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D56802

Sigma-Aldrich

1,2-Dichlorobenzene

ReagentPlus®, 99%

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

vapor density

5.1 (vs air)

Quality Level

vapor pressure

1.2 mmHg ( 20 °C)
1.6 mmHg ( 35 °C)

product line

ReagentPlus®

Assay

99%

form

liquid

autoignition temp.

1198 °F

expl. lim.

9.2 %

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.)

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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1 of 3

This Item
270598256412
vibrant-m

D56802

1,2-Dichlorobenzene

vibrant-m

270598

1,2-Dichlorobenzene

vibrant-m

256412

1,2,4-Trichlorobenzene

Quality Level

100

Quality Level

100

Quality Level

100

autoignition temp.

1198 °F

autoignition temp.

1198 °F

autoignition temp.

1060 °F

vapor density

5.1 (vs air)

vapor density

5.1 (vs air)

vapor density

>6 (vs air)

expl. lim.

9.2 %

expl. lim.

9.2 %

expl. lim.

6.6 %, 150 °F

density

1.306 g/mL at 25 °C (lit.)

density

1.306 g/mL at 25 °C (lit.)

density

1.454 g/mL at 25 °C (lit.)

Application

1,2-Dichlorobenzene can be used as a solvent:
  • In the Wohl-Ziegler bromination of methoxyimino-o-tolyl-acetic acid methyl esters.
  • To synthesize poly(butyleneterephthalate) copolyesters via polycondensation.

Legal Information

ReagentPlus 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


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Benzylic Brominations with N-Bromosuccinimide in 1, 2-Dichlorobenzene: Effective Preparation of (2-Bromomethyl-phenyl)-Methoxyiminoacetic Acid Methyl Ester
Lee S, et al.
Clean Technologies and Environmental Policy, 22, 269-273 (2016)
Synthesis and characterization of poly (butylene terephthalate) copolyesters derived from threitol
Ittobane N, et al.
Polymer Composites, 29, S817-S825 (2021)
Daisuke Mori et al.
ACS applied materials & interfaces, 3(8), 2924-2927 (2011-07-07)
We have fabricated polymer/polymer blend solar cells consisting of poly(3-hexylthiophene) as the electron donor and poly{2,7-(9,9-didodecylfluorene)-alt-5,5-[4',7'-bis(2-thienyl)-2',1',3'-benzothiadiazole]} as the acceptor. The power conversion efficiency (PCE) was strongly dependent on solvents employed for spin coating. The best PCE of 2.0% was obtained
Cecile A Lagadec et al.
Chemical communications (Cambridge, England), 48(63), 7817-7819 (2012-07-05)
We demonstrate that linear-dendritic shape-isomerism can have an impact on the gelation potential of peptides based on lysine, but the architectural effects can be inverted depending on the choice of functional groups, with the nature of these protecting groups dominating
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

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