H-N-Me-Ala-OH.HCl

Modify Date: 2024-01-03 13:16:43

H-N-Me-Ala-OH.HCl Structure
H-N-Me-Ala-OH.HCl structure
Common Name H-N-Me-Ala-OH.HCl
CAS Number 3913-67-5 Molecular Weight 139.581
Density 1.0±0.1 g/cm3 Boiling Point 190.1±23.0 °C at 760 mmHg
Molecular Formula C4H10ClNO2 Melting Point 300 °C
MSDS Chinese USA Flash Point 68.8±22.6 °C

 Use of H-N-Me-Ala-OH.HCl


H-N-Me-Ala-OH is an alanine derivative[1].

 Names

Name N-methyl-L-alanine
Synonym More Synonyms

 H-N-Me-Ala-OH.HCl Biological Activity

Description H-N-Me-Ala-OH is an alanine derivative[1].
Related Catalog
Target

Human Endogenous Metabolite

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):1793-1019.

 Chemical & Physical Properties

Density 1.0±0.1 g/cm3
Boiling Point 190.1±23.0 °C at 760 mmHg
Melting Point 300 °C
Molecular Formula C4H10ClNO2
Molecular Weight 139.581
Flash Point 68.8±22.6 °C
Exact Mass 139.040009
PSA 49.33000
LogP -0.44
Vapour Pressure 0.2±0.7 mmHg at 25°C
Index of Refraction 1.436
Storage condition Store at RT.

 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 2922499990

 Customs

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%

 Articles13

More Articles
Three-dimensional quantitative structure-activity relationship analyses of substrates of the human proton-coupled amino acid transporter 1 (hPAT1).

Bioorg. Med. Chem. 19 , 6409-18, (2011)

The proton-coupled amino acid transporter hPAT1 has recently gained much interest due to its ability to transport small drugs thereby allowing their oral administration. A three-dimensional quantitati...

1H-NMR and 13C-NMR investigation of complexes of Mn2+ with ocytocin analogues in (2H6)dimethylsulfoxide.

Eur. J. Biochem. 240(1) , 118-24, (1996)

Several ocytocin analogues were synthesised by substitution of the Pro residue with sarcosine or N-methylalanine, the glutamine residue with threonine and one of the cysteines with 2-mercaptopropionic...

Transport of L-alanine in cultured human fibroblasts: evidence for two kinetically distinguishable systems.

J. Cell Physiol. 109(1) , 37-43, (1981)

The transport of L-alanine in human diploid fibroblasts was investigated. Transport measurements were performed on subcultures between the third and eighth passages with subconfluent cells growing on ...

 Synonyms

(2S)-2-(Methylamino)propanoic acid
N-Methyl-L-alanine hydrochloride (1:1)
(S)-2-Methylaminopropanoic acid
L-Alanine, N-methyl-, hydrochloride (1:1)
N-Methyl-L-alanine
QVY1&M1 &&L or S Form
MFCD06801364
N-methyl-L-alanine zwitterion
L-Alanine, N-methyl-
H-N-Me-Ala-OH
N-Me-Ala-OH.HCl
H-N-Me-Ala-OH.HCl
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