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Details

Stereochemistry ACHIRAL
Molecular Formula C2H3Cl3
Molecular Weight 133.404
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of TRICHLOROETHANE

SMILES

CC(Cl)(Cl)Cl

InChI

InChIKey=UOCLXMDMGBRAIB-UHFFFAOYSA-N
InChI=1S/C2H3Cl3/c1-2(3,4)5/h1H3

HIDE SMILES / InChI

Molecular Formula C2H3Cl3
Molecular Weight 133.404
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

1,1,1-trichloroethane (methyl chloroform) is a colorless liquid or vapour with a sharp sweet smell. It dissolves in water and other chemicals and easily evaporates into the air. TCE is non-flammable. Trichloroethane is used as a solvent and degreasing agent in industry. It is an ingredient in consumer products such as household cleaners, glues, and aerosol sprays. Methyl chloroform is also used as a chemical intermediate in the production of vinylidene chloride. It was formerly used as a food and grain fumigant. Excessive absorption of this substance through the lungs or gastrointestinal tract produces central nervous system (CNS) depression proportional to the amount absorbed. Mild liver and kidney dysfunction may occur transiently following recovery from CNS depression. The consumption of trichloroethane has been banned by the 1987 Montreal Protocol because of its ozone-depleting potential.

CNS Activity

Curator's Comment: Excessive absorption of trichloroethane through the lungs or gastrointestinal tract produces central nervous system (CNS) depression proportional to the amount absorbed.

Approval Year

Doses

Doses

DosePopulationAdverse events​
735 ppm multiple, respiratory
Studied dose
Dose: 735 ppm
Route: respiratory
Route: multiple
Dose: 735 ppm
Sources:
healthy, 16 years
Health Status: healthy
Age Group: 16 years
Sex: M
Sources:
Other AEs: Death...
17718 ppm multiple, respiratory
Studied dose
Dose: 17718 ppm
Route: respiratory
Route: multiple
Dose: 17718 ppm
Sources:
healthy, 27 years
Health Status: healthy
Age Group: 27 years
Sex: M
Sources:
Other AEs: Hepatitis...
Other AEs:
Hepatitis
Sources:
1380 ppm 1 times / day single, respiratory
Studied dose
Dose: 1380 ppm, 1 times / day
Route: respiratory
Route: single
Dose: 1380 ppm, 1 times / day
Sources:
healthy, 30 to 60 years
Health Status: healthy
Age Group: 30 to 60 years
Sex: M
Sources:
Other AEs: Anesthesia...
1 % 1 times / day single, topical
Studied dose
Dose: 1 %, 1 times / day
Route: topical
Route: single
Dose: 1 %, 1 times / day
Sources:
healthy, 30 years
Health Status: healthy
Age Group: 30 years
Sex: M
Sources:
Other AEs: Contact dermatitis...
Other AEs:
Contact dermatitis
Sources:
90 % multiple, topical
Studied dose
Dose: 90 %
Route: topical
Route: multiple
Dose: 90 %
Sources:
healthy, 31 years
Health Status: healthy
Age Group: 31 years
Sex: M
Sources:
Other AEs: Paresthesia distal...
Other AEs:
Paresthesia distal
Sources:
1 oz 1 times / day single, oral
Studied dose
Dose: 1 oz, 1 times / day
Route: oral
Route: single
Dose: 1 oz, 1 times / day
Sources:
healthy, 47 years
Health Status: healthy
Age Group: 47 years
Sex: M
Sources:
Other AEs: Nausea, Vomiting...
Other AEs:
Nausea
Vomiting
Diarrhea
Sources:
AEs

