JPS6241593B2 - - Google Patents
Info
- Publication number
- JPS6241593B2 JPS6241593B2 JP55063459A JP6345980A JPS6241593B2 JP S6241593 B2 JPS6241593 B2 JP S6241593B2 JP 55063459 A JP55063459 A JP 55063459A JP 6345980 A JP6345980 A JP 6345980A JP S6241593 B2 JPS6241593 B2 JP S6241593B2
- Authority
- JP
- Japan
- Prior art keywords
- formaldehyde
- solution
- bisguanamine
- stabilizer
- methanol
- 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
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 claims description 52
- 125000002947 alkylene group Chemical group 0.000 claims description 10
- 239000008098 formaldehyde solution Substances 0.000 claims description 10
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 45
- 239000003381 stabilizer Substances 0.000 description 20
- VZXTWGWHSMCWGA-UHFFFAOYSA-N 1,3,5-triazine-2,4-diamine Chemical compound NC1=NC=NC(N)=N1 VZXTWGWHSMCWGA-UHFFFAOYSA-N 0.000 description 9
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 6
- 238000000034 method Methods 0.000 description 6
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 5
- 238000000921 elemental analysis Methods 0.000 description 5
- 150000002148 esters Chemical class 0.000 description 5
- 238000002844 melting Methods 0.000 description 5
- 230000008018 melting Effects 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- 230000000087 stabilizing effect Effects 0.000 description 5
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 4
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 4
- 239000004372 Polyvinyl alcohol Substances 0.000 description 4
- 150000001241 acetals Chemical class 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 4
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 4
- -1 polyoxyethylene lauryl ether Polymers 0.000 description 4
- 229920002451 polyvinyl alcohol Polymers 0.000 description 4
- 150000005846 sugar alcohols Polymers 0.000 description 4
- GZVHEAJQGPRDLQ-UHFFFAOYSA-N 6-phenyl-1,3,5-triazine-2,4-diamine Chemical compound NC1=NC(N)=NC(C=2C=CC=CC=2)=N1 GZVHEAJQGPRDLQ-UHFFFAOYSA-N 0.000 description 3
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 3
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- 239000002202 Polyethylene glycol Substances 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 150000002170 ethers Chemical class 0.000 description 3
- 239000000194 fatty acid Substances 0.000 description 3
- 229920001223 polyethylene glycol Polymers 0.000 description 3
- 239000000600 sorbitol Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- KBPLFHHGFOOTCA-UHFFFAOYSA-N 1-Octanol Chemical compound CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 description 2
- BBMCTIGTTCKYKF-UHFFFAOYSA-N 1-heptanol Chemical compound CCCCCCCO BBMCTIGTTCKYKF-UHFFFAOYSA-N 0.000 description 2
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 2
- NAMCDLUESQLMOZ-UHFFFAOYSA-N 6-ethyl-1,3,5-triazine-2,4-diamine Chemical compound CCC1=NC(N)=NC(N)=N1 NAMCDLUESQLMOZ-UHFFFAOYSA-N 0.000 description 2
- ZHNUHDYFZUAESO-UHFFFAOYSA-N Formamide Chemical compound NC=O ZHNUHDYFZUAESO-UHFFFAOYSA-N 0.000 description 2
- 229920000877 Melamine resin Polymers 0.000 description 2
- NJYZCEFQAIUHSD-UHFFFAOYSA-N acetoguanamine Chemical compound CC1=NC(N)=NC(N)=N1 NJYZCEFQAIUHSD-UHFFFAOYSA-N 0.000 description 2
- 238000004458 analytical method Methods 0.000 description 2
- 239000000084 colloidal system Substances 0.000 description 2
