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16856-13-6

16856-13-6 structure
16856-13-6 structure

Name L-Aspartic acid β-methyl ester hydrochloride
Synonyms (2S)-2-Amino-4-methoxy-4-oxobutanoic acid hydrochloride (1:1)
L-Aspartatic Acid 4-Methyl Ester Hydrochloride
4-Methyl L-Aspartate Hydrochloride
EINECS 240-880-5
L-Asparitc acid 4-methyl ester HCl
L-Aspartic acid, 4-methyl ester, hydrochloride (1:1)
MFCD00038972
H-Asp(OMe)-OH.HCl
H-Asp(OMe)-OH·HCl
(S)-2-Amino-4-methoxy-4-oxobutanoic acid hydrochloride
beta-Methyl L-aspartate hydrochloride
β-Methyl L-aspartate hydrochloride
Description β-Methyl L-aspartate hydrochloride 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.

Density 1.299g/cm3
Boiling Point 301.7ºC at 760mmHg
Melting Point 191-193°C
Molecular Formula C5H10ClNO4
Molecular Weight 183.590
Flash Point 136.3ºC
Exact Mass 183.029831
PSA 89.62000
LogP 0.46370
Vapour Pressure 0.000242mmHg at 25°C
Storage condition −20°C
Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Hazard Codes Xi
RIDADR NONH for all modes of transport
WGK Germany 3
HS Code 2922509090
HS Code 2922509090
Summary 2922509090. other amino-alcohol-phenols, amino-acid-phenols and other amino-compounds with oxygen function. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%