Description
Specifications Table
Product Name – 4-BROMOACETANILIDE 98% For Synthesis
Quantity/Pack Size – 100 g, 500 g
Form – Solid (Powder/Crystals)
Grade – For Synthesis
Application – Organic synthesis, chemical research
Product Overview
4-Bromoacetanilide 98% is a high-purity chemical compound designed for synthesis applications, offering exceptional reactivity and stability in organic reactions. This synthesis-grade reagent is meticulously processed to ensure minimal impurities, making it a reliable choice for laboratory experiments requiring precise chemical transformations. Its brominated structure enhances its utility in substitution reactions, while the acetanilide backbone provides stability under varying conditions. The compound is commonly used in the preparation of pharmaceutical intermediates, specialty chemicals, and advanced materials. With a purity of 98%, it meets stringent quality standards, ensuring consistent results in research and development workflows. The solid form, typically powder or crystals, allows for easy handling and accurate measurement. Whether used in small-scale experiments or larger synthesis projects, this compound delivers dependable performance, making it a staple in chemical laboratories. Proper storage in a cool, dry place preserves its integrity, while adherence to standard lab safety protocols ensures safe handling.
FAQs
1. What is the chemical structure of 4-Bromoacetanilide?
4-Bromoacetanilide features a bromine atom at the para position of an acetanilide molecule, with the formula C8H8BrNO.
2. Is this compound compatible with aqueous solutions?
It has limited solubility in water but dissolves well in organic solvents like ethanol, acetone, and dichloromethane.
3. Are there any alternatives to 4-Bromoacetanilide for similar applications?
Alternatives include 4-bromoaniline or 4-iodoacetanilide, depending on the specific reaction requirements.
4. What is the recommended storage condition for this compound?
Store in a tightly sealed container in a cool, dry place, away from direct sunlight and moisture.
5. Can this compound be used in halogenation reactions?
Yes, the bromine substituent makes it suitable for further halogenation or nucleophilic substitution reactions.
