Details
Stereochemistry | ACHIRAL |
Molecular Formula | 2C15H14N4O.H2O |
Molecular Weight | 550.611 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
O.CC1=CC=NC2=C1NC(=O)C3=C(N=CC=C3)N2C4CC4.CC5=CC=NC6=C5NC(=O)C7=C(N=CC=C7)N6C8CC8
InChI
InChIKey=KMTLSXAXTLQBKJ-UHFFFAOYSA-N
InChI=1S/2C15H14N4O.H2O/c2*1-9-6-8-17-14-12(9)18-15(20)11-3-2-7-16-13(11)19(14)10-4-5-10;/h2*2-3,6-8,10H,4-5H2,1H3,(H,18,20);1H2
Molecular Formula | H2O |
Molecular Weight | 18.0153 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Molecular Formula | C15H14N4O |
Molecular Weight | 266.2979 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Approval Year
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 21:18:13 UTC 2023
by
admin
on
Fri Dec 15 21:18:13 UTC 2023
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Record UNII |
B7XF2TD73C
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Record Status |
Validated (UNII)
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Record Version |
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-
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Common Name | English | ||
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Systematic Name | English |
Code System | Code | Type | Description | ||
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1460714
Created by
admin on Fri Dec 15 21:18:13 UTC 2023 , Edited by admin on Fri Dec 15 21:18:13 UTC 2023
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PRIMARY | |||
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DBSALT002723
Created by
admin on Fri Dec 15 21:18:13 UTC 2023 , Edited by admin on Fri Dec 15 21:18:13 UTC 2023
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PRIMARY | |||
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100000127941
Created by
admin on Fri Dec 15 21:18:13 UTC 2023 , Edited by admin on Fri Dec 15 21:18:13 UTC 2023
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PRIMARY | |||
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NEVIRAPINE HEMIHYDRATE
Created by
admin on Fri Dec 15 21:18:13 UTC 2023 , Edited by admin on Fri Dec 15 21:18:13 UTC 2023
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PRIMARY | Description: A white to almost white powder. Solubility: Practically insoluble in water, sparingly to slightly soluble in dichloromethane R, slightly soluble in methanol R. Category: Antiretroviral (Non-Nucleoside Reverse Transcriptase Inhibitor). Storage: Nevirapine should be kept in a well-closed container. Labelling: The designation on the container should state whether the substance is the hemihydrate or is in the anhydrous form. Definition: Nevirapine contains not less than 98.0% and not more than 102.0% of nevirapine (C15H14N4O), calculated with reference to the anhydrous substance. | ||
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9959243
Created by
admin on Fri Dec 15 21:18:13 UTC 2023 , Edited by admin on Fri Dec 15 21:18:13 UTC 2023
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PRIMARY | |||
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2462459
Created by
admin on Fri Dec 15 21:18:13 UTC 2023 , Edited by admin on Fri Dec 15 21:18:13 UTC 2023
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PRIMARY | |||
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DTXSID30176606
Created by
admin on Fri Dec 15 21:18:13 UTC 2023 , Edited by admin on Fri Dec 15 21:18:13 UTC 2023
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PRIMARY | |||
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B7XF2TD73C
Created by
admin on Fri Dec 15 21:18:13 UTC 2023 , Edited by admin on Fri Dec 15 21:18:13 UTC 2023
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PRIMARY | |||
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B7XF2TD73C
Created by
admin on Fri Dec 15 21:18:13 UTC 2023 , Edited by admin on Fri Dec 15 21:18:13 UTC 2023
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PRIMARY | |||
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SUB34149
Created by
admin on Fri Dec 15 21:18:13 UTC 2023 , Edited by admin on Fri Dec 15 21:18:13 UTC 2023
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PRIMARY | |||
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220988-26-1
Created by
admin on Fri Dec 15 21:18:13 UTC 2023 , Edited by admin on Fri Dec 15 21:18:13 UTC 2023
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PRIMARY |
Related Record | Type | Details | ||
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PARENT -> SALT/SOLVATE | |||
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BASIS OF STRENGTH->SUBSTANCE |
ASSAY (HPLC)
EP
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ANHYDROUS->SOLVATE |
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Related Record | Type | Details | ||
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IMPURITY -> PARENT |
Amount Not Specified
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||
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IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
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IMPURITY -> PARENT |
The test is not valid unless the resolution between nevirapine and nevirapine impurity B RS is not less than 5. In the chromatogram obtained with solution (3) the peak due to impurity (B) is eluted at a relative retention of about 0.7 with reference to nevirapine (retention time about 7.6 minutes).
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IMPURITY -> PARENT |
Amount Not Specified
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||
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IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
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IMPURITY -> PARENT |
UNSPECIFIED
EP
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IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
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Related Record | Type | Details | ||
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ACTIVE MOIETY |