CZ3898A3 - Koncentrované stabilní prostředky na změkčování tkanin obsahující chelatační činidla - Google Patents
Koncentrované stabilní prostředky na změkčování tkanin obsahující chelatační činidla Download PDFInfo
- Publication number
- CZ3898A3 CZ3898A3 CZ9838A CZ3898A CZ3898A3 CZ 3898 A3 CZ3898 A3 CZ 3898A3 CZ 9838 A CZ9838 A CZ 9838A CZ 3898 A CZ3898 A CZ 3898A CZ 3898 A3 CZ3898 A3 CZ 3898A3
- Authority
- CZ
- Czechia
- Prior art keywords
- methyl
- dimethyl
- hexanediol
- pentanediol
- heptanediol
- Prior art date
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- 239000004744 fabric Substances 0.000 title claims abstract description 44
- 239000002738 chelating agent Substances 0.000 title claims abstract description 37
- 238000002360 preparation method Methods 0.000 title description 38
- 239000000203 mixture Substances 0.000 claims abstract description 200
- 239000002253 acid Substances 0.000 claims abstract description 31
- 235000014113 dietary fatty acids Nutrition 0.000 claims abstract description 31
- 239000000194 fatty acid Substances 0.000 claims abstract description 31
- 229930195729 fatty acid Natural products 0.000 claims abstract description 31
- 150000004665 fatty acids Chemical class 0.000 claims abstract description 31
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 25
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 14
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims abstract description 12
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 12
- 229910052740 iodine Inorganic materials 0.000 claims abstract description 12
- 239000011630 iodine Substances 0.000 claims abstract description 12
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 12
- 239000001257 hydrogen Substances 0.000 claims abstract description 11
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims abstract description 11
- 238000004458 analytical method Methods 0.000 claims abstract description 8
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims abstract description 7
- GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 claims abstract description 5
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims abstract description 5
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims abstract description 5
- 239000002904 solvent Substances 0.000 claims description 199
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 64
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 51
- 239000004480 active ingredient Substances 0.000 claims description 44
- 150000001875 compounds Chemical class 0.000 claims description 40
- 239000004014 plasticizer Substances 0.000 claims description 26
- 125000004417 unsaturated alkyl group Chemical group 0.000 claims description 23
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims description 20
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims description 18
- 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 claims description 18
- 229960003330 pentetic acid Drugs 0.000 claims description 18
- YPFDHNVEDLHUCE-UHFFFAOYSA-N 1,3-propanediol Substances OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 claims description 16
- 125000004432 carbon atom Chemical group C* 0.000 claims description 16
- 239000003974 emollient agent Substances 0.000 claims description 16
- 150000001450 anions Chemical class 0.000 claims description 13
- 229920000166 polytrimethylene carbonate Polymers 0.000 claims description 12
- DNIAPMSPPWPWGF-VKHMYHEASA-N (+)-propylene glycol Chemical compound C[C@H](O)CO DNIAPMSPPWPWGF-VKHMYHEASA-N 0.000 claims description 9
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims description 8
- 238000002834 transmittance Methods 0.000 claims description 6
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 claims description 5
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 claims description 5
- KIWBPDUYBMNFTB-UHFFFAOYSA-N Ethyl hydrogen sulfate Chemical compound CCOS(O)(=O)=O KIWBPDUYBMNFTB-UHFFFAOYSA-N 0.000 claims description 5
- 229910002651 NO3 Inorganic materials 0.000 claims description 5
