Chemical structure of 1,1,-Bis (4-Chlorophenyl)-2,2,2-Trichloroethane 4,4'-DTT | 50-29-3
SKU: S2426

Ethyl trifluoroacetate | 383-63-1 | Sarchem Labs

SKU: S2426

Description

9794

Synonym : ethyl trifluoroacetate, trifluoroacetic acid ethyl ester, ethyltrifluoroacetate, acetic acid, trifluoro-, ethyl ester, trifluoroacetic acid, ethyl ester, ethyl trifluoroethanoate, unii-a6tzk6x11x, acetic acid, 2,2,2-trifluoro-, ethyl ester, a6tzk6x11x, ethyl ester of trifluoroacetic acid

Boiling Point 62°C
Color Colorless
UN Number 2924
Formula Weight 142.08
Physical Form Clear Liquid at 20°C
Chemical Name or Material Ethyl Trifluoroacetate

SPECIFICATION

AppearanceN/A
Content of ZincN/A
Boiling PointN / A
Melting PointN/A
Vapor PressureN/A
% Volatile by WeightN/A
Solubility in WaterN/A
DensityN/A
pH of Liquid, Typical (10% soln)N/A
Specific Gravity ApproxN/A
OdorN/A
pHN/A
Flash PointN/A
Ignition temperatureN/A
Lower exposure limitN/A
Upper exposure limitN/A

Safety Information

Classification of the substance or mixture

GHS Label elements, including precautionary statements

Hazards not otherwise classified (HNOC) or not covered by GHS

 

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Ethyl trifluoroacetate | 383-63-1 FAQs

Because it can engage in various organic processes, including esterifications and acylations, ethyl trifluoroacetate is frequently employed to synthesize medicines, agrochemicals, and other speciality chemicals.

The ethyl trifluoroacetate structure, with an ethyl group linked to the trifluoroacetate moiety, is highly reactive and stable, making it ideal for chemical synthesis and industrial uses.

Ethyl trifluoroacetate boiling point is around 105°C, indicating its volatility and appropriateness for reactions that need heat and regulated conditions.

The trifluoroacetic acid structure is composed of a carboxylic acid group (-COOH) coupled with a trifluoromethyl group (-CF3), which gives it distinct features such as high acidity and excellent solubility in polar liquids.

This compound's stable ethyl trifluoroacetate structure makes it very reactive in organic synthesis, allowing for selective acylation and generating a variety of fluorinated intermediates.