CS208477B2 - Freshening and hydrophobous means for the leathers - Google Patents

Freshening and hydrophobous means for the leathers Download PDF

Info

Publication number: CS208477B2
Authority: CS; Czechoslovakia
Prior art keywords: formula; carbon atoms; alkyl; group; leather
Prior art date: 1977-07-02

Application number

CS784408A

Other languages

Czech (cs)

English (en)

Inventor

Gustav Hudec

Karl-Heinz Keil

Volker Koehler

Joachim Ribka

Kurt Rosenbusch

Original Assignee

Cassella Ag

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.)

1977-07-02

Filing date

1978-07-03

Publication date

1981-09-15

1978-07-03 Application filed by Cassella Ag filed Critical Cassella Ag

1981-09-15 Publication of CS208477B2 publication Critical patent/CS208477B2/cs

Links

XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 61
239000000203 mixture Substances 0.000 claims description 44
125000004432 carbon atom Chemical group C* 0.000 claims description 38
125000000217 alkyl group Chemical group 0.000 claims description 36
150000001875 compounds Chemical class 0.000 claims description 33
230000002209 hydrophobic effect Effects 0.000 claims description 32
239000002979 fabric softener Substances 0.000 claims description 25
239000003995 emulsifying agent Substances 0.000 claims description 23
125000003342 alkenyl group Chemical group 0.000 claims description 18
239000003760 tallow Chemical group 0.000 claims description 14
244000060011 Cocos nucifera Species 0.000 claims description 12
235000013162 Cocos nucifera Nutrition 0.000 claims description 12
238000000034 method Methods 0.000 claims description 12
239000003960 organic solvent Substances 0.000 claims description 12
239000000243 solution Substances 0.000 claims description 8
229910052739 hydrogen Inorganic materials 0.000 claims description 7
239000001257 hydrogen Substances 0.000 claims description 7
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 6
239000012875 nonionic emulsifier Substances 0.000 claims description 5
239000007864 aqueous solution Substances 0.000 claims description 4
239000012874 anionic emulsifier Substances 0.000 claims description 3
125000005041 acyloxyalkyl group Chemical group 0.000 claims description 2
125000005037 alkyl phenyl group Chemical group 0.000 claims description 2
239000004744 fabric Substances 0.000 claims description 2
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 2
125000004079 stearyl group Chemical group [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])C([H])([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 claims description 2
125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 1
125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims 1
125000003710 aryl alkyl group Chemical group 0.000 claims 1
125000001589 carboacyl group Chemical group 0.000 claims 1
239000003792 electrolyte Substances 0.000 claims 1
239000010985 leather Substances 0.000 description 73
229910052757 nitrogen Inorganic materials 0.000 description 36
-1 alkenyl sulfates Chemical class 0.000 description 28
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 27
239000000460 chlorine Substances 0.000 description 23
239000000047 product Substances 0.000 description 21
239000003925 fat Substances 0.000 description 17
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 15
239000003795 chemical substances by application Substances 0.000 description 15
239000011734 sodium Substances 0.000 description 15
IGFHQQFPSIBGKE-UHFFFAOYSA-N 4-nonylphenol Chemical compound CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 14
229940100389 Sulfonylurea Drugs 0.000 description 14
238000006243 chemical reaction Methods 0.000 description 14
239000007795 chemical reaction product Substances 0.000 description 14
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 13
229910052801 chlorine Inorganic materials 0.000 description 13
239000000194 fatty acid Substances 0.000 description 12
229910052717 sulfur Inorganic materials 0.000 description 12
235000014113 dietary fatty acids Nutrition 0.000 description 11
239000000839 emulsion Substances 0.000 description 11
