Bupropion
Bupropion | |
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Molecular structure via molpic | |
Molecular formula | C13H18ClNO |
Molecular mass | 239.74 g/mol |
Appearance | Pale yellow oil |
Melting point | 233-234 °C |
Boiling point | 52 °C |
Solubility | Very hygroscopic and susceptible to decomposition |
Chirality | racemic |
Identifiers [] | |
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IUPAC name | 2-(tert-butylamino)-1-(3-chlorophenyl)propan-1-one |
Cannonical SMILES | CC(C(=O)C1=CC(=CC=C1)Cl)NC(C)(C)C |
InChI | InChI=1S/C13H18ClNO/c1-9(15-13(2,3)4)12(16)10-6-5-7-11(14)8-10/h5-9,15H,1-4H3 |
InChIKey | SNPPWIUOZRMYNY-UHFFFAOYSA-N |
Dosing |
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Insufflated [] | |
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Threshold | 1 - 26.250000000000007 mg |
Light | 26.250000000000007 - 75 mg |
Common | 75 - 150 mg |
Strong | 150 mg |
Heavy | 150 - 222.49999999999997 mg |
Oral [] | |
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Threshold | 1 - 82.50000000000001 tablet |
Light | 82.50000000000001 - 150 tablet |
Common | 150 - 300 tablet |
Strong | 300 - 450 tablet |
Heavy | 450 - 600 tablet |
Statistically derived dosages by Sernyl |
Bupropion (also known as Amfebutamone, Amfebutamon, Wellbutrin, 34841-39-9, amfebutamonum, Amfebutamona, Elontril, (+-)-Bupropion, Wellbatrin or Amfebutamonum [INN-Latin]) is a depressant substance of the methcathinone class.
Chemistry
Bupropion is typically prepared in the form of its amine salts hydrobromide, hydrochloride and maleate.
Bupropion is a racemic mixture of two optical stereoisomers.