Skip to product information
1 of 2

TCI

CAS 15484-80-7

Vinyl 4-tert-Butylbenzoate TCI B1386

Vinyl 4-tert-Butylbenzoate TCI B1386

Chemical Identity

CAS No.
15484-80-7
PubChem
CID 84940·SID 87564308
Formula
C13H16O2
Molecular weight
204.26 g/mol
Purity
>98.0%(GC)
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
ethenyl 4-tert-butylbenzoate
SMILES
CC(C)(C)C1=CC=C(C=C1)C(=O)OC=C
InChIKey
ZLHVSEPPILCZHH-UHFFFAOYSA-N
Regular price Rp 530.250,00
Regular price Rp 386.400,00 Sale price Rp 530.250,00
Sale Sold out
Shipping calculated at checkout.
Volume
Quantity
Pembayaran hanya melalui request quotation dan dilakukan setelah tim kami menghubungi Anda. Mohon cantumkan nomor WhatsApp aktif untuk konfirmasi pesanan & pembuatan invoice. Estimasi pengiriman 2-4 minggu setelah pembayaran.

Dokumen Keamanan & Mutu

CoA (Certificate of Analysis)

Spesifik per batch produksi — diterbitkan dan dikirim bersama barang sesuai nomor lot yang Anda terima.

Contoh CoA segera tersedia.

💬 Minta CoA via WhatsApp

View full details

Vinyl 4-tert-Butylbenzoate is a chemical compound widely used in scientific experiments, particularly in the fields of materials science and organic chemistry. As a monomer, it plays a crucial role in polymerization reactions, making it essential for the synthesis of new polymers or the modification of existing ones. Its chemical structure allows it to participate effectively in various synthetic processes, contributing to the development of advanced materials with tailored properties. This compound is commonly found in laboratory settings where researchers are working on polymer-based projects or exploring new chemical reactions.

One of the key attributes of Vinyl 4-tert-Butylbenzoate is its stable molecular structure and good reactivity, which enable efficient chemical reactions. It is also non-polar, allowing it to dissolve easily in organic solvents such as ethers and benzene. These properties make it a preferred choice for applications requiring non-reactive solvents. Its solubility and chemical stability ensure reliable results in experimental setups, making it a versatile reagent in both academic and industrial research environments.

In Indonesian laboratories, Vinyl 4-tert-Butylbenzoate is used extensively in scientific research and higher education. It is a common material in polymerization studies, organic compound modifications, and the development of new materials. Its availability supports various experimental needs, contributing to the advancement of scientific knowledge and innovation in the region.

TCI brochures (PDF)

  • Polymerization studies benefit from Vinyl 4-tert-Butylbenzoate due to its role as a monomer in creating new polymer structures.
  • Organic compound modification experiments use this reagent for altering molecular structures and enhancing material properties.
  • Material development research relies on Vinyl 4-tert-Butylbenzoate for synthesizing advanced polymers with specific functional characteristics.
  • Educational institutions incorporate this compound into teaching labs to demonstrate polymerization mechanisms and chemical reactivity.
  • Industrial research applications utilize this material for the production of specialty polymers and polymer-based products.

Brand TCI
CAS number 15484-80-7
Molecular formula —
Purity —
Category Materials Science > Polymer/Macromolecule Reagents > Monomers
Pack sizes As per supplier specifications
Physical form Liquid
Storage Store in a cool, dry place away from direct sunlight

Vinyl 4-tert-Butylbenzoate should be stored in a cool, dry environment, away from direct sunlight and sources of heat. It is recommended to keep the compound in a sealed container made of glass or inert plastic to prevent contamination and maintain its chemical integrity. Due to its non-polar nature, it is important to use appropriate safety measures when handling the material, such as wearing gloves and protective eyewear. In laboratory settings, it should be stored separately from incompatible substances to avoid any potential chemical interactions. Proper ventilation should be ensured when working with this reagent to minimize exposure risks. Following these guidelines ensures safe and effective use in both academic and research environments.

—