H-Ala-Obzl.HCl

Names

[ Name ]:
H-Ala-Obzl.HCl

[Synonym ]:
L-Alanine benzyl ester hydrochloride
EINECS 226-920-4
MFCD00054340
Alanine, phenylmethyl ester, hydrochloride (1:1)
Benzyl alaninate hydrochloride (1:1)
L-Alaninebenzylesterhydrochloride

Chemical & Physical Properties

[ Density]:
1.1g/cm3

[ Boiling Point ]:
293ºC at 760 mmHg

[ Melting Point ]:
135 to 145ºC

[ Molecular Formula ]:
C₁₀H₁₄ClNO₂

[ Molecular Weight ]:
215.677

[ Flash Point ]:
131ºC

[ Exact Mass ]:
215.071304

[ PSA ]:
52.32000

[ LogP ]:
2.57930

[ Index of Refraction ]:
1.53

[ Storage condition ]:
−20°C

MSDS

Safety Information

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

[ Hazard Codes ]:
Xi

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2922499990

Customs

[ HS Code ]: 2922499990

[ Summary ]:
HS:2922499990 other amino-acids, other than those containing more than one kind of oxygen function, and their esters; salts thereof VAT:17.0% Tax rebate rate:9.0% Supervision conditions:AB(certificate of inspection for goods inward,certificate of inspection for goods outward) MFN tariff:6.5% General tariff:30.0%

Articles

The Benzyl Ester Group of Amino Acid Monomers Enhances Substrate Affinity and Broadens the Substrate Specificity of the Enzyme Catalyst in Chemoenzymatic Copolymerization.

Biomacromolecules 17 , 314-23, (2016)

The chemoenzymatic polymerization of amino acid monomers by proteases involves a two-step reaction: the formation of a covalent acyl-intermediate complex between the protease and the carboxyl ester gr...

Positively charged microemulsions for topical application.

Int. J. Pharm. 346 , 119-123, (2008)

The study reports pig-skin permeation and skin accumulation of miconazole nitrate (MCZ) from positively charged microemulsions containing water, 1-decanol/1-dodecanol (2:1, w/w), lecithin and/or decyl...

Synthesis, QSAR and anti-HIV activity of new 5-benzylthio-1,3,4-oxadiazoles derived from α-amino acids.

J. Enzyme Inhib. Med. Chem. 26 , 668-680, (2011)

2-(1-[(4-Chloro/methylphenylsulfonylamino)alkyl]-5-thioxo-4,5-dihydro-1,3,4-oxadiazoles (4a-e) were synthesized, in four steps, via the sulfonyl derivatives of l-amino acids (l-alanine, l-methionine a...