• 5-Vinyl-1,3-benzodioxole (CAS 7315-32-4) - TCI E1467 - AMI Scientific
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TCI

CAS 7315-32-4

5-Vinyl-1,3-benzodioxole TCI E1467

5-Vinyl-1,3-benzodioxole TCI E1467
Rp 5.577.600,00
Rp 5.577.600,00
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5-Vinyl-1,3-benzodioxole with CAS number 7315-32-4 is a functional benzodioxole-derived monomer equipped with a reactive vinyl group, making it an important raw material for polymer and copolymer synthesis in the laboratory. In materials research practice, this monomer acts as a building block that can be polymerized through a free-radical mechanism, producing polymers with a benzodioxole backbone that imparts distinctive thermal, optical, and chemical resistance properties. This TCI product is supplied in a 250-milligram package, which is highly suitable for small-scale studies, reaction condition optimization, and the preparation of polymers with controlled molecular weight in materials chemistry laboratories.

The main advantage of this compound lies in the combination of a reactive vinyl group and a thermally stable benzodioxole ring. The vinyl group enables the monomer to participate in radical polymerization as well as copolymerization with other monomers such as styrene, acrylates, or maleimides, allowing the final polymer properties to be engineered according to research requirements. At the same time, the presence of the benzodioxole ring contributes polarity, good thermal stability, and potential for aromatic interactions, which can influence solubility, film-forming behavior, and the overall performance of the resulting macromolecules in advanced material applications.

In Indonesian laboratories, particularly those focused on materials science, polymer chemistry, and advanced materials research at universities and research institutions, this monomer is typically used in small-batch polymerization experiments, screening of reaction conditions, and the development of novel functional polymers. The 250-milligram packaging is convenient for initial trials and feasibility studies, enabling researchers to explore monomer behavior without committing to large quantities. It is also well suited for collaborative projects and student training in polymer synthesis, supporting the growth of local expertise in specialty monomer chemistry.

  • Free-radical polymerization studies: The reactive vinyl group enables clean radical polymerization under standard initiator conditions, making this monomer an ideal candidate for investigating polymerization kinetics, conversion rates, and polymer architecture in bench-scale experiments.
  • Copolymer synthesis: It readily copolymerizes with monomers such as styrene, acrylates, or maleimides, allowing researchers to incorporate benzodioxole functionality into copolymers and systematically tune thermal, optical, and mechanical properties for target applications.
  • Controlled molecular weight polymer preparation: Because the monomer polymerizes predictably in small quantities, it supports the synthesis of polymers with controlled molecular weight and narrow distribution when used with appropriate initiator and chain-transfer systems in the laboratory.
  • Functional material development: The benzodioxole ring imparts polarity and thermal stability, making this monomer useful for developing functional polymers intended for coatings, optical films, and specialty materials with enhanced chemical resistance.
  • Reaction condition optimization: The 250-milligram pack size is ideal for rapid screening of solvents, temperatures, and initiator systems, enabling efficient optimization of polymerization conditions before scaling up to larger synthesis batches.

Brand TCI
CAS number 7315-32-4
Molecular formula —
Purity —
Category Materials Science > Polymer/Macromolecule Reagents > Monomers
Pack sizes —
Physical form —
Storage keep the container tightly closed in a cool, dry, well-ventilated area
  • Product name: 5-Vinyl-1,3-benzodioxole (product code: E1467)

Store this monomer in its original, tightly sealed container in a cool, dry, well-ventilated area, away from direct sunlight, heat sources, and ignition sources. Keep the container closed when not in use to prevent moisture uptake and contamination. Use appropriate personal protective equipment, including laboratory gloves, safety goggles, and a laboratory coat, when handling the material. Work in a fume hood or well-ventilated area to minimize exposure to vapors or dust. Avoid contact with skin and eyes, and do not ingest the material. Keep it away from incompatible substances and strong oxidizing agents. Follow standard laboratory waste disposal procedures for chemical waste, and in case of accidental spillage, contain the material and clean it up promptly using suitable absorbent materials.

Note: where the physical form was not stated in the source data, no specific form has been assumed; all technical details above are taken directly from the Indonesian reference version.

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