWHGIFFBLHNNEZ-UHFFFAOYSA-N 2,2,3,3-tetramethylbutane-1,4-diol Chemical compound OCC(C)(C)C(C)(C)CO UWHGIFFBLHNNEZ-UHFFFAOYSA-N 0.000 description 1
- QPBYBLZYMNWGMO-UHFFFAOYSA-N 2,2,3-trimethyloxirane Chemical compound CC1OC1(C)C QPBYBLZYMNWGMO-UHFFFAOYSA-N 0.000 description 1
- RFXKPBYAIZDRIL-UHFFFAOYSA-N 2,2-dimethylcyclohexane-1,3-diol Chemical compound CC1(C)C(O)CCCC1O RFXKPBYAIZDRIL-UHFFFAOYSA-N 0.000 description 1
- UYZUYVVDLFXCCV-UHFFFAOYSA-N 2,2-dimethylhexane-1,6-diol Chemical compound OCC(C)(C)CCCCO UYZUYVVDLFXCCV-UHFFFAOYSA-N 0.000 description 1
- IIKPOMFCVYWGDB-UHFFFAOYSA-N 2,2-dimethylhexane-3,4-diol Chemical compound CCC(O)C(O)C(C)(C)C IIKPOMFCVYWGDB-UHFFFAOYSA-N 0.000 description 1
- JOEVSHWHIUYQJN-UHFFFAOYSA-N 2,3,3-trimethylbutane-1,2-diol Chemical compound CC(C)(C)C(C)(O)CO JOEVSHWHIUYQJN-UHFFFAOYSA-N 0.000 description 1
- VZYDKJOUEPFKMW-UHFFFAOYSA-N 2,3-dihydroxybenzenesulfonic acid Chemical compound OC1=CC=CC(S(O)(=O)=O)=C1O VZYDKJOUEPFKMW-UHFFFAOYSA-N 0.000 description 1
- KWTBLNQFVMFKHW-UHFFFAOYSA-N 2,4-dimethylhexane-1,6-diol Chemical compound OCC(C)CC(C)CCO KWTBLNQFVMFKHW-UHFFFAOYSA-N 0.000 description 1
- FVYBULURWSSTRW-UHFFFAOYSA-N 2,5-dimethylhexane-1,2-diol Chemical compound CC(C)CCC(C)(O)CO FVYBULURWSSTRW-UHFFFAOYSA-N 0.000 description 1
- XSNQECSCDATQEL-SECBINFHSA-N 2,6-dimethyl-7-octen-2-ol Chemical compound C=C[C@@H](C)CCCC(C)(C)O XSNQECSCDATQEL-SECBINFHSA-N 0.000 description 1
- HJMSSELHASGURL-UHFFFAOYSA-N 2,6-dimethylcyclohexane-1,4-diol Chemical compound CC1CC(O)CC(C)C1O HJMSSELHASGURL-UHFFFAOYSA-N 0.000 description 1
- ZAPOEKZHEPVHAT-UHFFFAOYSA-N 2,6-dimethylhept-5-ene-1,2-diol Chemical compound CC(C)=CCCC(C)(O)CO ZAPOEKZHEPVHAT-UHFFFAOYSA-N 0.000 description 1
- BEARMGATPGLSKG-UHFFFAOYSA-N 2,6-dimethyloct-7-en-2-yl acetate Chemical compound C=CC(C)CCCC(C)(C)OC(C)=O BEARMGATPGLSKG-UHFFFAOYSA-N 0.000 description 1
- RBQDTYIKRSQHLY-UHFFFAOYSA-N 2,7-dimethylideneoct-4-ene-1,8-diol Chemical compound OCC(=C)CC=CCC(=C)CO RBQDTYIKRSQHLY-UHFFFAOYSA-N 0.000 description 1
- XFSNGEVVHCZELD-UHFFFAOYSA-N 2,7-dimethylocta-3,5-diene-2,7-diol Chemical compound CC(C)(O)C=CC=CC(C)(C)O XFSNGEVVHCZELD-UHFFFAOYSA-N 0.000 description 1
- YBGRBTWDGJERRR-UHFFFAOYSA-N 2,7-dimethylocta-5,7-diene-1,4-diol Chemical compound OCC(C)CC(O)C=CC(C)=C YBGRBTWDGJERRR-UHFFFAOYSA-N 0.000 description 1
- BWMWJUZQBRXRNM-UHFFFAOYSA-N 2-(2,2-dimethylpropyl)propane-1,3-diol Chemical compound CC(C)(C)CC(CO)CO BWMWJUZQBRXRNM-UHFFFAOYSA-N 0.000 description 1
- KKSCGTQXLBSZAA-UHFFFAOYSA-N 2-(2-hydroxycyclohexyl)oxycyclohexan-1-ol Chemical compound OC1CCCCC1OC1C(O)CCCC1 KKSCGTQXLBSZAA-UHFFFAOYSA-N 0.000 description 1
- UOMUPZRYELCVFC-UHFFFAOYSA-N 2-(2-methylpropyl)butane-1,4-diol Chemical compound CC(C)CC(CO)CCO UOMUPZRYELCVFC-UHFFFAOYSA-N 0.000 description 1
- CNSSIRNAFSJOFW-UHFFFAOYSA-N 2-(2-phenylethyl)propane-1,3-diol Chemical compound OCC(CO)CCC1=CC=CC=C1 CNSSIRNAFSJOFW-UHFFFAOYSA-N 0.000 description 1
- FVDOZPZAGYXWRS-UHFFFAOYSA-N 2-(3-methylbut-2-enyl)butane-1,3-diol Chemical compound CC(O)C(CO)CC=C(C)C FVDOZPZAGYXWRS-UHFFFAOYSA-N 0.000 description 1
- VWQPAMYYOLDISD-UHFFFAOYSA-N 2-(3-methylbutyl)propane-1,3-diol Chemical compound CC(C)CCC(CO)CO VWQPAMYYOLDISD-UHFFFAOYSA-N 0.000 description 1
- AWNOGHRWORTNEI-UHFFFAOYSA-N 2-(6,6-dimethyl-4-bicyclo[3.1.1]hept-3-enyl)ethyl acetate Chemical compound CC(=O)OCCC1=CCC2C(C)(C)C1C2 AWNOGHRWORTNEI-UHFFFAOYSA-N 0.000 description 1
- ROKSAUSPJGWCSM-UHFFFAOYSA-N 2-(7,7-dimethyl-4-bicyclo[3.1.1]hept-3-enyl)ethanol Chemical compound C1C2C(C)(C)C1CC=C2CCO ROKSAUSPJGWCSM-UHFFFAOYSA-N 0.000 description 1
- OHWMJHMSUDKMGL-UHFFFAOYSA-N 2-(hydroxymethyl)cyclohexan-1-ol Chemical compound OCC1CCCCC1O OHWMJHMSUDKMGL-UHFFFAOYSA-N 0.000 description 1
- DNRJTBAOUJJKDY-UHFFFAOYSA-N 2-Acetyl-3,5,5,6,8,8-hexamethyl-5,6,7,8- tetrahydronaphthalene Chemical compound CC(=O)C1=C(C)C=C2C(C)(C)C(C)CC(C)(C)C2=C1 DNRJTBAOUJJKDY-UHFFFAOYSA-N 0.000 description 1
- LBLYYCQCTBFVLH-UHFFFAOYSA-N 2-Methylbenzenesulfonic acid Chemical compound CC1=CC=CC=C1S(O)(=O)=O LBLYYCQCTBFVLH-UHFFFAOYSA-N 0.000 description 1
- HMKKIXGYKWDQSV-SDNWHVSQSA-N 2-Pentyl-3-phenyl-2-propenal Chemical compound CCCCC\C(C=O)=C/C1=CC=CC=C1 HMKKIXGYKWDQSV-SDNWHVSQSA-N 0.000 description 1
- MJTPMXWJHPOWGH-UHFFFAOYSA-N 2-Phenoxyethyl isobutyrate Chemical compound CC(C)C(=O)OCCOC1=CC=CC=C1 MJTPMXWJHPOWGH-UHFFFAOYSA-N 0.000 description 1
- JKXYOQDLERSFPT-UHFFFAOYSA-N 2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-(2-octadecoxyethoxy)ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethanol Chemical compound CCCCCCCCCCCCCCCCCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCO JKXYOQDLERSFPT-UHFFFAOYSA-N 0.000 description 1
- VFBJXXJYHWLXRM-UHFFFAOYSA-N 2-[2-[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyloxy]ethylsulfanyl]ethyl 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoate Chemical compound CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(CCC(=O)OCCSCCOC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)=C1 VFBJXXJYHWLXRM-UHFFFAOYSA-N 0.000 description 1
- MLEVHXGDYIRFBV-UHFFFAOYSA-N 2-but-2-enyl-2-methylbutane-1,3-diol Chemical compound CC=CCC(C)(CO)C(C)O MLEVHXGDYIRFBV-UHFFFAOYSA-N 0.000 description 1
- QOOXGUCQYVVEFD-UHFFFAOYSA-N 2-butyl-2-methylpropane-1,3-diol Chemical compound CCCCC(C)(CO)CO QOOXGUCQYVVEFD-UHFFFAOYSA-N 0.000 description 1
- YIEIFUSLOJKTEE-UHFFFAOYSA-N 2-butylbutane-1,4-diol Chemical compound CCCCC(CO)CCO YIEIFUSLOJKTEE-UHFFFAOYSA-N 0.000 description 1
- RZYZEPWXXPYLQY-UHFFFAOYSA-N 2-cyclopent-2-en-1-ylpropane-1,3-diol Chemical compound OCC(CO)C1CCC=C1 RZYZEPWXXPYLQY-UHFFFAOYSA-N 0.000 description 1
- BDAHAEQIBHATPB-UHFFFAOYSA-N 2-ethyl-3,3-dimethylbutane-1,2-diol Chemical compound CCC(O)(CO)C(C)(C)C BDAHAEQIBHATPB-UHFFFAOYSA-N 0.000 description 1
- RDKBBSDNTZSMHK-UHFFFAOYSA-N 2-ethyl-3-methylpentane-1,2-diol Chemical compound CCC(C)C(O)(CC)CO RDKBBSDNTZSMHK-UHFFFAOYSA-N 0.000 description 1
- TVNYBRISSUFYFY-UHFFFAOYSA-N 2-ethyl-4-methylpentane-1,2-diol Chemical compound CCC(O)(CO)CC(C)C TVNYBRISSUFYFY-UHFFFAOYSA-N 0.000 description 1
- NACLMQVDUHEFQS-UHFFFAOYSA-N 2-ethylhexane-1,2-diol Chemical compound CCCCC(O)(CC)CO NACLMQVDUHEFQS-UHFFFAOYSA-N 0.000 description 1
- AJKXDPSHWRTFOZ-UHFFFAOYSA-N 2-ethylhexane-1,6-diol Chemical compound CCC(CO)CCCCO AJKXDPSHWRTFOZ-UHFFFAOYSA-N 0.000 description 1
- GMLXBSIHGBBDAR-UHFFFAOYSA-N 2-ethylpentane-1,2-diol Chemical compound CCCC(O)(CC)CO GMLXBSIHGBBDAR-UHFFFAOYSA-N 0.000 description 1
- PJXHBTZLHITWFX-UHFFFAOYSA-N 2-heptylcyclopentan-1-one Chemical compound CCCCCCCC1CCCC1=O PJXHBTZLHITWFX-UHFFFAOYSA-N 0.000 description 1
- YEGNTQBFSQBGJT-UHFFFAOYSA-N 2-heptylundecan-1-ol Chemical compound CCCCCCCCCC(CO)CCCCCCC YEGNTQBFSQBGJT-UHFFFAOYSA-N 0.000 description 1
- XULHFMYCBKQGEE-UHFFFAOYSA-N 2-hexyl-1-Decanol Chemical compound CCCCCCCCC(CO)CCCCCC XULHFMYCBKQGEE-UHFFFAOYSA-N 0.000 description 1
- LYUCYGUJPUGIQI-UHFFFAOYSA-N 2-hydroxy-n,n-dimethyloctadecan-1-amine oxide Chemical compound CCCCCCCCCCCCCCCCC(O)C[N+](C)(C)[O-] LYUCYGUJPUGIQI-UHFFFAOYSA-N 0.000 description 1
- RIWRBSMFKVOJMN-UHFFFAOYSA-N 2-methyl-1-phenylpropan-2-ol Chemical compound CC(C)(O)CC1=CC=CC=C1 RIWRBSMFKVOJMN-UHFFFAOYSA-N 0.000 description 1
- NDAPOJOHGRLBMF-UHFFFAOYSA-N 2-methyl-1-phenylpropane-1,3-diol;1-phenylbutane-1,3-diol Chemical compound CC(O)CC(O)C1=CC=CC=C1.OCC(C)C(O)C1=CC=CC=C1 NDAPOJOHGRLBMF-UHFFFAOYSA-N 0.000 description 1
- HGECJFVPNUYRJZ-UHFFFAOYSA-N 2-methyl-2-(4-propan-2-ylphenyl)propanal Chemical compound CC(C)C1=CC=C(C(C)(C)C=O)C=C1 HGECJFVPNUYRJZ-UHFFFAOYSA-N 0.000 description 1
