GB465200A - Improvements in the manufacture and production of valuable condensation products containing nitrogen, phosphorus or sulphur - Google Patents
Improvements in the manufacture and production of valuable condensation products containing nitrogen, phosphorus or sulphurInfo
- Publication number
- GB465200A GB465200A GB2382435A GB2382435A GB465200A GB 465200 A GB465200 A GB 465200A GB 2382435 A GB2382435 A GB 2382435A GB 2382435 A GB2382435 A GB 2382435A GB 465200 A GB465200 A GB 465200A
- Authority
- GB
- United Kingdom
- Prior art keywords
- compounds
- quaternary ammonium
- treated
- products
- dimethylsulphate
- 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
Links
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 title abstract 6
- 239000007859 condensation product Substances 0.000 title abstract 4
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 title abstract 3
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 title abstract 3
- 239000005864 Sulphur Substances 0.000 title abstract 3
- 229910052757 nitrogen Inorganic materials 0.000 title abstract 3
- 229910052698 phosphorus Inorganic materials 0.000 title abstract 3
- 239000011574 phosphorus Substances 0.000 title abstract 3
- 238000004519 manufacturing process Methods 0.000 title 2
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 abstract 18
- 229940117927 ethylene oxide Drugs 0.000 abstract 18
- 239000000047 product Substances 0.000 abstract 14
- VAYGXNSJCAHWJZ-UHFFFAOYSA-N dimethyl sulfate Chemical compound COS(=O)(=O)OC VAYGXNSJCAHWJZ-UHFFFAOYSA-N 0.000 abstract 12
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical class S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 abstract 10
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 abstract 9
- -1 dichlordiethylether Chemical compound 0.000 abstract 9
- 150000003856 quaternary ammonium compounds Chemical class 0.000 abstract 9
- 239000004721 Polyphenylene oxide Substances 0.000 abstract 8
- 229920000570 polyether Polymers 0.000 abstract 8
- 125000001453 quaternary ammonium group Chemical group 0.000 abstract 8
- 239000007795 chemical reaction product Substances 0.000 abstract 7
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 abstract 6
- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 abstract 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 abstract 6
- QGLWBTPVKHMVHM-KTKRTIGZSA-N (z)-octadec-9-en-1-amine Chemical compound CCCCCCCC\C=C/CCCCCCCCN QGLWBTPVKHMVHM-KTKRTIGZSA-N 0.000 abstract 5
- REYJJPSVUYRZGE-UHFFFAOYSA-N Octadecylamine Chemical compound CCCCCCCCCCCCCCCCCCN REYJJPSVUYRZGE-UHFFFAOYSA-N 0.000 abstract 5
- 150000001875 compounds Chemical class 0.000 abstract 5
- 150000002148 esters Chemical class 0.000 abstract 5
- 150000002170 ethers Chemical class 0.000 abstract 5
- VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical compound NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 abstract 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 abstract 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 abstract 4
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 abstract 4
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 abstract 4
- FOCAUTSVDIKZOP-UHFFFAOYSA-N chloroacetic acid Chemical compound OC(=O)CCl FOCAUTSVDIKZOP-UHFFFAOYSA-N 0.000 abstract 4
- 238000004043 dyeing Methods 0.000 abstract 4
- 125000001033 ether group Chemical group 0.000 abstract 4
- KRGNEXKRYVRWOD-UHFFFAOYSA-N octadecyl(2,2,2-trihydroxyethyl)azanium;hydroxide Chemical compound [OH-].CCCCCCCCCCCCCCCCCC[NH2+]CC(O)(O)O KRGNEXKRYVRWOD-UHFFFAOYSA-N 0.000 abstract 4
- FATBGEAMYMYZAF-KTKRTIGZSA-N oleamide Chemical class CCCCCCCC\C=C/CCCCCCCC(N)=O FATBGEAMYMYZAF-KTKRTIGZSA-N 0.000 abstract 4
- FSYKKLYZXJSNPZ-UHFFFAOYSA-N sarcosine Chemical compound C[NH2+]CC([O-])=O FSYKKLYZXJSNPZ-UHFFFAOYSA-N 0.000 abstract 4
- LPCUKVLKMNSRFQ-UHFFFAOYSA-N 1,2,2,2-tetrahydroxyethylazanium;hydroxide Chemical compound [OH-].[NH3+]C(O)C(O)(O)O LPCUKVLKMNSRFQ-UHFFFAOYSA-N 0.000 abstract 3
- RZBQPWHJXAYARL-UHFFFAOYSA-N 2-n-dodecylpropane-1,2-diamine Chemical class CCCCCCCCCCCCNC(C)CN RZBQPWHJXAYARL-UHFFFAOYSA-N 0.000 abstract 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 abstract 3
