H3379
Hydantoic acid
Synonym(s):
N-Carbamoylglycine
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About This Item
Linear Formula:
H2NCONHCH2CO2H
CAS Number:
Molecular Weight:
118.09
UNSPSC Code:
12352200
PubChem Substance ID:
EC Number:
207-328-5
MDL number:
InChI key
KZVRXPPUJQRGFN-UHFFFAOYSA-N
InChI
1S/C3H6N2O3/c4-3(8)5-1-2(6)7/h1H2,(H,6,7)(H3,4,5,8)
SMILES string
NC(=O)NCC(O)=O
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signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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K Shimada et al.
Journal of chromatography, 339(2), 331-337 (1985-05-03)
An analytical method for determining phenytoin and its metabolites in the urine of epileptic patients is described. The analysis was performed for the m- and p-isomers of hydroxyphenytoin, the oxidative products of phenytoin, using gas chromatography. As an internal standard
H Yamada et al.
Biochimie, 62(5-6), 395-399 (1980-01-01)
Bacterial dihydropyrimidinase was shown to catalyze the hydrolytic cleavage of various 5-substituted hydantoins to the corresponding N-carbamyl-D-amino acids under alkaline conditions. Therefore, an enzymatic method for preparing the D-forms of phenylglycine-related amino acids was developed using immobilized bacterial cells with
Violina T Angelova et al.
Organic & biomolecular chemistry, 5(17), 2835-2840 (2007-08-19)
The hydrolysis of iminohydantoins generates the same tetrahedral intermediate as that obtained in the cyclization of hydantoic acid amides to hydantoins. The ratio of the products of imine hydrolysis under kinetic control is determined by the relative height of the
Y Yamagata et al.
Origins of life, 11(4), 317-320 (1981-12-01)
Electric discharges between a pair of carbon electrodes were continued for 50 days in a vessel of 5 liters in volume which initially contained nitrogen at a pressure of 15 cm Hg and 200 ml of water. The pressure in
R Forster et al.
Mutation research, 298(2), 71-79 (1992-12-01)
Ames tests have been performed with imidazole and its principal metabolites, hydantoin and hydantoic acid. N-Acetyl-imidazole, a potential metabolite resulting from the action of intestinal bacteria, and histamine, a structurally related compound which is widely distributed in mammalian tissues, have
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