4-Pentyloxyphenylboronic Acid

Product Overview

4-Pentyloxyphenylboronic Acid is a specialized organic compound belonging to the arylboronic acid family. Recognized for its stability and reactivity, this chemical serves as a critical building block in modern medicinal chemistry and organic synthesis. Our facility produces this compound under strict quality management systems to ensure consistency across batches. The molecule features a pentyloxy substituent on the phenyl ring, which influences its electronic properties and solubility profile, making it particularly suitable for specific cross-coupling reactions.

As a leading supplier in the fine chemicals sector, we understand the demanding requirements of research laboratories and production plants. This product is synthesized using advanced catalytic methods to achieve high purity levels. The presence of the boronic acid group allows for versatile functionalization, enabling chemists to construct complex molecular architectures efficiently. Whether used in small-scale discovery or large-scale manufacturing, our material provides a reliable foundation for your synthetic pathways.

Technical Specifications

We adhere to rigorous analytical standards to guarantee the quality of 4-Pentyloxyphenylboronic Acid. Each batch undergoes comprehensive testing using HPLC, NMR, and Karl Fischer titration. The following table outlines the key physical and chemical parameters typically associated with our standard grade material.

Please note that specific parameters may vary slightly depending on the production batch. A Certificate of Analysis (COA) is provided with every shipment to verify compliance with the agreed specifications. Our quality control team is available to discuss custom purity requirements for specialized applications.

Industrial Applications

The primary application of 4-Pentyloxyphenylboronic Acid lies in the field of pharmaceutical intermediates. It is extensively utilized in Suzuki-Miyaura cross-coupling reactions, which are pivotal for forming carbon-carbon bonds. This capability is essential for synthesizing biaryl structures found in numerous active pharmaceutical ingredients (APIs). The pentyloxy chain offers specific steric and electronic effects that can enhance reaction yields or selectivity in certain catalytic cycles.

• Key reagent for palladium-catalyzed coupling reactions.
• Building block for developing novel therapeutic agents.
• Used in the synthesis of liquid crystals and functional materials.
• Supports research in organic electronics and polymer chemistry.

Beyond pharmaceuticals, this boronic acid derivative finds utility in material science. Researchers utilize it to develop advanced polymers and optoelectronic materials where precise molecular orientation is required. The stability of the boronic acid group under various conditions makes it a preferred choice for multi-step synthesis routes.

Storage and Handling

Proper storage is essential to maintain the integrity of 4-Pentyloxyphenylboronic Acid. The product should be kept in a cool, dry, and well-ventilated area away from direct sunlight and heat sources. Containers must remain tightly closed to prevent moisture absorption, which can lead to the formation of boronic anhydrides. We recommend storing the material at ambient temperatures below 25°C.

Safety is our priority. This compound is classified under transport hazard class 3. Personnel handling this chemical should wear appropriate personal protective equipment, including gloves and safety goggles. In case of spillage, standard chemical cleanup procedures should be followed. We provide comprehensive Safety Data Sheets (SDS) with every order to ensure compliance with local safety regulations. Our packaging options include 25kg drums, with custom solutions available upon request to suit your logistics needs.