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Details

Stereochemistry RACEMIC
Molecular Formula C20H28N.Br
Molecular Weight 362.347
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of EMEPRONIUM BROMIDE

SMILES

[Br-].CC[N+](C)(C)C(C)CC(C1=CC=CC=C1)C2=CC=CC=C2

InChI

InChIKey=UVKFSMBPRQBNCH-UHFFFAOYSA-M
InChI=1S/C20H28N.BrH/c1-5-21(3,4)17(2)16-20(18-12-8-6-9-13-18)19-14-10-7-11-15-19;/h6-15,17,20H,5,16H2,1-4H3;1H/q+1;/p-1

HIDE SMILES / InChI

Molecular Formula BrH
Molecular Weight 80.912
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C20H28N
Molecular Weight 282.443
Charge 1
Count
Stereochemistry MIXED
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

Substance Class Chemical
Created
by admin
on Fri Dec 15 18:03:47 UTC 2023
Edited
by admin
on Fri Dec 15 18:03:47 UTC 2023
Record UNII
WZM699L2TL
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
EMEPRONIUM BROMIDE
INN   MART.   MI   WHO-DD  
INN  
Official Name English
BENZENEPROPANAMINIUM, N-ETHYL-N,N,.ALPHA.-TRIMETHYL-.GAMMA.-PHENYL-, BROMIDE (1:1)
Systematic Name English
Emepronium bromide [WHO-DD]
Common Name English
CETIPRIN
Brand Name English
EMEPRONIUM BROMIDE [MART.]
Common Name English
RESTENACHT
Brand Name English
AMMONIUM, ETHYLDIMETHYL(1-METHYL-3,3-DIPHENYLPROPYL)-, BROMIDE
Systematic Name English
URO-RIPIRIN
Brand Name English
ETHYLDIMETHYL(1-METHYL-3,3-DIPHENYLPROPYL)AMMONIUM BROMIDE
Systematic Name English
HEXANIUM
Systematic Name English
EMEPRONIUM BROMIDE [MI]
Common Name English
BENZENEPROPANAMINIUM, N-ETHYL-N,N,.ALPHA.-TRIMETHYL-.GAMMA.-PHENYL-, BROMIDE
Systematic Name English
emepronium bromide [INN]
Common Name English
RIPIRIN
Brand Name English
Code System Code Type Description
EPA CompTox
DTXSID50875265
Created by admin on Fri Dec 15 18:03:47 UTC 2023 , Edited by admin on Fri Dec 15 18:03:47 UTC 2023
PRIMARY
WIKIPEDIA
EMEPRONIUM BROMIDE
Created by admin on Fri Dec 15 18:03:47 UTC 2023 , Edited by admin on Fri Dec 15 18:03:47 UTC 2023
PRIMARY
PUBCHEM
71820
Created by admin on Fri Dec 15 18:03:47 UTC 2023 , Edited by admin on Fri Dec 15 18:03:47 UTC 2023
PRIMARY
ChEMBL
CHEMBL2110805
Created by admin on Fri Dec 15 18:03:47 UTC 2023 , Edited by admin on Fri Dec 15 18:03:47 UTC 2023
PRIMARY
MERCK INDEX
m4885
Created by admin on Fri Dec 15 18:03:47 UTC 2023 , Edited by admin on Fri Dec 15 18:03:47 UTC 2023
PRIMARY Merck Index
SMS_ID
100000080217
Created by admin on Fri Dec 15 18:03:47 UTC 2023 , Edited by admin on Fri Dec 15 18:03:47 UTC 2023
PRIMARY
EVMPD
SUB06504MIG
Created by admin on Fri Dec 15 18:03:47 UTC 2023 , Edited by admin on Fri Dec 15 18:03:47 UTC 2023
PRIMARY
NCI_THESAURUS
C169941
Created by admin on Fri Dec 15 18:03:47 UTC 2023 , Edited by admin on Fri Dec 15 18:03:47 UTC 2023
PRIMARY
RXCUI
71481
Created by admin on Fri Dec 15 18:03:47 UTC 2023 , Edited by admin on Fri Dec 15 18:03:47 UTC 2023
PRIMARY RxNorm
FDA UNII
WZM699L2TL
Created by admin on Fri Dec 15 18:03:47 UTC 2023 , Edited by admin on Fri Dec 15 18:03:47 UTC 2023
PRIMARY
ECHA (EC/EINECS)
222-786-6
Created by admin on Fri Dec 15 18:03:47 UTC 2023 , Edited by admin on Fri Dec 15 18:03:47 UTC 2023
PRIMARY
INN
2414
Created by admin on Fri Dec 15 18:03:47 UTC 2023 , Edited by admin on Fri Dec 15 18:03:47 UTC 2023
PRIMARY
CAS
3614-30-0
Created by admin on Fri Dec 15 18:03:47 UTC 2023 , Edited by admin on Fri Dec 15 18:03:47 UTC 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
PARENT -> SALT/SOLVATE
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY