Understanding Aripiprazole Specifications: What Manufacturers and Buyers Need to Know
For professionals in the chemical and pharmaceutical industries, understanding the detailed specifications of a compound like Aripiprazole (CAS 129722-12-9) is fundamental to successful sourcing and application. This white powder intermediate is a critical component, and its precise characteristics dictate its suitability for various synthesis processes.
At the forefront of Aripiprazole specifications is its purity. A minimum assay of ≥99.9% signifies an exceptionally high level of chemical integrity. For pharmaceutical intermediates, such stringent purity is non-negotiable. It minimizes the risk of unwanted side reactions, ensures the predictability of synthesis pathways, and directly impacts the quality and safety of the final Active Pharmaceutical Ingredient (API). As a manufacturer, achieving and verifying this purity is a core commitment.
The physical appearance of Aripiprazole is specified as a White Powder. This visual characteristic is an initial indicator of quality and consistency. Deviations from this appearance could suggest contamination or degradation, making it a crucial quality control parameter for both manufacturers and buyers when assessing a batch. This uniformity is key when you purchase Aripiprazole.
Key physical and chemical properties provide further insight into Aripiprazole's behavior and suitability for specific applications. The melting point of 139°C is a critical identifier and purity indicator. A sharp melting point within this range suggests a pure substance, while a broader or lower range might indicate impurities. The boiling point, listed as 646.2±55.0 °C, is also important for understanding its thermal stability and behavior under various processing conditions.
Density (1.263±0.06 g/cm³) and storage conditions (2-8°C) are other vital specifications. Maintaining the recommended storage temperature is crucial for preserving the compound's stability and preventing degradation. For buyers, understanding these requirements helps in planning for storage and handling, ensuring the material remains viable from the supplier to the end-user.
As a manufacturer and supplier of Aripiprazole in China, NINGBO INNO PHARMCHEM CO.,LTD. places immense importance on these specifications. We ensure that every batch we supply adheres to these defined parameters. For procurement managers looking to buy Aripiprazole or obtain an Aripiprazole supplier quote, requesting and scrutinizing the Certificate of Analysis (CoA) that details these specifications is a standard best practice. This transparency builds trust and guarantees that you receive the high-quality Aripiprazole for sale that your projects demand.
In conclusion, the detailed specifications of Aripiprazole (CAS 129722-12-9) are not mere technical data points; they are the bedrock of its application in demanding industries. Understanding and prioritizing these specifications when sourcing this vital intermediate ensures success in pharmaceutical manufacturing and advanced chemical synthesis.
Perspectives & Insights
Agile Reader One
“This white powder intermediate is a critical component, and its precise characteristics dictate its suitability for various synthesis processes.”
Logic Vision Labs
“It minimizes the risk of unwanted side reactions, ensures the predictability of synthesis pathways, and directly impacts the quality and safety of the final Active Pharmaceutical Ingredient (API).”
Molecule Origin 88
“Deviations from this appearance could suggest contamination or degradation, making it a crucial quality control parameter for both manufacturers and buyers when assessing a batch.”