N-(Chloromethyl)phthalimide, 97% | ALF-A12018-14 | Thermofisher

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N-(Chloromethyl)phthalimide, 97% | ALF-A12018-14 | Thermofisher

97% pure N-(Chloromethyl)phthalimide, a key reagent for organic synthesis. White crystalline solid with high reactivity for chloromethylation and phthalimide derivatives.

Original price was: ₹9,018.00.Current price is: ₹8,116.00.

Description

Specifications Table

Product Name – N-(Chloromethyl)phthalimide
Quantity/Pack Size – 25g
Form – Crystalline solid
Grade – 97% pure
Application – Organic synthesis, chloromethylation, phthalimide derivatives

Product Overview

N-(Chloromethyl)phthalimide, 97% pure, is a versatile reagent widely used in organic synthesis for chloromethylation reactions. This high-purity compound appears as a white crystalline solid, offering excellent stability and reactivity under controlled conditions. Its molecular structure combines a phthalimide ring with a chloromethyl group, enabling selective functionalization in synthetic pathways. The 97% purity ensures minimal impurities, making it ideal for precise chemical transformations where consistency is critical. The compound is particularly valued for its role in introducing phthalimide protective groups or as a precursor in the synthesis of complex organic molecules. Its solubility in common organic solvents like dichloromethane and acetone further enhances its utility in laboratory settings. Proper handling and storage are recommended to maintain its integrity, as exposure to moisture or elevated temperatures may affect its performance.

FAQs

1. What is the shelf life of N-(Chloromethyl)phthalimide when stored properly?

When stored in a cool, dry place away from direct sunlight and moisture, this compound retains its stability for up to 24 months from the date of manufacture.

2. Is this compound compatible with aqueous solutions?

N-(Chloromethyl)phthalimide has limited solubility in water but dissolves well in organic solvents like dichloromethane, THF, or acetone for most applications.

3. Are there any safer alternatives for chloromethylation reactions?

Alternatives like N-(bromomethyl)phthalimide or N-(iodomethyl)phthalimide can be used, but reactivity and yield may vary based on the specific reaction conditions.

4. How should I dispose of unused or expired N-(Chloromethyl)phthalimide?

Follow local chemical waste disposal guidelines. Neutralize with a suitable reagent if required, then dispose of in designated hazardous waste containers.

5. Can this compound be used in microwave-assisted synthesis?

Yes, but caution is advised as rapid heating may lead to decomposition. Optimize reaction parameters like temperature and time for best results.

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