N-Me-DL-Ala-OH.HCl

Modify Date: 2024-01-02 10:05:01

N-Me-DL-Ala-OH.HCl Structure
N-Me-DL-Ala-OH.HCl structure
Common Name N-Me-DL-Ala-OH.HCl
CAS Number 600-21-5 Molecular Weight 103.120
Density 1.0±0.1 g/cm3 Boiling Point 190.1±23.0 °C at 760 mmHg
Molecular Formula C4H9NO2 Melting Point 317CºC
MSDS Chinese USA Flash Point 68.8±22.6 °C

 Use of N-Me-DL-Ala-OH.HCl


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

 Names

Name 2-(methylamino)propanoic acid
Synonym More Synonyms

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

Description H-N-Me-DL-Ala-OH is an alanine 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):1793-1021.

 Chemical & Physical Properties

Density 1.0±0.1 g/cm3
Boiling Point 190.1±23.0 °C at 760 mmHg
Melting Point 317CºC
Molecular Formula C4H9NO2
Molecular Weight 103.120
Flash Point 68.8±22.6 °C
Exact Mass 103.063332
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

 Synthetic Route

 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%

 Articles16

More Articles
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 ...

Monomeric sarcosine oxidase: 2. Kinetic studies with sarcosine, alternate substrates, and a substrate analogue.

Biochemistry 39 , 8825-9, (2000)

Monomeric sarcosine oxidase (MSOX) is a flavoenzyme that catalyzes the oxidative demethylation of sarcosine (N-methylglycine) to yield glycine, formaldehyde, and hydrogen peroxide. MSOX can oxidize ot...

 Synonyms

2-(methylamino)propionic acid
2-(Methylamino)propanoic acid
2-(N-methylamino)propionic acid
N-Me-DL-Ala-OH.HCl
Alanine, N-methyl-
N-|A-Methyl-DL-alanine
L-Alanine,N-methyl
N-Methyl-D-Alanine
N-Methyl-DL-alanine
MFCD00063136
N-Methylalanine
N-Methyl-Alanine
Alanine,N-methyl-,L
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