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Details

Stereochemistry ACHIRAL
Molecular Formula C6H4Cl2
Molecular Weight 147.002
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 1,4-DICHLOROBENZENE

SMILES

ClC1=CC=C(Cl)C=C1

InChI

InChIKey=OCJBOOLMMGQPQU-UHFFFAOYSA-N
InChI=1S/C6H4Cl2/c7-5-1-2-6(8)4-3-5/h1-4H

HIDE SMILES / InChI

Molecular Formula C6H4Cl2
Molecular Weight 147.002
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Paradichlorobenzene is a chlorinated aromatic hydrocarbon. It is a fumigant insecticide and repellent. Paradichlorobenzene turns directly from a solid into a gas, a process called sublimation. The target organisms are molds, mildews, and insects, but paradichlorobenzene can also be toxic to people and other animals. Most pesticide products containing paradichlorobenzene in the U.S. are used to control clothes moths in airtight containers. Paradichlorobenzene was first registered for use in the United States in 1942, and it is sometimes called 1,4-dichlorobenzene.

CNS Activity

Curator's Comment: Paradichlorobenzene crosses the blood-brain barrier, causing demyelination of nerve fibers and consequent leukoencephalopathy.

Approval Year

TargetsConditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
PubMed

PubMed

TitleDatePubMed
Organic air pollutants inside and outside residences in Shimizu, Japan: levels, sources and risks.
2006-08-01
Analysis of chemical contamination within a canal in a Mexican border colonia.
2006-04
Genotoxicity and toxicity assessment in urban hydrographic basins.
2006-01-31
Higher triplet excited states of benzophenones and bimolecular triplet energy transfer measured by using nanosecond-picosecond two-color/two-laser flash photolysis.
2005-11-04
Carcinogenicity and chronic toxicity in mice and rats exposed by inhalation to para-dichlorobenzene for two years.
2005-10
Gas chromatography-mass spectroscopy analysis of emissions from cement when using ultrasonically driven tools.
2005-10
Rhodococcus phenolicus sp. nov., a novel bioprocessor isolated actinomycete with the ability to degrade chlorobenzene, dichlorobenzene and phenol as sole carbon sources.
2005-10
Determination of 1,2-dibromoethane, 1,4-dichlorobenzene and naphthalene residues in honey by gas chromatography--mass spectrometry using purge and trap thermal desorption extraction.
2005-08-12
Tissue-dependent distribution and accumulation of chlorobenzenes by vegetables in urban area.
2005-08
Communication and re-use of chemical information in bioscience.
2005-07-18
Cross-linking of polyolefins: a study by thermoporosimetry with benzene derivatives as swelling solvents.
2005-06-13
A thermodynamically based method to quantify true sorption hysteresis.
2005-05-13
A field comparison of volatile organic compound measurements using passive organic vapor monitors and stainless steel canisters.
2005-05-01
Thirteen-week inhalation toxicity of p-dichlorobenzene in mice and rats.
2005-05
Effects of perinatal combined exposure to 1,4-dichlorobenzene and 1,1-dichloro-2, 2-bis (p-chlorophenyl) ethylene on rat male offspring.
2005-05
Structure of toluene6.4-ZSM-5 and the toluene disproportionation reaction on ZSM-5.
2005-04
Children's exposure to volatile organic compounds as determined by longitudinal measurements in blood.
2005-03
Structure relationship for catalytic dechlorination rate of dichlorobenzenes in water.
