CA2226564C - Concentrated, stable fabric softening compositions with low organic solvent level - Google Patents
Concentrated, stable fabric softening compositions with low organic solvent level Download PDFInfo
- Publication number
- CA2226564C CA2226564C CA002226564A CA2226564A CA2226564C CA 2226564 C CA2226564 C CA 2226564C CA 002226564 A CA002226564 A CA 002226564A CA 2226564 A CA2226564 A CA 2226564A CA 2226564 C CA2226564 C CA 2226564C
- Authority
- CA
- Canada
- Prior art keywords
- methyl
- dimethyl
- pentanediol
- hexanediol
- butanediol
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 188
- 239000004744 fabric Substances 0.000 title claims abstract description 20
- 239000003960 organic solvent Substances 0.000 title description 4
- 239000002904 solvent Substances 0.000 claims abstract description 117
- 239000002979 fabric softener Substances 0.000 claims abstract description 42
- 150000002009 diols Chemical class 0.000 claims abstract description 37
- 150000001875 compounds Chemical class 0.000 claims abstract description 31
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 claims description 589
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 claims description 565
- YPFDHNVEDLHUCE-UHFFFAOYSA-N 1,3-propanediol Substances OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 claims description 458
- 229920000166 polytrimethylene carbonate Polymers 0.000 claims description 456
- DNIAPMSPPWPWGF-VKHMYHEASA-N (+)-propylene glycol Chemical compound C[C@H](O)CO DNIAPMSPPWPWGF-VKHMYHEASA-N 0.000 claims description 449
- RUOPINZRYMFPBF-UHFFFAOYSA-N pentane-1,3-diol Chemical compound CCC(O)CCO RUOPINZRYMFPBF-UHFFFAOYSA-N 0.000 claims description 296
- GLOBUAZSRIOKLN-UHFFFAOYSA-N pentane-1,4-diol Chemical compound CC(O)CCCO GLOBUAZSRIOKLN-UHFFFAOYSA-N 0.000 claims description 290
- AVIYEYCFMVPYST-UHFFFAOYSA-N hexane-1,3-diol Chemical compound CCCC(O)CCO AVIYEYCFMVPYST-UHFFFAOYSA-N 0.000 claims description 280
- UNVGBIALRHLALK-UHFFFAOYSA-N 1,5-Hexanediol Chemical compound CC(O)CCCCO UNVGBIALRHLALK-UHFFFAOYSA-N 0.000 claims description 256
- HTXVEEVTGGCUNC-UHFFFAOYSA-N heptane-1,3-diol Chemical compound CCCCC(O)CCO HTXVEEVTGGCUNC-UHFFFAOYSA-N 0.000 claims description 224
- TXGJTWACJNYNOJ-UHFFFAOYSA-N hexane-2,4-diol Chemical compound CCC(O)CC(C)O TXGJTWACJNYNOJ-UHFFFAOYSA-N 0.000 claims description 224
- -1 2-ethyl- Chemical group 0.000 claims description 187
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims description 182
- QVTWBMUAJHVAIJ-UHFFFAOYSA-N hexane-1,4-diol Chemical compound CCC(O)CCCO QVTWBMUAJHVAIJ-UHFFFAOYSA-N 0.000 claims description 182
- ALQSHHUCVQOPAS-UHFFFAOYSA-N Pentane-1,5-diol Chemical compound OCCCCCO ALQSHHUCVQOPAS-UHFFFAOYSA-N 0.000 claims description 180
- 235000013772 propylene glycol Nutrition 0.000 claims description 168
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 claims description 161
- BMRWNKZVCUKKSR-UHFFFAOYSA-N butane-1,2-diol Chemical compound CCC(O)CO BMRWNKZVCUKKSR-UHFFFAOYSA-N 0.000 claims description 160
- PFURGBBHAOXLIO-UHFFFAOYSA-N cyclohexane-1,2-diol Chemical compound OC1CCCCC1O PFURGBBHAOXLIO-UHFFFAOYSA-N 0.000 claims description 160
- 238000000034 method Methods 0.000 claims description 160
- XLMFDCKSFJWJTP-UHFFFAOYSA-N pentane-2,3-diol Chemical compound CCC(O)C(C)O XLMFDCKSFJWJTP-UHFFFAOYSA-N 0.000 claims description 131
- GTCCGKPBSJZVRZ-UHFFFAOYSA-N pentane-2,4-diol Chemical compound CC(O)CC(C)O GTCCGKPBSJZVRZ-UHFFFAOYSA-N 0.000 claims description 121
- WCVRQHFDJLLWFE-UHFFFAOYSA-N pentane-1,2-diol Chemical compound CCCC(O)CO WCVRQHFDJLLWFE-UHFFFAOYSA-N 0.000 claims description 118
- OHMBHFSEKCCCBW-UHFFFAOYSA-N hexane-2,5-diol Chemical compound CC(O)CCC(C)O OHMBHFSEKCCCBW-UHFFFAOYSA-N 0.000 claims description 112
