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Details

Stereochemistry ACHIRAL
Molecular Formula C21H26N2O
Molecular Weight 322.4439
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of BENZYLFENTANYL

SMILES

CCC(=O)N(C1CCN(CC2=CC=CC=C2)CC1)C3=CC=CC=C3

InChI

InChIKey=POQDXIFVWVZVML-UHFFFAOYSA-N
InChI=1S/C21H26N2O/c1-2-21(24)23(19-11-7-4-8-12-19)20-13-15-22(16-14-20)17-18-9-5-3-6-10-18/h3-12,20H,2,13-17H2,1H3

HIDE SMILES / InChI

Approval Year

Unknown
149124
Targets

Targets

Primary TargetPharmacologyConditionPotency
Mu-type opioid receptor
61
Target ID: P35372|||G8XRH8|||Q5TDA1|||Q9UN57
Gene ID: 4988.0
Gene Symbol: OPRM1
Target Organism: Homo sapiens (Human)
Binding Agent
1076
 213.0 nM [Ki]
Patents

Patents

20060252797
5
WO2014153099A2
2
Name Type Language
FENTANYL RELATED COMPOUND F
USP  
Preferred Name English
BENZYLFENTANYL
Common Name English
PROPANAMIDE, N-PHENYL-N-(1-(PHENYLMETHYL)-4-PIPERIDINYL)-
Systematic Name English
FENTANYL RELATED COMPOUND F [USP IMPURITY]
Common Name English
FENTANYL CITRATE IMPURITY H [EP IMPURITY]
Common Name English
1-BENZYL-4-(N-PHENYLPROPIONAMIDO)PIPERIDINE
Systematic Name English
FENTANYL IMPURITY K [EP IMPURITY]
Common Name English
R-4129
Code English
NSC-73402
Code English
N-BENZYLFENTANYL
Common Name English
Benzyl fentanyl
Common Name English
Classification Tree Code System Code
WIKIPEDIA List_of_fentanyl_analogues
Created by admin on Mon Mar 31 19:01:26 GMT 2025 , Edited by admin on Mon Mar 31 19:01:26 GMT 2025
DEA NO. 8334
Created by admin on Mon Mar 31 19:01:26 GMT 2025 , Edited by admin on Mon Mar 31 19:01:26 GMT 2025
Code System Code Type Description
WEB RESOURCE
BENZYLFENTANYL
Created by admin on Mon Mar 31 19:01:26 GMT 2025 , Edited by admin on Mon Mar 31 19:01:26 GMT 2025
PRIMARY
CAS
1474-02-8
Created by admin on Mon Mar 31 19:01:26 GMT 2025 , Edited by admin on Mon Mar 31 19:01:26 GMT 2025
PRIMARY
FDA UNII
9BV2D1A57H
Created by admin on Mon Mar 31 19:01:26 GMT 2025 , Edited by admin on Mon Mar 31 19:01:26 GMT 2025
PRIMARY
EPA CompTox
DTXSID00163705
Created by admin on Mon Mar 31 19:01:26 GMT 2025 , Edited by admin on Mon Mar 31 19:01:26 GMT 2025
PRIMARY
WIKIPEDIA
BENZYLFENTANYL
Created by admin on Mon Mar 31 19:01:26 GMT 2025 , Edited by admin on Mon Mar 31 19:01:26 GMT 2025
PRIMARY Benzylfentanyl has a Ki of 213nM at the mu opioid receptor, binding around 200x less strongly than fentanyl itself. Side effects of fentanyl analogs are similar to those of fentanyl itself, which include itching, nausea and potentially serious respiratory depression, which can be life-threatening. Fentanyl analogs have killed hundreds of people throughout Europe and the former Soviet republics since the most recent resurgence in use began in Estonia in the early 2000s, and novel derivatives continue to appear.
DRUG BANK
DB09182
Created by admin on Mon Mar 31 19:01:26 GMT 2025 , Edited by admin on Mon Mar 31 19:01:26 GMT 2025
PRIMARY
PUBCHEM
252141
Created by admin on Mon Mar 31 19:01:26 GMT 2025 , Edited by admin on Mon Mar 31 19:01:26 GMT 2025
PRIMARY
NSC
73402
Created by admin on Mon Mar 31 19:01:26 GMT 2025 , Edited by admin on Mon Mar 31 19:01:26 GMT 2025
PRIMARY
ECHA (EC/EINECS)
216-014-7
Created by admin on Mon Mar 31 19:01:26 GMT 2025 , Edited by admin on Mon Mar 31 19:01:26 GMT 2025
PRIMARY
ACTIVE MOIETY
Structure of BENZYLFENTANYL
NIH
NCATS
PRIVACY NOTICE
ACCESSIBILITY
DISCLAIMER
HHS VULNERABILITY DISCLOSURE
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