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 claims description 5
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims description 5
- 125000002947 alkylene group Chemical group 0.000 claims description 5
- JZMJDSHXVKJFKW-UHFFFAOYSA-M methyl sulfate(1-) Chemical compound COS([O-])(=O)=O JZMJDSHXVKJFKW-UHFFFAOYSA-M 0.000 claims description 5
- 239000003021 water soluble solvent Substances 0.000 claims description 5
- 239000003153 chemical reaction reagent Substances 0.000 claims description 4
- YACKEPLHDIMKIO-UHFFFAOYSA-N methylphosphonic acid Chemical class CP(O)(O)=O YACKEPLHDIMKIO-UHFFFAOYSA-N 0.000 claims description 4
- MGFYIUFZLHCRTH-UHFFFAOYSA-N nitrilotriacetic acid Chemical compound OC(=O)CN(CC(O)=O)CC(O)=O MGFYIUFZLHCRTH-UHFFFAOYSA-N 0.000 claims description 4
- RUOJZAUFBMNUDX-UHFFFAOYSA-N propylene carbonate Chemical compound CC1COC(=O)O1 RUOJZAUFBMNUDX-UHFFFAOYSA-N 0.000 claims description 3
- VKZRWSNIWNFCIQ-UHFFFAOYSA-N 2-[2-(1,2-dicarboxyethylamino)ethylamino]butanedioic acid Chemical compound OC(=O)CC(C(O)=O)NCCNC(C(O)=O)CC(O)=O VKZRWSNIWNFCIQ-UHFFFAOYSA-N 0.000 claims 1
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 claims 1
- MXBDBLBKBBAYGD-UHFFFAOYSA-N P(O)(O)=O.C Chemical compound P(O)(O)=O.C MXBDBLBKBBAYGD-UHFFFAOYSA-N 0.000 claims 1
- -1 e.g. Chemical group 0.000 abstract description 90
- 125000001424 substituent group Chemical group 0.000 abstract description 14
- 230000005540 biological transmission Effects 0.000 abstract description 4
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 abstract 1
- 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 217
- 238000000034 method Methods 0.000 description 202
- 239000002585 base Substances 0.000 description 95
- VNAWKNVDKFZFSU-UHFFFAOYSA-N 2-ethyl-2-methylpropane-1,3-diol Chemical compound CCC(C)(CO)CO VNAWKNVDKFZFSU-UHFFFAOYSA-N 0.000 description 79
- 150000002009 diols Chemical class 0.000 description 66
- 238000006243 chemical reaction Methods 0.000 description 44
- 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 description 43
- PFURGBBHAOXLIO-UHFFFAOYSA-N cyclohexane-1,2-diol Chemical compound OC1CCCCC1O PFURGBBHAOXLIO-UHFFFAOYSA-N 0.000 description 42
- AKPLTHZVVWBOPT-UHFFFAOYSA-N 2,2-diethylbutane-1,3-diol Chemical compound CCC(CC)(CO)C(C)O AKPLTHZVVWBOPT-UHFFFAOYSA-N 0.000 description 40
- 239000000047 product Substances 0.000 description 38
- 229940015975 1,2-hexanediol Drugs 0.000 description 36
- ZTQSAGDEMFDKMZ-UHFFFAOYSA-N Butyraldehyde Chemical compound CCCC=O ZTQSAGDEMFDKMZ-UHFFFAOYSA-N 0.000 description 36
- QXKKYNIWAYERHT-UHFFFAOYSA-N 2,2-dimethylbutane-1,3-diol Chemical compound CC(O)C(C)(C)CO QXKKYNIWAYERHT-UHFFFAOYSA-N 0.000 description 35
- 239000011541 reaction mixture Substances 0.000 description 32
- 239000007788 liquid Substances 0.000 description 29
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 28
- 239000000126 substance Substances 0.000 description 27
- FHKSXSQHXQEMOK-UHFFFAOYSA-N hexane-1,2-diol Chemical compound CCCCC(O)CO FHKSXSQHXQEMOK-UHFFFAOYSA-N 0.000 description 26
- 239000002979 fabric softener Substances 0.000 description 25
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 22
- 239000000243 solution Substances 0.000 description 22
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 21
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 21
- 229920006395 saturated elastomer Polymers 0.000 description 21
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 20
- AMIMRNSIRUDHCM-UHFFFAOYSA-N Isopropylaldehyde Chemical compound CC(C)C=O AMIMRNSIRUDHCM-UHFFFAOYSA-N 0.000 description 20
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 19
- WERYXYBDKMZEQL-UHFFFAOYSA-N 1,4-butanediol Substances OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 18
- 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
- 239000003795 chemical substances by application Substances 0.000 description 18
- 238000009833 condensation Methods 0.000 description 18
- 230000005494 condensation Effects 0.000 description 18
