Fluoroethylene carbonate (FEC) - ≥99.5% , CAS No.114435-02-8

CAS: 114435-02-8 Cat. No.: F1491912 Molecular Weight: 106.05 EC Number: 483-360-5

GRADE & PURITY ≥99.5%

Synonyms

Fluoroethylene carbonate | 4-Fluoro-2-oxo-1,3-dioxolane | 4-fluoro-1,3-dioxolan-2-one | EN300-243587 | AS-19415 | 1,3-Dioxolan-2-one, 4-fluoro- | FEC, Lithium Ion Battery Grade

Storage

Store at 2-8°C,Argon charged

Shipped In

Wet ice

Overview

Anhydrous fluoroethylene carbonate (FEC) is a synthetic, organic compound that belongs to the class of compounds known as carbonates. It is a clear, colorless liquid that is highly stable and resistant to hydrolysis, making it an ideal choice for use in a variety of chemical reactions and processes. Fluoroethylene carbonate is typically produced by the reaction of fluoroacetic acid and carbon dioxide.
Application
Battery-grade fluoroethylene carbonate (FEC) is an essential ingredient in high-quality lithium-ion battery electrolytes. Its unique properties, such as its ability to form a stable SEI layer on the anode, help improve the safety, reliability, and performance of lithium-ion batteries. In particular, the addition of battery-grade FEC to the electrolyte can significantly enhance the rate capability, capacity retention, and low-temperature performance of lithium-ion batteries. Battery-grade FEC is compatible with a range of materials used in lithium-ion batteries, including lithium metal, graphite, silicon, and metal oxide cathodes, making it a versatile electrolyte additive. As the demand for high-performance lithium-ion batteries continues to grow in various applications, including electric vehicles and portable electronics, the use of battery-grade FEC as an electrolyte additive is becoming increasingly important in the development of advanced battery technologies.

Specifications

Synonyms

Fluoroethylene carbonate | 4-Fluoro-2-oxo-1, 3-dioxolane | 4-fluoro-1, 3-dioxolan-2-one | EN300-243587 | AS-19415 | 1, 3-Dioxolan-2-one, 4-fluoro- | FEC, Lithium Ion Battery Grade

Specifications & Purity

≥99.5%

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.

Note

The water content of these electrolyte solutions is extremely low; Please operate in an inert and moisture free environment (glove box). Keep the container tightly sealed. Keep away from heat and fire sources. Store in a cool and dry place. Avoid storing with oxidant

Purity

≥99.5%

Names and Identifiers

• Canonical Smiles: C1C(OC(=O)O1)F
• IUPAC Name: 4-fluoro-1,3-dioxolan-2-one
• InChIKey: SBLRHMKNNHXPHG-UHFFFAOYSA-N
• INCHI: 1S/C3H3FO3/c4-2-1-6-3(5)7-2/h2H,1H2
• Isomeric SMILES: C1C(OC(=O)O1)F
• WGK Germany: 1
• Molecular Weight: 106.05
• Reaxy-Rn: 8613769
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=8613769&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Class Organic carbonic acids and derivatives
      • Subclass Carbonic acid diesters

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Class: Organic carbonic acids and derivatives
• Subclass: Carbonic acid diesters
• Intermediate Tree Nodes: Not available
• Direct Parent: Carbonic acid diesters
• Alternative Parents: 1,3-dioxolanes Oxacyclic compounds Organofluorides Organic oxides Hydrocarbon derivatives Carbonyl compounds Alkyl fluorides
• Molecular Framework: Aliphatic heteromonocyclic compounds
• Substituents: Carbonic acid diester - Meta-dioxolane - Oxacycle - Organoheterocyclic compound - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organofluoride - Organohalogen compound - Carbonyl group - Alkyl halide - Alkyl fluoride - Aliphatic heteromonocyclic compound
• Description: This compound belongs to the class of organic compounds known as carbonic acid diesters. These are compounds comprising the carbonic acid diester functional group.
• 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，Air sensitive，Heat sensitive
• Refractive Index: 1.4
• Flash Point(°C): 102 °C
• Boil Point(°C): 210°C
• Melt Point(°C): 20°C
• Molecular Weight: 106.050 g/mol
• XLogP3: -0.300
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 0
• Exact Mass: 106.007 Da
• Monoisotopic Mass: 106.007 Da
• Topological Polar Surface Area: 35.500 Ų
• Heavy Atom Count: 7
• Formal Charge: 0
• Complexity: 92.200
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 1
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1

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