- DUQRSLHVBMIFRX-UHFFFAOYSA-N 2-methyl-2-phenyloctadecanoic acid Chemical compound CCCCCCCCCCCCCCCCC(C)(C(O)=O)C1=CC=CC=C1 DUQRSLHVBMIFRX-UHFFFAOYSA-N 0.000 description 1
- ONKWQHDQGCUIEB-UHFFFAOYSA-N 2-methyl-2-propan-2-ylbutane-1,4-diol Chemical compound CC(C)C(C)(CO)CCO ONKWQHDQGCUIEB-UHFFFAOYSA-N 0.000 description 1
- IQYONWMXEQRXIO-UHFFFAOYSA-N 2-methylheptane-3,4-diol Chemical compound CCCC(O)C(O)C(C)C IQYONWMXEQRXIO-UHFFFAOYSA-N 0.000 description 1
- BSJQMNIJQVVJPX-UHFFFAOYSA-N 2-methylhexane-1,2-diol Chemical compound CCCCC(C)(O)CO BSJQMNIJQVVJPX-UHFFFAOYSA-N 0.000 description 1
- LJSJWFGNXJMAFG-UHFFFAOYSA-N 2-methylhexane-3,4-diol Chemical compound CCC(O)C(O)C(C)C LJSJWFGNXJMAFG-UHFFFAOYSA-N 0.000 description 1
- QSFGULCWYYRYGP-UHFFFAOYSA-N 2-methylideneoct-4-ene-1,8-diol Chemical compound OCCCC=CCC(=C)CO QSFGULCWYYRYGP-UHFFFAOYSA-N 0.000 description 1
- RHYUFGNCUXTFTC-UHFFFAOYSA-N 2-pentylpropane-1,3-diol Chemical compound CCCCCC(CO)CO RHYUFGNCUXTFTC-UHFFFAOYSA-N 0.000 description 1
- WLJVXDMOQOGPHL-PPJXEINESA-N 2-phenylacetic acid Chemical compound O[14C](=O)CC1=CC=CC=C1 WLJVXDMOQOGPHL-PPJXEINESA-N 0.000 description 1
- SNCPNGLMZQUXGY-UHFFFAOYSA-N 2-phenylbutane-1,2-diol Chemical compound CCC(O)(CO)C1=CC=CC=C1 SNCPNGLMZQUXGY-UHFFFAOYSA-N 0.000 description 1
- DCNMHZIUXXXJIC-UHFFFAOYSA-N 2-phenylbutane-1,3-diol Chemical compound CC(O)C(CO)C1=CC=CC=C1 DCNMHZIUXXXJIC-UHFFFAOYSA-N 0.000 description 1
- ZVFOERMFRFPDRR-UHFFFAOYSA-N 2-phenylbutane-2,3-diol Chemical compound CC(O)C(C)(O)C1=CC=CC=C1 ZVFOERMFRFPDRR-UHFFFAOYSA-N 0.000 description 1
- MHRUHQMTCFFKOR-UHFFFAOYSA-N 2-propan-2-ylpentane-1,5-diol Chemical compound CC(C)C(CO)CCCO MHRUHQMTCFFKOR-UHFFFAOYSA-N 0.000 description 1
- BJLRAKFWOUAROE-UHFFFAOYSA-N 2500-83-6 Chemical compound C12C=CCC2C2CC(OC(=O)C)C1C2 BJLRAKFWOUAROE-UHFFFAOYSA-N 0.000 description 1
- LVHOAHHFUNMKQA-UHFFFAOYSA-N 3,3-dihydroxy-2,2,5,5-tetramethyl-4-oxohexanoic acid Chemical compound CC(C)(C)C(=O)C(O)(O)C(C)(C)C(O)=O LVHOAHHFUNMKQA-UHFFFAOYSA-N 0.000 description 1
- BQNVNLVPNSRNBZ-UHFFFAOYSA-N 3,3-dimethylcyclopentane-1,2-diol Chemical compound CC1(C)CCC(O)C1O BQNVNLVPNSRNBZ-UHFFFAOYSA-N 0.000 description 1
- JRQXGXRNKMLMPA-UHFFFAOYSA-N 3,3-dimethylhexane-1,6-diol Chemical compound OCCC(C)(C)CCCO JRQXGXRNKMLMPA-UHFFFAOYSA-N 0.000 description 1
- VYZKQGGPNIFCLD-UHFFFAOYSA-N 3,3-dimethylhexane-2,2-diol Chemical class CCCC(C)(C)C(C)(O)O VYZKQGGPNIFCLD-UHFFFAOYSA-N 0.000 description 1
- QULIOZDJZXKLNY-UHFFFAOYSA-N 3,4,5-trihydroxy-2-propylbenzoic acid Chemical compound CCCC1=C(O)C(O)=C(O)C=C1C(O)=O QULIOZDJZXKLNY-UHFFFAOYSA-N 0.000 description 1
- IBYMEIXDADKDCM-UHFFFAOYSA-N 3,4-dimethylhexane-1,6-diol Chemical compound OCCC(C)C(C)CCO IBYMEIXDADKDCM-UHFFFAOYSA-N 0.000 description 1
- RJOVKNVJGPMWDT-UHFFFAOYSA-N 3,4-dimethylhexane-3,4-diol Chemical compound CCC(C)(O)C(C)(O)CC RJOVKNVJGPMWDT-UHFFFAOYSA-N 0.000 description 1
- FFIQNIBSZCBOLR-UHFFFAOYSA-N 3,4-dimethylpentane-1,2-diol Chemical compound CC(C)C(C)C(O)CO FFIQNIBSZCBOLR-UHFFFAOYSA-N 0.000 description 1
- SAJMVUGWBCJISP-UHFFFAOYSA-N 3,5,7-trimethyldecanoic acid Chemical compound CCCC(C)CC(C)CC(C)CC(O)=O SAJMVUGWBCJISP-UHFFFAOYSA-N 0.000 description 1
- GGZBFCBGBFRGPA-UHFFFAOYSA-N 3,5-dimethylhex-5-ene-2,4-diol Chemical compound CC(O)C(C)C(O)C(C)=C GGZBFCBGBFRGPA-UHFFFAOYSA-N 0.000 description 1
- GOLORTLGFDVFDW-UHFFFAOYSA-N 3-(1h-benzimidazol-2-yl)-7-(diethylamino)chromen-2-one Chemical compound C1=CC=C2NC(C3=CC4=CC=C(C=C4OC3=O)N(CC)CC)=NC2=C1 GOLORTLGFDVFDW-UHFFFAOYSA-N 0.000 description 1
- XGHAAJWWNQHCQI-UHFFFAOYSA-N 3-(2-methylpropoxy)propane-1,2-diol Chemical compound CC(C)COCC(O)CO XGHAAJWWNQHCQI-UHFFFAOYSA-N 0.000 description 1
- BWVZAZPLUTUBKD-UHFFFAOYSA-N 3-(5,6,6-Trimethylbicyclo[2.2.1]hept-1-yl)cyclohexanol Chemical compound CC1(C)C(C)C2CC1CC2C1CCCC(O)C1 BWVZAZPLUTUBKD-UHFFFAOYSA-N 0.000 description 1
- KSXHXCWTPJPLAT-UHFFFAOYSA-N 3-[3-(trifluoromethyl)phenyl]benzaldehyde Chemical compound FC(F)(F)C1=CC=CC(C=2C=C(C=O)C=CC=2)=C1 KSXHXCWTPJPLAT-UHFFFAOYSA-N 0.000 description 1
- NHQDETIJWKXCTC-UHFFFAOYSA-N 3-chloroperbenzoic acid Chemical compound OOC(=O)C1=CC=CC(Cl)=C1 NHQDETIJWKXCTC-UHFFFAOYSA-N 0.000 description 1
- MGXLIHQUEDFVCW-UHFFFAOYSA-N 3-ethylhexane-2,2-diol Chemical class CCCC(CC)C(C)(O)O MGXLIHQUEDFVCW-UHFFFAOYSA-N 0.000 description 1
- HZGQHYCPLPOYSG-UHFFFAOYSA-N 3-ethylhexane-2,3-diol Chemical compound CCCC(O)(CC)C(C)O HZGQHYCPLPOYSG-UHFFFAOYSA-N 0.000 description 1
- ZISGOYMWXFOWAM-UHFFFAOYSA-N 3-methyl-2-pentylcyclopentan-1-one Chemical compound CCCCCC1C(C)CCC1=O ZISGOYMWXFOWAM-UHFFFAOYSA-N 0.000 description 1
- WPZKBFKHGKBLSW-UHFFFAOYSA-N 3-methyl-2-propan-2-ylbutane-1,2-diol Chemical compound CC(C)C(O)(CO)C(C)C WPZKBFKHGKBLSW-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
- OHPBIRBXCGMCRJ-UHFFFAOYSA-N 3-methylheptane-1,2-diol Chemical compound CCCCC(C)C(O)CO OHPBIRBXCGMCRJ-UHFFFAOYSA-N 0.000 description 1
- MSCWGJFHWUZSAO-UHFFFAOYSA-N 3-methylhexane-1,2-diol Chemical compound CCCC(C)C(O)CO MSCWGJFHWUZSAO-UHFFFAOYSA-N 0.000 description 1
- ZKOHOMNDHMAYRX-UHFFFAOYSA-N 3-methylhexane-3,4-diol Chemical compound CCC(O)C(C)(O)CC ZKOHOMNDHMAYRX-UHFFFAOYSA-N 0.000 description 1
- HTLBMZKXJYNJSK-UHFFFAOYSA-N 3-naphthalen-2-yl-1,2-oxazol-5-amine Chemical compound O1C(N)=CC(C=2C=C3C=CC=CC3=CC=2)=N1 HTLBMZKXJYNJSK-UHFFFAOYSA-N 0.000 description 1
- FAZRWYMHXGYVGX-UHFFFAOYSA-N 3-phenylbutane-1,2-diol Chemical compound OCC(O)C(C)C1=CC=CC=C1 FAZRWYMHXGYVGX-UHFFFAOYSA-N 0.000 description 1
- ZTKZJXGLCCVMLJ-UHFFFAOYSA-N 3-propoxypropane-1,2-diol Chemical compound CCCOCC(O)CO ZTKZJXGLCCVMLJ-UHFFFAOYSA-N 0.000 description 1
- VMQLTMBUIHNHTR-UHFFFAOYSA-N 4,5-dimethylcyclohex-4-ene-1,2-diol Chemical compound CC1=C(C)CC(O)C(O)C1 VMQLTMBUIHNHTR-UHFFFAOYSA-N 0.000 description 1
- INIOTLARNNSXAE-UHFFFAOYSA-N 4,8-dimethyl-2-propan-2-ylidene-3,3a,4,5,6,8a-hexahydro-1h-azulen-6-ol Chemical compound CC1CC(O)C=C(C)C2CC(=C(C)C)CC12 INIOTLARNNSXAE-UHFFFAOYSA-N 0.000 description 1
- MQBIZQLCHSZBOI-UHFFFAOYSA-N 4-(4-Methyl-3-pentenyl)-3-cyclohexene-1-carboxaldehyde Chemical compound CC(C)=CCCC1=CCC(C=O)CC1 MQBIZQLCHSZBOI-UHFFFAOYSA-N 0.000 description 1
- IKTHMQYJOWTSJO-UHFFFAOYSA-N 4-Acetyl-6-tert-butyl-1,1-dimethylindane Chemical compound CC(=O)C1=CC(C(C)(C)C)=CC2=C1CCC2(C)C IKTHMQYJOWTSJO-UHFFFAOYSA-N 0.000 description 1
- UAOCKRSKPFWKKI-UHFFFAOYSA-N 4-ethylhexane-2,3-diol Chemical compound CCC(CC)C(O)C(C)O UAOCKRSKPFWKKI-UHFFFAOYSA-N 0.000 description 1
- HQDUPXREPYCQCS-UHFFFAOYSA-N 4-methylheptane-1,2-diol Chemical compound CCCC(C)CC(O)CO HQDUPXREPYCQCS-UHFFFAOYSA-N 0.000 description 1
- LVJCJDMIBZEIJA-UHFFFAOYSA-N 4-methylheptane-3,4-diol Chemical compound CCCC(C)(O)C(O)CC LVJCJDMIBZEIJA-UHFFFAOYSA-N 0.000 description 1
- IMHLMIRSHNHXBC-UHFFFAOYSA-N 4-methylhexane-1,2-diol Chemical compound CCC(C)CC(O)CO IMHLMIRSHNHXBC-UHFFFAOYSA-N 0.000 description 1
- YGUMVDWOQQJBGA-UHFFFAOYSA-N 5-[(4-anilino-6-morpholin-4-yl-1,3,5-triazin-2-yl)amino]-2-[2-[4-[(4-anilino-6-morpholin-4-yl-1,3,5-triazin-2-yl)amino]-2-sulfophenyl]ethenyl]benzenesulfonic acid Chemical class C=1C=C(C=CC=2C(=CC(NC=3N=C(N=C(NC=4C=CC=CC=4)N=3)N3CCOCC3)=CC=2)S(O)(=O)=O)C(S(=O)(=O)O)=CC=1NC(N=C(N=1)N2CCOCC2)=NC=1NC1=CC=CC=C1 YGUMVDWOQQJBGA-UHFFFAOYSA-N 0.000 description 1
- WJTFBTYHZZKPPA-UHFFFAOYSA-N 5-ethylhept-1-ene-3,5-diol Chemical compound CCC(O)(CC)CC(O)C=C WJTFBTYHZZKPPA-UHFFFAOYSA-N 0.000 description 1