- QWGRWMMWNDWRQN-UHFFFAOYSA-N 2-methylpropane-1,3-diol Chemical compound OCC(C)CO QWGRWMMWNDWRQN-UHFFFAOYSA-N 0.000 description 17
- XPFCZYUVICHKDS-UHFFFAOYSA-N 3-methylbutane-1,3-diol Chemical compound CC(C)(O)CCO XPFCZYUVICHKDS-UHFFFAOYSA-N 0.000 description 17
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical class CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 17
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 17
- HGBOYTHUEUWSSQ-UHFFFAOYSA-N valeric aldehyde Natural products CCCCC=O HGBOYTHUEUWSSQ-UHFFFAOYSA-N 0.000 description 17
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 16
- 239000000463 material Substances 0.000 description 16
- 229940043375 1,5-pentanediol Drugs 0.000 description 15
- 150000001299 aldehydes Chemical class 0.000 description 15
- BMRWNKZVCUKKSR-UHFFFAOYSA-N butane-1,2-diol Chemical compound CCC(O)CO BMRWNKZVCUKKSR-UHFFFAOYSA-N 0.000 description 15
- 238000004821 distillation Methods 0.000 description 15
- UQGLNXPQGUMNRU-UHFFFAOYSA-N heptane-1,6-diol Chemical compound CC(O)CCCCCO UQGLNXPQGUMNRU-UHFFFAOYSA-N 0.000 description 15
- 229960004063 propylene glycol Drugs 0.000 description 15
- OGRCRHSHBFQRKO-UHFFFAOYSA-N heptane-1,4-diol Chemical compound CCCC(O)CCCO OGRCRHSHBFQRKO-UHFFFAOYSA-N 0.000 description 14
- MZQZXSHFWDHNOW-UHFFFAOYSA-N 1-phenylpropane-1,2-diol Chemical compound CC(O)C(O)C1=CC=CC=C1 MZQZXSHFWDHNOW-UHFFFAOYSA-N 0.000 description 13
- RWLALWYNXFYRGW-UHFFFAOYSA-N 2-Ethyl-1,3-hexanediol Chemical compound CCCC(O)C(CC)CO RWLALWYNXFYRGW-UHFFFAOYSA-N 0.000 description 13
- AVIYEYCFMVPYST-UHFFFAOYSA-N hexane-1,3-diol Chemical compound CCCC(O)CCO AVIYEYCFMVPYST-UHFFFAOYSA-N 0.000 description 13
- 235000013772 propylene glycol Nutrition 0.000 description 13
- 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 description 12
- JCYHHICXJAGYEL-UHFFFAOYSA-N 3-butoxypropane-1,2-diol Chemical compound CCCCOCC(O)CO JCYHHICXJAGYEL-UHFFFAOYSA-N 0.000 description 12
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 12
- AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 description 12
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 12
- 150000005690 diesters Chemical class 0.000 description 12
- 238000003756 stirring Methods 0.000 description 12
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 11
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 description 11
- 229940083957 1,2-butanediol Drugs 0.000 description 11
- 229940035437 1,3-propanediol Drugs 0.000 description 11
- UNVGBIALRHLALK-UHFFFAOYSA-N 1,5-Hexanediol Chemical compound CC(O)CCCCO UNVGBIALRHLALK-UHFFFAOYSA-N 0.000 description 11
- AUGLSFONVIKZLA-UHFFFAOYSA-N 2-methylheptane-3,5-diol Chemical compound CCC(O)CC(O)C(C)C AUGLSFONVIKZLA-UHFFFAOYSA-N 0.000 description 11
- SVTBMSDMJJWYQN-UHFFFAOYSA-N 2-methylpentane-2,4-diol Chemical compound CC(O)CC(C)(C)O SVTBMSDMJJWYQN-UHFFFAOYSA-N 0.000 description 11
- JHWQMXKQJVAWKI-UHFFFAOYSA-N 3-phenylpropane-1,2-diol Chemical compound OCC(O)CC1=CC=CC=C1 JHWQMXKQJVAWKI-UHFFFAOYSA-N 0.000 description 11
- 229910052799 carbon Inorganic materials 0.000 description 11
- NNYOSLMHXUVJJH-UHFFFAOYSA-N heptane-1,5-diol Chemical compound CCC(O)CCCCO NNYOSLMHXUVJJH-UHFFFAOYSA-N 0.000 description 11
- 239000010410 layer Substances 0.000 description 11
- 238000004519 manufacturing process Methods 0.000 description 11
- 229910052757 nitrogen Inorganic materials 0.000 description 11
- IOMHEFJNPZANMF-UHFFFAOYSA-N 2-methylheptane-2,6-diol Chemical compound CC(O)CCCC(C)(C)O IOMHEFJNPZANMF-UHFFFAOYSA-N 0.000 description 10
- LPEVSCRXBSHMOZ-UHFFFAOYSA-N 2-propylbutane-1,4-diol Chemical compound CCCC(CO)CCO LPEVSCRXBSHMOZ-UHFFFAOYSA-N 0.000 description 10
- ZMWAURRHTDCQCX-UHFFFAOYSA-N 3-methylheptane-2,4-diol Chemical compound CCCC(O)C(C)C(C)O ZMWAURRHTDCQCX-UHFFFAOYSA-N 0.000 description 10
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 10
- 150000002170 ethers Chemical class 0.000 description 10
- 238000010438 heat treatment Methods 0.000 description 10
- HTXVEEVTGGCUNC-UHFFFAOYSA-N heptane-1,3-diol Chemical compound CCCCC(O)CCO HTXVEEVTGGCUNC-UHFFFAOYSA-N 0.000 description 10