AEs

AESignificanceDosePopulation
Death
735 ppm multiple, respiratory
Studied dose
Dose: 735 ppm
Route: respiratory
Route: multiple
Dose: 735 ppm
Sources:
healthy, 16 years
Health Status: healthy
Age Group: 16 years
Sex: M
Sources:
Hepatitis
17718 ppm multiple, respiratory
Studied dose
Dose: 17718 ppm
Route: respiratory
Route: multiple
Dose: 17718 ppm
Sources:
healthy, 27 years
Health Status: healthy
Age Group: 27 years
Sex: M
Sources:
Anesthesia
1380 ppm 1 times / day single, respiratory
Studied dose
Dose: 1380 ppm, 1 times / day
Route: respiratory
Route: single
Dose: 1380 ppm, 1 times / day
Sources:
healthy, 30 to 60 years
Health Status: healthy
Age Group: 30 to 60 years
Sex: M
Sources:
Contact dermatitis
1 % 1 times / day single, topical
Studied dose
Dose: 1 %, 1 times / day
Route: topical
Route: single
Dose: 1 %, 1 times / day
Sources:
healthy, 30 years
Health Status: healthy
Age Group: 30 years
Sex: M
Sources:
Paresthesia distal
90 % multiple, topical
Studied dose
Dose: 90 %
Route: topical
Route: multiple
Dose: 90 %
Sources:
healthy, 31 years
Health Status: healthy
Age Group: 31 years
Sex: M
Sources:
Diarrhea
1 oz 1 times / day single, oral
Studied dose
Dose: 1 oz, 1 times / day
Route: oral
Route: single
Dose: 1 oz, 1 times / day
Sources:
healthy, 47 years
Health Status: healthy
Age Group: 47 years
Sex: M
Sources:
Nausea
1 oz 1 times / day single, oral
Studied dose
Dose: 1 oz, 1 times / day
Route: oral
Route: single
Dose: 1 oz, 1 times / day
Sources:
healthy, 47 years
Health Status: healthy
Age Group: 47 years
Sex: M
Sources:
Vomiting
1 oz 1 times / day single, oral
Studied dose
Dose: 1 oz, 1 times / day
Route: oral
Route: single
Dose: 1 oz, 1 times / day
Sources:
healthy, 47 years
Health Status: healthy
Age Group: 47 years
Sex: M
Sources:
Overview

