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2886-33-1

2886-33-1 structure
2886-33-1 structure

Name L-Aspartic acid dibenzyl ester 4-toluenesulfonate
Synonyms 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
Description H-Asp(OBzl)-Obzl.TosOH is an aspartic acid derivative[1].
Related Catalog
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.

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
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