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 10
- 238000010992 reflux Methods 0.000 description 10
- 150000003839 salts Chemical class 0.000 description 10
- 239000011734 sodium Substances 0.000 description 10
- 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 description 9
- FWRDQCHWQGNXNZ-UHFFFAOYSA-N 2,2,3-trimethylbutane-1,3-diol Chemical compound CC(C)(O)C(C)(C)CO FWRDQCHWQGNXNZ-UHFFFAOYSA-N 0.000 description 9
- BGQUJDPWPVVEGV-UHFFFAOYSA-N 2,2-dimethylhexane-1,3-diol Chemical compound CCCC(O)C(C)(C)CO BGQUJDPWPVVEGV-UHFFFAOYSA-N 0.000 description 9
- ALVVFCGEWCJMES-UHFFFAOYSA-N 2-ethyl-3-methylpentane-1,3-diol Chemical compound CCC(CO)C(C)(O)CC ALVVFCGEWCJMES-UHFFFAOYSA-N 0.000 description 9
- JVZZUPJFERSVRN-UHFFFAOYSA-N 2-methyl-2-propylpropane-1,3-diol Chemical compound CCCC(C)(CO)CO JVZZUPJFERSVRN-UHFFFAOYSA-N 0.000 description 9
- WPIMUZQTFDJTFU-UHFFFAOYSA-N 2-methylheptane-2,5-diol Chemical compound CCC(O)CCC(C)(C)O WPIMUZQTFDJTFU-UHFFFAOYSA-N 0.000 description 9
- BTVWZWFKMIUSGS-UHFFFAOYSA-N 2-methylpropane-1,2-diol Chemical compound CC(C)(O)CO BTVWZWFKMIUSGS-UHFFFAOYSA-N 0.000 description 9
- SQAJRDHPLTWZQT-UHFFFAOYSA-N 3-methylhexane-1,6-diol Chemical compound OCCC(C)CCCO SQAJRDHPLTWZQT-UHFFFAOYSA-N 0.000 description 9
- POWFRZFDXPVABI-UHFFFAOYSA-N 6-methylheptane-2,4-diol Chemical compound CC(C)CC(O)CC(C)O POWFRZFDXPVABI-UHFFFAOYSA-N 0.000 description 9
- MFBMFHMAWZBOEZ-UHFFFAOYSA-N 6-methylheptane-2,5-diol Chemical compound CC(C)C(O)CCC(C)O MFBMFHMAWZBOEZ-UHFFFAOYSA-N 0.000 description 9
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 9
- 230000008901 benefit Effects 0.000 description 9
- 230000015572 biosynthetic process Effects 0.000 description 9
- 150000002081 enamines Chemical class 0.000 description 9
- ACCCMOQWYVYDOT-UHFFFAOYSA-N hexane-1,1-diol Chemical class CCCCCC(O)O ACCCMOQWYVYDOT-UHFFFAOYSA-N 0.000 description 9
- GLOBUAZSRIOKLN-UHFFFAOYSA-N pentane-1,4-diol Chemical compound CC(O)CCCO GLOBUAZSRIOKLN-UHFFFAOYSA-N 0.000 description 9
- 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 description 8
- LHOBKFFUEUQRQX-UHFFFAOYSA-N 2,2,4-trimethylpentane-1,5-diol Chemical compound OCC(C)CC(C)(C)CO LHOBKFFUEUQRQX-UHFFFAOYSA-N 0.000 description 8
- DEPDXIXAMMDTBV-UHFFFAOYSA-N 2-ethylpentane-1,5-diol Chemical compound CCC(CO)CCCO DEPDXIXAMMDTBV-UHFFFAOYSA-N 0.000 description 8
- GSQFUEPQVUSAPE-UHFFFAOYSA-N 2-methylpentane-2,3-diol Chemical compound CCC(O)C(C)(C)O GSQFUEPQVUSAPE-UHFFFAOYSA-N 0.000 description 8
- AREOBENUACTGHH-UHFFFAOYSA-N 3-methylheptane-3,5-diol Chemical compound CCC(O)CC(C)(O)CC AREOBENUACTGHH-UHFFFAOYSA-N 0.000 description 8
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 8
- 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 8
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 8
- 150000007513 acids Chemical class 0.000 description 8
- 125000001924 fatty-acyl group Chemical group 0.000 description 8
- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 8
- 239000004615 ingredient Substances 0.000 description 8
- WYNVIVRXHYGNRT-UHFFFAOYSA-N octane-3,5-diol Chemical compound CCCC(O)CC(O)CC WYNVIVRXHYGNRT-UHFFFAOYSA-N 0.000 description 8
- IVDFJHOHABJVEH-UHFFFAOYSA-N pinacol Chemical compound CC(C)(O)C(C)(C)O IVDFJHOHABJVEH-UHFFFAOYSA-N 0.000 description 8
- 229910052708 sodium Inorganic materials 0.000 description 8
- 238000003786 synthesis reaction Methods 0.000 description 8
- 150000000185 1,3-diols Chemical class 0.000 description 7
- 150000000190 1,4-diols Chemical class 0.000 description 7
- UZOYKBBAMVVEMJ-UHFFFAOYSA-N 1-(3-methylphenyl)propane-1,3-diol Chemical compound CC1=CC=CC(C(O)CCO)=C1 UZOYKBBAMVVEMJ-UHFFFAOYSA-N 0.000 description 7
- YTCRRFFBEJJVLV-UHFFFAOYSA-N 2-butan-2-ylpropane-1,3-diol Chemical compound CCC(C)C(CO)CO YTCRRFFBEJJVLV-UHFFFAOYSA-N 0.000 description 7
- OTKHZEOSBVSFCJ-UHFFFAOYSA-N 2-butylbutane-1,3-diol Chemical compound CCCCC(CO)C(C)O OTKHZEOSBVSFCJ-UHFFFAOYSA-N 0.000 description 7
- RMEZNLDVMHNLHR-UHFFFAOYSA-N 2-ethylbutane-1,2-diol Chemical compound CCC(O)(CC)CO RMEZNLDVMHNLHR-UHFFFAOYSA-N 0.000 description 7
