Skip to Content
Merck
All Photos(3)

Key Documents

View All Documentation

K6625

Sigma-Aldrich

2-Ketohexanoic acid sodium salt

97.0-103.0%

Synonym(s):

α-Ketocaproic acid sodium salt, 2-Ketocaproic acid sodium salt

Sign Into View Organizational & Contract Pricing
All Photos(3)

About This Item

Linear Formula:
C6H9O3Na
CAS Number:
13022-85-0
Molecular Weight:
152.12
MDL number:
MFCD00013063
UNSPSC Code:
12352100
PubChem Substance ID:
57654321
NACRES:
NA.22

Quality Level

200

Assay

97.0-103.0%

form

powder

mp

240 °C (dec.) (lit.)

storage temp.

2-8°C

SMILES string

[Na].CCCCC(=O)C(O)=O

InChI

1S/C6H10O3.Na/c1-2-3-4-5(7)6(8)9;/h2-4H2,1H3,(H,8,9);/q;+1/p-1

InChI key

WDCARDDLMCHULC-UHFFFAOYSA-M

Looking for similar products? Visit Product Comparison Guide

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
0000336112
0000269146
SLCQ1293
SLCM6026
SLCD8612

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Customers Also Viewed

Slide 1 of 1

1 of 1

3-Hydroxybutyric acid 95%

Sigma-Aldrich

166898

3-Hydroxybutyric acid

S Lenzen et al.
The Journal of biological chemistry, 260(23), 12629-12634 (1985-10-15)
High aminotransferase activities catalyzing the reactions between L-glutamate and L-glutamine and the aliphatic ketomonocarboxylic acids 2-ketoisocaproate, 2-ketocaproate, and 2-ketoisovalerate were observed in pancreatic B-cell mitochondria. While maximal rates of transamination with L-glutamate were observed in the presence of micromolar concentrations
W J Malaisse
Diabete & metabolisme, 9(4), 313-320 (1983-12-01)
Insulin release evoked by nutrient secretagogues invariably coincides with an increase in the catabolism of exogenous and/or endogenous nutrients in pancreatic islet cells, resulting in an increased generation rate of reducing equivalents and ATP, and an increase in O2 consumption.
M U Javed et al.
Journal of enzyme inhibition, 10(3), 187-193 (1996-01-01)
An LDH isoenzyme was purified to homogeneity from uromastix testes and its inhibition spectrum towards known LDH isoenzyme inhibitors studied. Platinum compounds inhibited the enzyme in the forward reaction (pyruvate-->lactate) only, n-hexanediol and colchicine showed no inhibition and gossypol acetic
S A Metz
The Journal of pharmacology and experimental therapeutics, 238(3), 809-818 (1986-09-01)
Activation of an islet phospholipase A2 may contribute to glucose-induced insulin release. In order to simulate the accumulation of the resultant hydrolytic products (arachidonic acid, AA; its lipoxygenase-derived oxygenation product 12-hydroxyeicosatetraenoic acid; and lysophospholipids) without many of the other concomitants
S Lenzen et al.
The Journal of biological chemistry, 257(12), 6631-6633 (1982-06-25)
2-Ketocaproate and 2-ketoisocaproate were equally potent insulin secretagogues. The insulin secretory potency of L-leucine was less than half of that of the keto acids and L-norleucine did not induce any insulin release by isolated islets and by the perfused pancreas
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service