Propionyl chloride typically (CH3CH2COCl) is a valuable reagent within the realm 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 volatile compound at room temperature. Its density is slightly 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 cool and dry location, away from incompatible 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, swiftly 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 bulk amount of one hundred grams of Propionyl Chloride, characterized by its CAS P280: Wear protective gloves/protective clothing/eye protection/face protection number 79-03-8. This compound is widely utilized in various chemical synthesis applications. Purchase 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 creating a variety of chemicals, including pharmaceuticals, agrochemicals, and polymers. Its reactivity makes it a valuable reagent in organic chemistry reactions. Opt for this reliable source for your Propionyl Chloride needs.
SDS : Propionyl Chloride CH3CH2COCl
Propionyl chloride serves as an extremely hazardous chemical compound. It possesses the chemical formula CH3CH2COCl. Propionyl chloride is highly reactive and can lead to significant injury upon exposed tissues. Handling of propionyl chloride must be undertaken with extreme care following all relevant procedures.
Detailed information concerning potential hazards and safe handling practices for propionyl chloride is essential for ensuring the protection of individuals engaged with this chemical. The SDS provides essential data on:
* Health risks associated with propionyl chloride
* Procedures for safe use
* Emergency response protocols
* Proper handling and containment
* Equipment necessary for safe handling
Refer to the SDS before employing propionyl chloride. Adhering to 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 functions as a versatile chemical in organic synthesis, widely utilized for the formation of propionate esters and amides. Its potent carbonyl group readily participates electrophilic attacks, enabling the creation of complex organic molecules. Furthermore, propionyl chloride is instrumental in the manufacture of various medications, agrochemicals, and food additives.
In some chemical procedures, propionyl chloride can interact with alcohols to form esters, while reaction with amines results amides. Its resistance under various environments makes it a important tool in the field 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—A Key Tool in Organic Synthesis
Propionyl chloride serves as a widely utilized reagent in organic synthesis owing to its remarkable reactivity. This colorless liquid, characterized by a pungent odor, readily undergoes nucleophilic substitution reactions, making it an indispensable tool for forming a diverse range of organic molecules. From simple esters to complex heterocyclic rings, propionyl chloride contributes a pivotal role in bringing about molecular modifications.
Its ability to engage in various chemical groups further enhances its utility.
For instance, propionyl chloride can be utilized in the creation of:
* Esters with aromatic rings
* Amides
* Carboxylic acids
This versatile reagent finds applications numerous industries, amongst 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.