Sodium L-lactate - AR, 60% in water , CAS No.867-56-1

CAS: 867-56-1 Cat. No.: S108837 Formula: C₃H₅NaO₃ Peso molecolare: 112.06 Beilstein Registry Number: 4567087 Numero EC: 212-762-3 PubChem CID: 23664767

GRADE & PURITY AR, 60% in water

Synonyms

L-Lactic acidsodium salt | Sarcolactic acidsodium salt | (S)-2-Hydroxypropionic acidsodium salt

Storage

Store at 2-8°C,Argon charged

Shipped In

Wet ice

Panoramica

A simple 3 carbon sugar produced from pyruvate via LDH in mammals.

Specifications

Sinonimi

L-Lactic acidsodium salt | Sarcolactic acidsodium salt | (S)-2-Hydroxypropionic acidsodium salt

Specifiche e purezza

AR, 60% in water

Meccanismi biochimici e fisiologici

Sodium L-lactate is produced from pyruvate by the enzyme Lacate Dehydrogenase. Lactate production occurs during anaerobic glycolysis or in proliferatively active cells.

Condizioni di conservazione di stoccaggio

Store at 2-8°C,Argon charged

Spedito in

Wet ice

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Grado

AR

Nomi e identificatori

Pubchem Sid

508810634

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/508810634

Sorrisi canonici

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

IUPAC Name

sodium;(2S)-2-hydroxypropanoate

InChIKey

NGSFWBMYFKHRBD-DKWTVANSSA-M

INCHI

1S/C3H6O3.Na/c1-2(4)3(5)6;/h2,4H,1H3,(H,5,6);/q;+1/p-1/t2-;/m0./s1

Isomeri SMILES

C[C@@H](C(=O)[O-])O.[Na+]

WGK Germania

1

PubChem CID

23664767

Peso molecolare

112.06

Beilstein

4567087

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Classe Carboxylic acids and derivatives
      • Subclass Carboxylic acid derivatives

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Classe: Carboxylic acids and derivatives
• Subclass: Carboxylic acid derivatives
• Intermediate Tree Nodes: Not available
• Direct Parent: Carboxylic acid salts
• Alternative Parents: Secondary alcohols Monocarboxylic acids and derivatives Carboxylic acids Organic zwitterions Organic sodium salts Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Secondary alcohol - Carboxylic acid salt - Organic alkali metal salt - Monocarboxylic acid or derivatives - Carboxylic acid - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organic sodium salt - Organic salt - Organic zwitterion - Organooxygen compound - Carbonyl group - Alcohol - Aliphatic acyclic compound
• Descrizione: This compound belongs to the class of organic compounds known as carboxylic acid salts. These are ionic derivatives of carboxylic acid.
• External Descriptors: Not available

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

Obiettivi associati (umani)

CA2 Tclin Carbonic anhydrase II (17698 Activities)

Discover Target: CA2

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Obiettivi associati (non umani)

Carbonic anhydrase (69 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Meccanismi d'azione

Proprietà chimiche e fisiche

• Solubilità: Soluble in water (50 mg/ml).
• Sensibilità: Moisture sensitive.
• Indice di rifrazione: 1.422-1.425
• Punto di fusione (°C): 163-165°C
• Peso molecolare: 112.060 g/mol
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 1
• Exact Mass: 112.014 Da
• Monoisotopic Mass: 112.014 Da
• Topological Polar Surface Area: 60.400 Ų
• Heavy Atom Count: 7
• Formal Charge: 0
• Complexity: 63.200
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 1
• 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

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