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8.08259

Sigma-Aldrich

2,2,2-Trifluoroethanol

for synthesis

Synonym(s):

2,2,2-Trifluoroethanol

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About This Item

Empirical Formula (Hill Notation):
C2H3F3O
CAS Number:
Molecular Weight:
100.04
MDL number:
UNSPSC Code:
12352104
EC Index Number:
200-913-6
NACRES:
NA.22

vapor pressure

70.9 hPa ( 20 °C)

Quality Level

Assay

≥99% (GC)

form

liquid

potency

240 mg/kg LD50, oral (Rat)
1680 mg/kg LD50, skin (Rat)

expl. lim.

8.4-28.8 % (v/v)

pH

7

bp

73.6 °C/1013 hPa

mp

-43.5 °C

transition temp

flash point 30 °C

density

1.38 g/cm3 at 25 °C

storage temp.

2-30°C

InChI

1S/C2H3F3O/c3-2(4,5)1-6/h6H,1H2

InChI key

RHQDFWAXVIIEBN-UHFFFAOYSA-N

General description

2,2,2-Trifluoroethanol (TFE) is a fluorinated compound used as a solvent in organic synthesis. Peptides and proteins are experimentally studied using TEE as a cosolvent. In TFE, hydrogen peroxide is effective for oxidizing sulfur compounds.

Application

2,2,2-Trifluoroethanol is used as a solvent:
  • In the preparation of nylon/Ag composite nanofibers by electrospinning method.
  • To study the combination of two polymers PANI (polyaniline) and PHB (polyhydroxy-butyrate).

Features and Benefits

2,2,2-Trifluoroethanol is more acidic than ethanol due to the presence of electronegative trifluoromethyl group.

Signal Word

Danger

Hazard Classifications

Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Eye Dam. 1 - Flam. Liq. 3 - Repr. 1B - STOT RE 2 Inhalation

Target Organs

Blood

Storage Class Code

3 - Flammable liquids

WGK

WGK 1

Flash Point(F)

86.0 °F - closed cup

Flash Point(C)

30 °C - closed cup


Certificates of Analysis (COA)

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Protocols

Fmoc resin cleavage and deprotection are crucial steps for peptide synthesis, yielding the desired peptide after resin detachment.

Fmoc resin cleavage and deprotection are crucial steps for peptide synthesis, yielding the desired peptide after resin detachment.

Fmoc resin cleavage and deprotection are crucial steps for peptide synthesis, yielding the desired peptide after resin detachment.

Fmoc resin cleavage and deprotection are crucial steps for peptide synthesis, yielding the desired peptide after resin detachment.

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