- IDEOPBXRUBNYBN-UHFFFAOYSA-N 2-methylbutane-2,3-diol Chemical compound CC(O)C(C)(C)O IDEOPBXRUBNYBN-UHFFFAOYSA-N 0.000 description 7
- DXWLGCKTCQEDOO-UHFFFAOYSA-N 2-methylheptane-2,4-diol Chemical compound CCCC(O)CC(C)(C)O DXWLGCKTCQEDOO-UHFFFAOYSA-N 0.000 description 7
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- DVSDBMFJEQPWNO-UHFFFAOYSA-N methyllithium Chemical compound C[Li] DVSDBMFJEQPWNO-UHFFFAOYSA-N 0.000 description 1
- 239000003658 microfiber Substances 0.000 description 1
- 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 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 150000002823 nitrates Chemical class 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- BCYQTARIMBPDNP-UHFFFAOYSA-N non-8-ene-2,4-diol Chemical compound CC(O)CC(O)CCCC=C BCYQTARIMBPDNP-UHFFFAOYSA-N 0.000 description 1
- VOPCSIHRGQNUCF-UHFFFAOYSA-N non-8-ene-2,5-diol Chemical compound CC(O)CCC(O)CCC=C VOPCSIHRGQNUCF-UHFFFAOYSA-N 0.000 description 1
- FVXBCDWMKCEPCL-UHFFFAOYSA-N nonane-1,1-diol Chemical class CCCCCCCCC(O)O FVXBCDWMKCEPCL-UHFFFAOYSA-N 0.000 description 1
- DQZRAEOPSNPXSQ-UHFFFAOYSA-N oct-2-ene-1,4-diol Chemical compound CCCCC(O)C=CCO DQZRAEOPSNPXSQ-UHFFFAOYSA-N 0.000 description 1
- DZTXWUVWSFDEKI-UHFFFAOYSA-N oct-2-ene-1,7-diol Chemical compound CC(O)CCCC=CCO DZTXWUVWSFDEKI-UHFFFAOYSA-N 0.000 description 1
- MTNZKIPFTFNUDB-UHFFFAOYSA-N oct-6-ene-1,5-diol Chemical compound CC=CC(O)CCCCO MTNZKIPFTFNUDB-UHFFFAOYSA-N 0.000 description 1
- QSQGNBGEHSFMAA-UHFFFAOYSA-N octane-1,2,3-triol Chemical compound CCCCCC(O)C(O)CO QSQGNBGEHSFMAA-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
- ONGUKKAIGDNAGC-UHFFFAOYSA-N octane-2,6-diol Chemical compound CCC(O)CCCC(C)O ONGUKKAIGDNAGC-UHFFFAOYSA-N 0.000 description 1
- UJWVPVVMYOBBIY-UHFFFAOYSA-N octane-3,4-diol Chemical compound CCCCC(O)C(O)CC UJWVPVVMYOBBIY-UHFFFAOYSA-N 0.000 description 1
- BCKOQWWRTRBSGR-UHFFFAOYSA-N octane-3,6-diol Chemical compound CCC(O)CCC(O)CC BCKOQWWRTRBSGR-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
- 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
- 150000007524 organic acids Chemical class 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000007800 oxidant agent Substances 0.000 description 1
- 230000001590 oxidative effect Effects 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
- 239000000312 peanut oil Substances 0.000 description 1
- RGSFGYAAUTVSQA-UHFFFAOYSA-N pentamethylene Natural products C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 description 1
- KHIWWQKSHDUIBK-UHFFFAOYSA-N periodic acid Chemical compound OI(=O)(=O)=O KHIWWQKSHDUIBK-UHFFFAOYSA-N 0.000 description 1
- 239000003444 phase transfer catalyst Substances 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 125000002467 phosphate group Chemical group [H]OP(=O)(O[H])O[*] 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229910003446 platinum oxide Inorganic materials 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
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 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
- 239000003755 preservative agent Substances 0.000 description 1
- KIWATKANDHUUOB-UHFFFAOYSA-N propan-2-yl 2-hydroxypropanoate Chemical compound CC(C)OC(=O)C(C)O KIWATKANDHUUOB-UHFFFAOYSA-N 0.000 description 1
- 229940032159 propylene carbonate Drugs 0.000 description 1
- 125000006239 protecting group Chemical group 0.000 description 1
- 238000005086 pumping Methods 0.000 description 1
- 238000005956 quaternization reaction Methods 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 238000003303 reheating Methods 0.000 description 1
- 235000009566 rice Nutrition 0.000 description 1
- 235000005713 safflower oil Nutrition 0.000 description 1
- 239000003813 safflower oil Substances 0.000 description 1
- 239000012047 saturated solution Substances 0.000 description 1
- 150000003335 secondary amines Chemical class 0.000 description 1
- 238000009958 sewing Methods 0.000 description 1
- 239000010802 sludge Substances 0.000 description 1
