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Ethyl trifluoroacetate

CAS No.
383-63-1
Chemical Name:
Ethyl trifluoroacetate
Synonyms
ETHYL 2,2,2-TRIFLUOROACETATE;ETFA;TFAET;TRIFLUOROACETIC ACID ETHYL ESTER;CF3COOC2H5;RARECHEM AL BI 0416;2,2,2-Trifluoroacetic acid ethyl ester;cb1020;fd06h11;wu:fd06h11
CBNumber:
CB6349488
Molecular Formula:
C4H5F3O2
Molecular Weight:
142.08
MDL Number:
MFCD00000419
MOL File:
383-63-1.mol
MSDS File:
SDS
Last updated:2024-12-18 14:08:57

Ethyl trifluoroacetate 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.)
Flash point 30 °F
storage temp. 2-8°C
solubility 4g/l
pka 0.43[at 20 ℃]
form Liquid
Specific Gravity 1.194
color Clear
PH 4 (4g/l, H2O, 20℃)
Water Solubility HYDROLYSIS
Sensitive Moisture Sensitive
BRN 1761411
Stability Hygroscopic, Moisture Sensitive, Volatile
InChIKey STSCVKRWJPWALQ-UHFFFAOYSA-N
LogP 0.79-1.032 at 25℃
CAS DataBase Reference 383-63-1(CAS DataBase Reference)
FDA UNII A6TZK6X11X
NIST Chemistry Reference Acetic acid, trifluoro-, ethyl ester(383-63-1)
EPA Substance Registry System Ethyl trifluoroacetate (383-63-1)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictogramsGHS hazard pictogramsGHS hazard pictograms
GHS02,GHS05,GHS07
Signal word  Danger
Hazard statements  H225-H302-H315-H318-H335
Precautionary statements  P210-P261-P280-P305+P351+P338
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
NFPA 704
3
2 0

Ethyl trifluoroacetate price More Price(36)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich E50000 Ethyl trifluoroacetate 99% 383-63-1 25g $33.2 2024-03-01 Buy
Sigma-Aldrich E50000 Ethyl trifluoroacetate 99% 383-63-1 100g $110 2024-03-01 Buy
TCI Chemical T0432 Ethyl Trifluoroacetate >99.0%(GC) 383-63-1 25g $35 2024-03-01 Buy
TCI Chemical T0432 Ethyl Trifluoroacetate >99.0%(GC) 383-63-1 100g $98 2024-03-01 Buy
Alfa Aesar A11520 Ethyl trifluoroacetate, 99% 383-63-1 50g $51.9 2024-03-01 Buy
Product number Packaging Price Buy
E50000 25g $33.2 Buy
E50000 100g $110 Buy
T0432 25g $35 Buy
T0432 100g $98 Buy
A11520 50g $51.9 Buy

Ethyl trifluoroacetate Chemical Properties,Uses,Production

Chemical Properties

Colorless to yellow liquid

Uses

Ethyl 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.

Uses

Widely used in the synthetic process of medicine, pesticides and organic intermediate.

Uses

Ethyl 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.

Preparation

Trifluoroacetic 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%.

Definition

ChEBI: 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 Explosibility

Highly flammable

Purification Methods

Fractionate 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.]

354-32-5
64-17-5
383-63-1
Synthesis of Ethyl trifluoroacetate from Trifluoroacetyl chloride and Ethanol
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View Lastest Price from Ethyl trifluoroacetate manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Ethyl trifluoroacetate pictures 2024-12-20 Ethyl trifluoroacetate
383-63-1
US $0.00 / KG 1KG 99% 200mt Jinan Finer Chemical Co., Ltd
Ethyl trifluoroacetate pictures 2024-11-01 Ethyl trifluoroacetate
383-63-1
US $1.00 / KG 1KG 99% 10 mt Hebei Weibang Biotechnology Co., Ltd
Ethyl trifluoroacetate pictures 2024-10-29 Ethyl trifluoroacetate
383-63-1
US $0.00 / kg 20kg 99% 20 tons Qingdao RENAS Polymer Material Co., Ltd.
ETHYL TRIFLUOROACETATE TIMTEC-BB SBB008466 Threetrifluoroacetic acid ethyl ester cb1020 fd06h11 wu:fd06h11 aceticacid,trifluoro-,ethylester Ethyl ester of Trifluoroacetic acid Ethyl trifluoroethanoate ethylperfluoroacetate Trifluoressigsαureethylester trifluoro-aceticaciethylester VITAS-BB TBB000648 3,4,5-Trimethoxybenzenesulfonic Acid Sodium ETHYL TRIFLUOROACETATE 98% (GC) Ethyl trifluoroacetate,99% Ethyl trifluoroacetate 99% 2,2,2-TRIFLOUROETHYL ACETATE (TFAET) Ethyltrifluoracetat trifluoroacetatic acid ethyl ester Ethyl trifluoroacetate, 98+% Ethyl trifluoroaceta Trifluoroacetic acid ethyl Ethyl 4-trifluoroacetate Ethyl trifluoroacetate, 99% 100ML Ethyl trifluoroacetate, 99% 25ML Ethyl trifluoroacetate or Propyl ester Ethyltrifuoroacetate Ethyltrifluoroacetate(ETFA) Ethyl Trifluoroacetate > ETHYL TRIFLUOROACETATE For Synthesis RARECHEM AL BI 0416 ETHYL 2,2,2-TRIFLUOROACETATE TRIFLUOROACETIC ACID ETHYL ESTER CF3COOC2H5 TFAET ETFA 2,2,2-Trifluoroacetic acid ethyl ester Sitagliptin Impurity 76 Ethyl trifluoroacetate(TFAE) Ethyl Trifluoroacetate 98% For Synthesis 383-63-1 CF3CO2C2H5 F3CCOOC2H5 C4H5F3O2 CF3CO2CH2CH3 Building Blocks Carbonyl Compounds C2 to C5 Organic Building Blocks Esters Fluorinated Building Blocks Fluorinating Reagents & Building Blocks for Fluorinated Biochemical Compounds organofluorine compounds Building Blocks C2 to C5 Carbonyl Compounds Chemical Synthesis