GB608186A - Method of preparing guanamine-aldehyde condensation products - Google Patents
Method of preparing guanamine-aldehyde condensation productsInfo
- Publication number
- GB608186A GB608186A GB499646A GB499646A GB608186A GB 608186 A GB608186 A GB 608186A GB 499646 A GB499646 A GB 499646A GB 499646 A GB499646 A GB 499646A GB 608186 A GB608186 A GB 608186A
- Authority
- GB
- United Kingdom
- Prior art keywords
- prepared
- formaldehyde
- guanamines
- butanol
- reacted
- 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
- 239000007859 condensation product Substances 0.000 title abstract 4
- 238000000034 method Methods 0.000 title 1
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 abstract 24
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 abstract 15
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 11
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 abstract 10
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 abstract 6
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 abstract 5
- 239000000047 product Substances 0.000 abstract 5
- VZXTWGWHSMCWGA-UHFFFAOYSA-N 1,3,5-triazine-2,4-diamine Chemical compound NC1=NC=NC(N)=N1 VZXTWGWHSMCWGA-UHFFFAOYSA-N 0.000 abstract 4
- PYGXAGIECVVIOZ-UHFFFAOYSA-N Dibutyl decanedioate Chemical compound CCCCOC(=O)CCCCCCCCC(=O)OCCCC PYGXAGIECVVIOZ-UHFFFAOYSA-N 0.000 abstract 4
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 abstract 4
- 239000000975 dye Substances 0.000 abstract 4
- 238000010438 heat treatment Methods 0.000 abstract 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 4
- XNCOSPRUTUOJCJ-UHFFFAOYSA-N Biguanide Chemical compound NC(N)=NC(N)=N XNCOSPRUTUOJCJ-UHFFFAOYSA-N 0.000 abstract 3
- 229940123208 Biguanide Drugs 0.000 abstract 3
- 125000001931 aliphatic group Chemical group 0.000 abstract 3
- 239000001913 cellulose Substances 0.000 abstract 3
- 229920002678 cellulose Polymers 0.000 abstract 3
- 239000000203 mixture Substances 0.000 abstract 3
- 229920000642 polymer Polymers 0.000 abstract 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 abstract 2
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 abstract 2
- 229920000877 Melamine resin Polymers 0.000 abstract 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 abstract 2
- 239000003513 alkali Substances 0.000 abstract 2
- 229910000147 aluminium phosphate Inorganic materials 0.000 abstract 2
- 239000004202 carbamide Substances 0.000 abstract 2
- 150000002148 esters Chemical class 0.000 abstract 2
- 150000002170 ethers Chemical class 0.000 abstract 2
- 239000004744 fabric Substances 0.000 abstract 2
- 230000003301 hydrolyzing effect Effects 0.000 abstract 2
- 239000004922 lacquer Substances 0.000 abstract 2
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 abstract 2
- -1 methylol compounds Chemical class 0.000 abstract 2
- 239000000123 paper Substances 0.000 abstract 2
- 239000000049 pigment Substances 0.000 abstract 2
- 229920005989 resin Polymers 0.000 abstract 2
- 239000011347 resin Substances 0.000 abstract 2
- 239000004753 textile Substances 0.000 abstract 2
- UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 abstract 2
- ZUHMEUFBTDOKPX-UHFFFAOYSA-N 6-[2-(4,6-diamino-1,3,5-triazin-2-yl)ethyl]-1,3,5-triazine-2,4-diamine Chemical compound NC1=NC(N)=NC(CCC=2N=C(N)N=C(N)N=2)=N1 ZUHMEUFBTDOKPX-UHFFFAOYSA-N 0.000 abstract 1
- VVYBFJSLGGZKFD-UHFFFAOYSA-N 6-[4-(4,6-diamino-1,3,5-triazin-2-yl)butyl]-1,3,5-triazine-2,4-diamine Chemical compound NC1=NC(N)=NC(CCCCC=2N=C(N)N=C(N)N=2)=N1 VVYBFJSLGGZKFD-UHFFFAOYSA-N 0.000 abstract 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 abstract 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 abstract 1
- 239000003082 abrasive agent Substances 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 150000001298 alcohols Chemical class 0.000 abstract 1
- 150000004703 alkoxides Chemical class 0.000 abstract 1
- 239000011230 binding agent Substances 0.000 abstract 1
- 238000005266 casting Methods 0.000 abstract 1
- 239000003054 catalyst Substances 0.000 abstract 1
- 239000008199 coating composition Substances 0.000 abstract 1
- 239000007799 cork Substances 0.000 abstract 1
- QGBSISYHAICWAH-UHFFFAOYSA-N dicyandiamide Chemical compound NC(N)=NC#N QGBSISYHAICWAH-UHFFFAOYSA-N 0.000 abstract 1
