3-Methylvaline

Modify Date: 2024-01-02 20:09:46

3-Methylvaline Structure
3-Methylvaline structure
Common Name 3-Methylvaline
CAS Number 33105-81-6 Molecular Weight 131.173
Density 1.0±0.1 g/cm3 Boiling Point 217.7±23.0 °C at 760 mmHg
Molecular Formula C6H13NO2 Melting Point 299-301ºC
MSDS USA Flash Point 85.5±22.6 °C

 Use of 3-Methylvaline


2-Amino-3,3-dimethylbutanoic acid is a leucine derivative[1].

 Names

Name 2-amino-3,3-dimethylbutanoic acid
Synonym More Synonyms

 3-Methylvaline Biological Activity

Description 2-Amino-3,3-dimethylbutanoic acid is a leucine 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 1.0±0.1 g/cm3
Boiling Point 217.7±23.0 °C at 760 mmHg
Melting Point 299-301ºC
Molecular Formula C6H13NO2
Molecular Weight 131.173
Flash Point 85.5±22.6 °C
Exact Mass 131.094635
PSA 63.32000
LogP 0.55
Vapour Pressure 0.1±0.9 mmHg at 25°C
Index of Refraction 1.464
Storage condition Store at RT.
Water Solubility H2O: 0.1 g/mL, clear, colorless | soluble

 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 29224995

 Synthetic Route

 Articles9

More Articles
Highly selective asymmetric acetate aldol reactions of an N-acetyl thiazolidinethione reagent.

Org. Lett. 6 , 23-25, (2004)

[reaction: see text] A highly diastereoselective acetate aldol reaction that uses a tert-leucine-derived thiazolidinethione auxiliary and dichlorophenylborane has been developed. The reaction proceeds...

Scaleable catalytic asymmetric Strecker syntheses of unnatural alpha-amino acids.

Nature 461(7266) , 968-70, (2009)

Alpha-amino acids are the building blocks of proteins and are widely used as components of medicinally active molecules and chiral catalysts. Efficient chemo-enzymatic methods for the synthesis of ena...

An efficient and selective enzymatic oxidation system for the synthesis of enantiomerically pure D-tert-leucine.

Org. Lett. 5(20) , 3649-50, (2003)

[reaction: see text] d-tert-Leucine was prepared with an enantiomeric excess of >99% by an enzyme-catalyzed oxidative resolution of the racemic mixture of dl-tert-leucine with use of leucine dehydroge...

 Synonyms

L-2-(tert-butyl)glycine
tert-leucine
L-Tert-Leucine
L-tert-leucin
(S)-2-Amino-3,3-dimethylbutyric acid
LEUCINE,L
2-tert-butyl-glycine
DL-Tert-Leucine
3-Methylvaline
(S)-2-Amino-4-methylpentanoic acid
T-BUTYL GLYCINE
DL-tert-Butylglycine
L-2-amino-3,3-dimethylbutanoic acid
(2S)-2-amino-3,3-dimethylbutanoic acid
3-Methyl-L-valine
L-Valine, 3-methyl-
L-2-tert-Butylglycine
Valine, 3-methyl-
(S)-2-Amino-3,3-dimethylbutanoic acid
3-Methyl valine
t-Butylglycine
h-dl-tle-oh
L-α-tert-Butylglycine
dl-t-butylglycine
L-tert
H-L-LEU-OH
QVYZX1&1&1 &&L or S Form
2-Amino-3,3-dimethylbutanoic acid
2-amino-3,3-dimethyl-butyric acid
tert-butylglycine
MFCD00065933
H-Tle-OH
Top Suppliers:I want be here



Get all suppliers and price by the below link:

3-Methylvaline suppliers


Price: ¥35/1g

Reference only. check more 3-Methylvaline price