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144657

Sigma-Aldrich

Trifluoroacetamide

97%

Synonym(s):

2,2,2-Trifluoroacetamide

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About This Item

Linear Formula:
CF3CONH2
CAS Number:
Molecular Weight:
113.04
Beilstein:
1753625
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

97%

form

solid

bp

162.5 °C (lit.)

mp

65-70 °C (lit.)

functional group

amide

SMILES string

NC(=O)C(F)(F)F

InChI

1S/C2H2F3NO/c3-2(4,5)1(6)7/h(H2,6,7)

InChI key

NRKYWOKHZRQRJR-UHFFFAOYSA-N

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General description

Trifluoroacetamide is a good quencher of tryptophan fluorescence.

Application

Trifluoroacetamide was used as probe for determination of membrane potential and extra/intracellular volume of erythrocytes by fluorine-19 NMR studies.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

13 - Non Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Chengquan Tan et al.
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The roots of Platycodon grandiflorus are widely used as a crude drug. The active components include a variety of triterpenoid saponins. Recent studies have revealed that Cyt P450 monooxygenases (P450s) function as triterpene oxidases in triterpenoid saponin biosynthesis in many
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Frontiers in plant science, 8, 2098-2098 (2018-01-13)
Glycine, the simplest amino acid in nature and one of the most abundant free amino acids in soil, is regarded as a model nutrient in organic nitrogen studies. To date, many studies have focused on the uptake, metabolism and distribution
P Midoux et al.
Biochimica et biophysica acta, 801(1), 16-25 (1984-09-07)
Trifluoroacetamide was found to be a good quencher of tryptophan fluorescence, and the quenching was shown to proceed via both a dynamic and a static process. The respective quenching constants were determined by the measurement of the decrease of the
Melody Anne de Laat et al.
PloS one, 13(6), e0200070-e0200070 (2018-06-30)
Hyperinsulinemia is a major risk factor for equine laminitis, a debilitating and painful foot condition. Sweet taste receptor (T1R2/3) inhibitors have been used to reduce the insulin and glucose responses to oral carbohydrates in other species. However, their effect in

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