229930195729 fatty acid Natural products 0.000 description 11
QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 10
150000004665 fatty acids Chemical class 0.000 description 10
150000003254 radicals Chemical class 0.000 description 10
KHWQFISNNNRGLV-UHFFFAOYSA-N 2,4,6-tributylphenol Chemical compound CCCCC1=CC(CCCC)=C(O)C(CCCC)=C1 KHWQFISNNNRGLV-UHFFFAOYSA-N 0.000 description 9
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 9
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 8
239000012948 isocyanate Substances 0.000 description 8
235000020094 liqueur Nutrition 0.000 description 8
238000002844 melting Methods 0.000 description 8
230000008018 melting Effects 0.000 description 8
239000003921 oil Substances 0.000 description 7
235000019198 oils Nutrition 0.000 description 7
238000002360 preparation method Methods 0.000 description 7
RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 6
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 6
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 6
239000004480 active ingredient Substances 0.000 description 6
239000006185 dispersion Substances 0.000 description 6
229930195733 hydrocarbon Natural products 0.000 description 6
150000002430 hydrocarbons Chemical class 0.000 description 6
230000008569 process Effects 0.000 description 6
HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 5
239000002253 acid Substances 0.000 description 5
239000002671 adjuvant Substances 0.000 description 5
150000001412 amines Chemical class 0.000 description 5
229910021529 ammonia Inorganic materials 0.000 description 5
239000012043 crude product Substances 0.000 description 5
239000000975 dye Substances 0.000 description 5
230000000694 effects Effects 0.000 description 5
238000005470 impregnation Methods 0.000 description 5
150000002513 isocyanates Chemical class 0.000 description 5
239000000314 lubricant Substances 0.000 description 5
150000003839 salts Chemical class 0.000 description 5
239000002904 solvent Substances 0.000 description 5
RFFLAFLAYFXFSW-UHFFFAOYSA-N 1,2-dichlorobenzene Chemical compound ClC1=CC=CC=C1Cl RFFLAFLAYFXFSW-UHFFFAOYSA-N 0.000 description 4
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
239000004166 Lanolin Substances 0.000 description 4
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical group CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 4
URLKBWYHVLBVBO-UHFFFAOYSA-N Para-Xylene Chemical group CC1=CC=C(C)C=C1 URLKBWYHVLBVBO-UHFFFAOYSA-N 0.000 description 4
238000009835 boiling Methods 0.000 description 4
229910052799 carbon Inorganic materials 0.000 description 4
238000004043 dyeing Methods 0.000 description 4
235000019388 lanolin Nutrition 0.000 description 4
229940039717 lanolin Drugs 0.000 description 4
239000007788 liquid Substances 0.000 description 4
IVSZLXZYQVIEFR-UHFFFAOYSA-N m-xylene Chemical group CC1=CC=CC(C)=C1 IVSZLXZYQVIEFR-UHFFFAOYSA-N 0.000 description 4
ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid group Chemical group C(CCCCCCC\C=C/CCCCCCCC)(=O)O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 4
IPCSVZSSVZVIGE-UHFFFAOYSA-N palmitic acid group Chemical group C(CCCCCCCCCCCCCCC)(=O)O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 4
230000035515 penetration Effects 0.000 description 4
239000001993 wax Substances 0.000 description 4
WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 3
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 3
244000126014 Valeriana officinalis Species 0.000 description 3
235000013832 Valeriana officinalis Nutrition 0.000 description 3
150000007513 acids Chemical class 0.000 description 3
125000000129 anionic group Chemical group 0.000 description 3
MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 3
229960001701 chloroform Drugs 0.000 description 3
125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 3
210000000003 hoof Anatomy 0.000 description 3
238000005461 lubrication Methods 0.000 description 3
229910052751 metal Inorganic materials 0.000 description 3
239000002184 metal Substances 0.000 description 3
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
230000007935 neutral effect Effects 0.000 description 3