- AFDGVGXTGJRHOY-UHFFFAOYSA-N 5-methylcyclohept-5-ene-1,3-diol Chemical compound CC1=CCC(O)CC(O)C1 AFDGVGXTGJRHOY-UHFFFAOYSA-N 0.000 description 1
- VDOXKUPNOQSLCM-UHFFFAOYSA-N 5-methylheptane-1,2-diol Chemical compound CCC(C)CCC(O)CO VDOXKUPNOQSLCM-UHFFFAOYSA-N 0.000 description 1
- CKTLYOSMORMIIG-UHFFFAOYSA-N 5-methylheptane-3,4-diol Chemical compound CCC(C)C(O)C(O)CC CKTLYOSMORMIIG-UHFFFAOYSA-N 0.000 description 1
- PTXXRZSKRORMHV-UHFFFAOYSA-N 5-methylhexane-1,2-diol Chemical compound CC(C)CCC(O)CO PTXXRZSKRORMHV-UHFFFAOYSA-N 0.000 description 1
- ADTDSDFUDNTLSC-UHFFFAOYSA-N 6,6-dimethylcyclohex-3-ene-1,2-diol Chemical compound CC1(C)CC=CC(O)C1O ADTDSDFUDNTLSC-UHFFFAOYSA-N 0.000 description 1
- LJSJTXAZFHYHMM-UHFFFAOYSA-N 7-methyloctyl acetate Chemical compound CC(C)CCCCCCOC(C)=O LJSJTXAZFHYHMM-UHFFFAOYSA-N 0.000 description 1
- QGFSQVPRCWJZQK-UHFFFAOYSA-N 9-Decen-1-ol Chemical compound OCCCCCCCCC=C QGFSQVPRCWJZQK-UHFFFAOYSA-N 0.000 description 1
- NJYQVLBJCYPWOL-UHFFFAOYSA-N 9-methoxyoctadecanoic acid Chemical compound CCCCCCCCCC(OC)CCCCCCCC(O)=O NJYQVLBJCYPWOL-UHFFFAOYSA-N 0.000 description 1
- RZVAJINKPMORJF-UHFFFAOYSA-N Acetaminophen Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-UHFFFAOYSA-N 0.000 description 1
- YPZUZOLGGMJZJO-UHFFFAOYSA-N Ambronide Chemical compound C1CC2C(C)(C)CCCC2(C)C2C1(C)OCC2 YPZUZOLGGMJZJO-UHFFFAOYSA-N 0.000 description 1
- 235000017060 Arachis glabrata Nutrition 0.000 description 1
- 244000105624 Arachis hypogaea Species 0.000 description 1
- 235000010777 Arachis hypogaea Nutrition 0.000 description 1
- 235000018262 Arachis monticola Nutrition 0.000 description 1
- 229910015900 BF3 Inorganic materials 0.000 description 1
- 239000004857 Balsam Substances 0.000 description 1
- 239000005711 Benzoic acid Substances 0.000 description 1
- 235000003717 Boswellia sacra Nutrition 0.000 description 1
- 240000007551 Boswellia serrata Species 0.000 description 1
- 235000012035 Boswellia serrata Nutrition 0.000 description 1
- 239000004322 Butylated hydroxytoluene Substances 0.000 description 1
- NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 description 1
- BKLRYIVOMGBLCG-UHFFFAOYSA-N C(=CC)C(CO)CCCO.CC(C(CO)CC=C)C(C)O Chemical compound C(=CC)C(CO)CCCO.CC(C(CO)CC=C)C(C)O BKLRYIVOMGBLCG-UHFFFAOYSA-N 0.000 description 1
- AWQJAAWVEAAHTL-UHFFFAOYSA-N C(C)(C)C1C(C(C1)O)O.C(CC)C1C(C(C1)O)O.C(C)C1C(C(C1C)O)O Chemical compound C(C)(C)C1C(C(C1)O)O.C(CC)C1C(C(C1)O)O.C(C)C1C(C(C1C)O)O AWQJAAWVEAAHTL-UHFFFAOYSA-N 0.000 description 1
- BPJVCLCEOOBWLB-UHFFFAOYSA-N C(C)(C)C1C(C(C1)O)O.C(CC)C1C(C(C1)O)O.C(C)C1C(C(C1C)O)O.C(C)(C)C1(C(CC1)O)O Chemical compound C(C)(C)C1C(C(C1)O)O.C(CC)C1C(C(C1)O)O.C(C)C1C(C(C1C)O)O.C(C)(C)C1(C(CC1)O)O BPJVCLCEOOBWLB-UHFFFAOYSA-N 0.000 description 1
- XTRPBWCPKOJMBS-UHFFFAOYSA-N C(C)C(C(C)(O)C)C(C)O.C(C)C(CCO)(CCO)C Chemical compound C(C)C(C(C)(O)C)C(C)O.C(C)C(CCO)(CCO)C XTRPBWCPKOJMBS-UHFFFAOYSA-N 0.000 description 1
- UKVBCZKAIPKHOO-UHFFFAOYSA-N C(C)C(CO)(C(C)C)O.CC(CO)(CO)C(C)C Chemical compound C(C)C(CO)(C(C)C)O.CC(CO)(CO)C(C)C UKVBCZKAIPKHOO-UHFFFAOYSA-N 0.000 description 1
- GNKBVYCIPSOXQO-UHFFFAOYSA-N C(C)C(CO)(CC(C)O)C.C(C)C(C(CO)C)(CC)O Chemical compound C(C)C(CO)(CC(C)O)C.C(C)C(C(CO)C)(CC)O GNKBVYCIPSOXQO-UHFFFAOYSA-N 0.000 description 1
- QTDNFLYORDNJBP-UHFFFAOYSA-N C(C)C(CO)C(C(C)O)C.C(C)C(CO)(CC(C)O)C.C(C)C(C(CO)C)(CC)O Chemical compound C(C)C(CO)C(C(C)O)C.C(C)C(CO)(CC(C)O)C.C(C)C(C(CO)C)(CC)O QTDNFLYORDNJBP-UHFFFAOYSA-N 0.000 description 1
- DSJPTAOBLBXWBB-UHFFFAOYSA-N C(C)C1(C(C(CC1)=C)O)O.CC1(C(CC(C1)=C)(O)C)O Chemical compound C(C)C1(C(C(CC1)=C)O)O.CC1(C(CC(C1)=C)(O)C)O DSJPTAOBLBXWBB-UHFFFAOYSA-N 0.000 description 1
- YKAOMWZBOSUNPD-UHFFFAOYSA-N C(CCC)OCC(CO)O.C(CCC)OCC(O)CO Chemical compound C(CCC)OCC(CO)O.C(CCC)OCC(O)CO YKAOMWZBOSUNPD-UHFFFAOYSA-N 0.000 description 1
- KORJIHIXRMHJBH-UHFFFAOYSA-N C1(=CC=CC=C1)C(C(C)O)O.C1(=CC=CC=C1)C(CO)O Chemical compound C1(=CC=CC=C1)C(C(C)O)O.C1(=CC=CC=C1)C(CO)O KORJIHIXRMHJBH-UHFFFAOYSA-N 0.000 description 1
- UIICFTOJBFHJFR-UHFFFAOYSA-N C1(=CC=CC=C1)CC(C(C)O)O.C1(=CC=CC=C1)C(CO)CCO Chemical compound C1(=CC=CC=C1)CC(C(C)O)O.C1(=CC=CC=C1)C(CO)CCO UIICFTOJBFHJFR-UHFFFAOYSA-N 0.000 description 1
- LSKPMLVNRCDUPZ-UHFFFAOYSA-N C1(=CC=CC=C1)OC(CO)CO.C1(=CC=CC=C1)CC(C)OCC(CO)O.C1(=CC=CC=C1)CCOCC(CO)O.C(C1=CC=CC=C1)OCC(CO)O.C1(=CC=CC=C1)OCC(CO)O Chemical compound C1(=CC=CC=C1)OC(CO)CO.C1(=CC=CC=C1)CC(C)OCC(CO)O.C1(=CC=CC=C1)CCOCC(CO)O.C(C1=CC=CC=C1)OCC(CO)O.C1(=CC=CC=C1)OCC(CO)O LSKPMLVNRCDUPZ-UHFFFAOYSA-N 0.000 description 1
- ZVVUKQHFDNWFBF-UHFFFAOYSA-N C1(=CCCC1)C(CO)CO.CC(C)=C1C(CCC1O)O Chemical compound C1(=CCCC1)C(CO)CO.CC(C)=C1C(CCC1O)O ZVVUKQHFDNWFBF-UHFFFAOYSA-N 0.000 description 1
- XVYVTGQYIILMRE-UHFFFAOYSA-N CC(CC(CO)CO)(C)C.CC(CCC)C(CO)CO.C(C)C(CC)C(CO)CO.CC(C(C)C)C(CO)CO.CC(CC)(C)C(CO)CO Chemical compound CC(CC(CO)CO)(C)C.CC(CCC)C(CO)CO.C(C)C(CC)C(CO)CO.CC(C(C)C)C(CO)CO.CC(CC)(C)C(CO)CO XVYVTGQYIILMRE-UHFFFAOYSA-N 0.000 description 1
- CGFGARRDUSYCAG-UHFFFAOYSA-N CC(CO)(CO)C(CC)C.C(C)C(CO)(CO)CCC.C(C)C(CO)(CO)C(C)C.C(CCC)C(CO)(CO)C.CC(CCC(CO)CO)C Chemical compound CC(CO)(CO)C(CC)C.C(C)C(CO)(CO)CCC.C(C)C(CO)(CO)C(C)C.C(CCC)C(CO)(CO)C.CC(CCC(CO)CO)C CGFGARRDUSYCAG-UHFFFAOYSA-N 0.000 description 1
- 125000006519 CCH3 Chemical group 0.000 description 1
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 1
- PBGWNXWNCSSXCO-UHFFFAOYSA-N Caprylsaeure-hexenylester Natural products CCCCCCCC(=O)OCCCCCC PBGWNXWNCSSXCO-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- OKTJSMMVPCPJKN-OUBTZVSYSA-N Carbon-13 Chemical compound [13C] OKTJSMMVPCPJKN-OUBTZVSYSA-N 0.000 description 1
- NPBVQXIMTZKSBA-UHFFFAOYSA-N Chavibetol Natural products COC1=CC=C(CC=C)C=C1O NPBVQXIMTZKSBA-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 240000008772 Cistus ladanifer Species 0.000 description 1
- 235000005241 Cistus ladanifer Nutrition 0.000 description 1
- KRKNYBCHXYNGOX-UHFFFAOYSA-K Citrate Chemical compound [O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O KRKNYBCHXYNGOX-UHFFFAOYSA-K 0.000 description 1
- JOZKFWLRHCDGJA-LLVKDONJSA-N Citronellyl acetate Natural products CC(=O)OCC[C@H](C)CCC=C(C)C JOZKFWLRHCDGJA-LLVKDONJSA-N 0.000 description 1
- 235000005979 Citrus limon Nutrition 0.000 description 1
- 244000131522 Citrus pyriformis Species 0.000 description 1
- 240000000560 Citrus x paradisi Species 0.000 description 1
- 241000640882 Condea Species 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 235000014493 Crataegus Nutrition 0.000 description 1
- 241001092040 Crataegus Species 0.000 description 1
- JPVYNHNXODAKFH-UHFFFAOYSA-N Cu2+ Chemical compound [Cu+2] JPVYNHNXODAKFH-UHFFFAOYSA-N 0.000 description 1
- 229920000858 Cyclodextrin Polymers 0.000 description 1
- CKLJMWTZIZZHCS-UHFFFAOYSA-N D-OH-Asp Natural products OC(=O)C(N)CC(O)=O CKLJMWTZIZZHCS-UHFFFAOYSA-N 0.000 description 1
- YZCKVEUIGOORGS-OUBTZVSYSA-N Deuterium Chemical compound [2H] YZCKVEUIGOORGS-OUBTZVSYSA-N 0.000 description 1
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 1
- QXNVGIXVLWOKEQ-UHFFFAOYSA-N Disodium Chemical class [Na][Na] QXNVGIXVLWOKEQ-UHFFFAOYSA-N 0.000 description 1
- RPWFJAMTCNSJKK-UHFFFAOYSA-N Dodecyl gallate Chemical compound CCCCCCCCCCCCOC(=O)C1=CC(O)=C(O)C(O)=C1 RPWFJAMTCNSJKK-UHFFFAOYSA-N 0.000 description 1
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical class OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- XRHCAGNSDHCHFJ-UHFFFAOYSA-N Ethylene brassylate Chemical compound O=C1CCCCCCCCCCCC(=O)OCCO1 XRHCAGNSDHCHFJ-UHFFFAOYSA-N 0.000 description 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
