107360

Ácido pirúvico

98%

• Sinónimos: αÁcido α-cetopropiónico, Ácido 2-oxopropiónico
• Fórmula lineal: CH₃COCOOH
• Número de CAS: 127-17-3
• Peso molecular: 88.06
• Beilstein/REAXYS Number: 506211
• EC Number: 204-824-3
• MDL number: MFCD00002585
• UNSPSC Code: 12352100
• eCl@ss: 39021320
• PubChem Substance ID: 24846765
• NACRES: NA.22

Propiedades

• assay: 98%
• refractive index: n20/D 1.428 (lit.)
• bp: 165 °C (lit.)
• mp: 11-12 °C (lit.)
• solubility: H₂O: miscible; alcohol: miscible; diethyl ether: miscible
• density: 1.267 g/mL at 25 °C (lit.)
• functional group: carboxylic acid
• 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

Descripción

Application

Pyruvic acid was used to study the cultivation of previously undescribed soil bacteria as micro colonies using soil substrate membrane system. Pyruvic acid was used to develop a new method for simultaneous determination of organic acids in red wine and must using liquid chromatography.

Biochem/physiol Actions

Pyruvic acid reacts with N-acetyl mannosamine by an aldol-type condensation to form sialic acid. Pyruvic acid is a component of commercial red seaweed polysaccharide. In muscle, pyruvic acid (derived from glycogen) is reduced to lactic acid during exertion, which is reoxidized and partially retransformed to glycogen during rest.

Información de seguridad

• pictograms: GHS05
• signalword: Danger
• hcodes: H314
• pcodes: P280 - P303 + P361 + P353 - P304 + P340 + P310 - P305 + P351 + P338 - P363 - P405
• Hazard Classifications: Eye Dam. 1 - Skin Corr. 1C
• Storage Class: 8A - Combustible corrosive hazardous materials
• wgk_germany: 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