The pharmaceutical industry operates under the most stringent quality demands, where every raw material must meet exacting standards to ensure patient safety and product efficacy. For chemical intermediates like 1-Phenylethanol (CAS 98-85-1), the classification of 'pharmaceutical grade' signifies a level of purity and reliability that is indispensable. This article delves into the importance of pharmaceutical grade 1-Phenylethanol, its key benefits, and how B2B buyers can effectively source it.

1-Phenylethanol, a secondary aromatic alcohol with the chemical formula C8H11O, is frequently used as a key intermediate in the synthesis of Active Pharmaceutical Ingredients (APIs) and various drug formulations. Its chemical structure lends itself to a variety of reactions, making it a valuable building block in complex pharmaceutical manufacturing processes. The requirement for pharmaceutical grade implies a rigorous quality control process, ensuring that the product is free from harmful contaminants and meets specific purity criteria, typically above 99.0% assay.

The benefits of using high-purity, pharmaceutical grade 1-Phenylethanol are manifold. Firstly, it guarantees consistency in chemical reactions, leading to predictable yields and minimal batch-to-batch variability in API production. This is crucial for maintaining the quality and regulatory compliance of pharmaceutical products. Secondly, it minimizes the risk of side reactions or the introduction of impurities that could compromise the safety or efficacy of the final drug. This adherence to quality is why many pharmaceutical companies actively seek out this specific grade.

When it comes to purchasing pharmaceutical grade 1-Phenylethanol (CAS 98-85-1), understanding the supplier landscape is key. Manufacturers in China have become significant global players in supplying high-quality chemical intermediates. For pharmaceutical companies looking to buy 1-Phenylethanol, partnering with a reputable manufacturer that specializes in pharmaceutical grade products is essential. This often means verifying their adherence to Good Manufacturing Practices (GMP) or similar quality management systems.

Key specifications to look for when sourcing pharmaceutical grade 1-Phenylethanol include an assay of ≥99.0%, low water content (≤1.0%), and extremely low levels of heavy metals (≤10 ppm) and other impurities (single impurity ≤0.10%, total impurity ≤0.5%). A comprehensive Certificate of Analysis (CoA) from the manufacturer is indispensable for verification and regulatory filings. Buyers should also inquire about packaging, typically in secure 200kg drums, and minimum order quantities, which are often set at 100kg.

In conclusion, pharmaceutical grade 1-Phenylethanol (CAS 98-85-1) is a critical component in the pharmaceutical supply chain. Its superior purity and quality are non-negotiable for ensuring the integrity of medicinal products. By carefully selecting manufacturers who can provide documented pharmaceutical grade material and adhere to stringent quality standards, pharmaceutical companies can secure a reliable and safe supply of this essential intermediate, thereby supporting their commitment to producing high-quality medicines.