Name | Dimethyl L-cystinate dihydrochloride |
---|---|
Synonyms |
Dimethyl L-cystinate dihydrochloride
L-CYSTINE DIETHYL DIHYDROCHLORIDE L-cystine-dimethylester dihydrochloride bis(glycine)-L-cystine dimethyl ether hydrochloride DIMETHYL CYSTINATE 2HCL (H-L-Cys-OMe)2 MFCD00012490 EINECS 251-261-4 L-Cystine-dimethyl Ester Dihydrochloride (2R,2'R)-Dimethyl 3,3'-disulfanediylbis(2-aminopropanoate) dihydrochloride Dimethyl L-Cystine dihydrochloride L-Cystine, dimethyl ester, hydrochloride (1:2) L-Cysteinedimethylester hydrochloride L-cystine dimethyl ester hydrochloride cystine-di-OMe dihydrochloride (H-Cys-OMe)2 . 2 HCl,(Disulfide bond) L-Cystine Dimethyl Ester 2HCl L-cysteine dimethyl ester dihydrochloride L-Cystine dimethyl ester dihydrochloride (H-Cys-OMe)2.2HCl L-Cystine, 1,1'-dimethyl ester, hydrochloride |
Description | Dimethyl 3,3'-disulfanediyl(2R,2'R)-bis(2-aminopropanoate) dihydrochloride 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 |
Boiling Point | 375.5ºC at 760 mmHg |
---|---|
Melting Point | 182-183 °C (dec.)(lit.) |
Molecular Formula | C8H18Cl2N2O4S2 |
Molecular Weight | 341.276 |
Flash Point | 180.9ºC |
Exact Mass | 340.008514 |
PSA | 155.24000 |
LogP | 2.37300 |
Symbol |
GHS07 |
---|---|
Signal Word | Warning |
Hazard Statements | H315-H319-H335 |
Precautionary Statements | P261-P305 + P351 + P338 |
Personal Protective Equipment | dust mask type N95 (US);Eyeshields;Gloves |
Hazard Codes | Xn: Harmful; |
Risk Phrases | R22;R36/37/38 |
Safety Phrases | S26-S36-S37/39 |
RIDADR | NONH for all modes of transport |
WGK Germany | 3 |
~98% 32854-09-4 |
Literature: Tetrahedron Letters, , vol. 55, # 6 p. 1132 - 1135 |
~% 32854-09-4
Detail
|
Literature: Australian Journal of Chemistry, , vol. 64, # 4 p. 443 - 453 |
Precursor 4 | |
---|---|
DownStream 4 | |