Nadolol EP Impurity A

Product Name Nadolol EP Impurity A
Alternate Names Nadolol Impurities, Impurities of Nadolol
CAT No. CS-O-13050
CAS No. Not Available
Category Impurities
Stock IN-Stock
Mol. Wt. 254.28 g/mol
Mol. For. C₁₃H₁₈O₅
Hazardous This is not a Hazardous Compound
COA View Sample COA
MSDS View Sample MSDS
Parent API Nadolol
Therapeutic Anti-Migraines
Controlled No
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Nadolol EP Impurity A is a chemical compound that is commonly used as an impurity reference standard in pharmaceutical research and development. It is a derivative of Nadolol, a beta-blocker medication that is used to treat high blood pressure and other cardiovascular conditions. Nadolol EP Impurity A is a byproduct of the synthesis of Nadolol and is present in small amounts in the final drug product. Chemically, Nadolol EP Impurity A is known as 5-(2,3-dihydroxypropoxy)-1,2,3,4-tetrahydronaphthalene-2-carboxylic acid. It is a white to off-white crystalline powder that is soluble in water and ethanol. The compound has a molecular weight of 268.25 g/mol. In pharmaceutical research, Nadolol EP Impurity A is used as a reference standard to ensure the purity and quality of Nadolol drug products. It is also used as a benchmark to develop and validate analytical methods for the detection and quantification of Nadolol in various matrices. Overall, Nadolol EP Impurity A is an important chemical compound in pharmaceutical research and development that plays a critical role in ensuring the safety and efficacy of Nadolol drug products.

Related Compounds

Nadolol EP Impurity C | NADOLOL IMPURITY 4 HCL | NADOLOL IMPURITY 6 | NADOLOL IMPURITY 7 HCL | Nadolol EP Impurity E | N-Nitroso-Nadolol | Nadolol EP Impurity B | De(2,3-dihydroxy) Nadolol Hydrochloride | cis-5,6,7,8-Tetrahydro-1,6,7-naphthalenetriol | Nadolol Epoxide Impurity | NADOLOL IMPURITY 8 | Nadolol EP Impurity D | Nadolol EP Impurity F | Nadolol EP Impurity G |

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