- 239000005770 Eugenol Substances 0.000 description 1
- 239000001263 FEMA 3042 Substances 0.000 description 1
- 239000004863 Frankincense Substances 0.000 description 1
- 239000005792 Geraniol Substances 0.000 description 1
- WHUUTDBJXJRKMK-UHFFFAOYSA-N Glutamic acid Natural products OC(=O)C(N)CCC(O)=O WHUUTDBJXJRKMK-UHFFFAOYSA-N 0.000 description 1
- SXRSQZLOMIGNAQ-UHFFFAOYSA-N Glutaraldehyde Chemical compound O=CCCCC=O SXRSQZLOMIGNAQ-UHFFFAOYSA-N 0.000 description 1
- 239000007818 Grignard reagent Substances 0.000 description 1
- DUKPKQFHJQGTGU-UHFFFAOYSA-N Hexyl salicylic acid Chemical compound CCCCCCOC(=O)C1=CC=CC=C1O DUKPKQFHJQGTGU-UHFFFAOYSA-N 0.000 description 1
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 1
- 239000003810 Jones reagent Substances 0.000 description 1
- CKLJMWTZIZZHCS-UWTATZPHSA-N L-Aspartic acid Natural products OC(=O)[C@H](N)CC(O)=O CKLJMWTZIZZHCS-UWTATZPHSA-N 0.000 description 1
- CKLJMWTZIZZHCS-REOHCLBHSA-N L-aspartic acid Chemical compound OC(=O)[C@@H](N)CC(O)=O CKLJMWTZIZZHCS-REOHCLBHSA-N 0.000 description 1
- WHUUTDBJXJRKMK-VKHMYHEASA-N L-glutamic acid Chemical compound OC(=O)[C@@H](N)CCC(O)=O WHUUTDBJXJRKMK-VKHMYHEASA-N 0.000 description 1
- 239000004869 Labdanum Substances 0.000 description 1
- 240000006240 Linum usitatissimum Species 0.000 description 1
- 235000004431 Linum usitatissimum Nutrition 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 1
- 244000024873 Mentha crispa Species 0.000 description 1
- 235000014749 Mentha crispa Nutrition 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- LRBQNJMCXXYXIU-PPKXGCFTSA-N Penta-digallate-beta-D-glucose Natural products OC1=C(O)C(O)=CC(C(=O)OC=2C(=C(O)C=C(C=2)C(=O)OC[C@@H]2[C@H]([C@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)[C@@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)[C@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)O2)OC(=O)C=2C=C(OC(=O)C=3C=C(O)C(O)=C(O)C=3)C(O)=C(O)C=2)O)=C1 LRBQNJMCXXYXIU-PPKXGCFTSA-N 0.000 description 1
- LQKRYVGRPXFFAV-UHFFFAOYSA-N Phenylmethylglycidic ester Chemical compound CCOC(=O)C1OC1(C)C1=CC=CC=C1 LQKRYVGRPXFFAV-UHFFFAOYSA-N 0.000 description 1
- QLZHNIAADXEJJP-UHFFFAOYSA-N Phenylphosphonic acid Chemical compound OP(O)(=O)C1=CC=CC=C1 QLZHNIAADXEJJP-UHFFFAOYSA-N 0.000 description 1
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical class OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 1
- 235000008331 Pinus X rigitaeda Nutrition 0.000 description 1
- 235000011613 Pinus brutia Nutrition 0.000 description 1
- 241000018646 Pinus brutia Species 0.000 description 1
- 229920002257 Plurafac® Polymers 0.000 description 1
- 240000002505 Pogostemon cablin Species 0.000 description 1
- 235000011751 Pogostemon cablin Nutrition 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- UVMRYBDEERADNV-UHFFFAOYSA-N Pseudoeugenol Natural products COC1=CC(C(C)=C)=CC=C1O UVMRYBDEERADNV-UHFFFAOYSA-N 0.000 description 1
- ISRUGXGCCGIOQO-UHFFFAOYSA-N Rhoden Chemical compound CNC(=O)OC1=CC=CC=C1OC(C)C ISRUGXGCCGIOQO-UHFFFAOYSA-N 0.000 description 1
- 101100137598 Saccharomyces cerevisiae (strain ATCC 204508 / S288c) PRM6 gene Proteins 0.000 description 1
- 235000019485 Safflower oil Nutrition 0.000 description 1
- 239000002262 Schiff base Substances 0.000 description 1
- 150000004753 Schiff bases Chemical class 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
- 235000016639 Syzygium aromaticum Nutrition 0.000 description 1
- 244000223014 Syzygium aromaticum Species 0.000 description 1
- DOOTYTYQINUNNV-UHFFFAOYSA-N Triethyl citrate Chemical compound CCOC(=O)CC(O)(C(=O)OCC)CC(=O)OCC DOOTYTYQINUNNV-UHFFFAOYSA-N 0.000 description 1
- YZCKVEUIGOORGS-NJFSPNSNSA-N Tritium Chemical compound [3H] YZCKVEUIGOORGS-NJFSPNSNSA-N 0.000 description 1
- 244000284012 Vetiveria zizanioides Species 0.000 description 1
- 235000007769 Vetiveria zizanioides Nutrition 0.000 description 1
- UAVFEMBKDRODDE-UHFFFAOYSA-N Vetiveryl acetate Chemical compound CC1CC(OC(C)=O)C=C(C)C2CC(=C(C)C)CC12 UAVFEMBKDRODDE-UHFFFAOYSA-N 0.000 description 1
- BGYHLZZASRKEJE-UHFFFAOYSA-N [3-[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyloxy]-2,2-bis[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyloxymethyl]propyl] 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoate Chemical compound CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(CCC(=O)OCC(COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)(COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)=C1 BGYHLZZASRKEJE-UHFFFAOYSA-N 0.000 description 1
- YIMQCDZDWXUDCA-UHFFFAOYSA-N [4-(hydroxymethyl)cyclohexyl]methanol Chemical compound OCC1CCC(CO)CC1 YIMQCDZDWXUDCA-UHFFFAOYSA-N 0.000 description 1
- JEDZLBFUGJTJGQ-UHFFFAOYSA-N [Na].COCCO[AlH]OCCOC Chemical compound [Na].COCCO[AlH]OCCOC JEDZLBFUGJTJGQ-UHFFFAOYSA-N 0.000 description 1
- 150000001242 acetic acid derivatives Chemical class 0.000 description 1
- NUPSHWCALHZGOV-UHFFFAOYSA-N acetic acid n-decyl ester Natural products CCCCCCCCCCOC(C)=O NUPSHWCALHZGOV-UHFFFAOYSA-N 0.000 description 1
- KCQUJORJVXQRST-UHFFFAOYSA-N acetic acid;ethane-1,2-diamine Chemical compound CC(O)=O.CC(O)=O.CC(O)=O.CC(O)=O.CC(O)=O.NCCN KCQUJORJVXQRST-UHFFFAOYSA-N 0.000 description 1
- 150000000476 acetylides Chemical class 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 239000002671 adjuvant Substances 0.000 description 1
- 239000005456 alcohol based solvent Substances 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 125000004450 alkenylene group Chemical group 0.000 description 1
- 125000005210 alkyl ammonium group Chemical group 0.000 description 1
- 150000001347 alkyl bromides Chemical class 0.000 description 1
- 150000001350 alkyl halides Chemical class 0.000 description 1
- 125000005529 alkyleneoxy group Chemical group 0.000 description 1
- GUUHFMWKWLOQMM-NTCAYCPXSA-N alpha-hexylcinnamaldehyde Chemical compound CCCCCC\C(C=O)=C/C1=CC=CC=C1 GUUHFMWKWLOQMM-NTCAYCPXSA-N 0.000 description 1
- GUUHFMWKWLOQMM-UHFFFAOYSA-N alpha-n-hexylcinnamic aldehyde Natural products CCCCCCC(C=O)=CC1=CC=CC=C1 GUUHFMWKWLOQMM-UHFFFAOYSA-N 0.000 description 1
- WUOACPNHFRMFPN-UHFFFAOYSA-N alpha-terpineol Chemical compound CC1=CCC(C(C)(C)O)CC1 WUOACPNHFRMFPN-UHFFFAOYSA-N 0.000 description 1
- YPZUZOLGGMJZJO-LQKXBSAESA-N ambroxan Chemical compound CC([C@@H]1CC2)(C)CCC[C@]1(C)[C@@H]1[C@]2(C)OCC1 YPZUZOLGGMJZJO-LQKXBSAESA-N 0.000 description 1
- 229940062909 amyl salicylate Drugs 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- RUVINXPYWBROJD-UHFFFAOYSA-N anethole Chemical compound COC1=CC=C(C=CC)C=C1 RUVINXPYWBROJD-UHFFFAOYSA-N 0.000 description 1
- 239000004663 anionic softener Substances 0.000 description 1
- 239000012300 argon atmosphere Substances 0.000 description 1
- 235000010323 ascorbic acid Nutrition 0.000 description 1
- 229960005070 ascorbic acid Drugs 0.000 description 1
- 239000011668 ascorbic acid Substances 0.000 description 1
- 229960005261 aspartic acid Drugs 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- SRSXLGNVWSONIS-UHFFFAOYSA-N benzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC=CC=C1 SRSXLGNVWSONIS-UHFFFAOYSA-N 0.000 description 1
- 229940092714 benzenesulfonic acid Drugs 0.000 description 1
- 235000010233 benzoic acid Nutrition 0.000 description 1
- 229960004365 benzoic acid Drugs 0.000 description 1
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 1
- 239000012965 benzophenone Substances 0.000 description 1
- 229940007550 benzyl acetate Drugs 0.000 description 1
