247081
3,5-Bis(trifluoromethyl)phenol
95%
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About This Item
Linear Formula:
(CF3)2C6H3OH
CAS Number:
Molecular Weight:
230.11
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
206-488-3
Beilstein/REAXYS Number:
2123670
MDL number:
Assay:
95%
Form:
liquid
InChI key
ODSXJQYJADZFJX-UHFFFAOYSA-N
InChI
1S/C8H4F6O/c9-7(10,11)4-1-5(8(12,13)14)3-6(15)2-4/h1-3,15H
SMILES string
Oc1cc(cc(c1)C(F)(F)F)C(F)(F)F
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.)
functional group
fluoro
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.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
10 - Combustible liquids
wgk
WGK 3
flash_point_f
235.4 °F - closed cup
flash_point_c
113 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
Regulatory Information
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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)
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
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
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