α-Ketobutyric acid sodium salt, 98%

Name: α-Ketobutyric acid sodium salt, 98% | 2013-26-5
Brand: J&K Chemical
SKU: JK282985_5_G
Price: 191.9 USD
Availability: OutOfStock

Cat. No JK282985_5_G

Vendor: J&K Chemical

Product Information

Product Name

α-Ketobutyric acid sodium salt, 98%

Brand Name

J&K

Product Number

282985

CAS

2013-26-5

Molecular Formula

C4H5NaO3

Molecular Weight

124.07

Certificate of Analysis (COA)

COA not found

General Information

Synonyms

Sodium α-ketobutyrate,2-Oxobutyric acid sodium salt,Sodium 2-oxobutyrate

PubChem CID

23673454

IUPAC Name

sodium 2-oxobutanoate

InChI Key

SUAMAHKUSIHRMR-UHFFFAOYSA-M

SMILES

CCC(=O)C(=O)O-.Na+

Properties

Melting Point

210

Safety Information

Storage Condition

Store at 2-8℃

Application

a-Ketobutyric acid sodium salt is widely utilized in research focused on:

Metabolic Studies: This compound serves as a key intermediate in metabolic pathways, allowing researchers to study energy metabolism and the role of ketone bodies in various physiological conditions.
Biochemical Research: It is often used in enzyme assays and biochemical experiments to investigate the activity of specific enzymes involved in amino acid metabolism.
Pharmaceutical Development: The compound is explored for its potential therapeutic effects, particularly in the development of treatments for metabolic disorders and neurological conditions.
Food Industry: It is used as a food additive and flavoring agent, enhancing the taste and nutritional profile of various products, particularly in health-focused formulations.
Animal Nutrition: This sodium salt is incorporated into animal feed to improve growth performance and metabolic health in livestock, showcasing its benefits in agricultural applications.

References Data Source From Pubchem

An easy and sensitive assay for acetohydroxyacid synthases based on the simultaneous detection of substrates and products in a single step

Publication Name: Analytical and Bioanalytical Chemistry

Publication Date: 2024-10-23

DOI: 10.1007/s00216-024-05613-1

New insights in the targets of action of dimethyl fumarate in endothelial cells: effects on energetic metabolism and serine synthesis in vitro and in vivo

Publication Name: Communications Biology

Publication Date: 2023-10-25

DOI: 10.1038/s42003-023-05443-4

Synthesis of a 13C-methylene-labeled isoleucine precursor as a useful tool for studying protein side-chain interactions and dynamics

Publication Name: Journal of Biomolecular NMR

Publication Date: 2023-10-11

DOI: 10.1007/s10858-023-00427-2

Site-Specific Isotope Labeling of FliG for Studying Structural Dynamics Using Nuclear Magnetic Resonance Spectroscopy

Publication Name: Methods in molecular biology (Clifton, N.J.)

Publication Date: 2023

DOI: 10.1007/978-1-0716-3060-0_6

The methyl 13C-edited/13C-filtered transferred NOE for studying protein interactions with short linear motifs

Publication Name: Journal of Biomolecular NMR

Publication Date: 2020-09-30

DOI: 10.1007/s10858-020-00340-y

α-Ketobutyric acid sodium salt, 98%

Product Information

General Information

Properties

Safety Information

Application

References Data Source From Pubchem

An easy and sensitive assay for acetohydroxyacid synthases based on the simultaneous detection of substrates and products in a single step

New insights in the targets of action of dimethyl fumarate in endothelial cells: effects on energetic metabolism and serine synthesis in vitro and in vivo

Synthesis of a 13C-methylene-labeled isoleucine precursor as a useful tool for studying protein side-chain interactions and dynamics

Site-Specific Isotope Labeling of FliG for Studying Structural Dynamics Using Nuclear Magnetic Resonance Spectroscopy

The methyl 13C-edited/13C-filtered transferred NOE for studying protein interactions with short linear motifs