- 235000009518 sodium iodide Nutrition 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 239000004328 sodium tetraborate Substances 0.000 description 1
- 235000010339 sodium tetraborate Nutrition 0.000 description 1
- HUAUNKAZQWMVFY-UHFFFAOYSA-M sodium;oxocalcium;hydroxide Chemical compound [OH-].[Na+].[Ca]=O HUAUNKAZQWMVFY-UHFFFAOYSA-M 0.000 description 1
- 239000002689 soil Substances 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
- 239000003549 soybean oil Substances 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 229940014800 succinic anhydride Drugs 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000002600 sunflower oil Substances 0.000 description 1
- 239000003784 tall oil Substances 0.000 description 1
- 239000003760 tallow Substances 0.000 description 1
- RKSOPLXZQNSWAS-UHFFFAOYSA-N tert-butyl bromide Chemical compound CC(C)(C)Br RKSOPLXZQNSWAS-UHFFFAOYSA-N 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 125000001412 tetrahydropyranyl group Chemical group 0.000 description 1
- 238000004809 thin layer chromatography Methods 0.000 description 1
- 101150068774 thyX gene Proteins 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-O triethanolammonium Chemical compound OCC[NH+](CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-O 0.000 description 1
- 229910052722 tritium Inorganic materials 0.000 description 1
- 239000006097 ultraviolet radiation absorber Substances 0.000 description 1
- 238000005292 vacuum distillation Methods 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 238000004383 yellowing Methods 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M23/00—Treatment of fibres, threads, yarns, fabrics or fibrous goods made from such materials, characterised by the process
- D06M23/10—Processes in which the treating agent is dissolved or dispersed in organic solvents; Processes for the recovery of organic solvents thereof
-
- 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
-
- 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
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Emergency Medicine (AREA)
- Health & Medical Sciences (AREA)
- Dispersion Chemistry (AREA)
- Textile Engineering (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Peptides Or Proteins (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Detergent Compositions (AREA)
- Cosmetics (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US105795P | 1995-07-11 | 1995-07-11 | |
US62101996A | 1996-03-22 | 1996-03-22 |
Publications (1)
Publication Number | Publication Date |
---|---|
CZ3898A3 true CZ3898A3 (cs) | 1998-08-12 |
Family
ID=26668492
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CZ9838A CZ3898A3 (cs) | 1995-07-11 | 1996-07-11 | Koncentrované stabilní prostředky na změkčování tkanin obsahující chelatační činidla |
CZ9862A CZ6298A3 (cs) | 1995-07-11 | 1996-07-11 | Materiál, který je schopen tvořit čiré, koncentrované, biodegradovatelné avivážní prostředky látek, vodný, stabilní avivážní prostředek pro látky, způsob jeho výroby, výrobek, který ho obsahuje, předem připravená směs složek ho obsahující, směs rozpouštědel pro jeho výrobu a způsob její výroby |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CZ9862A CZ6298A3 (cs) | 1995-07-11 | 1996-07-11 | Materiál, který je schopen tvořit čiré, koncentrované, biodegradovatelné avivážní prostředky látek, vodný, stabilní avivážní prostředek pro látky, způsob jeho výroby, výrobek, který ho obsahuje, předem připravená směs složek ho obsahující, směs rozpouštědel pro jeho výrobu a způsob její výroby |
Country Status (15)
Country | Link |
---|---|
EP (2) | EP0839180A1 (ko) |
JP (2) | JP3916666B2 (ko) |
KR (3) | KR100274684B1 (ko) |
CN (3) | CN1195369A (ko) |
AR (1) | AR002814A1 (ko) |
AT (1) | ATE233804T1 (ko) |
AU (2) | AU6636596A (ko) |
BR (2) | BR9609823A (ko) |
CA (2) | CA2226564C (ko) |
CZ (2) | CZ3898A3 (ko) |
DE (1) | DE69626521T2 (ko) |
HU (2) | HUP9802207A3 (ko) |
MX (2) | MX9800381A (ko) |
TR (1) | TR199800029T1 (ko) |
WO (2) | WO1997003172A1 (ko) |
