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Catalog Number:
14092
CAS Number:
383-63-1
Trifluoroacétate d'éthyle
Purity:
≥ 99% (GC)
Synonym(s):
Ester éthylique de l'acide trifluoroacétique
Hazmat
Documents
$20.00 /100 g
Taille
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Product Information

Ethyl trifluoroacetate is a versatile chemical compound widely utilized in organic synthesis and various industrial applications. Known for its trifluoromethyl group, this compound serves as an effective reagent in the preparation of fluorinated compounds, which are increasingly important in pharmaceuticals and agrochemicals. Its unique properties allow it to act as a solvent and an intermediate in the synthesis of complex molecules, making it invaluable for researchers and industry professionals alike. Ethyl trifluoroacetate is particularly beneficial in the production of fluorinated esters, which are essential in the development of advanced materials and specialty chemicals.

In addition to its role in synthesis, ethyl trifluoroacetate is recognized for its stability and ease of handling, which enhances its appeal for laboratory use. Its applications extend to the production of fine chemicals and as a building block in the creation of various fluorinated compounds, offering significant advantages over similar compounds due to its trifluoromethyl functionality. This makes it a preferred choice for those looking to innovate in chemical synthesis and product development.

Synonyms
Ester éthylique de l'acide trifluoroacétique
CAS Number
383-63-1
Purity
≥ 99% (GC)
Molecular Formula
C4H5F3O2
Molecular Weight
142.1
MDL Number
MFCD00000419
PubChem ID
9794
Density
1,194 g/mL à 25 °C (Lit.)
Appearance
Liquide clair et incolore
Conditions
Conserver à 0 - 8 °C
General Information
Synonyms
Ester éthylique de l'acide trifluoroacétique
CAS Number
383-63-1
Purity
≥ 99% (GC)
Molecular Formula
C4H5F3O2
Molecular Weight
142.1
MDL Number
MFCD00000419
PubChem ID
9794
Density
1,194 g/mL à 25 °C (Lit.)
Appearance
Liquide clair et incolore
Conditions
Conserver à 0 - 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Oui
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Ethyl trifluoroacetate is widely utilized in research focused on:

  • Synthesis of Fluorinated Compounds: It serves as a key reagent in the synthesis of various fluorinated organic compounds, which are valuable in pharmaceuticals and agrochemicals.
  • Intermediate in Drug Development: This compound is often used as an intermediate in the production of active pharmaceutical ingredients (APIs), enhancing the efficiency of drug formulation processes.
  • Analytical Chemistry: Ethyl trifluoroacetate is employed in analytical techniques such as gas chromatography and mass spectrometry, aiding in the detection and quantification of substances in complex mixtures.
  • Fluorination Reactions: It is utilized in fluorination reactions, providing a method to introduce fluorine atoms into organic molecules, which can improve their biological activity and stability.
  • Polymer Chemistry: The compound finds application in polymer chemistry, where it can be used to modify polymer properties, enhancing their performance in various industrial applications.

Citations