Propionyl chloride often (CH3CH2COCl) is a valuable reagent within the field of organic synthesis. This colorless to pale yellow substance 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 volatile compound at room temperature. Its density is reasonably higher than that of water, indicating its tendency to settle upon contact.
Due to its reactive nature, propionyl chloride should always be stored in a refrigerated and humid-controlled location, away from reactive 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 P280: Wear protective gloves/protective clothing/eye protection/face protection 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.
100g Propionyl Chloride CAS 79-03-8 for Chemical Synthesis
This offering presents a quantity supply 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 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 reactions. Choose this reliable source for your Propionyl Chloride needs.
SDS : Propionyl Chloride CH3CH2COCl
Propionyl chloride acts as an extremely hazardous chemical compound. It possesses the chemical formula CH3CH2COCl. Propionyl chloride is highly reactive and can cause severe damage to the skin, eyes, and respiratory tract. Utilization of propionyl chloride must be undertaken with extreme care following all relevant regulations.
Full documentation regarding the safety precautions for propionyl chloride is mandatory for ensuring the well-being of individuals engaged with this chemical. The SDS provides essential data on:
* Health risks associated with propionyl chloride
* Guidelines for minimizing risk
* Emergency response protocols
* Conditions for safe storage
* Protective gear
Seek guidance from the SDS before handling, using, or storing propionyl chloride. Adhering to the information provided in the SDS is indispensable for preventing accidents and ensuring a safe working environment.
Uses of Propionyl Chloride in Organic Chemistry
Propionyl chloride serves as a versatile chemical in organic synthesis, widely applied for the synthesis of propionate esters and amides. Its potent carbonyl group readily engages nucleophilic attacks, enabling the assembly of complex organic structures. Moreover, propionyl chloride is crucial in the production of various medications, herbicides, and flavoring agents.
In some organic procedures, propionyl chloride can combine with alcohols to form esters, while combination with amines yields amides. Its stability under various conditions makes it a valuable tool in the realm of organic synthesis.
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li Propionyl chloride is commonly applied in the production of propionic acid and its derivatives.
li It can be used to produce 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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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 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 compounds. From simple esters to complex heterocyclic cycles, propionyl chloride performs a pivotal role in facilitating chemical reactions.
Its ability to interact with various chemical groups greatly improves its utility.
For instance, propionyl chloride can be utilized in the synthesis of:
* Esters with aromatic rings
* Amides
* Carboxylic acids
This versatile reagent is employed in numerous industries, including 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.