Olmesartan Medoxomil EP Impurity D

Product Name Olmesartan Medoxomil EP Impurity D
Alternate Names Olmesartan Impurities, Impurities of Olmesartan
CAT No. CS-T-62583
CAS No. 1020157-01-0
Category Impurities
Stock IN-Stock
Mol. Wt. 800.90 g/mol
Mol. For. C₄₈H₄₄N₆O₆
Hazardous This is a Hazardous Compound
COA View Sample COA
MSDS View Sample MSDS
Parent API Olmesartan
Purity Not less than 95 %
Therapeutic Anti-Hypertensives
Smileys O=C(OCC(OC1=O)=C(O1)C)C2=C(C(C)(O)C)N=C(CCC)N2CC3=CC=C(C=C3)C4=C(C=CC=C4)C5=NN(N=N5)C(C6=CC=CC=C6)(C7=CC=CC=C7)C8=CC=CC=C8
Canonical Smiles CCCC1=NC(=C(N1CC2=CC=C(C=C2)C3=CC=CC=C3C4=NN(N=N4)C(C5=CC=CC=C5)(C6=CC=CC=C6)C7=CC=CC=C7)C(=O)OCC8=C(OC(=O)O8)C)C(C)(C)O
InchIKey KKYFOXOGKNDKRS-UHFFFAOYSA-N
Inchl InChI=1S/C48H44N6O6/c1-5-17-41-49-43(47(3,4)57)42(45(55)58-31-40-32(2)59-46(56)60-40)53(41)30-33-26-28-34(29-27-33)38-24-15-16-25-39(38)44-50-52-54(51-44)48(35-18-9-6-10-19-35,36-20-11-7-12-21-36)37-22-13-8-14-23-37/h6-16,18-29,57H,5,17,30-31H2,1-4H3
IUPAC (5-methyl-2-oxo-1,3-dioxol-4-yl)methyl 5-(2-hydroxypropan-2-yl)-2-propyl-3-[[4-[2-(2-trityltetrazol-5-yl)phenyl]phenyl]methyl]imidazole-4-carboxylate
Controlled No
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Olmesartan Medoxomil EP Impurity D is a chemical compound that is used in the production of Olmesartan Medoxomil, a medication used to treat hypertension. It is classified as an impurity, which means that it is an unintended byproduct of the manufacturing process. Impurities can sometimes be harmful or cause unwanted side effects, which is why they are closely monitored during drug production. Chemically, Olmesartan Medoxomil EP Impurity D is a derivative of Olmesartan Medoxomil, which is an angiotensin II receptor antagonist. This means that it works by blocking the action of a hormone called angiotensin II, which is responsible for narrowing blood vessels and increasing blood pressure. Olmesartan Medoxomil EP Impurity D is not an active ingredient in itself, but it can affect the purity and potency of Olmesartan Medoxomil. To ensure the safety and effectiveness of Olmesartan Medoxomil, it is important to control the levels of Olmesartan Medoxomil EP Impurity D during manufacturing. This is done through various quality control measures, such as testing raw materials and monitoring the production process. By minimizing impurities like Olmesartan Medoxomil EP Impurity D, pharmaceutical companies can ensure that patients receive a safe and effective medication.

Related Compounds

Olmesartan Medoxomil Impurity G | Methoxy impurity of Trityl Olmesartan Medoxomil | Olmesartan Medoxomil N-Oxide | Olmesartan Medoxomil Impurity 1 | Olmesartan Dimer Ester Impurity 2 | N-alkylated Olmesartan | azide impurity of Olmesartan | Olmesartan Dimer Ester Impurity 1 | Olmesartan Medoxomil EP Impurity C (1-methylethyl) | Olmesartan Methyl Ketone | Olmesartan medoxomil methyl ether | ethyl 5-(prop-1-en-2-yl)-2-propyl-1H-imidazole-4-carboxylate | Olmesartan Dimer | Olmesartan Methyl Ester | Butyl analogue of trityl Olmesartan medoxomil | N-Nitroso Olmesartan | Olmesartan Medoxomil Ester Dimer | N-Nitroso Olmesartan Intermediate 1 | Olmesartan Impurity 23 | N-Trityl Olmesartan Ethyl Ester | Olmesartan Medoxomil EP Impurity B | Nitroso Olmesartan | Olmesartan Ethyl Ester | Olmesartan Anhydro Acid Ethyl Ester | Ethyl analogue of trityl Olmesartan medoxomil | Olmesartan Nitroso Impurity 1 | Dehydro Olmesartan | Olmesartan EP Impurity C | Olmesartan Impurity 34 | Olmesartan Medoxomil Impurity E | N-1 Trityl Ethyl Methyl Olmesartan | O-Methyl Ether Olmesartan Acid | N1-Nitrosamine Olmesartan Medoxomil | n-Butyl Olmesartan Medoxomil | Ethyl Olmesartan Medoxomil | ethyl 5-acetyl-2-propyl-1-((2'-(1-trityl-1H-tetrazol-5-yl)-[1,1'-biphenyl]-4-yl)methyl)-1H-imidazole | Olmesartan Dimer Impurity | Olmesartan N1-Trityl Impurity | Olmesartan trityl alcohol | Dehydro N2-Triphenylmethyl Olmesartan | Olmesartan N2-Trityl Impurity | Dehydro Olmesartan-2-trityl Medoxomil |

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