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

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