(3,4-Dimethoxyphenyl)acetonitrile
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Technical Description
Verapamil Impurity 12 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:
Buy 92040-70-5 Purchase 92040-70-5 Order 92040-70-5 Enquire 92040-70-5 92040-70-5 price 92040-70-5 supplier 92040-70-5 manufacturer 92040-70-5 exporter Verapamil Impurity 12 for method validation Verapamil Impurity 12 reference standard Verapamil Impurity 12 for ANDA filing Verapamil Impurity 12 for forced degradation studies Verapamil Impurity 12 identification standard Verapamil Impurity 12 for DMF filing Verapamil Impurity 12 HPLC standard Verapamil Impurity 12 supplier Verapamil Impurity 12 manufacturer Verapamil Impurity 12 distributor
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.
Verapamil Impurity 12
CAT. No. V180045 · CAS 92040-70-5 ·
219.30 g/mol
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