Pyruvic acid - ≥98%(T) , CAS No.127-17-3

CAS: 127-17-3 Cat. No.: P104138 Formula: C₃H₄O₃ Peso molecolare: 88.06 Beilstein Registry Number: 506211 Numero EC: 204-824-3

QUALITÀ & PUREZZA ≥98%(T)

Synonyms

13C Labeled pyruvic acid | Brenztraubensaeure | 2-Oxopropansaure | bmse000112 | B3CFF0AD-2F35-484C-B062-4AC88A1B2830 | Tox21_303284 | C00022 | EINECS 204-824-3 | 2-Oxopropanoic acid, Pyroracemic acid | AKOS000118803 | AMY6082 | Pyruvic acid (natural) | Py

Storage

Store at 2-8°C,Argon charged

Shipped In

Wet ice

Panoramica

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.

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.

Specifiche

Sinonimi

13C Labeled pyruvic acid | Brenztraubensaeure | 2-Oxopropansaure | bmse000112 | B3CFF0AD-2F35-484C-B062-4AC88A1B2830 | Tox21_303284 | C00022 | EINECS 204-824-3 | 2-Oxopropanoic acid, Pyroracemic acid | AKOS000118803 | AMY6082 | Pyruvic acid (natural) | Py

Specifiche e purezza

≥98%(T)

Meccanismi biochimici e fisiologici

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

Condizioni di conservazione di stoccaggio

Store at 2-8°C,Argon charged

Spedito in

Wet ice

Questo prodotto richiede spedizione a catena fredda. I servizi di terra e altri servizi economici non sono disponibili.

Purezza

≥98%(T)

Nomi e identificatori

Pubchem Sid

508811713

Sorrisi canonici

CC(=O)C(=O)O

IUPAC Name

2-oxopropanoic acid

InChIKey

LCTONWCANYUPML-UHFFFAOYSA-N

INCHI

1S/C3H4O3/c1-2(4)3(5)6/h1H3,(H,5,6)

Isomeri SMILES

CC(=O)C(=O)O

WGK Germania

3

Numero UN

3265

Peso molecolare

88.06

Beilstein

506211

Reaxy-Rn

506211

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=506211&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Classe Keto acids and derivatives
      • Subclass Alpha-keto acids and derivatives

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Classe: Keto acids and derivatives
• Subclass: Alpha-keto acids and derivatives
• Intermediate Tree Nodes: Not available
• Direct Parent: Alpha-keto acids and derivatives
• Alternative Parents: Alpha-hydroxy ketones Monocarboxylic acids and derivatives Carboxylic acids Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Alpha-keto acid - Alpha-hydroxy ketone - Ketone - Monocarboxylic acid or derivatives - Carboxylic acid - Carboxylic acid derivative - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Carbonyl group - Aliphatic acyclic compound
• Descrizione: This compound belongs to the class of organic compounds known as alpha-keto acids and derivatives. These are organic compounds containing an aldehyde substituted with a keto group on the adjacent carbon.
• External Descriptors: Oxo fatty acids

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

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Meccanismi d'azione

Proprietà chimiche e fisiche

• Solubilità: Miscible with chloroform and methanol.
• Sensibilità: Heat,Light & Air Sensitive.
• Indice di rifrazione: 1.426-1.43
• Punto di infiammabilità (°F): 82℃
• Punto di infiammabilità (°C): 82℃
• Punto di ebollizione (°C): 165℃
• Punto di fusione (°C): 11-13 °C
• Peso molecolare: 88.060 g/mol
• XLogP3: -0.300
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 1
• Exact Mass: 88.016 Da
• Monoisotopic Mass: 88.016 Da
• Topological Polar Surface Area: 54.400 Ų
• Heavy Atom Count: 6
• Formal Charge: 0
• Complexity: 84.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1