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Guanidine nitrate is the chemical compound with the formula [C(NH 2) 3]NO 3. It is a colorless, water-soluble salt. It is produced on a large scale and finds use as precursor for nitroguanidine, [1] fuel in pyrotechnics and gas generators. Its correct name is guanidinium nitrate, but the colloquial term guanidine nitrate is widely used.
The general structure of a guanidine. Guanidines are a group of organic compounds sharing a common functional group with the general structure (R 1 R 2 N)(R 3 R 4 N)C=N−R 5. The central bond within this group is that of an imine, and the group is related structurally to amidines and ureas.
The guanidinium nitrate intermediate may also be produced via the Boatright–Mackay–Roberts (BMR) process, in which molten urea is reacted with molten ammonium nitrate in the presence of silica gel. [3] [4] This process had been commercialized because of its attractive economic features. 2 NH 2 CONH 2 + NH 4 NO 3 → [C(NH 2) 3]NO 3 + 2 NH 3 ...
Guanidine nitrate; Guanidinium chloride; Guanidinium thiocyanate This page was last edited on 23 October 2021, at 14:51 (UTC). Text is available under the Creative ...
The general structure of a guanidine. Subcategories. This category has the following 9 subcategories, out of 9 total. A. Acylguanidines (8 P) ...
Pimagedine, also known as aminoguanidine, is an investigational drug for the treatment of diabetic nephropathy that is no longer under development as a drug. [1] Pimagedine functions as an inhibitor of diamine oxidase and nitric oxide synthase.
Petrunkin and Petrunkin (1927, 1928) appear to be the first who studied the binding of GnHCl to gelatin and a mixture of thermally denatured protein from brain extract. . Greenstein (1938, 1939), however, appears to be the first to discover the high denaturing action of guanidinium halides and thiocyanates in following the liberation of sulfhydryl groups in ovalbumin and other proteins as a ...
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