Trifluoroethyl acetate - Names and Identifiers
Name | 2,2,2-trifluoroethyl acetate
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Synonyms | Trifluoroethyl acetate 2,2,2-trifluoroethyl acetate 2,2,2-TRIFLUOROETHYL ACETATE 2,2,2-Trifluoroethanol acetate Acetic acid 2,2,2-trifluoroethyl ester 2,2,2-Trifluoroethyl ethanoate, Acetic acid 2,2,2-trifluoroethyl ester 2-Acetoxy-1,1,1-trifluoroethane, 1-(2,2,2-Trifluoroethoxy)ethan-1-one, 2,2,2-Trifluoroethyl ethanoate
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CAS | 406-95-1
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EINECS | 671-427-3 |
InChI | InChI=1/C4H5F3O2/c1-3(8)9-2-4(5,6)7/h2H2,1H3 |
Trifluoroethyl acetate - Physico-chemical Properties
Molecular Formula | C4H5F3O2
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Molar Mass | 142.08 |
Density | 1,258 g/cm3 |
Boling Point | 78 °C |
Flash Point | 11°C |
Water Solubility | Soluble in water (16 g/L) (25°C) |
Specific Gravity | 1.258 |
BRN | 1757502 |
Refractive Index | 1.3202 |
Trifluoroethyl acetate - Risk and Safety
Hazard Symbols | F - Flammable
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Risk Codes | 11 - Highly Flammable
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Safety Description | S16 - Keep away from sources of ignition.
S23 - Do not breathe vapour.
S24/25 - Avoid contact with skin and eyes.
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UN IDs | 3272 |
Hazard Note | Flammable |
Hazard Class | 3 |
Packing Group | III |
Trifluoroethyl acetate - Introduction
2,2,2-trifluoroethyl acetate(2,2,2-trifluoroethyl acetate) is an organic compound. The following is a description of its nature, use, preparation and safety information:
Nature:
-Appearance: 2,2,2-trifluoroethyl acetate is a colorless liquid.
-Boiling point: about 90-95 ℃.
-Density: about 1.24g/cm³.
-Melting point: about -62 ℃.
-Relative molecular mass: about 132.1g/mol.
-Solubility: 2,2,2-trifluoroethyl acetate is soluble in organic solvents, such as alcohols and ethers.
Use:
- 2,2,2-trifluoroethyl acetate are often used as important organic synthesis intermediates.
-It can be used in the synthesis and production of dyes, coatings, adhesives and cosmetics.
-This compound can also be used as a thinner for paints and varnishes.
Preparation Method:
The preparation of 2,2,2-trifluoroethyl acetate is usually carried out by the following steps:
1. First, acetic acid is reacted with 2,2, 2-trifluoroethanol to generate ethyl trifluoroacetate.
2. The reaction can be accelerated using an acidic catalyst (such as sulfuric acid).
Safety Information:
- 2,2,2-trifluoroethyl acetate is an organic compound and should be handled with care. Wear appropriate personal protective equipment such as protective gloves, masks and goggles during operation.
-It has a certain degree of volatility, so avoid inhalation or contact with skin during operation. In case of accidental contact, rinse immediately with plenty of water and seek medical attention immediately.
-Its placement and use should be away from open flames and high temperature sources.
-Please store properly to avoid reaction with oxidants, strong acids or strong bases.
-Waste disposal should comply with local regulations and can be consulted with relevant authorities.
Last Update:2024-04-09 21:01:54