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G6104

Glycinamide hydrochloride

Name: Glycinamide hydrochloride
Brand: ALDRICH

98%

Synonym(s):

2-Aminoacetamide hydrochloride, Aminoacetamide hydrochloride, Glycine amide hydrochloride

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About This Item

Linear Formula:

NH₂CH₂CONH₂ · HCl

CAS Number:

1668-10-6

Molecular Weight:

110.54

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24895244

EC Number:

216-789-1

Beilstein/REAXYS Number:

3554199

MDL number:

MFCD00013008

Assay:

98%

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Properties

Quality Level

100

assay

98%

mp

204 °C (dec.) (lit.)

SMILES string

Cl.NCC(N)=O

InChI

1S/C2H6N2O.ClH/c3-1-2(4)5;/h1,3H2,(H2,4,5);1H

InChI key

WKNMKGVLOWGGOU-UHFFFAOYSA-N

Description

Application

Buffer useful in the physiological pH range.

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Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Theoretical study of the effect of water in the process of proton transfer of glycinamide.

Yong Sun et al.

The journal of physical chemistry. B, 109(12), 5919-5926 (2006-07-21)

For the purpose of investigating the tautomerism from glycinamide (G) to glycinamidic acid (G*) induced by proton transfer, we carried out a study of structural interconversion of the two tautomers and the relative stabilizing influences of water during the tautomerization

Activity of the small modified amino acid alpha-hydroxy glycineamide on in vitro and in vivo human immunodeficiency virus type 1 capsid assembly and infectivity.

Samir Abdurahman et al.

Antimicrobial agents and chemotherapy, 52(10), 3737-3744 (2008-07-23)

Upon maturation of the human immunodeficiency virus type 1 (HIV-1) virion, proteolytic cleavage of the Gag precursor protein by the viral protease is followed by morphological changes of the capsid protein p24, which will ultimately transform the virus core from

A potential prebiotic route to adenine from hypoxanthine.

Irene M Lagoja et al.

Chemistry & biodiversity, 2(7), 923-927 (2006-12-29)

A possible reaction mechanism for the dehydration of glycinamide (3) and N,N'-diformylurea (4) yielding hypoxanthine (2) has been investigated. Furthermore, a potential prebiotic route converting hypoxanthine (2) into adenine (1) via phosphate activation followed by substitution reaction with NH3 was

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Global Trade Item Number

SKU	GTIN
G6104-25G	04061833638811
G6104-5G	04061831813753