- XVEOUOTUJBYHNL-UHFFFAOYSA-N heptane-2,4-diol Chemical compound CCCC(O)CC(C)O XVEOUOTUJBYHNL-UHFFFAOYSA-N 0.000 claims description 111
- XTVHTJKQKUOEQA-UHFFFAOYSA-N heptane-2,5-diol Chemical compound CCC(O)CCC(C)O XTVHTJKQKUOEQA-UHFFFAOYSA-N 0.000 claims description 92
- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 claims description 83
- OZIMXLFSRSPFAS-UHFFFAOYSA-N heptane-2,6-diol Chemical compound CC(O)CCCC(C)O OZIMXLFSRSPFAS-UHFFFAOYSA-N 0.000 claims description 76
- OGRCRHSHBFQRKO-UHFFFAOYSA-N heptane-1,4-diol Chemical compound CCCC(O)CCCO OGRCRHSHBFQRKO-UHFFFAOYSA-N 0.000 claims description 72
- UQGLNXPQGUMNRU-UHFFFAOYSA-N heptane-1,6-diol Chemical compound CC(O)CCCCCO UQGLNXPQGUMNRU-UHFFFAOYSA-N 0.000 claims description 71
- NNYOSLMHXUVJJH-UHFFFAOYSA-N heptane-1,5-diol Chemical compound CCC(O)CCCCO NNYOSLMHXUVJJH-UHFFFAOYSA-N 0.000 claims description 60
- BQWORYKVVNTRAW-UHFFFAOYSA-N heptane-3,5-diol Chemical compound CCC(O)CC(O)CC BQWORYKVVNTRAW-UHFFFAOYSA-N 0.000 claims description 60
- OWBTYPJTUOEWEK-UHFFFAOYSA-N butane-2,3-diol Chemical compound CC(O)C(C)O OWBTYPJTUOEWEK-UHFFFAOYSA-N 0.000 claims description 59
- QCIYAEYRVFUFAP-UHFFFAOYSA-N hexane-2,3-diol Chemical compound CCCC(O)C(C)O QCIYAEYRVFUFAP-UHFFFAOYSA-N 0.000 claims description 42
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 37
- 239000000194 fatty acid Substances 0.000 claims description 37
- 229930195729 fatty acid Natural products 0.000 claims description 37
- 150000004665 fatty acids Chemical class 0.000 claims description 37
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 35
- POFSNPPXJUQANW-UHFFFAOYSA-N hexane-3,4-diol Chemical compound CCC(O)C(O)CC POFSNPPXJUQANW-UHFFFAOYSA-N 0.000 claims description 34
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 26
- SXCBDZAEHILGLM-UHFFFAOYSA-N heptane-1,7-diol Chemical compound OCCCCCCCO SXCBDZAEHILGLM-UHFFFAOYSA-N 0.000 claims description 22
- MHIBEGOZTWERHF-UHFFFAOYSA-N heptane-1,1-diol Chemical class CCCCCCC(O)O MHIBEGOZTWERHF-UHFFFAOYSA-N 0.000 claims description 21
- 125000001183 hydrocarbyl group Chemical group 0.000 claims description 21
- JHWQMXKQJVAWKI-UHFFFAOYSA-N 3-phenylpropane-1,2-diol Chemical compound OCC(O)CC1=CC=CC=C1 JHWQMXKQJVAWKI-UHFFFAOYSA-N 0.000 claims description 18
- QCHAHMKQNICNLC-UHFFFAOYSA-N cyclobut-3-ene-1,2-diol Chemical compound OC1C=CC1O QCHAHMKQNICNLC-UHFFFAOYSA-N 0.000 claims description 18
- 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 17
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims description 17
- 229910052740 iodine Inorganic materials 0.000 claims description 17
- BTANRVKWQNVYAZ-UHFFFAOYSA-N butan-2-ol Chemical compound CCC(C)O BTANRVKWQNVYAZ-UHFFFAOYSA-N 0.000 claims description 16
- VCVOSERVUCJNPR-UHFFFAOYSA-N cyclopentane-1,2-diol Chemical compound OC1CCCC1O VCVOSERVUCJNPR-UHFFFAOYSA-N 0.000 claims description 16
- 125000001424 substituent group Chemical group 0.000 claims description 16
- WYNVIVRXHYGNRT-UHFFFAOYSA-N octane-3,5-diol Chemical compound CCCC(O)CC(O)CC WYNVIVRXHYGNRT-UHFFFAOYSA-N 0.000 claims description 15
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims description 13
- FHKSXSQHXQEMOK-UHFFFAOYSA-N hexane-1,2-diol Chemical compound CCCCC(O)CO FHKSXSQHXQEMOK-UHFFFAOYSA-N 0.000 claims description 13
- 239000011630 iodine Substances 0.000 claims description 13
- 229940015975 1,2-hexanediol Drugs 0.000 claims description 12
- PAWKNQDIXPJKSO-UHFFFAOYSA-N octa-1,7-diene-3,6-diol Chemical compound C=CC(O)CCC(O)C=C PAWKNQDIXPJKSO-UHFFFAOYSA-N 0.000 claims description 12
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 claims description 12
- 229920006395 saturated elastomer Polymers 0.000 claims description 12
- 239000003021 water soluble solvent Substances 0.000 claims description 12
- DCTMXCOHGKSXIZ-UHFFFAOYSA-N (R)-1,3-Octanediol Chemical compound CCCCCC(O)CCO DCTMXCOHGKSXIZ-UHFFFAOYSA-N 0.000 claims description 11
