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103213-32-7

103213-32-7 structure
103213-32-7 structure

Name FMOC-S-trityl-L-cysteine
Synonyms Fmoc-Cys(Trt)-OH
(2R)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-tritylsulfanylpropanoic acid
Fmoc-S-Trityl-L-Cysteine
N-Fmoc-S-trityl-L-cysteine
Cysteine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-S-(triphenylmethyl)-
(2R)-2-{[(9H-Fluoren-9-ylmethoxy)carbonyl]amino}-3-(tritylsulfanyl)propanoic acid
N-(9-Fluorenyl methoxy carbonyl)-S-trityl-L-cysteine
Na-Fmoc-Ng-trityl-L-glutamine
N-[(9H-Fluoren-9-ylMethoxy)carbonyl]-S-(triphenylMethyl)-L-cysteine
N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-S-tritylcysteine
MFCD00038538
2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(tritylthio)propanoic acid
Description Fmoc-Cys(Trt)-OH is a cysteine 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):1793-807.

Density 1.3±0.1 g/cm3
Boiling Point 763.4±60.0 °C at 760 mmHg
Melting Point 170-173 °C(lit.)
Molecular Formula C37H31NO4S
Molecular Weight 585.711
Flash Point 415.5±32.9 °C
Exact Mass 585.197388
PSA 100.93000
LogP 9.96
Vapour Pressure 0.0±2.7 mmHg at 25°C
Index of Refraction 1.656
Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Hazard Codes Xi: Irritant;
Risk Phrases R36/37/38
Safety Phrases S22-S24/25
RIDADR NONH for all modes of transport
WGK Germany 3
HS Code 2930909090
HS Code 2930909090
Summary 2930909090. other organo-sulphur compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%