A metabolite of mirtazapine
Related Products
Technical Support & Resources

Information provided in the product description is from published literature. Due to the nature of scientific experimentation, your results (e.g., selectivity and effective concentrations) or specific application for this product may differ. If you have questions about how this product fits your application, please contact our technical support staff.

Visit our FAQ

Contact Us

Toll Free Phone (USA and Canada Only): (888) 526-5351
Direct Phone: (734) 975-3888

Request Technical Support

Technical Support Request

To streamline the process attach the appropriate questionnaire to your inquiry.

Download IHC QuestionnaireDownload WB Questionnaire

View Our Privacy Statement for details on how we use and protect your data. In addition, this site is protected by hCaptcha and its Privacy Policy and Terms of Service apply.

Mirtazapine N-oxide

Item No. 34214

Technical Information
Formal Name
1,2,3,4,10,14b-hexahydro-2-methyl-pyrazino[2,1-a]pyrido[2,3-c][2]benzazepine, 2-oxide
CAS Number
155172-12-6
Molecular Formula
C17H19N3O
Formula Weight
Purity
≥95% (mixture of diastereomers)
A solid
Methanol: Soluble
SMILES
C[N+]1(CC2N(CC1)C3=NC=CC=C3CC4=CC=CC=C24)[O-]
InChi Code
InChI=1S/C17H19N3O/c1-20(21)10-9-19-16(12-20)15-7-3-2-5-13(15)11-14-6-4-8-18-17(14)19/h2-8,16H,9-12H2,1H3
InChi Key
GAFCUVMEBFTFQJ-UHFFFAOYSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
Recommended Products

Certificates of Analysis & Batch Specific Data

Provide batch numbers separated by commas to download or request available product inserts, QC sheets, certificates of analysis, data packs, and GC-MS data.

    Add

    Add

    Add

    Add

    Product Description

    Mirtazapine N-oxide is a metabolite of mirtazapine.1 It is formed from mirtazapine by the cytochrome P450 (CYP) isoforms CYP1A2 and CYP3A4 in human liver microsomes.

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Störmer, E., von Moltke, L.L., Shader, R.I., et alMetabolism of the antidepressant mirtazapine in vitro: Contribution of cytochromes P-450 1A2, 2D6, and 3A4. Drug Metab. Dispos. 28(10), 1168-1175 (2000).