K6625
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
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
97.0-103.0%
Form:
powder
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
Related Categories
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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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
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
The stimulus-secretion coupling of amino acid-induced insulin release. Synergistic effects of L-glutamine and 2-keto acids upon insulin secretion.
A Sener et al.
Biochimica et biophysica acta, 677(1), 32-38 (1981-09-18)
Analysis of beta-hydroxy-beta-methyl butyrate in plasma by gas chromatography and mass spectrometry.
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
Global Trade Item Number
| SKU | GTIN |
|---|---|
| K6625-250MG | 04061833944776 |
| K6625-1G | 04061833944769 |
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