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A flow chemistry system in combination with solid-supported reagents and scavengers was used to perform fluorination reactions in a continuous mode.   Using an inline analysis method, the effect of the solid supported reagents and scavengers on the product stream can be investigated.  Read more »

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Cyclopentadecanone monooxygenase (CPDMO), a Baeyer-Villiger monooxygenase (BVMO), is an enzyme proven to be effective in the biotransformation of large and small cyclic ketones to lactones and offers high chemo-, regio-, and enantioselectivity. Read more »

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The desire to gain major improvements in product quality, yield, synthetic route, cycle time and safety in chemical processes have become key driving factors for chemists and engineers working in the chemical development and manufacturing environment in the pharmaceutical and fine chemical industries. In order to achieve these goals, scientists are actively seeking alternative chemical development methods such as modern continuous flow reactor technologies. These technologies provide the opportunity to address many of these issues as they allow for rapid testing, optimization, and scaling of chemical sequences, many of which are unsafe for batch operations.

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There are several interesting upcoming crystallization conferences and meetings. Read more »

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In Situ Monitoring of Supersaturation and Polymorphic Form of Piracetam during Batch Cooling Crystallization

Mark Barrett and others at the University College Dublin (UCD) recently published a paper Read more »

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On January 25, 2012, I attended an excellent session at the IFPAC Conference where a series of presenters including Lonza, Hovione, Merck, Pfizer, and Bristol-Myers Squibb presented the value of Process Analytical Technology (PAT) and Quality by Design (QbD) within a CRO/CMO (Contract Research Organization/Contract Manufacturing Organization). Read more »

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Transferring a crystallization to manufacturing or a contract partner is a critical step.

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Chemists and Engineers need to quickly develop repeatable crystallization processes with fast cycle times. Read more »

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USP dissolution testing is a standard method in pharmaceutical industry to characterize dissolution performance of solid dosage forms. Read more »

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