NO128575B - - Google Patents
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- Publication number
- NO128575B NO128575B NO218169A NO218169A NO128575B NO 128575 B NO128575 B NO 128575B NO 218169 A NO218169 A NO 218169A NO 218169 A NO218169 A NO 218169A NO 128575 B NO128575 B NO 128575B
- Authority
- NO
- Norway
- Prior art keywords
- dialkylhydantoin
- group
- reaction
- formaldehyde
- added
- Prior art date
Links
- WSFSSNUMVMOOMR-UHFFFAOYSA-N formaldehyde Substances O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 claims description 58
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims description 23
- 229920005989 resin Polymers 0.000 claims description 18
- 239000011347 resin Substances 0.000 claims description 18
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims description 16
- 239000004202 carbamide Substances 0.000 claims description 13
- 238000000034 method Methods 0.000 claims description 13
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 claims description 12
- 238000006243 chemical reaction Methods 0.000 claims description 12
- 150000001875 compounds Chemical class 0.000 claims description 11
- 125000000524 functional group Chemical group 0.000 claims description 8
- 239000002904 solvent Substances 0.000 claims description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 7
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 claims description 6
- 230000002378 acidificating effect Effects 0.000 claims description 5
- 238000001704 evaporation Methods 0.000 claims description 5
- 230000008020 evaporation Effects 0.000 claims description 5
- 238000004519 manufacturing process Methods 0.000 claims description 5
- 239000003960 organic solvent Substances 0.000 claims description 5
- 125000000217 alkyl group Chemical group 0.000 claims description 4
- 239000007864 aqueous solution Substances 0.000 claims description 4
- 230000001588 bifunctional effect Effects 0.000 claims description 4
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- RXKJFZQQPQGTFL-UHFFFAOYSA-N dihydroxyacetone Chemical compound OCC(=O)CO RXKJFZQQPQGTFL-UHFFFAOYSA-N 0.000 claims description 4
- 150000002576 ketones Chemical class 0.000 claims description 4
- 239000003795 chemical substances by application Substances 0.000 claims description 2
- WJRBRSLFGCUECM-UHFFFAOYSA-N hydantoin Chemical compound O=C1CNC(=O)N1 WJRBRSLFGCUECM-UHFFFAOYSA-N 0.000 claims description 2
- 229940091173 hydantoin Drugs 0.000 claims description 2
- 239000011541 reaction mixture Substances 0.000 claims 2
- 239000000243 solution Substances 0.000 description 29
- 229920003002 synthetic resin Polymers 0.000 description 18
- 239000000057 synthetic resin Substances 0.000 description 18
- 239000000047 product Substances 0.000 description 17
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 12
- YIROYDNZEPTFOL-UHFFFAOYSA-N 5,5-Dimethylhydantoin Chemical compound CC1(C)NC(=O)NC1=O YIROYDNZEPTFOL-UHFFFAOYSA-N 0.000 description 10
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 10
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 10
- 235000013877 carbamide Nutrition 0.000 description 10
- 239000000834 fixative Substances 0.000 description 10
- 238000002844 melting Methods 0.000 description 9
- 230000008018 melting Effects 0.000 description 8
- 235000019256 formaldehyde Nutrition 0.000 description 7
- 239000000203 mixture Substances 0.000 description 7
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 6
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 229920001577 copolymer Polymers 0.000 description 5
- 150000004985 diamines Chemical group 0.000 description 5
- 230000000694 effects Effects 0.000 description 4
- 238000006386 neutralization reaction Methods 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 3
- 239000008266 hair spray Substances 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- 239000000443 aerosol Substances 0.000 description 2
