Propionyl Chloride (CH3CH2COCl): Physical Properties and Handling

Propionyl chloride typically (CH3CH2COCl) is a valuable reagent within the realm of organic synthesis. This colorless to pale yellow solution possesses a pungent, irritating odor that necessitates careful 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 submerge upon contact.

Due to its reactive nature, propionyl chloride should always be stored in a cool and humid-controlled location, away from harmful substances such as strong bases and oxidizing agents. During handling, personal protective equipment is essential to minimize the risk of skin or eye contact and inhalation exposure. In case of accidental exposure, immediately 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 substantial amount of 100g 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 safely to ensure integrity during transportation.

Propionyl chloride plays a crucial role in generating diverse chemicals, including pharmaceuticals, agrochemicals, and polymers. Its reactivity makes it a valuable reagent in organic chemistry transformations. Opt for this reliable source for your Propionyl Chloride needs.

SDS : Propionyl Chloride CH3CH2COCl

Propionyl chloride acts as a dangerous chemical compound. It possesses the chemical formula CH3CH2COCl. Propionyl chloride is highly reactive and can result in damage to the skin, eyes, and respiratory tract. Handling of propionyl chloride requires meticulous attention following all relevant regulations.

Full documentation regarding the safety precautions for propionyl chloride is crucial for ensuring the protection of individuals exposed to this chemical. The SDS provides crucial details on:

* Potential hazards associated with propionyl chloride

* Safe handling practices

* Emergency response protocols

* Storage requirements

* Personal protective equipment (PPE)

Refer to the SDS before employing propionyl chloride. Strict observation of the information provided in the SDS is paramount for preventing accidents and ensuring a safe working environment.

Uses of Propionyl Chloride in Organic Chemistry

Propionyl chloride acts as a versatile compound in organic synthesis, widely applied for the introduction of propionate esters and amides. Its potent carbonyl group readily participates ionic , substitutions, enabling the creation of complex organic structures. Furthermore, propionyl chloride is instrumental in the production of various drugs, agrochemicals, and food additives.

In some organic procedures, propionyl chloride can react with alcohols to form esters, while interaction with amines results amides. Its durability under various environments makes it a important tool in the scope of organic synthesis.

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li Propionyl chloride is commonly employed in the production of propionic acid and its derivatives.

li It can be used to H331: Toxic if inhaled 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.

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Preparation and Analysis 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 acts as a widely utilized reagent in organic synthesis owing to their remarkable reactivity. This colorless liquid, characterized by a pungent odor, readily undergoes attacks from nucleophiles, making it an indispensable tool for forming a diverse range of organic molecules. From common esters to complex heterocyclic rings, propionyl chloride plays a pivotal role in achieving desired transformations.

Its ability to interact with various molecular moieties further enhances its utility.

For instance, propionyl chloride can be applied in the creation of:

* Benzene-based esters

* Amides

* Carboxylic acids

This versatile reagent plays a role in numerous industries, such as pharmaceuticals, agrochemicals, and polymers.

Its powerful nature and relative ease of handling have cemented its position as a staple reagent in the chemist's arsenal.

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