Sodium pyruvate - PharmPure™, ≥98% , CAS No.113-24-6

CAS: 113-24-6 Cat. No.: GMP1526388 Fórmula: C₃H₃NaO₃ Peso molecular: 110.04 Beilstein Registry Number: 3568341 Número CE: 204-024-4 PubChem CID: 23662274

GRADE & PURITY PharmPure™, ≥98%

Storage

Store at 2-8°C

Shipped In

Wet ice

Visão geral

Sodium pyruvate, derived from pyruvic acid, finds extensive use in cell biology, cell culture, and biochemical research. As the end-product of the glycolysis pathway, where glucose is converted into pyruvate with the energetic production of ATP (Adenosine Triphosphate), pyruvate serves as an intermediary in numerous metabolic pathways, including sugar metabolism. While cells naturally synthesize sodium pyruvate as an intermediate metabolite in glycolysis, it isn′t universally necessary as a supplement for all cell cultures. However, if cells have been cultivated in a medium enriched with sodium pyruvate, it′s advisable to continue its use as cell growth may diminish without it.Sodium pyruvate is frequently incorporated into cell culture formulations to fortify broths and media, enhancing cell survival by providing an easily-accessible carbohydrate energy source alongside glucose. It′s often added to the growth medium, particularly for rapidly proliferating cells like tumor cells. Furthermore, it participates in amino acid metabolism and initiates the Krebs cycle. Cells can readily utilize sodium pyruvate as a carbon source for energy production and crucial metabolic pathways, eliminating the need for biosynthetic production from glucose or amino acids.Certain cell lines require supplemental pyruvate in the culture media due to their inability to convert glucose or amino acids into pyruvate. Additionally, sodium pyruvate serves as a free radical scavenger, effectively quenching reactive oxygen species (ROS) and contributing to cellular health and viability.

Specifications

Especificações e pureza

PharmPure™, ≥98%

Mecanismos bioquímicos e fisiológicos

Sodium Pyruvate has shown antioxidant properties and protective effects against oxygen radicals. Pyruvate is produced as part of glycolysis and is an intermediate in many metabolic pathways. It can be converted into acetyl CoA and enter the TCA Cycle.Sodi

Aplicação

Sodium pyruvate has been used:To culture MCF7 ρ0 (human breast cancer cell line) cells as parent cells. As a supplement in extracellular flux (XF) assay media to incubate cells for measuring oxygen consumption rate (OCR). Aas a supplement in minimum essen

Condições de armazenamento de armazenamento

Store at 2-8°C

Enviado em

Wet ice

Este produto requer transporte de cadeia fria. Serviços terrestres e outros serviços econômicos não estão disponíveis.

Grau

PharmPure™

Nota

Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.

Pureza

≥98%

Nomes e identificadores

Sorrisos canónicos

CC(=O)C(=O)[O-].[Na+]

IUPAC Name

sodium;2-oxopropanoate

InChIKey

DAEPDZWVDSPTHF-UHFFFAOYSA-M

INCHI

1S/C3H4O3.Na/c1-2(4)3(5)6;/h1H3,(H,5,6);/q;+1/p-1

SMILES isoméricas

CC(=O)C(=O)[O-].[Na+]

WGK Alemanha

3

PubChem CID

23662274

Peso molecular

110.04

Beilstein

3568341

Reaxy-Rn

3568341

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: Ketones Carboxylic acid salts Monocarboxylic acids and derivatives Carboxylic acids Organic sodium salts Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Alpha-keto acid - Ketone - Carboxylic acid salt - Organic alkali metal salt - Monocarboxylic acid or derivatives - Carboxylic acid - Carboxylic acid derivative - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organic sodium salt - Organic salt - Organooxygen compound - Carbonyl group - Aliphatic acyclic compound
• Descrição: 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: organic sodium salt

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

Propriedades químicas e físicas

• Solubilidade: Soluble in water.
• Sensibilidade: heat sensitive
• Ponto de fusão (°C): ＞300°C
• Peso molecular: 110.040 g/mol
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 1
• Exact Mass: 109.998 Da
• Monoisotopic Mass: 109.998 Da
• Topological Polar Surface Area: 57.200 Ų
• Heavy Atom Count: 7
• Formal Charge: 0
• Complexity: 88.200
• 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: 2

XLogP3