Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C16H28N2O4.H3O4P |
Molecular Weight | 410.3997 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 3 / 3 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
OP(O)(O)=O.CCOC(=O)C1=C[C@@H](OC(CC)CC)[C@H](NC(C)=O)[C@@H](N)C1
InChI
InChIKey=PGZUMBJQJWIWGJ-ONAKXNSWSA-N
InChI=1S/C16H28N2O4.H3O4P/c1-5-12(6-2)22-14-9-11(16(20)21-7-3)8-13(17)15(14)18-10(4)19;1-5(2,3)4/h9,12-15H,5-8,17H2,1-4H3,(H,18,19);(H3,1,2,3,4)/t13-,14+,15+;/m0./s1
Molecular Formula | H3O4P |
Molecular Weight | 97.9952 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Molecular Formula | C16H28N2O4 |
Molecular Weight | 312.4045 |
Charge | 0 |
Count |
|
Stereochemistry | ABSOLUTE |
Additional Stereochemistry | No |
Defined Stereocenters | 3 / 3 |
E/Z Centers | 0 |
Optical Activity | UNSPECIFIED |
Approval Year
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 16:25:33 UTC 2023
by
admin
on
Fri Dec 15 16:25:33 UTC 2023
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Record UNII |
4A3O49NGEZ
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Record Status |
Validated (UNII)
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Record Version |
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-
Download
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Classification Tree | Code System | Code | ||
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NCI_THESAURUS |
C281
Created by
admin on Fri Dec 15 16:25:34 UTC 2023 , Edited by admin on Fri Dec 15 16:25:34 UTC 2023
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Code System | Code | Type | Description | ||
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DTXSID0044230
Created by
admin on Fri Dec 15 16:25:34 UTC 2023 , Edited by admin on Fri Dec 15 16:25:34 UTC 2023
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PRIMARY | |||
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SUB12544MIG
Created by
admin on Fri Dec 15 16:25:34 UTC 2023 , Edited by admin on Fri Dec 15 16:25:34 UTC 2023
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PRIMARY | |||
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m8256
Created by
admin on Fri Dec 15 16:25:34 UTC 2023 , Edited by admin on Fri Dec 15 16:25:34 UTC 2023
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PRIMARY | Merck Index | ||
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KK-62
Created by
admin on Fri Dec 15 16:25:34 UTC 2023 , Edited by admin on Fri Dec 15 16:25:34 UTC 2023
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PRIMARY | |||
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C29305
Created by
admin on Fri Dec 15 16:25:34 UTC 2023 , Edited by admin on Fri Dec 15 16:25:34 UTC 2023
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PRIMARY | |||
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1479304
Created by
admin on Fri Dec 15 16:25:34 UTC 2023 , Edited by admin on Fri Dec 15 16:25:34 UTC 2023
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PRIMARY | |||
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CHEMBL1229
Created by
admin on Fri Dec 15 16:25:34 UTC 2023 , Edited by admin on Fri Dec 15 16:25:34 UTC 2023
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PRIMARY | |||
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4A3O49NGEZ
Created by
admin on Fri Dec 15 16:25:34 UTC 2023 , Edited by admin on Fri Dec 15 16:25:34 UTC 2023
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PRIMARY | |||
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7799
Created by
admin on Fri Dec 15 16:25:34 UTC 2023 , Edited by admin on Fri Dec 15 16:25:34 UTC 2023
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PRIMARY | |||
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78000
Created by
admin on Fri Dec 15 16:25:34 UTC 2023 , Edited by admin on Fri Dec 15 16:25:34 UTC 2023
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PRIMARY | |||
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100000091466
Created by
admin on Fri Dec 15 16:25:34 UTC 2023 , Edited by admin on Fri Dec 15 16:25:34 UTC 2023
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PRIMARY | |||
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4A3O49NGEZ
Created by
admin on Fri Dec 15 16:25:34 UTC 2023 , Edited by admin on Fri Dec 15 16:25:34 UTC 2023
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PRIMARY | |||
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204255-11-8
Created by
admin on Fri Dec 15 16:25:34 UTC 2023 , Edited by admin on Fri Dec 15 16:25:34 UTC 2023
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PRIMARY | |||
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OSELTAMIVIR PHOSPHATE
Created by
admin on Fri Dec 15 16:25:34 UTC 2023 , Edited by admin on Fri Dec 15 16:25:34 UTC 2023