- 229960002903 benzyl benzoate Drugs 0.000 description 1
- JGQFVRIQXUFPAH-UHFFFAOYSA-N beta-citronellol Natural products OCCC(C)CCCC(C)=C JGQFVRIQXUFPAH-UHFFFAOYSA-N 0.000 description 1
- 230000033228 biological regulation Effects 0.000 description 1
- LSVYFFDZLQBSCB-UHFFFAOYSA-N bis(1,2,6,10-tetramethylcyclododeca-2,5,9-trien-1-yl)methanone Chemical compound C1CC(C)=CCCC(C)=CCC=C(C)C1(C)C(=O)C1(C)C(C)=CCC=C(C)CCC=C(C)CC1 LSVYFFDZLQBSCB-UHFFFAOYSA-N 0.000 description 1
- 229920001400 block copolymer Polymers 0.000 description 1
- 229910021538 borax Inorganic materials 0.000 description 1
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
- 239000004327 boric acid Substances 0.000 description 1
- WTEOIRVLGSZEPR-UHFFFAOYSA-N boron trifluoride Chemical compound FB(F)F WTEOIRVLGSZEPR-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
- 238000005282 brightening Methods 0.000 description 1
- 230000031709 bromination Effects 0.000 description 1
- 238000005893 bromination reaction Methods 0.000 description 1
- 229960003168 bronopol Drugs 0.000 description 1
- RFAZFSACZIVZDV-UHFFFAOYSA-N butan-2-one Chemical compound CCC(C)=O.CCC(C)=O RFAZFSACZIVZDV-UHFFFAOYSA-N 0.000 description 1
- 239000001273 butane Substances 0.000 description 1
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 1
- CZBZUDVBLSSABA-UHFFFAOYSA-N butylated hydroxyanisole Chemical compound COC1=CC=C(O)C(C(C)(C)C)=C1.COC1=CC=C(O)C=C1C(C)(C)C CZBZUDVBLSSABA-UHFFFAOYSA-N 0.000 description 1
- 235000010354 butylated hydroxytoluene Nutrition 0.000 description 1
- 229940095259 butylated hydroxytoluene Drugs 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 150000001669 calcium Chemical class 0.000 description 1
- 239000001110 calcium chloride Substances 0.000 description 1
- 229910001628 calcium chloride Inorganic materials 0.000 description 1
- SJEZDMHBMZPMME-UHFFFAOYSA-L calcium;(3,5-ditert-butyl-4-hydroxyphenyl)methyl-ethoxyphosphinate Chemical compound [Ca+2].CCOP([O-])(=O)CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1.CCOP([O-])(=O)CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 SJEZDMHBMZPMME-UHFFFAOYSA-L 0.000 description 1
- CREMABGTGYGIQB-UHFFFAOYSA-N carbon carbon Chemical compound C.C CREMABGTGYGIQB-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 150000001767 cationic compounds Chemical class 0.000 description 1
- 239000002752 cationic softener Substances 0.000 description 1
- SVURIXNDRWRAFU-OGMFBOKVSA-N cedrol Chemical compound C1[C@]23[C@H](C)CC[C@H]3C(C)(C)[C@@H]1[C@@](O)(C)CC2 SVURIXNDRWRAFU-OGMFBOKVSA-N 0.000 description 1
- 229940026455 cedrol Drugs 0.000 description 1
- PCROEXHGMUJCDB-UHFFFAOYSA-N cedrol Natural products CC1CCC2C(C)(C)C3CC(C)(O)CC12C3 PCROEXHGMUJCDB-UHFFFAOYSA-N 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- FOCAUTSVDIKZOP-UHFFFAOYSA-N chloroacetic acid Chemical compound OC(=O)CCl FOCAUTSVDIKZOP-UHFFFAOYSA-N 0.000 description 1
- 229940106681 chloroacetic acid Drugs 0.000 description 1
- DHNRXBZYEKSXIM-UHFFFAOYSA-N chloromethylisothiazolinone Chemical compound CN1SC(Cl)=CC1=O DHNRXBZYEKSXIM-UHFFFAOYSA-N 0.000 description 1
- 229930003633 citronellal Natural products 0.000 description 1
- 235000000983 citronellal Nutrition 0.000 description 1
- 239000001926 citrus aurantium l. subsp. bergamia wright et arn. oil Substances 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 229910052570 clay Inorganic materials 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 230000000536 complexating effect Effects 0.000 description 1
- 239000008139 complexing agent Substances 0.000 description 1
- 238000006482 condensation reaction Methods 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 229910001431 copper ion Inorganic materials 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- BLBJUGKATXCWET-UHFFFAOYSA-N cyclaprop Chemical compound C12CC=CC2C2CC(OC(=O)CC)C1C2 BLBJUGKATXCWET-UHFFFAOYSA-N 0.000 description 1
- 150000001925 cycloalkenes Chemical class 0.000 description 1
- 229940097362 cyclodextrins Drugs 0.000 description 1
- ZXIJMRYMVAMXQP-UHFFFAOYSA-N cycloheptene Chemical class C1CCC=CCC1 ZXIJMRYMVAMXQP-UHFFFAOYSA-N 0.000 description 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- WJVTUJNZYOAXID-UHFFFAOYSA-N cyclooct-2-ene-1,4-diol Chemical compound OC1CCCCC(O)C=C1 WJVTUJNZYOAXID-UHFFFAOYSA-N 0.000 description 1
- DNJRSNYMHOVSGB-UHFFFAOYSA-N cyclooctane-1,3-diol Chemical compound OC1CCCCCC(O)C1 DNJRSNYMHOVSGB-UHFFFAOYSA-N 0.000 description 1
- UYDJAHJCGZTTHB-UHFFFAOYSA-N cyclopentane-1,1-diol Chemical compound OC1(O)CCCC1 UYDJAHJCGZTTHB-UHFFFAOYSA-N 0.000 description 1
- VCVOSERVUCJNPR-UHFFFAOYSA-N cyclopentane-1,2-diol Chemical compound OC1CCCC1O VCVOSERVUCJNPR-UHFFFAOYSA-N 0.000 description 1
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
- YSRSBDQINUMTIF-UHFFFAOYSA-N decane-1,2-diol Chemical compound CCCCCCCCC(O)CO YSRSBDQINUMTIF-UHFFFAOYSA-N 0.000 description 1
- GHVNFZFCNZKVNT-UHFFFAOYSA-N decanoic acid Chemical class CCCCCCCCCC(O)=O GHVNFZFCNZKVNT-UHFFFAOYSA-N 0.000 description 1
- 238000004042 decolorization Methods 0.000 description 1
- SQIFACVGCPWBQZ-UHFFFAOYSA-N delta-terpineol Natural products CC(C)(O)C1CCC(=C)CC1 SQIFACVGCPWBQZ-UHFFFAOYSA-N 0.000 description 1
- 230000003745 detangling effect Effects 0.000 description 1
- 229910052805 deuterium Inorganic materials 0.000 description 1
- 150000001990 dicarboxylic acid derivatives Chemical class 0.000 description 1
- 150000001991 dicarboxylic acids Chemical class 0.000 description 1
- XSNQECSCDATQEL-UHFFFAOYSA-N dihydromyrcenol Chemical compound C=CC(C)CCCC(C)(C)O XSNQECSCDATQEL-UHFFFAOYSA-N 0.000 description 1
- 229930008394 dihydromyrcenol Natural products 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 238000006471 dimerization reaction Methods 0.000 description 1
- IQDGSYLLQPDQDV-UHFFFAOYSA-N dimethylazanium;chloride Chemical compound Cl.CNC IQDGSYLLQPDQDV-UHFFFAOYSA-N 0.000 description 1
- USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical compound C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 description 1
- ZPWVASYFFYYZEW-UHFFFAOYSA-L dipotassium hydrogen phosphate Chemical compound [K+].[K+].OP([O-])([O-])=O ZPWVASYFFYYZEW-UHFFFAOYSA-L 0.000 description 1
- 229910000396 dipotassium phosphate Inorganic materials 0.000 description 1
- 235000019797 dipotassium phosphate Nutrition 0.000 description 1
- SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 1
- 230000008034 disappearance Effects 0.000 description 1
- WAJKHNTVDCZXPH-UHFFFAOYSA-N disodium acetylide Chemical compound [Na+].[Na+].[C-]#[C-] WAJKHNTVDCZXPH-UHFFFAOYSA-N 0.000 description 1
- BNIILDVGGAEEIG-UHFFFAOYSA-L disodium hydrogen phosphate Chemical compound [Na+].[Na+].OP([O-])([O-])=O BNIILDVGGAEEIG-UHFFFAOYSA-L 0.000 description 1
- 229910000397 disodium phosphate Inorganic materials 0.000 description 1
- 235000019800 disodium phosphate Nutrition 0.000 description 1
- UQGFMSUEHSUPRD-UHFFFAOYSA-N disodium;3,7-dioxido-2,4,6,8,9-pentaoxa-1,3,5,7-tetraborabicyclo[3.3.1]nonane Chemical compound [Na+].[Na+].O1B([O-])OB2OB([O-])OB1O2 UQGFMSUEHSUPRD-UHFFFAOYSA-N 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- DDXLVDQZPFLQMZ-UHFFFAOYSA-M dodecyl(trimethyl)azanium;chloride Chemical compound [Cl-].CCCCCCCCCCCC[N+](C)(C)C DDXLVDQZPFLQMZ-UHFFFAOYSA-M 0.000 description 1
- QYDYPVFESGNLHU-UHFFFAOYSA-N elaidic acid methyl ester Natural products CCCCCCCCC=CCCCCCCCC(=O)OC QYDYPVFESGNLHU-UHFFFAOYSA-N 0.000 description 1
- 239000003792 electrolyte Substances 0.000 description 1
