36627
1,2,4-三氯苯
PESTANAL®, analytical standard
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关于此项目
经验公式（希尔记法）:
C6H3Cl3
化学文摘社编号:
分子量:
181.45
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
EC Number:
204-428-0
Beilstein/REAXYS Number:
956819
MDL number:
InChI key
PBKONEOXTCPAFI-UHFFFAOYSA-N
InChI
1S/C6H3Cl3/c7-4-1-2-5(8)6(9)3-4/h1-3H
SMILES string
Clc1ccc(Cl)c(Cl)c1
grade
analytical standard
vapor density
>6 (vs air)
vapor pressure
1 mmHg ( 40 °C)
product line
PESTANAL®
autoignition temp.
1060 °F
shelf life
limited shelf life, expiry date on the label
expl. lim.
6.6 %, 150 °F
technique(s)
HPLC: suitable, gas chromatography (GC): suitable
refractive index
n20/D 1.571 (lit.)
bp
214 °C (lit.)
mp
16 °C (lit.)
density
1.454 g/mL at 25 °C (lit.)
application(s)
agriculture
environmental
format
neat
Quality Level
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General description
1,2,4-Trichlorobenzene can be used as a solvent for industrial purposes. It can also find applications as a termiticide and lubricant for household uses.
Application
1,2,4-Trichlorobenzene may be used as an eluent in order to determine the polydispersity index and also the molecular weight of benzo[c][1,2,5]oxadiazole based copolymers using high-temperature gel-permeation chromatography (GPC).
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Legal Information
PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Skin Irrit. 2
存储类别
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk
WGK 3
flash_point_f
235.4 °F - closed cup
flash_point_c
113.0 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
危险化学品
此项目有
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Journal of Materials Chemistry, 5(11), 2892-2898 (2017)
National study of chemical residues in fish Volume II (1993)
Tatyana Balandina et al.
Chemical communications (Cambridge, England), 49(22), 2207-2209 (2013-02-12)
STM brings to light chirality aspects of the self-assembly of a functionalized helicene at the interface between a liquid and the solid substrates, gold and graphite. This reveals conditions for conglomerate formation.
Ernest Marco-Urrea et al.
Bioresource technology, 100(23), 5757-5762 (2009-07-21)
Extracellular hydroxyl radical ((*)OH) production via quinone redox cycling in Trametes versicolor, grown in a chemically defined medium, was investigated to degrade trichloroethylene (TCE), perchloroethylene (PCE), 1,2,4- and 1,3,5-trichlorobenzene (TCB). The activity of the enzymes catalyzing the quinone redox cycle
Vijai Elango et al.
Chemosphere, 84(2), 247-253 (2011-05-03)
Using inoculum from a microcosm study that exhibited aerobic transformation of cis-1,2-dichloroethene (cDCE) and trichloroethene (TCE) commensurate with biodegradation of monoaromatic compounds, enrichment cultures were developed by providing benzene, chlorobenzene (CB), dichlorobenzene (DCB) isomers and 1,2,4-trichlorobenzene as carbon and energy
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