Propionyl chloride commonly (CH3CH2COCl) is a valuable reagent within the realm of organic synthesis. This colorless to pale yellow liquid possesses a pungent, irritating odor that necessitates prudent handling. With a boiling point of approximately 79 °C and a melting point around -60 °C, propionyl chloride exists as a evaporative compound at room temperature. Its density is slightly higher than that of water, indicating its tendency to sink upon contact.
Due to its reactive nature, propionyl chloride should always be stored in a cool and humid-controlled location, away from incompatible substances such as strong bases and oxidizing agents. During handling, safety gear is essential to minimize the risk of skin or eye contact and inhalation exposure. In case of accidental exposure, promptly flush affected areas with copious amounts of water and seek medical attention.
- Physical Properties
- Appearance: Colorless to pale yellow liquid
- Odor: Pungent, irritating
- Boiling Point: Approximately 79 °C
- Melting Point: Around -60 °C
- Density: Slightly higher than water
- Handling Precautions
- Store in a cool, dry location away from incompatible substances.
- Wear personal protective equipment (gloves, goggles, respirator) during handling.
- In case of exposure, flush affected areas with water and seek medical attention.
High Purity Propionyl Chloride CAS 79-03-8 for Sale
This offering presents a bulk amount of exactly one hundred grams of Propionyl Chloride, characterized by its CAS number 79-03-8. This compound is widely utilized in various chemical synthesis applications. Acquire this high purity Propionyl Chloride for your research endeavors or industrial processes. It arrives packaged securely to ensure integrity during transportation.
Propionyl chloride plays a crucial role in generating a variety of chemicals, including pharmaceuticals, agrochemicals, and polymers. Its reactivity makes it a valuable reagent in organic chemistry processes. Choose this reliable source for more info your Propionyl Chloride needs.
SDS : Propionyl Chloride CH3CH2COCl
Propionyl chloride serves as a hazardous chemical compound. It possesses the chemical formula CH3CH2COCl. Propionyl chloride is extremely reactive and can result in injury upon skin, eyes, and respiratory system. Storage of propionyl chloride requires meticulous attention following all relevant regulations.
Detailed information concerning potential hazards and safe handling practices for propionyl chloride is essential for ensuring the protection of individuals involved in this chemical. The SDS provides crucial details on:
* Possible dangers associated with propionyl chloride
* Procedures for safe use
* Immediate actions to take in case of exposure
* Conditions for safe storage
* Equipment necessary for safe handling
Refer to the SDS before handling, using, or storing propionyl chloride. Strict observation of the information provided in the SDS is crucial for preventing accidents and ensuring a safe working environment.
Uses of Propionyl Chloride in Organic Chemistry
Propionyl chloride functions as a versatile compound in organic synthesis, widely applied for the formation of propionate esters and amides. Its reactive carbonyl group readily undergoes ionic , substitutions, enabling the assembly of complex organic compounds. Furthermore, propionyl chloride is crucial in the synthesis of various drugs, herbicides, and food additives.
In some chemical procedures, propionyl chloride can react with alcohols to form esters, while reaction with amines yields amides. Its stability under various conditions makes it a valuable tool in the field of organic synthesis.
ul
li Propionyl chloride is commonly employed in the production of propionic acid and its derivatives.
li It can be used to synthesize esters and amides, which are important building blocks in organic chemistry.
li Propionyl chloride is also used in the synthesis of pharmaceuticals, agrochemicals, and flavoring agents.
ul
Production and Evaluation of Propionyl Chloride
Propionyl chloride is a/represents/serves as a widely used acyl chloride in organic synthesis. Its synthesis/preparation/manufacture typically involves the reaction/combination/interaction of propionic acid with a chlorinating agent, such as thionyl chloride or phosphorus pentachloride. The resulting/produced/obtained propionyl chloride can be characterized/may be identified/is evaluated by various methods, including gas chromatography/infrared spectroscopy/melting point determination.
- Gas chromatography/Infrared Spectroscopy/Nuclear Magnetic Resonance/NMR/, allows for the identification/confirmation/analysis of the product's structure and purity.
- Melting point/temperature/range provides evidence/proof/indication of the compound's identity, as it is a characteristic property.
- Titration/Chemical Analysis/Quantitative Assay can be used to determine the concentration/amount/percentage of propionyl chloride in a solution.
Propionyl Chloride (CH3CH2COCl): A Versatile Reagent
Propionyl chloride is a widely utilized reagent in organic synthesis owing to its' efficiency. This colorless liquid, characterized by a sharp fragrance, readily undergoes reaction with nucleophiles, making it an indispensable tool for forming a diverse range of organic compounds. From common esters to complex heterocyclic systems, propionyl chloride plays a pivotal role in achieving desired transformations.
Its ability to participate various chemical groups further enhances its utility.
For instance, propionyl chloride can be utilized in the preparation of:
* Esters with aromatic rings
* Amides
* Carboxylic acids
This versatile reagent finds applications numerous industries, such as pharmaceuticals, agrochemicals, and polymers.
Its high reactivity and relative ease of handling have cemented its position as a staple reagent in the chemist's arsenal.