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1113-60-6

Basic Information
CAS No.: 1113-60-6
Name: -Hydroxypyruvic acid
Article Data: 49
Molecular Structure:
Molecular Structure of 1113-60-6 (-Hydroxypyruvic acid)
Formula: C3H4 O4
Molecular Weight: 104.062
Synonyms: Pyruvicacid, hydroxy- (6CI,8CI); 2-Oxo-3-hydroxypropionic acid; 3-Hydroxypyruvic acid;Hydroxypyruvic acid; b-Hydroxypyruvic acid
Density: 1.546g/cm3
Melting Point: 202℃ (ethanol )
Boiling Point: 252.9°Cat760mmHg
Flash Point: 121°C
PSA: 74.60000
LogP: -1.36760
Synthetic route
56-81-5

glycerol

A

79-14-1

glycolic Acid

B

1113-60-6

3-hydroxy-2-oxopropionic acid

C

96-26-4

dihydroxyacetone

Conditions
ConditionsYield
With pyridine; dodecacarbonyl triosmium; dihydrogen peroxide In acetonitrile at 60℃; for 13h; Kinetics; Temperature;A 8%
B 1.5%
C 7.5%
With pyridine; dodecacarbonyl triosmium; dihydrogen peroxide In acetonitrile at 60℃; for 5h; Kinetics; Temperature;A 4%
B 2.7%
C 8.3%
312-84-5

D-Serine

1113-60-6

3-hydroxy-2-oxopropionic acid

Conditions
ConditionsYield
With D-amino acid oxide ase from rat's kidney; oxygen
With 2,2'-azinobis(3-ethylbenzthiazolinesulfonate); recombinant Trigonopsis variabilis D-amino acid oxidase, Arg169Ala/Arg220Ala mutant; horseradish peroxidase at 30℃; pH=8; Kinetics; Reagent/catalyst; Temperature; aq. phosphate buffer; Enzymatic reaction;
With human D-amino acid oxidase; Aspergillus niger catalase; flavin adenine dinucleotide at 37℃; for 0.25h; pH=8.3; aq. phosphate buffer; Enzymatic reaction;
4294-45-5

DL-threo-β-hydroxyaspartic acid

127-65-1

chloroamine-T

A

1113-60-6

3-hydroxy-2-oxopropionic acid

B

131543-46-9

Glyoxal

Conditions
ConditionsYield
reag.die neutralen Salze;
87-69-4

L-Tartaric acid

1113-60-6

3-hydroxy-2-oxopropionic acid

Conditions
ConditionsYield
Electrolysis.Elektrolyse in wss. Loesung an Platin;
96-26-4

dihydroxyacetone

1113-60-6

3-hydroxy-2-oxopropionic acid

Conditions
ConditionsYield
With copper(I) sulfate; copper(II) sulfate at 80℃;
1113-59-3

bromopyruvic acid

1113-60-6

3-hydroxy-2-oxopropionic acid

Conditions
ConditionsYield
With sodium hydroxide; water
With sodium hydroxide In water
With alkaline buffer
With lithium hydroxide Yield given;
With alkaline buffer Rate constant; Kinetics; the mechanism of the reaction was investigated by polarography in aqueous solution;
127-17-3

2-oxo-propionic acid

1113-60-6

3-hydroxy-2-oxopropionic acid

Conditions
ConditionsYield
With iodine; glycine
473-81-4

glyceric acid

1113-60-6

3-hydroxy-2-oxopropionic acid

Conditions
ConditionsYield
With αβ-dihydroxyacid dehydratase EC 4.2.1.9 of Salmonella typhimurium Product distribution; αβ-dihydroxyacid dehydratase activity;
With Fructose 1,6-bisphosphate; Bacillus stearothermophilus; triethanolamine hydrochloride; NADH at 25℃; Rate constant; Equilibrium constant; also in presence of Gln102 or Asn enzyme;
1113-60-6

3-hydroxy-2-oxopropionic acid

Conditions
ConditionsYield
With benzylviologen cation radical In water at 25℃; Equilibrium constant; cell free extract of Proteus vulgaris (potassium phosphate buffer pH 7.0), Vmax;
1113-60-6

3-hydroxy-2-oxopropionic acid

Conditions
ConditionsYield
With Fructose 1,6-bisphosphate; oxidized form of nicotineamide adenine dinucleotide In water at 25℃; Rate constant; pH 8.5, reaction in the presence of L-lactate dehydrogenase from Bacillus stearothermophilus (BSLDH 102R) or other enzymes;
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