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Aminoform

Chemical Designations - Synonyms Aminoform Ammoform Hexamine Metheneamine Urotropin Chemical Formula CSH12N4. [Pg.199]

Only 1,3,5,7-tetraazaadamantane is known. It is also called hexamethylenetetramine (93) (HMT), hexamine, aminoform, ammoform, cyctamin, cystogen, formin, uritone, urotropin, and methenamine. It is listed by the last name in the Merck Index. It is prepared from formaldehyde and ammonia. The chemistry of this well-known compound is not discussed in this review. [Pg.98]

Based on features of their interaction with ChE, anti-cholinesterase substances are classified as reversible and irreversible inhibitors. Referred to the reversible anti-cholinesterase substances are quaternary ammonium compounds and aminoformic acid esters OPC are referred to the irreversible anti-cholinesterase substances. [Pg.102]

Synonyms ammonium aminoformate ammonium carbonate anhydride... [Pg.29]

Hexamethylenetetramine and Derivatives. Hexamethylenetetramine (HMTAj, Hexamethyleneamine, Hexin, Urotropine, Hexamine, Formincystogen, Aminoform, Hex, Naphthamine or Uriton (Ger)... [Pg.79]

Amidoazourolic Acid. See Aminoazaurolic Acid Amidocarbonic Acid. See Carbamic Acid or Aminoformic Acid... [Pg.171]

Carbamic Acid Amidocarbonic Acid or Aminoformic ActW(called Carbamidsaure Kohlensaure-monoamid or Aminoameisensaure in Get) HaN.COOH mw 61.04, N 22.95 the theoretical, first simplest aminoacid known in aq solns, are called carbamates, and other derivs. The prepn props of aq solns of carbamic acid and its salts are described in detail in Refs 1 2. See also Refs 3 4... [Pg.435]

Ester-amides (derivatives of aminoformic acid, NH2COOH)... [Pg.1372]

Hexamine is also known as hexamethylenetetramine, aminoform, crystamine, methenamine or formin. It was first prepared in 1859 by Butlerov of Russia. It is a white, crystalline powder with a slight amine odor. It is soluble in water, alcohol, and chloroform, but it is insoluble in ether. However the aqueous solutions exhibit inverse solubility, i.e., less hexamine dissolves as the temperature increases. The hydrate, (CHi N O can be crystallized from the aqueous solution at temperatures below 14°C. Some additional properties are listed in Table 17.1. [Pg.333]

Such substrates are seldom used but tert-butyl (I - I -W-methoxy-A-methylcar-bamoyl)-3-methylbutyl]carbamoyl -2-phenylethyl aminoformate (44) gave 3-ben-zyl-6-isobutyl-2(l//)-pyrazinone (45) (21%) by two deprotections (LiAlH4 and HC1—dioxane) and a final cyclization in acetonitrile during 13 h.1510... [Pg.9]

Hexamethlyenetetraminc is quite a mouthful to say but is a perfect fuel for AN explosives due to its high stability. For its manufacture from ammonia water and formaldehyde solution see KITCHEN IMPROVISED PLASTIC EXPLOSIVES. It can also be bought as ration heating tablets from any army surplus store (eg. Hexamine fuel tabs). Also available under the following names "Ammoform", "Hexamethylenamine", "Aminoform", "Ammoform", "Formin, "Urotropin". [Pg.35]

Synonyms. Aminoform Esammina Formine Hexamethylen-amine Hexamethylenetetramine Methenamine Urotropine. Proprietary Names. Antihydral Urotropina. [Pg.654]

SYNS ACETO HMT AMINOFORM AMMOFORM AMMONIOFORMALDEHYDE CYSTAMIN CYSTOGEN ESAMETILENTETRAMINA (ITAUAN) FORNtAMINE FORMIN HEXAFORM ... [Pg.719]

Kobashi, K. (1992) Urease activity of /fe/Zcobacterpytor/. /. Clin. Pathol.. 45.367-368. Urechollne " bethanechol chloride, urethane inn (ethyl carbamate ethyl aminoformate ethyl urethane NSC 746) was formerly used clinically as a HYPNOTIC, and can be used as a GENERAL ANAESTHETIC in small animals. It has been used as an anticanCER agent in treating chronic myeloid leukaemia. [Pg.285]

Ethyl N- 1 -[(A-(2,2-diethoxyethyl)-A-methylcarbamoyl]-2-phenylethyl aminoformate (17) gave ethyl 2-benzyl-4-methyl-3-oxo-l,2,3,4-tetrahydropy-razinecarboxylate (18) [HCl, MeCN, 20°C, 1 h yield unstated ( %)] analogues likewise. ... [Pg.5]

Derivatives of aminoformic acid react with ChE similarly to OPC, i.e. in two stages with establishing a covalent bond. A degree of the anti-cholinesterase action of carbamates depends upon strength of the complexes formed. Evidently, the phosphorylated ChE becomes disabled for a more prolonged period, as compared with the carbamylated ChE. Rapidity of the initial activity restoration of the enzyme inhibited by carbamates is determined, respectively, by the carbamylated enzyme hydrolysis speed, which depends upon the inhibitor structure. Carbamy-... [Pg.155]

Methernamine, formamine, hexamine, utrotropin, metramine, HMTA, aminoform. Frequently but erroneously called hexam-ethyleneamine. [Pg.12]

AMINOFORM (100-97-0) Combustible solid (flash point 482°F/250°C). Incompatible with acids, l-bromopentaborane(9), organic anhydrides, isocyanates, vinyl acetate, acrylates, substituted allyls, alkylene oxides, epichlorohydrin, iodine, iodoform, ketones, aldehydes, alcohols, glycols, phenols, cresols, caprolactam solution, sodium peroxide, strong oxidizers. Attacks aluminum, copper, lead, tin, zinc, and their alloys, and some plastics, rubber, and coatings. [Pg.85]

M, Carbamic Acid. Aminoformic acid aminometban -dcirid, NHjCOOH. Not known in the free state. Its salts tccur is blood and urine of mammals, la salts, e.g ammonium carbamate, and its esters, such Kite ethyl ester (urethan), are entered separately. [Pg.269]

Ester-Amides (Derivatives of Aminoformic Acid, NHjCOOH)... [Pg.425]


See other pages where Aminoform is mentioned: [Pg.425]    [Pg.9]    [Pg.425]    [Pg.375]    [Pg.594]    [Pg.1194]    [Pg.67]    [Pg.1507]    [Pg.1511]    [Pg.60]    [Pg.648]    [Pg.56]    [Pg.56]    [Pg.32]    [Pg.395]    [Pg.784]   
See also in sourсe #XX -- [ Pg.199 ]

See also in sourсe #XX -- [ Pg.199 ]

See also in sourсe #XX -- [ Pg.160 ]




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Aminoformic Acid

Ammonium aminoformate

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