α-ketoisovalerate

Base Information

Chemical Name:α-ketoisovalerate
CAS No.:2507-77-9
Molecular Formula:C₅H₇O₃
Molecular Weight:115.109
Hs Code.:

Synonyms:α-ketoisovalerate

Suppliers and Price of α-ketoisovalerate

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of α-ketoisovalerate

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

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Technology Process of α-ketoisovalerate

There total 1 articles about α-ketoisovalerate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: 72-18-4,25609-85-2,7004-03-7,921-10-8
L-valine

: 64-15-3
α-ketoglutarate

: 2507-77-9
α-ketoisovalerate

: 154679-07-9,11070-68-1
L-glutamate

Guidance literature:: With pyridoxal 5-triphosphate; branched-chain-amino-acid transaminase from E_. coli; In phosphate buffer; at 298.15 ℃; pH=7.18 - 7.24; Product distribution; Thermodynamic data; Equilibrium constant; Enzymatic reaction;
DOI:10.1006/jcht.2000.0686

Reference yield: 97.0%

: 2507-77-9
α-ketoisovalerate

: 72-18-4,25609-85-2,7004-03-7,921-10-8
L-valine

Guidance literature:: With ammonium formate; tris hydrochloride; nicotinamide adenine dinucleotide; formate dehydrogenase; phenylalanine dehydrogenase; In water; at 30 ℃; for 24h;

Reference yield:

: 2507-77-9
α-ketoisovalerate

: 4026-18-0,17407-55-5,17407-56-6,600-37-3
2-hydroxy-3-methylbutanoic acid

Guidance literature:: With 1,6-di-o-phosphonohex-2-ulofuranose; piperazine*HCl buffer; NADH; at 25 ℃; Rate constant; pH 6.0, reaction in the presence of L-lactate dehydrogenase from Bacillus stearothermophilus (BSLDH Q₁₀₂R) or other enzymes;
DOI:10.1021/ja00038a016