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical class CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 abstract 3
- 235000014113 dietary fatty acids Nutrition 0.000 abstract 3
- QKEFILMVJRWDRR-UHFFFAOYSA-M dodecyl-(2-hydroxyethyl)-dimethylazanium;hydroxide Chemical compound [OH-].CCCCCCCCCCCC[N+](C)(C)CCO QKEFILMVJRWDRR-UHFFFAOYSA-M 0.000 abstract 3
- 239000000194 fatty acid Substances 0.000 abstract 3
- 229930195729 fatty acid Natural products 0.000 abstract 3
- OMEMQVZNTDHENJ-UHFFFAOYSA-N n-methyldodecan-1-amine Chemical compound CCCCCCCCCCCCNC OMEMQVZNTDHENJ-UHFFFAOYSA-N 0.000 abstract 3
- NLKNQRATVPKPDG-UHFFFAOYSA-M potassium iodide Chemical compound [K+].[I-] NLKNQRATVPKPDG-UHFFFAOYSA-M 0.000 abstract 3
- 150000003839 salts Chemical class 0.000 abstract 3
- FKNWPJMXOOXOKG-JJKGCWMISA-N (2R,3S,4R,5R)-1,1-diaminohexane-1,2,3,4,5,6-hexol ethene Chemical compound NC(O)([C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO)N.C=C FKNWPJMXOOXOKG-JJKGCWMISA-N 0.000 abstract 2
- KULQACNMKIDJNN-GASJEMHNSA-N (2r,3s,4r,5r)-1-aminohexane-1,2,3,4,5,6-hexol Chemical compound NC(O)[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO KULQACNMKIDJNN-GASJEMHNSA-N 0.000 abstract 2
- DEWLEGDTCGBNGU-UHFFFAOYSA-N 1,3-dichloropropan-2-ol Chemical compound ClCC(O)CCl DEWLEGDTCGBNGU-UHFFFAOYSA-N 0.000 abstract 2
- PBLNBZIONSLZBU-UHFFFAOYSA-N 1-bromododecane Chemical compound CCCCCCCCCCCCBr PBLNBZIONSLZBU-UHFFFAOYSA-N 0.000 abstract 2
- LHORZPMPPHTXFQ-UHFFFAOYSA-N 1-chloroethanesulfonic acid Chemical compound CC(Cl)S(O)(=O)=O LHORZPMPPHTXFQ-UHFFFAOYSA-N 0.000 abstract 2
- SZIFAVKTNFCBPC-UHFFFAOYSA-N 2-chloroethanol Chemical compound OCCCl SZIFAVKTNFCBPC-UHFFFAOYSA-N 0.000 abstract 2
- PLIKAWJENQZMHA-UHFFFAOYSA-N 4-aminophenol Chemical compound NC1=CC=C(O)C=C1 PLIKAWJENQZMHA-UHFFFAOYSA-N 0.000 abstract 2
- 229920002955 Art silk Polymers 0.000 abstract 2
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 abstract 2
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 abstract 2
- 239000005977 Ethylene Substances 0.000 abstract 2
- CTKINSOISVBQLD-UHFFFAOYSA-N Glycidol Chemical compound OCC1CO1 CTKINSOISVBQLD-UHFFFAOYSA-N 0.000 abstract 2
- 108010077895 Sarcosine Proteins 0.000 abstract 2
- 235000021355 Stearic acid Nutrition 0.000 abstract 2
- 229910000147 aluminium phosphate Inorganic materials 0.000 abstract 2
- 150000003868 ammonium compounds Chemical class 0.000 abstract 2
- 125000004429 atom Chemical group 0.000 abstract 2
- KCXMKQUNVWSEMD-UHFFFAOYSA-N benzyl chloride Chemical compound ClCC1=CC=CC=C1 KCXMKQUNVWSEMD-UHFFFAOYSA-N 0.000 abstract 2
- 229940073608 benzyl chloride Drugs 0.000 abstract 2
- 238000004061 bleaching Methods 0.000 abstract 2
- RDHPKYGYEGBMSE-UHFFFAOYSA-N bromoethane Chemical compound CCBr RDHPKYGYEGBMSE-UHFFFAOYSA-N 0.000 abstract 2
- 125000004432 carbon atom Chemical group C* 0.000 abstract 2
- OTDMAGSUUOTZNQ-UHFFFAOYSA-N carboxymethyl-dodecyl-dimethylazanium;chloride Chemical compound [Cl-].CCCCCCCCCCCC[N+](C)(C)CC(O)=O OTDMAGSUUOTZNQ-UHFFFAOYSA-N 0.000 abstract 2
- 229920002678 cellulose Chemical class 0.000 abstract 2
- 239000001913 cellulose Chemical class 0.000 abstract 2
- NEHMKBQYUWJMIP-UHFFFAOYSA-N chloromethane Chemical compound ClC NEHMKBQYUWJMIP-UHFFFAOYSA-N 0.000 abstract 2
- FKKYVFKDQPNXNO-UHFFFAOYSA-N dibutyl(2,2-dimethoxyethyl)azanium hydroxide Chemical compound [OH-].CCCC[NH+](CCCC)CC(OC)OC FKKYVFKDQPNXNO-UHFFFAOYSA-N 0.000 abstract 2
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 abstract 2
- WNAHIZMDSQCWRP-UHFFFAOYSA-N dodecane-1-thiol Chemical compound CCCCCCCCCCCCS WNAHIZMDSQCWRP-UHFFFAOYSA-N 0.000 abstract 2
- 229910052736 halogen Inorganic materials 0.000 abstract 2
- 150000002367 halogens Chemical group 0.000 abstract 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 2
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 abstract 2
- 239000012948 isocyanate Substances 0.000 abstract 2
- 150000002513 isocyanates Chemical class 0.000 abstract 2
- DBNYMXPUYZOHQN-UHFFFAOYSA-N n'-[2-(octadecylamino)ethyl]ethane-1,2-diamine Chemical compound CCCCCCCCCCCCCCCCCCNCCNCCN DBNYMXPUYZOHQN-UHFFFAOYSA-N 0.000 abstract 2
