Structure via PubChem · Public domain (PubChem)
1,2,4-trichlorobenzene
Sign in to saveAlso known as unsym-trichlorobenzene, 1,2,4-trichlorobenzol, 1,2,4-Trichlorbenzol, 1,2,5-trichlorobenzene, as-trichlorobenzene, 1,2,4-tris(chloranyl)benzene
1,2,4-Trichlorobenzene is an organochlorine compound, one of three isomers of trichlorobenzene. It is a derivative of benzene with three chloride substituents. It is a colorless liquid used as a solvent for a variety of compounds and materials.
Chemical data
- Formula
- C6H3Cl3
- Molecular weight
- 181.4 g/mol
- IUPAC name
- 1,2,4-trichlorobenzene
- SMILES
- C1=CC(=C(C=C1Cl)Cl)Cl
- InChIKey
- PBKONEOXTCPAFI-UHFFFAOYSA-N
- XLogP
- 4
- Polar surface area
- 0 Ų
- H-bond donors
- 0
- H-bond acceptors
- 0
- Formal charge
- 0
via PubChem
Drug data · ChEMBL
- Molecule type
- Small molecule
via ChEMBL · EBI
Wikidata facts
- Subclass of
- trichlorobenzene
- Mass
- 179.93
Show 14 more facts
- chemical formula
- C₆H₃Cl₃
- vapor pressure
- 1
- NIOSH Pocket Guide ID
- 0627
- density
- 1.45
- melting point
- 17.0
- boiling point
- 213.5
- flash point
- 222
- solubility
- 0.003
- lower flammable limit
- 2.5
- upper flammable limit
- 6.6
- ceiling exposure limit
- 40
- canonical SMILES
- C1=CC(=C(C=C1Cl)Cl)Cl
- Commons category
- 1,2,4-Trichlorobenzene
- ionization energy
- 9.04
via Wikidata · CC0
~1 min read
Encyclopedic overview
4 sectionsContents
- Production and uses
- Safety
- See also
- References
1,2,4-Trichlorobenzene is an organochlorine compound, one of three isomers of trichlorobenzene. It is a derivative of benzene with three chloride substituents. It is a colorless liquid used as a solvent for a variety of compounds and materials.
==Production and uses== Depending on the conditions and additives (e.g., sulfur), it can be the main product from the chlorination of benzene. It is virtually the exclusive product from the chlorination of 1,4-dichlorobenzene. It is also the main product from the dehydrochlorination of hexachlorocyclohexane.
Excerpted from Wikipedia’s “1,2,4-trichlorobenzene” article, available under the CC BY-SA 4.0 licence.