Lithium L-lactate - ≥98%(T) , CAS No.27848-80-2

CAS: 27848-80-2 Cat. No.: L133140 Molecular Weight: 96.01

GRADE & PURITY ≥98%(T)

Synonyms

Lithium (S)-2-hydroxypropanoate | Lithium L-lactate | L-Lactic acid lithium salt | MFCD00065512 | Propanoic acid,2-hydroxy-,lithium salt(1:1),(2S)- | AKOS024462570 | lithium(1+) (2S)-2-hydroxypropanoate | HY-D0884 | Lithium L-lactate, >=98% (titration) |

Storage

Store at 2-8°C

Shipped In

Wet ice

Specifications

Synonyms

Lithium (S)-2-hydroxypropanoate | Lithium L-lactate | L-Lactic acid lithium salt | MFCD00065512 | Propanoic acid, 2-hydroxy-, lithium salt(1:1), (2S)- | AKOS024462570 | lithium(1+) (2S)-2-hydroxypropanoate | HY-D0884 | Lithium L-lactate, >=98% (titration) |

Specifications & Purity

≥98%(T)

Biochemical and Physiological Mechanisms

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

Shipped In

Wet ice

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

Purity

≥98%(T)

Names and Identifiers

• Pubchem Sid: 504769666
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504769666
• Canonical Smiles: [Li+].CC(C(=O)[O-])O
• IUPAC Name: lithium;(2S)-2-hydroxypropanoate
• InChIKey: GKQWYZBANWAFMQ-DKWTVANSSA-M
• INCHI: 1S/C3H6O3.Li/c1-2(4)3(5)6;/h2,4H,1H3,(H,5,6);/q;+1/p-1/t2-;/m0./s1
• Isomeric SMILES: [Li+].C[C@@H](C(=O)[O-])O
• Molecular Weight: 96.01
• Reaxy-Rn: 3568332
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=3568332&ln=

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 Organic lithium salts Monocarboxylic acids and derivatives Carboxylic acids Organic zwitterions Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Secondary alcohol - Carboxylic acid salt - Organic lithium salt - Organic alkali metal salt - Monocarboxylic acid or derivatives - Carboxylic acid - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - 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

Chemical and Physical Properties

• Solubility: Solubility in Water almost transparency
• Sensitivity: Hygroscopic
• Specific Rotation[α]: -14° (C=5,H2O)
• Melt Point(°C): 253-255°C
• Molecular Weight: 96.000 g/mol
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 1
• Exact Mass: 96.0399 Da
• Monoisotopic Mass: 96.0399 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

References

1. Yiyin Yang, Kangzhou Xie, Donglin Tang.  (2023)  Non-Isocyanate Polyurethanes by Alcoholysis of Alkyl Bisurea with Li Salt-Assisted Melting: Synthesis and Properties.  MACROMOLECULAR CHEMISTRY AND PHYSICS,  224  (8): (2200448).  [PMID:] [10.1002/macp.202200448]