1,3-Divinylbenzene (stabilized with TBC) TCI D6174

Chemical Identity

Other names: 1,3-Diethenylbenzene (stabilized with TBC) · m-Divinylbenzene (stabilized with TBC) · m-Vinylstyrene (stabilized with TBC)
CAS No.: 108-57-6
PubChem: CID 7941
Formula: C10H10
Molecular weight: 130.19 g/mol
Purity: >98.0%(GC)
Storage: 0-10°C
Reference databases: ChEBI·ChemSpider·ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 1,3-bis(ethenyl)benzene
SMILES: C=CC1=CC(=CC=C1)C=C
InChIKey: PRJNEUBECVAVAG-UHFFFAOYSA-N

Rp 2.809.800,00

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1,3-Divinylbenzene (stabilized with TBC) is a chemical compound widely used as a building block in various laboratory applications. It is a key reagent in organic chemistry due to its aromatic structure and two vinyl groups positioned at the 1 and 3 positions of the benzene ring. This compound plays a crucial role in the synthesis of complex organic molecules, making it an essential component in research and development settings. Its versatility allows it to participate in multiple reaction types, including addition and substitution reactions, which are fundamental in chemical synthesis.

The properties that make 1,3-Divinylbenzene a preferred choice include its stability and non-polar nature, which facilitate solubility in organic solvents. The stabilization with tert-butylcatechol (TBC) ensures that the compound remains chemically stable during storage and use, reducing the risk of degradation. This stability is particularly important in laboratory environments where long-term storage and repeated use are common. Additionally, its reactivity and compatibility with various functional groups make it a valuable tool in synthetic chemistry.

In Indonesian laboratories, 1,3-Divinylbenzene is commonly used in organic chemistry research, especially in academic institutions and research centers. Its role in the synthesis of polymers and other chemical compounds makes it a popular choice for both educational and industrial applications. The compound’s reliability and performance in controlled laboratory conditions ensure consistent results in chemical experiments and processes.

Related TCI products

Organic synthesis applications benefit from 1,3-Divinylbenzene due to its reactivity and ability to form cross-linked polymers.
Polymer research utilizes this compound for creating cross-linked structures, enhancing the mechanical properties of the final product.
Chemical reaction testing often involves this compound because of its stability and compatibility with various functional groups.
Teaching laboratories use it to demonstrate key organic chemistry concepts, such as addition and substitution reactions.
Industrial chemical development relies on this compound for the synthesis of complex molecules and materials.

Brand	TCI
CAS number	108-57-6
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes	Available in various quantities as per supplier specifications
Physical form	Liquid
Storage	Store in a cool, dry place away from light and incompatible materials

This compound should be stored in a cool, dry environment, away from direct sunlight and sources of heat. It is recommended to keep it in a sealed container to prevent exposure to air and moisture. Due to its non-polar nature, it is advisable to use containers made of materials that are chemically inert, such as glass or high-density polyethylene. In laboratory settings, it is important to handle the compound with care, using appropriate personal protective equipment. Ensure that the storage area is well-ventilated to minimize the risk of inhalation of vapors. Always follow standard safety protocols to maintain a safe working environment.

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