- 125000000217 alkyl group Chemical group 0.000 claims description 11
- ACCCMOQWYVYDOT-UHFFFAOYSA-N hexane-1,1-diol Chemical class CCCCCC(O)O ACCCMOQWYVYDOT-UHFFFAOYSA-N 0.000 claims description 11
- WHYBHJWYBIXOPS-UHFFFAOYSA-N 1-phenylbutane-2,3-diol Chemical compound CC(O)C(O)CC1=CC=CC=C1 WHYBHJWYBIXOPS-UHFFFAOYSA-N 0.000 claims description 10
- LNCZPZFNQQFXPT-UHFFFAOYSA-N 2-phenyl-1,2-propanediol Chemical compound OCC(O)(C)C1=CC=CC=C1 LNCZPZFNQQFXPT-UHFFFAOYSA-N 0.000 claims description 10
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 10
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 claims description 10
- GRRYTPLUXFDFCG-UHFFFAOYSA-N cyclohex-3-ene-1,2-diol Chemical compound OC1CCC=CC1O GRRYTPLUXFDFCG-UHFFFAOYSA-N 0.000 claims description 10
- NWVFBFHOQGKOIF-UHFFFAOYSA-N cyclohex-4-ene-1,2-diol Chemical compound OC1CC=CCC1O NWVFBFHOQGKOIF-UHFFFAOYSA-N 0.000 claims description 10
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 10
- XFVAWWPVJMMDGC-UHFFFAOYSA-N octa-2,7-diene-1,6-diol Chemical compound OCC=CCCC(O)C=C XFVAWWPVJMMDGC-UHFFFAOYSA-N 0.000 claims description 10
- HOWLAKMIIWUJEJ-UHFFFAOYSA-N octane-2,4-diol Chemical compound CCCCC(O)CC(C)O HOWLAKMIIWUJEJ-UHFFFAOYSA-N 0.000 claims description 10
- BCKOQWWRTRBSGR-UHFFFAOYSA-N octane-3,6-diol Chemical compound CCC(O)CCC(O)CC BCKOQWWRTRBSGR-UHFFFAOYSA-N 0.000 claims description 10
- ORTVZLZNOYNASJ-UPHRSURJSA-N (z)-but-2-ene-1,4-diol Chemical compound OC\C=C/CO ORTVZLZNOYNASJ-UPHRSURJSA-N 0.000 claims description 9
- GIJUUECDGIVMIX-UHFFFAOYSA-N 3-(2-hydroxyethyl)cyclohexan-1-ol Chemical compound OCCC1CCCC(O)C1 GIJUUECDGIVMIX-UHFFFAOYSA-N 0.000 claims description 9
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 9
- ORXQCSFBMXUINI-UHFFFAOYSA-N hept-1-ene-3,5-diol Chemical compound CCC(O)CC(O)C=C ORXQCSFBMXUINI-UHFFFAOYSA-N 0.000 claims description 9
- IKSZUZSICAXOHV-UHFFFAOYSA-N hept-6-ene-2,4-diol Chemical compound CC(O)CC(O)CC=C IKSZUZSICAXOHV-UHFFFAOYSA-N 0.000 claims description 9
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 9
- IHUYEFNGFUUZQV-UHFFFAOYSA-N oct-7-ene-1,3-diol Chemical compound OCCC(O)CCCC=C IHUYEFNGFUUZQV-UHFFFAOYSA-N 0.000 claims description 9
- YHSJEDVJYGRFHX-UHFFFAOYSA-N 1-(2-hydroxyethyl)cyclohexan-1-ol Chemical compound OCCC1(O)CCCCC1 YHSJEDVJYGRFHX-UHFFFAOYSA-N 0.000 claims description 8
- 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 8
- XEXSBXKKNKXLTA-UHFFFAOYSA-N 7-Octen-1,6-diol Natural products OCCCCCC(O)C=C XEXSBXKKNKXLTA-UHFFFAOYSA-N 0.000 claims description 8
- 125000004432 carbon atom Chemical group C* 0.000 claims description 8
- 150000002170 ethers Chemical class 0.000 claims description 8
- DQFFSJKSYARNCX-UHFFFAOYSA-N hept-3-ene-2,6-diol Chemical compound CC(O)CC=CC(C)O DQFFSJKSYARNCX-UHFFFAOYSA-N 0.000 claims description 8
- RPRMJMJEESOAHE-UHFFFAOYSA-N hept-6-ene-1,4-diol Chemical compound OCCCC(O)CC=C RPRMJMJEESOAHE-UHFFFAOYSA-N 0.000 claims description 8
- ZNZZFXONMYVVGZ-UHFFFAOYSA-N heptane-3,4-diol Chemical compound CCCC(O)C(O)CC ZNZZFXONMYVVGZ-UHFFFAOYSA-N 0.000 claims description 8
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims description 8
- LWNYCVKZZKMXJZ-UHFFFAOYSA-N octa-2,5-diene-1,7-diol Chemical compound CC(O)C=CCC=CCO LWNYCVKZZKMXJZ-UHFFFAOYSA-N 0.000 claims description 8
- AZVKGHXATHHFRF-UHFFFAOYSA-N octane-2,5-diol Chemical compound CCCC(O)CCC(C)O AZVKGHXATHHFRF-UHFFFAOYSA-N 0.000 claims description 8
- PAXWQLGKYISPNH-UHFFFAOYSA-N octane-2,7-diol Chemical compound CC(O)CCCCC(C)O PAXWQLGKYISPNH-UHFFFAOYSA-N 0.000 claims description 8
- 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 7
- ADXMFHMYYFZEGM-HWKANZROSA-N (5e)-hepta-1,5-diene-3,4-diol Chemical compound C\C=C\C(O)C(O)C=C ADXMFHMYYFZEGM-HWKANZROSA-N 0.000 claims description 7
