Description

Dipentafluorophenylcarbonate (DPFPC) is a high-purity fluorinated organic compound with the molecular formula C₁₃F₁₀O₃ and CAS number 59483-84-0. This specialized chemical, also known as bis(2,3,4,5,6-pentafluorophenyl) carbonate, features two pentafluorophenyl groups bonded to a central carbonate moiety, making it a valuable reagent for advanced synthetic applications. Its unique perfluorinated aromatic structure enhances reactivity and stability under demanding conditions, particularly in nucleophilic substitution reactions and polymer chemistry. DPFPC is supplied as a crystalline solid with exceptional purity (>98%), ensuring consistent performance in research and industrial processes. Ideal for use in organic synthesis, materials science, and pharmaceutical intermediates, this compound is packaged under inert conditions to maintain integrity.

Properties

• CAS Number: 59483-84-0
• Complexity: 439
• IUPAC Name: bis(2,3,4,5,6-pentafluorophenyl) carbonate
• InChI: InChI=1S/C13F10O3/c14-1-3(16)7(20)11(8(21)4(1)17)25-13(24)26-12-9(22)5(18)2(15)6(19)10(12)23
• InChI Key: IOVVFSGCNWQFQT-UHFFFAOYSA-N
• Exact Mass: 393.96877548
• Molecular Formula: C13F10O3
• Molecular Weight: 394.12
• SMILES: C1(=C(C(=C(C(=C1F)F)F)F)F)OC(=O)OC2=C(C(=C(C(=C2F)F)F)F)F
• Topological: 35.5
• Monoisotopic Mass: 393.96877548
• Synonyms: 59483-84-0, DPFPC, Dipentafluorophenylcarbonate, DTXSID40208184, Phenol, pentafluoro-, carbonate (2:1), DTXCID60130675, Bis(pentafluorophenyl) carbonate, Bis(pentafluorophenyl)carbonate, Bis(perfluorophenyl) carbonate, bis(perfluorophenyl)carbonate, bis(2,3,4,5,6-pentafluorophenyl) carbonate, MFCD00368353, Pentafluorophenyl carbonate, C13F10O3, Carbonic Acid Bis(pentafluorophenyl) Ester, di-pentafluorphenylcarbonate, SCHEMBL34317, IOVVFSGCNWQFQT-UHFFFAOYSA-N, BBL100135, STK077845, AKOS008901256, Bis(pentafluorophenyl) carbonate, 97%, CS-W011714, FB38526, AS-11126, BP-31253, SY016222, B3604, AG-690/11959240

Application

Dipentafluorophenylcarbonate (DPFPC) serves as a versatile building block in the synthesis of fluorinated polymers and specialty materials, where its carbonate linkage enables controlled polymerization. It is widely employed in pharmaceutical research for constructing fluorinated drug analogs, leveraging the electron-withdrawing properties of pentafluorophenyl groups to modulate reactivity. Additionally, DPFPC finds use as a coupling agent in peptide synthesis and as a precursor for high-performance coatings with enhanced thermal and chemical resistance.

Safety and Hazards

GHS Hazard Statements

• H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]
• H319 (100%): Causes serious eye irritation [Warning Serious eye damage/eye irritation]
• H335 (100%): May cause respiratory irritation [Warning Specific target organ toxicity, single exposure; Respiratory tract irritation]

Precautionary Statements

• P261, P264, P264+P265, P271, P280, P302+P352, P304+P340, P305+P351+P338, P319, P321, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501

Hazard Classes and Categories

• Skin Irrit. 2 (100%)
• Eye Irrit. 2 (100%)
• STOT SE 3 (100%)

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Disclaimer: Sold exclusively for laboratory research. Prohibited for commercial use, diagnostics, or human/animal applications. Buyers assume all compliance liability.