Mefentanyl
| 3-MF | |
|---|---|
| Molecular structure via molpic based on CDK |
| Physical properties [] | |
|---|---|
| Molecular mass | 350.5 g/mol [1] |
| Melting point | Crystals from isopropanol. MP: 272-8-273.6 °C /3-Methylfentanyl hydrochloride/ [1] |
| Predicted LogP | 4.5 [1] |
| Structural Identifiers [] | |
|---|---|
| Molecular formula | C23H30N2O [1] |
| IUPAC name | N-[3-methyl-1-(2-phenylethyl)piperidin-4-yl]-N-phenylpropanamide [1] |
| SMILES | CCC(=O)N(C1CCN(CC1C)CCC2=CC=CC=C2)C3=CC=CC=C3 [1] |
| InChI | InChI=1S/C23H30N2O/c1-3-23(26)25(21-12-8-5-9-13-21)22-15-17-24(18-19(22)2)16-14-20-10-6-4-7-11-20/h4-13,19,22H,3,14-18H2,1-2H3 [1] |
| InChIKey | MLQRZXNZHAOCHQ-UHFFFAOYSA-N [1] |
Mefentanyl (also known as 3-Methylfentanyl, 3-Methylfentanil, DEA No. 9813, N-(3-Methyl-1-(2-phenylethyl)-4-piperidinyl)-N-phenylpropanamide, Chebi:61092, Propanamide, N-(3-methyl-1-(2-phenylethyl)-4-piperidinyl)-N-phenyl-, QVU94XE61A, 3-methyl-fentanyl, N-(3-methyl-1-(2-phenylethyl)piperidin-4-yl)-N-phenylpropanamide or F-7209) is a opioid substance of the phenethylpiperidine class.
Chemistry
Stereochemistry []
Mefentanyl is a racemic mixture of the diastereomers.
| Stereoisomerism |
|---|
| Stereoisomer enumberation with rdkit |
Subjective effects []
Legal status []
- Australia: Mefentanyl is a Unscheduled substance.
- Brazil: Mefentanyl is a F1 substance.
- Canada: Mefentanyl is a Schedule I substance.
- New Zealand: Mefentanyl is a Unscheduled substance.
- United Kingdom: Mefentanyl is a Class A substance.
- Germany: Mefentanyl is a Anlage I substance.
- United States: Mefentanyl is a Schedule I under the "Controlled Substances Act (CSA)".
- United Nations: Mefentanyl is a Unscheduled substance.
See also []
- Opioid
- Substituted phenethylpiperidines (fentalogs)
External links []
References []
National Center for Biotechnology Information. PubChem Compound Summary for CID 61996, Mefentanyl. Accessed May 25, 2026. https://pubchem.ncbi.nlm.nih.gov/compound/61996