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TCI

CAS 939-97-9

4-tert-Butylbenzaldehyde TCI B1760

4-tert-Butylbenzaldehyde TCI B1760

Chemical Identity

CAS No.
939-97-9
PubChem
CID 70324·SID 87564655
Formula
C11H14O
Molecular weight
162.23 g/mol
Purity
>95.0%(GC)
Reference databases
ChEBI·ChemSpider·ECHA·Wikipedia
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
4-tert-butylbenzaldehyde
SMILES
CC(C)(C)C1=CC=C(C=C1)C=O
InChIKey
OTXINXDGSUFPNU-UHFFFAOYSA-N
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4-Tert-Butylbenzaldehyde is a chemical compound widely used in organic synthesis reactions within laboratory settings. It is a versatile building block that plays a key role in the development of complex molecules, particularly in the fields of pharmaceutical and industrial chemistry. Its molecular structure consists of an aldehyde group attached to a benzene ring, with a tert-butyl group at the 4-position. This unique structure makes it an essential component in various synthetic pathways, enabling chemists to create a wide range of functional derivatives.

The compound is valued for its chemical stability and reactivity, which are crucial for successful synthetic outcomes. Its high boiling and melting points facilitate controlled heating and cooling processes in laboratory experiments. Additionally, its clear molecular structure allows for easy identification through analytical techniques such as infrared (IR) and nuclear magnetic resonance (NMR) spectroscopy. These properties make it a reliable and efficient reagent for both research and industrial applications.

In Indonesian laboratories, 4-Tert-Butylbenzaldehyde is commonly used in organic chemistry research, especially in academic institutions and research centers. It is a fundamental reagent in the synthesis of aromatic compounds, pharmaceutical intermediates, and fragrance materials. Its availability and reliability make it a preferred choice for chemists working on complex molecular structures and functional group transformations.

  • Organic synthesis reactions benefit from 4-Tert-Butylbenzaldehyde due to its reactivity and structural versatility, enabling the formation of complex aromatic derivatives.
  • Pharmaceutical research utilizes this compound as a building block for the synthesis of drug molecules, contributing to the development of therapeutic agents.
  • Industrial chemical production relies on this reagent for the creation of specialty chemicals and fragrance compounds, supporting diverse manufacturing needs.
  • Spectroscopic analysis is enhanced by the compound’s clear molecular structure, making it ideal for IR and NMR studies in analytical chemistry.
  • Educational institutions use it as a teaching tool to demonstrate organic reaction mechanisms and synthetic strategies in undergraduate and graduate courses.

Brand TCI
CAS number 939-97-9
Molecular formula —
Purity —
Category Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes Available in various quantities as per standard laboratory supply formats
Physical form Liquid
Storage Store in a cool, dry place away from direct sunlight and incompatible materials

4-Tert-Butylbenzaldehyde 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 high-density polyethylene to prevent contamination and evaporation. Due to its chemical nature, it should be kept separate from strong oxidizing agents and reactive substances. In laboratory settings, proper ventilation is essential to minimize exposure. Always handle with care, using appropriate personal protective equipment such as gloves and safety goggles. Regular monitoring of storage conditions ensures the compound remains stable and suitable for use in chemical experiments.

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