Therapeutic Uses
Anti-Migraines
Storage Condition
Store at refrigerator (2-8°C) for long term storage
Synonyms
Nadolol USP Related Compound G
Application Notes
Useful research chemical for a range of applications
Purity by HPLC
Not less than 90%
Hazard Compound
No -Refer MSDS for accurate information
Nadolol EP Impurity G is a drug product that is used as an analytical standard for HPLC, as well as in research and development of drugs.
Refund Policy
We are committed to offering products of the highest quality in order to meet the needs of our customers, and have elaborate systems in
place to ensure that material specifications, their certification and all handling and storage conditions are communicated at the time of
material handover.
We have invested in the highest quality packaging materials and use international logistics partners to service our customers. While all
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basis. If there is no other option, we will either replace your product(s) or issue a refund or account credit, whichever you prefer.
If there is an issue with one or more of our products, our policy is that it must be reported to us within 45 days of your receiving shipment.
While we will always address product issues after the 45 day return window has passed, we cannot issue a refund or account credit. As
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Nadolol EP Impurity G usage and description
Nadolol EP Impurity G is a chemical compound that is commonly used as an impurity standard in the pharmaceutical industry. It is a derivative of the drug Nadolol, which is a beta-blocker used to treat high blood pressure and other heart conditions. Nadolol EP Impurity G is considered an important reference standard for quality control and analytical testing of Nadolol.
Chemically, Nadolol EP Impurity G has the molecular formula C17H20ClNO3S and a molecular weight of 355.86 g/mol. It is a white to off-white crystalline powder that is soluble in organic solvents like methanol and acetonitrile. Nadolol EP Impurity G is stable under normal storage conditions and has a purity level of not less than 98%.
In terms of usage, Nadolol EP Impurity G is primarily used as a reference standard in the development and validation of analytical methods for the determination of Nadolol in pharmaceutical products. It is also used as a marker for the identification of Nadolol in drug substances and formulations. Nadolol EP Impurity G serves as an important tool for ensuring the quality and consistency of Nadolol-based medications, which is crucial for patient safety and effective treatment outcomes.
In conclusion, Nadolol EP Impurity G is a valuable reference standard for the pharmaceutical industry, playing a vital role in the quality control and analytical testing of Nadolol-based drugs. Its chemical properties and stability make it an ideal impurity standard for analytical laboratories and pharmaceutical manufacturers.