- 238000001035 drying Methods 0.000 abstract 1
- 239000003995 emulsifying agent Substances 0.000 abstract 1
- 239000000839 emulsion Substances 0.000 abstract 1
- 239000002657 fibrous material Substances 0.000 abstract 1
- 239000010985 leather Substances 0.000 abstract 1
- 239000002184 metal Substances 0.000 abstract 1
- 238000000465 moulding Methods 0.000 abstract 1
- 239000000025 natural resin Substances 0.000 abstract 1
- 230000007935 neutral effect Effects 0.000 abstract 1
- 239000003960 organic solvent Substances 0.000 abstract 1
- 239000004014 plasticizer Substances 0.000 abstract 1
- LETVJWLLIMJADE-UHFFFAOYSA-N pyridazin-3-amine Chemical class NC1=CC=CN=N1 LETVJWLLIMJADE-UHFFFAOYSA-N 0.000 abstract 1
- 239000012429 reaction media Substances 0.000 abstract 1
- 239000012260 resinous material Substances 0.000 abstract 1
- 239000012265 solid product Substances 0.000 abstract 1
- 239000002904 solvent Substances 0.000 abstract 1
- 229920003002 synthetic resin Polymers 0.000 abstract 1
- 239000000057 synthetic resin Substances 0.000 abstract 1
- 235000020357 syrup Nutrition 0.000 abstract 1
- 239000006188 syrup Substances 0.000 abstract 1
- 239000002966 varnish Substances 0.000 abstract 1
- 239000000080 wetting agent Substances 0.000 abstract 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
- C08G12/30—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen of aldehydes with heterocyclic compounds with substituted triazines
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Phenolic Resins Or Amino Resins (AREA)
Abstract
Condensation products are prepared by heating formaldehyde or a polymer thereof and one or more guanamines of the general formula <FORM:0608186/IV(a)/1> where R is a substituted or unsubstituted divalent straight-chain aliphatic or phenylene radical (see Group IV (a)). The reaction medium may be water or an organic solvent. An alcohol may be present during the reaction or the product may be reacted with an alcohol. A list of suitable alcohols is included in the Specification. Melamine, urea, phenol, aniline, dicyandiamide or thiourea may be mixed with the guanamine. Impure mixtures of guanamine with guanides or aminodiazines obtained by reacting two mols. of biguanide with one mol. of a dicarboxylic acid in a solvent such as methanol and, if desired, in presence of a catalyst such as a metal alkoxide may be used. The products may be used, if desired, with other resinous material in drying oil varnishes, for treating fibrous materials such as paper, textiles or leather, as a binder for abrasives or cork, for moulding compositions, as casting resins, in coating compositions, if desired together with cellulose derivatives, natural or synthetic resins, and plasticisers, for affixing dyes to fabrics, particularly of cellulose or its derivatives, or for insolubilising dyes, lakes or pigments. Aqueous syrups or emulsions are particularly useful for treating textiles or paper (see Group VIII). They may also contain wetting agents and compatible emulsifiers, of which a list is to be found in the Specification. By keeping the time and temperature of the reaction low, it is possible to obtain ethers of the methylol guanamine in substantially monomeric condition. The condensation products may be cured to the insoluble condition by heating under acid, basic or neutral conditions. In example (1), sebacoguanamine is condensed with formaldehyde. The solid product is soluble in ethanol, butanol and hot water. It may be reacted with or dissolved in alcohol to yield a lacquer, or is suitable for modifying resins formed from formaldehyde and urea and/or melamine; (2) a lacquer is prepared by heating formalin, sebacoguanamine and butanol for some time, adding phosphoric acid and dehydrating; (3) succinoguanamine is condensed with formaldehyde in presence of triethanolamine. The product is heated with butanol, yielding a film-forming solution; (4) adipoguanamine is condensed with formalin and the product reacted with butanol; (5) terephthaloguanamine is reacted with formalin and then with butanol. The product may be mixed with phosphoric acid to yield a film-forming composition which hardens on baking. Sebacoguanamine is prepared