239000012188 paraffin wax Substances 0.000 description 3
239000000376 reactant Substances 0.000 description 3
238000010992 reflux Methods 0.000 description 3
XSQUKJJJFZCRTK-UHFFFAOYSA-N urea group Chemical group NC(=O)N XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 3
235000016788 valerian Nutrition 0.000 description 3
ALSTYHKOOCGGFT-KTKRTIGZSA-N (9Z)-octadecen-1-ol Chemical compound CCCCCCCC\C=C/CCCCCCCCO ALSTYHKOOCGGFT-KTKRTIGZSA-N 0.000 description 2
SCYULBFZEHDVBN-UHFFFAOYSA-N 1,1-Dichloroethane Chemical compound CC(Cl)Cl SCYULBFZEHDVBN-UHFFFAOYSA-N 0.000 description 2
KVNYFPKFSJIPBJ-UHFFFAOYSA-N 1,2-diethylbenzene Chemical compound CCC1=CC=CC=C1CC KVNYFPKFSJIPBJ-UHFFFAOYSA-N 0.000 description 2
VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 description 2
GJYCVCVHRSWLNY-UHFFFAOYSA-N 2-butylphenol Chemical compound CCCCC1=CC=CC=C1O GJYCVCVHRSWLNY-UHFFFAOYSA-N 0.000 description 2
GIWHJVQUZDWFDI-UHFFFAOYSA-N 2-chloro-n-(oxomethylidene)ethanesulfonamide Chemical compound ClCCS(=O)(=O)N=C=O GIWHJVQUZDWFDI-UHFFFAOYSA-N 0.000 description 2
DLFVBJFMPXGRIB-UHFFFAOYSA-N Acetamide Chemical compound CC(N)=O DLFVBJFMPXGRIB-UHFFFAOYSA-N 0.000 description 2
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 description 2
IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
YNQLUTRBYVCPMQ-UHFFFAOYSA-N Ethylbenzene Chemical compound CCC1=CC=CC=C1 YNQLUTRBYVCPMQ-UHFFFAOYSA-N 0.000 description 2
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
DCXXMTOCNZCJGO-UHFFFAOYSA-N Glycerol trioctadecanoate Natural products CCCCCCCCCCCCCCCCCC(=O)OCC(OC(=O)CCCCCCCCCCCCCCCCC)COC(=O)CCCCCCCCCCCCCCCCC DCXXMTOCNZCJGO-UHFFFAOYSA-N 0.000 description 2
DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 description 2
IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 2
REYJJPSVUYRZGE-UHFFFAOYSA-N Octadecylamine Chemical compound CCCCCCCCCCCCCCCCCCN REYJJPSVUYRZGE-UHFFFAOYSA-N 0.000 description 2
OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 2
CYTYCFOTNPOANT-UHFFFAOYSA-N Perchloroethylene Chemical group ClC(Cl)=C(Cl)Cl CYTYCFOTNPOANT-UHFFFAOYSA-N 0.000 description 2
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
XSTXAVWGXDQKEL-UHFFFAOYSA-N Trichloroethylene Chemical group ClC=C(Cl)Cl XSTXAVWGXDQKEL-UHFFFAOYSA-N 0.000 description 2
239000013543 active substance Substances 0.000 description 2
239000012752 auxiliary agent Substances 0.000 description 2
235000013871 bee wax Nutrition 0.000 description 2
235000015278 beef Nutrition 0.000 description 2
239000012166 beeswax Substances 0.000 description 2
230000008901 benefit Effects 0.000 description 2
230000001680 brushing effect Effects 0.000 description 2
239000004202 carbamide Substances 0.000 description 2
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238000000576 coating method Methods 0.000 description 2
229940096386 coconut alcohol Drugs 0.000 description 2
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238000001035 drying Methods 0.000 description 2
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125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
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238000009472 formulation Methods 0.000 description 2
238000009963 fulling Methods 0.000 description 2
125000005843 halogen group Chemical group 0.000 description 2
238000010438 heat treatment Methods 0.000 description 2
IRHTZOCLLONTOC-UHFFFAOYSA-N hexacosan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCO IRHTZOCLLONTOC-UHFFFAOYSA-N 0.000 description 2
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201000006747 infectious mononucleosis Diseases 0.000 description 2
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125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
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125000001117 oleyl group Chemical group [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])=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 2
150000002924 oxiranes Chemical class 0.000 description 2
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239000007921 spray Substances 0.000 description 2
238000005507 spraying Methods 0.000 description 2