- 238000006482 condensation reaction Methods 0.000 description 2
- MWKFXSUHUHTGQN-UHFFFAOYSA-N decan-1-ol Chemical compound CCCCCCCCCCO MWKFXSUHUHTGQN-UHFFFAOYSA-N 0.000 description 2
- QGBSISYHAICWAH-UHFFFAOYSA-N dicyandiamide Chemical compound NC(N)=NC#N QGBSISYHAICWAH-UHFFFAOYSA-N 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- 235000019253 formic acid Nutrition 0.000 description 2
- 235000011187 glycerol Nutrition 0.000 description 2
- OMJZDDSTIUIRDT-UHFFFAOYSA-N hexadecanedinitrile Chemical compound N#CCCCCCCCCCCCCCCC#N OMJZDDSTIUIRDT-UHFFFAOYSA-N 0.000 description 2
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 2
- MMEAFPSLRJDLRM-UHFFFAOYSA-N octadecanedinitrile Chemical compound N#CCCCCCCCCCCCCCCCCC#N MMEAFPSLRJDLRM-UHFFFAOYSA-N 0.000 description 2
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 2
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 description 2
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 2
- 230000006641 stabilisation Effects 0.000 description 2
- 238000011105 stabilization Methods 0.000 description 2
- UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- FZNYFWOTWAPTCI-UHFFFAOYSA-N 2-n-benzyl-1,3,5-triazine-2,4,6-triamine Chemical compound NC1=NC(N)=NC(NCC=2C=CC=CC=2)=N1 FZNYFWOTWAPTCI-UHFFFAOYSA-N 0.000 description 1
- CVKGSDYWCFQOKU-UHFFFAOYSA-N 2-n-butyl-1,3,5-triazine-2,4,6-triamine Chemical compound CCCCNC1=NC(N)=NC(N)=N1 CVKGSDYWCFQOKU-UHFFFAOYSA-N 0.000 description 1
- FHEJGRHXJIQFRP-UHFFFAOYSA-N 2-n-cyclohexyl-1,3,5-triazine-2,4,6-triamine Chemical compound NC1=NC(N)=NC(NC2CCCCC2)=N1 FHEJGRHXJIQFRP-UHFFFAOYSA-N 0.000 description 1
- STMSRQMGUCRAKM-UHFFFAOYSA-N 2-n-ethyl-1,3,5-triazine-2,4,6-triamine Chemical compound CCNC1=NC(N)=NC(N)=N1 STMSRQMGUCRAKM-UHFFFAOYSA-N 0.000 description 1
- CTRPRMNBTVRDFH-UHFFFAOYSA-N 2-n-methyl-1,3,5-triazine-2,4,6-triamine Chemical compound CNC1=NC(N)=NC(N)=N1 CTRPRMNBTVRDFH-UHFFFAOYSA-N 0.000 description 1
- JIHOVGXINXMLLR-UHFFFAOYSA-N 2-n-phenyl-1,3,5-triazine-2,4,6-triamine Chemical compound NC1=NC(N)=NC(NC=2C=CC=CC=2)=N1 JIHOVGXINXMLLR-UHFFFAOYSA-N 0.000 description 1
- VTGYMXCBLHTEOQ-UHFFFAOYSA-N 2-n-propyl-1,3,5-triazine-2,4,6-triamine Chemical compound CCCNC1=NC(N)=NC(N)=N1 VTGYMXCBLHTEOQ-UHFFFAOYSA-N 0.000 description 1
- MANZJYLLDYENIU-UHFFFAOYSA-N 2-nonylpropanedinitrile Chemical compound CCCCCCCCCC(C#N)C#N MANZJYLLDYENIU-UHFFFAOYSA-N 0.000 description 1
- 239000001856 Ethyl cellulose Substances 0.000 description 1
- ZZSNKZQZMQGXPY-UHFFFAOYSA-N Ethyl cellulose Chemical compound CCOCC1OC(OC)C(OCC)C(OCC)C1OC1C(O)C(O)C(OC)C(CO)O1 ZZSNKZQZMQGXPY-UHFFFAOYSA-N 0.000 description 1
- 108010010803 Gelatin Proteins 0.000 description 1
- 238000004566 IR spectroscopy Methods 0.000 description 1
- FLVIGYVXZHLUHP-UHFFFAOYSA-N N,N'-diethylthiourea Chemical compound CCNC(=S)NCC FLVIGYVXZHLUHP-UHFFFAOYSA-N 0.000 description 1
- MGJKQDOBUOMPEZ-UHFFFAOYSA-N N,N'-dimethylurea Chemical compound CNC(=O)NC MGJKQDOBUOMPEZ-UHFFFAOYSA-N 0.000 description 1
- XGEGHDBEHXKFPX-UHFFFAOYSA-N N-methylthiourea Natural products CNC(N)=O XGEGHDBEHXKFPX-UHFFFAOYSA-N 0.000 description 1
- 238000005481 NMR spectroscopy Methods 0.000 description 1
- 229930040373 Paraformaldehyde Natural products 0.000 description 1
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 1
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
- MBHRHUJRKGNOKX-UHFFFAOYSA-N [(4,6-diamino-1,3,5-triazin-2-yl)amino]methanol Chemical compound NC1=NC(N)=NC(NCO)=N1 MBHRHUJRKGNOKX-UHFFFAOYSA-N 0.000 description 1
