Skip to product information
1 of 2

TCI

CAS 6939-93-1

4-Bromoisophthalic Acid TCI B1260

4-Bromoisophthalic Acid TCI B1260

Chemical Identity

CAS No.
6939-93-1
PubChem
CID 81361·SID 87564194
Formula
C8H5BrO4
Molecular weight
245.03 g/mol
Purity
>97.0%(GC)(T)
Reference databases
ECHA
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
4-bromobenzene-1,3-dicarboxylic acid
SMILES
C1=CC(=C(C=C1C(=O)O)C(=O)O)Br
InChIKey
MSQIEZXCNYUWHN-UHFFFAOYSA-N
Regular price Rp 3.710.700,00
Regular price Rp 2.594.550,00 Sale price Rp 3.710.700,00
Sale Sold out
Shipping calculated at checkout.
Berat
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

4-Bromoisophthalic Acid is a chemical compound widely used as a foundational building block in the synthesis of complex organic compounds. It is derived from isophthalic acid with the addition of a bromine group, which enhances its reactivity and versatility in various chemical reactions. This compound plays a crucial role in laboratory settings, particularly in the development of new materials and pharmaceuticals. Its structural simplicity and functional groups make it an essential tool for chemists working on synthetic pathways.

The compound is valued for its high reactivity and stability, making it a preferred choice for researchers. Its two carboxylic acid groups allow for a wide range of chemical modifications, including substitution, esterification, and coupling reactions. These properties enable it to be used in multiple synthetic strategies, offering flexibility in experimental design. Its compatibility with various reagents such as bases, alcohols, and catalysts further enhances its utility in laboratory applications.

In Indonesian laboratories, 4-Bromoisophthalic Acid is commonly used in organic chemistry research, especially in academic and research institutions. Its role in the synthesis of heterocyclic compounds, pharmaceuticals, and industrial chemicals makes it a key reagent for scientists and students alike. The compound's reliability and consistent performance contribute to its widespread use in both educational and professional settings.

  • Organic synthesis is greatly enhanced by 4-Bromoisophthalic Acid due to its reactivity and ability to participate in multiple reaction types.
  • Pharmaceutical research benefits from its use in the development of new drug compounds through structural modifications.
  • Industrial chemical production utilizes this compound for the creation of specialized materials and functional chemicals.
  • Academic research relies on its availability and versatility for teaching and experimental purposes in chemistry courses.
  • Heterocyclic compound synthesis is supported by its ability to undergo substitution and coupling reactions effectively.

Brand TCI
CAS number 6939-93-1
Molecular formula —
Purity —
Category Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes Available in various quantities as per standard laboratory supply
Physical form Solid
Storage Store in a cool, dry place away from moisture and direct sunlight

4-Bromoisophthalic Acid should be stored in a cool, dry place, away from moisture and direct sunlight. It is recommended to use airtight containers to prevent exposure to air and humidity. Due to its reactivity, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles. It is important to ensure proper ventilation in the laboratory when working with this compound. Avoid contact with incompatible substances to maintain its stability and effectiveness. Regular inspection of storage conditions helps in maintaining the integrity of the compound for long-term use.

—