Name | L-Aspartic acid dibenzyl ester 4-toluenesulfonate |
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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]. |
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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 |
Boiling Point | 455.3ºC at 760 mmHg |
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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 |
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Hazard Codes | Xi |
Safety Phrases | S22-S24/25 |
RIDADR | NONH for all modes of transport |
WGK Germany | 3 |