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36707

Supelco

1,2-Dichlorobenzene

PESTANAL®, analytical standard

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About This Item

Empirical Formula (Hill Notation):
C6H4Cl2
CAS Number:
Molecular Weight:
147.00
Beilstein:
606078
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.04

grade

analytical standard

Quality Level

vapor density

5.1 (vs air)

vapor pressure

1.2 mmHg ( 20 °C)
1.6 mmHg ( 35 °C)

product line

PESTANAL®

autoignition temp.

1198 °F

shelf life

limited shelf life, expiry date on the label

expl. lim.

9.2 %

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

refractive index

n20/D 1.551 (lit.)

bp

178-180 °C (lit.)

mp

−18-−17 °C (lit.)

density

1.306 g/mL at 25 °C (lit.)

application(s)

agriculture
environmental

format

neat

SMILES string

Clc1ccccc1Cl

InChI

1S/C6H4Cl2/c7-5-3-1-2-4-6(5)8/h1-4H

InChI key

RFFLAFLAYFXFSW-UHFFFAOYSA-N

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Application

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

Pictograms

Exclamation markEnvironment

Signal Word

Warning

Hazard Classifications

Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1B - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

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

WGK

WGK 2

Flash Point(F)

150.8 °F - closed cup

Flash Point(C)

66.0 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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1,4-Dichlorobenzene for synthesis

Sigma-Aldrich

8.03226

1,4-Dichlorobenzene

1,3-Dichlorobenzene puriss., ≥99.0% (GC)

Sigma-Aldrich

35350

1,3-Dichlorobenzene

Supelco

Supelco

40025

1,4-Dichlorobenzene solution

Alexander S Filatov et al.
Inorganic chemistry, 49(4), 1626-1633 (2010-01-14)
The first example of a reversible [Cu(4)] <--> [Cu(6)] interconversion for polynuclear copper(I) complexes under controlled experimental settings is reported. It illustrates the key role of specific crystal growth conditions for accessing the target cluster nuclearity that consequently determines physical
Marina V Ivanova et al.
International journal of nanomedicine, 7, 403-415 (2012-02-16)
Carbon nanotubes (CNTs) are novel materials with considerable potential in many areas related to nanomedicine. However, a major limitation in the development of CNT-based therapeutic nanomaterials is a lack of reliable and reproducible data describing their chemical and structural composition.
Eric Vejerano et al.
Environmental science & technology, 45(2), 589-594 (2010-12-09)
Previous studies have shown environmentally persistent free radicals (EPFRs) form when chlorine- and hydroxy-substituted benzenes chemisorb on Cu(II)O-containing surfaces under postcombustion conditions. This paper reports the formation of EPFRs on silica particles containing 5% Fe(III)(2)O(3). The EPFRs are formed by
Sungmin Chin et al.
Chemosphere, 75(9), 1206-1209 (2009-03-10)
This study examined the catalytic oxidation of 1,2-dichlorobenzene on V(2)O(5)/TiO(2) nanoparticles. The V(2)O(5)/TiO(2) nanoparticles were synthesized by the thermal decomposition of vanadium oxytripropoxide and titanium tetraisopropoxide. The effects of the synthesis conditions, such as the synthesis temperature and precursor heating
Ivan Guryanov et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 15(46), 12837-12845 (2009-10-23)
The effect of microwave (MW) irradiation and ionic liquids (IL) on the cycloaddition of azomethine ylides to [60]fullerene has been investigated by screening the reaction protocol with regard to the IL medium composition, the applied MW power, and the simultaneous

Protocols

US EPA Method TO-17: GC Analysis of Volatiles on VOCOL® after Collection/Desorption using Air Toxics Tube

US EPA Method 8260 describes the analysis of volatile organic compounds in solid wastes and ground waters. This application illustrates the analysis of many compounds commonly analyzed by this method using purge and trap coupled to GC-MS.

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