- PWMWNFMRSKOCEY-UHFFFAOYSA-N 1-Phenyl-1,2-ethanediol Chemical compound OCC(O)C1=CC=CC=C1 PWMWNFMRSKOCEY-UHFFFAOYSA-N 0.000 claims description 7
- IOZFUGDROBQPNP-UHFFFAOYSA-N 1-methylcyclohexane-1,2-diol Chemical compound CC1(O)CCCCC1O IOZFUGDROBQPNP-UHFFFAOYSA-N 0.000 claims description 7
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims description 7
- KUQWZSZYIQGTHT-UHFFFAOYSA-N hexa-1,5-diene-3,4-diol Chemical compound C=CC(O)C(O)C=C KUQWZSZYIQGTHT-UHFFFAOYSA-N 0.000 claims description 7
- DZTXWUVWSFDEKI-UHFFFAOYSA-N oct-2-ene-1,7-diol Chemical compound CC(O)CCCC=CCO DZTXWUVWSFDEKI-UHFFFAOYSA-N 0.000 claims description 7
- ONGUKKAIGDNAGC-UHFFFAOYSA-N octane-2,6-diol Chemical compound CCC(O)CCCC(C)O ONGUKKAIGDNAGC-UHFFFAOYSA-N 0.000 claims description 7
- RUOJZAUFBMNUDX-UHFFFAOYSA-N propylene carbonate Chemical compound CC1COC(=O)O1 RUOJZAUFBMNUDX-UHFFFAOYSA-N 0.000 claims description 7
- 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 6
- MWSXXXZZOZFTPR-OWOJBTEDSA-N (e)-hex-3-ene-1,6-diol Chemical compound OCC\C=C\CCO MWSXXXZZOZFTPR-OWOJBTEDSA-N 0.000 claims description 6
- FNEWEOQQGPJOHL-UHFFFAOYSA-N 1-ethylcyclopentane-1,2-diol Chemical compound CCC1(O)CCCC1O FNEWEOQQGPJOHL-UHFFFAOYSA-N 0.000 claims description 6
- 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 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
- YMQBYIZMIOBDOD-UHFFFAOYSA-N 1-propan-2-ylcyclobutane-1,2-diol Chemical compound CC(C)C1(O)CCC1O YMQBYIZMIOBDOD-UHFFFAOYSA-N 0.000 claims description 6
- 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 6
- PFXRPUFYSLHDMF-UHFFFAOYSA-N 3-(hydroxymethyl)cyclohexan-1-ol Chemical compound OCC1CCCC(O)C1 PFXRPUFYSLHDMF-UHFFFAOYSA-N 0.000 claims description 6
- BQNJVHGCZBNKBG-UHFFFAOYSA-N 3-phenylbutane-1,3-diol Chemical compound OCCC(O)(C)C1=CC=CC=C1 BQNJVHGCZBNKBG-UHFFFAOYSA-N 0.000 claims description 6
- NSMIMJYEKVSYMT-SNVBAGLBSA-N 8-hydroxylinalool Natural products OCC(C)=CCC[C@](C)(O)C=C NSMIMJYEKVSYMT-SNVBAGLBSA-N 0.000 claims description 6
- PTCYLOJKSMVJTR-SNVBAGLBSA-N Rosiridol Natural products CC(=CC[C@@H](O)C(=CCO)C)C PTCYLOJKSMVJTR-SNVBAGLBSA-N 0.000 claims description 6
- 239000002253 acid Substances 0.000 claims description 6
- 150000001450 anions Chemical class 0.000 claims description 6
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 6
- 239000011575 calcium Substances 0.000 claims description 6
- 229910052791 calcium Inorganic materials 0.000 claims description 6
- NSMIMJYEKVSYMT-UHFFFAOYSA-N cis-8-Hydroxylinalool Natural products OCC(C)=CCCC(C)(O)C=C NSMIMJYEKVSYMT-UHFFFAOYSA-N 0.000 claims description 6
- DCYPPXGEIQTVPI-UHFFFAOYSA-N cycloheptane-1,2-diol Chemical compound OC1CCCCCC1O DCYPPXGEIQTVPI-UHFFFAOYSA-N 0.000 claims description 6
- 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 6
- OKEPQQSIXVXWIE-UHFFFAOYSA-N hepta-2,6-diene-1,4-diol Chemical compound OCC=CC(O)CC=C OKEPQQSIXVXWIE-UHFFFAOYSA-N 0.000 claims description 6
- 239000004615 ingredient Substances 0.000 claims description 6
- 159000000003 magnesium salts Chemical class 0.000 claims description 6
- 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 5
- ROGXKDQQAVRTSA-GGWOSOGESA-N (2e,6e)-octa-2,6-diene-1,8-diol Chemical compound OC\C=C\CC\C=C\CO ROGXKDQQAVRTSA-GGWOSOGESA-N 0.000 claims description 5
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 claims description 5
- ROUNKFJLNCHQLL-UHFFFAOYSA-N 1,2-dimethylcyclohexane-1,3-diol Chemical compound CC1C(O)CCCC1(C)O ROUNKFJLNCHQLL-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 5
- ZHOKPKCKZNPBOA-UHFFFAOYSA-N 1,4-dimethylcyclopentane-1,2-diol Chemical compound CC1CC(O)C(C)(O)C1 ZHOKPKCKZNPBOA-UHFFFAOYSA-N 0.000 claims description 5
- BGZGQDDKQNYZID-UHFFFAOYSA-N 1-(hydroxymethyl)cyclohexan-1-ol Chemical compound OCC1(O)CCCCC1 BGZGQDDKQNYZID-UHFFFAOYSA-N 0.000 claims description 5
