Propionyl Chloride (CH3CH2COCl) - 100g

This bulk supply of this compound weighs a precise 100g. It is a colorless solution with a pungent odor. Propionyl Chloride plays a role in various chemical reactions, including the preparation of esters, amides, and other organic compounds. Always handle with care as Propionyl Chloride is corrosive to living tissues.

Properties of CAS 79-03-8

CAS this compound, formally identified as 4,6-Dimethyl-1-methylpiperidin-3-ol, possesses a myriad of fascinating physical and chemical properties. This colorless to light yellow liquid exhibits a characteristic fragrance. At standard conditions, its melting point is approximately -88°C while the boiling point is roughly 156°C.

  • This exhibits a density of 0.99 g/cm³ and its volatility is low
  • 4,6-Dimethyl-1-methylpiperidin-3-ol is dissolves in a variety of solvents including water, ethanol, and acetone.
  • CAS 79-03-8 reacts in the presence of various reagents under certain situations, leading to diverse processes

Safety Data Sheet for

This Information Sheet provides vital details regarding the attributes of Propionyl Chloride (CH3CH2COCl). It describes the potential hazards associated with this substance, along with measures for handling. Users should thoroughly read this document to ensure a safe and operational setting.

  • Major points covered in this information pack 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 reagent in organic synthesis, owing to its reactive 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 reacts with alcohols or amines. Furthermore, it plays a crucial role in the manufacture of esters by interacting with alcohols under appropriate circumstances.

The employment of propionyl chloride extends to the preparation of amides, where it couples with amines. This versatile reagent also finds application in P303+361: IF ON SKIN (or hair): Remove/Take off immediately all contaminated clothing. Rinse skin with water/shower the transformation of existing organic molecules, such as the introduction of acetyl groups into compounds.

  • Instances of propionyl chloride's implementations in organic synthesis comprise:
  • The synthesis of pharmaceuticals, such as ibuprofen.
  • An generation of agrochemicals, like pesticides and herbicides.
  • An construction of fragrances and flavors.

Guidelines for Managing Propionyl Chloride (CH3CH2COCl)

Propionyl chloride possesses highly reactive chemical substance that demands careful handling and storage practices to minimize potential hazards. Prior 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 well-ventilated area, separated from incompatible materials such as strong oxidizing agents and bases. Ensure proper ventilation in the storage room to mitigate 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 eyes.

In case of accidental exposure, promptly wash the affected area with plenty of water for at least 20 minutes.

It is crucial to consult the material safety data sheet (MSDS) for detailed 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 volatile chemical compound widely utilized in various industrial processes. Its chemical properties make it an important reagent for the production of diverse compounds. To ensure its safe and effective application, detailed analytical characterization is essential.

Various characterization techniques are employed to comprehensively analyze propionyl chloride. These include instrumental methods such as infrared spectroscopy, which provide valuable information about its composition. Additionally, thermal analysis measurements contribute to a complete understanding of this useful compound.

  • Chemical characterization techniques are instrumental in identifying the functional groups and structure of propionyl chloride.
  • Analytical methods allow for the separation and quantification of impurities present in propionyl chloride samples.
  • Thermal analysis 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.

Leave a Reply

Your email address will not be published. Required fields are marked *