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Details

Stereochemistry ACHIRAL
Molecular Formula C2HCl5
Molecular Weight 202.294
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PENTACHLOROETHANE

SMILES

ClC(Cl)C(Cl)(Cl)Cl

InChI

InChIKey=BNIXVQGCZULYKV-UHFFFAOYSA-N
InChI=1S/C2HCl5/c3-1(4)2(5,6)7/h1H

HIDE SMILES / InChI

Molecular Formula C2HCl5
Molecular Weight 202.294
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
[Health risk analysis of VOC/SVOC contaminated soil in an abandoned chemical plant].
2010-02
Discrimination of carcinogens by hepatic transcript profiling in rats following 28-day administration.
2009-11-13
Mechanism of base-promoted dehydrochlorination of pentachloroethane: concerted or stepwise?
2009-04-16
Important bioactive molecules of erythrocytes in colorectal cancer patients after colectomy.
2008-02-27
Carbon and chlorine isotope effects during abiotic reductive dechlorination of polychlorinated ethanes.
2007-07-01
Oxygenases and dehalogenases: molecular approaches to efficient degradation of chlorinated environmental pollutants.
2006-10
Direct electrochemistry and electrochemical catalysis of immobilized hemoglobin in an ethanol-water mixture.
2006-08
Hydration/expansion and cation charge compensation modulate the Brønsted basicity of distorted clay water.
2006-03-28
Biochemical and molecular characterization of a tetrachloroethene dechlorinating Desulfitobacterium sp. strain Y51: a review.
2005-12
Reduction of chlorinated ethanes by nanosized zero-valent iron: kinetics, pathways, and effects of reaction conditions.
2005-08-15
Total degradation of pentachloroethane by an engineered Alcaligenes strain expressing a modified camphor monooxygenase and a hybrid dioxygenase.
2004-06
Reduction of halogenated ethanes by green rust.
2004-01
Linear free-energy relationship analysis of the fate of chlorinated 1- and 2-carbon compounds by redox-manipulated smectite clay minerals.
2003-10
Dehydrochlorination of 1,1,1-trichloroethane and pentachloroethane by microbially reduced ferruginous smectite.
2003-05
Dechlorination of pentachloroethane by commercial Fe and ferruginous smectite.
2002-06
Oxidized cellulose esters: I. Preparation and characterization of oxidized cellulose acetates--a new class of biodegradable polymers.
2002
Branchial elimination of superhydrophobic organic compounds by rainbow trout (Oncorhynchus mykiss).
2001-11-01
Transformation of chlorinated aliphatic compounds by ferruginous smectite.
2001-02-15
A physiologically based toxicokinetic model for lake trout (Salvelinus namaycush).
2001-01
Tetrachloroethane, pentachloroethane, and hexachloroethane: genetic and biochemical studies.
1989
Patents

Patents

Substance Class Chemical
Created
by admin
on Mon Mar 31 21:05:35 GMT 2025
Edited
by admin
on Mon Mar 31 21:05:35 GMT 2025
Record UNII
QOJ9TH7LDL
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
PENTACHLOROETHANE [MI]
Preferred Name English
PENTACHLOROETHANE
MI  
Systematic Name English
PENTACHLOROETHANE [IARC]
Common Name English
Classification Tree Code System Code
EPA PESTICIDE CODE 598300
Created by admin on Mon Mar 31 21:05:35 GMT 2025 , Edited by admin on Mon Mar 31 21:05:35 GMT 2025
IARC Pentachloroethane
Code System Code Type Description
PUBCHEM
6419
Created by admin on Mon Mar 31 21:05:36 GMT 2025 , Edited by admin on Mon Mar 31 21:05:36 GMT 2025
PRIMARY
MESH
C016036
Created by admin on Mon Mar 31 21:05:35 GMT 2025 , Edited by admin on Mon Mar 31 21:05:35 GMT 2025
PRIMARY
WIKIPEDIA
PENTACHLOROETHANE
Created by admin on Mon Mar 31 21:05:35 GMT 2025 , Edited by admin on Mon Mar 31 21:05:35 GMT 2025
PRIMARY
ECHA (EC/EINECS)
200-925-1
Created by admin on Mon Mar 31 21:05:35 GMT 2025 , Edited by admin on Mon Mar 31 21:05:35 GMT 2025
PRIMARY
MERCK INDEX
m8487
Created by admin on Mon Mar 31 21:05:36 GMT 2025 , Edited by admin on Mon Mar 31 21:05:36 GMT 2025
PRIMARY Merck Index
EPA CompTox
DTXSID7021104
Created by admin on Mon Mar 31 21:05:36 GMT 2025 , Edited by admin on Mon Mar 31 21:05:36 GMT 2025
PRIMARY
CAS
76-01-7
Created by admin on Mon Mar 31 21:05:35 GMT 2025 , Edited by admin on Mon Mar 31 21:05:35 GMT 2025
PRIMARY
FDA UNII
QOJ9TH7LDL
Created by admin on Mon Mar 31 21:05:36 GMT 2025 , Edited by admin on Mon Mar 31 21:05:36 GMT 2025
PRIMARY
HSDB
2034
Created by admin on Mon Mar 31 21:05:36 GMT 2025 , Edited by admin on Mon Mar 31 21:05:36 GMT 2025
PRIMARY