- KELMAQQLJLWUAY-UHFFFAOYSA-N 2-(2-hydroxyethyl)cyclohexan-1-ol Chemical compound OCCC1CCCCC1O KELMAQQLJLWUAY-UHFFFAOYSA-N 0.000 claims description 5
- BVDKYMGISZDCIY-UHFFFAOYSA-N 2-phenylbutane-1,4-diol Chemical compound OCCC(CO)C1=CC=CC=C1 BVDKYMGISZDCIY-UHFFFAOYSA-N 0.000 claims description 5
- BQNVNLVPNSRNBZ-UHFFFAOYSA-N 3,3-dimethylcyclopentane-1,2-diol Chemical compound CC1(C)CCC(O)C1O BQNVNLVPNSRNBZ-UHFFFAOYSA-N 0.000 claims description 5
- LTIMVARCDQKGLB-UHFFFAOYSA-N 3,4-dimethylcyclopentane-1,2-diol Chemical compound CC1CC(O)C(O)C1C LTIMVARCDQKGLB-UHFFFAOYSA-N 0.000 claims description 5
- HRFAQTLGZYUGEP-UHFFFAOYSA-N 3,5-dimethylcyclopentane-1,2-diol Chemical compound CC1CC(C)C(O)C1O HRFAQTLGZYUGEP-UHFFFAOYSA-N 0.000 claims description 5
- DLRLJRUDHDJCSW-UHFFFAOYSA-N 3-ethyl-4-methylcyclobutane-1,2-diol Chemical compound CCC1C(C)C(O)C1O DLRLJRUDHDJCSW-UHFFFAOYSA-N 0.000 claims description 5
- VFRVYGUCOZPHEQ-UHFFFAOYSA-N 3-methylcyclohexane-1,2-diol Chemical compound CC1CCCC(O)C1O VFRVYGUCOZPHEQ-UHFFFAOYSA-N 0.000 claims description 5
- ZHYNWTRHGRBVIM-UHFFFAOYSA-N 3-propylcyclobutane-1,2-diol Chemical compound CCCC1CC(O)C1O ZHYNWTRHGRBVIM-UHFFFAOYSA-N 0.000 claims description 5
- CNDPNCDBQDTLGU-UHFFFAOYSA-N 4,4-dimethylcyclohexane-1,3-diol Chemical compound CC1(C)CCC(O)CC1O CNDPNCDBQDTLGU-UHFFFAOYSA-N 0.000 claims description 5
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- MCQKYGSUZXPJQU-UHFFFAOYSA-N 5-methylheptane-2,3-diol Chemical compound CCC(C)CC(O)C(C)O MCQKYGSUZXPJQU-UHFFFAOYSA-N 0.000 description 1
- CXIXEMXKCTZXTQ-UHFFFAOYSA-N 5-methylhexane-1,3-diol Chemical compound CC(C)CC(O)CCO CXIXEMXKCTZXTQ-UHFFFAOYSA-N 0.000 description 1
- ARBBSOILKXUDJE-UHFFFAOYSA-N 5-methylhexane-1,4-diol Chemical compound CC(C)C(O)CCCO ARBBSOILKXUDJE-UHFFFAOYSA-N 0.000 description 1
- LNFDWQCEHXSMLT-UHFFFAOYSA-N 5-methylhexane-1,5-diol Chemical compound CC(C)(O)CCCCO LNFDWQCEHXSMLT-UHFFFAOYSA-N 0.000 description 1
- GSOCFGPQNAFJLB-UHFFFAOYSA-N 6-methylheptane-1,2-diol Chemical compound CC(C)CCCC(O)CO GSOCFGPQNAFJLB-UHFFFAOYSA-N 0.000 description 1
- FZDKHFNKZOXGAZ-UHFFFAOYSA-N 6-methylheptane-3,4-diol Chemical compound CCC(O)C(O)CC(C)C FZDKHFNKZOXGAZ-UHFFFAOYSA-N 0.000 description 1
- FIMGSRKZYWEKNE-UHFFFAOYSA-N 6-methyloctane-1,1-diol Chemical class CCC(C)CCCCC(O)O FIMGSRKZYWEKNE-UHFFFAOYSA-N 0.000 description 1
- FNTAEYHVVSEWCZ-UHFFFAOYSA-N 8-methyldecane-5,5-diol Chemical class CCCCC(O)(O)CCC(C)CC FNTAEYHVVSEWCZ-UHFFFAOYSA-N 0.000 description 1
- JYNWXPWCJIAFGW-UHFFFAOYSA-N CC(C(O)O)(C(CC(C)(C)C)(C)C)C Chemical class CC(C(O)O)(C(CC(C)(C)C)(C)C)C JYNWXPWCJIAFGW-UHFFFAOYSA-N 0.000 description 1
- XLKQRRQTHZPANU-UHFFFAOYSA-N CC(CCC(C)O)O.CC(CC(CC)O)O.C(CCCCCO)O.C(CCCC(C)O)O.C(CCC(CC)O)O.CC(CCO)(CCC)O Chemical compound CC(CCC(C)O)O.CC(CC(CC)O)O.C(CCCCCO)O.C(CCCC(C)O)O.C(CCC(CC)O)O.CC(CCO)(CCC)O XLKQRRQTHZPANU-UHFFFAOYSA-N 0.000 description 1
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- OKTJSMMVPCPJKN-OUBTZVSYSA-N Carbon-13 Chemical compound [13C] OKTJSMMVPCPJKN-OUBTZVSYSA-N 0.000 description 1
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- 101100532699 Drosophila melanogaster scyl gene Proteins 0.000 description 1
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- 241000231687 Heza Species 0.000 description 1
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- 235000019485 Safflower oil Nutrition 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
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- 125000001931 aliphatic group Chemical group 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
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- 125000003368 amide group Chemical group 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 235000006708 antioxidants Nutrition 0.000 description 1