Families Citing this family (33)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA2260920C (en) * | 1996-07-19 | 2002-04-16 | The Procter & Gamble Company | Concentrated fabric softening composition and highly unsaturated fabric softener compound therefor |
WO1998008924A2 (en) * | 1996-08-30 | 1998-03-05 | The Procter & Gamble Company | Concentrated premix with reduced flammability for forming fabric softening composition |
AU7578198A (en) * | 1997-05-19 | 1998-12-11 | Procter & Gamble Company, The | Clear or translucent fabric softener compositions using mixture of solvents |
BR9811584A (pt) * | 1997-07-29 | 2000-08-22 | Procter & Gamble | Composição concentrada estável, de preferência transparente, para amaciamento de tecidos contendo amaciante de tecidos de amina |
JP4049996B2 (ja) * | 1997-08-18 | 2008-02-20 | ザ プロクター アンド ギャンブル カンパニー | 透明液体布地柔軟化組成物 |
US6875735B1 (en) * | 1997-11-24 | 2005-04-05 | The Procter & Gamble Company | Clear or translucent aqueous fabric softener compositions containing high electrolyte content and optional phase stabilizer |
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 |
EP1018541A1 (de) * | 1999-01-07 | 2000-07-12 | Goldschmidt Rewo GmbH & Co. KG | Klare Weichspülmittelformulierungen |
US6916781B2 (en) | 1999-03-02 | 2005-07-12 | The Procter & Gamble Company | Concentrated, stable, translucent or clear, fabric softening compositions |
US6995131B1 (en) | 1999-05-10 | 2006-02-07 | The Procter & Gamble Company | Clear or translucent aqueous fabric softener compositions containing high electrolyte and optional phase stabilizer |
GB9915964D0 (en) | 1999-07-07 | 1999-09-08 | Unilever Plc | Fabric conditioning composition |
WO2001085892A1 (en) * | 2000-05-11 | 2001-11-15 | The Procter & Gamble Company | Highly concentrated fabric softener compositions and articles containing such compositions |
CA2410189A1 (en) * | 2000-05-24 | 2001-11-24 | The Procter & Gamble Company | A fabric softening composition comprising a malodor controlling agent |
DE10046434A1 (de) * | 2000-09-20 | 2002-04-04 | Cognis Deutschland Gmbh | Verfahren zur Herstellung von verzweigten Alkoholen und/oder Kohlenwasserstoffen |
US6946501B2 (en) | 2001-01-31 | 2005-09-20 | The Procter & Gamble Company | Rapidly dissolvable polymer films and articles made therefrom |
DE10320433A1 (de) * | 2003-05-08 | 2005-02-17 | Henkel Kgaa | Frostresistente Konditioniermittel |
DE602004015129D1 (de) * | 2003-10-16 | 2008-08-28 | Procter & Gamble | Wässrige zusammensetzungen mit vesikeln mit gewisser vesikeldurchlässigkeit |
JP4611422B2 (ja) * | 2005-05-12 | 2011-01-12 | ザ プロクター アンド ギャンブル カンパニー | 凍結融解条件下で安定な布地柔軟化組成物 |
JP4579055B2 (ja) * | 2005-06-01 | 2010-11-10 | 花王株式会社 | 透明又は半透明の液体柔軟剤組成物 |
CN1940045B (zh) * | 2005-09-27 | 2010-09-22 | 深圳市城洁宝环保科技有限公司 | 粘胶清除液 |
CN101454433B (zh) * | 2006-05-31 | 2011-08-17 | 阿克佐诺贝尔股份有限公司 | 具有改进的软化和抗静电性能的水性衣物洗涤剂组合物 |
GB0714589D0 (en) * | 2007-07-27 | 2007-09-05 | Unilever Plc | Fabric softening composition |
EP2231531B1 (en) * | 2007-12-14 | 2012-04-04 | Unilever N.V. | Builder system for a detergent composition |
US8232239B2 (en) * | 2010-03-09 | 2012-07-31 | Ecolab Usa Inc. | Liquid concentrated fabric softener composition |
US11261402B2 (en) | 2016-01-25 | 2022-03-01 | The Procter & Gamble Company | Treatment compositions |
EP3408365A1 (en) | 2016-01-25 | 2018-12-05 | The Procter and Gamble Company | Treatment compositions |
US9896648B2 (en) | 2016-03-02 | 2018-02-20 | The Procter & Gamble Company | Ethoxylated diols and compositions containing ethoxylated diols |
US9840684B2 (en) | 2016-03-02 | 2017-12-12 | The Procter & Gamble Company | Compositions containing alkyl sulfates and/or alkoxylated alkyl sulfates and a solvent comprising a diol |
US9790454B2 (en) | 2016-03-02 | 2017-10-17 | The Procter & Gamble Company | Compositions containing alkyl sulfates and/or alkoxylated alkyl sulfates and a solvent comprising a diol |
US9856440B2 (en) | 2016-03-02 | 2018-01-02 | The Procter & Gamble Company | Compositions containing anionic surfactant and a solvent comprising butanediol |
CN106242954B (zh) * | 2016-08-01 | 2019-03-15 | 山东一诺威新材料有限公司 | 聚醚胺用低分子量聚醚多元醇的制备方法 |
