643564
3-(Trifluoromethyl)pyridine
97%
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About This Item
Empirical Formula (Hill Notation):
C6H4F3N
CAS Number:
Molecular Weight:
147.10
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
223-268-2
MDL number:
Assay:
97%
InChI key
JTZSFNHHVULOGJ-UHFFFAOYSA-N
InChI
1S/C6H4F3N/c7-6(8,9)5-2-1-3-10-4-5/h1-4H
SMILES string
FC(F)(F)c1cccnc1
assay
97%
refractive index
n20/D 1.418
bp
113-115 °C (lit.)
density
1.276 g/mL at 25 °C
functional group
fluoro
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 2 Oral - Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
3 - Flammable liquids
wgk
WGK 2
flash_point_f
73.4 °F - closed cup
flash_point_c
23 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Regulatory Information
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P M Hext et al.
Toxicology, 72(1), 61-75 (1992-01-01)
The accumulation of [methyl-14C]3-trifluoromethylpyridine (14C-3-FMP) by rat olfactory and hepatic tissue in vivo and in vitro has been investigated. 14C-3-FMP accumulates rapidly and selectively in both tissues in vivo, with an appreciable proportion of this activity being associated with the
B A Gaskell et al.
Toxicology, 50(1), 57-68 (1988-06-01)
Rats exposed by inhalation to 3-trifluoromethylpyridine (3-FMP) for 10, 30 or 90 days showed an unusual response in the nasal passages. Focal histological change including reduction in the number of cell layers, disorganisation, vacuolation and minimal necrosis was confined to
B A Gaskell et al.
Toxicology, 62(1), 35-51 (1990-05-14)
The effects of a single exposure to 3-trifluoromethyl pyridine (3FMP), were investigated in two studies. In the first study, rats were exposed nose only to 0, 50 or 800 ppm 3FMP for periods of 15 min to 4 h. Half
Malcolm E Tessensohn et al.
Chemphyschem : a European journal of chemical physics and physical chemistry, 18(16), 2250-2257 (2017-06-14)
The voltammetric behavior of 2,3,5,6-tetramethyl-1,4-phenylenediamine was found to be able to differentiate the hydrogen acceptor abilities of electroinactive pyridine compounds in acetonitrile. Weak and strong hydrogen acceptors were distinguished through the onset of a third oxidation process that came about
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