- MJCJUDJQDGGKOX-UHFFFAOYSA-N n-dodecyldodecan-1-amine Chemical compound CCCCCCCCCCCCNCCCCCCCCCCCC MJCJUDJQDGGKOX-UHFFFAOYSA-N 0.000 abstract 2
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 abstract 2
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 abstract 2
- 239000003921 oil Substances 0.000 abstract 2
- 229940113162 oleylamide Drugs 0.000 abstract 2
- 239000012188 paraffin wax Substances 0.000 abstract 2
- XYFCBTPGUUZFHI-UHFFFAOYSA-O phosphonium Chemical compound [PH4+] XYFCBTPGUUZFHI-UHFFFAOYSA-O 0.000 abstract 2
- 150000004714 phosphonium salts Chemical class 0.000 abstract 2
- 229920000223 polyglycerol Polymers 0.000 abstract 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 2
- 150000004023 quaternary phosphonium compounds Chemical class 0.000 abstract 2
- 229940043230 sarcosine Drugs 0.000 abstract 2
- 239000000344 soap Substances 0.000 abstract 2
- JVBXVOWTABLYPX-UHFFFAOYSA-L sodium dithionite Chemical compound [Na+].[Na+].[O-]S(=O)S([O-])=O JVBXVOWTABLYPX-UHFFFAOYSA-L 0.000 abstract 2
- 235000011121 sodium hydroxide Nutrition 0.000 abstract 2
- 239000007858 starting material Substances 0.000 abstract 2
- 239000008117 stearic acid Substances 0.000 abstract 2
- 150000005846 sugar alcohols Polymers 0.000 abstract 2
- RWSOTUBLDIXVET-UHFFFAOYSA-O sulfonium Chemical compound [SH3+] RWSOTUBLDIXVET-UHFFFAOYSA-O 0.000 abstract 2
- 239000004753 textile Substances 0.000 abstract 2
- 125000003396 thiol group Chemical group [H]S* 0.000 abstract 2
- RIOQSEWOXXDEQQ-UHFFFAOYSA-N triphenylphosphine Chemical compound C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-N 0.000 abstract 2
- 238000005406 washing Methods 0.000 abstract 2
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 abstract 1
- RPMFWLKUMRBVKZ-KTKRTIGZSA-N (z)-n,n-bis(2-hydroxyethyl)octadec-9-en-1-amine oxide Chemical compound CCCCCCCC\C=C/CCCCCCCC[N+]([O-])(CCO)CCO RPMFWLKUMRBVKZ-KTKRTIGZSA-N 0.000 abstract 1
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 abstract 1
- GEYOCULIXLDCMW-UHFFFAOYSA-N 1,2-phenylenediamine Chemical compound NC1=CC=CC=C1N GEYOCULIXLDCMW-UHFFFAOYSA-N 0.000 abstract 1
- YVSNBDFDMHIXBF-UHFFFAOYSA-N 1-(chloromethylsulfanyl)dodecane Chemical compound CCCCCCCCCCCCSCCl YVSNBDFDMHIXBF-UHFFFAOYSA-N 0.000 abstract 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 abstract 1
- JFGQHAHJWJBOPD-UHFFFAOYSA-N 3-hydroxy-n-phenylnaphthalene-2-carboxamide Chemical compound OC1=CC2=CC=CC=C2C=C1C(=O)NC1=CC=CC=C1 JFGQHAHJWJBOPD-UHFFFAOYSA-N 0.000 abstract 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 abstract 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 abstract 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 abstract 1
- KXDHJXZQYSOELW-UHFFFAOYSA-N Carbamic acid Chemical class NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 abstract 1
- 229920000742 Cotton Polymers 0.000 abstract 1
- 229920001353 Dextrin Chemical class 0.000 abstract 1
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 abstract 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 abstract 1
- 241000322338 Loeseliastrum Species 0.000 abstract 1
- 229920000715 Mucilage Polymers 0.000 abstract 1
- 239000005642 Oleic acid Substances 0.000 abstract 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 abstract 1
- DIOYAVUHUXAUPX-KHPPLWFESA-N Oleoyl sarcosine Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)N(C)CC(O)=O DIOYAVUHUXAUPX-KHPPLWFESA-N 0.000 abstract 1
- 229920002472 Starch Chemical class 0.000 abstract 1
- 241000607479 Yersinia pestis Species 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 239000000980 acid dye Substances 0.000 abstract 1
- 150000007513 acids Chemical class 0.000 abstract 1
- 239000000853 adhesive Substances 0.000 abstract 1
- 150000001408 amides Chemical class 0.000 abstract 1
- 239000000981 basic dye Substances 0.000 abstract 1
- UENWRTRMUIOCKN-UHFFFAOYSA-N benzyl thiol Chemical compound SCC1=CC=CC=C1 UENWRTRMUIOCKN-UHFFFAOYSA-N 0.000 abstract 1
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 abstract 1
- 238000009835 boiling Methods 0.000 abstract 1
- 238000010000 carbonizing Methods 0.000 abstract 1
- 239000003638 chemical reducing agent Substances 0.000 abstract 1
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- 239000002537 cosmetic Substances 0.000 abstract 1