CA3105523A1 (en) * | 2018-07-18 | 2020-01-23 | Symrise Ag | A detergent composition |
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CA913309A (en) * | 1968-08-01 | 1972-10-31 | A. Gluck Bruno | Fabric softening compositions |
DK131432A (ko) * | 1968-12-09 | |||
US3756950A (en) * | 1971-03-08 | 1973-09-04 | Lever Brothers Ltd | Fabric softening compositions |
US3920564A (en) * | 1972-09-20 | 1975-11-18 | Colgate Palmolive Co | Softener-detergent composition |
US4298480A (en) * | 1978-12-11 | 1981-11-03 | Colgate Palmolive Co. | Detergent softener compositions |
GB8312619D0 (en) * | 1983-05-07 | 1983-06-08 | Procter & Gamble | Surfactant compositions |
ATE105331T1 (de) * | 1987-06-16 | 1994-05-15 | Cotelle Sa | Konzentrierte weichmacher. |
GB8914054D0 (en) * | 1989-06-19 | 1989-08-09 | Unilever Plc | Fabric softening composition |
ES2080241T3 (es) * | 1991-09-27 | 1996-02-01 | Procter & Gamble | Composiciones suavizantes de tejidos concentradas. |
CZ276994A3 (en) * | 1992-05-12 | 1995-04-12 | Procter & Gamble | Concentrated agent for softening fabrics and containing biodegradable fabric softeners |
DE4307186A1 (de) * | 1993-03-08 | 1994-09-15 | Henkel Kgaa | Wäßrige Textilweichmacher-Zusammensetzung |
US5490944A (en) * | 1994-08-11 | 1996-02-13 | Colgate-Palmolive Company | Liquid fabric softener compositions |
US5460736A (en) * | 1994-10-07 | 1995-10-24 | The Procter & Gamble Company | Fabric softening composition containing chlorine scavengers |
US5525245A (en) * | 1994-12-21 | 1996-06-11 | Colgate-Palmolive Company | Clear, concentrated liquid fabric softener compositions |
DE69632129D1 (de) * | 1995-04-27 | 2004-05-13 | Goldschmidt Chemical Corp | Diol enthaltende zusammensetzungen |
ES2174913T3 (es) * | 1995-09-18 | 2002-11-16 | Procter & Gamble | Composiciones estabilizadas suavizantes de tejidos. |
-
1996
- 1996-07-11 HU HU9802207A patent/HUP9802207A3/hu unknown
- 1996-07-11 AU AU66365/96A patent/AU6636596A/en not_active Abandoned
- 1996-07-11 JP JP50599197A patent/JP3916666B2/ja not_active Expired - Fee Related
- 1996-07-11 KR KR1019980700197A patent/KR100274684B1/ko not_active IP Right Cessation
- 1996-07-11 EP EP96926070A patent/EP0839180A1/en not_active Ceased
- 1996-07-11 CA CA002226564A patent/CA2226564C/en not_active Expired - Fee Related
- 1996-07-11 CZ CZ9838A patent/CZ3898A3/cs unknown
- 1996-07-11 AT AT96924436T patent/ATE233804T1/de not_active IP Right Cessation
- 1996-07-11 TR TR1998/00029T patent/TR199800029T1/xx unknown
- 1996-07-11 WO PCT/US1996/011572 patent/WO1997003172A1/en not_active Application Discontinuation
- 1996-07-11 KR KR1019997011199A patent/KR100263216B1/ko not_active IP Right Cessation
- 1996-07-11 AU AU64889/96A patent/AU6488996A/en not_active Abandoned
- 1996-07-11 HU HU9802404A patent/HUP9802404A3/hu unknown
- 1996-07-11 DE DE69626521T patent/DE69626521T2/de not_active Expired - Lifetime
- 1996-07-11 BR BR9609823A patent/BR9609823A/pt not_active Application Discontinuation
- 1996-07-11 EP EP96924436A patent/EP0842250B1/en not_active Expired - Lifetime
- 1996-07-11 CZ CZ9862A patent/CZ6298A3/cs unknown
- 1996-07-11 CN CN96196787A patent/CN1195369A/zh active Pending
- 1996-07-11 BR BR9609800A patent/BR9609800A/pt not_active Application Discontinuation
- 1996-07-11 CA CA002226550A patent/CA2226550C/en not_active Expired - Fee Related
- 1996-07-11 JP JP9505982A patent/JPH11506810A/ja active Pending
- 1996-07-11 WO PCT/US1996/011556 patent/WO1997003169A1/en not_active Application Discontinuation
- 1996-07-11 CN CN96196853A patent/CN1107716C/zh not_active Expired - Fee Related
- 1996-07-11 MX MX9800381A patent/MX9800381A/es unknown
- 1996-07-11 MX MX9800382A patent/MX9800382A/es unknown
- 1996-07-11 KR KR1019980700196A patent/KR100263870B1/ko not_active IP Right Cessation
- 1996-07-12 AR ARP960103546A patent/AR002814A1/es not_active Application Discontinuation
-
2002
- 2002-09-17 CN CNB021432295A patent/CN1232692C/zh not_active Expired - Fee Related
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PD00 | Pending as of 2000-06-30 in czech republic |