AnodyneWiki

Fentanyl

Fentanyl
Fentanyl
Salts
[]
Fentanyl citrate
Generated by the Chemistry Development Kit (http://github.com/cdk)
Fentanyl hydrochloride
Generated by the Chemistry Development Kit (http://github.com/cdk)
Molecular structure via molpic based on CDK
Rotamer
[]
Conformer structure via 3Dmol.js
Enable javascript to view conformer structure via 3Dmol.js
Physical properties
[]
336.5 g/mol [1]
AppearanceCrystals [1]
Melting point83-84 [1]
DecompositionWhen heated to decomposition it emits toxic fumes of /nitrogen oxides/. [1]
Solubility0.74mg/mL [1]
[1]
Structural Identifiers
[]
C22H28N2O [1]
N-phenyl-N-[1-(2-phenylethyl)piperidin-4-yl]propanamide [1]
CCC(=O)N(C1CCN(CC1)CCC2=CC=CC=C2)C3=CC=CC=C3 [1]
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]
InChIKeyPJMPHNIQZUBGLI-UHFFFAOYSA-N [1]
Pharmacokinetics[]
Elimination half-lifeIntravaneous: 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 actionIntravaneous: 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.

 []

Fentanyl is a achiral mixture.

There are currently 3 reagent-interactions on

ReagentColor change
Marquis
Mecke
Mandelin

Pharmacology

In the () fentanyl acts In the () fentanyl acts as a analgesic (), anesthetic (), anesthetics, general (), fentanyl (), fentanyl (), opioid anesthetic (), opioid () and phenylpiperidine derivative ().[1]

Interactions []

induction / inhibition
bonzi / Fentanyl []
0xea / Fentanyl []
Routes:
  • Intravenous (15 - 375mcg)
    Onset: 5 - 10 s
    Comeup: 30 s
    Duration: 60 - 120 m
  • Subcutaneous (50 - 250mcg)
    Onset: 7 - 8 m
    Comeup: 10 m
    Duration: 60 - 120 m
  • Vaporized (250 - 1000mcg)
    Onset: 5 - 10 s
    Comeup: 30 s
    Duration: ?
Salts:
  • D-Tartrate
  • Citrate
Source:
  • Fentanyl: DNM Germany
Indication:Effects:After Effects:Notes:
  • intravenously using volumetric liquid dosing only. eyeballing or measuring out single injections would likely be deadly.
  • intravenous injection of unsanitary solution repeatedly lead to the development of soars all around my body(unrelated to venipuncture)

Experience reports

 []

  • 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 []

External links []

References []

  1. National Center for Biotechnology Information. PubChem Compound Summary for CID 3345, Fentanyl. Accessed May 24, 2026. https://pubchem.ncbi.nlm.nih.gov/compound/3345

  2. 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

  3. Instanyl EPAR. July 20, 2009. Accessed May 24, 2026. https://www.ema.europa.eu/en/medicines/human/EPAR/instanyl

  4. Effentora EPAR. April 4, 2008. Accessed May 24, 2026. https://www.ema.europa.eu/en/medicines/human/EPAR/effentora

  5. 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