High-Purity Hydrochlorothiazide Impurity C CAS 402824-96-8: Chemical Properties, Applications & Suppliers
Essential impurity standard for Hydrochlorothiazide quality control and analysis.
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Hydrochlorothiazide EP Impurity C
This product serves as a critical reference standard for the pharmaceutical industry, specifically for the quality control and analysis of Hydrochlorothiazide. Its established purity and characterization are vital for ensuring the safety and efficacy of pharmaceutical products, making it an indispensable tool in drug substance analysis.
- Accurate monitoring of Hydrochlorothiazide impurity levels is crucial, and this reference standard, Hydrochlorothiazide EP Impurity C CAS 402824-96-8, provides the benchmark for such assessments.
- As a Dimer Impurity C type, understanding its chemical synthesis of Hydrochlorothiazide impurity C allows for better process control in drug manufacturing.
- The chemical properties of this compound, including its solubility in DMSO and methanol, are well-documented, aiding in its analytical application.
- Sourcing this high-purity pharmaceutical impurity standard from reliable suppliers is key to maintaining robust quality assurance systems.
Key Advantages
Ensured Purity and Accuracy
With a purity of ≥95%, this standard offers reliable results for buy Hydrochlorothiazide EP Impurity C in your laboratory, crucial for meeting stringent regulatory requirements in pharmaceutical impurity reference standard applications.
Critical for Quality Control
This Hydrochlorothiazide EP Impurity C is essential for effective Hydrochlorothiazide quality control, helping manufacturers identify and quantify impurities as part of comprehensive drug substance analysis.
Comprehensive Chemical Data
Detailed CAS 402824-96-8 chemical properties, including its structure and solubility, are readily available, supporting its effective use in various analytical methods.
Key Applications
Pharmaceutical Quality Control
Utilizing the Hydrochlorothiazide EP Impurity C CAS 402824-96-8 as a reference standard is paramount for laboratories performing quality control on Hydrochlorothiazide formulations.
Analytical Method Development
Researchers can leverage the known chemical properties of this Hydrochlorothiazide dimer impurity to develop and validate analytical methods for impurity profiling.
Regulatory Compliance
Adhering to pharmaceutical impurity standards and guidelines is critical; this product aids in meeting regulatory requirements for drug purity.
Drug Substance Analysis
Its role as a reference standard makes it indispensable for thorough drug substance analysis, ensuring product integrity and safety.