Skip to Content
MilliporeSigma
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

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
SLCD8612
SLBV1708
SLBL7699V
SLBK7898V
SLBF0752V

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, 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
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
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
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.
S Nissen et al.
Analytical biochemistry, 188(1), 17-19 (1990-07-01)
A method for measuring the branched chain hydroxy acid beta-hydroxy-beta-methyl butyrate (HMB, a product of leucine catabolism) has been described. A [2H6]HMB internal standard was added to plasma and standards, and samples were extracted with diethyl ether, backextracted into neutral
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