Candesartan Cilexetil EP Impurity I

Product Name Candesartan Cilexetil EP Impurity I
Alternate Names Candesartan Impurities, Impurities of Candesartan
CAT No. CS-O-07487
CAS No. 139481-69-9
Category Impurities
Stock IN-Stock
Mol. Wt. 454.48 g/mol
Mol. For. C₂₅H₂₂N₆O₃
Hazardous This is a Hazardous Compound
COA View Sample COA
MSDS View Sample MSDS
Parent API Candesartan
Purity >98%
Therapeutic Anti-Hypertensives
Smileys CCOC1=NC2=CC=CC(=C2N1CC3=CC=C(C=C3)C4=CC=CC=C4C5=NNN=N5)C(=O)OC
Canonical Smiles CCOC1=NC2=CC=CC(=C2N1CC3=CC=C(C=C3)C4=CC=CC=C4C5=NNN=N5)C(=O)OC
InchIKey RBPFEPGTRLLUKI-UHFFFAOYSA-N
Inchl InChI=1S/C25H22N6O3/c1-3-34-25-26-21-10-6-9-20(24(32)33-2)22(21)31(25)15-16-11-13-17(14-12-16)18-7-4-5-8-19(18)23-27-29-30-28-23/h4-14H,3,15H2,1-2H3,(H,27,28,29,30)
IUPAC methyl 2-ethoxy-3-[[4-[2-(2H-tetrazol-5-yl)phenyl]phenyl]methyl]benzimidazole-4-carboxylate
Controlled No
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Candesartan cilexetil EP impurity I is a chemical compound that is commonly used as a reference standard in pharmaceutical research and development. It is an impurity that is formed during the synthesis of candesartan cilexetil, which is an angiotensin II receptor blocker used in the treatment of hypertension and congestive heart failure. The chemical information of candesartan cilexetil EP impurity I is vital for drug manufacturers, as it helps to ensure the quality and safety of the final product. The impurity is typically analyzed using high-performance liquid chromatography (HPLC) and mass spectrometry (MS) techniques to determine its structure and purity. Furthermore, the usage of candesartan cilexetil EP impurity I is not limited to pharmaceutical research and development. It can also be used in the detection and quantification of candesartan cilexetil impurities in environmental and biological samples. In conclusion, candesartan cilexetil EP impurity I is an important reference standard in the pharmaceutical industry. Its chemical information and usage are critical in ensuring the quality and safety of candesartan cilexetil, as well as in detecting and quantifying impurities in various samples.

Related Compounds

Candesartan Cilexetil EP Impurity E | Candesartan Cilexetil N1-Trityl Methoxy Analog | Candesartan Cilexetil EP Impurity A | N-Trityl Candesartan Trityl Ester | Candesartan Methyl Ester N1-Trityl Analog | Candesartan Nitro impurity | Candesartan Bromo N2-Trityl Impurity | N2-Trityl Candesartan Cilexetil | N2-Trityl Candesartan | Candesartan N2-Ethyl Impurity | Candesartan Methyl Ester N1-Trityl Methoxy Analog | Candesartan Benzimidazole Methoxy Methyl Ester | Candesartan Cilexetil Desethyl N2-Trityl Analog | Candesartan Cilexetil EP Impurity F | Candesartan Bromo N1-Trityl Impurity | Candesartan Ethyl Ester Desethyl N1-Cilexetil Analog | Candesartan Cilexetil EP Impurity C | Candesartan Methyl Ester Desethyl Analog | Candesartan Cilexetil N2-Trityl Methoxy Analog | Candesartan Ethyl Ester N1-Cilexetil Analog | Candesartan N1-Trityl Impurity | Candesartan Impurity 2 | Candesartan Ethyl Ester Desethyl Analog | Candesartan Desethyl Analog | Candesartan Cilexetil Methoxy Analogue | N-Trityl Candesartan Methyl Ester Methoxy Analogue | Candesartan N1-Trityl Methoxy Analog | N-Nitroso Candesartan | Candesartan Cilexetil EP Impurity D | Candesartan Ethyl Ester Desethyl N2-Cilexetil Analog | Candesartan Ethyl Ester N2-Trityl Analog | Candesartan Cilexetil EP impurity B | Candesartan Cilexetil EP Impurity H | Candesartan N2-Trityl Methoxy Analog | Candesartan Ethyl Ester N2-Cilexetil Analog | Candesartan Cilexetil Desethyl N1-Trityl Analog |

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