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Merck
CN

643564

Sigma-Aldrich

3-三氟甲基吡啶

97%

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About This Item

经验公式(希尔记法):
C6H4F3N
CAS号:
分子量:
147.10
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

方案

97%

折射率

n20/D 1.418

沸点

113-115 °C (lit.)

密度

1.276 g/mL at 25 °C

官能团

fluoro

SMILES字符串

FC(F)(F)c1cccnc1

InChI

1S/C6H4F3N/c7-6(8,9)5-2-1-3-10-4-5/h1-4H

InChI key

JTZSFNHHVULOGJ-UHFFFAOYSA-N

象形图

FlameSkull and crossbones

警示用语:

Danger

危险分类

Acute Tox. 2 Oral - Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3

靶器官

Respiratory system

储存分类代码

3 - Flammable liquids

WGK

WGK 2

闪点(°F)

73.4 °F - closed cup

闪点(°C)

23 °C - closed cup

个人防护装备

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

法规信息

新产品

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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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
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
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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