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1113-60-6

1113-60-6 Structure

1113-60-6 Structure
IdentificationBack Directory
[Name]

-Hydroxypyruvic acid
[CAS]

1113-60-6
[Synonyms]

3-Hydroxypyruvate
hydroxypyruvic aci
3-hydroxypyruvicaci
3-HYDROXYPYRUVIC ACID
β-hydroxypyruvic acid
β-hydroxy Pyruvic Acid
-Hydroxypyruvic acid
3-HYDROXY-2-OXOPROPIONICACID
3-hydroxy-2-oxopropanoic acid
B-hydroxypyruvic acid free acid
Propanoic acid, 3-hydroxy-2-oxo-
Decanoic acid, ester with 2-ethyl-2-(hydroxymethy)-1,3-propanediol octanoate
[Molecular Formula]

C3H4O4
[MDL Number]

MFCD00083380
[MOL File]

1113-60-6.mol
[Molecular Weight]

104.06
Chemical PropertiesBack Directory
[Melting point ]

202℃ (ethanol )
[Boiling point ]

252.9±23.0 °C(Predicted)
[density ]

1.546±0.06 g/cm3(Predicted)
[FEMA ]

3843 | 3-HYDROXY-2-OXOPROPIONIC ACID
[storage temp. ]

2-8°C
[solubility ]

10mg/mL in PBS, pH7.2
[form ]

Solid
[pka]

2.19±0.54(Predicted)
[color ]

Off-white to light brown
[Odor]

at 1.00 % in propylene glycol. sour radish cabbage
[Odor Type]

sour
[JECFA Number]

635
[InChI]

1S/C3H4O4/c4-1-2(5)3(6)7/h4H,1H2,(H,6,7)
[InChIKey]

HHDDCCUIIUWNGJ-UHFFFAOYSA-N
[SMILES]

OC(C(CO)=O)=O || OC(C(CO)=O)=O
[LogP]

-2.04
Safety DataBack Directory
[Hazard Codes ]

C
[Risk Statements ]

22-34
[Safety Statements ]

26-36/37/39-45
[RIDADR ]

UN3261 8/PG 3
[WGK Germany ]

3
[Storage Class]

8A - Combustible corrosive hazardous materials
[Hazard Classifications]

Acute Tox. 4 Oral
Skin Corr. 1B
Hazard InformationBack Directory
[Chemical Properties]

White crystalline powder. Boiling point 257°C. Soluble in water (50g/L, 20°C) and white oil (<100g/kg, 20°C).
[Occurrence]

Reported found in blue cheese, provolone cheese, beer and cocoa
[Uses]

β-Hydroxypyruvic Acid is a metabolite involved in the pathway of carbon in photorespiration. It can also be used to treat fiber.
[Definition]

ChEBI: A 2-oxo monocarboxylic acid that is pyruvic acid in which one of the methyl hydrogens is substituted by a hydroxy group. It is an intermediate involved in the glycine and serine metabolism.
[Biochem/physiol Actions]

Metabolite involved in the pathway of carbon in photorespiration.
[in vivo]

Hydroxypyruvic acid (intravenous injection; 100 mg/ml; slowly over 10 min) increases the 5-h urinary oxalate and glycolate excretion to 0.68% (6.56 μmol) and 0.53% (5.10 μmol) in control rats, in addition, it increases to 2.43% (23.36 μmol) and 0.79% (7.59 μmol) of the dose in the vitamin-B6-deficient rats[1].

Animal Model:SD rat[1]
Dosage:100 mg/ml; slowly over 10 min
Administration:Intravenous injection
Result:Led to a significant increase of urinary oxalate and glycolate excretion in both control and vitamin-B6-deficient rats, but these changes are exaggerated in the vitamin-B6-deficient group.
[IC 50]

Human Endogenous Metabolite
[storage]

Store at -20°C
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