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PRIMARY | Description: A white to off-white powder. Solubility: Freely soluble in water and in methanol. Category: Antiviral. Storage: Oseltamivir phosphate should be kept in a well-closed container, protected from light. Additional information: Oseltamivir phosphate may show polymorphism. Definition: Oseltamivir phosphate contains not less than 97.5% and not more than 102.0% of oseltamivir phosphate (C16H28N2O4, H3PO4) using Assay method A, and not less than 98.5% and not more than 101.0% of oseltamivir phosphate (C16H28N2O4, H3PO4) using Assay method B, both calculated with reference to the anhydrous substance. | ||
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259275
Created by
admin on Fri Dec 15 16:25:34 UTC 2023 , Edited by admin on Fri Dec 15 16:25:34 UTC 2023
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PRIMARY | RxNorm | ||
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7798
Created by
admin on Fri Dec 15 16:25:34 UTC 2023 , Edited by admin on Fri Dec 15 16:25:34 UTC 2023
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DB00198
Created by
admin on Fri Dec 15 16:25:34 UTC 2023 , Edited by admin on Fri Dec 15 16:25:34 UTC 2023
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PRIMARY |
Related Record | Type | Details | ||
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BASIS OF STRENGTH->SUBSTANCE |
ASSAY (HPLC)
USP
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BASIS OF STRENGTH->SUBSTANCE |
ASSAY (HPLC)
EP
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PARENT -> SALT/SOLVATE |
Related Record | Type | Details | ||
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IMPURITY -> PARENT |
Use the chromatogram obtained with solution (4) to identify the peaks due to impurities A, B, C and D. The impurity peaks are eluted at the following relative retention with reference to oseltamivir phosphate (retention time about 19 minutes): impurity A about 0.16. The test is not valid unless the resolution between the peaks due to impurities A and B and that between the peaks due to impurities C and D is at least 1.3.
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IMPURITY -> PARENT |
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IMPURITY -> PARENT |
UNSPECIFIED
EP
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IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (HPLC/UV)
USP
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IMPURITY -> PARENT |
UNSPECIFIED
EP
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IMPURITY -> PARENT |
UNSPECIFIED
EP
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IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
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IMPURITY -> PARENT |
Use the chromatogram obtained with solution (4) to identify the peaks due to impurities A, B, C and D. The impurity peaks are eluted at the following relative retention with reference to oseltamivir phosphate (retention time about 19 minutes): impurity C about 0.51. The test is not valid unless the resolution between the peaks due to impurities A and B and that between the peaks due to impurities C and D is at least 1.3.
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IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
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IMPURITY -> PARENT |
Use the chromatogram obtained with solution (4) to identify the peaks due to impurities A, B, C and D. The impurity peaks are eluted at the following relative retention with reference to oseltamivir phosphate (retention time about 19 minutes): impurity B about 0.17. The test is not valid unless the resolution between the peaks due to impurities A and B and that between the peaks due to impurities C and D is at least 1.3.
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IMPURITY -> PARENT |
UNSPECIFIED
EP
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IMPURITY -> PARENT |
Use the chromatogram obtained with solution (4) to identify the peaks due to impurities A, B, C and D. The impurity peaks are eluted at the following relative retention with reference to oseltamivir phosphate (retention time about 19 minutes): impurity D about 0.55. The test is not valid unless the resolution between the peaks due to impurities A and B and that between the peaks due to impurities C and D is at least 1.3.
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IMPURITY -> PARENT |
UNSPECIFIED
EP
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IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (HPLC/UV)
USP
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IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (GC)
EP
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Related Record | Type | Details | ||
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ACTIVE MOIETY |