
Education Journalist | Study Abroad Lead
Tetrachloroethylene (C2Cl4) is a molecule consisting of carbon and chlorine and is widely used as a fluid for dry cleaning of fabrics. It is also known as tetrachloroethene or perchloroethylene which is volatile in nature. It is a colourless liquid that is also used widely as an automotive brake cleaner. However, this compound is known to be carcinogenic and a contaminant of groundwater and therefore, it is now being replaced by the process where detergent with liquified carbon dioxide and hydrogen peroxide is used.
| Table of Contents |
Key takeaways: Tetrachloroethylene, hydrogen peroxide, organic solvent, covalent bonds, carbon dioxide
Tetrachloroethylene
[Click Here for Sample Questions]
Tetrachloroethylene is an organic solvent that is volatile in nature. Tetrachloroethylene molecules are made up of two carbon atoms linked by double covalent bonds and four chlorine atoms linked by single covalent bonds, as seen in the structure below.

Structure of tetrachloroethylene
Properties of Tetrachloroethylene
[Click Here for Sample Questions]
The IUPAC name of tetrachloroethylene is 1,1,2,2-tetrachloroethene. The formula for the compound is:
- Empirical formula: CCl2
- Molecular formula: C2Cl4 or Cl2C=CCl2
Physical properties
The physical properties of Tetrachloroethylene (C2Cl4) are as follows:
- Even at a concentration of 1ppm, people may smell its presence.
- It is denser than water.
- It is non-flammable.
- It's an excellent organic compound solvent.
- It is both volatile and extremely stable.
| Molecular mass | 165.82 g/mol |
| Appearance | Clear, colorless liquid |
| Odor | Mild, chloroform like |
| Density | 1.622 g/cm3 |
| Melting point | -19oC (-2oF; 254 K) |
| Boiling point | 121.1oC (250oF; 394.2K) |
| Solubility in water | 0.15g/L at 25oC |
| Vapor pressure | 14mmHg at 20oC or 18.47 mmHg at 25oC |
Chemical properties
The chemical properties of tetrachloroethylene are:
- Reaction with water - Dichloromethane and oxygen are produced when it combines with water.
C2Cl4 + 2H2O → 2CH2Cl2 + O2
Tetrachloroethylene dichloromethane + oxygen
- Reaction with alkali - It creates formic acid and sodium chloride when it combines with alkalis like sodium hydroxide.
4NaOH + C2Cl4 → 2HCO2H + 4NaCl
Sodium hydroxide formic + acid sodium chloride
Production of tetrachloroethylene
[Click Here for Sample Questions]
The production of tetrachloroethylene takes place in the following way:
- In 1821, British scientist and chemist Michael Faraday used thermal breakdown of hexachloroethane to create tetrachloroethylene for the first time.
C2Cl6 → C2Cl4 + Cl2
The chlorination of light hydrocarbons at high temperatures produces the majority of tetrachloroethylene. Because hexachloroethane is created and thermally decomposes, the procedure is linked to Faraday's discovery. Carbon tetrachloride, hydrogen chloride, and hexachlorobutadiene are some of the byproducts.
- There have been a number of additional approaches explored. Tetrachloroethylene is created when 1,2-dichloroethane is heated to 400oC with chlorine.
ClCH2CH2Cl + 3Cl2 → Cl2C=CCl2 + 4 HCl
A combination of potassium chloride and aluminium chloride, or activated carbon, can accelerate this process. Trichloroethylene is a significant byproduct that may be removed using distillation.
Uses of tetrachloroethylene
[Click Here for Sample Questions]
The uses of tetrachloroethylene are as follows:
- It is extensively used for cloth dry cleaning. It's also known as a dry cleaning fluid for this reason.
- Many organic compounds and processes use it as a solvent.
- It's used to clean grease from metal parts in the automotive and other sectors.
- Paint strippers and spot removers contain tetrachloroethylene as one of the active components.
- It's an anthelmintic that's mostly used to treat hookworm infestations.
Things to remember
- Tetrachloroethylene molecules have two carbon atoms joined together by double covalent bonds and four chlorine atoms linked together by single covalent bonds.
- Other names for tetrachloroethylene are tetrachloroethene or perchloroethylene.
- It is used in dry cleaning clothes and therefore also goes by the name ‘dry cleaning fluid’.
- It is a stable organic solvent that is volatile, clear and has a chloroform-like smell.
- Michael Faraday was the first to synthesize this compound in 1821.
- Due to its carcinogenicity and ability to contaminate the groundwater, alternatives like hydrogen peroxide and detergents in liquified carbon dioxide are being used.
Sample Questions
Ques. What are the uses of tetrachloroethylene? (3 marks)
Ans. Tetrachloroethene is a synthetic chemical used in the dry cleaning of materials, notably clothing.
- It's also utilized in the degreasing of metal components and the production of other chemicals.
- As it dissolves oil and filth without harming clothes, it is utilized as a powerful dry-cleaning solvent.
- Tetrachloroethylene is one of the active ingredients in paint strippers and spot removers.
- However, because this molecule is known to be carcinogenic and a groundwater pollutant, it is presently being substituted with liquified carbon dioxide and hydrogen peroxide and detergent.
