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Documenti

198994

Sigma-Aldrich

Sodium 3-methyl-2-oxobutyrate

greener alternative

95%

Sinonimo/i:

α-Ketoisovaleric acid sodium salt, 2-Keto-3-methylbutyric acid sodium salt, 3-Methyl-2-oxobutanoic acid sodium salt, 3-Methyl-2-oxobutyric acid sodium salt, Ketovaline sodium salt

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About This Item

Formula condensata:
(CH3)2CHCOCOONa
Numero CAS:
3715-29-5
Peso molecolare:
138.10
Beilstein:
4334552
Numero CE:
223-062-2
Numero MDL:
MFCD00002581
Codice UNSPSC:
12352100
ID PubChem:
24851887
NACRES:
NA.22

Saggio

95%

Forma fisica

solid

Punteggio alternativa più verde

old score: 14
new score: 9
Find out more about DOZN™ Scoring

Caratteristiche più verdi

Waste Prevention
Atom Economy
Safer Solvents and Auxiliaries
Learn more about the Principles of Green Chemistry.

sustainability

Greener Alternative Product

Punto di fusione

220-230 °C (dec.) (lit.)

Solubilità

water: soluble 100 mg/mL, clear, colorless

Categoria alternativa più verde

, Re-engineered

Stringa SMILE

[Na+].CC(C)C(=O)C([O-])=O

InChI

1S/C5H8O3.Na/c1-3(2)4(6)5(7)8;/h3H,1-2H3,(H,7,8);/q;+1/p-1
WIQBZDCJCRFGKA-UHFFFAOYSA-M

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Categorie correlate

Applicazioni

Sodium 3-methyl-2-oxobutyrate (3-Methyl-2-oxobutanoic acid sodium salt) was used in the synthesis of (S)-2-hydroxy-3-methylbutanoic acid.

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

Eyeshields, Gloves, type N95 (US)

Certificati d'analisi (COA)

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2-Ketobutyric acid sodium salt hydrate ≥95%

Sigma-Aldrich

464422

2-Ketobutyric acid sodium salt hydrate

An evaluation of the substrate specificity and asymmetric synthesis potential of the cloned L-lactate dehydrogenase from Bacillus stearothermophilus.
Canadian Journal of Chemistry, 67(6), 1065-1070 (1989)
Frances H A Huisman et al.
Biochemistry, 51(11), 2289-2297 (2012-02-23)
α-Isopropylmalate synthase (α-IPMS) catalyzes the metal-dependent aldol reaction between α-ketoisovalerate (α-KIV) and acetyl-coenzyme A (AcCoA) to give α-isopropylmalate (α-IPM). This reaction is the first committed step in the biosynthesis of leucine in bacteria. α-IPMS is homodimeric, with monomers consisting of
Marta de la Plaza et al.
Journal of molecular microbiology and biotechnology, 17(2), 96-100 (2008-11-27)
The alpha-ketoisovalerate decarboxylase (Kivd) is a unique lactococcal key enzyme in the decarboxylation of branched-chain alpha-keto acids derived from branched-chain amino acids transamination into aldehydes. These products are important aroma compounds produced during cheese ripening. In this study, the Kivd
Taro Murakami et al.
Journal of nutritional science and vitaminology, 51(1), 48-50 (2005-05-27)
Branched-chain alpha-keto acid dehydrogenase kinase (BDK) phosphorylates and inactivates the branched-chain alpha-keto acid dehydrogenase complex (BCKDC), which is the rate-limiting enzyme in the branched-chain amino acid catabolism. BDK has been believed to be bound to the BCKDC. However, recent our
Isabel Ayala et al.
Journal of biomolecular NMR, 43(2), 111-119 (2008-12-31)
A strategy for the introduction of ((1)H,(13)C-methyl)-alanine into perdeuterated proteins is described. Specific protonation of alanine methyl groups to a level of 95% can be achieved by overexpressing proteins in M9/D(2)O based bacterial growth medium supplemented with 800 mg/l of
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