This substantial amount of Propionyl Chloride (CH3CH2COCl) weighs a precise 100g. It is a colorless substance with a sharp odor. Propionyl Chloride finds applications in various synthetic processes, including the synthesis of esters, amides, and other organic compounds. Always handle with care as Propionyl Chloride is harmful to the human body.
Properties of CAS 79-03-8
CAS this compound, formally identified as cyclohexanone, possesses a myriad of remarkable physical and chemical properties. This colorless to light yellow solution exhibits a characteristic fragrance. At standard ambient conditions, its melting point is around -90°C while the boiling point is approximately 154°C.
- The exhibits a density of 0.97 g/cm³ and its volatility is moderately high
- CAS 79-03-8 is dissolves in a variety of compounds including water, ethanol, and acetone.
- Cyclohexanone reacts with various substances under certain conditions, leading to various processes
Product Information for Propionyl Chloride
This Information Sheet provides comprehensive details regarding the characteristics of Propionyl Chloride (CH3CH2COCl). It describes the dangers associated with this chemical, along with appropriate safety precautions for handling. Users should carefully review this document to guarantee a safe and workplace.
- Major points covered in this sheet contain: chemical identification, hazards identification, first aid measures, firefighting measures, accidental release measures, handling and storage, exposure controls/personal protection, physical and chemical properties, stability and reactivity, toxicological information, ecological information, disposal considerations, regulatory information, transportation information
Applications of Propionyl Chloride in Organic Synthesis
Propionyl chloride acts as a versatile chemical intermediate in organic synthesis, owing to its electrophilic acyl group. It can be readily utilized in a variety of reactions to construct complex molecules with diverse structures. One prominent application is the formation of ketones through acylation processes, where propionyl chloride reacts with alcohols or amines. Furthermore, it plays a crucial role in the manufacture of esters by interacting with alcohols under appropriate circumstances.
The use of propionyl chloride extends to the preparation of amides, where it transforms with amines. This versatile reagent also finds relevance in the alteration of existing organic molecules, such as the introduction of acetyl groups into compounds.
- Examples of propionyl chloride's implementations in organic synthesis include:
- An synthesis of pharmaceuticals, such as ibuprofen.
- An manufacturing of agrochemicals, like pesticides and herbicides.
- A construction of fragrances and flavors.
Storing and Handling Propionyl Chloride (CH3CH2COCl)
Propionyl chloride possesses highly reactive chemical substance that demands careful handling and storage practices to minimize potential hazards. Always handling propionyl chloride, ensure you don appropriate personal protective equipment such as chemical-resistant gloves, eye protection, and a lab coat.
Store propionyl chloride in a temperature-controlled area, away from incompatible materials such as strong oxidizing agents and bases. Ensure proper ventilation in the storage room to reduce the risk of vapor buildup.
When transferring propionyl chloride, use suitable equipment, such as a glass transfer pipette or Teflon tubing, and avoid contact with eyes.
Should of accidental exposure, immediately flush the affected area with plenty of water for at least 30 minutes.
It is crucial to review the material safety data sheet (MSDS) for detailed information on handling, storage, and emergency procedures related to propionyl chloride.
Analytical Characterization of Propionyl Chloride (CAS 79-03-8)
Propionyl chloride, with the CAS number 79.03.8, is a reactive chemical compound widely utilized in various industrial processes. Its physical properties make it an important reagent for the synthesis of diverse compounds. To ensure its safe and effective application, detailed analytical characterization is crucial.
Various experimental techniques are employed to comprehensively analyze propionyl chloride. P304+340: IF INHALED: Remove victim to fresh air and keep at rest in a position comfortable for breathing These include spectroscopic such as infrared spectroscopy, which provide valuable information about its composition. Additionally, thermal analysis measurements contribute to a complete understanding of this versatile compound.
- Physicochemical characterization techniques are instrumental in identifying the functional groups and structure of propionyl chloride.
- Chromatographic methods allow for the separation and quantification of impurities present in propionyl chloride samples.
- Boiling point measurement provides insights into the thermal stability and properties of propionyl chloride.
The results obtained from these analytical characterizations enable the proper handling, storage, and application of propionyl chloride in various industrial settings. By understanding its chemical and physical characteristics, safety precautions can be implemented effectively, minimizing potential hazards.