- 238000004855 creaseproofing Methods 0.000 abstract 1
- HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 abstract 1
- 239000007857 degradation product Substances 0.000 abstract 1
- FYGDTMLNYKFZSV-MRCIVHHJSA-N dextrin Chemical class O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)OC1O[C@@H]1[C@@H](CO)OC(O[C@@H]2[C@H](O[C@H](O)[C@H](O)[C@H]2O)CO)[C@H](O)[C@H]1O FYGDTMLNYKFZSV-MRCIVHHJSA-N 0.000 abstract 1
- 229940079919 digestives enzyme preparation Drugs 0.000 abstract 1
- 239000000982 direct dye Substances 0.000 abstract 1
- 239000000975 dye Substances 0.000 abstract 1
- 239000003925 fat Substances 0.000 abstract 1
- 235000019197 fats Nutrition 0.000 abstract 1
- 150000004665 fatty acids Chemical class 0.000 abstract 1
- 239000008396 flotation agent Substances 0.000 abstract 1
- 238000009963 fulling Methods 0.000 abstract 1
- 239000008103 glucose Substances 0.000 abstract 1
- 239000003292 glue Substances 0.000 abstract 1
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 abstract 1
- 229910000041 hydrogen chloride Inorganic materials 0.000 abstract 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 abstract 1
- 239000004922 lacquer Substances 0.000 abstract 1
- 239000000314 lubricant Substances 0.000 abstract 1
- 125000005341 metaphosphate group Chemical group 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 229940050176 methyl chloride Drugs 0.000 abstract 1
- YWFWDNVOPHGWMX-UHFFFAOYSA-N n,n-dimethyldodecan-1-amine Chemical compound CCCCCCCCCCCCN(C)C YWFWDNVOPHGWMX-UHFFFAOYSA-N 0.000 abstract 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 abstract 1
- 239000003346 palm kernel oil Substances 0.000 abstract 1
- 235000019865 palm kernel oil Nutrition 0.000 abstract 1
- 239000000123 paper Substances 0.000 abstract 1
- 239000000825 pharmaceutical preparation Substances 0.000 abstract 1
- 229940127557 pharmaceutical product Drugs 0.000 abstract 1
- 125000005496 phosphonium group Chemical group 0.000 abstract 1
- 229920001223 polyethylene glycol Polymers 0.000 abstract 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 abstract 1
- 239000011347 resin Substances 0.000 abstract 1
- 229920005989 resin Polymers 0.000 abstract 1
- 239000000243 solution Substances 0.000 abstract 1
- 239000002904 solvent Substances 0.000 abstract 1
- 238000009987 spinning Methods 0.000 abstract 1
- 239000008107 starch Chemical class 0.000 abstract 1
- 235000019698 starch Nutrition 0.000 abstract 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical compound [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 abstract 1
- UWHCKJMYHZGTIT-UHFFFAOYSA-N tetraethylene glycol Chemical compound OCCOCCOCCOCCO UWHCKJMYHZGTIT-UHFFFAOYSA-N 0.000 abstract 1
- 239000000984 vat dye Substances 0.000 abstract 1
- 238000004078 waterproofing Methods 0.000 abstract 1
- 239000001993 wax Substances 0.000 abstract 1
- 238000009736 wetting Methods 0.000 abstract 1
- 210000002268 wool Anatomy 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C381/00—Compounds containing carbon and sulfur and having functional groups not covered by groups C07C301/00 - C07C337/00
- C07C381/12—Sulfonium compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/54—Quaternary phosphonium compounds
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
- D06P1/00—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
- D06P1/44—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders
- D06P1/60—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders using compositions containing polyethers
- D06P1/607—Nitrogen-containing polyethers or their quaternary derivatives
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
- D06P1/00—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
- D06P1/44—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders
- D06P1/60—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders using compositions containing polyethers
- D06P1/607—Nitrogen-containing polyethers or their quaternary derivatives
- D06P1/6076—Nitrogen-containing polyethers or their quaternary derivatives addition products of amines and alkylene oxides or oxiranes
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
