4-tert-Butylphenol TCI B0230

Chemical Identity

CAS No.: 98-54-4
PubChem: CID 7393·SID 87563350
Formula: C10H14O
Molecular weight: 150.22 g/mol
Purity: >98.0%(GC)
Reference databases: ChEBI·ChemSpider·ECHA·Wikipedia

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 4-tert-butylphenol
SMILES: CC(C)(C)C1=CC=C(C=C1)O
InChIKey: QHPQWRBYOIRBIT-UHFFFAOYSA-N

Rp 557.550,00

~~Rp 405.300,00~~ Rp 557.550,00

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Berat 25g 500g

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4-Tert-Butylphenol is a chemical compound widely used in various laboratory reactions due to its versatility and chemical stability. As a building block in organic chemistry, it serves as a fundamental component for the synthesis of more complex molecules. Its structure, featuring a phenolic ring with a tert-butyl group, provides a stable yet reactive platform for chemical modifications. This makes it a valuable resource for chemists seeking to explore substitution and oxidation reactions under controlled conditions.

The compound’s key properties include its high boiling and melting points, which facilitate handling during heating and cooling processes in the lab. These characteristics make it suitable for reactions that require elevated temperatures or specific thermal conditions. Additionally, its reactivity can be precisely controlled, allowing for tailored chemical transformations. The stability of 4-tert-Butylphenol ensures it remains a reliable reagent in diverse experimental setups.

In Indonesian laboratories, 4-tert-Butylphenol is commonly used in organic chemistry research, particularly in the synthesis of aromatic compounds and their derivatives. It plays a crucial role in projects involving the modification of phenolic structures, supporting both academic and industrial research initiatives. Its availability and chemical properties make it a preferred choice for chemists working in various research fields.

Related TCI products

Organic synthesis of aromatic compounds where stable and reactive phenolic derivatives are required.
Oxidation reactions that benefit from the controlled reactivity of the tert-butyl group.
Substitution reactions in which the phenolic ring serves as a starting point for structural modifications.
Research projects focused on the development of new chemical intermediates and functional groups.
Industrial applications involving the production of specialty chemicals and pharmaceutical precursors.

Brand	TCI
CAS number	98-54-4
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 and incompatible materials

4-Tert-Butylphenol 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 potential reactivity, it should be stored away from strong oxidizing agents and incompatible substances. The container should be made of materials that are chemically inert to the compound, such as glass or high-density polyethylene. In laboratory settings, proper ventilation is essential to minimize inhalation risks. Always handle the compound with appropriate personal protective equipment, including gloves and safety goggles, to ensure safe usage and storage.

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