4,6-Di-tert-butyl-m-cresol TCI D1432

Chemical Identity

Other names: 2,4-Di-tert-butyl-5-hydroxytoluene · 2,4-Di-tert-butyl-5-methylphenol
CAS No.: 497-39-2
Formula: C15H24O
Molecular weight: 220.36 g/mol
Purity: >96.0%(GC)
Storage: 0-10°C

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 2,4-ditert-butyl-5-methylphenol
SMILES: CC1=CC(=C(C=C1C(C)(C)C)C(C)(C)C)O
InChIKey: WYSSJDOPILWQDC-UHFFFAOYSA-N
MDL: MDL00059208
PubChem: CID 10346

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4,6-Di-tert-butyl-m-cresol is a chemical compound widely used in organic synthesis reactions within laboratory settings. It serves as a building block for the creation of more complex chemical structures, particularly in the field of organic chemistry. This compound is commonly found in laboratories as a stable and reliable reagent, offering a foundation for various synthetic pathways. Its utility stems from its aromatic structure and the protective tert-butyl groups, which enhance its chemical stability and reactivity control.

The compound's unique properties make it a preferred choice in laboratory environments. Its aromatic ring structure provides a stable base for chemical modifications, while the tert-butyl groups shield the hydroxyl group from unwanted side reactions. This stability ensures consistent performance in synthetic processes, reducing the risk of degradation or unpredictable outcomes. Additionally, its moderate reactivity allows for controlled reactions, making it suitable for a wide range of applications without the need for extreme reaction conditions.

In Indonesian laboratories, 4,6-Di-tert-butyl-m-cresol is frequently used in organic chemistry research, especially in the synthesis of aromatic compounds and their derivatives. Its availability and chemical stability make it a relevant material for academic and industrial research projects. It is particularly valuable in the development of new chemical materials and in the study of aromatic substitution reactions. Its reliability and consistent performance make it a trusted component in both educational and research settings.

Organic synthesis of aromatic compounds due to its stable aromatic structure and protective tert-butyl groups.
Development of new chemical materials through controlled substitution reactions on its aromatic ring.
Research in synthetic pathways requiring predictable and stable reagents for complex molecule formation.
Educational use in teaching organic chemistry principles and reaction mechanisms.
Industrial applications in the production of specialty chemicals and pharmaceutical intermediates.

Brand	TCI
CAS number	497-39-2
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes	Available in various sizes as per standard laboratory supply
Physical form	Solid
Storage	Store in a cool, dry place away from direct sunlight

This compound should be stored in a cool, dry environment, away from direct sunlight and sources of heat. It is recommended to use airtight containers to prevent moisture absorption and maintain its chemical integrity. Due to its moderate reactivity, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. It is important to ensure proper ventilation in the laboratory when working with this compound to minimize exposure. Avoid contact with incompatible substances to prevent any potential chemical interactions. Proper storage and handling practices will help maintain its stability and ensure safe usage in laboratory settings.

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