Propionyl chloride often (CH3CH2COCl) is a valuable reagent within the sphere 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 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, 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.
High Purity Propionyl Chloride CAS 79-03-8 for Sale
This offering presents a substantial amount of exactly one hundred grams of Propionyl Chloride, characterized by its CAS 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 click here plays a crucial role in generating diverse 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 a hazardous chemical compound. It presents with the formula CH3CH2COCl. Propionyl chloride is extremely reactive and can cause severe harmful effects on exposed tissues. Handling of propionyl chloride requires meticulous attention following all relevant safety guidelines.
Detailed information concerning potential hazards and safe handling practices for propionyl chloride is mandatory for ensuring the protection of individuals exposed to this chemical. The SDS provides vital information on:
* Possible dangers associated with propionyl chloride
* Guidelines for minimizing risk
* Immediate actions to take in case of exposure
* Conditions for safe storage
* Protective gear
Refer to the SDS before handling, using, or storing propionyl chloride. Strict observation of the information provided in the SDS is paramount for preventing accidents and ensuring a safe working environment.
Applications of Propionyl Chloride in Organic Chemistry
Propionyl chloride acts as a versatile compound in organic synthesis, widely utilized for the synthesis of propionate esters and amides. Its reactive carbonyl group readily engages ionic attacks, enabling the assembly of complex organic molecules. Furthermore, propionyl chloride is crucial in the manufacture of various medications, agrochemicals, and ingredients.
In some organic procedures, propionyl chloride can combine with alcohols to form esters, while interaction with amines produces amides. Its durability under various conditions makes it a important tool in the field 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
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 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 cycles, propionyl chloride contributes a pivotal role in achieving desired transformations.
Its ability to interact with various molecular moieties further enhances its utility.
For instance, propionyl chloride can be employed in the preparation of:
* Benzene-based esters
* Amides
* Carboxylic acids
This versatile reagent finds applications numerous industries, including 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.