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ChemicalBook--->CAS DataBase List--->7004-03-7

7004-03-7

7004-03-7 Structure

7004-03-7 Structure
IdentificationBack Directory
[Name]

Valine
[CAS]

7004-03-7
[Synonyms]

CB4875617
Valine USP/EP/BP
DL-Aminovaleic Acid
1-2-Amino-3-methylbutyric acid
[EINECS(EC#)]

200-773-6
[Molecular Formula]

C5H11NO2
[MDL Number]

MFCD00064220
[MOL File]

7004-03-7.mol
Chemical PropertiesBack Directory
[Melting point ]

315° C (under decomposition).
[solubility ]

9% soluble in water, practically insoluble in alcohol and oils.
[form ]

Leafy crystals
[Odor]

virtually odorless
Raw materials And Preparation ProductsBack Directory
[Preparation Products]

L-Valine-->D-Valine-->(2S)-2-[[2-chloro-4-(trifluoromethyl)phenyl]amino]-3-methyl-butanoate
Hazard InformationBack Directory
[Description]

Valine(2-amino-3-methylbutyric acid) is one of the 20 amino acids that make up proteins. It is an essential 8 amino acids and glucogenic amino acids for the human body. And Valine works with isoleucine and leucine to promote normal body growth, repair tissues, regulate blood sugar, and provide the required energy.
[Chemical Properties]

Valine(2-amino-3-methylbutyric acid) is one of the 20 amino acids that make up proteins. It is an essential 8 amino acids and glucogenic amino acids for the human body. And Valine works with isoleucine and leucine to promote normal body growth, repair tissues, regulate blood sugar, and provide the required energy.
[Physical properties]

Valine, White crystal or crystalline powder; odorless, slightly sweet and then bitter. Soluble in water, almost insoluble in ethanol.
[Definition]

ChEBI: L-valine is the L-enantiomer of valine. It has a role as a nutraceutical, a micronutrient, a human metabolite, an algal metabolite, a Saccharomyces cerevisiae metabolite, an Escherichia coli metabolite and a mouse metabolite. It is a pyruvate family amino acid, a proteinogenic amino acid, a valine and a L-alpha-amino acid. It is a conjugate base of a L-valinium. It is a conjugate acid of a L-valinate. It is an enantiomer of a D-valine. It is a tautomer of a L-valine zwitterion.
[Synthesis]

Valine can be synthesized by hydrolysis of aminoisobutyronitrile which is obtained by amination and cyanation of aminoisoaldehyde.
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