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Ethyl trifluoroacetate

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Company Name: Hangzhou Qiwei Pharmatech Co.,Ltd
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Products Intro: Product Name:Ethyl trifluoroacetate*
CAS:383-63-1
Purity:0.99 Package:5KG;1KG
Company Name: Shandong Dexiang International Trade Co., Ltd
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Products Intro: Product Name:Ethyl trifluoroacetate
CAS:383-63-1
Purity:99% Package:25kg Remarks:Industrial grade
Company Name: Hebei Weibang Biotechnology Co., Ltd
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Products Intro: Product Name:Ethyl trifluoroacetate
CAS:383-63-1
Purity:99% Package:200KG;1.00;USD
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Products Intro: Product Name:Ethyl Trifluoroacetate
CAS:383-63-1
Purity:99% Package:1KG;10.70;USD
Company Name: Capot Chemical Co.,Ltd.
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Products Intro: Product Name:Ethyl trifluoroacetate
CAS:383-63-1
Purity:98%(Min,GC) Package:100g;1kg;5kg,10kg,25kg,50kg

Ethyl trifluoroacetate manufacturers

  • Ethyl trifluoroacetate
  • Ethyl trifluoroacetate pictures
  • $0.00 / 200kg
  • 2024-10-29
  • CAS:383-63-1
  • Min. Order: 20kg
  • Purity: 99%
  • Supply Ability: 20 tons
Ethyl trifluoroacetate Basic information
Product Name:Ethyl trifluoroacetate
Synonyms:ETHYL TRIFLUOROACETATE;TIMTEC-BB SBB008466;Threetrifluoroacetic acid ethyl ester;cb1020;fd06h11;wu:fd06h11;aceticacid,trifluoro-,ethylester;Ethyl ester of Trifluoroacetic acid
CAS:383-63-1
MF:C4H5F3O2
MW:142.08
EINECS:206-851-6
Product Categories:organofluorine compounds;Building Blocks;C2 to C5;Carbonyl Compounds;Chemical Synthesis;Esters;Organic Building Blocks;Fluoro-Aliphatics ;Acetics acid and esters;Organic Fluorides;Fluorinated Building Blocks;Fluorinating Reagents & Building Blocks for Fluorinated Biochemical Compounds;Synthetic Organic Chemistry;Pharmaceutical intermediates;top;383-63-1;K00001;bc0001
Mol File:383-63-1.mol
Ethyl trifluoroacetate Structure
Ethyl trifluoroacetate Chemical Properties
Melting point -78 °C
Boiling point 60-62 °C(lit.)
density 1.194 g/mL at 25 °C(lit.)
vapor pressure 18.5kPa at 20℃
refractive index n20/D 1.307(lit.)
Fp 30 °F
storage temp. 2-8°C
solubility 4g/l
pka0.43[at 20 ℃]
form Liquid
Specific Gravity1.194
color Clear
PH4 (4g/l, H2O, 20℃)
Water Solubility HYDROLYSIS
Sensitive Moisture Sensitive
BRN 1761411
Stability:Hygroscopic, Moisture Sensitive, Volatile
InChIKeySTSCVKRWJPWALQ-UHFFFAOYSA-N
LogP0.79-1.032 at 25℃
CAS DataBase Reference383-63-1(CAS DataBase Reference)
NIST Chemistry ReferenceAcetic acid, trifluoro-, ethyl ester(383-63-1)
EPA Substance Registry SystemEthyl trifluoroacetate (383-63-1)
Safety Information
Hazard Codes F,Xn,C
Risk Statements 11-22-37/38-41-34
Safety Statements 9-16-26-36/39-45-36/37/39
RIDADR UN 1993 3/PG 2
WGK Germany 1
Hazard Note Flammable/Corrosive
TSCA T
HazardClass 3
PackingGroup II
HS Code 29159080
MSDS Information
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Ethyl trifluoroacetate English
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Ethyl trifluoroacetate Usage And Synthesis
Chemical PropertiesColorless to yellow liquid
UsesEthyl Trifluoroacetate is an intermediate used in the synthesis of various pharmaceutically active molecules and agricultural products. Ethyl Trifluoroacetate is also useful for the preparation of tri fluoroacylated compounds.
UsesWidely used in the synthetic process of medicine, pesticides and organic intermediate.
UsesEthyl trifluoroacetate is used as an intermediate in organic synthesis to prepare organic fluorine compounds like 3-ethyl-1-methylimidazolium trifluoroacetate (EMITA). It is involved in the syntheses of various pharmaceutically active molecules and agricultural products. It is also useful for the preparation of tri fluoroacylated compounds.
PreparationTrifluoroacetic acid and ethanol were used as starting materials with strong-acid cation exchange resin as catalysts at 40 ~ 50 she℃. Add ethanol drop and temperature rising reflux divides the mixture of water and ethanol. After that, collect the mix of thick product ethanol and Ethyl trifluoroacetate. The crude product collected is added a small amount of water, and layering can obtain a content of more than 99.5%. The qualified product Ethyl trifluoroacetate, whose moisture is less than 0.1%, yields more than 95%.
DefinitionChEBI: TRIFLUOROACETIC ACID ETHYL ESTER is an organohalogen compound. It is functionally related to a carboxylic acid.
Synthesis Reference(s)Journal of the American Chemical Society, 72, p. 3527, 1950 DOI: 10.1021/ja01164a056
Flammability and ExplosibilityHighly flammable
Purification MethodsFractionate it through a long Vigreux column (p 11). IR has max at 1800 (CO2) and 1000 (OCO) cm-1 [Fuson et al. J Chem Phys 20 1627 1952, Bergman J Org Chem 23 476 1958]. [Beilstein 2 IV 463.]
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