Fentanyl
| Fentanyl | |
|---|---|
| Salts [] | |
|---|---|
| Fentanyl citrate | |
| Fentanyl hydrochloride | |
| Molecular structure via molpic based on CDK |
| Physical properties [] | |
|---|---|
| Molecular mass | 336.5 g/mol [1] |
| Appearance | Crystals [1] |
| Melting point | 83-84 [1] |
| Decomposition | When heated to decomposition it emits toxic fumes of /nitrogen oxides/. [1] |
| Solubility | 0.74mg/mL [1] |
| Predicted LogP | 4 [1] |
| Structural Identifiers [] | |
|---|---|
| Molecular formula | C22H28N2O [1] |
| IUPAC name | N-phenyl-N-[1-(2-phenylethyl)piperidin-4-yl]propanamide [1] |
| SMILES | CCC(=O)N(C1CCN(CC1)CCC2=CC=CC=C2)C3=CC=CC=C3 [1] |
| InChI | InChI=1S/C22H28N2O/c1-2-22(25)24(20-11-7-4-8-12-20)21-14-17-23(18-15-21)16-13-19-9-5-3-6-10-19/h3-12,21H,2,13-18H2,1H3 [1] |
| InChIKey | PJMPHNIQZUBGLI-UHFFFAOYSA-N [1] |
| Pharmacokinetics[] | |
|---|---|
| Elimination half-life | Intravaneous: 6 mins (T1/2 α) 1 hours (T1/2 β) 16 hours (T1/2 ɣ)Intranasal: 15 – 25 hoursTransdermal: 20 – 27 hoursSublingual: 5 – 13.5 hoursBuccal: 3.2 – 6.4 hours |
| Duration of action | Intravaneous: 30 – 60 minutes[5] |
Fentanyl (also known as Phentanyl, Fentanil, Fentanest, Duragesic, Sublimase, Fentanylum, Durogesic, Fentanila, Matrifen or Duragesic-100) is a opioid substance of the phenethylpiperidine class.
Chemistry
Salts []
Fentanyl is typically found in the form of its citrate and hydrochloride salts.
Stereochemistry []
Fentanyl is a achiral mixture.
Reagents
There are currently 3 reagent-interactions on DrugsPRO
| Reagent | Color change |
|---|---|
| Marquis | |
| Mecke | |
| Mandelin |
Pharmacology
ATC Classification
In the nervous system (N) fentanyl acts In the nervous system (N) fentanyl acts as a analgesic (N02), anesthetic (N01), anesthetics, general (N01A), fentanyl (N01AH01), fentanyl (N02AB03), opioid anesthetic (N01AH), opioid (N02A) and phenylpiperidine derivative (N02AB).[1]Interactions []
| CYP3A4 | induction / inhibition |
|---|
Subjective effects []
| bonzi / Fentanyl [] | |
|---|---|
| 0xea / Fentanyl [] | |
|---|---|
Routes:
| |
Experience reports
Erowid
There are currently 26 experience reports involving fentanyl on Erowid: []
- "Legal experiences with Fentanyl" by Soren
- "Various Methods of Ingestion" by Cactushead
- "Lollipop Flop" by WeaponX
- "Smoke Smoke Yes" by W
- "Chillin' for a While" by Paul
- "Lollipops vs. Patches" by ML
- "Care and Comfort" by Dozer
- "On a Cigarette" by rusty s.
- "Licit Experiences" by murky303
- "Why Fight?" by May
- "Pleasurable Poppies" by OxyFace
- "Got Sucked in and Couldn't Stop" by Junkie Scientist
- "A Shortcut to Death" by Bran Man
- "Baking Soda Method" by SpinePAIN E101
- "Good Effin Times" by Sm0ke42o
- "Long Term Medical Use, Withdrawal, Overdosing" by Namaste
- "Lucid Dreaming" by Legend
- "One Single Drop" by Eltigre
- "I Need to Be Careful With This Substance" by Noble Experimenter
- "On the Good Ship Lollipop" by Matt Himself
- "I Decided to Detox Myself" by Selfguineapig
- "A Day of Bliss, a Night of Nirvana" by Zilla
- "Unbelievable Wave After Wave of Soothing Warmth" by An Evilbeast
- "Euphoric Vomiting" by phallout
- "Relaxation on a Blotter" by Psych0naut
- "A Wonderful Three Days" by cs
Legal status []
- Australia: Fentanyl is a S8 substance.
- Brazil: Fentanyl is a Class A1 substance.
- Canada: Fentanyl is a Schedule I substance.
- Germany: Fentanyl is a Anlage III substance.
- New Zealand: Fentanyl is a Class B substance.
- United Kingdom: Fentanyl is a Class A substance.
- United States: Fentanyl is a Controlled Substances Act#Schedule II|Schedule II substance.
- European Union: Fentanyl is a prescription only substance.[3][4]
- United Nations: Fentanyl is a Schedule I narcotic under the "Single Convention on Narcotic Drugs 1961".
See also []
- Opioid
- Substituted phenethylpiperidines (fentalogs)
External links []
References []
National Center for Biotechnology Information. PubChem Compound Summary for CID 3345, Fentanyl. Accessed May 24, 2026. https://pubchem.ncbi.nlm.nih.gov/compound/3345
U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. Fentanyl. UNII: UF599785JZ. Global Substance Registration System. Accessed May 24, 2026. https://gsrs.ncats.nih.gov/ginas/app/beta/substances/UF599785JZ
Instanyl EPAR. July 20, 2009. Accessed May 24, 2026. https://www.ema.europa.eu/en/medicines/human/EPAR/instanyl
Effentora EPAR. April 4, 2008. Accessed May 24, 2026. https://www.ema.europa.eu/en/medicines/human/EPAR/effentora
Guideline for administration of fentanyl for pain relief in labour. RCP. Accessed May 24, 2026. http://rcp.nshealth.ca/sites/default/files/clinical-practice-guidelines/fentanyl.pdf