2-Methoxy-4-vinylphenol (stabilized with TBC) TCI M3600

Description

2-Methoxy-4-vinylphenol, also known as 4-vinylguaiacol, is an aromatic phenolic compound characterized by a reactive vinyl group and a methoxy substituent on its benzene ring. In the laboratory, it serves as an important building block and starting material for organic synthesis, particularly for constructing more complex molecular structures through polymerization, copolymerization, and various functional group transformations. As a vinyl monomer, it provides a strategic starting point for designing functional polymers, resins, pharmaceutical intermediates, and fine chemicals. Its significance also extends to natural product research, since this compound is a natural aroma component found in coffee, beer, and wine, making it a frequent subject of study in food chemistry and analytical chemistry.

This compound is selected because of its balanced combination of reactivity and stability. The vinyl group enables addition reactions, radical polymerization, and copolymerization with a wide range of other monomers, giving synthetic chemists considerable flexibility in tailoring material properties. At the same time, the phenolic hydroxyl group provides natural antioxidant character and permits further modification through reactions such as esterification and etherification, expanding the range of accessible derivatives. This dual functionality makes the compound versatile for both polymer science and small-molecule synthesis, while its stability, reinforced by TBC stabilization, ensures dependable handling and consistent performance in routine laboratory workflows.

In Indonesian laboratories, this product is typically used by research groups in universities, research institutes, and industrial R&D facilities working in polymer chemistry, organic synthesis, and natural product studies. It functions as a reliable monomer for preparing functional polymers and resins, and as a synthetic intermediate in the development of pharmaceutical and fine chemical compounds. Because it is also a recognized aroma component of coffee, beer, and wine, it is frequently employed as a reference material in food chemistry and analytical laboratories studying flavor compounds and their behavior. Its availability as a stabilized reagent makes it a convenient and dependable choice for these applications.

Laboratory Applications

• Monomer for radical polymerization: The reactive vinyl group readily participates in radical polymerization and copolymerization, enabling researchers to build functional polymers with controlled composition and tailored material properties.
• Building block for organic synthesis: As a versatile non-heterocyclic building block, it serves as a strategic intermediate for constructing complex molecular frameworks through addition, esterification, and etherification reactions.
• Preparation of functional polymers and resins: Its balanced reactivity and modifiable phenolic hydroxyl group allow incorporation into polymer backbones and resin formulations to achieve specific functional characteristics.
• Pharmaceutical and fine chemical intermediate: The vinyl and phenolic functionalities offer multiple derivatization pathways, making it a useful starting material for synthesizing specialty chemicals and bioactive intermediates.
• Analytical standard in food chemistry: As a natural aroma component of coffee, beer, and wine, it is used as a reference compound in analytical and flavor studies to identify and quantify this volatile phenolic compound.

Specifications

• Brand: TCI
• Product name: M3600 2-Methoxy-4-vinylphenol (stabilized with TBC)
• CAS number: 7786-61-0
• Category: Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
• Stabilization: Stabilized with TBC (tert-butylcatechol), as stated in the product name
• Storage note: store in a cool, dark, and tightly sealed container, away from heat and direct sunlight (see Handling and Storage)

Handling and Storage

2-Methoxy-4-vinylphenol is a reactive vinyl compound, and although it is supplied stabilized with TBC to inhibit premature polymerization, it should still be stored under cool, dry, and dark conditions in a tightly sealed container. Keeping the container tightly closed when not in use minimizes exposure to air and moisture, which helps preserve the effectiveness of the stabilizer and the quality of the product. It is advisable to store the material away from heat sources, open flames, and direct sunlight, and to keep it separate from strong oxidizing agents and polymerization initiators. Standard laboratory precautions apply: wear appropriate personal protective equipment such as gloves and safety glasses, work in a well-ventilated area or fume hood, and avoid inhalation of vapors and contact with skin or eyes. Always consult the Safety Data Sheet before handling.

*Assumption: pack size and physical form were not stated in the reference data, so these details are intentionally omitted rather than invented.*