238000003756 stirring Methods 0.000 description 2
150000005846 sugar alcohols Polymers 0.000 description 2
125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 description 2
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235000021355 Stearic acid Nutrition 0.000 description 1
HVWGGPRWKSHASF-UHFFFAOYSA-N Sulfuric acid, monooctadecyl ester Chemical compound CCCCCCCCCCCCCCCCCCOS(O)(=O)=O HVWGGPRWKSHASF-UHFFFAOYSA-N 0.000 description 1
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 1
238000006887 Ullmann reaction Methods 0.000 description 1
240000006365 Vitis vinifera Species 0.000 description 1
235000014787 Vitis vinifera Nutrition 0.000 description 1
238000005299 abrasion Methods 0.000 description 1
239000000980 acid dye Substances 0.000 description 1
230000009471 action Effects 0.000 description 1
239000000654 additive Substances 0.000 description 1
150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
239000003513 alkali Substances 0.000 description 1
150000001447 alkali salts Chemical class 0.000 description 1
150000001336 alkenes Chemical class 0.000 description 1
150000004996 alkyl benzenes Chemical class 0.000 description 1
125000002947 alkylene group Chemical group 0.000 description 1
150000001408 amides Chemical class 0.000 description 1
239000000908 ammonium hydroxide Substances 0.000 description 1
150000001449 anionic compounds Chemical class 0.000 description 1
239000004668 anionic fabric softener Substances 0.000 description 1
229940053200 antiepileptics fatty acid derivative Drugs 0.000 description 1
150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
125000004429 atom Chemical group 0.000 description 1
239000002585 base Substances 0.000 description 1
125000002511 behenyl group Chemical group [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])C([H])([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])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
230000009286 beneficial effect Effects 0.000 description 1
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SUMDYPCJJOFFON-UHFFFAOYSA-N beta-hydroxyethanesulfonic acid Natural products OCCS(O)(=O)=O SUMDYPCJJOFFON-UHFFFAOYSA-N 0.000 description 1
239000008280 blood Substances 0.000 description 1
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GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
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QARVLSVVCXYDNA-UHFFFAOYSA-N bromobenzene Chemical compound BrC1=CC=CC=C1 QARVLSVVCXYDNA-UHFFFAOYSA-N 0.000 description 1
239000000872 buffer Substances 0.000 description 1
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229940080284 cetyl sulfate Drugs 0.000 description 1
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125000001309 chloro group Chemical group Cl* 0.000 description 1
150000008422 chlorobenzenes Chemical class 0.000 description 1
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239000000470 constituent Substances 0.000 description 1
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238000001816 cooling Methods 0.000 description 1
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150000004292 cyclic ethers Chemical class 0.000 description 1
125000002704 decyl group Chemical group [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])C([H])([H])C([H])([H])* 0.000 description 1
239000003599 detergent Substances 0.000 description 1
235000019961 diglycerides of fatty acid Nutrition 0.000 description 1
239000002270 dispersing agent Substances 0.000 description 1
JRBPAEWTRLWTQC-UHFFFAOYSA-N dodecylamine Chemical compound CCCCCCCCCCCCN JRBPAEWTRLWTQC-UHFFFAOYSA-N 0.000 description 1
238000005108 dry cleaning Methods 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
LSTFJMBLMONQOP-UHFFFAOYSA-N ethenylsulfonylurea Chemical compound NC(=O)NS(=O)(=O)C=C LSTFJMBLMONQOP-UHFFFAOYSA-N 0.000 description 1
229960003750 ethyl chloride Drugs 0.000 description 1
150000002191 fatty alcohols Chemical class 0.000 description 1
230000002349 favourable effect Effects 0.000 description 1
210000003608 fece Anatomy 0.000 description 1
235000021323 fish oil Nutrition 0.000 description 1