- 125000004104 aryloxy group Chemical group 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- UDKULWJCCCNZCF-UHFFFAOYSA-M bis(2-dodecanoyloxyethyl)-dimethylazanium;chloride Chemical compound [Cl-].CCCCCCCCCCCC(=O)OCC[N+](C)(C)CCOC(=O)CCCCCCCCCCC UDKULWJCCCNZCF-UHFFFAOYSA-M 0.000 description 1
- 238000009835 boiling Methods 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
- 239000006227 byproduct Substances 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000003240 coconut oil Substances 0.000 description 1
- 235000019864 coconut oil Nutrition 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 230000003750 conditioning effect Effects 0.000 description 1
- MFXVLOBVCPRXDJ-UHFFFAOYSA-N cycloheptane-1,3-diol Chemical compound OC1CCCCC(O)C1 MFXVLOBVCPRXDJ-UHFFFAOYSA-N 0.000 description 1
- FDODVZVWGKVMBO-UHFFFAOYSA-N cyclohex-2-ene-1,4-diol Chemical compound OC1CCC(O)C=C1 FDODVZVWGKVMBO-UHFFFAOYSA-N 0.000 description 1
- FPQOEJPNPFCPNQ-UHFFFAOYSA-N cyclohex-4-ene-1,3-diol Chemical compound OC1CC=CC(O)C1 FPQOEJPNPFCPNQ-UHFFFAOYSA-N 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
- NUUPJBRGQCEZSI-UHFFFAOYSA-N cyclopentane-1,3-diol Chemical compound OC1CCC(O)C1 NUUPJBRGQCEZSI-UHFFFAOYSA-N 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
- 230000001419 dependent effect Effects 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 229910052805 deuterium Inorganic materials 0.000 description 1
- ACOHUVFYOFOGIG-JDVCJPALSA-M dimethyl-bis[2-[(z)-octadec-9-enoyl]oxyethyl]azanium;chloride Chemical compound [Cl-].CCCCCCCC\C=C/CCCCCCCC(=O)OCC[N+](C)(C)CCOC(=O)CCCCCCC\C=C/CCCCCCCC ACOHUVFYOFOGIG-JDVCJPALSA-M 0.000 description 1
- IQDGSYLLQPDQDV-UHFFFAOYSA-N dimethylazanium;chloride Chemical compound Cl.CNC IQDGSYLLQPDQDV-UHFFFAOYSA-N 0.000 description 1
- REZZEXDLIUJMMS-UHFFFAOYSA-M dimethyldioctadecylammonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCC[N+](C)(C)CCCCCCCCCCCCCCCCCC REZZEXDLIUJMMS-UHFFFAOYSA-M 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229960004756 ethanol Drugs 0.000 description 1
- 150000002190 fatty acyls Chemical group 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- 235000021588 free fatty acids Nutrition 0.000 description 1
- 238000007429 general method Methods 0.000 description 1
- VWLBUYNYKAHDHY-UHFFFAOYSA-N heptane-1,7-diol heptane-2,3-diol heptane-2,4-diol heptane-2,5-diol heptane-2,6-diol heptane-3,4-diol heptane-3,5-diol 3-methylheptane-1,2-diol Chemical compound CCC(CC(CC)O)O.C(CCCCCCO)O.CCC(C(CCC)O)O.CC(CCCC(C)O)O.CC(CCC(CC)O)O.CC(CC(CCC)O)O.CC(C(CCCC)O)O.CC(C(CO)O)CCCC VWLBUYNYKAHDHY-UHFFFAOYSA-N 0.000 description 1
- ZYXQFVIQXIIONQ-UHFFFAOYSA-N hexa-1,3-diene-3,4-diol Chemical compound CCC(O)=C(O)C=C ZYXQFVIQXIIONQ-UHFFFAOYSA-N 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 238000004900 laundering Methods 0.000 description 1
- AKDNDOBRFDICST-UHFFFAOYSA-N methylazanium;methyl sulfate Chemical compound [NH3+]C.COS([O-])(=O)=O AKDNDOBRFDICST-UHFFFAOYSA-N 0.000 description 1
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-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
- GDUWKVCUIFEAGC-UHFFFAOYSA-N octane-1,6-diol Chemical compound CCC(O)CCCCCO GDUWKVCUIFEAGC-UHFFFAOYSA-N 0.000 description 1
- WWZKQHOCKIZLMA-UHFFFAOYSA-N octanoic acid Chemical compound CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 235000019198 oils Nutrition 0.000 description 1
- 125000002811 oleoyl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])/C([H])=C([H])\C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 230000020477 pH reduction Effects 0.000 description 1
- 230000036961 partial effect Effects 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 125000002467 phosphate group Chemical class [H]OP(=O)(O[H])O[*] 0.000 description 1
- IVDFJHOHABJVEH-UHFFFAOYSA-N pinacol Chemical compound CC(C)(O)C(C)(C)O IVDFJHOHABJVEH-UHFFFAOYSA-N 0.000 description 1
