Fentanyl hydrochlorideProduct ingredient for Fentanyl

Name
Fentanyl hydrochloride
Drug Entry
Fentanyl

Fentanyl, a potent opioid agonist, was developed in the 1950s to fill a need for strong and rapid analgesia.8 Because of these characteristics, fentanyl is commonly used to treat chronic cancer pain or in anesthesia.Label,15,16,17,18,19,20,21 Fentanyl is related to other opioids like morphine and oxycodone.

Fentanyl's high potency has also made it a common adulterant in illicit drugs, especially heroin.8 In 2017, 47600 overdose deaths in the United States involved some opioid (over 2/3 of all overdose deaths).22 Opioid overdoses kill an average of 11 Canadians daily.23

Fentanyl was FDA approved in 1968.Label,15,16,17,18,19,20,21

Accession Number
DBSALT001226
Structure
Synonyms
Fentanyl HCl
UNII
59H156XY46
CAS Number
1443-54-5
Weight
Average: 372.94
Monoisotopic: 372.1968413
Chemical Formula
C22H29ClN2O
InChI Key
LHCBOXPPRUIAQT-UHFFFAOYSA-N
InChI
InChI=1S/C22H28N2O.ClH/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;1H
IUPAC Name
N-phenyl-N-[1-(2-phenylethyl)piperidin-4-yl]propanamide hydrochloride
SMILES
Cl.CCC(=O)N(C1CCN(CCC2=CC=CC=C2)CC1)C1=CC=CC=C1
ChemSpider
75734
ChEMBL
CHEMBL1201159
Predicted Properties
PropertyValueSource
Water Solubility0.024 mg/mLALOGPS
logP4.12ALOGPS
logP3.82Chemaxon
logS-4.2ALOGPS
pKa (Strongest Basic)8.77Chemaxon
Physiological Charge1Chemaxon
Hydrogen Acceptor Count2Chemaxon
Hydrogen Donor Count0Chemaxon
Polar Surface Area23.55 Å2Chemaxon
Rotatable Bond Count6Chemaxon
Refractivity103.48 m3·mol-1Chemaxon
Polarizability38.68 Å3Chemaxon
Number of Rings3Chemaxon
Bioavailability1Chemaxon
Rule of FiveYesChemaxon
Ghose FilterYesChemaxon
Veber's RuleYesChemaxon
MDDR-like RuleYesChemaxon