GB466957A - Manufacture of 2:4:6-triamino-1:3:5-triazine - Google Patents

Manufacture of 2:4:6-triamino-1:3:5-triazine

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Publication number
GB466957A
GB466957A GB3501035A GB3501035A GB466957A GB 466957 A GB466957 A GB 466957A GB 3501035 A GB3501035 A GB 3501035A GB 3501035 A GB3501035 A GB 3501035A GB 466957 A GB466957 A GB 466957A
Authority
GB
United Kingdom
Prior art keywords
dicyandiamide
ammonia
heated
autoclave
cyanamide
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
Application number
GB3501035A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
BASF Schweiz AG
Original Assignee
Gesellschaft fuer Chemische Industrie in Basel CIBA
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.)
Filing date
Publication date
Application filed by Gesellschaft fuer Chemische Industrie in Basel CIBA filed Critical Gesellschaft fuer Chemische Industrie in Basel CIBA
Priority to GB3501035A priority Critical patent/GB466957A/en
Publication of GB466957A publication Critical patent/GB466957A/en
Expired legal-status Critical Current

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  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

Abstract

2 : 4 : 6 - Triamino - 1 : 3 : 5 - triazine (melamine) is prepared by heating to above 100 DEG C., dicyandiamide or cyanamide in the presence of ammonia under anhydrous conditions or in the presence of less than 20 per cent of water calculated on the weight of dicyandiamide or cyanamide. Preferably a solid or liquid diluent, e.g. liquid ammonia, which acts as a heat buffer is employed. In examples: (1) ammonia gas is forced under pressure into an autoclave containing dicyandiamide and methyl alcohol, benzine, ethyl alcohol or nitrobenzene and heat applied; melamine is obtained by filtering and washing the product; (2) dicyandiamide is heated in an autoclave with liquid ammonia; (3) dried dicyandiamide is mixed with iron powder and heated in a sealed tube or is heated in the presence of ammonia gas in an autoclave; when the ammonia is not introduced part of the dicyandiamide furnishes the required ammonia by decomposition; (4) dicyandiamide is heated in a flask in the presence of copper bronze to 185--190 DEG C.; (5) a mixture of cyanamide and methylalcohol is saturated with ammonia and heated in a sealed tube; (6) liquid ammonia is introduced into an autoclave containing dicyandiamide and methyl alcohol and heat applied; (7) dicyandiamide is mixed with 22 per cent aqueous ammonia and heated in a bomb. Zinc powder, magnesium oxide, asbestine and dioxane are mentioned as diluents.
GB3501035A 1935-12-17 1935-12-17 Manufacture of 2:4:6-triamino-1:3:5-triazine Expired GB466957A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB3501035A GB466957A (en) 1935-12-17 1935-12-17 Manufacture of 2:4:6-triamino-1:3:5-triazine

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB3501035A GB466957A (en) 1935-12-17 1935-12-17 Manufacture of 2:4:6-triamino-1:3:5-triazine

Publications (1)

Publication Number Publication Date
GB466957A true GB466957A (en) 1937-06-09

Family

ID=10372723

Family Applications (1)

Application Number Title Priority Date Filing Date
GB3501035A Expired GB466957A (en) 1935-12-17 1935-12-17 Manufacture of 2:4:6-triamino-1:3:5-triazine

Country Status (1)

Country Link
GB (1) GB466957A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2559617A (en) * 1951-07-10 Manufacture of melamine
US2567847A (en) * 1951-09-11 Preparation of substituted
DE752869C (en) * 1938-01-30 1952-11-10 Ig Farbenindustrie Ag Process for the production of 2, 4, 6-triamino-1, 3, 5-triazine (melamine)
US3177215A (en) * 1961-03-14 1965-04-06 Standard Oil Co Process for the production of melamine from hydrogen cyanide by way of cyanamide

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2559617A (en) * 1951-07-10 Manufacture of melamine
US2567847A (en) * 1951-09-11 Preparation of substituted
DE752869C (en) * 1938-01-30 1952-11-10 Ig Farbenindustrie Ag Process for the production of 2, 4, 6-triamino-1, 3, 5-triazine (melamine)
US3177215A (en) * 1961-03-14 1965-04-06 Standard Oil Co Process for the production of melamine from hydrogen cyanide by way of cyanamide

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