Skip to Content
Merck

T63002

2,2,2-Trifluoroethanol

ReagentPlus®, ≥99%

Synonym(s):

Trifluoroethyl alcohol

Sign In to View Organizational & Contract Pricing.

Select a Size

Pricing and availability is not currently available.

About This Item

Linear Formula:
CF3CH2OH
CAS Number:
Molecular Weight:
100.04
UNSPSC Code:
12191601
NACRES:
NA.21
PubChem Substance ID:
EC Number:
200-913-6
Beilstein/REAXYS Number:
1733203
MDL number:
Assay:
≥99%
Bp:
77-80 °C (lit.)
Vapor pressure:
70 mmHg ( 25 °C)

Skip To

Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

Product Name

2,2,2-Trifluoroethanol, ReagentPlus®, ≥99%

InChI

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

InChI key

RHQDFWAXVIIEBN-UHFFFAOYSA-N

SMILES string

OCC(F)(F)F

vapor density

3.5 (vs air)

vapor pressure

70 mmHg ( 25 °C)

product line

ReagentPlus®

assay

≥99%

form

liquid

autoignition temp.

~896 °F

expl. lim.

42 %

dilution

(for general lab use)

refractive index

n20/D 1.3 (lit.)

pH

7

bp

77-80 °C (lit.)

mp

−44 °C (lit.)

density

1.373 g/mL at 25 °C (lit.)

Quality Level

Looking for similar products? Visit Product Comparison Guide

Compare Similar Items

View Full Comparison

Show Differences

1 of 4

This Item
8.0825991683426237
Quality Level

100

Quality Level

200

Quality Level

100

Quality Level

200

assay

≥99%

assay

≥99% (GC)

assay

≥99.5% (GC)

assay

99% (CP)

form

liquid

form

liquid

form

-

form

liquid

bp

77-80 °C (lit.)

bp

73.6 °C/1013 hPa

bp

77-80 °C (lit.)

bp

77-80 °C (lit.)

vapor density

3.5 (vs air)

vapor density

-

vapor density

3.5 (vs air)

vapor density

-

autoignition temp.

~896 °F

autoignition temp.

-

autoignition temp.

~896 °F

autoignition temp.

-

Application

2,2,2-Trifluoroethanol can be used as a solvent:
  • In the synthesis of 2-amino-3-cyano-4H-chromene and tetrahydrobenzo[b]pyran derivatives by catalyst free one-pot condensation of aldehydes, malononitrile and resorcinol or dimedone.
  • In the N-formylation of amines with formic acid in the presence of heterogeneous ZIF-8 (zeolitic imidazolate framework) catalyst.
  • In the preparation of 2-substituted-2,3-dihydro-4(1H)-quinazolinone derivatives by condensation of anthranilamide with alkyl, aryl, or heteroaryl ketones or aldehydes.
  • In the mild and selective oxidation of sulfur compounds using H2O2(hydrogen peroxide).

Features and Benefits

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

General description

2,2,2-Trifluoroethanol (TFE) is an organic compound with the chemical formula CF3CH2OH. TFE is a commonly used solvent in organic synthesis. It can also be used as a cosolvent in the experimental study of proteins and peptides.

Legal Information

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

signalword

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

3 - Flammable liquids

wgk

WGK 1

flash_point_f

86.0 °F - closed cup

flash_point_c

30 °C - closed cup


Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Hannah A Strobel et al.
Tissue engineering. Part A, 24(19-20), 1492-1503 (2018-05-05)
Tissue-engineered human blood vessels may enable in vitro disease modeling and drug screening to accelerate advances in vascular medicine. Existing methods for tissue-engineered blood vessel (TEBV) fabrication create homogenous tubes not conducive to modeling the focal pathologies characteristic of certain
Feifei Xu et al.
Clinical proteomics, 17, 3-3 (2020-02-12)
Cancer stem cells (CSCs) are reported to be responsible for tumor initiation, progression, metastasis, and therapy resistance where P-glycoprotein (P-gp) as well as other glycoproteins are involved. Identification of these glycoprotein markers is critical for understanding the resistance mechanism and
Erin K Zess et al.
PLoS biology, 17(7), e3000373-e3000373 (2019-07-23)
Autophagy-related protein 8 (ATG8) is a highly conserved ubiquitin-like protein that modulates autophagy pathways by binding autophagic membranes and a number of proteins, including cargo receptors and core autophagy components. Throughout plant evolution, ATG8 has expanded from a single protein
Deborah Chang et al.
Molecular & cellular proteomics : MCP, 19(9), 1533-1545 (2020-07-01)
Influenza A virus (IAV) mutates rapidly, resulting in antigenic drift and poor year-to-year vaccine effectiveness. One challenge in designing effective vaccines is that genetic mutations frequently cause amino acid variations in IAV envelope protein hemagglutinin (HA) that create new N-glycosylation
Jie E Yang et al.
Scientific reports, 10(1), 7939-7939 (2020-05-16)
Enteroviruses support cell-to-cell viral transmission prior to their canonical lytic spread of virus. Poliovirus (PV), a prototype for human pathogenic positive-sense RNA enteroviruses, and picornaviruses in general, transport multiple virions en bloc via infectious extracellular vesicles, 100~1000 nm in diameter, secreted

Questions

Reviews

No rating value

Active Filters

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service