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Merck
CN

D56802

1,2-Dichlorobenzene

ReagentPlus®, 99%

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About This Item

Empirical Formula (Hill Notation):
C6H4Cl2
CAS Number:
95-50-1
Molecular Weight:
147.00
UNSPSC Code:
12191501
NACRES:
NA.04
PubChem Substance ID:
329798810
EC Number:
202-425-9
Beilstein/REAXYS Number:
606078
MDL number:
MFCD00000535
Assay:
99%
Bp:
178-180 °C (lit.)
Vapor pressure:
1.2 mmHg ( 20 °C)
1.6 mmHg ( 35 °C)

Key Documents

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Product Name

1,2-Dichlorobenzene, ReagentPlus®, 99%

InChI key

RFFLAFLAYFXFSW-UHFFFAOYSA-N

InChI

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

SMILES string

Clc1ccccc1Cl

vapor density

5.1 (vs air)

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 %

dilution

(for general lab use)

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.)

Quality Level

100

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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

wgk

WGK 2

pictograms

Exclamation markEnvironment
GHS07,GHS09

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

flash_point_f

150.8 °F - closed cup

flash_point_c

66.0 °C - closed cup

Regulatory Information

危险化学品
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Certificates of Analysis (COA)

Lot/Batch Number
SDBB5522
SHBT1602
SHBT0950
SHBS9178
SDBB2411

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Synthesis and characterization of poly (butylene terephthalate) copolyesters derived from threitol
Ittobane N, et al.
Polymer Composites, 29, S817-S825 (2021)
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)
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
Bimalendu Adhikari et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 17(41), 11488-11496 (2011-09-29)
The N-terminally pyrene-conjugated oligopeptide, Py-Phe-Phe-Ala-OMe, (Py=pyrene 1-butyryl acyl) forms transparent, stable, supramolecular fluorescent organogels in various organic solvents. One of these organogels was thoroughly studied using various techniques including transmission electron microscopy (TEM), field-emission scanning electron microscopy (FESEM), atomic force
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