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1791-13-5

1791-13-5 structure
1791-13-5 structure

Name ditert-butyl (2S)-2-aminobutanedioate,hydrochloride
Synonyms L-Aspartic acid, bis(1,1-dimethylethyl) ester, hydrochloride (1:1)
H-Asp(OtBu)-OtBu,HCl
aspartic acid di-t-butyl ester hydrochloride
(S)-Di-tert-butyl 2-aminosuccinate hydrochloride
H-Asp(OtBu)-OtBu·HCl
di-t-Bu-L-aspartic acid
L-Aspartic Acid Di-tert-butyl Ester Hydrochloride
Bis(2-methyl-2-propanyl) L-aspartate hydrochloride (1:1)
Di-tert-butyl L-aspartate hydrochloride (1:1)
Di-tert-butyl L-Aspartate Hydrochloride
aspartic acid di-tert-butyl ester hydrochloride
H-Asp(OtBu)-OtBu.HCl
H-Asp(OBut)-ObutHCL
Description H-Asp(OtBu)-OtBu.HCl 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 339.8ºC at 760 mmHg
Melting Point 150 °C(dec.)
Molecular Formula C12H24ClNO4
Molecular Weight 281.776
Flash Point 159.3ºC
Exact Mass 281.139374
PSA 78.62000
LogP 2.88950
Vapour Pressure 6.39E-05mmHg at 25°C
Storage condition −20°C
Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
RIDADR NONH for all modes of transport
WGK Germany 3
HS Code 2922499990
Precursor  1

DownStream  1

HS Code 2922499990
Summary HS:2922499990 other amino-acids, other than those containing more than one kind of oxygen function, and their esters; salts thereof VAT:17.0% Tax rebate rate:9.0% Supervision conditions:AB(certificate of inspection for goods inward,certificate of inspection for goods outward) MFN tariff:6.5% General tariff:30.0%