- D06P1/00—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
- D06P1/44—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders
- D06P1/60—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders using compositions containing polyethers
- D06P1/613—Polyethers without nitrogen
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
- D06P1/00—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
- D06P1/44—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders
- D06P1/655—Compounds containing ammonium groups
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
- D06P1/00—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
- D06P1/44—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders
- D06P1/655—Compounds containing ammonium groups
- D06P1/66—Compounds containing ammonium groups containing quaternary ammonium groups
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
- D06P5/00—Other features in dyeing or printing textiles, or dyeing leather, furs, or solid macromolecular substances in any form
- D06P5/13—Fugitive dyeing or stripping dyes
- D06P5/138—Fugitive dyeing or stripping dyes fugitive dyeing
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- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Paper (AREA)
Abstract
Products useful as assistants in the textile, paper, lacquer, tanning and rubber industries are obtained by introducing one or more ether or polyether radicles into quaternary ammonium or phosphonium compounds or ternary sulphonium compounds by condensing the latter with polyhydric alcohols or etherifying derivatives thereof having at most six carbon atoms or with polyether compounds containing atoms or groups such as halogen which react with the said quaternary ammonium or phosphonium or ternary sulphonium compounds. Specified components are: ethylene and propylene oxides, glycide, epichlorhydrin, dichlorhydrin, dichlordiethylether, glycol, glycerol, polyglycerol, glycolchlorhydrin, polyglycerolchloride and a -chlor tetraethylene glycol. The quaternary phosphonium and ammonium compounds and the ternary sulphonium compounds may contain hydroxyl, carboxylic, amino or mercapto groups which react with the second components. The same products may also be produced from any compound containing nitrogen, phosphorus or sulphur by first introducing the ether group or groups and then converting the resulting ethers into quaternary ammonium or ternary sulphonium compounds. Thus, diethylbutanolamine, asymdimethylethylenediamine or sarcosine may be treated with ethyleneoxide and quaternary ammonium compounds produced by a final treatment with dimethylsulphate, ethylbromide or benzylchloride. The following starting materials which contain radicles of high molecular weight are advantageously employed: dodecyldimethyl hydroxyethylammoniumhydroxide, stearyltrihydroxyethyl ammoniumhydroxide, dimethyloxyethyldibutylammoniumhydroxide, the monooleicester of tetrahydroxyethylammoniumhydroxide, dodecyldimethylcarboxymethylammoniumchloride (from dodecyldimethylamine and chloracetic acid), the reaction product of ethylenediamine with octodecyldimethylchlorethylammoniumchloride (from octodecyldimethylamine and ethylenechloride), the reaction product of dimethyl sulphate with stearyldiethylenetriamine, the quaternary ammonium compounds of oleylpiperazine (from piperazine and oleylsulphuric ester), quaternary ammonium compounds obtained by adding on dodecyl bromide, dodecahydroxymethylchloride or dodecathio methylchloride to tetramethyl-b -hydroxypropylenediamine, oleyldihydroxyethylamineoxide (from oleylamine, ethyleneoxide and hydrogen peroxide), stearylamine, oleylamine, dodecylmethylamine, didodecylamine, octodecylethylenediamine, dodecylpropylenediamine, and polyether derivatives of oleic acid amides of ethylenediamine, triethylenetetramine or ethylene diaminosorbitol (from glucose and ethylenediamine followed by reduction) and polyether derivatives of the reaction product of triethylenetetramine or aminosorbitol with trichlorinated paraffin wax or of oleylamide of piperazine. The high molecular radicle may however be introduced when the ethers are converted into quaternary ammonium or ternary