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CAS 5435-64-3

3,5,5-Trimethylhexanal TCI T0940

3,5,5-Trimethylhexanal TCI T0940

Chemical Identity

CAS No.
5435-64-3
PubChem
CID 21574·SID 87576758
Formula
C9H18O
Molecular weight
142.24 g/mol
Purity
>90.0%(GC)
Reference databases
ChEBI·ChemSpider·ECHA
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
3,5,5-trimethylhexanal
SMILES
CC(CC=O)CC(C)(C)C
InChIKey
WTPYRCJDOZVZON-UHFFFAOYSA-N
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3,5,5-Trimethylhexanal is an organic compound widely used in chemical reactions for the synthesis of complex molecules. As an aldehyde, it possesses reactive functional groups that enable participation in various chemical transformations, including reduction, oxidation, and substitution reactions. This versatility makes it a valuable tool in synthetic chemistry, where it serves as a building block for the creation of aromatic compounds, esters, and other high-reactivity substances. Its role in laboratory settings is crucial for both educational and research purposes, supporting the development of new chemical structures and methodologies.

The compound’s simple yet reactive molecular structure contributes to its popularity among chemists. It has a relatively stable boiling and melting point, which facilitates heating and cooling processes during experiments. Its liquid form also allows for easy handling and use in a variety of reaction scales, from small-scale experiments to larger industrial applications. These properties make it a preferred choice for laboratories seeking reliable and efficient chemical reagents.

In Indonesian laboratories, 3,5,5-Trimethylhexanal is extensively used in both academic and research environments. It is commonly found in university chemistry departments and research institutions, where it supports fundamental and advanced chemical experiments. Its availability and affordability make it a favored material for a wide range of chemical projects, contributing to the growth of scientific research in the region.

  • Used in the synthesis of aromatic compounds due to its reactivity and ability to participate in various chemical transformations.
  • Applied in esterification reactions because of its aldehyde group, which can undergo substitution and condensation reactions.
  • Utilized in organic synthesis for creating complex molecules through oxidation and reduction processes.
  • Employed in educational settings to teach fundamental chemical reactions and synthetic techniques.
  • Integrated into research projects requiring high-reactivity compounds for the development of new chemical structures.

Brand TCI
CAS number 5435-64-3
Molecular formula —
Purity —
Category Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes Available in various quantities as per standard laboratory supply
Physical form Liquid
Storage Store in a cool, dry place away from direct sunlight

3,5,5-Trimethylhexanal should be stored in a cool, dry environment, away from direct sunlight and sources of heat. It is recommended to use airtight containers made of glass or polyethylene to prevent contamination and evaporation. Due to its reactive nature, it should be handled in a well-ventilated area, and appropriate personal protective equipment, such as gloves and goggles, should be worn. Avoid contact with incompatible materials, and ensure that storage areas are secure to prevent accidental spills or exposure. Regular monitoring of storage conditions is essential to maintain the compound’s stability and effectiveness in laboratory applications.

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