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

CAS: 867-56-1 Cat. No.: S108837 Molecular Weight: 112.06 Beilstein Registry Number: 4567087 EC Number: 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

Overview

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

Specifications

Synonyms

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

Specifications & Purity

AR, 60% in water

Biochemical and Physiological Mechanisms

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

Storage

Store at 2-8°C, Argon charged

Shipped In

Wet ice

This product requires cold chain shipping. Ground and other economy services are not available.

Grade

AR

Names and Identifiers

• Canonical Smiles: 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
• Isomeric SMILES: C[C@@H](C(=O)[O-])O.[Na+]
• WGK Germany: 1
• PubChem CID: 23664767
• Molecular Weight: 112.06
• Beilstein: 4567087

Taxonomic Classification

Taxonomy Tree

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

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Class: 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
• Description: 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

Associated Targets(Human)

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

Associated Targets(non-human)

Carbonic anhydrase (69 Activities)

Explore this target

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

Mechanisms of Action

Chemical and Physical Properties

• Solubility: Soluble in water (50 mg/ml).
• Sensitivity: Moisture sensitive.
• Refractive Index: 1.422-1.425
• Melt Point(°C): 163-165°C
• Molecular Weight: 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

XLogP3

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