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Merck
CN

36627

Supelco

1,2,4-三氯苯

PESTANAL®, analytical standard

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About This Item

经验公式(希尔记法):
C6H3Cl3
CAS号:
分子量:
181.45
Beilstein:
956819
EC 号:
MDL编号:
UNSPSC代码:
41116107
PubChem化学物质编号:
NACRES:
NA.24

等级

analytical standard

质量水平

蒸汽密度

>6 (vs air)

蒸汽压

1 mmHg ( 40 °C)

产品线

PESTANAL®

自燃温度

1060 °F

保质期

limited shelf life, expiry date on the label

expl. lim.

6.6 %, 150 °F

技术

HPLC: suitable
gas chromatography (GC): suitable

折射率

n20/D 1.571 (lit.)

bp

214 °C (lit.)

mp

16 °C (lit.)

密度

1.454 g/mL at 25 °C (lit.)

应用

agriculture
environmental

格式

neat

SMILES字符串

Clc1ccc(Cl)c(Cl)c1

InChI

1S/C6H3Cl3/c7-4-1-2-5(8)6(9)3-4/h1-3H

InChI key

PBKONEOXTCPAFI-UHFFFAOYSA-N

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相关类别

一般描述

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.

应用

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.

法律信息

PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany

象形图

Exclamation markEnvironment

警示用语:

Warning

危险声明

危险分类

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Skin Irrit. 2

储存分类代码

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3

闪点(°F)

235.4 °F - closed cup

闪点(°C)

113.0 °C - closed cup

个人防护装备

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

法规信息

危险化学品

Choose from one of the most recent versions:

分析证书(COA)

Lot/Batch Number

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If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

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Novel benzo [c][1, 2, 5] oxadiazole-naphthalenediimide based copolymer for high-performance air-stable n-type field-effect transistors exhibiting high electron mobility of 2.43 cm 2 V- 1 s- 1
Zhao Z, et al.
Journal of Materials Chemistry, 5(11), 2892-2898 (2017)
National study of chemical residues in fish Volume II (1993)
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
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.
Journal of hazardous materials, 166(2-3), 1141-1147 (2009-01-31)
The degradation of 1,2,3-, 1,3,5- and 1,2,4-trichlorobenzene (TCB) by the white-rot fungus Trametes versicolor was studied. Time course experiments showed a degradation rate of 2.27 and 2.49 nmol d(-1)mg(-1) dry weight of biomass during the first 4d of incubation in

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