- 238000001493 electron microscopy Methods 0.000 description 1
- 230000001804 emulsifying effect Effects 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 238000005265 energy consumption Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- NYNCZOLNVTXTTP-UHFFFAOYSA-N ethyl 2-(1,3-dioxoisoindol-2-yl)acetate Chemical compound C1=CC=C2C(=O)N(CC(=O)OCC)C(=O)C2=C1 NYNCZOLNVTXTTP-UHFFFAOYSA-N 0.000 description 1
- LZCLXQDLBQLTDK-UHFFFAOYSA-N ethyl 2-hydroxypropanoate Chemical class CCOC(=O)C(C)O LZCLXQDLBQLTDK-UHFFFAOYSA-N 0.000 description 1
- 229960002217 eugenol Drugs 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 125000005313 fatty acid group Chemical group 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000000834 fixative Substances 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 230000008014 freezing Effects 0.000 description 1
- 238000007710 freezing Methods 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- LRBQNJMCXXYXIU-QWKBTXIPSA-N gallotannic acid Chemical compound OC1=C(O)C(O)=CC(C(=O)OC=2C(=C(O)C=C(C=2)C(=O)OC[C@H]2[C@@H]([C@@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)[C@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)[C@@H](OC(=O)C=3C=C(OC(=O)C=4C=C(O)C(O)=C(O)C=4)C(O)=C(O)C=3)O2)OC(=O)C=2C=C(OC(=O)C=3C=C(O)C(O)=C(O)C=3)C(O)=C(O)C=2)O)=C1 LRBQNJMCXXYXIU-QWKBTXIPSA-N 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- HIGQPQRQIQDZMP-UHFFFAOYSA-N geranil acetate Natural products CC(C)=CCCC(C)=CCOC(C)=O HIGQPQRQIQDZMP-UHFFFAOYSA-N 0.000 description 1
- 229940113087 geraniol Drugs 0.000 description 1
- HIGQPQRQIQDZMP-DHZHZOJOSA-N geranyl acetate Chemical compound CC(C)=CCC\C(C)=C\COC(C)=O HIGQPQRQIQDZMP-DHZHZOJOSA-N 0.000 description 1
- 230000002070 germicidal effect Effects 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- 235000013922 glutamic acid Nutrition 0.000 description 1
- 239000004220 glutamic acid Substances 0.000 description 1
- 150000002314 glycerols Chemical class 0.000 description 1
- 150000004795 grignard reagents Chemical class 0.000 description 1
- 235000008216 herbs Nutrition 0.000 description 1
- UFLHIIWVXFIJGU-UHFFFAOYSA-N hex-3-en-1-ol Natural products CCC=CCCO UFLHIIWVXFIJGU-UHFFFAOYSA-N 0.000 description 1
- IPCSVZSSVZVIGE-UHFFFAOYSA-M hexadecanoate Chemical compound CCCCCCCCCCCCCCCC([O-])=O IPCSVZSSVZVIGE-UHFFFAOYSA-M 0.000 description 1
- 229950004531 hexyldecanoic acid Drugs 0.000 description 1
- 239000012456 homogeneous solution Substances 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 239000005457 ice water Substances 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 238000003780 insertion Methods 0.000 description 1
- 230000037431 insertion Effects 0.000 description 1
- 229930002839 ionone Natural products 0.000 description 1
- 150000002499 ionone derivatives Chemical class 0.000 description 1
- 235000000396 iron Nutrition 0.000 description 1
- HEBMCVBCEDMUOF-UHFFFAOYSA-N isochromane Chemical compound C1=CC=C2COCCC2=C1 HEBMCVBCEDMUOF-UHFFFAOYSA-N 0.000 description 1
- SVURIXNDRWRAFU-UHFFFAOYSA-N juniperanol Natural products C1C23C(C)CCC3C(C)(C)C1C(O)(C)CC2 SVURIXNDRWRAFU-UHFFFAOYSA-N 0.000 description 1
- ACKFDYCQCBEDNU-UHFFFAOYSA-J lead(2+);tetraacetate Chemical compound [Pb+2].CC([O-])=O.CC([O-])=O.CC([O-])=O.CC([O-])=O ACKFDYCQCBEDNU-UHFFFAOYSA-J 0.000 description 1
- 229930007744 linalool Natural products 0.000 description 1
- UWKAYLJWKGQEPM-UHFFFAOYSA-N linalool acetate Natural products CC(C)=CCCC(C)(C=C)OC(C)=O UWKAYLJWKGQEPM-UHFFFAOYSA-N 0.000 description 1
- 125000005647 linker group Chemical group 0.000 description 1
- 150000002632 lipids Chemical class 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 150000007931 macrolactones Chemical class 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- NXPHGHWWQRMDIA-UHFFFAOYSA-M magnesium;carbanide;bromide Chemical compound [CH3-].[Mg+2].[Br-] NXPHGHWWQRMDIA-UHFFFAOYSA-M 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
- IPWBXORAIBJDDQ-UHFFFAOYSA-N methyl 2-hexyl-3-oxocyclopentane-1-carboxylate Chemical compound CCCCCCC1C(C(=O)OC)CCC1=O IPWBXORAIBJDDQ-UHFFFAOYSA-N 0.000 description 1
- QJQYPZZUKLQGGT-UHFFFAOYSA-N methyl hypobromite Chemical class COBr QJQYPZZUKLQGGT-UHFFFAOYSA-N 0.000 description 1
- QYDYPVFESGNLHU-KHPPLWFESA-N methyl oleate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OC QYDYPVFESGNLHU-KHPPLWFESA-N 0.000 description 1
- 229940073769 methyl oleate Drugs 0.000 description 1
- 125000005527 methyl sulfate group Chemical group 0.000 description 1
- 239000012022 methylating agents Substances 0.000 description 1
- BEGLCMHJXHIJLR-UHFFFAOYSA-N methylisothiazolinone Chemical compound CN1SC=CC1=O BEGLCMHJXHIJLR-UHFFFAOYSA-N 0.000 description 1
- DVSDBMFJEQPWNO-UHFFFAOYSA-N methyllithium Chemical compound C[Li] DVSDBMFJEQPWNO-UHFFFAOYSA-N 0.000 description 1
- YACKEPLHDIMKIO-UHFFFAOYSA-N methylphosphonic acid Chemical compound CP(O)(O)=O YACKEPLHDIMKIO-UHFFFAOYSA-N 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 125000002757 morpholinyl group Chemical group 0.000 description 1
- DZJFABDVWIPEIM-UHFFFAOYSA-N n,n-bis(2-hydroxyethyl)dodecan-1-amine oxide Chemical compound CCCCCCCCCCCC[N+]([O-])(CCO)CCO DZJFABDVWIPEIM-UHFFFAOYSA-N 0.000 description 1
- BACGZXMASLQEQT-UHFFFAOYSA-N n,n-diethyldecan-1-amine oxide Chemical compound CCCCCCCCCC[N+]([O-])(CC)CC BACGZXMASLQEQT-UHFFFAOYSA-N 0.000 description 1
- RSVIRMFSJVHWJV-UHFFFAOYSA-N n,n-dimethyloctan-1-amine oxide Chemical compound CCCCCCCC[N+](C)(C)[O-] RSVIRMFSJVHWJV-UHFFFAOYSA-N 0.000 description 1
- WWRMRGSSMGHJPF-UHFFFAOYSA-N n-dodecyl-n-methylhydroxylamine Chemical compound CCCCCCCCCCCCN(C)O WWRMRGSSMGHJPF-UHFFFAOYSA-N 0.000 description 1
- WNGXRJQKUYDBDP-UHFFFAOYSA-N n-ethyl-n-methylhexadecan-1-amine oxide Chemical compound CCCCCCCCCCCCCCCC[N+](C)([O-])CC WNGXRJQKUYDBDP-UHFFFAOYSA-N 0.000 description 1
- NCDCLPBOMHPFCV-UHFFFAOYSA-N n-hexyl n-hexanoate Natural products CCCCCCOC(=O)CCCCC NCDCLPBOMHPFCV-UHFFFAOYSA-N 0.000 description 1
- PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical compound C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 1
- 239000005445 natural material Substances 0.000 description 1
- 229920005615 natural polymer Polymers 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 150000002823 nitrates Chemical class 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- MGFYIUFZLHCRTH-UHFFFAOYSA-N nitrilotriacetic acid Chemical class OC(=O)CN(CC(O)=O)CC(O)=O MGFYIUFZLHCRTH-UHFFFAOYSA-N 0.000 description 1
- BKIMMITUMNQMOS-UHFFFAOYSA-N nonane Chemical class CCCCCCCCC BKIMMITUMNQMOS-UHFFFAOYSA-N 0.000 description 1
- XFVAWWPVJMMDGC-UHFFFAOYSA-N octa-2,7-diene-1,6-diol Chemical compound OCC=CCCC(O)C=C XFVAWWPVJMMDGC-UHFFFAOYSA-N 0.000 description 1
- NELAVKWPGRMFEQ-UHFFFAOYSA-N octane-1,4-diol Chemical compound CCCCC(O)CCCO NELAVKWPGRMFEQ-UHFFFAOYSA-N 0.000 description 1
- ZKRNQSNKDPEUOH-UHFFFAOYSA-N octane-1,5-diol Chemical compound CCCC(O)CCCCO ZKRNQSNKDPEUOH-UHFFFAOYSA-N 0.000 description 1
- QUADBKCRXGFGAX-UHFFFAOYSA-N octane-1,7-diol Chemical compound CC(O)CCCCCCO QUADBKCRXGFGAX-UHFFFAOYSA-N 0.000 description 1
- GBJVLVHKCGSHIA-UHFFFAOYSA-N octane-4,4-diol Chemical class CCCCC(O)(O)CCC GBJVLVHKCGSHIA-UHFFFAOYSA-N 0.000 description 1
- WWZKQHOCKIZLMA-UHFFFAOYSA-N octanoic acid Chemical compound CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 1
- JPMIIZHYYWMHDT-UHFFFAOYSA-N octhilinone Chemical compound CCCCCCCCN1SC=CC1=O JPMIIZHYYWMHDT-UHFFFAOYSA-N 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 150000002889 oleic acids Chemical class 0.000 description 1
