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Olmesartan Impurity 39
Olmesartan Impurity 39
Technical Description
Olmesartan Impurity 39 is listed by Simson Pharma as a impurity standards for laboratory research, analytical development and quality-control workflows.
Suitability is method- and purpose-specific. Before use, verify the product name, catalogue number, chemical identifiers, storage requirements and the information reported in the current product or batch documentation. Your laboratory remains responsible for method qualification or validation.
Product Applications & Regulatory Search Terms:
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![Structure of 1H-Imidazole-5-carboxylic acid, 4-acetyl-2-propyl-1-[[2`-(2H-tetrazol-5-yl)[1,1`-biphenyl]-4-yl]methyl]-, (5-methyl-2-oxo-1,3-dioxol-4-yl)methyl ester](https://www.simsonpharma.com/admin/uploads/products/O020099.jpg)
DISCLAIMER
This page supports product identification and initial technical
evaluation. Specifications, assigned values, pack options, availability and documentation may vary by
product or batch; verify the applicable details in the current quotation, label and supplied records before
use. The purchaser or importer is responsible for determining method suitability and meeting local
regulatory, transport and import requirements.
For research, analytical and quality-control use only. Not for human
or veterinary consumption, and not for use as a medicine.
Olmesartan Impurity 39
CAT. No. O020095 · CAS NA ·
210.15 g/mol
✕
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