Tenoxicam impurity mixture CRS, 0.0042 mg

Tenoxicam impurity mixture is a European Pharmacopoeia chemical reference substance, prescribed under Ph. Eur. monograph 1156. It is intended for identification and quantification of a specified impurity.

Identity is established by EDQM catalogue code Y0001114, current batch 3. The batch in distribution is valid until 31 January 2027.

Application

Reference standards of the European Pharmacopoeia are used in the tests and assays of the official Ph. Eur. methods, by analysts competent in those methods. Typical use is in pharmaceutical quality control — release and stability testing, method development and validation, and system suitability checks in chromatographic analysis. As an impurity standard, it supports the related-substances test for the corresponding monograph.

Packaging and storage

Supplied as 0.0042 mg per vial. One vial per sales unit. Store refrigerated at +5 °C ± 3 °C. Ships at ambient temperature.

Notes

• For laboratory analytical use only. Not for human or veterinary consumption, and not for therapeutic, diagnostic or food use.
• Reference standards are non-returnable once dispatched, except where faulty, damaged or incorrectly supplied. Please report any damage within one working day of delivery, with photographs.