Propionyl chloride typically (CH3CH2COCl) is a valuable reagent within the field of organic synthesis. Product Specifications This colorless to pale yellow liquid 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 vaporous 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 well-ventilated and dry location, away from incompatible 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, 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.
Obtain Propionyl Chloride CAS 79-03-8
This offering presents a bulk 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 securely to ensure integrity during transportation.
Propionyl chloride plays a crucial role in synthesizing a variety of chemicals, including pharmaceuticals, agrochemicals, and polymers. Its reactivity makes it a valuable reagent in organic chemistry transformations. Choose 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 highly reactive and can lead to significant injury upon skin, eyes, and respiratory system. Utilization of propionyl chloride should be performed cautiously following all relevant safety guidelines.
A comprehensive Safety Data Sheet (SDS) for propionyl chloride is mandatory for ensuring the protection of individuals engaged with this chemical. The SDS provides vital information on:
* Potential hazards associated with propionyl chloride
* Safe handling practices
* Emergency response protocols
* Proper handling and containment
* Protective gear
Refer to 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 reagent in organic synthesis, widely utilized for the introduction of propionate esters and amides. Its reactive carbonyl group readily engages ionic attacks, enabling the construction of complex organic structures. Additionally, propionyl chloride is instrumental in the manufacture of various medications, herbicides, and ingredients.
In some synthetic procedures, propionyl chloride can react with alcohols to form esters, while interaction with amines yields amides. Its stability under various circumstances makes it a valuable tool in the realm of organic synthesis.
ul
li Propionyl chloride is commonly employed in the production of propionic acid and its derivatives.
li It can be used to create 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.
ul
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 is a widely utilized reagent in organic synthesis owing to its remarkable reactivity. This colorless liquid, characterized by an acrid smell, readily undergoes attacks from nucleophiles, making it an indispensable tool for constructing a diverse range of organic compounds. 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 significantly amplifies its utility.
For instance, propionyl chloride can be employed in the synthesis of:
* Benzene-based esters
* Amides
* Carboxylic acids
This versatile reagent is employed in numerous industries, such as pharmaceuticals, agrochemicals, and polymers.
Its powerful nature and simplicity of use have cemented its position as a staple reagent in the chemist's arsenal.