by reacting biguanide and butyl sebacate in methanol and purified by dissolving in ethanol and acetic acid, suspending the acetate in water and hydrolysing it with alkali. The other guanamines used in the example are prepared in a similar manner with appropriate esters in place of butyl sebacate.ALSO:Ethers of methylol guanamines may be prepared in substantially monomeric condition by keeping the time and temperature of the reaction low. The methylol compounds are formed from formaldehyde or a polymer thereof and a guanamine of the general formula <FORM:0608186/IV(b)/1> where R is a straight chain aliphatic or phenylene radical. The alcohol may be present during the reaction or the preformed methylol compound may be reacted with the alcohol. Sebacoguanamine is prepared by reacting biguanide and butyl sebacate in methanol and purified by dissolving in ethanol and acetic acid suspending the acetate in water and hydrolysing it with alkali. Other guanamines may be prepared in a similar manner with appropriate esters in place of butyl sebacate.ALSO:Condensation products prepared by heating formaldehyde or a polymer thereof and one or more guanamines of the general formula <FORM:0608186/IV (c)/1> where R is a substituted or unsubstituted divalent straight chain aliphatic or phenylene radical (see Group IV (a)) may be used for affixing dyes to fabrics particularly of cellulose or its derivatives or for insolubilising dyes, lakes or pigments.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB499646A GB608186A (en) | 1946-02-18 | 1946-02-18 | Method of preparing guanamine-aldehyde condensation products |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB499646A GB608186A (en) | 1946-02-18 | 1946-02-18 | Method of preparing guanamine-aldehyde condensation products |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB608186A true GB608186A (en) | 1948-09-10 |
Family
ID=9787753
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB499646A Expired GB608186A (en) | 1946-02-18 | 1946-02-18 | Method of preparing guanamine-aldehyde condensation products |
Country Status (1)
| Country | Link |
|---|---|
| GB (1) | GB608186A (en) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2653143A (en) * | 1952-03-12 | 1953-09-22 | Rohm & Haas | Condensation products of bis-aminotriazines |
| US3434983A (en) * | 1966-06-20 | 1969-03-25 | Standard Oil Co | Stain-resistant composition comprising 2,2' - (1,2 - cyclobutylene) bis 4,6 - diamine-5 - triazine - melamin - aldehyde reaction product and a filler |
| US4359500A (en) | 1980-08-08 | 1982-11-16 | E. I. Du Pont De Nemours And Company | Alkylated isoadipoguanamine-formaldehyde crosslinking resin and improved coating compositions produced therefrom |
| US4365053A (en) | 1980-08-08 | 1982-12-21 | E. I. Du Pont De Nemours And Company | Alkylated isoadipoguanamine-formaldehyde crosslinking resin and improved coating compositions produced therefrom |
| US4370427A (en) | 1980-08-08 | 1983-01-25 | E. I. Du Pont De Nemours And Company | Alkylated isoadipoguanamine-formaldehyde crosslinking resin and improved coating compositions produced therefrom |
-
1946
- 1946-02-18 GB GB499646A patent/GB608186A/en not_active Expired
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2653143A (en) * | 1952-03-12 | 1953-09-22 | Rohm & Haas | Condensation products of bis-aminotriazines |
| US3434983A (en) * | 1966-06-20 | 1969-03-25 | Standard Oil Co | Stain-resistant composition comprising 2,2' - (1,2 - cyclobutylene) bis 4,6 - diamine-5 - triazine - melamin - aldehyde reaction product and a filler |
| US4359500A (en) | 1980-08-08 | 1982-11-16 | E. I. Du Pont De Nemours And Company | Alkylated isoadipoguanamine-formaldehyde crosslinking resin and improved coating compositions produced therefrom |
| US4365053A (en) | 1980-08-08 | 1982-12-21 | E. I. Du Pont De Nemours And Company | Alkylated isoadipoguanamine-formaldehyde crosslinking resin and improved coating compositions produced therefrom |
| US4370427A (en) | 1980-08-08 | 1983-01-25 | E. I. Du Pont De Nemours And Company | Alkylated isoadipoguanamine-formaldehyde crosslinking resin and improved coating compositions produced therefrom |
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