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1,3-Dichloropropene

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Identification
Molecular formula
C3H4Cl2
CAS number
542-75-6
IUPAC name
1,3-dichloroprop-1-ene
State
State
1,3-Dichloropropene is a liquid under room temperature conditions, typically appearing as a colorless to light yellow liquid.
Melting point (Celsius)
-97.80
Melting point (Kelvin)
175.35
Boiling point (Celsius)
112.36
Boiling point (Kelvin)
385.51
General information
Molecular weight
110.98g/mol
Molar mass
110.9760g/mol
Density
1.2180g/cm3
Appearence
1,3-Dichloropropene is a colorless liquid with a chloroform-like odor. It can appear in pure form but is often found in technical-grade mixtures of cis- and trans-isomers.
Comment on solubility

Solubility of 1,3-Dichloroprop-1-ene

1,3-Dichloroprop-1-ene, with the chemical formula C3H4Cl2, exhibits interesting solubility characteristics. Being a chlorinated hydrocarbon, its solubility can be influenced by several factors:

  • Polarity: The presence of chlorine atoms increases the polarity of the molecule. However, 1,3-dichloroprop-1-ene is still predominantly nonpolar.
  • Solvent Compatibility: It is more soluble in organic solvents such as ethanol, acetone, and dichloromethane than in water due to its nonpolar characteristics.
  • Temperature Influence: Like many organic compounds, its solubility tends to increase with temperature.

In general, you can expect 1,3-dichloroprop-1-ene to have limited solubility in water, which can be characterized as:

  1. Low solubility due to its nonpolar nature.
  2. Higher affinity for organic solvents.

Overall, understanding the solubility behavior of this compound is essential for its applications in various chemical processes. As always, remember that solubility is influenced by chemical structure and the nature of the solvents used.

Interesting facts

Exciting Facts about 1,3-Dichloroprop-1-ene

1,3-Dichloroprop-1-ene is a fascinating compound that belongs to the class of alkenes. This molecule captures the attention of chemists due to its unique structure and diverse applications. Here are some interesting aspects about this compound:

  • Reactivity: The presence of two chlorine atoms at the 1 and 3 positions makes 1,3-dichloroprop-1-ene a versatile intermediate in organic synthesis. It can undergo various reactions, including nucleophilic substitutions and eliminations, making it valuable in the development of complex organic molecules.
  • Use in Agriculture: This compound plays a role in the agricultural sector. It serves as an active ingredient in some pesticides and herbicides, helping in the control of pests and weeds. This can be particularly beneficial in sustainable farming practices.
  • Chemical Reactions: 1,3-Dichloroprop-1-ene can participate in polymerization reactions. Researchers explore its potential to form polymers, leading to innovative materials with distinct properties.
  • Environmental Considerations: As with many chlorinated compounds, 1,3-dichloroprop-1-ene raises important questions regarding environmental safety and health. Understanding its behavior in the environment is crucial for assessing its impact on ecosystems.
  • Structural Significance: The compound's unique double bond and the positioning of chlorine atoms influence its chemical properties significantly, making it a subject of study in understanding reaction mechanisms in organic chemistry.

In conclusion, 1,3-dichloroprop-1-ene stands out as a remarkable compound with multiple facets that appeal to both synthetic chemists and environmental scientists. The balance between its utility and potential risks continues to fuel research and discussions in chemical science.

Synonyms
1,3-DICHLOROPROPENE
542-75-6
1,3-Dichloro-1-propene
1, 3-Dichloropropene
DTXSID1022057
1,3 dichloropropene
1,3-dichioropropene
Telone II, technical grade (without epichlorohydrin)
Telone II, technical grade (with 1% epichlorohydrin)
1,3-dichloro-prop-1-ene
SCHEMBL33877
SCHEMBL9643561
CHEMBL3561804
cis-/trans-1,3-Dichloropropene
1,3-Dichloropropene (cis+trans)
UOORRWUZONOOLO-UHFFFAOYSA-N
AKOS025117018
DB-354178
D0405
NS00007908