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Trichloroethylene chemical structure, C2HCl3, CAS 79-01-6
2D chemical structure

Key facts

What buyers check first

Appearance
Colorless liquid (unless dyed blue)
Melting point
-84.7 °C
Boiling point
87.2 °C
Density
Relative density (water = 1): 1.5 (20 °C)
Flash point
>93.3
HS code
290322
Category
Chlorinated and fluorinated solvents
UN number
UN 1710
Illustrative photo, 200 litre blue HDPE drums of liquid in a warehouse
Typical packagingIllustrative packaging image, not the actual product

What is Trichloroethylene?

Plain description, key identifiers and synonyms

Trichloroethene is a member of the class of chloroethenes that is ethene substituted by chloro groups at positions 1, 1 and 2. It has a role as an inhalation anaesthetic and a mouse metabolite.

Identifiers

Registry numbers, names and line notations, tap to copy

IUPAC name
1,1,2-trichloroethene
CAS number
79-01-6 CAS number cross-checkedOther or deprecated CAS: 123919-09-5
EC number
201-167-4
Molecular formula
C2HCl3
UNII
290YE8AR51
MDL number
MFCD00000838
InChIKey
XSTXAVWGXDQKEL-UHFFFAOYSA-N
InChI
InChI=1S/C2HCl3/c3-1-2(4)5/h1H
SMILES (canonical and isomeric)
C(=C(Cl)Cl)Cl

Synonyms

  • Trichloroethene
  • 1,1,2-Trichloroethene
  • Ethinyl trichloride
  • 1,1,2-Trichloroethylene
  • Ethene, trichloro-
  • Ethylene trichloride
  • Germalgene
  • Westrosol
  • Densinfluat
  • Narkosoid
  • Trethylene
  • Acetylene trichloride
  • Anamenth
  • Narcogen
  • Trilene
  • Trichlorethylene
  • Chlorilen
  • Chlorylen
  • Threthylen
  • Trichloran
  • Trichloren
  • Trielene
  • Trielina
  • Trieline
  • Trimar
Show all 39 synonyms
  • Tri-Clene
  • triciene
  • Trichloraethen
  • Benzinol
  • Blacosolv
  • Blancosolv
  • Cecolene
  • Circosolv
  • Crawhaspol
  • Lethurin
  • Petzinol
  • Threthylene
  • Algylen
  • Dukeron

Physical and chemical properties

Measured values and descriptors computed from the structure

Physical and chemical properties

Measured values, check the supplier specification for your grade

Appearance
Colorless liquid (unless dyed blue)exp.
Odour
Ethereal odorexp.
Taste
Sweet burning tasteexp.
Melting point
-84.7 °Cexp.
Boiling point
87.2 °Cexp.
Density
Relative density (water = 1): 1.5 (20 °C)exp.
Flash point
>93.3exp.
Autoignition temperature
420 °Cexp.
Solubility
In water, range of 999-1,472 mg/L at 25 °C (average of 1,118 mg/L) /7 measured values/exp.
Vapour pressure
69 mm Hg at 25 °Cexp.

Values vary by grade. Ask suppliers for the COA or TDS of the batch you buy.

Computed descriptors

Calculated from the structure, useful for screening and formulation

Molecular weight
131.39 g/molcalc.
Exact mass
129.9144 Dacalc.
LogP (octanol/water)
2.5calc.
Topological polar surface area
0 Ųcalc.
Hydrogen bond donors
0calc.
Hydrogen bond acceptors
0calc.
Rotatable bonds
0calc.
Heavy atoms
5calc.
Rings
0calc.
Aromatic rings
0calc.
Fraction sp3 carbons
0calc.
Formal charge
0calc.
Stereocentres
0calc.
Lipinski rule of five
Passes (0 violations)calc.

Calculated for screening. Confirm critical figures with the supplier.