Ques. What are the potential sources of exposure to tetrachloroethylene? (3 marks)
Ans. Tetrachloroethylene concentrations in ambient air have decreased in recent decades as the use of tetrachloroethylene has decreased. Tetrachloroethylene has also been found in drinking water sources affected by contaminated groundwater.
Occupational exposure to tetrachloroethylene occurs mostly in industries that use the chemical (for example, numerous dry-cleaning establishments) and in companies that manufacture it. Over the last few decades, new dry-cleaning technology and procedures have resulted in significantly lower occupational exposure.
Ques. What are the minor effects of being exposed to tetrachloroethylene? (3 marks)
Ans. Acute inhalation exposure of humans to tetrachloroethylene vapours causes irritation of the upper respiratory tract and eyes, kidney dysfunction, and, at lower concentrations, neurological effects such as reversible mood and behavioural changes, coordination impairment, dizziness, headache, sleepiness, and unconsciousness. Acute inhalation exposure to high amounts of tetrachloroethylene has been shown to have consequences on the liver, kidneys, and central nervous system (CNS) in animals. Tetrachloroethylene toxicity from inhalation and oral exposure was shown to be minimal in acute animal studies in mice.
Ques. What are the chronic effects of being exposed to tetrachloroethylene? (5 marks)
Ans. In chronic cases, one can suffer from the following:
- In humans, the main impacts of prolonged inhalation exposure to tetrachloroethylene are neurological effects, such as sensory complaints including headaches, cognitive and motor neurobehavioral deficits, and colour vision abnormalities.
- Other human impacts include liver damage, renal effects, immunological and hematologic effects, and effects on development and reproduction, all of which are more common at greater doses.
- Chronic inhalation exposure to tetrachloroethylene has been shown to have effects on the liver, kidneys, and CNS in animal studies.
Ques. What are the possible reproductive or developmental effects faced by exposure to tetrachloroethylene? (3 marks)
Ans. The possible reproductive/developmental effects of tetrachloroethylene are as follows:
- In investigations of persons occupationally exposed to tetrachloroethylene, unfavourable reproductive consequences such as menstruation problems, changed sperm structure, and lower fertility have been documented. The evidence, however, is inconclusive.
- Some investigations of pregnant women who were exposed to tetrachloroethylene and other solvents in their drinking water imply a link between tetrachloroethylene exposure and birth abnormalities, although definite conclusions cannot be formed due to the limitations of these research.
- In animals exposed to high amounts of tetrachloroethylene by inhalation, increased foetal resorptions and effects on the foetus have been recorded.
Ques. What is the association of tetrachloroethylene to cancer? (3 marks)
Ans. Tetrachloroethylene can be associated to cancer in the following ways:
- Studies of dry cleaners exposed to tetrachloroethylene have found links between tetrachloroethylene exposure and numerous forms of cancer, including bladder cancer, non-Hodgkin lymphoma, and multiple myeloma. There's also some evidence of links to esophageal cancer, renal cancer, cervical cancer, and breast cancer.
- Inhalation and gavage (experimentally inserting the chemical in the stomach) exposure in mice resulted in an increased incidence of liver cancers, whereas inhalation exposure in rats resulted in kidney and mononuclear cell leukemias.
- Based on suggestive data in epidemiological studies and definitive evidence in rats (mononuclear cell leukaemia) and mice, the EPA has categorised tetrachloroethylene as probably carcinogenic to humans by all routes of exposure (increased incidence of liver tumours). Tetrachloroethylene is classed as possibly harmful to humans by the International Agency for Research on Cancer (IARC) (Group 2A).
Ques. What are the physical properties of tetrachloroethylene? (3 marks)
Ans. The physical properties of tetrachloroethylene are as follows:
- Tetrachloroethylene is a colourless, non-flammable liquid with a distinct sweet odour that has a 1 ppm olfactory threshold.
- Tetrachloroethylene has the chemical formula C2Cl4 and a molecular weight of 165.82 g/mol.
- At 25 °C, tetrachloroethylene has a vapour pressure of 18.47 mm Hg and a log octanol/water partition coefficient (log Kow) of 3.40.
Ques. What is the distribution of tetrachloroethylene in the environment and what are its degradation products? (4 marks)
Ans. The distribution of tetrachloroethylene in the environment is predicted to be 76.39 percent to 99.69 percent in the air, 0.23 percent to 23.2 percent in the water, 0.06-7 percent in the soil, and the rest in the sediment and biota. The lifespan in the atmosphere is predicted to be around 2 months in the Southern Hemisphere and 5–6 months in the Northern Hemisphere, according to a survey conducted in 1987.
Phosgene, trichloroacetyl chloride, hydrogen chloride, carbon dioxide, and carbon monoxide are some of the degradation products that have been seen in a laboratory. Tetrachloroethylene is a persistent organic compound that is destroyed by hydrolysis. Trichloroethylene, dichloroethylene, vinyl chloride, ethylene, and ethane are some of the breakdown products produced by reductive dechlorination under anaerobic circumstances. Where CFC-11 (CCl3F) is 1, it has an ozone depletion potential of 0.005.
Read Also:






Comments