H-Asp(OMe)-OH·HCl

Modify Date: 2024-01-02 12:58:41

H-Asp(OMe)-OH·HCl Structure
H-Asp(OMe)-OH·HCl structure
Common Name H-Asp(OMe)-OH·HCl
CAS Number 16856-13-6 Molecular Weight 183.590
Density 1.299g/cm3 Boiling Point 301.7ºC at 760mmHg
Molecular Formula C5H10ClNO4 Melting Point 191-193°C
MSDS Chinese USA Flash Point 136.3ºC

 Use of H-Asp(OMe)-OH·HCl


β-Methyl L-aspartate hydrochloride is an aspartic acid derivative[1].

 Names

Name L-Aspartic acid β-methyl ester hydrochloride
Synonym More Synonyms

 H-Asp(OMe)-OH·HCl Biological Activity

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.

 Chemical & Physical Properties

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

 Safety Information

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

 Customs

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%

 Articles3

More Articles
Syntheses of S-enantiomers of hanishin, longamide B, and longamide B methyl ester from L-aspartic acid beta-methyl ester: establishment of absolute stereochemistry.

J. Org. Chem. 70 , 9081-9084, (2005)

[reaction: see text] Total syntheses of enantiopure hanishin, longamide B, and longamide B methyl ester are described. Absolute configurations of these natural products have been established.

Enzymatic synthesis of a CCK-4 tripeptide fragment.

Di Yi Jun Yi Da Xue Xue Bao 23 , 289-292, (2003)

To synthesize a tripeptide derivative Phac-Met-Asp(OMe)-Phe -NH2, which is a fragment of the gastrin C-terminal tetrapeptide CCK-4, by enzymatic reaction.Three free enzymes, alpha-chymotrypsin, papain...

Practical synthesis of (R)-4-mercaptopyrrolidine-2-thione from L-aspartic acid. Preparation of a novel orally active 1-beta-methylcarbapenem, TA-949.

J. Org. Chem. 65 , 517-522, (2000)

A facile and economical synthesis of a novel orally active 1-beta-methylcarbapenem, TA-949 (1), is described. The key process involves an efficient synthesis of the C-2 side chain (R)-4-mercaptopyrrol...

 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
Top Suppliers:I want be here





Get all suppliers and price by the below link:

H-Asp(OMe)-OH·HCl suppliers


Price: ¥45/5g

Reference only. check more H-Asp(OMe)-OH·HCl price