230000037406 food intake Effects 0.000 description 1
235000019253 formic acid Nutrition 0.000 description 1
235000015203 fruit juice Nutrition 0.000 description 1
229940052308 general anesthetics halogenated hydrocarbons Drugs 0.000 description 1
ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
229960002449 glycine Drugs 0.000 description 1
235000013905 glycine and its sodium salt Nutrition 0.000 description 1
238000000227 grinding Methods 0.000 description 1
JEGUKCSWCFPDGT-UHFFFAOYSA-N h2o hydrate Chemical compound O.O JEGUKCSWCFPDGT-UHFFFAOYSA-N 0.000 description 1
150000008282 halocarbons Chemical class 0.000 description 1
239000008233 hard water Substances 0.000 description 1
230000035876 healing Effects 0.000 description 1
125000002818 heptacosyl group Chemical group [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])C([H])([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])C([H])([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
235000019514 herring Nutrition 0.000 description 1
LPTIRUACFKQDHZ-UHFFFAOYSA-N hexadecyl sulfate;hydron Chemical compound CCCCCCCCCCCCCCCCOS(O)(=O)=O LPTIRUACFKQDHZ-UHFFFAOYSA-N 0.000 description 1
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239000000976 ink Substances 0.000 description 1
239000001023 inorganic pigment Substances 0.000 description 1
PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
CAHGCLMLTWQZNJ-BQNIITSRSA-N lanosterol Chemical compound C([C@@]12C)C[C@H](O)C(C)(C)[C@@H]1CCC1=C2CC[C@]2(C)[C@@H]([C@@H](CCC=C(C)C)C)CC[C@]21C CAHGCLMLTWQZNJ-BQNIITSRSA-N 0.000 description 1
125000002463 lignoceryl group Chemical group [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])C([H])([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])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
239000000944 linseed oil Substances 0.000 description 1
235000021388 linseed oil Nutrition 0.000 description 1
239000010871 livestock manure Substances 0.000 description 1
239000006210 lotion Substances 0.000 description 1
230000001050 lubricating effect Effects 0.000 description 1
125000002960 margaryl group Chemical group [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])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
239000000463 material Substances 0.000 description 1
239000000155 melt Substances 0.000 description 1
150000002736 metal compounds Chemical class 0.000 description 1
BLPITTLHXKDNPJ-UHFFFAOYSA-N methylsulfonylurea Chemical compound CS(=O)(=O)NC(N)=O BLPITTLHXKDNPJ-UHFFFAOYSA-N 0.000 description 1
239000002480 mineral oil Substances 0.000 description 1
239000001788 mono and diglycerides of fatty acids Substances 0.000 description 1
125000002819 montanyl group Chemical group [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])C([H])([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])C([H])([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])C([H])([H])[H] 0.000 description 1
125000001421 myristyl group Chemical group [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])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
BPWDRXCIUKMAOL-UHFFFAOYSA-N n-butyldodecan-1-amine Chemical compound CCCCCCCCCCCCNCCCC BPWDRXCIUKMAOL-UHFFFAOYSA-N 0.000 description 1
RDXBZXWKSIEKKS-UHFFFAOYSA-N n-ethyldecan-1-amine Chemical compound CCCCCCCCCCNCC RDXBZXWKSIEKKS-UHFFFAOYSA-N 0.000 description 1
ZCYXXKJEDCHMGH-UHFFFAOYSA-N nonane Chemical compound CCCC[CH]CCCC ZCYXXKJEDCHMGH-UHFFFAOYSA-N 0.000 description 1
BKIMMITUMNQMOS-UHFFFAOYSA-N normal nonane Natural products CCCCCCCCC BKIMMITUMNQMOS-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
OXUCOTSGWGNWGC-UHFFFAOYSA-N octane Chemical compound CCCCCCC[CH2-] OXUCOTSGWGNWGC-UHFFFAOYSA-N 0.000 description 1
JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
239000012860 organic pigment Substances 0.000 description 1
FWFGVMYFCODZRD-UHFFFAOYSA-N oxidanium;hydrogen sulfate Chemical compound O.OS(O)(=O)=O FWFGVMYFCODZRD-UHFFFAOYSA-N 0.000 description 1
239000002540 palm oil Substances 0.000 description 1
125000000913 palmityl group Chemical group [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])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
