643564
3-(Trifluoromethyl)pyridine
97%
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About This Item
Formula empirica (notazione di Hill):
C6H4F3N
Numero CAS:
Peso molecolare:
147.10
Numero CE:
Numero MDL:
Codice UNSPSC:
12352100
ID PubChem:
NACRES:
NA.22
Prodotti consigliati
Saggio
97%
Indice di rifrazione
n20/D 1.418
P. ebollizione
113-115 °C (lit.)
Densità
1.276 g/mL at 25 °C
Gruppo funzionale
fluoro
Stringa SMILE
FC(F)(F)c1cccnc1
InChI
1S/C6H4F3N/c7-6(8,9)5-2-1-3-10-4-5/h1-4H
JTZSFNHHVULOGJ-UHFFFAOYSA-N
Avvertenze
Danger
Indicazioni di pericolo
Consigli di prudenza
Classi di pericolo
Acute Tox. 2 Oral - Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3
Organi bersaglio
Respiratory system
Codice della classe di stoccaggio
3 - Flammable liquids
Classe di pericolosità dell'acqua (WGK)
WGK 2
Punto d’infiammabilità (°F)
73.4 °F - closed cup
Punto d’infiammabilità (°C)
23 °C - closed cup
Dispositivi di protezione individuale
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
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I clienti hanno visto anche
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, 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
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
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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