N‐Nitroso Ganirelix - aquigenbio/blog GitHub Wiki

Category: Impurity Standards – Ganirelix

Overview

N-Nitroso Ganirelix is a high-quality reference standard offered by AquigenBio. With the molecular formula C₈₀H₁₁₂ClN₁₉O₁₄ and a molecular weight of about 1599.3 Da, it is designed to support analytical method development, method validation, quality control (QC), and Abbreviated New Drug Applications (ANDA).

This impurity standard is thoroughly characterized and may be traceable to pharmacopeial references such as USP or EP, where applicable. It is intended strictly for analytical use and not for human administration.

Safety and Handling

When working with N-Nitroso Ganirelix, it is essential to follow strict laboratory safety practices:

Review the Safety Data Sheet (SDS) before use.

Wear suitable PPE including gloves, lab coat, safety goggles, and respirator if required.

Handle under proper ventilation to prevent exposure.

Prevent contamination and store in labeled, secure containers.

Follow waste disposal guidelines in line with local regulations.

Train staff in safe handling, emergency protocols, and incident reporting.

Related Products

AquigenBio also supplies a wide range of Ganirelix impurity standards to complement N-Nitroso Ganirelix in impurity profiling and analytical method development:

Ganirelix Acetate Impurity A – a characterized impurity standard for analytical studies.

Ganirelix Acetate Impurity B – useful in validation and QC testing.

Ganirelix Acetate Impurity C – an important impurity reference for research applications.

Ganirelix Acetate Impurity D – a structural variation ideal for comparative studies.

Ganirelix Impurity 1 – supports impurity profiling and QC requirements.

Ganirelix Impurity 2 – a related impurity standard widely used in method validation.

Conclusion

N-Nitroso Ganirelix, along with its related impurity standards, plays a vital role in pharmaceutical research and regulatory support. By offering high-quality, reliable standards, AquigenBio ensures accuracy in analytical testing, impurity profiling, and global compliance.