125000002460 pentacosyl group Chemical group [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])C([H])([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])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
125000002958 pentadecyl group Chemical group [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])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
239000003208 petroleum Substances 0.000 description 1
239000008194 pharmaceutical composition Substances 0.000 description 1
150000002989 phenols Chemical class 0.000 description 1
WVDDGKGOMKODPV-ZQBYOMGUSA-N phenyl(114C)methanol Chemical compound O[14CH2]C1=CC=CC=C1 WVDDGKGOMKODPV-ZQBYOMGUSA-N 0.000 description 1
239000011505 plaster Substances 0.000 description 1
229920000642 polymer Polymers 0.000 description 1
229920002451 polyvinyl alcohol Polymers 0.000 description 1
239000000843 powder Substances 0.000 description 1
230000002035 prolonged effect Effects 0.000 description 1
125000004368 propenyl group Chemical group C(=CC)* 0.000 description 1
125000001453 quaternary ammonium group Chemical group 0.000 description 1
239000011541 reaction mixture Substances 0.000 description 1
230000009257 reactivity Effects 0.000 description 1
238000001953 recrystallisation Methods 0.000 description 1
235000020095 red wine Nutrition 0.000 description 1
238000005096 rolling process Methods 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
230000002393 scratching effect Effects 0.000 description 1
238000007789 sealing Methods 0.000 description 1
230000035945 sensitivity Effects 0.000 description 1
239000000344 soap Substances 0.000 description 1
239000011877 solvent mixture Substances 0.000 description 1
239000000600 sorbitol Substances 0.000 description 1
239000003549 soybean oil Substances 0.000 description 1
235000012424 soybean oil Nutrition 0.000 description 1
239000012177 spermaceti Substances 0.000 description 1
229940084106 spermaceti Drugs 0.000 description 1
210000000952 spleen Anatomy 0.000 description 1
239000007858 starting material Substances 0.000 description 1
239000008117 stearic acid Substances 0.000 description 1
238000003860 storage Methods 0.000 description 1
NVBFHJWHLNUMCV-UHFFFAOYSA-N sulfamide Chemical class NS(N)(=O)=O NVBFHJWHLNUMCV-UHFFFAOYSA-N 0.000 description 1
150000003871 sulfonates Chemical group 0.000 description 1
238000006277 sulfonation reaction Methods 0.000 description 1
150000003457 sulfones Chemical class 0.000 description 1
238000009988 textile finishing Methods 0.000 description 1
229920001169 thermoplastic Polymers 0.000 description 1
239000004416 thermosoftening plastic Substances 0.000 description 1
125000002469 tricosyl group Chemical group [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])C([H])([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])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
125000002889 tridecyl group Chemical group [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])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
GBXQPDCOMJJCMJ-UHFFFAOYSA-M trimethyl-[6-(trimethylazaniumyl)hexyl]azanium;bromide Chemical compound [Br-].C[N+](C)(C)CCCCCC[N+](C)(C)C GBXQPDCOMJJCMJ-UHFFFAOYSA-M 0.000 description 1
125000002948 undecyl group Chemical group [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])C([H])([H])C([H])([H])[H] 0.000 description 1
235000013311 vegetables Nutrition 0.000 description 1
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
229920002554 vinyl polymer Polymers 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
- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
- D06M13/322—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing nitrogen
- D06M13/402—Amides imides, sulfamic acids
- D06M13/438—Sulfonamides ; Sulfamic acids
- 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
- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
- D06M13/322—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing nitrogen
- D06M13/402—Amides imides, sulfamic acids
- D06M13/432—Urea, thiourea or derivatives thereof, e.g. biurets; Urea-inclusion compounds; Dicyanamides; Carbodiimides; Guanidines, e.g. dicyandiamides

