Candesartan Cilexetil EP impurity B
| Product Name | Candesartan Cilexetil EP impurity B |
|---|---|
| Alternate Names | Candesartan Impurities, Impurities of Candesartan |
| CAT No. | CS-O-11779 |
| CAS No. | 869631-11-8 |
| Category | Impurities |
| Stock | IN-Stock |
| Mol. Wt. | 582.61 g/mol |
| Mol. For. | C₃₁H₃₀N₆O₆ |
| Hazardous | This is a Hazardous Compound |
| COA | View Sample COA |
| MSDS | View Sample MSDS |
| Parent API | Candesartan |
| Purity | 95% |
| Therapeutic | Anti-Hypertensives |
| Smileys | O=C(N1)N(C(C1=CC=C2)=C2C(OC(C)OC(OC3CCCCC3)=O)=O)CC4=CC=C(C5=C(C6=NN=NN6)C=CC=C5)C=C4 |
| Controlled | No |
| Shipping | Free for purchase above 1000$ |
| Delivery | In-Stock, products will be dispatched within 24 hours via FedEx for USA, Europe, and other countries. |
| Return | Returns/replacement accepted if you are not satisfied with the quality of the product, (please send us an email with the reason/issues which are facing, within 15 days, after receipt of the product). |
| Ordering | Place your order online or by email sales@clearsynth.com |
Candesartan Cilexetil EP impurity B, also known as (2-[(2'-carboxybiphenyl-4-yl)methyl]-1H-benzimidazol-6-yl)acetic acid, is a chemical impurity that is commonly found in pharmaceutical products that contain Candesartan Cilexetil. This impurity can be formed during the synthesis of Candesartan Cilexetil and can be present in small amounts in the final product.
Candesartan Cilexetil EP impurity B is a white or off-white crystalline powder that is sparingly soluble in water and soluble in methanol and acetonitrile. It has a molecular weight of 361.4 g/mol and a melting point range of 235-240°C.
The usage of Candesartan Cilexetil EP impurity B is not recommended in pharmaceutical formulations as it is considered an impurity. However, it is important to monitor the levels of this impurity in Candesartan Cilexetil formulations as it can affect the purity and quality of the final product. Regulatory agencies such as the United States Pharmacopeia (USP) have set limits on impurities in pharmaceutical products, including Candesartan Cilexetil, to ensure the safety and efficacy of the product.
In conclusion, Candesartan Cilexetil EP impurity B is an impurity that can be present in pharmaceutical products containing Candesartan Cilexetil. It is important to monitor and control the levels of this impurity to ensure the quality and safety of the final product.
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Related Compounds
Candesartan Ethyl Ester Desethyl Analog | Candesartan N2-Ethyl Impurity | Candesartan Ethyl Ester Desethyl N2-Cilexetil Analog | Candesartan Cilexetil EP Impurity F | N-Trityl Candesartan Trityl Ester | Candesartan N2-Trityl Methoxy Analog | Candesartan Ethyl Ester N2-Cilexetil Analog | Candesartan Benzimidazole Methoxy Methyl Ester | Candesartan Cilexetil EP Impurity D | Candesartan N1-Trityl Methoxy Analog | Candesartan Bromo N1-Trityl Impurity | Candesartan Cilexetil N1-Trityl Methoxy Analog | Candesartan Impurity 2 | Candesartan Ethyl Ester N2-Trityl Analog | Candesartan Ethyl Ester N1-Cilexetil Analog | N-Nitroso Candesartan | Candesartan Ethyl Ester Desethyl N1-Cilexetil Analog | Candesartan Cilexetil EP Impurity I | Candesartan Cilexetil EP Impurity A | Candesartan Methyl Ester N1-Trityl Analog | Candesartan Desethyl Analog | Candesartan N1-Trityl Impurity | Candesartan Cilexetil Methoxy Analogue | N-Trityl Candesartan Methyl Ester Methoxy Analogue | Candesartan Methyl Ester Desethyl Analog | N2-Trityl Candesartan | Candesartan Cilexetil EP Impurity C | Candesartan Cilexetil Desethyl N2-Trityl Analog | Candesartan Bromo N2-Trityl Impurity | N2-Trityl Candesartan Cilexetil | Candesartan Methyl Ester N1-Trityl Methoxy Analog | Candesartan Cilexetil EP Impurity E | Candesartan Cilexetil Desethyl N1-Trityl Analog | Candesartan Cilexetil N2-Trityl Methoxy Analog | Candesartan Nitro impurity | Candesartan Cilexetil EP Impurity H |