2-Methyl-L-serine

Modify Date: 2025-08-27 07:05:35

2-Methyl-L-serine Structure
2-Methyl-L-serine structure
Common Name 2-Methyl-L-serine
CAS Number 5424-29-3 Molecular Weight 119.119
Density 1.3±0.1 g/cm3 Boiling Point 345.8±32.0 °C at 760 mmHg
Molecular Formula C4H9NO3 Melting Point 253-263ºC
MSDS USA Flash Point 162.9±25.1 °C

 Use of 2-Methyl-L-serine


2-Amino-3-hydroxy-2-methylpropanoic acid is a serine derivative[1].

 Names

Name .α.-Methyl-DL-serine
Synonym More Synonyms

 2-Methyl-L-serine Biological Activity

Description 2-Amino-3-hydroxy-2-methylpropanoic acid is a serine 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 1.3±0.1 g/cm3
Boiling Point 345.8±32.0 °C at 760 mmHg
Melting Point 253-263ºC
Molecular Formula C4H9NO3
Molecular Weight 119.119
Flash Point 162.9±25.1 °C
Exact Mass 119.058243
PSA 83.55000
LogP -1.23
Vapour Pressure 0.0±1.7 mmHg at 25°C
Index of Refraction 1.513

 Safety Information

Personal Protective Equipment Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Hazard Codes Xi
Safety Phrases S24/25
RIDADR NONH for all modes of transport
WGK Germany 3
HS Code 2922509090

 Synthetic Route

 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%

 Articles11

More Articles
Drug design, in vitro pharmacology, and structure-activity relationships of 3-acylamino-2-aminopropionic acid derivatives, a novel class of partial agonists at the glycine site on the N-methyl-D-aspartate (NMDA) receptor complex.

J. Med. Chem. 52 , 5093-107, (2009)

Retaining agonistic activity at the glycine coagonist site of the NMDA receptor in molecules derived from glycine or d-serine has proven to be difficult because in the vicinity of the alpha-amino acid...

The requirement of phosphorylation on a threonine residue in the acute regulation of steroidogenesis in MA-10 mouse Leydig cells.

J. Steroid Biochem. Mol. Biol. 46(3) , 337-47, (1993)

In the present study we have used several non-phosphorylatable analogs of the amino acids threonine and serine to determine the role of phosphorylation in the acute regulation of steroidogenesis in MA...

Control of chemoselectivity in Dieckmann ring closures leading to tetramic acids.

Org. Biomol. Chem. 9 , 6663, (2011)

An efficient strategy for the control of the chemoselectivity in Dieckmann ring closures leading to tetramic acids derived from serine and α-methyl serine is reported, and this provides pathways to di...

 Synonyms

Serine,2-methyl-,DL
2-methylserine
Serine, 2-methyl-, DL-
DL-A-METHYLSERINE
Dl-serine,2-methyl
2-methyl-DL-serine
DL-Serine, 2-methyl-
A-METHYL-D,L-SERINE
L-Serine, 2-methyl-
DL-2-Methylserine
DL-2-Me-Ser-OH
2-Methyl-L-serine
Alpha-Methyl-D,L-serine
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