Category:
Preclinical Research Services
CAS NO:
17460-13-8
Standard:
USP, EP,
Glucosamine sulfate Impurity 12 is a critical reference standard used in the pharmaceutical industry for quality control of glucosamine sulfate APIs. This impurity arises from specific degradation pathways or synthesis byproducts during manufacturing processes.
Store under inert atmosphere at controlled temperatures below -20°C to prevent degradation. Handle with appropriate PPE due to potential sensitization risks. Not intended for direct clinical use but strictly for analytical validation purposes only.