Lithium acetate dihydrate - PrimorTrace™, ≥99.99% metals basis, used for Separation of saturated and unsaturated fatty acids. Used in the pharmaceutical industry for preparing diuretics and as raw materials for lithium-ion batteries various applications ,

CAS: 6108-17-4 Cat. No.: L105192 Formula: CH₃COOLi·2H₂O Peso molecolare: 102.02 Beilstein Registry Number: 3564320 Numero EC: 612-081-5

GRADE & PURITY PrimorTrace™, ≥99.99% metals basis

Synonyms

DTXSID40209954 | IAQLJCYTGRMXMA-UHFFFAOYSA-M | Lithium acetate dihydrate, BioXtra | T460029GB5 | Lithium acetate dihydrate, Vetec(TM) reagent grade | LiOAc-2H2O | Lithium acetate dihydrate, Reagent Grade | Lithium acetate dihydrate, purum p.a., crystalliz

Storage

Room temperature,Desiccated

Shipped In

Normal

Panoramica

Prone to deliquescence, soluble in water and alcohol, with a nearly neutral aqueous solution.

Specifications

Sinonimi

DTXSID40209954 | IAQLJCYTGRMXMA-UHFFFAOYSA-M | Lithium acetate dihydrate, BioXtra | T460029GB5 | Lithium acetate dihydrate, Vetec(TM) reagent grade | LiOAc-2H2O | Lithium acetate dihydrate, Reagent Grade | Lithium acetate dihydrate, purum p.a., crystalliz

Specifiche e purezza

PrimorTrace™, ≥99.99% metals basis

Applicazione

Separation of saturated and unsaturated fatty acids. Used in the pharmaceutical industry for preparing diuretics and as raw materials for lithium-ion batteries

Condizioni di conservazione di stoccaggio

Room temperature,Desiccated

Spedito in

Normal

Grado

PrimorTrace™

Purezza

≥99.99% metals basis

Nomi e identificatori

Pubchem Sid

508816768

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/508816768

Sorrisi canonici

[Li+].CC(=O)[O-].O.O

IUPAC Name

lithium;acetate;dihydrate

InChIKey

IAQLJCYTGRMXMA-UHFFFAOYSA-M

INCHI

1S/C2H4O2.Li.2H2O/c1-2(3)4;;;/h1H3,(H,3,4);;2*1H2/q;+1;;/p-1

Isomeri SMILES

[Li+].CC(=O)[O-].O.O

Peso molecolare

102.02

Beilstein

3564320

Reaxy-Rn

3573992

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=3573992&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Classe Carboxylic acids and derivatives
      • Subclass Carboxylic acid derivatives
        • Level5 Carboxylic acid salts
          • Level6 Acetate salts

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Classe: Carboxylic acids and derivatives
• Subclass: Carboxylic acid derivatives
• Intermediate Tree Nodes: Carboxylic acid salts
• Direct Parent: Acetate salts
• Alternative Parents: Organic lithium salts Monocarboxylic acids and derivatives Carboxylic acids Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Acetate salt - Organic lithium salt - Organic alkali metal salt - Monocarboxylic acid or derivatives - Carboxylic acid - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organic salt - Organooxygen compound - Carbonyl group - Aliphatic acyclic compound
• Descrizione: This compound belongs to the class of organic compounds known as acetate salts. These are organic compounds containing acetic acid as its acid component.
• 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

Proprietà chimiche e fisiche

• Sensibilità: Moisture sensitive
• Punto di fusione (°C): 53-56 °C (lit.)
• Peso molecolare: 102.000 g/mol
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 0
• Exact Mass: 102.05 Da
• Monoisotopic Mass: 102.05 Da
• Topological Polar Surface Area: 42.100 Ų
• Heavy Atom Count: 7
• Formal Charge: 0
• Complexity: 34.600
• 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: 4

XLogP3