Sibutramine | |
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Salts [] | |
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Sibutramine hydrochloride | |
Sibutramine mesylate | |
Sibutramine maleate | |
Molecular structure via molpic | |
Conformer structure via 3Dmol.js | |
Molecular formula | C17H26ClN[1] |
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Molecular mass | 279.8 g/mol[1] |
Predicted LogP | 5.4[1] |
Melting point | 191-192 °C[1] |
Decomposition | When heated to decomposition, material emits very toxic fumes of /hydrogen chloride/ and /nitrogen oxides/. Emits toxic fumes[1] |
Solubility | 9.40e-04 g/L[1] |
Chirality | racemic[2] |
Identifiers [] | |
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IUPAC name | 1-[1-(4-chlorophenyl)cyclobutyl]-N,N,3-trimethylbutan-1-amine[1] |
SMILES | CC(C)CC(C1(CCC1)C2=CC=C(C=C2)Cl)N(C)C[1] |
InChI | InChI=1S/C17H26ClN/c1-13(2)12-16(19(3)4)17(10-5-11-17)14-6-8-15(18)9-7-14/h6-9,13,16H,5,10-12H2,1-4H3[1] |
InChIKey | UNAANXDKBXWMLN-UHFFFAOYSA-N[1] |
Dosing | |
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Elimination half-life | 1 hour (sibutramine), 14 hours (M1) & 16 hours (M2) |
Sibutramine
(Redirected from (+)-Sibutramine)
Sibutramine (also known as Medaria, Butramin, Sibutramina, (+/-)-Sibutramine, racemic sibutramine, Cf-alli, Sibutraminum, Smr000238156, S-Sibutramine or BTS 54 524) is a stimulant substance of the amphetamine class.
Chemistry
Sibutramine is typically found in the form of its hydrochloride, mesylate and maleate salts.
Stereochemistry
(RS)-Sibutramine is a racemic mixture of the optical stereoisomers:
Stereoisomers [] |
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Legal status
- Brazil: Sibutramine is a B2 substance.
- United States: Sibutramine is a Schedule IV substance.
See also
External links
- Sibutramine (Wikipedia)
- Sibutramine / (+)-Sibutramine / (-)-Sibutramine (Wikidata)
- Sibutramine (DrugBank)
- Sibutramine / (+)-Sibutramine / (-)-Sibutramine (PubChem)
- Sibutramine / (-)-Sibutramine (ChEMBL)
- Sibutramine (ChEBI)
- Sibutramine / (+)-Sibutramine / (-)-Sibutramine (Common Chemistry)
- Sibutramine (HMDB)
- Sibutramine (KEGG)
- Sibutramine / (+)-Sibutramine / (-)-Sibutramine (UNII)
- Sibutramine / (+)-Sibutramine / (-)-Sibutramine (EPA DSSTox)