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1,2,3-Trichlorobutane

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Identification
Molecular formula
C4H7Cl3
CAS number
503-19-3
IUPAC name
1,2,3-trichlorobutane
State
State

This compound is a liquid at room temperature.

Melting point (Celsius)
-11.00
Melting point (Kelvin)
262.15
Boiling point (Celsius)
187.00
Boiling point (Kelvin)
460.15
General information
Molecular weight
147.44g/mol
Molar mass
147.4440g/mol
Density
1.2540g/cm3
Appearence

1,2,3-Trichlorobutane is a colorless liquid that might emit a mild, sweet odor similar to other chlorinated hydrocarbons. This compound is typically clear and free from any suspended particles.

Comment on solubility

Solubility of 1,2,3-Trichlorobutane

1,2,3-Trichlorobutane, with the chemical formula C4H7Cl3, is a chlorinated hydrocarbon that showcases particular solubility characteristics due to its unique molecular structure. Here’s a closer look at its solubility:

  • Solvent Interactions: This compound is generally more soluble in organic solvents such as alcohols, ethers, and aromatic hydrocarbons.
  • Aqueous Solubility: 1,2,3-trichlorobutane has limited solubility in water. The presence of multiple chlorine atoms increases polarity, but the hydrocarbon portion of the molecule hinders its ability to dissolve in water effectively.
  • Environmental Considerations: Due to its chlorinated structure, 1,2,3-trichlorobutane may exhibit different behaviors in various environments, impacting its solubility based on pH and temperature.

In summary, while 1,2,3-trichlorobutane finds good solubility in non-polar to slightly polar organic solvents, its aqueous solubility remains quite limited, making it essential to choose solvents wisely when working with this compound.

Interesting facts

Interesting Facts About 1,2,3-Trichlorobutane

1,2,3-Trichlorobutane is a fascinating organochlorine compound often explored in the field of organic chemistry and environmental science. Its structural nuances and reactions contribute to its importance.

Key Characteristics:

  • Chlorination Process: This compound is synthesized through the chlorination of butane, where chlorine atoms replace hydrogen atoms at the 1st, 2nd, and 3rd positions of the butane chain.
  • Applications: It finds utility as an intermediate in organic synthesis, particularly in the production of pesticides and other chemical products.
  • Environmental Impact: Being a chlorinated hydrocarbon, 1,2,3-trichlorobutane is often scrutinized for its potential environmental effects, especially in relation to soil and water contamination.
  • Health Considerations: It has been studied for its toxicological effects, emphasizing the need for safety measures when handling such compounds in laboratory settings.

Fun Fact:

The compound's chlorinated structure makes it a subject of study for understanding halogen reactivity in organic chemistry, as halogens often participate in a variety of chemical reactions.

In summary, 1,2,3-trichlorobutane serves not only as a useful toolkit for organic synthesis but also as a reminder of the responsibility that comes with working with chemical compounds. As researchers and students delve into its properties, they uncover the delicate balance between utilizing such compounds and understanding their implications on health and the environment.

Synonyms
1,2,3-Trichlorobutane
18338-40-4
BUTANE, 1,2,3-TRICHLORO-
BRN 1733310
DTXSID30871280
3-01-00-00285 (Beilstein Handbook Reference)
DTXCID10818951
1,2,3-Trichlorobutane.
1,2,3-trichloro-butane
SCHEMBL246604
SCHEMBL1398526
SCHEMBL7845597
SCHEMBL11049787
RMZZAEDPBSKZOM-UHFFFAOYSA-N
AKOS006385274