2005-03
[Experimental study on repairing segmental bone defects with three bio-bone derived materials].
2005-02
Catalytic dechlorination kinetics of p-dichlorobenzene over Pd/Fe catalysts.
2005-02
Priority volatile organic compounds in surface waters of the southern North Sea.
2005-01
Levels of polychlorinated biphenyls in 1,4-dichlorobenzene mothballs.
2005
Advanced oxidation degradation of dichlorobenzene in water by the UV/H2O2 process.
2005
Photochemical organic oxidations and dechlorinations with a mu-oxo bridged heme/non-heme diiron complex.
2004-12-27
C1 to C9 volatile organic compound measurements in urban air.
2004-12-01
Formation of PCDD/Fs and PCBs in the process of production of 1,4-dichlorobenzene.
2004-12
Snoring in primary school children and domestic environment: a Perth school based study.
2004-11-04
[Dechlorination of p-dichlorobenzene by metallic catalytic reduction technology].
2004-11
Evaluation of solubilizing ability of humic aggregate basing on the phase-separation model.
2004-11
Symptoms in relation to chemicals and dampness in newly built dwellings.
2004-10
Outdoor, indoor, and personal exposure to VOCs in children.
2004-10
1,4-dichlorobenzene marine risk assessment with special reference to the OSPARCOM region: North Sea.
2004-10
Effects of four chlorobenzenes on serum sex steroids and hepatic microsome enzyme activities in crucian carp, Carassius auratus.
2004-10
Effects of perinatal combined exposure to 1,4-dichlorobenzene and 1,1-dichloro-2, 2-bis (p-chlorophenyl) ethylene (p,p'-DDE) on rat female offspring.
2004-09
Analysis of volatile and semivolatile hydrocarbons recovered from steam-classified municipal solid waste.
2004-07-16
On line biomonitors used as a tool for toxicity reduction evaluation of in situ groundwater remediation techniques.
2004-07-15
Electrochemistry of metal phthalocyanines in organic solvents at variable pressure.
2004-07-12
Polychlorinated dibenzo-p-dioxins and polychlorinated dibenzofurans in 1,4-dichlorobenzene mothballs.
2004-07
Electrochemical reduction of organohalogen compound by noble metal sintered electrode.
2004-07
Fate of volatile organic compounds in constructed wastewater treatment wetlands.
2004-04-01
Emission of volatile organic compounds during composting of municipal solid wastes.
2004-04
Diffusion-based calibration for solid-phase microextraction of benzene, toluene, ethylbenzene, p-xylene and chlorobenzenes from aqueous samples.
2004-01-30
[Interdisciplinary diagnostics in the outpatient treatment department of an environmental medical centre - report on experience with 400 patients].
2004-01
Analysis of BTEX and other substituted benzenes in water using headspace SPME-GC-FID: method validation.
2004-01
[Hygienic standards of the occupational air quality established by the Experts on Chemical Agents, 2002].
2004
Ambient, indoor and personal exposure relationships of volatile organic compounds in Mexico City Metropolitan Area.
2004
Differences in source emission rates of volatile organic compounds in inner-city residences of New York City and Los Angeles.
2004
Spatial and temporal variability of priority volatile organic compounds in the Scheldt estuary.
2003-10-01
Bacterial community dynamics during biostimulation and bioaugmentation experiments aiming at chlorobenzene degradation in groundwater.
2003-08
1,4-Dichlorobenzene.
2002
Patents

