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270598

Sigma-Aldrich

1,2-Dichlorobenzene

suitable for HPLC, 99%

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Empirical Formula (Hill Notation):
C6H4Cl2
CAS Number:
95-50-1
Molecular Weight:
147.00
Beilstein:
606078
EC Number:
202-425-9
MDL number:
MFCD00000535
UNSPSC Code:
12190000
PubChem Substance ID:
329752954
NACRES:
NA.21

vapor density

5.1 (vs air)

Quality Level

100

vapor pressure

1.2 mmHg ( 20 °C)
1.6 mmHg ( 35 °C)

Assay

99%

form

liquid

autoignition temp.

1198 °F

purified by

glass distillation

expl. lim.

9.2 %

technique(s)

HPLC: suitable

impurities

<0.020% water

evapn. residue

<0.0005%

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.)

λ

H2O reference

UV absorption

λ: 296 nm Amax: 1.00
λ: 300 nm Amax: 0.30
λ: 305 nm Amax: 0.20
λ: 335 nm Amax: 0.05
λ: 375-400 nm Amax: 0.01

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


  • Microstructure regulation and enhanced VOC removal performance of carbon aerogels by surface carbon nanotube grown.: This study presents a new method to enhance the removal of volatile organic compounds, including 1,2-Dichlorobenzene, using surface-modified carbon aerogels (Cheng et al., 2024) (Cheng et al., 2024).

  • Role of Electronegativity in Environmentally Persistent Free Radicals (EPFRs) Formation on ZnO.: This research investigates how surface chemistry affects the formation of persistent free radicals, including those from 1,2-Dichlorobenzene on zinc oxide surfaces (Ahmed et al., 2024) (Ahmed et al., 2024).

  • Cu(I) Complexes Catalyzed the Dehydrogenation of N-Heterocycles.: This article discusses the application of copper(I) complexes in catalyzing the dehydrogenation of N-heterocycles, including reactions involving 1,2-Dichlorobenzene derivatives (Shen et al., 2024) (Shen et al., 2024).

  • New Features of Laboratory-Generated EPFRs from 1,2-Dichlorobenzene (DCB) and 2-Monochlorophenol (MCP).: This publication explores the characteristics of laboratory-generated free radicals from 1,2-Dichlorobenzene, shedding light on its environmental impact and degradation processes (Khachatryan et al., 2024) (Khachatryan et al., 2024).

  • Estimate of the C-Cl photoionization cross section and absolute photoionization cross sections of chlorinated organic compounds.: This study provides critical data on the photoionization properties of chlorinated organic compounds, including 1,2-Dichlorobenzene, which is important for understanding its behavior in atmospheric chemistry (Chen et al., 2024) (Chen et al., 2024).

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Pictograms

Exclamation markEnvironment
GHS07,GHS09

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

WGK

WGK 2

Flash Point(F)

closed cup

Flash Point(C)

closed cup

Regulatory Information

危险化学品

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Y Chen et al.
Physical chemistry chemical physics : PCCP, 14(41), 14142-14151 (2012-08-08)
In this perspective article, we discuss the dynamic instability of charge carrier transport in a range of popular organic semiconductors. We observe that in many cases field-effect mobility, an important parameter used to characterize the performance of organic field-effect transistors
Adsorption of 1, 2-dichlorobenzene from water to carbon nanotubes.
Peng X, et al.
Chemical Physics Letters, 376(1), 154-158 (2003)
Catalytic oxidation of 1, 2-dichlorobenzene over supported transition metal oxides.
Krishnamoorthy S, et al.
J. Catal., 193(2), 264-272 (2000)
Sébastien Haar et al.
Scientific reports, 5, 16684-16684 (2015-11-18)
Due to a unique combination of electrical and thermal conductivity, mechanical stiffness, strength and elasticity, graphene became a rising star on the horizon of materials science. This two-dimensional material has found applications in many areas of science ranging from electronics
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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