H-Gly-NH2.HCl

Suppliers

Names

[ Name ]:
H-Gly-NH2.HCl

[Synonym ]:
Acetamide, 2-amino-, monohydrochloride
2-Aminoacetamide hydrochloride
Glycinamide hydrochloride (1:1)
MFCD00013008
Glycine amide hydrochloride
Glycinamide, monohydrochloride
EINECS 216-789-1
2-aminoacetamide,hydrochloride
Acetamide, 2-amino-, hydrochloride (1:1)
H-Gly-NH2.HCl
Glycinamidehydrochloride

Chemical & Physical Properties

[ Density]:
1.122g/cm3

[ Boiling Point ]:
281.3ºC at 760mmHg

[ Melting Point ]:
204 °C (dec.)(lit.)

[ Molecular Formula ]:
C₂H₇ClN₂O

[ Molecular Weight ]:
110.54

[ Exact Mass ]:
110.024689

[ PSA ]:
69.11000

[ LogP ]:
0.63300

[ Vapour Pressure ]:
0.00359mmHg at 25°C

[ Storage condition ]:
Store at RT.

[ Water Solubility ]:
H2O: 0.1 g/mL, clear

MSDS

Click to get detail MSDS

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ Hazard Codes ]:
Xi:Irritant

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S22-S24/25-S37/39-S26

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
29241900

Precursor & DownStream

Precursor

DownStream

2-(benzylamino)acetamide
Boc-glycinamide
z-gly-nh2
5-phenyl-1h-pyrazin-2-one
N-(2-Amino-2-oxoethyl)-2-propenamide
2-Hydroxy-6-Methylpyrazine
5-Methylpyrazin-2-ol
Glycinamide
Z-Gly-Gly-NH2
Oxiracetam

Customs

[ HS Code ]: 2924199090

[ Summary ]:
2924199090. other acyclic amides (including acyclic carbamates) and their derivatives; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

Articles

Preparation of guanine and diaminopurine from biuret. Part III.

Chem. Biodivers. 4(4) , 818-22, (2007)

Because of their potential prebiotic origin and relative chemical stability, urea, biuret, formic acid, and glycine amide might have played a role in the assembly process of purine bases. In this pape...

Identification of quinoline, carboline and glycinamide compounds in cow milk using HRMS and NMR.

Food Chem. 141(3) , 1888-94, (2013)

The aim of this work was to characterise new UV-absorbing compounds (UAC) in cow milk in order to gain an overview of the molecular diversity of the minor bioactive constituents, that could be used to...

Synthesis of (-)-quinocarcin by directed condensation of alpha-amino aldehydes.

J. Am. Chem. Soc. 127(48) , 16796-7, (2005)

An enantioselective synthesis of the natural antiproliferative agent quinocarcin was achieved by the directed condensation of optically active alpha-amino aldehyde intermediates. Condensation of the N...