- SPTSIOTYTJZTOG-UHFFFAOYSA-N acetic acid;octadecanoic acid Chemical compound CC(O)=O.CCCCCCCCCCCCCCCCCC(O)=O SPTSIOTYTJZTOG-UHFFFAOYSA-N 0.000 description 1
- PXAJQJMDEXJWFB-UHFFFAOYSA-N acetone oxime Chemical compound CC(C)=NO PXAJQJMDEXJWFB-UHFFFAOYSA-N 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 229920002301 cellulose acetate Polymers 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- AVQYXBDAZWIFTO-UHFFFAOYSA-N dodecanedinitrile Chemical compound N#CCCCCCCCCCCC#N AVQYXBDAZWIFTO-UHFFFAOYSA-N 0.000 description 1
- 125000005745 ethoxymethyl group Chemical group [H]C([H])([H])C([H])([H])OC([H])([H])* 0.000 description 1
- 235000019325 ethyl cellulose Nutrition 0.000 description 1
- 229920001249 ethyl cellulose Polymers 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 239000008273 gelatin Substances 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 235000011852 gelatine desserts Nutrition 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 239000001866 hydroxypropyl methyl cellulose Substances 0.000 description 1
- 235000010979 hydroxypropyl methyl cellulose Nutrition 0.000 description 1
- 229920003088 hydroxypropyl methyl cellulose Polymers 0.000 description 1
- UFVKGYZPFZQRLF-UHFFFAOYSA-N hydroxypropyl methyl cellulose Chemical compound OC1C(O)C(OC)OC(CO)C1OC1C(O)C(O)C(OC2C(C(O)C(OC3C(C(O)C(O)C(CO)O3)O)C(CO)O2)O)C(CO)O1 UFVKGYZPFZQRLF-UHFFFAOYSA-N 0.000 description 1
- 125000004184 methoxymethyl group Chemical group [H]C([H])([H])OC([H])([H])* 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 1
- XGEGHDBEHXKFPX-NJFSPNSNSA-N methylurea Chemical compound [14CH3]NC(N)=O XGEGHDBEHXKFPX-NJFSPNSNSA-N 0.000 description 1
- 229920002866 paraformaldehyde Polymers 0.000 description 1
- 239000001814 pectin Substances 0.000 description 1
- 235000010987 pectin Nutrition 0.000 description 1
- 229920001277 pectin Polymers 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 229920000151 polyglycol Polymers 0.000 description 1
- 239000010695 polyglycol Substances 0.000 description 1
- 229920000259 polyoxyethylene lauryl ether Polymers 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 229920001290 polyvinyl ester Polymers 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 125000005767 propoxymethyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])[#8]C([H])([H])* 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- JTOFSXGLSGTDCB-UHFFFAOYSA-N tetradecanedinitrile Chemical compound N#CCCCCCCCCCCCCC#N JTOFSXGLSGTDCB-UHFFFAOYSA-N 0.000 description 1
- RMWAOHBYAMMDGT-UHFFFAOYSA-N tridecanedinitrile Chemical compound N#CCCCCCCCCCCCC#N RMWAOHBYAMMDGT-UHFFFAOYSA-N 0.000 description 1
- UOCLRXFKRLRMKV-UHFFFAOYSA-N trolnitrate phosphate Chemical compound OP(O)(O)=O.OP(O)(O)=O.[O-][N+](=O)OCCN(CCO[N+]([O-])=O)CCO[N+]([O-])=O UOCLRXFKRLRMKV-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D251/00—Heterocyclic compounds containing 1,3,5-triazine rings
- C07D251/02—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings
- C07D251/12—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
- C07D251/14—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hydrogen or carbon atoms directly attached to at least one ring carbon atom
- C07D251/16—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hydrogen or carbon atoms directly attached to at least one ring carbon atom to only one ring carbon atom
