trans-1,2-Cyclohexanedimethanol TCI C2362

Chemical Identity

Other names: trans-1,2-Bis(hydroxymethyl)cyclohexane
CAS No.: 25712-33-8
PubChem: CID 11217323·SID 87561418
Formula: C8H16O2
Molecular weight: 144.21 g/mol
Purity: >98.0%(GC)

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: [(1R,2R)-2-(hydroxymethyl)cyclohexyl]methanol
SMILES: C1CCC(C(C1)CO)CO
InChIKey: XDODWINGEHBYRT-YUMQZZPRSA-N

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Trans-1,2-Cyclohexanedimethanol is a chemical compound widely utilized in laboratory settings as a foundational building block for complex molecular synthesis. It plays a crucial role in organic chemistry by serving as a versatile intermediate in various reactions. Its unique molecular structure, featuring two methanol groups attached to a cyclohexane ring, provides a stable yet reactive platform for chemical transformations. This compound is essential for researchers aiming to construct more complex molecules through substitution or coupling reactions.

The compound's chemical properties make it a preferred choice in laboratory applications. Its stability under certain conditions, combined with its ability to react with acids, bases, and alkali metals, allows for a wide range of synthetic possibilities. The hydrophobic nature of the cyclohexane ring influences its solubility in organic solvents, making it suitable for reactions requiring specific solvent environments. These characteristics make it a reliable and adaptable reagent for chemical synthesis.

In Indonesian laboratories, Trans-1,2-Cyclohexanedimethanol is commonly used in organic chemistry research, particularly in undergraduate and postgraduate studies. It is an integral part of experiments designed to explore molecular structures and reaction mechanisms. Its availability and chemical versatility make it a standard reagent in both academic and industrial research settings across Indonesia.

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Organic synthesis experiments benefit from its reactivity and structural versatility, allowing the construction of complex molecules.
It is ideal for coupling reactions due to its ability to participate in various chemical transformations under controlled conditions.
In structural chemistry studies, it serves as a model compound for understanding ring-based molecular behavior and reactivity.
Its solubility in organic solvents makes it suitable for reactions requiring non-aqueous environments.
It is frequently used in teaching laboratories to demonstrate fundamental concepts in chemical synthesis and reaction mechanisms.

Brand	TCI
CAS number	25712-33-8
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes	Available in various quantities as per supplier specifications
Physical form	Liquid
Storage	Store in a cool, dry place away from direct sunlight

Trans-1,2-Cyclohexanedimethanol should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep it in a tightly sealed container to prevent exposure to air and moisture. Due to its hydrophobic nature, it is best stored in glass or polyethylene containers to avoid contamination. Laboratory personnel should handle the compound with care, using appropriate personal protective equipment such as gloves and safety goggles. It should be kept away from incompatible materials like strong oxidizing agents. Regular monitoring of storage conditions ensures the compound remains suitable for use in chemical experiments.

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