YOUR TRUSTED ROTIGOTINE MANUFACTURER FOR ALL YOUR NEEDS

OUR CORE PHILOSOPHY: LEADING SUPPLIER AND EXPORTER OF CAS 59729-32-7 COMPOUND

In the world of pharmaceutical manufacture there is no room for error. If there is an impurity or inconsistency in one of the intermediates, the final drug product may be ineffective or unsafe.

We have a complete Quality Management System in place which meets the strictest international standards. Our facilities are designed and maintained according to the current Good Manufacturing Practices (cGMP) guideline set by regulatory bodies such as US FDA, EMA, PMDA.

The three elements of our quality promise:

• Raw Material Vigilance: We purchase it from the qualified suppliers and every raw material is subjected to stringent tests before entering our production line.
• In-Process Control: We monitor our manufacturing processes continuously to make sure that they are kept within validated parameters.
• Analytical Excellence: Our state-of-the-art QC labs are equipped with instrumentation, providing complete traceability & characterization.
• Stability Assurance: Many tests are undertaken to ensure every batch we deliver is stable and offers long shelf life.

USES AND INDUSTRIAL APPLICATIONS OF CAS NO: 59729-32-7

Citalopram Hydrobromide (CAS 59729-32-7) is a selective serotonin reuptake inhibitor (SSRI) which is widely used in the pharmaceutical industry for the treatment of major depressive disorders and other mental health related problems. It is also used as a reference standard for pharmaceutical use and for analytical, research and quality control purposes.

• Used as active pharmaceutical ingredient (API) in antidepressant preparations
• Used often for major depression and some anxiety disorders
• Is a selective serotonin reuptake inhibitor (SSRI), which increases the amount of serotonin in the brain
• Reference standard for quality control and method validation of pharmaceuticals
• Applied in analytical laboratories in HPLC, LC-MS and other pharmaceutical testing techniques
• For pharmaceutical research and drug development
• Clinical toxicology and forensic analysis for identification and quantitation of drugs

PURITY STANDARDS, STORAGE CONDITIONS, AND QUALITY ASSURANCE

CAS No. 59729-32-7 is produced under a strict pharmaceutical quality system to guarantee purity, safety and performance.

Key highlights:

• Manufactured with highest purity and controlled level of impurities as required by the pharmaceutical industry
• Made in accordance to Good Manufacturing Practice (GMP) and strong quality management systems
• Validated analytical methods (HPLC, GC, IR and related substance analysis) were used to test
• Kept in a cool, dry and well-ventilated location away from direct heat, moisture and sun
• Provided in enclosed containers that are kept dry and stable during storage and transit

OUR MANUFACTURING CAPABILITIES: SCALE AND FLEXIBILITY

We are aware that there is no one size fits all. Your molecule has special needs and challenges and, that is why, we’ve designed our infrastructure to be as flexible and adaptable as possible. We have developed a strong manufacturing infrastructure to enable the scale-up of your product from the bench to commercial production.

Key features:

• Kilogram to Ton Scale: Small tasks for clinical trials or a large ton of commercial applications, we can help you.
• Multi-Purpose Reactors: Our reactor fleet can be set up in a variety of arrangements to suit the process requirements.
• Specialized Technologies: We have the in-house equipment for high pressure hydrogenation, cryogenic reactions, chromatographic purification, distillation and fractionation.
• Versatile Intermediates: We are highly experienced in preparing high purity, high yield, complex chiral intermediates, building blocks and advanced intermediates.

OUR R&D EXPERTISE: HIGH-QUALITY CAS NO. 59729-32-7 MANUFACTURER

Our R&D group isn’t just a bunch of chemists, it’s a team of problem solvers who want your process to be successful. The team take the time to work closely with you to locate possible constraints, to observe safety and to enhance yield.

• Process Feasibility: Start by comprehensive assessment of proposed synthetic route for scalability, safety, cost-effectiveness
• Process Optimization: Optimization of reaction parameters to achieve maximum yield, purity and minimum waste
• Impurity Profiling: We identify these impurities, synthesize and control them to ensure the superior quality product
• Tech Transfer: We support and document the transfer of the optimized process from our research lab to our manufacturing facilities smoothly and efficiently

SUPPLY CHAIN SECURITY AND GLOBAL REACH

Reliability is the most important currency in the world of global supply chains. We give you security and confidence so that your supply chain can continue without any hindrances. Our strong supply chain management system gives us the ability to execute our commitments, even in the face of global market changes.

Our supply chain is our advantage:

• Dual-Sourcing Strategy: We have strong supplier relationships with several qualified suppliers for critical raw materials and are able to move production between our facilities to manage risk.
• Inventory Management: Co-ordination with partners to predict the demand and strategically managing stock to ensure timely deliveries.
• Global Logistics: Our logistics personnel have the expertise to deal with all shipment, customs and documentation requirements to get your product where you want it and on time.

YOUR SUCCESS IS OUR MISSION: PREMIER CAS No. 59729-32-7 SUPPLIERS

In an industry where the consequence of failure is high, reliability, quality and expertise are irreplaceable in an industry where human health is the consequence of failure. In the case of human health, there’s nothing quite like reliability, quality, and expertise. We are ready to serve you as your strategic partner in getting your crucial pharmaceutical products to market.

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