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4-chlorobutyl acetate

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Identification
Molecular formula
C6H11ClO2
CAS number
6962-92-1
IUPAC name
4-chlorobutyl acetate
State
State

At room temperature, 4-chlorobutyl acetate is in a liquid state.

Melting point (Celsius)
-75.00
Melting point (Kelvin)
198.15
Boiling point (Celsius)
161.00
Boiling point (Kelvin)
434.15
General information
Molecular weight
150.61g/mol
Molar mass
150.6080g/mol
Density
0.9987g/cm3
Appearence

4-Chlorobutyl acetate is a clear, colorless liquid. It exhibits an ester-like odor typical of many acetate compounds.

Comment on solubility

Solubility of 4-chlorobutyl acetate

4-chlorobutyl acetate, with the chemical formula C5H10ClO2, exhibits interesting solubility characteristics that are essential for its applications. Generally, its solubility can be summarized as follows:

  • Solvent Compatibility: 4-chlorobutyl acetate is known to be soluble in a range of organic solvents. This includes polar solvents like ethanol and acetone.
  • Water Solubility: Moderate water solubility is observed. However, it is important to note that solubility in water is limited due to the hydrophobic alkyl chain associated with the molecule.
  • Temperature Effect: Increased temperature generally enhances the solubility of 4-chlorobutyl acetate in both organic and polar solvents. As temperature rises, kinetic energy increases, often leading to higher dissolution rates.

Understanding the solubility of 4-chlorobutyl acetate is crucial for various industrial and laboratory processes. As stated, its solubility behavior makes it a versatile compound in organic synthesis and solvent applications.

Interesting facts

Interesting Facts about 4-Chlorobutyl Acetate

4-Chlorobutyl acetate is an intriguing compound with various applications and properties that make it noteworthy in the field of chemistry. Here are a few compelling facts about this compound:

  • Chemical Identity: The compound belongs to the class of esters, which are characterized by the presence of a carbonyl group adjacent to an ether link. This specific compound contains a chlorine atom, which enhances its reactivity compared to other butyl esters.
  • Applications:
    • Used primarily as a solvent in various industrial processes.
    • It serves as an intermediate in the synthesis of agrochemicals and pharmaceuticals.
    • Plays a role in the formulation of coatings, adhesives, and sealants due to its effective solvating properties.
  • Reactivity: The presence of the chlorine atom makes 4-chlorobutyl acetate more reactive, allowing it to participate in nucleophilic substitution reactions.
  • Safety: Like many organic compounds, it can pose certain health hazards. Proper handling and storage are essential to mitigate risks associated with inhalation or skin contact.
  • Environmental Impact: Chlorinated compounds often raise concerns about environmental impact. Researching and implementing sustainable practices in its use and disposal is important for minimizing ecological harm.

In summary, 4-Chlorobutyl acetate is a versatile compound with significant industrial applications, but it also carries certain safety and environmental considerations. As chemistry continues to evolve, understanding these compounds and their implications is vital for future innovations.

Synonyms
4-Chlorobutyl acetate
1-Butanol, 4-chloro-, 1-acetate
EINECS 230-158-8
BRN 1749681
AI3-16503
PYLDCZJUHYVOAF-UHFFFAOYSA-
DTXSID20884344
4-02-00-00147 (Beilstein Handbook Reference)
DTXCID501023791
230-158-8
inchi=1/c6h11clo2/c1-6(8)9-5-3-2-4-7/h2-5h2,1h3
pyldczjuhyvoaf-uhfffaoysa-n
6962-92-1
4-chlorobutylacetate
1-Acetoxy-4-chlorobutane
4-Chloro-n-butyl acetate
1-Chloro-4-acetoxybutane
1-BUTANOL, 4-CHLORO-, ACETATE
4-Chloro-1-butanol acetate
4-Chlorbut-1-ylacetat
NSC 53492
NSC 54074
Acetic Acid 4-Chlorobutyl Ester
acetic acid 4-chloro-butyl ester
.omega.-Chlorobutyl acetate
delta-Chlorobutyl acetate
4-Chlorbut-1-ylacetat [German]
MFCD00001013
.delta.-Chlorobutyl acetate
4-Chlorobutyl acetate, 98%
SCHEMBL1270067
NSC53492
NSC54074
NSC-53492
NSC-54074
AKOS006221691
CS-W010967
FS-4206
A1098
NS00044344
EN300-66013
H10679
F0001-1810