Skip to product information
1 of 1

TCI

CAS 336-59-4

Heptafluorobutyric Anhydride TCI H0337

Heptafluorobutyric Anhydride TCI H0337

Chemical Identity

Other names
Perfluorobutyric Anhydride
CAS No.
336-59-4
Formula
C8F14O3
Molecular weight
410.06 g/mol
Purity
>95.0%(T)
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
2,2,3,3,4,4,4-heptafluorobutanoyl 2,2,3,3,4,4,4-heptafluorobutanoate
SMILES
C(=O)(C(C(C(F)(F)F)(F)F)(F)F)OC(=O)C(C(C(F)(F)F)(F)F)(F)F
InChIKey
UFFSXJKVKBQEHC-UHFFFAOYSA-N
MDL
MDL00000432
PubChem
CID 67643
Regular price Rp 2.279.550,00
Regular price Sale price Rp 2.279.550,00
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 4-5 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

Heptafluorobutyric Anhydride (HFBA) is a fluorinated chemical compound widely used in laboratory settings for the synthesis of complex organic molecules. As a key building block in fluorinated chemistry, HFBA plays a crucial role in organic reactions, particularly in fluorine substitution processes. Its unique molecular structure, rich in fluorine atoms, enables it to participate in various chemical transformations, making it a versatile reagent in synthetic chemistry. HFBA is commonly employed in research and development to create fluorinated compounds with specific functional properties, such as enhanced stability and reactivity.

HFBA is known for its high reactivity and ability to react with a range of functional groups, including amines, alcohols, and phenols. This reactivity makes it an ideal choice for modifying organic compounds with fluorine atoms, which can significantly alter the physical and chemical properties of the resulting molecules. Its effectiveness in fluorination reactions has made it a preferred reagent in both academic and industrial research. The compound's ability to introduce fluorine into carbon chains is particularly valuable in the development of pharmaceuticals and advanced materials.

In Indonesian laboratories, HFBA is frequently used in organic chemistry research, especially in the fields of pharmaceuticals and materials science. Its role in synthesizing fluorinated compounds is essential for creating compounds with unique properties that are used in various applications. Due to its chemical reactivity, HFBA is a critical component in the study of fluorinated molecules, contributing to advancements in chemical research and innovation.

  • Fluorination Reactions: HFBA is ideal for introducing fluorine atoms into organic molecules, enhancing their stability and reactivity for specialized applications.
  • Organic Synthesis: Its reactivity with amines, alcohols, and phenols makes it a valuable reagent in the synthesis of complex organic compounds.
  • Pharmaceutical Research: HFBA is used to develop fluorinated compounds with improved pharmacological properties, supporting drug discovery and development.
  • Materials Science: The compound is employed in the creation of fluorinated materials with unique physical and chemical characteristics.
  • Analytical Chemistry: HFBA is used in the preparation of standards and reagents for analytical procedures requiring fluorinated compounds.

Brand TCI
CAS number 336-59-4
Molecular formula —
Purity —
Category Chemistry > Building Blocks > Fluorinated Building Blocks
Pack sizes Available in various quantities as per supplier specifications
Physical form Solid or liquid, depending on the specific product variant
Storage Requires storage in a cool, dry, and well-ventilated area away from moisture and heat

HFBA should be stored in a cool, dry, and well-ventilated area, away from moisture and direct sunlight. It is recommended to use airtight containers made of materials compatible with fluorinated compounds to prevent contamination and degradation. Due to its reactivity and potential toxicity, HFBA should be handled with appropriate personal protective equipment, including gloves, goggles, and a fume hood. Laboratory personnel should be trained in safe handling procedures and emergency response protocols. Proper labeling and storage conditions are essential to ensure the safety of both the compound and the laboratory environment.

—