Propionyl chloride often (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 volatile compound at room temperature. Its density is slightly 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, protective clothing 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.
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. more info 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 carefully 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 transformations. Opt for this reliable source for your Propionyl Chloride needs.
SDS : Propionyl Chloride CH3CH2COCl
Propionyl chloride serves as a hazardous chemical compound. It has the formula CH3CH2COCl. Propionyl chloride is very reactive and can cause severe harmful effects on exposed tissues. 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 well-being of individuals involved in this chemical. The SDS provides crucial details on:
* Possible dangers associated with propionyl chloride
* Safe handling practices
* First aid measures
* Storage requirements
* Personal protective equipment (PPE)
Seek guidance from the SDS before employing propionyl chloride. Adhering to the information provided in the SDS is indispensable for preventing accidents and ensuring a safe working environment.
Applications of Propionyl Chloride in Organic Chemistry
Propionyl chloride functions as a versatile chemical in organic synthesis, widely utilized for the formation of propionate esters and amides. Its active carbonyl group readily engages ionic , substitutions, enabling the construction of complex organic molecules. Moreover, propionyl chloride is instrumental in the manufacture of various medications, herbicides, and flavoring agents.
In some chemical procedures, propionyl chloride can combine with alcohols to form esters, while interaction with amines results amides. Its stability under various circumstances makes it a important tool in the scope 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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Synthesis and Characterization 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 Key Tool in Organic Synthesis
Propionyl chloride serves 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 structures. From simple esters to complex heterocyclic cycles, propionyl chloride contributes a pivotal role in facilitating chemical reactions.
Its ability to engage in various functional groups further enhances its utility.
For instance, propionyl chloride can be employed in the preparation of:
* Benzene-based esters
* Amides
* Carboxylic acids
This versatile reagent plays a role in numerous industries, such as pharmaceuticals, agrochemicals, and polymers.
Its strong propensity to react and relative ease of handling have cemented its position as a staple reagent in the chemist's arsenal.