sulphonium compounds. The products may be condensed with chlorethane sulphonic acid, chloracetic acid, fatty acid chlorides, chlorcarbonic esters, isocyanates or treated with phosphoric acid or sulphonating agents. The wetting, dispersing, levelling, washing and softening properties of the products make them useful in the following processes; bleaching, bucking, carbonizing, mercerizing, stripping, printing, mordanting, fulling, dressing, waterproofing, crease-proofing and combating pests. They may also be added to artificial silk spinning solutions, lubricants, textile oils, shoe polishes, pharmaceutical products, cosmetics and flotation agents. They may be used in dyeing with acetate artificial silk dyes, and with vat, acid, substantive and basic dyes. The products may be used in association with soaps, sulphuric esters and sulphonic acids, condensation products of fatty acid chlorides with albumen degradation products, aminocarboxylic acids, condensation products of alkyleneoxides with hydroxy, carboxy, amino or mercapto compounds, starch, dextrine, cellulose derivatives, sulphite cellulose, ortho-, pyro- or meta-phosphates, Glauber's salts, glue, mucilages, resins, waxes, oils, fats, solvents, cyclohexanol, hydrogen peroxide and other per compounds and reducing agents such as sodium hydrosulphite. In examples: (1) stearylamine is treated with ethylene oxide and a quaternary ammonium compound formed by means of dimethylsulphate; the product may be added to bottoming or developing baths in dyeing with azo dyestuffs: (2) ethylenediamine or b : b -dibutyl ethylenediamine is treated with ethyleneoxide and a quaternary ammonium compound formed with octodecylbromide: (3) dodecyldimethylhydroxyethylammoniumhydroxide or stearyl trihydroxyethylammonium hydroxide is treated with ethylene oxide; a soap of stearylamine and stearic acid is treated with ethyleneoxide or a salt with stearic acid is formed from the quaternary ammonium base obtained from stearyltrihydroxyethylammonium hydroxide and ethylene oxide: (4) propylene oxide is reacted with tetrahydroxyethylammonium hydroxide: (5) methyldodecylamine is treated first with ethylene oxide and then with dimethylsulphate; the product may be used in dyeing with Naphthol AS. and as an assistant in association with oleylsarcosine in bleaching with sodium hydrosulphite: (6) quaternary ammonium compounds are obtained by treating with dimethylsulphate the products obtained from oleylamine and ethyleneoxide: (7) dimethylsulphate is added to the condensation product of oleylamine and ethylene oxide and the resulting quaternary salt sulphonated; the product may be used for dyeing mercerized calico with Hydronblau R: (8) stearylamine is treated first with ethyleneoxide and then with ethylene chlorhydrin; the product which may be used with enzyme preparations may be used for washing wool or cotton: (9) an amide obtained from ethylenediamine or phenylenediamine and oleic acid or dodecylpropylenediamine or paraaminophenol is treated with ethyleneoxide and a quaternary ammonium salt formed with dimethylsulphate. Specification 420,066 is referred to. Samples have been furnished under Sect. 2 (5) of products prepared as follows: (1) triphenylphosphine is heated with ethylenechlorhydrin in the presence of potassium iodide and a quaternary phosphonium base formed by treating with ethyleneoxide: (2) ethylenediamine is treated with ethylene oxide and high molecular residues of palm kernel oil introduced into the resulting quaternary base, which is finally sulphonated: (3) ethylenediamine is condensed with chloracetic acid, and the reaction product treated first with ethylene oxide and then with dimethylsulphate: (4) dodecylmercaptan is treated with ethyleneoxide and dimethylsulphate; a sulphonium base is obtained by boiling with caustic soda: (5) benzyl mercaptan is treated with ethyleneoxide and dimethylsulphate; a sulphonium base results on adding caustic soda. Dodecylhydroxy- and dodecylthio-methylchloride are obtained by reacting dodecylalcohol or dodecylmercaptan with formaldehyde in the presence of hydrogen chloride. Reference has been directed by the Comptroller to Specification 441,473.ALSO:Products