Metronidazole-OH-D₂ ISO 17034

1-(2-Hydroxyethyl)-2-hydroxymethyl-D₂-5-nitroimidazole

Metronidazole-OH-D₂ ISO 17034 (CAS 2196180-19-3) is a high-quality Reference Material produced and distributed by WITEGA Laboratorien Berlin-Adlershof GmbH. It supports robust LC-MS/MS and GC-MS workflows for quantitative analysis, calibration, method validation, and confirmatory analysis.

Manufactured under ISO 17034 competency requirements, this reference material is designed to ensure consistency, comparability, and long-term traceability. The deuterated hydroxy metabolite design helps minimize matrix effects and enables accurate isotope-dilution strategies. With clearly stated purity and accompanied documentation, you can build reliable calibration curves and demonstrate measurement reproducibility in regulated environments.

Analysts choose this reference material to optimize LC-MS/MS or GC-MS quantification, establish calibration ranges, and confirm analyte identity through retention time and ion ratio checks. It fits seamlessly into routine surveillance and specialized studies alike, from residue control to metabolism research and multi-residue method development.

• Ready for use in LC-MS/MS and GC-MS calibration and system suitability.
• Supports quantification and defensible method validation.
• Ideal for confirmatory analysis in regulated laboratories.
• Produced and distributed by WITEGA Laboratorien Berlin-Adlershof GmbH under ISO 17034.

Typical applications include:

• Regulated laboratories requiring traceable calibration and quality control.
• Pharmaceutical research focused on nitroimidazole metabolism studies.
• Residue control programs and compliance testing.
• Multi-residue method development and verification across complex matrices.

Use Metronidazole-OH-D₂ ISO 17034 (CAS 2196180-19-3) to establish linear calibration, assess accuracy and precision, and perform confirmatory analysis with confidence. Its robust documentation facilitates audits and harmonized reporting. Select this reference material to streamline validation, and maintain consistent performance across batches and instruments.