Understanding Pbf-Cl: Properties, Synthesis, and Handling
For chemists engaged in sophisticated organic synthesis and peptide development, a deep understanding of the reagents they utilize is crucial. 2,2,4,6,7-Pentamethyl-2,3-dihydrobenzofuran-5-sulfonyl chloride (Pbf-Cl, CAS 154445-78-0) is one such vital compound, primarily known for its efficacy as an arginine protecting group in Solid-Phase Peptide Synthesis (SPPS). This article delves into the intrinsic properties, common synthesis methodologies, and essential handling protocols for Pbf-Cl, providing valuable insights for laboratory professionals.
Chemically, Pbf-Cl is characterized by its molecular formula C13H17ClO3S and a molecular weight of approximately 288.79 g/mol. It presents as a gray solid with a melting point typically ranging between 58-71°C. The molecule features a robust 2,2,4,6,7-pentamethyl-2,3-dihydrobenzofuran core, to which a reactive sulfonyl chloride group (-SO2Cl) is attached. This sulfonyl chloride moiety is the key to its reactivity, allowing it to readily undergo nucleophilic substitution reactions, forming stable sulfonamides, sulfonates, and other derivatives.
The synthesis of Pbf-Cl commonly involves a two-step process starting from 2,3,5-trimethylphenol. The initial step, sulfonation, typically uses concentrated sulfuric acid to form the corresponding sulfonic acid intermediate. This is followed by chlorination, often employing chlorosulfonic acid or thionyl chloride, to convert the sulfonic acid into the desired sulfonyl chloride. Industrial-scale production often involves process optimization, such as utilizing continuous flow reactors and solvent recovery systems, to enhance efficiency, reduce waste, and maintain high purity levels, often exceeding 98%.
When considering the procurement of Pbf-Cl, understanding its stability and handling requirements is paramount. Pbf-Cl is sensitive to moisture and can hydrolyze to its corresponding sulfonic acid, a process accelerated by heat and extreme pH conditions. Therefore, it is recommended to store Pbf-Cl under an inert atmosphere (such as nitrogen or argon) at cold temperatures, typically -20°C, to preserve its reactivity and purity. When handling, it is crucial to use dry solvents and equipment, and to work in a well-ventilated area or fume hood, as sulfonyl chlorides can release corrosive gases like HCl upon reaction with moisture.
The GHS pictograms associated with Pbf-Cl often include the 'Corrosive' symbol, indicating that it can cause severe skin burns and eye damage. Appropriate personal protective equipment (PPE), including chemical-resistant gloves, safety goggles, and a lab coat, must be worn at all times. Proper disposal procedures should be followed, typically involving neutralization of any residual material before discarding it according to local regulations.
As a leading manufacturer and supplier of fine chemicals, NINGBO INNO PHARMCHEM CO.,LTD. is committed to providing Pbf-Cl that adheres to strict quality control measures. We ensure that our product meets the necessary specifications for purity and reactivity, supporting the critical applications of our clients in research and industry. Whether you are synthesizing complex peptides or exploring new organic transformations, understanding the nuances of Pbf-Cl is key to achieving successful outcomes. We encourage you to buy Pbf-Cl from us and experience the reliability and quality that our products offer.
Perspectives & Insights
Molecule Vision 7
“The molecule features a robust 2,2,4,6,7-pentamethyl-2,3-dihydrobenzofuran core, to which a reactive sulfonyl chloride group (-SO2Cl) is attached.”
Alpha Origin 24
“This sulfonyl chloride moiety is the key to its reactivity, allowing it to readily undergo nucleophilic substitution reactions, forming stable sulfonamides, sulfonates, and other derivatives.”
Future Analyst X
“The synthesis of Pbf-Cl commonly involves a two-step process starting from 2,3,5-trimethylphenol.”