Overview

CYP3A4CYP2C9CYP2D6hERG

OverviewOther

Other InhibitorOther SubstrateOther Inducer





Drug as perpetrator​

Drug as perpetrator​

TargetModalityActivityMetaboliteClinical evidence
likely
Drug as victim
Sourcing

Sourcing

Vendor/AggregatorIDURL
PubMed

PubMed

TitleDatePubMed
1,1,1-trichloroethane marine risk assessment with special reference to the OSPARCOM region: North Sea.
2004-10
Batch-test study on the dechlorination of 1,1,1-trichloroethane in contaminated aquifer material by zero-valent iron.
2004-10
Neurologic abnormalities in workers of a 1-bromopropane factory.
2004-09
Chlorinated hydrocarbon solvents.
2004-08
Biologic markers of exposure to chlorinated solvents.
2004-08
Trichloroethylene and cardiac malformations.
2004-08
Acute effects of 1,1,1-trichloroethane on human olfactory functioning.
2004-05-22
Intravenous self-administration of abused solvents and anesthetics in mice.
2004-02-06
Photolysis of chloral under atmospheric conditions.
2004-02-01
Rapid and sensitive static headspace gas chromatography-mass spectrometry method for the analysis of ethanol and abused inhalants in blood.
2004-01-25
Synthesis and protection of aryl sulfates using the 2,2,2-trichloroethyl moiety.
2004-01-22
Pi-halogen dimer interactions and the inclusion chemistry of a new tetrahalo aryl host.
2004-01-21
Changes in the regional emissions of greenhouse gases and ozone-depleting compounds.
2004-01-15
Reduction of halogenated ethanes by green rust.
2004-01
Ambient, indoor and personal exposure relationships of volatile organic compounds in Mexico City Metropolitan Area.
2004
Personal, indoor, and outdoor VOC exposures in a probability sample of children.
2004
Investigation of the inhibitory effect of silica on the degradation of 1,1,1-trichloroethane by granular iron.
2003-12-15
The effect of multicomponent diffusion on NAPL dissolution from spherical ternary mixtures.
2003-12
Comparative study of the effects of toluene, benzene, 1,1,1-trichloroethane, diethyl ether, and flurothyl on anxiety and nociception in mice.
2003-11-15
VOC removal from contaminated groundwater through membrane pervaporation. (II): 1,1,1-trichloroethane-SDS surfactant solution system.
2003-11
Adsorption of volatile organic compounds by pecan shell- and almond shell-based granular activated carbons.
2003-11
Linear free-energy relationship analysis of the fate of chlorinated 1- and 2-carbon compounds by redox-manipulated smectite clay minerals.
2003-10
Six interaction profiles for simple mixtures.
2003-10
Dissolution of entrapped DNAPLs in variable aperture fractures: experimental data and empirical model.
2003-09-15
Biofiltration of 1,1,1-trichloroethane by a trickle-bed air biofilter.
2003-09
Sorption of volatile organic compounds on typical carpet fibers.
2003-08
Environmental risk assessment of airborne trichloroacetic acid--a contribution to the discussion on the significance of anthropogenic and natural sources.
2003-07
Input of trichloroacetic acid into the vegetation of various climate zones--measurements on several continents.
2003-07
Fluxes of trichloroacetic acid between atmosphere, biota, soil, and groundwater.
2003-07
Quantitative structure-property relationships for physiologically based pharmacokinetic modeling of volatile organic chemicals in rats.
2003-06-15
Evaluation of toluene dependence and cross-sensitization to diazepam.
2003-05-16
Inhaled drugs of abuse enhance serotonin-3 receptor function.
2003-05-01
Dehydrochlorination of 1,1,1-trichloroethane and pentachloroethane by microbially reduced ferruginous smectite.
2003-05
Biodegradation of chlorinated solvents in a water unsaturated topsoil.
2003-04
Effects of inhaled toluene and 1,1,1-trichloroethane on seizures and death produced by N-methyl-D-aspartic acid in mice.
2003-03-18
An evaluation of Fourier transform infrared (FTIR) spectroscopy for detecting organic solvents in expired breath.
2003-03
Fast estimation of hydrogen-bonding donor and acceptor propensities: a GMIPp study.
2003-02-27
Evaluation of bacterial aerotaxis for its potential use in detecting the toxicity of chemicals to microorganisms.
2003-02-27
VOC exposures in a mixed-use university art building.
2003-02-07
Development of a new respirator for organic vapors with a breakthrough detector using a semiconductor gas sensor.
2003-02
Stable hydrogen, carbon and chlorine isotope measurements of selected chlorinated organic solvents.
2003-02
Continuing emissions of methyl chloroform from Europe.
2003-01-09
Trichloroacetic acid in Norway spruce/soil-system. I. Biodegradation in soil.
2003-01
[1,1, 1-trichloroethane-induced chronic active hepatitis].
2003-01