stated to have dispersing properties are obtained by introducing one or more ether or poly ether radicles into quaternary ammonium or phosphonium compounds or ternary sulphonium compounds by condensing the latter with polyhydric alcohols or etherifying derivatives thereof having at most six carbon atoms or with polyether compounds containing atoms or groups such as halogen, which react with the said quarternary ammonium or phosphonium or ternary sulphonium compounds. Specified components are: ethylene and propylene oxides, glycide, epichlorhydrin, dichlorhydrin, dichlordiethylether, glycol, glycerol, polyglycerol, glycolchlorhydrin and polyglycerolchloride. The quaternary phosphonium and ammonium compounds and the ternary sulphonium compounds may contain hydroxyl, carboxylic, amino or mercapto groups which react with the second components. The same products may also be produced from any compound containing nitrogen, phosphorus or sulphur by first introducing the ether group or groups and then converting the resulting ethers into quaternary ammonium or ternary sulphonium compounds. Thus, diethylbutanolamine, asym-dimethylethylenediamine or sarcosine may be treated with ethyleneoxide and quaternary ammonium compounds produced by a final treatment with dimethylsulphate, ethylbromide or benzylchloride. The following starting materials which contain radicles of high molecular weight are advantageously employed: dodecyldimethylhydroxyethylammoniumhydroxide, stearyltrihydroxyethylammonium hydroxide, dimethyloxyethyldibutyl ammoniumhydroxide, the monooleic ester of tetrahydroxyethylammoniumhydroxide, dodecyldimethylcarboxymethylammoniumchloride, the reaction product of ethylenediamine with octodecyldimethylchloroethylammoniumchloride, the reaction product of dimethylsulphate with stearyldiethylenetriamine, the quaternary ammonium compounds of oleylpiperazine, quaternary ammonium compounds obtained by adding on dodecyl bromide, dodecahydroxymethylchloride or dodecathiomethylchloride to tetramethyl-b -hydroxypropylenediamine, oleyldi--hydroxyethylamineoxide, stearylamine, oleylamine, dodecylmethylamine, didodecylamine, octodecylethylenediamine, dodecylpropylene - diamine, and polyether derivatives of oleic acid amides of ethylenediamine, triethylenetetramine or ethylene diaminosorbitol and poly ether derivatives of the reaction product of triethylenetetramine or aminosorbitol with trichlorinated paraffin wax or of the oleylamide of piperazine. The high molecular radicle may however be introduced when the ethers are converted into quaternary ammonium or ternary sulphonium compounds. The products may be condensed with chlorethanesulphonic acid, chloracetic acid, fatty acid chloride, chlorcarbonic esters, isocyanates or treated with phosphoric acid o
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2382435A GB465200A (en) | 1935-08-26 | 1935-08-26 | Improvements in the manufacture and production of valuable condensation products containing nitrogen, phosphorus or sulphur |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2382435A GB465200A (en) | 1935-08-26 | 1935-08-26 | Improvements in the manufacture and production of valuable condensation products containing nitrogen, phosphorus or sulphur |
Publications (1)
Publication Number | Publication Date |
---|---|
GB465200A true GB465200A (en) | 1937-04-26 |
Family
ID=10201895
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2382435A Expired GB465200A (en) | 1935-08-26 | 1935-08-26 | Improvements in the manufacture and production of valuable condensation products containing nitrogen, phosphorus or sulphur |
Country Status (1)
Country | Link |
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GB (1) | GB465200A (en) |
Cited By (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE879388C (en) * | 1938-05-15 | 1953-06-11 | Hoechst Ag | Process for the preparation of quaternary ammonium salts |
US3333005A (en) * | 1963-06-04 | 1967-07-25 | American Cyanamid Co | Quaternary organophosphonium halides and preparation thereof |
US3919283A (en) * | 1965-03-18 | 1975-11-11 | Ciba Geigy Ag | Sulfate derivatives of polyglycol compounds |
