33841-03-1
Nadolol EP Impurity G
CAS: 33841-03-1
Molecular Formula: C17H27NO2
33841-03-1 - Names and Identifiers
33841-03-1 - Physico-chemical Properties
| Molecular Formula | C17H27NO2 |
| Molar Mass | 277.4 |
| Storage Condition | 2-8°C |
33841-03-1 - Introduction
Nadolol EP Impurity G is an Impurity associated with Nadolol, a non-selective beta-blocker. Its chemical name is (5RS)-5-[2-[(1,1-dimenthyl-2-propyl) oxy]ethyl]-3-[4-hydroxy-3-(2-hydroxypan-2-yl) phenyl] oxolan-2-one.
Nadolol EP Impurity G is often used in pharmacy for the detection and quantitative analysis of harmful impurities in Nadolol. It belongs to one of the degradation products of Nadolol, and its presence may affect the efficacy and stability of nadolol.
Regarding the preparation method, Nadolol EP Impurity G can be produced by a transformation reaction of bacteria or yeast. Specific synthetic methods can be achieved by chemical synthesis or biosynthesis.
As for safety information, since Nadolol EP Impurity G is a degradation product of Nadolol, its role and safety need further research and evaluation. In pharmaceutical preparations and treatments, the content of Nadolol EP Impurity G should be controlled within the prescribed limits as far as possible to ensure the quality and efficacy of the drug. Therefore, in the process of using Nadolol, special attention should be paid to the formation and control of Nadolol EP Impurity G. In any case of drug use, the recommendations of the pharmacist or doctor should be followed, and the instructions for use and dosage guidelines should be strictly followed to ensure safe and effective medication.
Nadolol EP Impurity G is often used in pharmacy for the detection and quantitative analysis of harmful impurities in Nadolol. It belongs to one of the degradation products of Nadolol, and its presence may affect the efficacy and stability of nadolol.
Regarding the preparation method, Nadolol EP Impurity G can be produced by a transformation reaction of bacteria or yeast. Specific synthetic methods can be achieved by chemical synthesis or biosynthesis.
As for safety information, since Nadolol EP Impurity G is a degradation product of Nadolol, its role and safety need further research and evaluation. In pharmaceutical preparations and treatments, the content of Nadolol EP Impurity G should be controlled within the prescribed limits as far as possible to ensure the quality and efficacy of the drug. Therefore, in the process of using Nadolol, special attention should be paid to the formation and control of Nadolol EP Impurity G. In any case of drug use, the recommendations of the pharmacist or doctor should be followed, and the instructions for use and dosage guidelines should be strictly followed to ensure safe and effective medication.
Last Update：2024-04-09 22:09:11
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Product Name: Nadolol EP Impurity G Visit Supplier Webpage Request for quotation
CAS: 33841-03-1
Tel: 18301782025
Email: 3008007409@qq.com
Mobile: 18021002903
QQ: 3008007409
Wechat: 18301782025
CAS: 33841-03-1
Tel: 18301782025
Email: 3008007409@qq.com
Mobile: 18021002903
QQ: 3008007409
Wechat: 18301782025
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