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α-Ketoisovaleric Acid Sodium Salt (CAS 3715-29-5)

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Application:
α-Ketoisovaleric Acid Sodium Salt is an α-keto ester derivative
CAS Number:
3715-29-5
Purity:
≥96%
Molecular Weight:
138.10
Molecular Formula:
C5H7NaO3
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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α-Ketoisovaleric Acid Sodium Salt is a highly soluble white crystalline solid that holds value in the industrial sector. Its applications span across various industries, including leather tanning, dyeing, and food preservation. Furthermore, it serves as a precursor for formic acid production, which finds application in the manufacturing of pharmaceuticals and pesticides. It also plays a crucial role in laboratory settings, acting as a buffering agent and a reagent for organic compound synthesis. Additionally, it is utilized in catalyst preparation for organic compound synthesis and as a source of formate ions for the investigation of enzymatic reactions.

References:

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  2. NMR studies of DOXP reductoisomerase and its inhibitor complex.  |  Englert, NE., et al. 2011. Chembiochem. 12: 468-76. PMID: 21290548
  3. Differential isotope-labeling for Leu and Val residues in a protein by E. coli cellular expression using stereo-specifically methyl labeled amino acids.  |  Miyanoiri, Y., et al. 2013. J Biomol NMR. 57: 237-49. PMID: 24057411
  4. Profiling of chiral and achiral carboxylic acid metabolomics: synthesis and evaluation of triazine-type chiral derivatization reagents for carboxylic acids by LC-ESI-MS/MS and the application to saliva of healthy volunteers and diabetic patients.  |  Takayama, T., et al. 2015. Anal Bioanal Chem. 407: 1003-14. PMID: 25366977
  5. Characterization of cereulide synthetase, a toxin-producing macromolecular machine.  |  Alonzo, DA., et al. 2015. PLoS One. 10: e0128569. PMID: 26042597
  6. A novel approach for LC-MS/MS-based chiral metabolomics fingerprinting and chiral metabolomics extraction using a pair of enantiomers of chiral derivatization reagents.  |  Takayama, T., et al. 2015. Anal Chim Acta. 898: 73-84. PMID: 26526912
  7. Structural characterization of the Asf1-Rtt109 interaction and its role in histone acetylation.  |  Lercher, L., et al. 2018. Nucleic Acids Res. 46: 2279-2289. PMID: 29300933
  8. Evolution and diversification of the plant gibberellin receptor GID1.  |  Yoshida, H., et al. 2018. Proc Natl Acad Sci U S A. 115: E7844-E7853. PMID: 30068603
  9. Structural and dynamic studies of the peptidase domain from Clostridium thermocellum PCAT1.  |  Bhattacharya, S. and Palillo, A. 2022. Protein Sci. 31: 498-512. PMID: 34865273

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

α-Ketoisovaleric Acid Sodium Salt, 100 mg

sc-213205
100 mg
$230.00

α-Ketoisovaleric Acid Sodium Salt, 1 g

sc-213205A
1 g
$300.00

α-Ketoisovaleric Acid Sodium Salt, 5 g

sc-213205B
5 g
$380.00

α-Ketoisovaleric Acid Sodium Salt, 10 g

sc-213205C
10 g
$490.00