- 150000002902 organometallic compounds Chemical class 0.000 description 1
- 239000007800 oxidant agent Substances 0.000 description 1
- MUMZUERVLWJKNR-UHFFFAOYSA-N oxoplatinum Chemical compound [Pt]=O MUMZUERVLWJKNR-UHFFFAOYSA-N 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- IPCSVZSSVZVIGE-UHFFFAOYSA-N palmitic acid group Chemical group C(CCCCCCCCCCCCCCC)(=O)O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 1
- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 1
- QNGNSVIICDLXHT-UHFFFAOYSA-N para-ethylbenzaldehyde Natural products CCC1=CC=C(C=O)C=C1 QNGNSVIICDLXHT-UHFFFAOYSA-N 0.000 description 1
- 235000020232 peanut Nutrition 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- RGSFGYAAUTVSQA-UHFFFAOYSA-N pentamethylene Natural products C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 description 1
- 229960003330 pentetic acid Drugs 0.000 description 1
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
- MDHYEMXUFSJLGV-UHFFFAOYSA-N phenethyl acetate Chemical compound CC(=O)OCCC1=CC=CC=C1 MDHYEMXUFSJLGV-UHFFFAOYSA-N 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- WVDDGKGOMKODPV-ZQBYOMGUSA-N phenyl(114C)methanol Chemical compound O[14CH2]C1=CC=CC=C1 WVDDGKGOMKODPV-ZQBYOMGUSA-N 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 229940085991 phosphate ion Drugs 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 229910003446 platinum oxide Inorganic materials 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920005646 polycarboxylate Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 235000020777 polyunsaturated fatty acids Nutrition 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- CHKVPAROMQMJNQ-UHFFFAOYSA-M potassium bisulfate Chemical compound [K+].OS([O-])(=O)=O CHKVPAROMQMJNQ-UHFFFAOYSA-M 0.000 description 1
- 229910000343 potassium bisulfate Inorganic materials 0.000 description 1
- NTTOTNSKUYCDAV-UHFFFAOYSA-N potassium hydride Chemical compound [KH] NTTOTNSKUYCDAV-UHFFFAOYSA-N 0.000 description 1
- 229910000105 potassium hydride Inorganic materials 0.000 description 1
- 239000012286 potassium permanganate Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- KIWATKANDHUUOB-UHFFFAOYSA-N propan-2-yl 2-hydroxypropanoate Chemical class CC(C)OC(=O)C(C)O KIWATKANDHUUOB-UHFFFAOYSA-N 0.000 description 1
- 125000006239 protecting group Chemical group 0.000 description 1
- 238000005086 pumping 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
- 230000008929 regeneration Effects 0.000 description 1
- 238000011069 regeneration method Methods 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 229960004889 salicylic acid Drugs 0.000 description 1
- 239000012266 salt solution Substances 0.000 description 1
- 239000012047 saturated solution Substances 0.000 description 1
- 238000012216 screening Methods 0.000 description 1
- 150000003335 secondary amines Chemical class 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000012419 sodium bis(2-methoxyethoxy)aluminum hydride Substances 0.000 description 1
- WBHQBSYUUJJSRZ-UHFFFAOYSA-M sodium bisulfate Chemical compound [Na+].OS([O-])(=O)=O WBHQBSYUUJJSRZ-UHFFFAOYSA-M 0.000 description 1
- 229910000342 sodium bisulfate Inorganic materials 0.000 description 1
- 235000009518 sodium iodide Nutrition 0.000 description 1
- 239000004328 sodium tetraborate Substances 0.000 description 1
- 235000010339 sodium tetraborate Nutrition 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 238000000935 solvent evaporation Methods 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- RINCXYDBBGOEEQ-UHFFFAOYSA-N succinic anhydride Chemical class O=C1CCC(=O)O1 RINCXYDBBGOEEQ-UHFFFAOYSA-N 0.000 description 1
- 235000000346 sugar Nutrition 0.000 description 1
- 150000008163 sugars Chemical class 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000012209 synthetic fiber Substances 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 235000015523 tannic acid Nutrition 0.000 description 1
- 229920002258 tannic acid Polymers 0.000 description 1
- 229940033123 tannic acid Drugs 0.000 description 1
- 229940116411 terpineol Drugs 0.000 description 1
- 239000004250 tert-Butylhydroquinone Substances 0.000 description 1
- RKSOPLXZQNSWAS-UHFFFAOYSA-N tert-butyl bromide Chemical compound CC(C)(C)Br RKSOPLXZQNSWAS-UHFFFAOYSA-N 0.000 description 1
- 235000019281 tert-butylhydroquinone Nutrition 0.000 description 1
- 125000001412 tetrahydropyranyl group Chemical group 0.000 description 1
- 229930003799 tocopherol Natural products 0.000 description 1
- 239000011732 tocopherol Substances 0.000 description 1
- 235000019149 tocopherols Nutrition 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- DXNCZXXFRKPEPY-UHFFFAOYSA-N tridecanedioic acid Chemical compound OC(=O)CCCCCCCCCCCC(O)=O DXNCZXXFRKPEPY-UHFFFAOYSA-N 0.000 description 1
- 150000005691 triesters Chemical class 0.000 description 1
- 239000001069 triethyl citrate Substances 0.000 description 1
- VMYFZRTXGLUXMZ-UHFFFAOYSA-N triethyl citrate Natural products CCOC(=O)C(O)(C(=O)OCC)C(=O)OCC VMYFZRTXGLUXMZ-UHFFFAOYSA-N 0.000 description 1
- 235000013769 triethyl citrate Nutrition 0.000 description 1
- HVLUSYMLLVVXGI-USGGBSEESA-M trimethyl-[(z)-octadec-9-enyl]azanium;chloride Chemical compound [Cl-].CCCCCCCC\C=C/CCCCCCCC[N+](C)(C)C HVLUSYMLLVVXGI-USGGBSEESA-M 0.000 description 1
- 229910052722 tritium Inorganic materials 0.000 description 1
- MWOOGOJBHIARFG-UHFFFAOYSA-N vanillin Chemical compound COC1=CC(C=O)=CC=C1O MWOOGOJBHIARFG-UHFFFAOYSA-N 0.000 description 1
- 235000012141 vanillin Nutrition 0.000 description 1
- FGQOOHJZONJGDT-UHFFFAOYSA-N vanillin Natural products COC1=CC(O)=CC(C=O)=C1 FGQOOHJZONJGDT-UHFFFAOYSA-N 0.000 description 1
- 239000003039 volatile agent Substances 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 239000002023 wood Substances 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
- 239000008096 xylene Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- FUQAYSQLAOJBBC-PAPYEOQZSA-N β-caryophyllene alcohol Chemical compound C1C[C@](C2)(C)CCC[C@]2(O)[C@H]2CC(C)(C)[C@@H]21 FUQAYSQLAOJBBC-PAPYEOQZSA-N 0.000 description 1
- QUEDXNHFTDJVIY-UHFFFAOYSA-N γ-tocopherol Chemical class OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1 QUEDXNHFTDJVIY-UHFFFAOYSA-N 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
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/38—Cationic compounds
- C11D1/62—Quaternary ammonium compounds
-
- 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
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/38—Cationic compounds
- C11D1/645—Mixtures of compounds all of which are cationic
-
- 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
- C11D3/0005—Other compounding ingredients characterised by their effect
- C11D3/001—Softening compositions
- C11D3/0015—Softening compositions liquid
-
- 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
- C11D3/2003—Alcohols; Phenols
- C11D3/2041—Dihydric alcohols
- C11D3/2044—Dihydric alcohols linear
-
- 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
- C11D3/2003—Alcohols; Phenols
- C11D3/2041—Dihydric alcohols
- C11D3/2048—Dihydric alcohols branched
-
- 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
- C11D3/33—Amino carboxylic 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
- C11D3/2003—Alcohols; Phenols
- C11D3/2006—Monohydric alcohols
- C11D3/201—Monohydric alcohols linear
-
- 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
