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Glycinamide hydrochloride structure
Glycinamide hydrochloride structure

Glycinamide hydrochloride

Iupac Name:2-aminoacetamide;hydrochloride
CAS No.: 1668-10-6
Molecular Weight:110.54
Modify Date.: 2022-12-06 15:54
1. Names and Identifiers
1.1 Name
Glycinamide hydrochloride
1.2 Synonyms

Acetamide, 2-amino-, monohydrochloride Acetamide, 2-amino-,hydrochloride (1:1) Aminoacetamide hydrochloride GLYCINAMIDE HCI Glycinamide hydrochl GLYCINAMIDEHYDROCHLORIDE,BIOLOGICALBUFFER

1.3 CAS No.
1668-10-6
1.4 EINECS(EC#)
216-789-1
1.5 Molecular Formula
C2H7ClN2O (isomer)
1.6 Inchi
InChI=1S/C2H6N2O.ClH/c3-1-2(4)5;/h1,3H2,(H2,4,5);1H
1.7 InChIkey
WKNMKGVLOWGGOU-UHFFFAOYSA-N
1.8 Canonical Smiles
Cl.NCC(N)=O
1.9 Isomers Smiles
C(C(=O)N)N.Cl
2. Properties
2.1 Melting point
204?°C (dec.)(lit.)
2.1 pKa
8.20(at 20℃)
2.2 StorageTemp
Inert atmosphere,Room Temperature
3. Safety and Handling
3.1 Hazard Codes
Xi
3.1 Risk Statements
36/37/38
3.1 Safety Statements
22-24/25-37/39-26
3.1 WGK Germany
3
6. Other Information
6.0 BRN
3554199
6.1 Chemical Properties
Crystalline
6.2 Uses
Glycinamide hydrochloride is a buffer that is useful in the physiological pH range. And it is also used as a pharmaceutical intermediate, in the organic synthesis.
6.3 Uses
Glycinamide hydrochloride may be used in the synthesis of [M(glycinamidato-N,N′)(ptpy)2] where ptpy = 2-(p-tolyl)pyridinato) and M= Rh or Ir.
It may be used in the synthesis of the following glycinamide-based imidazolidinones:
  • (±)-2-(2-phenylpropyl)imidazolidin-4-one
  • (±)-2-(2,4,4-trimethylpentyl)imidazolidin-4-one
  • (±)-2-[(R)-2,6-dimethyl-5-heptenyl]imidazolidin-4-one
  • (5R,6S,9R)-6-isopropyl-9-methyl-1,4-diazaspiro[4.5]decan-2-one
  • (5S,6S,9R)-6-isopropyl-9-methyl-1,4-diazaspiro[4.5]decan-2-one
  • (±)-2-methyl-2-pentylimidazolidin-4-one
  • (±)-2-ethyl-2-(2-methylbutyl)imidazolidin-4-one
  • (±)-2-(undecan-2-yl)imidazolidin-4-one
  • (±)-2-pentylimidazolidin-4-one
  • 2-(2,4-dimethylcyclohex-3-en-1-yl)imidazolidin-4-one
6.4 Purification Methods
Crystallise the salt from EtOH, EtOH/H2O or MeOH. [Karmas & Spoerri J Am Chem Soc 74 1580 1952, Beilstein 4 IV 2358.]
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