Safety and hazards

GHS classification summary, not a safety data sheet

GHS signal word
Danger
GHS07: Harmful or irritant
Harmful or irritant
GHS08: Serious health hazard
Serious health hazard
120NFPA 704 rating

Hazard statements

  • H315Causes skin irritation.
  • H319Causes serious eye irritation.
  • H336May cause drowsiness or dizziness.
  • H341Suspected of causing genetic defects.
  • H350May cause cancer.
  • H412Harmful to aquatic life with long lasting effects.
Precautionary statements (19)
  • P203Obtain, read and follow all safety instructions before use.
  • P261Avoid breathing dust, fume, gas, mist, vapours or spray.
  • P264Wash skin thoroughly after handling.
  • P264 + P265Wash skin thoroughly after handling. Do not touch eyes.
  • P271Use only outdoors or in a well-ventilated area.
  • P273Avoid release to the environment.
  • P280Wear protective gloves, protective clothing, eye protection and face protection.
  • P302 + P352If on skin: Wash with plenty of water.
  • P304 + P340If inhaled: Remove person to fresh air and keep comfortable for breathing.
  • P305 + P351 + P338If in eyes: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing.
  • P318If exposed or concerned, get medical advice.
  • P319Get medical help if you feel unwell.
  • P321Specific treatment (see supplemental first aid instructions on the label).
  • P332 + P317If skin irritation occurs: Get medical help.
  • P337 + P317If eye irritation persists: Get medical help.
  • P362 + P364Take off contaminated clothing. And wash it before reuse.
  • P403 + P233Store in a well-ventilated place. Keep container tightly closed.
  • P405Store locked up.
  • P501Dispose of contents and container in accordance with local regulations.
UN number
UN 1710
Transport hazard class
6.1
Packing group
III

GHS classification summary, not a safety data sheet (SDS). Classifications can differ by supplier, grade and concentration. Always check the supplier's SDS.

Full safety data and first aid

Trichloroethylene suppliers

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Trichloroethylene price

Indicative price range per kg from live supplier offers

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Uses and applications

What the substance is used for, by industry and function

Trichloroethylene is used as chemical intermediate for the production of hydrofluorocarbons (e.g., HFC134a, HFC125), monochloroacetic acid, blowing agents, flame retardants, and some agricultural chemicals. The other major use is as solvent for vapor degreasing in the metal industry. ... Trichloroethylene is further used in solvent formulations for rubbers, adhesives, industrial paints, and in the manufacture of lithium-ion batteries.

Read more

In the production of poly(vinyl chloride), it serves as a chain-transfer agent to control the molecular mass distribution.

Metal degreasing, extraction solvent for oils, fats, waxes, solvent dyeing, dry-cleaning, refrigerant and heat-exchange liquid, fumigant, cleaning and drying electronic parts, diluent in paints and adhesives, textile processing, chemical intermediate, aerospace operations (flushing liquid oxygen).

Used as household cleaner, with trichloroethane it is used in most typewriter correction fluid.

The main use of trichloroethylene is in the vapor degreasing of metal parts. Trichloroethylene is used in consumer products such as typewriter correction fluids, paint removers/strippers, adhesives, spot removers, and rug-cleaning fluids.

Industrial uses: Refrigerants, Cleaning agent, Absorbent, Laboratory chemicals, Intermediate, Solvent.

Consumer uses: Solvent, Cleaning agent.

Use classes: Volatile organic compounds.

Pharmacological actions

  • Anesthetics, Inhalation
  • Solvents

Roles

  • anaesthetic
  • animal metabolite
  • eukaryotic metabolite
  • general anaesthetic
  • inhalation anaesthetic
  • mammalian metabolite
  • metabolite
  • mouse metabolite
  • pharmaceutical

Functional uses

  • Solubility enhancer
  • Solvent

Pharmacology

Trichloroethylene is a synthetic, light sensitive, volatile, colorless, liquid that is miscible with many non-polar organic solvents. Trichloroethylene is used mainly as a degreaser for metal parts. Upon combustion, it produces irritants and toxic gases. Occupational exposure to trichloroethylene is associated with excess incidences of liver cancer, kidney cancer and non-Hodgkin lymphoma. It is reasonably anticipated to be a human carcinogen. (NCI05)

How it is made

The production of trichloroethylene is mainly based on acetylene or ethylene. The acetylene route comprises acetylene chlorination to 1,1,2,2-tetrachloroethane followed by dehydrochlorination to trichloroethylene. In the ethylene-based processes, ethylene or ethylene-based chlorohydrocarbons, preferably 1,2-dichloroethane, are chlorinated or oxychlorinated and dehydrochlorinated in the same reactor. Tetrachloroethylene is obtained as a byproduct in substantial amounts.