US3958931A (en) * | 1965-03-18 | 1976-05-25 | Ciba-Geigy Ag | Wool dyeing with epihalohydrin or chloroacetamide quarternized polyglycolamine assisted dye solution |
US4132657A (en) | 1973-04-09 | 1979-01-02 | Gaf Corporation | Treatment of metal surfaces |
US4138371A (en) | 1976-04-07 | 1979-02-06 | Gaf Corporation | Washing method using amphoteric surface active agents |
GB2133028A (en) * | 1982-12-23 | 1984-07-18 | Procter & Gamble | Detergent compositions |
US4548744A (en) * | 1983-07-22 | 1985-10-22 | Connor Daniel S | Ethoxylated amine oxides having clay soil removal/anti-redeposition properties useful in detergent compositions |
US4551506A (en) | 1982-12-23 | 1985-11-05 | The Procter & Gamble Company | Cationic polymers having clay soil removal/anti-redeposition properties useful in detergent compositions |
GB2168364A (en) * | 1984-12-14 | 1986-06-18 | Sandoz Ltd | Sulphates of oxyalkylated amines and their use as dyeing assistants |
US4597898A (en) * | 1982-12-23 | 1986-07-01 | The Proctor & Gamble Company | Detergent compositions containing ethoxylated amines having clay soil removal/anti-redeposition properties |
GB2180249A (en) * | 1982-12-23 | 1987-03-25 | Procter & Gamble | Ethoxylated polyamino compounds |
US4659802A (en) | 1982-12-23 | 1987-04-21 | The Procter & Gamble Company | Cationic compounds having clay soil removal/anti-redeposition properties useful in detergent compositions |
US4661288A (en) | 1982-12-23 | 1987-04-28 | The Procter & Gamble Company | Zwitterionic compounds having clay soil removal/anti/redeposition properties useful in detergent compositions |
EP0665325A2 (en) * | 1994-01-26 | 1995-08-02 | Hoechst Aktiengesellschaft | Process for the manufacture of aminated cotton fibers |
-
1935
- 1935-08-26 GB GB2382435A patent/GB465200A/en not_active Expired
Cited By (17)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE879388C (en) * | 1938-05-15 | 1953-06-11 | Hoechst Ag | Process for the preparation of quaternary ammonium salts |
US3333005A (en) * | 1963-06-04 | 1967-07-25 | American Cyanamid Co | Quaternary organophosphonium halides and preparation thereof |
US3919283A (en) * | 1965-03-18 | 1975-11-11 | Ciba Geigy Ag | Sulfate derivatives of polyglycol compounds |
US3958931A (en) * | 1965-03-18 | 1976-05-25 | Ciba-Geigy Ag | Wool dyeing with epihalohydrin or chloroacetamide quarternized polyglycolamine assisted dye solution |
US4132657A (en) | 1973-04-09 | 1979-01-02 | Gaf Corporation | Treatment of metal surfaces |
US4138371A (en) | 1976-04-07 | 1979-02-06 | Gaf Corporation | Washing method using amphoteric surface active agents |
US4551506A (en) | 1982-12-23 | 1985-11-05 | The Procter & Gamble Company | Cationic polymers having clay soil removal/anti-redeposition properties useful in detergent compositions |
GB2133028A (en) * | 1982-12-23 | 1984-07-18 | Procter & Gamble | Detergent compositions |
GB2168708A (en) * | 1982-12-23 | 1986-06-25 | Procter & Gamble | Quaternany ammonium compounds |
US4597898A (en) * | 1982-12-23 | 1986-07-01 | The Proctor & Gamble Company | Detergent compositions containing ethoxylated amines having clay soil removal/anti-redeposition properties |
GB2180249A (en) * | 1982-12-23 | 1987-03-25 | Procter & Gamble | Ethoxylated polyamino compounds |
US4659802A (en) | 1982-12-23 | 1987-04-21 | The Procter & Gamble Company | Cationic compounds having clay soil removal/anti-redeposition properties useful in detergent compositions |
US4661288A (en) | 1982-12-23 | 1987-04-28 | The Procter & Gamble Company | Zwitterionic compounds having clay soil removal/anti/redeposition properties useful in detergent compositions |
US4548744A (en) * | 1983-07-22 | 1985-10-22 | Connor Daniel S | Ethoxylated amine oxides having clay soil removal/anti-redeposition properties useful in detergent compositions |
GB2168364A (en) * | 1984-12-14 | 1986-06-18 | Sandoz Ltd | Sulphates of oxyalkylated amines and their use as dyeing assistants |
EP0665325A2 (en) * | 1994-01-26 | 1995-08-02 | Hoechst Aktiengesellschaft | Process for the manufacture of aminated cotton fibers |
EP0665325A3 (en) * | 1994-01-26 | 1997-10-22 | Hoechst Ag | Process for the manufacture of aminated cotton fibers. |
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