Description
Specifications Table
Product Name – 4-METHOXYBENZYL CYANIDE 96% For Synthesis
Quantity/Pack Size – 100 ml
Form – Liquid
Grade – For Synthesis
Application – Organic synthesis, reagent in chemical reactions
Product Overview
4-Methoxybenzyl Cyanide 96% is a high-purity chemical reagent designed for precision in organic synthesis. This compound features a methoxy-substituted benzyl structure with a nitrile functional group, making it a versatile intermediate in various chemical transformations. The 96% purity ensures minimal impurities, reducing the need for additional purification steps and delivering reliable results in laboratory applications. Its liquid form allows for easy handling and accurate dosing, while the synthesis-grade classification guarantees consistency in experimental outcomes. The reagent is particularly valued for its stability under standard lab conditions, maintaining its integrity during storage and use. Whether used as a building block in complex molecule synthesis or as a reactive intermediate, this product meets the stringent requirements of research environments. The formulation is optimized for compatibility with common organic solvents, facilitating seamless integration into existing protocols. Rigorous quality control measures during production ensure batch-to-batch uniformity, making it a dependable choice for demanding synthetic procedures.
FAQs
1. What is the shelf life of 4-Methoxybenzyl Cyanide 96% when stored properly?
When stored in a cool, dry place away from direct sunlight and moisture, this reagent typically maintains its specified purity for 24 months from the date of manufacture. Always check the label for the exact expiration date and perform a quick purity verification if the product has been stored for an extended period.
2. Can this compound be used directly in aqueous reactions?
4-Methoxybenzyl Cyanide is primarily soluble in organic solvents like ethanol, acetone, or dichloromethane. While it has limited solubility in water, you may need to use co-solvents or emulsifiers if incorporating it into aqueous systems. Pre-testing with small quantities is recommended to assess compatibility with your specific reaction conditions.
3. What safety precautions should be taken while handling this chemical?
As with all nitrile compounds, proper laboratory safety measures are essential. Wear nitrile gloves, safety goggles, and a lab coat when handling. Work in a well-ventilated fume hood to avoid inhalation of vapors. The compound may cause skin and eye irritation, so immediate washing with plenty of water is advised in case of contact. Refer to the SDS for complete safety information.
4. How does the methoxy group influence the reactivity of this cyanide compound?
The methoxy substituent is an electron-donating group that increases the electron density on the benzyl ring, making the benzylic position more nucleophilic compared to unsubstituted benzyl cyanide. This modification can enhance reactivity in certain substitution reactions while potentially altering selectivity in other transformations. The exact impact depends on your specific reaction mechanism.
5. What alternatives exist if this specific purity grade is unavailable?
If 96% purity is not available, you might consider lower purity grades (typically 90-95%) for less sensitive applications, though additional purification may be required. For critical applications where higher purity is essential, you could explore custom synthesis options or alternative benzyl cyanide derivatives with similar functional groups that might serve your experimental needs.
