Propionyl chloride often (CH3CH2COCl) is a valuable reagent within the sphere of organic synthesis. 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 evaporative compound at room temperature. Its density is moderately 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 humid-controlled location, away from harmful 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, 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.
Obtain Propionyl Chloride CAS 79-03-8
This offering presents a bulk volume of 100g of Propionyl Chloride, characterized by its CAS number 79-03-8. 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 safely to ensure integrity during transportation.
Propionyl chloride plays a crucial role in synthesizing numerous chemicals, including pharmaceuticals, agrochemicals, and polymers. Its reactivity makes it a valuable reagent in organic chemistry transformations. Select this reliable source for your Propionyl Chloride needs.
Safety Data Sheet : Propionyl Chloride CH3CH2COCl
Propionyl chloride is a a dangerous chemical compound. It presents with the formula CH3CH2COCl. Propionyl chloride is highly reactive and can lead to significant harmful effects on exposed tissues. Storage of propionyl chloride requires meticulous attention following all relevant procedures.
A comprehensive Safety Data Sheet (SDS) for propionyl chloride is mandatory for ensuring the health and safety of individuals involved in this chemical. The SDS provides crucial details on:
* Potential hazards associated with propionyl chloride
* Procedures for safe Product Specifications use
* Immediate actions to take in case of exposure
* Storage requirements
* Personal protective equipment (PPE)
Always consult the SDS before handling, using, or storing propionyl chloride. Compliance with 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 applied for the formation of propionate esters and amides. Its reactive carbonyl group readily undergoes electrophilic attacks, enabling the creation of complex organic compounds. Additionally, propionyl chloride is crucial in the manufacture of various drugs, agrochemicals, and ingredients.
In some organic procedures, propionyl chloride can combine with alcohols to form esters, while interaction with amines yields amides. Its durability under various environments makes it a valuable tool in the realm 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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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 Chemical Workhorse
Propionyl chloride is a widely utilized reagent in organic synthesis owing to its' versatility. This colorless liquid, characterized by a sharp fragrance, readily undergoes nucleophilic substitution reactions, making it an indispensable tool for constructing a diverse range of organic structures. From common esters to complex heterocyclic rings, propionyl chloride contributes a pivotal role in bringing about molecular modifications.
Its ability to interact with various molecular moieties significantly amplifies its utility.
For instance, propionyl chloride can be employed in the synthesis of:
* Esters with aromatic rings
* Amides
* Carboxylic acids
This versatile reagent is employed in numerous industries, including pharmaceuticals, agrochemicals, and polymers.
Its strong propensity to react and convenient workability have cemented its position as a staple reagent in the chemist's arsenal.