H-Gly-NH2.HCl
Names
[ CAS No. ]:
1668-10-6
[ 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
Biological Activity
[Description]:
[Related Catalog]:
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
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
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
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...