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2-Chloroethyl N-propylcarbamate

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Identification
Molecular formula
C6H12ClNO2
CAS number
150-03-0
IUPAC name
2-chloroethyl N-propylcarbamate
State
State

At room temperature, 2-Chloroethyl N-propylcarbamate is a liquid. It is generally maintained and used in liquid form for various chemical applications.

Melting point (Celsius)
-34.00
Melting point (Kelvin)
239.00
Boiling point (Celsius)
104.00
Boiling point (Kelvin)
377.00
General information
Molecular weight
179.62g/mol
Molar mass
179.6200g/mol
Density
1.1480g/cm3
Appearence

2-Chloroethyl N-propylcarbamate is a liquid with a clear, colorless to pale yellow appearance. It is typically found as a clear, viscous liquid that is slightly soluble in water.

Comment on solubility

Solubility of 2-chloroethyl N-propylcarbamate

2-chloroethyl N-propylcarbamate, a chemical compound with a unique structure, exhibits intriguing solubility characteristics. Its solubility is influenced by several factors:

  • Polarity: The presence of the chloroethyl and carbamate groups imparts distinct polar characteristics to the compound, potentially enhancing its solubility in polar solvents such as water.
  • Hydrophobic Interactions: The N-propyl group may contribute hydrophobic properties, which can limit solubility in highly polar solvents.
  • Boiling Point: The molecular weight and structure of 2-chloroethyl N-propylcarbamate suggest it may have a moderate boiling point, impacting its volatility and solubility in various media.

In general, one can expect that:

  1. **Solubility in Water**: Given the polar nature of the carbamate group, it may demonstrate moderate water solubility.
  2. **Solubility in Organic Solvents**: The hydrophobic N-propyl group likely contributes to increased solubility in organic solvents such as ethanol and acetone.
  3. **Temperature Effects**: As with many compounds, solubility may increase with temperature, allowing for better dissolution in various solvents.

Overall, understanding the solubility profile of 2-chloroethyl N-propylcarbamate is crucial for its applications and interactions in chemical processes.

Interesting facts

Interesting Facts about 2-Chloroethyl N-Propylcarbamate

2-Chloroethyl N-propylcarbamate is a fascinating compound known for its versatile applications in various scientific fields. Here are some noteworthy aspects:

  • Biochemical Relevance: This compound is often investigated for its roles in biochemical processes, particularly as a probe in enzyme studies. Its structural features allow it to mimic natural substrates, enabling researchers to study enzymatic mechanisms with precision.
  • Industrial Applications: 2-Chloroethyl N-propylcarbamate is also utilized in the synthesis of pesticides and herbicides, showcasing its potential in agriculture for effective crop management.
  • Environmental Studies: The study of such compounds offers insights into environmental impact and remediation strategies. Scientists are keen on understanding the degradation pathways of carbamates as they seek ways to mitigate their effects on ecosystems.
  • Toxicological Investigations: With increasing attention on chemical safety, 2-chloroethyl N-propylcarbamate has become a subject of toxicology research. Studying its interaction with biological systems helps in assessing the risks associated with its usage.
  • Regulatory Considerations: Due to its chemical nature, it often falls under strict regulatory scrutiny in various countries. Understanding the regulations surrounding its use is essential for chemists and industries that deal with similar compounds.

Overall, 2-chloroethyl N-propylcarbamate exemplifies the intersection of chemistry with environmental science, agriculture, and health. Its diverse applications and the ongoing research surrounding it highlight the importance of continued exploration in the field of chemical compounds.

Synonyms
Propylcarbamic acid 2-chloroethyl ester
CARBAMIC ACID, PROPYL-, 2-CHLOROETHYL ESTER
20074-88-8
BRN 1756187
DTXSID30173897
4-04-00-00480 (Beilstein Handbook Reference)
DTXCID2096388
RefChem:332732
CB 4
AKOS006221682