- C11D3/2003—Alcohols; Phenols
- C11D3/2006—Monohydric alcohols
- C11D3/2017—Monohydric alcohols branched
-
- 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
- C11D3/2003—Alcohols; Phenols
- C11D3/2041—Dihydric alcohols
- C11D3/2058—Dihydric alcohols aromatic
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Emergency Medicine (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US62101996A | 1996-03-22 | 1996-03-22 | |
US08/679,694 US5747443A (en) | 1996-07-11 | 1996-07-11 | Fabric softening compound/composition |
Publications (1)
Publication Number | Publication Date |
---|---|
CZ304798A3 true CZ304798A3 (cs) | 1999-03-17 |
Family
ID=27088832
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CZ983047A CZ304798A3 (cs) | 1996-03-22 | 1997-03-05 | Biodegradovatelné látky pro změkčování tkanin a přípravky pro změkčování tkanin obsahující tyto látky |
Country Status (9)
Country | Link |
---|---|
EP (1) | EP0888424A1 (fr) |
JP (1) | JP3102894B2 (fr) |
CN (1) | CN1098350C (fr) |
AU (1) | AU2066597A (fr) |
BR (1) | BR9710409A (fr) |
CA (1) | CA2249587C (fr) |
CZ (1) | CZ304798A3 (fr) |
TR (1) | TR199801784T2 (fr) |
WO (1) | WO1997034972A1 (fr) |
Families Citing this family (19)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP3222145B2 (ja) | 1996-10-21 | 2001-10-22 | ザ、プロクター、エンド、ギャンブル、カンパニー | 濃縮布地柔軟化組成物 |
BR9713487A (pt) * | 1996-10-21 | 2002-11-26 | Procter & Gamble | Processos para a preparação de um composto ativo e de uma composição pré-misturada amaciante de tecidos e produtos abtidos por tais processos |
WO1998047991A1 (fr) * | 1997-05-19 | 1998-10-29 | The Procter & Gamble Company | Agent adoucissant derive de triethanolamine acyle |
WO1998057721A1 (fr) * | 1997-06-16 | 1998-12-23 | The Procter & Gamble Company | Procede permettant d'ameliorer l'odeur des solvants du commerce utilises dans les compositions d'adoucissants textiles |
JP2001520304A (ja) | 1997-10-23 | 2001-10-30 | ザ、プロクター、エンド、ギャンブル、カンパニー | 脂肪酸、石鹸、界面活性剤系、およびそれらをベースにした消費製品 |
US6992057B2 (en) * | 2000-02-22 | 2006-01-31 | The Procter & Gamble Company | Fatty acids, soaps, surfactant systems, and consumer products based thereon |
ZA991635B (en) * | 1998-03-02 | 1999-09-02 | Procter & Gamble | Concentrated, stable, translucent or clear, fabric softening compositions. |
US6486121B2 (en) | 1998-04-15 | 2002-11-26 | The Procter & Gamble Company | Softener active derived from acylated triethanolamine |
US6607715B1 (en) * | 1998-11-12 | 2003-08-19 | Croda, Inc. | Fatty ammonium quaternary compositions |
US6916781B2 (en) | 1999-03-02 | 2005-07-12 | The Procter & Gamble Company | Concentrated, stable, translucent or clear, fabric softening compositions |
DE60120567T2 (de) | 2000-01-19 | 2007-06-06 | Kao Corporation | Weichmacherzusammensetzung für die textilausrüstung |
GB0021765D0 (en) | 2000-09-05 | 2000-10-18 | Unilever Plc | A method of preparing fabric conditioning compositions |
GB0021766D0 (en) * | 2000-09-05 | 2000-10-18 | Unilever Plc | Fabric conditioning compositions |
US6770617B2 (en) | 2001-04-11 | 2004-08-03 | Kao Corporation | Softener composition |
GB0625069D0 (en) | 2006-12-15 | 2007-01-24 | Givaudan Sa | Compositions |
US11261402B2 (en) | 2016-01-25 | 2022-03-01 | The Procter & Gamble Company | Treatment compositions |
JP6738900B2 (ja) | 2016-01-25 | 2020-08-12 | ザ プロクター アンド ギャンブル カンパニーThe Procter & Gamble Company | 処理組成物 |
CN110157551B (zh) * | 2019-06-26 | 2021-04-30 | 广州市淳烨生物科技有限公司 | 一种高浓缩洗衣液 |
WO2023222325A1 (fr) * | 2022-05-19 | 2023-11-23 | Unilever Ip Holdings B.V. | Conditionneur de tissu concentré |
Family Cites Families (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB8312619D0 (en) * | 1983-05-07 | 1983-06-08 | Procter & Gamble | Surfactant compositions |
JPH01501492A (ja) * | 1987-06-16 | 1989-05-25 | コートル・ソシエテ・アノニム | 濃厚な柔軟剤組成物 |
GB8914054D0 (en) * | 1989-06-19 | 1989-08-09 | Unilever Plc | Fabric softening composition |
AU6271294A (en) * | 1993-03-01 | 1994-09-26 | Procter & Gamble Company, The | Concentrated biodegradable quaternary ammonium fabric softener compositions and compounds containing intermediate iodine value unsaturated fatty acid chains |
DE4307186A1 (de) * | 1993-03-08 | 1994-09-15 | Henkel Kgaa | Wäßrige Textilweichmacher-Zusammensetzung |
EP0637625A1 (fr) * | 1993-08-02 | 1995-02-08 | The Procter & Gamble Company | Emulsions superconcentrés avec adoucissants pour textiles |
JP3357453B2 (ja) * | 1993-09-10 | 2002-12-16 | 花王株式会社 | 液体柔軟仕上剤組成物並びに新規第4級アンモニウム塩並びに該塩の製造法 |
US5490944A (en) * | 1994-08-11 | 1996-02-13 | Colgate-Palmolive Company | Liquid fabric softener compositions |
US5500138A (en) * | 1994-10-20 | 1996-03-19 | The Procter & Gamble Company | Fabric softener compositions with improved environmental impact |
US5525245A (en) * | 1994-12-21 | 1996-06-11 | Colgate-Palmolive Company | Clear, concentrated liquid fabric softener compositions |
-
1997
- 1997-03-05 CA CA002249587A patent/CA2249587C/fr not_active Expired - Fee Related
- 1997-03-05 AU AU20665/97A patent/AU2066597A/en not_active Abandoned
- 1997-03-05 CZ CZ983047A patent/CZ304798A3/cs unknown
- 1997-03-05 JP JP09533490A patent/JP3102894B2/ja not_active Expired - Fee Related
- 1997-03-05 CN CN97194864A patent/CN1098350C/zh not_active Expired - Fee Related
- 1997-03-05 TR TR1998/01784T patent/TR199801784T2/xx unknown
- 1997-03-05 WO PCT/US1997/003374 patent/WO1997034972A1/fr not_active Application Discontinuation
- 1997-03-05 BR BR9710409A patent/BR9710409A/pt not_active Application Discontinuation
- 1997-03-05 EP EP97908858A patent/EP0888424A1/fr not_active Withdrawn
Also Published As
Publication number | Publication date |
---|---|
EP0888424A1 (fr) | 1999-01-07 |
AU2066597A (en) | 1997-10-10 |
CA2249587A1 (fr) | 1997-09-25 |
TR199801784T2 (en) | 1998-12-21 |
CN1098350C (zh) | 2003-01-08 |
CN1219953A (zh) | 1999-06-16 |
JPH11507095A (ja) | 1999-06-22 |
CA2249587C (fr) | 2001-12-18 |
BR9710409A (pt) | 1999-08-17 |
JP3102894B2 (ja) | 2000-10-23 |
WO1997034972A1 (fr) | 1997-09-25 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US5747443A (en) | Fabric softening compound/composition | |
CA2226564C (fr) | Composition d'adoucisseur de tissus stable et concentre ayant une faible teneur en solvant organique | |
US5877145A (en) | Concentrated fabric softening composition with good freeze/thaw recovery and highly unsaturated fabric softener compound therefor | |
CZ304798A3 (cs) | Biodegradovatelné látky pro změkčování tkanin a přípravky pro změkčování tkanin obsahující tyto látky | |
JP3222145B2 (ja) | 濃縮布地柔軟化組成物 | |
US5759990A (en) | Concentrated fabric softening composition with good freeze/thaw recovery and highly unsaturated fabric softener compound therefor | |
US6369025B1 (en) | Concentrated, water dispersible, stable, fabric softening compositions | |
US20060058215A1 (en) | Concentrated, stable, preferably clear, fabric softening composition | |
EP1352948A1 (fr) | Composition concentrée et stable d'adoucissement de linge | |
WO1998047991A1 (fr) | Agent adoucissant derive de triethanolamine acyle | |
JP3419464B2 (ja) | 濃縮布地柔軟化組成物およびそのための高不飽和布地柔軟剤化合物 | |
US6486121B2 (en) | Softener active derived from acylated triethanolamine | |
US20050202998A1 (en) | Concentrated, stable, translucent or clear, fabric softening compositions including chelants | |
CA2290409C (fr) | Agent adoucissant derive de triethanolamine acyle | |
CA2269352A1 (fr) | Composition concentree d'assouplissant de textile |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PD00 | Pending as of 2000-06-30 in czech republic |