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K6625

Sigma-Aldrich

2-Ketohexanoic acid sodium salt

97.0-103.0%

Synonym(s):

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

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About This Item

Linear Formula:
C6H9O3Na
CAS Number:
Molecular Weight:
152.12
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

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

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Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

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

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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
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
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
G P Butrimovitz et al.
Clinical chemistry, 29(8), 1518-1521 (1983-08-01)
We have developed an automated enzymatic assay for LDH-C4, a lactate dehydrogenase (EC 1.1.1.27) isoenzyme found exclusively in spermatozoa, as a marker of human spermatogenesis. LDH-C4 activity is assayed bichromatically in the Abbott ABA-100 spectrophotometer, with 2-oxohexanoate as substrate. As
G L Loy et al.
Analytical biochemistry, 185(1), 1-9 (1990-02-15)
Tracer methods using both carbon-13 and -14 have been utilized for determination of ovine fetal amino acid disposal and the results compared in seven animals. We infused [1-13C]leucine simultaneously with [1-14C]leucine into the fetal circulation of pregnant sheep chronically catheterized

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