H-Gly-Ala-OH

Suppliers

Names

[ CAS No. ]:
3695-73-6

[ Name ]:
H-Gly-Ala-OH

[Synonym ]:
EINECS 223-019-8
Gly-l-ala
Glycyl-DL-alanine
Glycine-alanine
Glycyl-L-alanine
Gly-Ala-OH
MFCD00065112
Glcylalanine
H-Gly-L-Ala-OH
UNII:44L9158R9G
N-glycylalanine
Gly-L-Ala-OH
Alanine, N-glycyl-, L-
L-Alanine, glycyl-
(S)-2-(2-Aminoacetamido)propanoic acid
Alanine, glycyl-
Glycylalanine
DL-Alanine, N-glycyl-
Gly-Ala
L-Alanine, N-glycyl-
N-Glycyl-L-alanine
H-GLY-ALA-OH
H-Gly-β-Ala-OH

Chemical & Physical Properties

[ Density]:
1.3±0.1 g/cm3

[ Boiling Point ]:
417.4±30.0 °C at 760 mmHg

[ Melting Point ]:
~ 230°C dec.

[ Molecular Formula ]:
C5H10N2O3

[ Molecular Weight ]:
146.145

[ Flash Point ]:
206.2±24.6 °C

[ Exact Mass ]:
146.069138

[ PSA ]:
92.42000

[ LogP ]:
-1.50

[ Vapour Pressure ]:
0.0±2.1 mmHg at 25°C

[ Index of Refraction ]:
1.498

[ Storage condition ]:
-15°C

MSDS

Safety Information

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

[ RIDADR ]:
NONH for all modes of transport

[ HS Code ]:
2924199090

Precursor & DownStream

Precursor

  • Z-Gly-Ala-OH
  • 2-(((benzyloxy)carbonyl)amino)acetic (isobutyl carbonic) anhydride
  • Z-Gly-Ala-OBzl
  • glycyl-L-alanine ethyl ester
  • N-(N,N-phthaloyl-glycyl)-L-alanine
  • N-(N,N-phthaloyl-glycyl)-L-alanin-ethyl ester
  • Cyclo(-ala-gly)

DownStream

  • H-Gly-DL-Ala-OH
  • L-alanine
  • Glycine
  • gly-d-ala
  • H-β-Ala-Gly-β-Ala-OH
  • L-Alanine,N-(chloroacetyl)- (9CI)

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

Charge-based interactions between peptides observed as the dominant force for association in aqueous solution.

Angew. Chem. Int. Ed. Engl. 47(47) , 9059-62, (2008)

Epstein-Barr virus latent genes.

Exp. Mol. Med. 47 , e131, (2015)

Latent Epstein-Barr virus (EBV) infection has a substantial role in causing many human disorders. The persistence of these viral genomes in all malignant cells, yet with the expression of limited late...

Dissociative electron attachment to glycyl-glycine, glycyl-alanine and alanyl-alanine.

Phys. Chem. Chem. Phys. 13(10) , 4600-6, (2011)

The processes of negative ions formation of dipeptides glycyl-glycine, glycyl-alanine and alanyl-alanine in the conditions of resonant electron capture have been studied with a help of negative ions m...


More Articles


Related Compounds

  • H-Gly-Ala-Asp-OH
  • H-Gly-Ala-Hyp-OH
  • H-Gly-Ala-Tyr-OH
  • H-Gly-Ala-Gly-OH
  • H-Gly-Ala-Phe-OH
  • H-Gly-Ala-Leu-OH
  • 2-[(2,5-dimethylphenoxy)methyl]-5,6-dimethyl-1H-benzimidazole
  • 5-methoxy-2-[(4-methylphenoxy)methyl]-1H-benzimidazole
  • N-((6-(4-chlorophenyl)-2,3-dihydroimidazo[2,1-b]thiazol-5-yl)methyl)-4-cyanobenzamide
  • 4-{[(1Z)-2-[4-(6-chloro-2-oxo-2H-chromen-3-yl)-1,3-thiazol-2-yl]-2-cyanoeth-1-en-1-yl]amino}benzamide
  • (E)-4-((2-cyano-2-(4-cyclopropylthiazol-2-yl)vinyl)amino)benzamide
  • 2-[(4-chloro-3-methylphenoxy)methyl]-5-methoxy-1H-benzimidazole
  • 4-(2-(2-(Cyclopropanecarboxamido)thiazol-4-yl)acetamido)benzamide
  • 4-(2-(2-(3-Cyclohexylureido)thiazol-4-yl)acetamido)benzamide
  • N-(4-{[(4-carbamoylphenyl)carbamoyl]methyl}-1,3-thiazol-2-yl)-4-chlorobenzamide
  • 6-({4-[4-(Trifluoromethyl)benzoyl]piperazin-1-yl}sulfonyl)-1-azatricyclo[6.3.1.0^{4,12}]dodeca-4(12),5,7-trien-11-one
The content on this webpage is sourced from various professional data sources. If you have any questions or concerns regarding the content, please feel free to contact service1@chemsrc.com.