Lithium trifluoroacetate - ≥95% , CAS No.2923-17-3

CAS: 2923-17-3 Cat. No.: L169327 Molecular Weight: 119.96 EC Number: 220-878-0

GRADE & PURITY ≥95%

Synonyms

SCHEMBL104453 | lithium 2,2,2-trifluoroacetate | lithium;2,2,2-trifluoroacetate | Trifluoroacetic acid lithium salt | Acetic acid, 2,2,2-trifluoro-, lithium salt (1:1) | ACETIC ACID,2,2,2-TRIFLUORO-, LITHIUM SALT (1:1) | AKOS005063529 | J-017445 | MFCD000

Storage

Room temperature,Argon charged

Shipped In

Normal

Specifications

Synonyms

SCHEMBL104453 | lithium 2, 2, 2-trifluoroacetate | lithium;2, 2, 2-trifluoroacetate | Trifluoroacetic acid lithium salt | Acetic acid, 2, 2, 2-trifluoro-, lithium salt (1:1) | ACETIC ACID, 2, 2, 2-TRIFLUORO-, LITHIUM SALT (1:1) | AKOS005063529 | J-017445 | MFCD000

Specifications & Purity

≥95%

Storage

Room temperature, Argon charged

Shipped In

Normal

Purity

≥95%

Names and Identifiers

• Pubchem Sid: 488200367
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488200367
• Canonical Smiles: [Li+].C(=O)(C(F)(F)F)[O-]
• IUPAC Name: lithium;2,2,2-trifluoroacetate
• InChIKey: HSFDLPWPRRSVSM-UHFFFAOYSA-M
• INCHI: 1S/C2HF3O2.Li/c3-2(4,5)1(6)7;/h(H,6,7);/q;+1/p-1
• Isomeric SMILES: [Li+].C(=O)(C(F)(F)F)[O-]
• WGK Germany: 3
• Molecular Weight: 119.96
• Reaxy-Rn: 4021523
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=4021523&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Class Carboxylic acids and derivatives
      • Subclass Alpha-halocarboxylic acids and derivatives

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Class: Carboxylic acids and derivatives
• Subclass: Alpha-halocarboxylic acids and derivatives
• Intermediate Tree Nodes: Not available
• Direct Parent: Alpha-halocarboxylic acids
• Alternative Parents: Carboxylic acid salts Organic metal halides Organic lithium salts Monocarboxylic acids and derivatives Carboxylic acids Organofluorides Organic oxides Hydrocarbon derivatives Carbonyl compounds Alkyl fluorides
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Alpha-halocarboxylic acid - Carboxylic acid salt - Organic metal halide - Organic lithium salt - Carboxylic acid - Organic alkali metal salt - Monocarboxylic acid or derivatives - Alkyl fluoride - Organooxygen compound - Organofluoride - Organohalogen compound - Organic salt - Hydrocarbon derivative - Organic oxide - Carbonyl group - Organic oxygen compound - Alkyl halide - Aliphatic acyclic compound
• Description: This compound belongs to the class of organic compounds known as alpha-halocarboxylic acids. These are carboxylic acids containing a halogen atom bonded to the alpha carbon atom.
• 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

• Sensitivity: Moisture sensitive.
• Molecular Weight: 120.000 g/mol
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 0
• Exact Mass: 120.001 Da
• Monoisotopic Mass: 120.001 Da
• Topological Polar Surface Area: 40.100 Ų
• Heavy Atom Count: 8
• Formal Charge: 0
• Complexity: 87.800
• 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: 2

XLogP3

References

1. Shikai Liu, Linyang Fang, He Ding, Yangyang Zhang, Wenting Li, Bin Liu, Shuming Dong, Boshi Tian, Lili Feng, Piaoping Yang.  (2022)  Alternative Strategy to Optimize Cerium Oxide for Enhanced X-ray-Induced Photodynamic Therapy.  ACS Nano,      [PMID:36378717] [10.1021/acsnano.2c08047]

2. Shikai Liu, Wenting Li, Hengxing Chen, Jialing Zhou, Shuming Dong, Pengyu Zang, Boshi Tian, He Ding, Shili Gai, Piaoping Yang, Yanli Zhao.  (2022)  On-Demand Generation of Peroxynitrite from an Integrated Two-Dimensional System for Enhanced Tumor Therapy.  ACS Nano,      [PMID:35666853] [10.1021/acsnano.1c11422]

3. Shuangshuang Lin, Haiming Hua, Jiyang Li, Peng Zhang, Jinbao Zhao.  (2020)  Lithium carboxylate: Effectively suppressing hydrogen evolution by self-introducing CO2 in aqueous electrolyte.  JOURNAL OF POWER SOURCES,      [PMID:] [10.1016/j.jpowsour.2020.228136]

4. Yuxuan Qiu, Songbin Liu, Junjie Wang, Yushuang Peng, Yutian Yu, Hongyuan Fei, Fengli Yang, Jiaqing Peng, Junjun Tan, Xinyu Ye.  (2025)  Local structure regulation of multiple upconversion emission selectivity in lanthanides highly-doped core-shell nanocrystals.  Journal of Materials Chemistry C,      [PMID:] [10.1039/D5TC00657K]