Read more

Some production is based on the catalytic hydrogenation of tetrachloroethylene coming from the chlorinolysis of C1 to C3 chlorohydrocarbons.

Until 1968, about 85% of United States production capacity of trichloroethylene was based on acetylene. The acetylene-based process consists of two steps: acetylene is first chlorinated to 1,1,2,2-tetrachloroethane, with a ferric chloride, phosphorus chloride or antimony chloride catalyst, and the product is then dehydrohalogenated to trichloroethylene. The current method of manufacture is from ethylene or 1,2-dichloroethane. In a process used by one plant in the United States, trichloroethylene is produced by noncatalytic chlorination of ethylene dichloride and other C2 hydrocarbons with a mixture of oxygen and chlorine or hydrogen chloride.

Prepn from sym-tetrachlorethane by elimination of (hydrochloric acid) (by boiling with lime) ..., by passing tetrachloroethane vapor over (calcium chloride) catalyst at 300 °C ..., without catalyst at 450-470 °C...

Regulatory status

Inventories, regulations and trade controls that list this substance

Europe

  • EU harmonised classification (CLP Annex VI)
    Index no: 602-027-00-9

Health and food

  • EU Cosmetics Regulation Annex II, prohibited in cosmetics
    Name: Trichloroethylene, Ref no: 645, Annex ref: II/645

United States

  • TSCA inventory (USA)
    Status: Active in US commerce, Regulatory flags: Section 6 risk management rule, significant new use rule

HS code and trade data

Customs classification and reported world trade statistics

Global trade

World import and export statistics for the HS code Trichloroethylene is traded under.

HS 2903.22Exact HS code

Unsaturated chlorinated derivatives of acyclic hydrocarbons: trichloroethylene

World exports in 2024
$31.2M
−20.6% vs 2023, imports $32.8M
2019 to 2024
Top exporters
  1. China57.2%
  2. Japan18.9%
  3. United States10.4%
Top importers
  1. South Korea9.8%
  2. India * partner reported8.8%
  3. Italy7.6%

* Partner reported figures, a lower bound.

Reported customs values in USD, not prices.Full trade data

The HS code shown for Trichloroethylene is indicative (it was matched by name in the HS nomenclature). Confirm the classification with your customs broker before shipping.

Frequently asked questions

Quick answers about Trichloroethylene, based on the data on this page

What is Trichloroethylene?

Trichloroethene is a member of the class of chloroethenes that is ethene substituted by chloro groups at positions 1, 1 and 2. It has a role as an inhalation anaesthetic and a mouse metabolite.

What is the CAS number of Trichloroethylene?

The CAS registry number of Trichloroethylene is 79-01-6. Other or deprecated CAS numbers: 123919-09-5.

What is the molecular formula and weight of Trichloroethylene?

The molecular formula of Trichloroethylene is C2HCl3 and its molar mass is 131.39 g/mol.

What is Trichloroethylene used for?

Trichloroethylene is used as chemical intermediate for the production of hydrofluorocarbons (e.g., HFC134a, HFC125), monochloroacetic acid, blowing agents, flame retardants, and some agricultural chemicals. The other major use is as solvent for vapor degreasing in the metal industry. ...

Is Trichloroethylene hazardous?

Trichloroethylene carries the GHS signal word "Danger". Main hazards: causes skin irritation, causes serious eye irritation, may cause drowsiness or dizziness. This summary is not an SDS, always read the supplier safety data sheet.

What is the HS code of Trichloroethylene?

Trichloroethylene is usually classified under HS code 290322 (Trichloroethylene). This is indicative, confirm it with your customs broker before shipping.

Where can I buy Trichloroethylene?

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What is the price of Trichloroethylene?

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Guides for buyers

Practical guides that help when you source, ship or handle Trichloroethylene

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Data last updated 7 Oct 2026. Details may have changed, please confirm them with the supplier. Report an error on this page
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