L-Aspartic acid dibenzyl ester 4-toluenesulfonate

Names

[ Name ]:
L-Aspartic acid dibenzyl ester 4-toluenesulfonate

[Synonym ]:
L-Aspartic acid, bis(phenylmethyl) ester, 4-methylbenzenesulfonate
TosOH
L-aspartic acid dibenzyl ester p-toluenesulfonate salt
H-Asp(OBzl)-OBzl·Tos-OH
1,4-Dibenzyl L-Aspartate p-Toluenesulfonate
MFCD00065188
L-Aspartic acid dibenzyl ester p-toluenesulfonate
EINECS 220-746-2
L-Aspartic Acid 1,4-Dibenzyl Ester p-Toluenesulfonate
L-Aspartic acid, bis(phenylmethyl) ester, 4-methylbenzenesulfonate (1:1)
H-Asp(OBzl)-OBzl
H-Asp(Obzl)-Obzl TosOH
L-Aspartic acid dibe
L-Asp-maleinimide
L-aspatic acid dibenzyl ester toluene-p-sulfonate salt
Dibenzyl L-aspartate 4-methylbenzenesulfonate
Dibenzyl L-aspartate 4-methylbenzenesulfonate (1:1)
(S)-Dibenzyl 2-aminosuccinate 4-methylbenzenesulfonate
H-Asp(OBzl)-OBzl·TosOH

Biological Activity

[Description]:

H-Asp(OBzl)-Obzl.TosOH is an aspartic acid 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

[ Boiling Point ]:
455.3ºC at 760 mmHg

[ Melting Point ]:
157-160 °C(lit.)

[ Molecular Formula ]:
C₂₅H₂₇NO₇S

[ Molecular Weight ]:
485.549

[ Exact Mass ]:
485.150818

[ PSA ]:
141.37000

[ LogP ]:
5.21340

[ Vapour Pressure ]:
1.78E-08mmHg at 25°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

Related Compounds

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