- 238000009833 condensation Methods 0.000 description 2
- 230000005494 condensation Effects 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 239000002304 perfume Substances 0.000 description 2
- 229920002689 polyvinyl acetate Polymers 0.000 description 2
- 239000011118 polyvinyl acetate Substances 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- 241000252073 Anguilliformes Species 0.000 description 1
- VOPWNXZWBYDODV-UHFFFAOYSA-N Chlorodifluoromethane Chemical compound FC(F)Cl VOPWNXZWBYDODV-UHFFFAOYSA-N 0.000 description 1
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 1
- SKZKKFZAGNVIMN-UHFFFAOYSA-N Salicilamide Chemical compound NC(=O)C1=CC=CC=C1O SKZKKFZAGNVIMN-UHFFFAOYSA-N 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- RSWGJHLUYNHPMX-ONCXSQPRSA-N abietic acid Chemical compound C([C@@H]12)CC(C(C)C)=CC1=CC[C@@H]1[C@]2(C)CCC[C@@]1(C)C(O)=O RSWGJHLUYNHPMX-ONCXSQPRSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000003929 acidic solution Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 230000001476 alcoholic effect Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000013065 commercial product Substances 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 239000003974 emollient agent Substances 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 239000004922 lacquer Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 231100000344 non-irritating Toxicity 0.000 description 1
- 230000009972 noncorrosive effect Effects 0.000 description 1
- 230000009965 odorless effect Effects 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- 125000005498 phthalate group Chemical class 0.000 description 1
- 150000003022 phthalic acids Chemical class 0.000 description 1
- 229920002006 poly(N-vinylimidazole) polymer Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 239000003380 propellant Substances 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 229960000581 salicylamide Drugs 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000005809 transesterification reaction Methods 0.000 description 1
- 238000005292 vacuum distillation Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G12/00—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen
- C08G12/02—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes
- C08G12/26—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes with heterocyclic compounds
- C08G12/34—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes with heterocyclic compounds and acyclic or carbocyclic compounds
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/84—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
- A61Q5/06—Preparations for styling the hair, e.g. by temporary shaping or colouring
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Chemical & Material Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Epidemiology (AREA)
- Birds (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Cosmetics (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19681770518 DE1770518C3 (de) | 1968-05-29 | 1968-05-29 | Verfahren zur Herstellung von Polykondensaten auf der Grundlage von 5,5-Oialkylhydantoinen und deren Verwendung |
Publications (1)
Publication Number | Publication Date |
---|---|
NO128575B true NO128575B (es) | 1973-12-10 |
Family
ID=5700541
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
NO218169A NO128575B (es) | 1968-05-29 | 1969-05-28 |
Country Status (13)
Country | Link |
---|---|
AT (1) | AT292309B (es) |
BE (1) | BE733793A (es) |
CH (2) | CH546802A (es) |
DE (1) | DE1770518C3 (es) |
DK (1) | DK122574B (es) |
ES (1) | ES367864A1 (es) |
FR (1) | FR2016100A1 (es) |
GB (1) | GB1278327A (es) |
IE (1) | IE32811B1 (es) |
IT (1) | IT998011B (es) |
NL (1) | NL160580C (es) |
NO (1) | NO128575B (es) |
SE (1) | SE373860B (es) |
