Dapagliflozin Alpha Isomer (CAS 1373321-04-0): Your Key to Pharmaceutical Quality
Precision, Purity, and Performance for Drug Development and Research.
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Dapagliflozin Alpha Isomer
As a vital component in the pharmaceutical landscape, Dapagliflozin Alpha Isomer serves as a critical reference standard. Its high purity and well-defined chemical structure are essential for accurate analytical method development and validation, ensuring the quality and safety of pharmaceutical products. This compound plays a significant role in the quality control processes for Dapagliflozin, supporting regulatory submissions and scientific research.
- High Purity for Reliable Results: With a purity exceeding 99%, this isomer is indispensable for precise pharmaceutical impurity quantification, guaranteeing the integrity of your analytical data.
- Foundation for Drug Development: Essential for robust analytical method development for Dapagliflozin, it aids in establishing reliable quality control protocols.
- Trusted in Scientific Research: Widely recognized as a key scientific research chemical standard, it supports various research endeavors in medicinal chemistry and drug discovery.
- Accelerate Your Projects: Leveraging custom synthesis of pharmaceutical intermediates ensures timely access to this critical standard, speeding up your project timelines.
Key Advantages Offered
Uncompromised Purity & Accuracy
Achieve superior accuracy in your analyses with our Dapagliflozin Alpha Isomer, a benchmark for Dapagliflozin reference standard applications, ensuring dependable and reproducible results.
Regulatory Compliance Support
Facilitate smoother regulatory submissions, such as ANDA and NDA, by utilizing a reference standard that adheres to stringent pharmaceutical quality guidelines.
Versatile Research Applications
Empower your R&D efforts with a compound essential for various studies, from understanding drug metabolism to developing novel analytical techniques for pharmaceutical impurities.
Key Applications
Analytical Method Development
Crucial for developing and optimizing HPLC methods for accurate quantification of Dapagliflozin and its related substances, aiding in pharmaceutical impurity quantification.
Quality Control (QC)
Serves as a vital Dapagliflozin reference standard in routine QC testing of API batches, ensuring product consistency and adherence to specifications.
Research and Development
A fundamental scientific research chemical standard used in pharmaceutical R&D for impurity profiling, stability studies, and new drug discovery.
Regulatory Submissions
Supports regulatory filings by providing well-characterized reference materials necessary for demonstrating product quality and safety to health authorities.