H-Gly-OBZl.HCl

Names

[ Name ]:
H-Gly-OBZl.HCl

[Synonym ]:
GLYCINE-OBZL HCL
GLYCINE BENZYL ESTER HCL
Benzyl glycinate HCl
Benzyl glycinate hydrochloride (1:1)
Benzyl glycinate hyd
N-Bn-glycine hydrochloride
GLYCINE BENZYL ESTERHCI
MFCD00035442
GLY-OBZLCL
Glycine, phenylmethyl ester, hydrochloride (1:1)
Glycine, N-(phenylmethyl)-, hydrochloride (1:1)
Benzyl glycinate
Gly benzyl ester hydrochloride
H2N-Gly-OBn*HCl
H-Gly-OBZl,HCl
benzyl 2-aminoacetate hydrochloride
Glycine benzyl ester hydrochloride
GlyOBn hydrochloride
Benzyl Glycinate Hydrochloride
H-Gly-OBzl.HCl,Benzylglycinate
Benzylglycinatehydrochloride
H-Gly-Obzl.HCl
N-Benzylglycine hydrochloride (1:1)
H-Gly-OBzl·HCl

Biological Activity

[Description]:

H-DL-Gly-OBzl.HCl is a Glycine (HY-Y0966) derivative[1].

[Related Catalog]:

Research Areas >> Others

Signaling Pathways >> Others >> Others

[In Vitro]

Amino acids and amino acid derivatives have been commercially used as ergogenic supplements. They influence the secretion of anabolic hormones, supply of fuel during exercise, mental performance during stress related tasks and prevent exercise induced muscle damage. They are recognized to be beneficial as ergogenic dietary substances[1].

[References]

[1]. Luckose F, et al. Effects of amino acid derivatives on physical, mental, and physiological activities. Crit Rev Food Sci Nutr. 2015;55(13):1793-1144.

Chemical & Physical Properties

[ Density]:
1.132g/cm3

[ Boiling Point ]:
245.5ºC at 760 mmHg

[ Melting Point ]:
138-140°C

[ Molecular Formula ]:
C₉H₁₂ClNO₂

[ Molecular Weight ]:
201.650

[ Flash Point ]:
110.3ºC

[ Exact Mass ]:
201.055649

[ PSA ]:
52.32000

[ LogP ]:
2.19080

[ Vapour Pressure ]:
0.0146mmHg at 25°C

[ Index of Refraction ]:
1.558

[ Storage condition ]:
−20°C

MSDS

Click to get detail MSDS

Safety Information

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

[ Hazard Codes ]:
Xi

[ Safety Phrases ]:
S22-S24/25

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

DownStream

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...

Synthesis of a metabolite of metoclopramide and its detection in human urine.

Il Farmaco 49 , 805-808, (1994)

The synthesis of 2-(4-amino-5-chloro-2-methoxybenzamido)acetic acid 2, a metabolite of metoclopramide 1, has been accomplished through the coupling of 4-amino-5-chloro-2-methoxybenzoic acid 4 with gly...

[Lengthening of the peptide chain at the C-terminal end of a glycosylamino acid].

Carbohydr. Res. 50 , 15-22, (1976)

An O-glycodipeptide was synthesized by lengthening the peptide chain on the C-terminal side of a glycosylamino acid unit. N-(Benzyloxycarbonyl)-3-O-(2,3,4,6-tetra-O-acetyl-beta-D-glucopyranosyl)-L-thr...