W387101
4-甲基-2-氧代戊酸 钠盐
97%
别名:
4-甲基-2-氧代戊酸钠盐, α-酮异己酸 钠盐, 4-Methyl-2-oxovaleric acid 钠盐, 4-甲基-2-氧代戊酸 钠盐, 酮亮氨酸 钠盐
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关于此项目
线性分子式:
(CH3)2CHCH2COCOONa
化学文摘社编号:
分子量:
152.12
NACRES:
NA.21
PubChem Substance ID:
UNSPSC Code:
12164502
FEMA Number:
3871
EC Number:
224-816-3
MDL number:
Beilstein/REAXYS Number:
4239297
InChI
1S/C6H10O3.Na/c1-4(2)3-5(7)6(8)9;/h4H,3H2,1-2H3,(H,8,9);/q;+1/p-1
SMILES string
[Na+].CC(C)CC(=O)C([O-])=O
InChI key
IXFAZKRLPPMQEO-UHFFFAOYSA-M
biological source
synthetic
assay
97%
mp
275 °C (dec.) (lit.)
application(s)
flavors and fragrances
documentation
see Safety & Documentation for available documents
food allergen
no known allergens
organoleptic
buttery
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Guoxing Fu et al.
Biochemistry, 50(29), 6292-6294 (2011-06-29)
D-Arginine dehydrogenase (DADH) catalyzes the flavin-dependent oxidative deamination of D-arginine and other D-amino acids to the corresponding imino acids. The 1.07 Å atomic-resolution structure of DADH crystallized with D-leucine unexpectedly revealed a covalent N(5) flavin adduct, instead of the expected
Li Qi et al.
Talanta, 81(4-5), 1554-1559 (2010-05-06)
A new strategy for the enantioseparation of D,L-amino acids employing the principle of ligand exchange capillary electrophoresis with Zn(II)-L-valine complex as a chiral selecting system in the presence of beta-cyclodextrin has been designed. Successful enantioseparation of label free and labeled
Benjamin Wax et al.
Journal of dietary supplements, 10(1), 6-16 (2013-01-30)
Glycine-arginine-α-ketoisocaproic acid (GAKIC) has been proposed to increase anaerobic high-intensity exercise performance in male subjects. However, the effects of GAKIC ingestion in female subjects have not been studied. Therefore, the purpose of this study was to investigate the effects of
Nelo Eidy Zanchi et al.
Amino acids, 40(4), 1015-1025 (2010-07-08)
Amino acids such as leucine and its metabolite α-ketoisocaproate (KIC), are returning to be the focus of studies, mainly because of their anti-catabolic properties, through inhibition of muscle proteolysis and enhancement of protein synthesis. It is clear that these effects
Chung-De Chen et al.
Journal of bacteriology, 194(22), 6206-6216 (2012-09-18)
Branched-chain aminotransferases (BCAT), which utilize pyridoxal 5'-phosphate (PLP) as a cofactor, reversibly catalyze the transfer of the α-amino groups of three of the most hydrophobic branched-chain amino acids (BCAA), leucine, isoleucine, and valine, to α-ketoglutarate to form the respective branched-chain
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