Sample Use Guides

In Vivo Use Guide
Curator's Comment: Paradichlorobenzene also has being shown to be administered subcutaneously in mice and rats at doses of 22-67 mg/kg/day https://www.ncbi.nlm.nih.gov/pubmed/17593412
Mice: In an MNT, male and female NMRI mice were treated orally with single dose of 2500mg/kg Paradichlorobenzen. Intraperitoneal treatments of male and female mice with 2 x 177.5 and 2 x 355mg/kg.
Route of Administration: Other
Significant dose-dependent increases of DNA fragmentation, as measured by the Comet assay, and of micronuclei frequency were obtained in primary kidney cells from both rats and humans with the following concentrations of Paradichlorobenzene: from 1.8 to 5.6 mM.
Substance Class Chemical
Created
by admin
on Mon Mar 31 17:33:16 GMT 2025
Edited
by admin
on Mon Mar 31 17:33:16 GMT 2025
Record UNII
D149TYB5MK
Record Status Validated (UNII)
Record Version
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Name Type Language
1,4-DICHLOROBENZENE
HSDB  
Systematic Name English
PARADICHLOROBENZENE
MART.   VANDF   WHO-DD  
Preferred Name English
DICHLORICIDE
Brand Name English
NSC-36935
Code English
BENZENE, 1,4-DICHLORO-
Common Name English
PARADICHLOROBENZENE [MART.]
Common Name English
Paradichlorobenzene [WHO-DD]
Common Name English
1,4-DICHLOROBENZENE [HSDB]
Common Name English
DICHLOROBENZENE, P-
Common Name English
P-DICHLOROBENZENE
MI  
Common Name English
P-DICHLOROBENZENE [MI]
Common Name English
PARADICHLOROBENZENE [VANDF]
Common Name English
PARACIDE
Common Name English
PARAMOTH
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C45386
Created by admin on Mon Mar 31 17:33:17 GMT 2025 , Edited by admin on Mon Mar 31 17:33:17 GMT 2025
EPA PESTICIDE CODE 61501
Created by admin on Mon Mar 31 17:33:17 GMT 2025 , Edited by admin on Mon Mar 31 17:33:17 GMT 2025
Code System Code Type Description
MERCK INDEX
m4336
Created by admin on Mon Mar 31 17:33:17 GMT 2025 , Edited by admin on Mon Mar 31 17:33:17 GMT 2025
PRIMARY Merck Index
MESH
C018511
Created by admin on Mon Mar 31 17:33:17 GMT 2025 , Edited by admin on Mon Mar 31 17:33:17 GMT 2025
PRIMARY
ECHA (EC/EINECS)
203-400-5
Created by admin on Mon Mar 31 17:33:17 GMT 2025 , Edited by admin on Mon Mar 31 17:33:17 GMT 2025
PRIMARY
PUBCHEM
4685
Created by admin on Mon Mar 31 17:33:17 GMT 2025 , Edited by admin on Mon Mar 31 17:33:17 GMT 2025
PRIMARY
NCI_THESAURUS
C44297
Created by admin on Mon Mar 31 17:33:17 GMT 2025 , Edited by admin on Mon Mar 31 17:33:17 GMT 2025
PRIMARY
CAS
106-46-7
Created by admin on Mon Mar 31 17:33:17 GMT 2025 , Edited by admin on Mon Mar 31 17:33:17 GMT 2025
PRIMARY
EPA CompTox
DTXSID1020431
Created by admin on Mon Mar 31 17:33:17 GMT 2025 , Edited by admin on Mon Mar 31 17:33:17 GMT 2025
PRIMARY
ALANWOOD
p-dichlorobenzene
Created by admin on Mon Mar 31 17:33:17 GMT 2025 , Edited by admin on Mon Mar 31 17:33:17 GMT 2025
PRIMARY
EVMPD
SUB22272
Created by admin on Mon Mar 31 17:33:17 GMT 2025 , Edited by admin on Mon Mar 31 17:33:17 GMT 2025
PRIMARY
SMS_ID
100000085829
Created by admin on Mon Mar 31 17:33:17 GMT 2025 , Edited by admin on Mon Mar 31 17:33:17 GMT 2025
PRIMARY
NSC
36935
Created by admin on Mon Mar 31 17:33:17 GMT 2025 , Edited by admin on Mon Mar 31 17:33:17 GMT 2025
PRIMARY
WIKIPEDIA
1,4-DICHLOROBENZENE
Created by admin on Mon Mar 31 17:33:17 GMT 2025 , Edited by admin on Mon Mar 31 17:33:17 GMT 2025
PRIMARY
FDA UNII
D149TYB5MK
Created by admin on Mon Mar 31 17:33:17 GMT 2025 , Edited by admin on Mon Mar 31 17:33:17 GMT 2025
PRIMARY
CHEBI
28618
Created by admin on Mon Mar 31 17:33:17 GMT 2025 , Edited by admin on Mon Mar 31 17:33:17 GMT 2025
PRIMARY
HSDB
523
Created by admin on Mon Mar 31 17:33:17 GMT 2025 , Edited by admin on Mon Mar 31 17:33:17 GMT 2025
PRIMARY
Related Record Type Details
ACTIVE MOIETY