Aicaigou LogoAicaigou LogoB2B WikiIndustrial Encyclopedia

Ethylboronic Acid

Updated: 2026-07-15

Overview

Ethylboronic acid is an organoboron compound primarily used as a reagent in organic synthesis. Its stability and reactivity make it a preferred choice for cross-coupling reactions, particularly in the pharmaceutical and agrochemical sectors. The compound is typically supplied as a crystalline solid and requires careful handling due to its sensitivity to moisture and air. As a boronic acid derivative, ethylboronic acid plays a critical role in modern synthetic chemistry. Its ability to form stable covalent bonds with carbon atoms under mild conditions has expanded its applications in drug discovery and material science.

Physical and Chemical Properties

4-乙基苯硼酸对乙基苯硼酸63139-21-9含量99%合成中间体上海宝杨宝欣生物科技有限公司

Ethylboronic acid is a white to off-white crystalline powder with a molecular weight of 73.89 g/mol. It melts at approximately 90-95°C and is soluble in common organic solvents such as tetrahydrofuran (THF) and ethanol. The compound is air-sensitive and may decompose upon prolonged exposure to moisture. Key chemical properties include its ability to participate in Suzuki-Miyaura cross-coupling reactions, where it acts as a nucleophilic partner. The boron-carbon bond in ethylboronic acid is relatively stable under anhydrous conditions but can hydrolyze in the presence of water, requiring careful storage and handling.

商家经验真实案例 · 安全可信
四氧化三锰工艺流程
本文详细解析四氧化三锰的生产工艺流程,包括原料处理、化学反应步骤及成品处理三大部分,帮助读者系统了解这一工业化学品的制造过程。

Main Applications

The primary application of ethylboronic acid is in Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds in organic synthesis. This reaction is particularly valuable in pharmaceutical manufacturing for creating complex molecular structures. Additional applications include its use as an intermediate in agrochemical production and materials science. In drug discovery, ethylboronic acid derivatives are explored for their potential biological activity, particularly in protease inhibition and boron neutron capture therapy (BNCT) research.

Safety and Storage

1-(1-乙氧基乙基)-4-吡唑硼酸频哪醇酯 CAS号1029716-44-6 健楚生物湖北健楚生物医药有限公司

Ethylboronic acid is classified as an irritant and should be handled with appropriate personal protective equipment (PPE), including gloves and eye protection. The compound is sensitive to moisture and air, requiring storage under inert atmosphere (e.g., nitrogen or argon) in a cool, dry environment. In case of skin contact, immediately wash with soap and water. For eye exposure, flush with copious amounts of water for at least 15 minutes and seek medical attention. Spills should be contained with inert absorbent material and disposed of according to local regulations.

商家经验真实案例 · 安全可信
皂基与脂肪酸钠之谜
本文解析皂基和脂肪酸钠的本质区别,从成分结构到应用场景全面对比,揭秘两者在清洁领域的独特价值与适用差异,帮助读者根据需求合理选择。

B2B Procurement Guide

When procuring ethylboronic acid, buyers should prioritize suppliers who provide certificates of analysis (CoA) detailing purity (>95%), moisture content, and heavy metal impurities. Bulk quantities (kilogram scale) typically offer better pricing, with reference prices ranging approximately $50-$200/kg depending on purity and supplier. Key procurement considerations include packaging quality (air-tight containers with proper seals), lead times, and the supplier's ability to provide technical support. For pharmaceutical applications, ensure the supplier complies with relevant Good Manufacturing Practice (GMP) standards and can provide documentation for regulatory compliance.

Related Manufacturers