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Details

Stereochemistry ACHIRAL
Molecular Formula C22H28N2O.ClH
Molecular Weight 372.931
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of FENTANYL HYDROCHLORIDE

SMILES

Cl.CCC(=O)N(C1CCN(CCC2=CC=CC=C2)CC1)C3=CC=CC=C3

InChI

InChIKey=LHCBOXPPRUIAQT-UHFFFAOYSA-N
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

HIDE SMILES / InChI
Molecular Formula ClH
Molecular Weight 36.461
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE
Molecular Formula C22H28N2O
Molecular Weight 336.4705
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Unknown
86413
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:39:16 UTC 2023
Edited
by admin
on Fri Dec 15 15:39:16 UTC 2023
Record UNII
59H156XY46
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
FENTANYL HYDROCHLORIDE
EMA EPAR   MART.   ORANGE BOOK   WHO-DD  
Common Name English
FENTANYL HYDROCHLORIDE [EMA EPAR]
Common Name English
FENTANYL HYDROCHLORIDE [ORANGE BOOK]
Common Name English
Fentanyl hydrochloride [WHO-DD]
Common Name English
FENTANYL HCL
Common Name English
FENTANYL HYDROCHLORIDE [MART.]
Common Name English
IONSYS
Brand Name English
PROPANAMIDE, N-PHENYL-N-(1-(2-PHENYLETHYL)-4-PIPERIDINYL)-, MONOHYDROCHLORIDE
Common Name English
FENTANYL HYDROCHLORIDE [JAN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C67413
Created by admin on Fri Dec 15 15:39:16 UTC 2023 , Edited by admin on Fri Dec 15 15:39:16 UTC 2023
NCI_THESAURUS C1506
Created by admin on Fri Dec 15 15:39:16 UTC 2023 , Edited by admin on Fri Dec 15 15:39:16 UTC 2023
EMA ASSESSMENT REPORTS IONSYS (WITHDRAWN: PAIN, POSTOPERATIVE)
Created by admin on Fri Dec 15 15:39:16 UTC 2023 , Edited by admin on Fri Dec 15 15:39:16 UTC 2023
Code System Code Type Description
EVMPD
SUB21234
Created by admin on Fri Dec 15 15:39:16 UTC 2023 , Edited by admin on Fri Dec 15 15:39:16 UTC 2023
PRIMARY
DRUG BANK
DBSALT001226
Created by admin on Fri Dec 15 15:39:16 UTC 2023 , Edited by admin on Fri Dec 15 15:39:16 UTC 2023
PRIMARY
RXCUI
1652097
Created by admin on Fri Dec 15 15:39:16 UTC 2023 , Edited by admin on Fri Dec 15 15:39:16 UTC 2023
PRIMARY RxNorm
NCI_THESAURUS
C61762
Created by admin on Fri Dec 15 15:39:16 UTC 2023 , Edited by admin on Fri Dec 15 15:39:16 UTC 2023
PRIMARY
PUBCHEM
83932
Created by admin on Fri Dec 15 15:39:16 UTC 2023 , Edited by admin on Fri Dec 15 15:39:16 UTC 2023
PRIMARY
CAS
1443-54-5
Created by admin on Fri Dec 15 15:39:16 UTC 2023 , Edited by admin on Fri Dec 15 15:39:16 UTC 2023
PRIMARY
FDA UNII
59H156XY46
Created by admin on Fri Dec 15 15:39:16 UTC 2023 , Edited by admin on Fri Dec 15 15:39:16 UTC 2023
PRIMARY
SMS_ID
100000092258
Created by admin on Fri Dec 15 15:39:16 UTC 2023 , Edited by admin on Fri Dec 15 15:39:16 UTC 2023
PRIMARY
ChEMBL
CHEMBL596
Created by admin on Fri Dec 15 15:39:16 UTC 2023 , Edited by admin on Fri Dec 15 15:39:16 UTC 2023
PRIMARY
EPA CompTox
DTXSID90162666
Created by admin on Fri Dec 15 15:39:16 UTC 2023 , Edited by admin on Fri Dec 15 15:39:16 UTC 2023
PRIMARY
Related Record Type Details
Structure of FENTANYL
PARENT -> SALT/SOLVATE
Related Record Type Details
Structure of FENTANYL
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