2 2′-Cyclouridine 99% Purity Medicine Intermediate CAS 3736-77-4 ISO Certified

Product Specifications

Overcoming Purity and Supply Challenges with 2,2'-Cyclouridine (CAS 3736-77-4)

In over a decade of serving chemical production and research facilities worldwide, we've witnessed how inconsistent raw material quality can derail critical projects. Researchers report yield losses from purity fluctuations as small as 0.5%, while manufacturers face costly production halts when suppliers fail to meet delivery deadlines. These challenges are particularly acute for specialized intermediates like 2,2'-Cyclouridine, where even minor impurities can compromise downstream synthesis.

Stabilizing Your Production with ISO-Certified 2,2'-Cyclouridine

Our 99% purity 2,2'-Cyclouridine addresses these pain points through rigorous manufacturing controls and a supply chain designed for industrial scale reliability. With a dedicated 20-ton annual production capacity and strategic warehousing across Asia, we ensure consistent availability from kilogram to ton-level orders—eliminating the production delays that plague projects relying on low-volume suppliers. This stability has made our Medicine Intermediate a trusted choice for pharmaceutical R&D labs and specialty chemical manufacturers across 50+ countries.

Industrial Applications of 2,2'-Cyclouridine

As a specialized Medicine Intermediate, 2,2'-Cyclouridine CAS 3736-77-4 finds primary use in pharmaceutical research and fine chemical synthesis. Its unique structural properties make it valuable for developing nucleoside-based compounds and studying biochemical pathways in laboratory settings. Industrial users leverage its high purity to ensure reproducibility in multi-step synthesis processes, where impurity accumulation can render entire batches unusable.

The Critical Role of Key Specifications in Synthesis

The 99% purity specification of our 2,2'-Cyclouridine directly impacts reaction efficiency—reducing side reactions that waste raw materials and complicate purification. Its defined melting point (239-240℃) provides a reliable quality control marker, ensuring batch-to-batch consistency critical for scale-up. The 456.3±55.0 °C boiling point data aids in process optimization for distillation-based purification steps, while the white powder appearance serves as an initial visual quality check before analytical testing. Together, these parameters form a quality framework that minimizes production risks.

Quality Assurance: From Production to Delivery

Choosing our ISO Certified Medicine Intermediate means investing in predictable outcomes rather than absorbing hidden costs. Inferior materials with unspecified impurities often require additional purification steps, increasing processing time by 30% or more. Our strict quality protocols—including HPLC analysis for every batch—ensure you receive material ready for immediate use, reducing lab waste and production downtime. With REACH compliance and full traceability documentation, we provide the regulatory assurance needed for international trade and strict manufacturing standards.

Our Commitment to Supply Chain Reliability

Certificate of Analysis & Documentation

Each shipment includes a batch-specific COA with purity test results, impurity profiles, and physical property data. Material Safety Data Sheets (MSDS) containing handling precautions and storage recommendations are provided with all orders. For critical applications requiring additional verification, we can supply raw HPLC chromatograms and NMR spectra upon request, ensuring complete transparency in our quality claims.

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 Order Process for Industrial Buyers

Initiate your purchase by submitting a detailed procurement list specifying required quantity and packaging preferences. Our technical team will confirm availability and provide a formal quotation within 24 hours, including delivery timelines based on your location. For first-time users, we offer small sample quantities for qualification testing prior to full-scale orders. Once specifications are confirmed, we arrange secure payment processing and coordinate shipping via sea or land transport, with full tracking provided until delivery.

Frequently Asked Questions