- XRVCFZPJAHWYTB-UHFFFAOYSA-N prenderol Chemical compound CCC(CC)(CO)CO XRVCFZPJAHWYTB-UHFFFAOYSA-N 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 229940032159 propylene carbonate Drugs 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 239000003813 safflower oil Substances 0.000 description 1
- 235000005713 safflower oil Nutrition 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 239000011877 solvent mixture Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 238000001308 synthesis method Methods 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 238000010257 thawing Methods 0.000 description 1
- 150000005691 triesters Chemical class 0.000 description 1
- 229910052722 tritium Inorganic materials 0.000 description 1
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 1
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 1
- HGBOYTHUEUWSSQ-UHFFFAOYSA-N valeric aldehyde Natural products CCCCC=O HGBOYTHUEUWSSQ-UHFFFAOYSA-N 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)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Emergency Medicine (AREA)
- Textile Engineering (AREA)
- Dispersion Chemistry (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Peptides Or Proteins (AREA)
- Detergent Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Cosmetics (AREA)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CA002438655A CA2438655A1 (en) | 1995-07-11 | 1996-07-11 | Concentrated, stable fabric softening compositions with low organic solvent level |
Applications Claiming Priority (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US105795P | 1995-07-11 | 1995-07-11 | |
US60,001,057 | 1995-07-11 | ||
US62101996A | 1996-03-22 | 1996-03-22 | |
US08/621,019 | 1996-03-22 | ||
PCT/US1996/011556 WO1997003169A1 (en) | 1995-07-11 | 1996-07-11 | Concentrated, stable fabric softening composition |
Related Child Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA002438655A Division CA2438655A1 (en) | 1995-07-11 | 1996-07-11 | Concentrated, stable fabric softening compositions with low organic solvent level |
Publications (2)
Publication Number | Publication Date |
---|---|
CA2226564A1 CA2226564A1 (en) | 1997-01-30 |
CA2226564C true CA2226564C (en) | 2003-10-28 |
Family
ID=26668492
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA002226564A Expired - Fee Related CA2226564C (en) | 1995-07-11 | 1996-07-11 | Concentrated, stable fabric softening compositions with low organic solvent level |
CA002226550A Expired - Fee Related CA2226550C (en) | 1995-07-11 | 1996-07-11 | Concentrated, stable fabric softening compositions including chelants |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA002226550A Expired - Fee Related CA2226550C (en) | 1995-07-11 | 1996-07-11 | Concentrated, stable fabric softening compositions including chelants |
Country Status (15)
Country | Link |
---|---|
EP (2) | EP0842250B1 (cs) |
JP (2) | JPH11506810A (cs) |
KR (3) | KR100274684B1 (cs) |
CN (3) | CN1107716C (cs) |
AR (1) | AR002814A1 (cs) |
AT (1) | ATE233804T1 (cs) |
AU (2) | AU6488996A (cs) |
BR (2) | BR9609823A (cs) |
CA (2) | CA2226564C (cs) |
CZ (2) | CZ6298A3 (cs) |
DE (1) | DE69626521T2 (cs) |
HU (2) | HUP9802404A3 (cs) |
MX (2) | MX9800381A (cs) |
TR (1) | TR199800029T1 (cs) |
WO (2) | WO1997003169A1 (cs) |
Families Citing this family (36)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CZ13399A3 (cs) * | 1996-07-19 | 1999-07-14 | The Procter & Gamble Company | Koncentrovaný přípravek na změkčování tkanin a jeho vysoce nenasycená účinná složka |
CA2264087A1 (en) * | 1996-08-30 | 1998-03-05 | Hugo Jean-Marie Demeyere | Concentrated premix with reduced flammability for forming fabric softening composition |
WO1998053035A1 (en) * | 1997-05-19 | 1998-11-26 | The Procter & Gamble Company | Clear or translucent fabric softener compositions using mixture of solvents |
