CZ3898A3 - Koncentrované stabilní prostředky na změkčování tkanin obsahující chelatační činidla - Google Patents

Koncentrované stabilní prostředky na změkčování tkanin obsahující chelatační činidla Download PDF

Info

Publication number: CZ3898A3
Authority: CZ; Czechia
Prior art keywords: methyl; dimethyl; hexanediol; pentanediol; heptanediol
Prior art date: 1995-07-11

Application number

CZ9838A

Other languages

Czech (cs)

English (en)

Inventor

Errol Hoffman Wahl

John Cort Severns

Scott William Waite

Frederick Anthony Hartman

Hugo Jean Marie Demwyere

Marc Johan Declercq

Alice Marie Ward

Original Assignee

The Procter & Gamble Company

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1995-07-11

Filing date

1996-07-11

Publication date

1998-08-12

1996-07-11 Application filed by The Procter & Gamble Company filed Critical The Procter & Gamble Company

1998-08-12 Publication of CZ3898A3 publication Critical patent/CZ3898A3/cs

Links

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
PMYMNKGSHYYMNT-UHFFFAOYSA-N 2-pentan-3-ylpropane-1,3-diol Chemical compound CCC(CC)C(CO)CO PMYMNKGSHYYMNT-UHFFFAOYSA-N 0.000 description 7
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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)

CZ9838A 1995-07-11 1996-07-11 Koncentrované stabilní prostředky na změkčování tkanin obsahující chelatační činidla CZ3898A3 (cs)

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 (zh)
JP (2)	JP3916666B2 (zh)
KR (3)	KR100274684B1 (zh)
CN (3)	CN1195369A (zh)
AR (1)	AR002814A1 (zh)
AT (1)	ATE233804T1 (zh)
AU (2)	AU6636596A (zh)
BR (2)	BR9609823A (zh)
CA (2)	CA2226564C (zh)
CZ (2)	CZ3898A3 (zh)
DE (1)	DE69626521T2 (zh)
HU (2)	HUP9802207A3 (zh)
MX (2)	MX9800381A (zh)
TR (1)	TR199800029T1 (zh)
WO (2)	WO1997003172A1 (zh)

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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 (zh) *	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

Also Published As

Publication number	Publication date
MX9800382A (es)	1998-04-30
AR002814A1 (es)	1998-04-29
CN1195369A (zh)	1998-10-07
HUP9802404A3 (en)	2000-06-28
EP0842250B1 (en)	2003-03-05
CN1232692C (zh)	2005-12-21
CA2226564C (en)	2003-10-28
JPH11509277A (ja)	1999-08-17
JP3916666B2 (ja)	2007-05-16
CA2226550A1 (en)	1997-01-30
KR100274684B1 (ko)	2001-01-15
HUP9802207A3 (en)	2000-11-28
CN1107716C (zh)	2003-05-07
CZ6298A3 (cs)	1998-06-17
EP0842250A1 (en)	1998-05-20
BR9609800A (pt)	1999-07-06
KR19990028894A (ko)	1999-04-15
AU6636596A (en)	1997-02-10
ATE233804T1 (de)	2003-03-15
BR9609823A (pt)	1999-07-06
WO1997003172A1 (en)	1997-01-30
JPH11506810A (ja)	1999-06-15
CA2226564A1 (en)	1997-01-30
HUP9802404A2 (hu)	1999-01-28
MX9800381A (es)	1998-04-30
EP0839180A1 (en)	1998-05-06
HUP9802207A2 (hu)	1999-01-28
CN1196082A (zh)	1998-10-14
DE69626521D1 (de)	2003-04-10
KR100263216B1 (ko)	2000-07-15
DE69626521T2 (de)	2003-12-24
AU6488996A (en)	1997-02-10
CN1436890A (zh)	2003-08-20
TR199800029T1 (xx)	1998-04-21
KR100263870B1 (ko)	2000-09-01
CA2226550C (en)	2002-02-19
KR19990028895A (ko)	1999-04-15
WO1997003169A1 (en)	1997-01-30

Legal Events

Date	Code	Title	Description
2000-06-30	PD00	Pending as of 2000-06-30 in czech republic

Publication	Publication Date	Title
CZ3898A3 (cs)	1998-08-12	Koncentrované stabilní prostředky na změkčování tkanin obsahující chelatační činidla
KR100262106B1 (ko)	2000-07-15	농축된, 수-분산성의, 안정한 직물 유연 조성물
US5759990A (en)	1998-06-02	Concentrated fabric softening composition with good freeze/thaw recovery and highly unsaturated fabric softener compound therefor
US5747443A (en)	1998-05-05	Fabric softening compound/composition
US5877145A (en)	1999-03-02	Concentrated fabric softening composition with good freeze/thaw recovery and highly unsaturated fabric softener compound therefor
DE69725605T2 (de)	2004-08-05	Trocken-aktivierte gewebekonditionierungs- und antistatische zusammensetzungen mit verbesseter parfüm-lebensdauer
JP3102894B2 (ja)	2000-10-23	布帛柔軟化化合物／組成物
US20060058216A1 (en)	2006-03-16	Concentrated, stable, preferably clear, fabric softening composition
ES2653942T3 (es)	2018-02-09	Composición de perfume
EP1352948A1 (en)	2003-10-15	Concentrated, stable, fabric softening composition
JP3419464B2 (ja)	2003-06-23	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
US20050202998A1 (en)	2005-09-15	Concentrated, stable, translucent or clear, fabric softening compositions including chelants
JP2009150035A (ja)	2009-07-09	液体柔軟剤組成物