The annual course of TCA formation in the lower troposphere: a modeling study.
2003
Kinetics of 1,1,1-trichloroethane transformation by iron sulfide and a methanogenic consortium.
2002-11-01
Microbial dehalorespiration with 1,1,1-trichloroethane.
2002-11-01
[Method for determining chlorinated solvent residues in dry cleaning fabrics with gas chromatography-mass spectrometry].
2002-11
Comparison of anaerobic dechlorinating enrichment cultures maintained on tetrachloroethene, trichloroethene, cis-dichloroethene and vinyl chloride.
2002-10
Tolerance to various toxicants by marine bacteria highly resistant to mercury.
2001-10-24
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 17:34:31 GMT 2025
Edited
by admin
on Mon Mar 31 17:34:31 GMT 2025
Record UNII
113C650IR1
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
TRICHLOROETHANE
II   INCI   MART.   VANDF  
INCI  
Official Name English
1,1,1-TRICHLOROETHANE
MI  
Preferred Name English
TRICHLOROETHANE [VANDF]
Common Name English
ALPHA-T
Common Name English
SOLVENT 111
Common Name English
1,1,1-TRICHLOROETHANE [USP-RS]
Common Name English
METHYLTRICHLOROMETHANE
Systematic Name English
TRICHLOROETHANE [MART.]
Common Name English
NSC-9367
Code English
RCRA-U226
Code English
UN-2831
Code English
1,1,1-TRICHLOROETHANE [MI]
Common Name English
CLEANITE
Brand Name English
CHLOROTHENE
Common Name English
TRICHLOROETHANE [II]
Common Name English
1,1,1 TRICHLOROETHANE
VANDF  
Systematic Name English
METHYLCHLOROFORM [HSDB]
Common Name English
1,1,1-TCE
Common Name English
1,1,1-TRICHLOROETHANE [IARC]
Common Name English
GENKLENE LB
Brand Name English
METHYLCHLOROFORM
HSDB  
Systematic Name English
1,1,1 TRICHLOROETHANE [VANDF]
Common Name English
.ALPHA.-TRICHLOROETHANE
Common Name English
Classification Tree Code System Code
CFR 21 CFR 216.24
Created by admin on Mon Mar 31 17:34:31 GMT 2025 , Edited by admin on Mon Mar 31 17:34:31 GMT 2025
IARC 1,1,1-Trichloroethane
CFR 21 CFR 310.502
Created by admin on Mon Mar 31 17:34:31 GMT 2025 , Edited by admin on Mon Mar 31 17:34:31 GMT 2025
EPA PESTICIDE CODE 81201
Created by admin on Mon Mar 31 17:34:31 GMT 2025 , Edited by admin on Mon Mar 31 17:34:31 GMT 2025
Code System Code Type Description
NCI_THESAURUS
C75637
Created by admin on Mon Mar 31 17:34:31 GMT 2025 , Edited by admin on Mon Mar 31 17:34:31 GMT 2025
PRIMARY
WIKIPEDIA
1,1,1-TRICHLOROETHANE
Created by admin on Mon Mar 31 17:34:31 GMT 2025 , Edited by admin on Mon Mar 31 17:34:31 GMT 2025
PRIMARY
HSDB
157
Created by admin on Mon Mar 31 17:34:31 GMT 2025 , Edited by admin on Mon Mar 31 17:34:31 GMT 2025
PRIMARY
EVMPD
SUB34322
Created by admin on Mon Mar 31 17:34:31 GMT 2025 , Edited by admin on Mon Mar 31 17:34:31 GMT 2025
PRIMARY
CHEBI
36015
Created by admin on Mon Mar 31 17:34:31 GMT 2025 , Edited by admin on Mon Mar 31 17:34:31 GMT 2025
PRIMARY
NCI_THESAURUS
C45678
Created by admin on Mon Mar 31 17:34:31 GMT 2025 , Edited by admin on Mon Mar 31 17:34:31 GMT 2025
CONCEPT Industrial Aid
ChEMBL
CHEMBL16080
Created by admin on Mon Mar 31 17:34:31 GMT 2025 , Edited by admin on Mon Mar 31 17:34:31 GMT 2025
PRIMARY
DAILYMED
113C650IR1
Created by admin on Mon Mar 31 17:34:31 GMT 2025 , Edited by admin on Mon Mar 31 17:34:31 GMT 2025
PRIMARY
ALANWOOD
methylchloroform
Created by admin on Mon Mar 31 17:34:31 GMT 2025 , Edited by admin on Mon Mar 31 17:34:31 GMT 2025
PRIMARY
ECHA (EC/EINECS)
200-756-3
Created by admin on Mon Mar 31 17:34:31 GMT 2025 , Edited by admin on Mon Mar 31 17:34:31 GMT 2025
PRIMARY
RS_ITEM_NUM
1601226
Created by admin on Mon Mar 31 17:34:31 GMT 2025 , Edited by admin on Mon Mar 31 17:34:31 GMT 2025
PRIMARY
FDA UNII
113C650IR1
Created by admin on Mon Mar 31 17:34:31 GMT 2025 , Edited by admin on Mon Mar 31 17:34:31 GMT 2025
PRIMARY
EPA CompTox
DTXSID0021381
Created by admin on Mon Mar 31 17:34:31 GMT 2025 , Edited by admin on Mon Mar 31 17:34:31 GMT 2025
PRIMARY
CAS
71-55-6
Created by admin on Mon Mar 31 17:34:31 GMT 2025 , Edited by admin on Mon Mar 31 17:34:31 GMT 2025
PRIMARY
MERCK INDEX
m11071
Created by admin on Mon Mar 31 17:34:31 GMT 2025 , Edited by admin on Mon Mar 31 17:34:31 GMT 2025
PRIMARY Merck Index
PUBCHEM
6278
Created by admin on Mon Mar 31 17:34:31 GMT 2025 , Edited by admin on Mon Mar 31 17:34:31 GMT 2025
PRIMARY
NSC
9367
Created by admin on Mon Mar 31 17:34:31 GMT 2025 , Edited by admin on Mon Mar 31 17:34:31 GMT 2025
PRIMARY
MESH
C024566
Created by admin on Mon Mar 31 17:34:31 GMT 2025 , Edited by admin on Mon Mar 31 17:34:31 GMT 2025
PRIMARY
SMS_ID
100000127975
Created by admin on Mon Mar 31 17:34:31 GMT 2025 , Edited by admin on Mon Mar 31 17:34:31 GMT 2025
PRIMARY
Related Record Type Details
ACTIVE MOIETY