Propionyl chloride typically (CH3CH2COCl) is a valuable reagent within the sphere of organic synthesis. This colorless to pale yellow solution 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 vaporous compound at room temperature. Its density is reasonably 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 well-ventilated and dry location, away from incompatible 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.
Obtain Propionyl Chloride CAS 79-03-8
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. Obtain 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 creating numerous chemicals, including pharmaceuticals, agrochemicals, and polymers. Its reactivity makes it a valuable reagent in organic chemistry processes. Select this reliable source for your Propionyl Chloride needs.
Material Safety Data Sheet : Propionyl Chloride CH3CH2COCl
Propionyl chloride acts as an extremely hazardous chemical compound. It has the formula CH3CH2COCl. Propionyl chloride is highly reactive and can lead to significant damage to exposed tissues. Storage of propionyl chloride should be performed cautiously following all relevant regulations.
Detailed information concerning potential hazards and safe handling practices for propionyl chloride is mandatory for ensuring the protection of individuals engaged with this chemical. The SDS provides essential data on:
* Possible dangers associated with propionyl chloride
* Safe handling practices
* Immediate actions to take in case of exposure
* Conditions for safe storage
* Equipment necessary for safe handling
Seek guidance from the SDS before interacting with, manipulating, or retaining propionyl chloride. Adhering to the information provided in the SDS is crucial for preventing accidents and ensuring a safe working environment.
Implementations of Propionyl Chloride in Organic Chemistry
Propionyl chloride acts as a versatile chemical in organic synthesis, widely employed for the synthesis of propionate esters and amides. Its reactive carbonyl group readily undergoes nucleophilic , substitutions, enabling the creation of complex organic structures. Moreover, propionyl chloride is crucial in the production of various medications, herbicides, and food additives.
In some organic procedures, propionyl chloride can interact with alcohols to form esters, while reaction with amines results amides. Its stability under various environments 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 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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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: A Chemical Workhorse
Propionyl chloride acts as a widely utilized reagent in organic synthesis H314: Causes severe skin burns and eye damage owing to their efficiency. This colorless liquid, characterized by an acrid smell, readily undergoes attacks from nucleophiles, making it an indispensable tool for forming a diverse range of organic molecules. From everyday esters to complex heterocyclic cycles, propionyl chloride contributes a pivotal role in bringing about molecular modifications.
Its ability to engage in various chemical groups greatly improves its utility.
For instance, propionyl chloride can be employed in the synthesis of:
* Esters with aromatic rings
* Amides
* Carboxylic acids
This versatile reagent finds applications numerous industries, amongst pharmaceuticals, agrochemicals, and polymers.
Its high reactivity and convenient workability have cemented its position as a staple reagent in the chemist's arsenal.