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Sodium lactate - 10mM in DMSO, high purity , CAS No.867-56-1

    Grade & Purity:
  • 10mM in DMSO
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Item Number
S426464
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S426464-1ml
1ml
Available within 4-8 weeks(?)
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$172.90
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Compound libraries (12325)

Basic Description

Synonyms Sodium L-lactate | 867-56-1 | sodium (S)-2-hydroxypropanoate | Sodium (S)-lactate | Sodium-L-lactate | L-Lactic acid sodium salt | Sodium lactate, l- | Propanoic acid, 2-hydroxy-, monosodium salt, (2S)- | (S)-2-Hydroxypropionic acid sodium salt | L-(+)-Lactic acid sodium s
Specifications & Purity 10mM in DMSO
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 Temp Store at -80°C
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Product Description

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

Taxonomic Classification

Taxonomy Tree

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

Associated Targets(Human)

CA2 Tclin Carbonic anhydrase II (17698 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Associated Targets(non-human)

Carbonic anhydrase (69 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Mechanisms of Action

Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References

Names and Identifiers

IUPAC Name sodium;(2S)-2-hydroxypropanoate
INCHI InChI=1S/C3H6O3.Na/c1-2(4)3(5)6;/h2,4H,1H3,(H,5,6);/q;+1/p-1/t2-;/m0./s1
InChIKey NGSFWBMYFKHRBD-DKWTVANSSA-M
Smiles CC(C(=O)[O-])O.[Na+]
Isomeric SMILES C[C@@H](C(=O)[O-])O.[Na+]
WGK Germany 1
PubChem CID 23664767
Molecular Weight 112.06
Beilstein 4567087

Certificates(CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Chemical and Physical Properties

Sensitivity Moisture sensitive.
Refractive Index 1.422-1.425
Melt Point(°C) 163-165°C
Molecular Weight 112.060 g/mol
XLogP3
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

Citations of This Product

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