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Merck

36707

1,2-Dichlorobenzene

PESTANAL®, analytical standard

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About This Item

Empirical Formula (Hill Notation):
C6H4Cl2
CAS Number:
Molecular Weight:
147.00
UNSPSC Code:
41116107
NACRES:
NA.04
PubChem Substance ID:
EC Number:
202-425-9
Beilstein/REAXYS Number:
606078
MDL number:
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Product Name

1,2-Dichlorobenzene, PESTANAL®, analytical standard

InChI key

RFFLAFLAYFXFSW-UHFFFAOYSA-N

InChI

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

SMILES string

Clc1ccccc1Cl

grade

analytical standard

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

Quality Level

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Legal Information

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

Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

pictograms

Exclamation markEnvironment

signalword

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

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

ppe

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


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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
Eranda Maligaspe et al.
The journal of physical chemistry. A, 114(1), 268-277 (2009-11-26)
Singlet-singlet energy transfer in self-assembled via axial coordination of imidazole-appended (at different positions of one of the meso-phenyl entities) free-base tetraphenylporphyrin, H(2)PIm, to either zinc phthalocyanine, ZnPc, or zinc naphthalocyanine, ZnNc, dyads is investigated in noncoordinating solvents, o-dichlorobenzene and toluene
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
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
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

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