Cefotiamhexetil Hydrochloride 99% Purity Medicine Intermediate CAS 4697-14-7 ISO Certified

Product Specifications

Overcoming Purity Fluctuations in Cefotiamhexetil Hydrochloride (CAS 4697-14-7) Production

In our 10+ years serving pharmaceutical intermediate manufacturers, we’ve witnessed how inconsistent purity of Cefotiamhexetil Hydrochloride disrupts synthesis processes—leading to unexpected副 reactions, failed batch validations, and costly production delays. Clients repeatedly highlight the challenge of sourcing a reliable 99% purity material that maintains specification across kilogram to ton-scale orders.

A Stable Supply Chain for Critical Medicine Intermediates

Our High Purity Cefotiamhexetil Hydrochloride for Pharmaceuticals addresses these pain points through a vertically integrated supply chain. With a dedicated 20t/year production line in Hangzhou and ISO-certified quality management, we deliver consistent material that meets the strict standards required for pharmaceutical intermediate synthesis. This stability has made us the trusted partner for 10,000+ industrial customers across 50+ countries.

Industrial Applications of Cefotiamhexetil Hydrochloride

As a Solid Medicine Intermediate CAS 4697-14-7, this compound serves as a key building block in the production of pharmaceutical active ingredients. Its primary industrial use lies in organic synthesis processes within controlled laboratory and manufacturing environments, where precise chemical properties are critical for downstream reactions. All applications must adhere to strict industrial protocols and safety standards.

Why Key Specifications Ensure Process Reliability

The >99% purity level of our Cefotiamhexetil Hydrochloride minimizes impurity interference, reducing side reactions that compromise product quality. Its defined boiling point (768.3℃ at 760 mmHg) provides consistent thermal behavior during synthesis, while the solid state ensures stable handling and metering. The molecular formula C15h14n2na2o6s2 confirms structural integrity, a critical factor for reproducible reaction outcomes in large-scale manufacturing.

Risk Mitigation Through Quality Assurance

Choosing ISO Certified Cefotiamhexetil Hydrochloride reduces the hidden costs of substandard materials: failed batch testing, production downtime, and regulatory non-compliance. Our material meets international quality standards, with each batch undergoing rigorous testing to ensure重金属控制 and impurity profiles that align with export requirements. Unlike unreliable suppliers, our stable production capacity guarantees consistent pricing and on-time delivery, protecting your production schedule from market volatility.

Our Quality Commitment: Beyond Compliance

Certificate of Analysis & Documentation

Each delivery includes a batch-specific Certificate of Analysis detailing purity, impurities, and physical properties, along with a Material Safety Data Sheet (MSDS) for safe handling. For qualifying orders, we can provide additional documentation including manufacturing process flow diagrams and stability studies upon request. Specific batch test data is retrievable by order number for audit purposes.

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 Industrial Procurement Process

Our transaction process is designed for industrial efficiency: submit your procurement list with required quantities, receive a detailed quotation including delivery timeline, and confirm your order with flexible payment terms. We offer sample testing for qualification purposes and provide dedicated account management throughout the ordering process. All shipments include full customs documentation for international logistics.

Frequently Asked Questions