Dl-4-Hydroxyphenylglycine 99% Purity Pharmaceutical Intermediate CAS 938-97-6

Product Specifications

Overcoming Purity and Supply Challenges with Dl-4-Hydroxyphenylglycine 99% CAS 938-97-6

We’ve witnessed countless production delays when pharmaceutical intermediates fail to meet purity standards—fluctuating impurity levels causing unexpected side reactions, inconsistent batch quality derailing research reproducibility, and unreliable suppliers missing critical delivery windows. In our 10+ years serving chemical manufacturers, these issues remain the top pain points for scaling production of pharmaceutical intermediates.

A Stable and Reliable Pharmaceutical Intermediate Supply Solution

Our Dl-4-Hydroxyphenylglycine addresses these challenges through consistent >99% purity and a supply chain designed for industrial scale. With a dedicated 20t/year production line and large warehousing capacity, we ensure steady availability from kilogram to ton-level orders, supporting your production continuity even during peak demand periods in the Asia-Pacific market.

Industrial Applications of Dl-4-Hydroxyphenylglycine

As a key Pharmaceutical Intermediate, this compound serves as a critical building block in organic synthesis processes within chemical manufacturing. Its high purity makes it suitable for laboratory research and industrial-scale production of fine chemicals, where structural integrity and impurity control are paramount for downstream reactions.

Why Key Specifications Matter in Production

The >99% purity of our Dl-4-Hydroxyphenylglycine minimizes副反应 (side reactions) and impurity interference, ensuring cleaner synthesis pathways and reducing purification costs. The defined boiling point of 446.3℃ at 760mmhg provides reliable process parameters for distillation and purification steps. Our standardized solid form ensures consistent handling and dissolution characteristics, while the 250kg/drum packaging optimizes storage efficiency and reduces material transfer losses in industrial settings.

Quality Assurance: Risks of Compromised Intermediates vs. Our Solution

Using substandard pharmaceutical intermediates risks batch failures, production downtime, and non-compliance with industry regulations. Our product adheres to strict quality control protocols aligned with industrial chemical standards, ensuring each batch meets consistent specifications. The stable supply chain eliminates sudden price volatility and delivery delays, providing predictable cost management for your manufacturing operations.

Our Quality Commitment: Beyond Compliance

Certificate of Analysis & Documentation

Each shipment includes a batch-specific COA and MSDS, providing full transparency of quality parameters. Detailed analytical data can be requested using your order reference, and additional documentation for regulatory compliance is available upon request.

Storage & Handling

• Store in a cool, dry, well-ventilated area, sealed and away from direct sunlight.
• Keep away from incompatible materials, food and feed sources.
• Handle with appropriate personal protective equipment (gloves, goggles, lab coat).
• Follow good industrial hygiene practices. Avoid inhalation and skin contact.
• Refer to MSDS for detailed storage and safety instructions.

Streamlined Procurement Process for Your Production Needs

Initiate your order by submitting your required quantity and specifications for a customized quotation. We offer sample evaluation to validate compatibility with your processes before full-scale procurement. Our standard transaction process ensures clarity from order confirmation to delivery, with dedicated support throughout the procurement cycle.

Frequently Asked Questions