Description

Specifications Table

Product Name – Cyclohexanol
Quantity/Pack Size – 100 ml
Form – Liquid
Grade – AR (Analytical Reagent)
Application – Solvent, organic synthesis, intermediate reactions

Product Overview

Cyclohexanol is a saturated aliphatic alcohol with a six-membered ring structure, widely recognized for its versatility in laboratory applications. This colorless to pale yellow liquid exhibits a characteristic camphor-like odor and serves as a crucial intermediate in organic synthesis. With a high boiling point of 161°C and miscibility in organic solvents, it functions effectively as a solvent for resins, oils, and waxes. The AR-grade purity ensures minimal impurities, making it suitable for precise analytical procedures and synthesis reactions where consistency is critical. Its hygroscopic nature requires proper storage in tightly sealed containers to prevent moisture absorption. Cyclohexanol’s chemical stability under standard conditions, combined with its reactivity with oxidizing agents, makes it a valuable reagent in esterification and dehydration processes. The compound’s low volatility at room temperature contributes to its safe handling in controlled laboratory environments.

FAQs

1. What is the typical shelf life of cyclohexanol when stored properly?

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

2. Can this grade of cyclohexanol be used for spectrophotometric analysis?

The AR grade offers high purity suitable for most analytical applications, though for UV spectrophotometry, additional purification may be required depending on specific wavelength requirements.

3. What safety precautions should be taken when handling cyclohexanol?

Use in a well-ventilated area with proper PPE including gloves and goggles. Avoid skin contact as it may cause irritation, and prevent inhalation of vapors which can be harmful at elevated temperatures.

4. How does cyclohexanol compare to cyclohexanone in terms of reactivity?

Cyclohexanol is less reactive than cyclohexanone due to the absence of a carbonyl group. It primarily undergoes substitution and elimination reactions rather than the addition reactions characteristic of ketones.