Families Citing this family (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3987010A (en) | 1968-05-29 | 1976-10-19 | Deutsche Texaco Aktiengesellschaft | Process for the production of film forming synthetic resins for hair fixatives |
US4035339A (en) | 1968-05-29 | 1977-07-12 | Deutsche Texaco Aktiengesellschaft | Process for the production of film forming synthetic resins for hair fixatives |
US4070320A (en) | 1968-05-29 | 1978-01-24 | Deutsche Texaco Aktiengesellschaft | Process for the production of film forming synthetic resins for hair fixatives |
US4035327A (en) | 1968-05-29 | 1977-07-12 | Deutsche Texaco Aktiengesellschaft | Process for the production of film forming synthetic resins for hair fixatives |
US4035358A (en) | 1968-05-29 | 1977-07-12 | Deutsche Texaco Aktiengesellschaft | Process for the production of film forming synthetic resins for hair fixatives |
US4035326A (en) | 1968-05-29 | 1977-07-12 | Deutsche Texaco Aktiengesellschaft | Process for the production of film forming synthetic resins for hair fixatives |
US4035432A (en) | 1968-05-29 | 1977-07-12 | Deutsche Texaco Aktiengesellschaft | Process for the production of film forming synthetic resins for hair fixatives |
DE2725078C3 (de) * | 1977-06-03 | 1981-10-01 | Th. Goldschmidt Ag, 4300 Essen | Verwendung von 5,5-Dimethyl-hydantoin als Modifizierungsmittel für Melamin-Formaldehyd-Vorkondensate |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2155863A (en) * | 1936-04-29 | 1939-04-25 | Du Pont | Resin compositions |
FR880185A (fr) * | 1941-03-25 | 1943-03-16 | Roehm & Haas Gmbh | Procédé pour préparer des produits de réaction à poids moléculaire élevé à partir de dioxo-imidazolidines et d'aldéhydes |
GB564424A (en) * | 1943-03-12 | 1944-09-27 | Du Pont | Resinous products formed from 3-methylol 5,5-dimethyl hydantoin |
US2956927A (en) * | 1956-06-01 | 1960-10-18 | Curtis Helene Ind Inc | 5, 5'-dialkylhydantoin-formaldehyde resin aerosol hair spray |
FR1307215A (fr) * | 1961-12-01 | 1962-10-19 | Basf Ag | Produits de condensation azotés et procédé pour leur production |
GB1048983A (en) * | 1962-05-21 | 1966-11-23 | Switzer Brothers Inc | Synthetic resin and pigment |
FR1519979A (fr) * | 1966-04-19 | 1968-04-05 | Oreal | Nouvelle composition pour le traitement des cheveux |
-
1968
- 1968-05-29 DE DE19681770518 patent/DE1770518C3/de not_active Expired
-
1969
- 1969-04-29 CH CH1589672A patent/CH546802A/xx not_active IP Right Cessation
- 1969-04-29 CH CH649969A patent/CH546803A/xx not_active IP Right Cessation
- 1969-05-16 AT AT467069A patent/AT292309B/de not_active IP Right Cessation
- 1969-05-21 GB GB2588269A patent/GB1278327A/en not_active Expired
- 1969-05-22 IE IE70769A patent/IE32811B1/xx unknown
- 1969-05-22 SE SE727769A patent/SE373860B/xx unknown
- 1969-05-27 NL NL6908028A patent/NL160580C/xx not_active IP Right Cessation
- 1969-05-28 DK DK289569A patent/DK122574B/da unknown
- 1969-05-28 NO NO218169A patent/NO128575B/no unknown
- 1969-05-29 BE BE733793D patent/BE733793A/xx unknown
- 1969-05-29 IT IT1752869A patent/IT998011B/it active
- 1969-05-29 FR FR6917634A patent/FR2016100A1/fr not_active Withdrawn
- 1969-05-29 ES ES367864A patent/ES367864A1/es not_active Expired
Also Published As
Publication number | Publication date |
---|---|
NL160580B (nl) | 1979-06-15 |
IT998011B (it) | 1976-01-20 |
ES367864A1 (es) | 1971-04-16 |
GB1278327A (en) | 1972-06-21 |
CH546803A (de) | 1974-03-15 |
AT292309B (de) | 1971-08-25 |
NL6908028A (es) | 1969-12-02 |
FR2016100A1 (es) | 1970-05-08 |
DE1770518A1 (de) | 1972-04-13 |
DE1770518C3 (de) | 1975-06-05 |
CH546802A (de) | 1974-03-15 |
DE1770518B2 (de) | 1974-10-03 |
DK122574B (da) | 1972-03-20 |
BE733793A (es) | 1969-11-03 |
IE32811B1 (en) | 1973-12-12 |
IE32811L (en) | 1969-11-29 |
NL160580C (nl) | 1979-11-15 |
SE373860B (es) | 1975-02-17 |
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