- C07D251/18—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hydrogen or carbon atoms directly attached to at least one ring carbon atom to only one ring carbon atom with nitrogen atoms directly attached to the two other ring carbon atoms, e.g. guanamines
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K15/00—Anti-oxidant compositions; Compositions inhibiting chemical change
- C09K15/04—Anti-oxidant compositions; Compositions inhibiting chemical change containing organic compounds
- C09K15/30—Anti-oxidant compositions; Compositions inhibiting chemical change containing organic compounds containing heterocyclic ring with at least one nitrogen atom as ring member
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Phenolic Resins Or Amino Resins (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19792919496 DE2919496A1 (de) | 1979-05-15 | 1979-05-15 | Neue bisguanamine |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS55162778A JPS55162778A (en) | 1980-12-18 |
| JPS6241593B2 true JPS6241593B2 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1987-09-03 |
Family
ID=6070751
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP6345980A Granted JPS55162778A (en) | 1979-05-15 | 1980-05-15 | Alkylenebisguanamine and stabilized formaldehyde aqueous solution containing same |
Country Status (17)
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2919496A1 (de) * | 1979-05-15 | 1980-12-04 | Degussa | Neue bisguanamine |
| DE3143920A1 (de) * | 1981-11-05 | 1983-05-11 | Degussa Ag, 6000 Frankfurt | Neue bismelamine |
| DE3509056A1 (de) * | 1985-03-14 | 1986-09-18 | Degussa Ag, 6000 Frankfurt | Verfahren zur herstellung von dodecamethylenbismelamin und dessen verwendung |
| DE3836047A1 (de) * | 1988-10-22 | 1990-04-26 | Degussa | Verfahren zur stabilisierung von waessrigen formaldehydloesungen |
| JPH09278700A (ja) * | 1996-04-17 | 1997-10-28 | Katayama Chem Works Co Ltd | 脂肪族アルデヒド水性溶液、その安定剤及び安定化方法 |
| US6150362A (en) * | 1997-12-12 | 2000-11-21 | Henkin; Jack | Triazine angiogenesis inhibitors |
| DE69814151T2 (de) * | 1997-12-12 | 2004-03-25 | Abbott Laboratories, Abbott Park | Triazin angiogenese-inhibitoren |
Family Cites Families (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2423353A (en) * | 1947-07-01 | Polymethylene diguanamines | ||
| US2000152A (en) * | 1932-06-29 | 1935-05-07 | Du Pont | Stabilization of formaldehyde solutions |
| US2237092A (en) * | 1939-11-28 | 1941-04-01 | American Cyanamid Co | Stabilization of formaldehyde solutions |
| US2642409A (en) * | 1951-05-15 | 1953-06-16 | Libbey Owens Ford Glass Co | Production of moldable compositions comprising an unsaturated alkyd and kaolin coated with a heterocyclic amine-formaldehyde resin |
| US2887409A (en) * | 1956-06-14 | 1959-05-19 | Jr William Julius Van Loo | Substituted guanamine-formaldehyde reaction products and the process for treating textiles therewith |
| DE1768915U (de) | 1958-04-02 | 1958-06-19 | Lutz Maschb K G | Vorrichtung zur verhinderung des verdrehens gefederter zugoesen. |
| US3137736A (en) * | 1958-06-24 | 1964-06-16 | Celanese Corp | Stabilization of formaldehyde solutions |
| US3183271A (en) * | 1961-12-01 | 1965-05-11 | Borden Co | Formaldehyde stabilization |
| GB1029039A (en) | 1963-04-18 | 1966-05-11 | Koei Kagaku Kogyo Kabushiki Ka | Improvements relating to the stabilization of aqueous formaldehyde solutions |
