Carfentanyl
| Carfentanyl | |
|---|---|
| Salts [] | |
|---|---|
| Carfentanyl citrate | |
| Molecular structure via molpic based on CDK |
| Physical properties [] | |
|---|---|
| Molecular mass | 394.5 g/mol [1] |
| Predicted LogP | 3.8 [1] |
| Structural Identifiers [] | |
|---|---|
| Molecular formula | C24H30N2O3 [1] |
| IUPAC name | methyl 1-(2-phenylethyl)-4-(N-propanoylanilino)piperidine-4-carboxylate [1] |
| SMILES | CCC(=O)N(C1=CC=CC=C1)C2(CCN(CC2)CCC3=CC=CC=C3)C(=O)OC [1] |
| InChI | InChI=1S/C24H30N2O3/c1-3-22(27)26(21-12-8-5-9-13-21)24(23(28)29-2)15-18-25(19-16-24)17-14-20-10-6-4-7-11-20/h4-13H,3,14-19H2,1-2H3 [1] |
| InChIKey | YDSDEBIZUNNPOB-UHFFFAOYSA-N [1] |
| Pharmacokinetics[] | |
|---|---|
| Elimination half-life | 7.7 hours |
Carfentanyl (also known as Carfentanil, Wildnil, Carfentanilum, carfentanilo, Carfentanila, 4-carbomethoxyfentanyl, (4-carbomethoxy fentanyl), Methyl 1-phenylethyl-4-(N-phenylpropionamido)isonipecotate, R 31833 or Chebi:61084) is a opioid substance of the phenethylpiperidine class.
Chemistry
Salts []
Carfentanyl is typically found in the form of its citrate salt.
Stereochemistry []
Carfentanyl is a achiral mixture.
Subjective effects []
Legal status []
- Australia: Carfentanyl is a S8 substance.
- Brazil: Carfentanyl is a F1 substance.
- Canada: Carfentanyl is a Schedule I substance.
- United Kingdom: Carfentanyl is a Class A substance.
- United States: Carfentanyl is a Schedule I under the "Controlled Substances Act (CSA)".
- Germany: Carfentanyl is a Anlage I substance.
See also []
External links []
References []
National Center for Biotechnology Information. PubChem Compound Summary for CID 62156, Carfentanyl. Accessed May 24, 2026. https://pubchem.ncbi.nlm.nih.gov/compound/62156
U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. Carfentanyl. UNII: LA9DTA2L8F. Global Substance Registration System. Accessed May 24, 2026. https://gsrs.ncats.nih.gov/ginas/app/beta/substances/LA9DTA2L8F