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线性分子式:
CH3COCOOH
化学文摘社编号:
分子量:
88.06
EC Number:
204-824-3
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
506211
MDL number:
eCl@ss:
39021320
grade
purum
assay
≥98.0% (T)
refractive index
n20/D 1.428 (lit.), n20/D 1.429
bp
165 °C (lit.)
mp
11-12 °C (lit.)
density
1.268 g/mL at 20 °C, 1.267 g/mL at 25 °C (lit.)
storage temp.
2-8°C
SMILES string
CC(=O)C(O)=O
InChI
1S/C3H4O3/c1-2(4)3(5)6/h1H3,(H,5,6)
InChI key
LCTONWCANYUPML-UHFFFAOYSA-N
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General description
Pyruvic acid is an α-keto-carboxylic acid. It is an metabolic intermediate and is a building unit for many biological compounds. Determination of pyruvic acid in blood and urine samples has been repoted.
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1 - Skin Corr. 1C
存储类别
8A - Combustible corrosive hazardous materials
wgk
WGK 1
flash_point_f
183.2 °F - closed cup
flash_point_c
84 °C - closed cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
法规信息
新产品
此项目有
Pyruvic acid. II. The determination of keto acids in blood and urine.
Friedemann TE and Haugen GE.
The Journal of Biological Chemistry, 147(415), 943-943 (1943)
Christian Henning et al.
The Journal of biological chemistry, 289(41), 28676-28688 (2014-08-29)
Maillard α-dicarbonyl compounds are known as central intermediates in advanced glycation end product (AGE) formation. Glucose is the primary source of energy for the human body, whereas l-threo-ascorbic acid (vitamin C) is an essential nutrient, involved in a variety of
Pyruvic acid, a unique component of an exocellular bacterial polysaccharide.
J H SLONEKER et al.
Nature, 194, 478-479 (1962-05-05)
Robert A Jacobs et al.
American journal of physiology. Endocrinology and metabolism, 304(7), E686-E694 (2013-02-07)
Lactate is an important intermediate metabolite in human bioenergetics and is oxidized in many different tissues including the heart, brain, kidney, adipose tissue, liver, and skeletal muscle. The mechanism(s) explaining the metabolism of lactate in these tissues, however, remains unclear.
Hannes Link et al.
Nature biotechnology, 31(4), 357-361 (2013-03-05)
Recent data suggest that the majority of proteins bind specific metabolites and that such interactions are relevant to metabolic and gene regulation. However, there are no methods to systematically identify functional allosteric protein-metabolite interactions. Here we present an experimental and
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