| GB1092657A (en) | 1963-12-28 | 1967-11-29 | Koei Chemical Company Ltd Koei | Improvements relating to the stabilization of aqueous formaldehyde solutions |
| DE1205073B (de) | 1964-04-03 | 1965-11-18 | Sueddeutsche Kalkstickstoff | Stabilisieren von waessrigen oder waessrig-methanolischen Formaldehydloesungen |
| US3518313A (en) | 1966-04-05 | 1970-06-30 | Kao Corp | Method of stabilizing aqueous formaldehyde |
| DE1643878A1 (de) | 1967-08-11 | 1970-09-24 | Degussa | Stabilisieren von Formaldehydloesungen I |
| FR1577912A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1968-09-04 | 1969-08-08 | ||
| DE2358856C3 (de) * | 1973-11-26 | 1981-05-21 | Basf Ag, 6700 Ludwigshafen | Verfahren zur Stabilisierung wäßriger Formaldehydlösungen |
| GB2003485B (en) * | 1977-08-30 | 1982-03-10 | Asahi Chemical Ind | Flame retardant resin composition comprising reaction product of polyguanamine compound and cyanuric or isocyanuric acid compound |
| DE2919496A1 (de) * | 1979-05-15 | 1980-12-04 | Degussa | Neue bisguanamine |
-
1979
- 1979-05-15 DE DE19792919496 patent/DE2919496A1/de active Granted
-
1980
- 1980-02-05 YU YU00294/80A patent/YU29480A/xx unknown
- 1980-02-27 NO NO800556A patent/NO158503C/no unknown
- 1980-03-07 NL NL8001399A patent/NL8001399A/nl not_active Application Discontinuation
- 1980-03-26 FR FR8006732A patent/FR2456735A1/fr active Granted
- 1980-04-18 DK DK167280A patent/DK149453C/da not_active IP Right Cessation
- 1980-05-05 US US06/146,247 patent/US4339578A/en not_active Expired - Lifetime
- 1980-05-07 IL IL60019A patent/IL60019A/xx unknown
- 1980-05-08 GB GB8015309A patent/GB2056436B/en not_active Expired
- 1980-05-12 AT AT0252580A patent/AT372070B/de not_active IP Right Cessation
- 1980-05-13 IT IT48659/80A patent/IT1188936B/it active
- 1980-05-13 BE BE6/47161A patent/BE883282A/fr not_active IP Right Cessation
- 1980-05-14 SE SE8003652A patent/SE435181B/sv not_active IP Right Cessation
- 1980-05-14 CA CA000351925A patent/CA1120477A/en not_active Expired
- 1980-05-14 BR BR8002985A patent/BR8002985A/pt not_active IP Right Cessation
- 1980-05-14 CH CH379880A patent/CH642363A5/de not_active IP Right Cessation
- 1980-05-15 JP JP6345980A patent/JPS55162778A/ja active Granted
-
1982
- 1982-02-05 US US06/346,255 patent/US4389333A/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| US4339578A (en) | 1982-07-13 |
| IT1188936B (it) | 1988-01-28 |
| NO158503B (no) | 1988-06-13 |
| ATA252580A (de) | 1983-01-15 |
| NL8001399A (nl) | 1980-11-18 |
| DK149453C (da) | 1986-11-17 |
| GB2056436A (en) | 1981-03-18 |
| NO158503C (no) | 1988-09-21 |
| GB2056436B (en) | 1983-05-25 |
| JPS55162778A (en) | 1980-12-18 |
| BR8002985A (pt) | 1980-12-23 |
| SE435181B (sv) | 1984-09-10 |
| DK149453B (da) | 1986-06-16 |
| IL60019A (en) | 1983-09-30 |
| YU29480A (en) | 1984-02-29 |
| BE883282A (fr) | 1980-11-13 |
| DK167280A (da) | 1980-11-16 |
| SE8003652L (sv) | 1980-11-16 |
| DE2919496C2 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1987-09-03 |
| CH642363A5 (de) | 1984-04-13 |
| FR2456735B1 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1984-12-28 |
| IT8048659A1 (it) | 1981-11-13 |
| CA1120477A (en) | 1982-03-23 |
| AT372070B (de) | 1983-08-25 |
| IL60019A0 (en) | 1980-07-31 |
| FR2456735A1 (fr) | 1980-12-12 |
| IT8048659A0 (it) | 1980-05-13 |
| NO800556L (no) | 1980-11-17 |
| US4389333A (en) | 1983-06-21 |
| DE2919496A1 (de) | 1980-12-04 |
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