Oseltamivir Acid Methyl Ester

Product Name Oseltamivir Acid Methyl Ester
Alternate Names Oseltamivir Impurities, Impurities of Oseltamivir
CAT No. CS-T-38115
CAS No. 208720-71-2
Category Impurities
Stock IN-Stock
Mol. Wt. 298.38 g/mol
Mol. For. C₁₅H₂₆N₂O₄
Hazardous This is a Hazardous Compound
COA View Sample COA
MSDS View Sample MSDS
Parent API Oseltamivir
Purity 95%
Therapeutic Antiretroviral / Anti-HIV
Smileys CCC(CC)OC1C=C(CC(C1NC(=O)C)N)C(=O)OC
Canonical Smiles CCC(CC)OC1C=C(CC(C1NC(=O)C)N)C(=O)OC
InchIKey HQFJHRGEFIDLDI-BFHYXJOUSA-N
Inchl InChI=1S/C15H26N2O4/c1-5-11(6-2)21-13-8-10(15(19)20-4)7-12(16)14(13)17-9(3)18/h8,11-14H,5-7,16H2,1-4H3,(H,17,18)/t12-,13+,14+/m0/s1
IUPAC methyl (3R,4R,5S)-4-acetamido-5-amino-3-pentan-3-yloxycyclohexene-1-carboxylate
Controlled No
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Oseltamivir Acid Methyl Ester, also known as Tamiflu, is an antiviral medication used to treat and prevent influenza. It is a prodrug, meaning it is metabolized in the body to its active form, oseltamivir carboxylate, which inhibits the neuraminidase enzyme of the influenza virus. This inhibition prevents the release of new viral particles from infected cells and helps to reduce the severity and duration of flu symptoms. Oseltamivir Acid Methyl Ester is typically administered orally in capsule form and is most effective when taken within 48 hours of the onset of symptoms. It is recommended for use in patients who are at least 2 weeks old and can be used to treat and prevent both type A and type B strains of influenza. The chemical structure of Oseltamivir Acid Methyl Ester includes a carboxylic acid group and a methyl ester group. It has a molecular weight of 312.4 g/mol and a melting point of 130-131°C. The compound is not very soluble in water but is soluble in polar organic solvents such as methanol and ethanol. While Oseltamivir Acid Methyl Ester is generally well-tolerated, some common side effects include nausea, vomiting, and headache. It is important to note that this medication is not a substitute for annual influenza vaccination and should only be used under the guidance of a healthcare professional.

Related Compounds

Oseltamivir EP Imp R | Oseltamivir EP Imp U | Oseltamivir Impurity 31 | Oseltamivir Impurity 32 | Oseltamivir RSR Isomer | Oseltamivir EP Impurity E HCl | Oseltamivir Phosphate Impurity B | Oseltamivir Impurity 6 | Oseltamivir 5-Desamino 5-(2-Formyl 5-Hydroxymethylpyrrol-1-yl) | Rac- Oseltamivir hydroxymethyl furan | Oseltamivir Nitroso Impurity 2 | Oseltamivir Related Compound B | Oseltamivir Nitroso Impurity 1 | Oseltamivir Impurity 23 | Oseltamivir Impurity 8 | OSELTAMIVIR CITRIC ACID ADDUCT | Oseltamivir Impurity 24 | Rel 4-N-Desacetyl-5-N-acetyl Oseltamivir Acid | Oseltamivir-Glucose Adduct 1 | Oseltamivir RSS Isomer | Oseltamivir Acid Methyl Ester Phosphate Salt | Oseltamivir EP Impurity B | Oseltamivir Impurity 52 | Oseltamivir Impurity 25 | Ethyl (3S, 4S, 5S)-4-acetamido-5-amino-3-(1- ethyl propoxy) cyclohex-1-ene-1-carboxylate | Oseltamivir Related Compound A | Oseltamivir Impurity 7 | Oseltamivir Impurity 15 | Oseltamivir Impurity 14 | Oseltamivir Impurity 4 | Oseltamivir Pyrrole analog | Oseltamivir Impurity 19 | Oseltamivir Impurity 22 | ethyl 4-(pentan-3-yloxy)benzoate | Oseltamivir impurity A | Acetamido azidesulfonamide | Oseltamivir Impurity 28 | OSELTAMIVIR CITRIC ACID ADDUCT 2 | ent-Oseltamivir Phosphate | Oseltamivir Impurity 41 | Oseltamivir Impurity 27 | Oseltamivir RRR Isomer | OSELTAMIVIR CITRIC ACID ADDUCT II | Oseltamivir Impurity 48 | Oseltamivir Impurity 26 | N-Nitroso Oseltamivir impurity | Oseltamivir Impurity 15 | Oseltamivir glucose adduct-2 | Oseltamivir diallyl amine impurity |

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