Description
Specifications Table
Product Name – 4-Chlorobutyryl chloride
Quantity/Pack Size – 100 ml
Form – Liquid
Grade – Laboratory Grade
Application – Organic synthesis, acylating agent
Product Overview
4-Chlorobutyryl chloride is a highly reactive acyl chloride used extensively in organic synthesis for introducing the 4-chlorobutyryl moiety into target molecules. This laboratory-grade reagent is valued for its purity and consistent performance in reactions such as Friedel-Crafts acylation, esterification, and amide formation. The compound’s chlorine substituent enhances its reactivity, making it a preferred choice for synthesizing pharmaceutical intermediates, agrochemicals, and specialty chemicals. Its liquid form ensures easy handling and precise dosing in laboratory settings. With a high degree of stability under recommended storage conditions, this reagent is ideal for researchers seeking reliable and reproducible results. The absence of impurities ensures minimal side reactions, making it suitable for sensitive applications. Whether used in small-scale experiments or larger synthetic processes, 4-chlorobutyryl chloride delivers exceptional performance, supporting the development of complex organic molecules with precision.
FAQs
1. What is the primary application of 4-chlorobutyryl chloride?
4-Chlorobutyryl chloride is primarily used as an acylating agent in organic synthesis, particularly for introducing the 4-chlorobutyryl group into various compounds.
2. Is this reagent compatible with standard glassware?
Yes, 4-chlorobutyryl chloride is compatible with standard borosilicate glassware, but it should be handled in a fume hood due to its corrosive nature.
3. What are the recommended storage conditions for this product?
Store 4-chlorobutyryl chloride in a cool, dry place, away from moisture and incompatible substances, in a tightly sealed container.
4. Are there any alternatives to 4-chlorobutyryl chloride for similar applications?
Alternatives include other acyl chlorides like butyryl chloride or chloroacetyl chloride, depending on the specific functional group required.
5. How should I handle this reagent safely?
Always wear appropriate personal protective equipment, including gloves and goggles, and handle the reagent in a well-ventilated area or fume hood.