CA2297032A1 (en) * | 1997-07-29 | 1999-02-11 | The Procter & Gamble Company | Concentrated, stable, preferably clear, fabric softening composition containing amine fabric softener |
WO1999009122A1 (en) * | 1997-08-18 | 1999-02-25 | The Procter & Gamble Company | Clear liquid fabric softening compositions |
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 |
US6966696B1 (en) | 1998-10-24 | 2005-11-22 | The Procter & Gamble Company | Methods for laundering delicate garments in a washing machine |
US6995124B1 (en) | 1998-10-24 | 2006-02-07 | The Procter & Gamble Company | Methods for laundering delicate garments in a washing machine |
US7185380B2 (en) | 1998-10-24 | 2007-03-06 | The Procter & Gamble Company | Methods for laundering delicate garments in a washing machine comprising a woven acrylic coated polyester garment container |
EP1018541A1 (de) * | 1999-01-07 | 2000-07-12 | Goldschmidt Rewo GmbH & Co. KG | Klare Weichspülmittelformulierungen |
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WO2003010265A1 (en) * | 2000-05-24 | 2003-02-06 | 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 |
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GB8914054D0 (en) * | 1989-06-19 | 1989-08-09 | Unilever Plc | Fabric softening composition |
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RU94046015A (ru) * | 1992-05-12 | 1996-10-10 | Дзе Проктер Энд Гэмбл Компани (US) | Концентрированная композиция замасливателя тканей, способ получения твердой порошковой композиции замасливателя, способ получения жидкой композиции замасливателя и способ замасливания тканей |
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-
1996
- 1996-07-11 CZ CZ9862A patent/CZ6298A3/cs unknown
- 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 MX MX9800381A patent/MX9800381A/es unknown
- 1996-07-11 CA CA002226564A patent/CA2226564C/en not_active Expired - Fee Related
- 1996-07-11 AT AT96924436T patent/ATE233804T1/de not_active IP Right Cessation
- 1996-07-11 HU HU9802404A patent/HUP9802404A3/hu unknown
- 1996-07-11 KR KR1019980700197A patent/KR100274684B1/ko not_active Expired - Fee Related
- 1996-07-11 MX MX9800382A patent/MX9800382A/es unknown
- 1996-07-11 JP JP50599197A patent/JP3916666B2/ja not_active Expired - Fee Related
- 1996-07-11 BR BR9609823A patent/BR9609823A/pt not_active Application Discontinuation
- 1996-07-11 AU AU64889/96A patent/AU6488996A/en not_active Abandoned
- 1996-07-11 CN CN96196853A patent/CN1107716C/zh not_active Expired - Fee Related
- 1996-07-11 KR KR1019980700196A patent/KR100263870B1/ko not_active Expired - Fee Related
- 1996-07-11 TR TR1998/00029T patent/TR199800029T1/xx unknown
- 1996-07-11 BR BR9609800A patent/BR9609800A/pt not_active Application Discontinuation
- 1996-07-11 EP EP96924436A patent/EP0842250B1/en not_active Expired - Lifetime
- 1996-07-11 CN CN96196787A patent/CN1195369A/zh active Pending
- 1996-07-11 WO PCT/US1996/011572 patent/WO1997003172A1/en not_active Application Discontinuation
- 1996-07-11 CA CA002226550A patent/CA2226550C/en not_active Expired - Fee Related
- 1996-07-11 DE DE69626521T patent/DE69626521T2/de not_active Expired - Lifetime
- 1996-07-11 CZ CZ9838A patent/CZ3898A3/cs unknown
- 1996-07-11 KR KR1019997011199A patent/KR100263216B1/ko not_active Expired - Fee Related
- 1996-07-11 AU AU66365/96A patent/AU6636596A/en not_active Abandoned
- 1996-07-11 EP EP96926070A patent/EP0839180A1/en not_active Ceased
- 1996-07-11 HU HU9802207A patent/HUP9802207A3/hu unknown
- 1996-07-12 AR ARP960103546A patent/AR002814A1/es not_active Application Discontinuation
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2002
- 2002-09-17 CN CNB021432295A patent/CN1232692C/zh not_active Expired - Fee Related
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