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247081

Sigma-Aldrich

3,5-Bis(trifluoromethyl)phenol

95%

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About This Item

Linear Formula:
(CF3)2C6H3OH
CAS Number:
349-58-6
Molecular Weight:
230.11
Beilstein:
2123670
EC Number:
206-488-3
MDL number:
MFCD00000386
UNSPSC Code:
12352100
PubChem Substance ID:
24854849
NACRES:
NA.22

Assay

95%

form

liquid

refractive index

n20/D 1.415 (lit.)

bp

97 °C/50 mmHg (lit.)

mp

20-21 °C (lit.)

density

1.511 g/mL at 25 °C (lit.)

SMILES string

Oc1cc(cc(c1)C(F)(F)F)C(F)(F)F

InChI

1S/C8H4F6O/c9-7(10,11)4-1-5(8(12,13)14)3-6(15)2-4/h1-3,15H

InChI key

ODSXJQYJADZFJX-UHFFFAOYSA-N

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Application

3,5-Bis(trifluoromethyl)phenol (BTMP) has been used as hydrogen donor in synergistic extraction of aluminium (III) and gallium (III) with 2,4-pentanedione in heptane.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

235.4 °F - closed cup

Flash Point(C)

113 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Steric effect of 3, 5-bis (trifluoromethyl) phenol as hydrogen-bond donor on outer-sphere complexation in the synergistic extraction of aluminium (III) and gallium (III) with 2, 4-pentanedione.
Imura H, et al.
Bulletin of the Chemical Society of Japan, 78(12), 2146-2151 (2005)
Douglas H Read et al.
Analytical sciences : the international journal of the Japan Society for Analytical Chemistry, 35(6), 671-677 (2019-02-19)
We describe for the first time hydrogen bonded acid (HBA) polymer, poly{methyl[3-(2-hydroxyl, 4,6-bistrifluoromethyl)phenyl]propylsiloxane}, (DKAP), as stationary phase for gas chromatography (μGC) of organophosphate (OP), chemical warfare agent (CWA) surrogates, dimethylmethylphosphonate (DMMP), diisopropylmethylphosphonate (DIMP), diethylmethylphosphonate (DEMP), and trimethylphosphate (TMP), with high
Nobuyuki Kakutani et al.
Xenobiotica; the fate of foreign compounds in biological systems, 51(1), 88-94 (2020-09-03)
The formation of reactive metabolites (RMs) is a problem in drug development that sometimes results in severe hepatotoxicity. As detecting RMs themselves is difficult, a covalent binding assay using expensive radiolabelled tracers is usually performed for candidate selection. This study

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