Propionyl Chloride (CH3CH2COCl) - 100g

This considerable quantity of the chemical reagent weighs one hundred grams. It is a clear substance with a pungent odor. Propionyl Chloride plays a role in various chemical reactions, including the preparation of diverse organic compounds. Exercise caution when handling as Propionyl Chloride is harmful to the human body.

Properties of CAS 79-03-8

CAS 79-03-8, formally recognized as cyclohexanone, possesses a myriad of interesting physical and chemical attributes. This colorless to light yellow liquid exhibits a characteristic fragrance. At standard ambient conditions, its melting point is approximately -88°C while the boiling point is approximately 158°C.

  • This exhibits a density of 0.97 g/cm³ and its volatility is high
  • 4,6-Dimethyl-1-methylpiperidin-3-ol is soluble in a variety of solvents including water, ethanol, and acetone.
  • The compound reacts with various substances under certain conditions, leading to numerous transformations

Safety Data Sheet for

This Technical Datasheet provides essential information regarding the characteristics of Propionyl Chloride (CH3CH2COCl). It describes the risks associated with this chemical, along with guidelines for storage. Users should thoroughly read this document to guarantee a safe and workplace.

  • Fundamental components covered in this document encompass: 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 is a versatile chemical intermediate in organic synthesis, owing to its functional acyl group. It can be readily incorporated in a variety of reactions to construct complex molecules with diverse architectures. One prominent application is the synthesis of ketones through acylation transformations, where propionyl chloride couples with alcohols or amines. Furthermore, it plays a crucial role in the production of esters by interacting with alcohols under appropriate conditions.

The employment of propionyl chloride extends to the preparation of amides, where it reacts with amines. This versatile reagent also finds application in the alteration of existing organic molecules, such as the introduction of acetyl groups into molecules.

  • Instances of propionyl chloride's uses in organic synthesis encompass:
  • An synthesis of pharmaceuticals, such as ibuprofen.
  • A manufacturing of agrochemicals, like pesticides and herbicides.
  • A production of fragrances and flavors.

Handling and Storage Propionyl Chloride (CH3CH2COCl)

Propionyl chloride is a highly reactive chemical substance that demands precise handling and storage practices to minimize potential hazards. Before handling propionyl chloride, ensure you utilize appropriate personal protective equipment P304+340: IF INHALED: Remove victim to fresh air and keep at rest in a position comfortable for breathing such as chemical-resistant gloves, eye protection, and a lab coat.

Store propionyl chloride in a temperature-controlled area, separated from incompatible materials such as strong oxidizing agents and bases. Ensure proper ventilation in the storage area to minimize the risk of vapor buildup.

When transferring propionyl chloride, use appropriate equipment, such as a glass transfer pipette or Teflon tubing, and avoid contact with skin.

Should of accidental exposure, immediately wash the affected area with plenty of water for at least 30 minutes.

It is crucial to refer the material safety data sheet (MSDS) for comprehensive information on handling, storage, and emergency procedures related to propionyl chloride.

Examining the Properties 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 chemical properties make it an important reagent for the manufacture of diverse products. To ensure its safe and effective application, detailed analytical characterization is necessary.

Various experimental techniques are employed to comprehensively analyze propionyl chloride. These include spectroscopic such as gas chromatography-mass spectrometry (GC-MS), which provide valuable information about its molecular weight. 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.
  • Separation 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 support the proper handling, storage, and application of propionyl chloride in various industrial settings. By understanding its chemical and physical properties, safety precautions can be implemented effectively, minimizing potential hazards.

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