Landscapes

Engineering & Computer Science (AREA)
Textile Engineering (AREA)
Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Treatment And Processing Of Natural Fur Or Leather (AREA)

CS784408A 1977-07-02 1978-07-03 Freshening and hydrophobous means for the leathers CS208477B2 (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE19772730042 DE2730042A1 (de)	1977-07-02	1977-07-02	Avivage- und hydrophobiermittel fuer zellulose-textilien und leder

Publications (1)

Publication Number	Publication Date
CS208477B2 true CS208477B2 (en)	1981-09-15

Family

ID=6013063

Family Applications (3)

Application Number	Title	Priority Date	Filing Date
CS784408A CS208477B2 (en)	1977-07-02	1978-07-03	Freshening and hydrophobous means for the leathers
CS784408A CS208476B2 (en)	1977-07-02	1978-07-03	Freshening and hydrophobous means for the textile materials from the cellulose or containing the cellulose
CS784408A CS208478B2 (en)	1977-07-02	1978-07-03	Method of making the sulphonyl urea

Family Applications After (2)

Application Number	Title	Priority Date	Filing Date
CS784408A CS208476B2 (en)	1977-07-02	1978-07-03	Freshening and hydrophobous means for the textile materials from the cellulose or containing the cellulose
CS784408A CS208478B2 (en)	1977-07-02	1978-07-03	Method of making the sulphonyl urea

Country Status (8)

Country	Link
US (1)	US4149979A (es)
EP (1)	EP0000201B1 (es)
BR (1)	BR7804208A (es)
CS (3)	CS208477B2 (es)
DE (2)	DE2730042A1 (es)
ES (2)	ES471328A1 (es)
HU (1)	HU177572B (es)
IT (1)	IT1118230B (es)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE2757582A1 (de) *	1977-12-23	1979-06-28	Cassella Ag	Verfahren zur herstellung lagerstabiler waessriger emulsionen von n.alkyl-n'-alkylol-harnstoffen und deren anwendung zum weichmachen von leder und textilmaterial

Family Cites Families (12)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
FR919464A (fr) *	1944-12-28	1947-03-10	Geigy Ag J R	Urées substituées et procédé de préparation de ces produits
US2487383A (en) *	1945-04-18	1949-11-08	Ciba Ltd	Urea derivatives and process of making same
FR1180621A (fr) *	1955-08-08	1959-06-08	Hoechst Ag	Sulfonylurées et leur procédé de préparation
US2976317A (en) *	1955-10-19	1961-03-21	Hoechst Ag	N(alkyl-, cycloalkyl-, and cycloalkylalkylsulfonyl)-n'(alkyl-, alkenyl-, cycloalkyl,and cycloalkylalkyl)-ureas
US3069466A (en) *	1959-04-21	1962-12-18	Anton Von Waldheim	New n1-halogenoalkyl-phenyl-sulfonyl-n2-substituted ureas, and the corresponding cyclohexyl compounds
US3420697A (en) *	1965-08-25	1969-01-07	Allied Chem	Perfluoroalkyl-substituted polyamide oil-repellency compound and textile materials treated therewith
BE686440A (es) *	1965-09-20	1967-02-15
CH1160169D (es) *	1968-08-01	1900-01-01
NL6908449A (es) *	1969-06-03	1970-12-07
BE790518A (fr) *	1971-10-26	1973-04-25	Bayer Ag	Production et application de perfluoro-alcane-sulfonamides
BE792563A (fr) *	1971-12-10	1973-06-12	Bayer Ag	Perfluoralcane sulfonamides et leur preparation
US3965015A (en) *	1972-08-01	1976-06-22	Colgate-Palmolive Company	Bleach-resistant fabric softener

1977
- 1977-07-02 DE DE19772730042 patent/DE2730042A1/de not_active Withdrawn
1978
- 1978-06-26 US US05/919,436 patent/US4149979A/en not_active Expired - Lifetime
- 1978-06-29 DE DE7878100278T patent/DE2860405D1/de not_active Expired
- 1978-06-29 EP EP78100278A patent/EP0000201B1/de not_active Expired
- 1978-06-30 HU HU78CA429A patent/HU177572B/hu unknown
- 1978-06-30 BR BR7804208A patent/BR7804208A/pt unknown
- 1978-06-30 IT IT25227/78A patent/IT1118230B/it active
- 1978-06-30 ES ES471328A patent/ES471328A1/es not_active Expired
- 1978-07-03 CS CS784408A patent/CS208477B2/cs unknown
- 1978-07-03 CS CS784408A patent/CS208476B2/cs unknown
- 1978-07-03 CS CS784408A patent/CS208478B2/cs unknown
1979
- 1979-03-15 ES ES478660A patent/ES478660A1/es not_active Expired

Also Published As

Publication number	Publication date
DE2730042A1 (de)	1979-01-11
CS208476B2 (en)	1981-09-15
ES471328A1 (es)	1979-09-01
EP0000201B1 (de)	1981-01-07
IT7825227A0 (it)	1978-06-30
EP0000201A1 (de)	1979-01-10
CS208478B2 (en)	1981-09-15
US4149979A (en)	1979-04-17
DE2860405D1 (en)	1981-02-26
BR7804208A (pt)	1979-04-03
ES478660A1 (es)	1979-07-01
IT1118230B (it)	1986-02-24
HU177572B (en)	1981-11-28

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