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Sigma-Aldrich

S-Ethyl trifluorothioacetate

97%

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About This Item

Linear Formula:
CF3COSC2H5
CAS Number:
Molecular Weight:
158.14
Beilstein:
1761564
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

97%

form

liquid

refractive index

n20/D 1.376 (lit.)

bp

90.5 °C (lit.)

density

1.234 g/mL at 25 °C (lit.)

SMILES string

CCSC(=O)C(F)(F)F

InChI

1S/C4H5F3OS/c1-2-9-3(8)4(5,6)7/h2H2,1H3

InChI key

VGGUKFAVHPGNBF-UHFFFAOYSA-N

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Application

S-Ethyl trifluorothioacetate was used to selectively trifluoroacetylate amino groups in proteins.

Pictograms

Flame

Signal Word

Danger

Hazard Statements

Hazard Classifications

Flam. Liq. 2

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

68.0 °F - closed cup

Flash Point(C)

20 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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S Doonan et al.
The Italian journal of biochemistry, 28(6), 441-455 (1979-11-01)
Results obtained as part of a study of the primary structure of mitochondrial aspartate aminotransferase from pig heart are described. In particular, the S-aminoethylated protein was digested with trypsin and with the lysine specific protease from A. mellea. In the
V D Mehta et al.
Bioconjugate chemistry, 5(3), 257-261 (1994-05-01)
Fluorinated proteins have been synthesized and characterized as potential in vivo 19F magnetic resonance imaging (MRI) and spectroscopy (MRS) agents. Proteins labeled with fluorine include bovine serum albumin, gamma-globulin, and purified immunoglobulin (IgG). The amino groups in proteins were selectively
M Kamo et al.
European journal of biochemistry, 255(1), 162-171 (1998-08-06)
A vapor of S-ethyltrifluorothioacetate was found to specifically cleave the amino side of serine and threonine peptide bonds. The cleavage reactions were carried out at 50 degrees C for 6 h-24 h or at 30 degrees C for 24 h.
K L Hastings et al.
Immunopharmacology and immunotoxicology, 17(1), 201-213 (1995-02-01)
Halothane hepatitis appears to result from an inappropriate immune response to the products of halothane metabolism. Attempts to produce an animal model for halothane hepatitis have been largely unsuccessful. Although guinea pigs produce neoantigens following treatment with halothane, the subsequent
María Eliana Defonsi Lestard et al.
The Journal of chemical physics, 131(21), 214303-214303 (2009-12-09)
The molecular structure and conformational properties of S-ethyl trifluorothioacetate, CF(3)COSCH(2)CH(3), were determined in the gas phase by electron diffraction and vibrational spectroscopy (IR and Raman). The experimental investigations were supplemented by ab initio (Moller Plesset of second order) and density

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