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 extreme 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 reasonably 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 well-ventilated and moisture-free 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 amount of 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 carefully to ensure integrity during transportation.
Propionyl chloride plays a crucial role in creating a variety of chemicals, including pharmaceuticals, agrochemicals, and polymers. Its reactivity makes it a valuable reagent in organic chemistry reactions. Select this reliable source for your Propionyl Chloride needs.
Safety Data Sheet : Propionyl Chloride CH3CH2COCl
Propionyl chloride serves as an extremely hazardous chemical compound. It has the formula CH3CH2COCl. Propionyl chloride is very reactive and can lead to significant injury upon exposed tissues. Handling of propionyl chloride must be undertaken with extreme care following all relevant safety guidelines.
A comprehensive Safety Data Sheet (SDS) for propionyl chloride is mandatory for ensuring the protection of individuals involved in this chemical. The SDS provides crucial details on:
* Health risks associated with propionyl chloride
* Procedures for safe use
* Emergency response protocols
* Storage requirements
* Equipment necessary for safe handling
Refer to the SDS before employing 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 acts as a versatile reagent in organic synthesis, widely utilized for the introduction of propionate esters and amides. Its potent carbonyl group readily engages ionic attacks, enabling the assembly of complex organic compounds. Furthermore, propionyl chloride is instrumental in the production of various medications, pesticides, and ingredients.
In some organic procedures, propionyl chloride can interact with alcohols to form esters, while reaction with amines results amides. Its durability under various environments makes it a significant tool in the scope of organic synthesis.
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li Propionyl chloride is commonly used 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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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 serves as a widely utilized reagent in organic synthesis owing to its' versatility. This colorless liquid, characterized by a sharp fragrance, readily undergoes reaction with nucleophiles, making it an indispensable tool for synthesizing a diverse range of organic structures. From simple esters to complex get more info heterocyclic rings, propionyl chloride plays a pivotal role in facilitating chemical reactions.
Its ability to interact with various molecular moieties significantly amplifies its utility.
For instance, propionyl chloride can be applied in the creation of:
* Esters with aromatic rings
* Amides
* Carboxylic acids
This versatile reagent plays a role in 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.