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Details

Stereochemistry ACHIRAL
Molecular Formula C9H24N2O
Molecular Weight 176.2997
Optical Activity NONE
Defined Stereocenters 0 / 2
E/Z Centers 0
Charge 2

SHOW SMILES / InChI
Structure of PROLONIUM

SMILES

C[N+](C)(C)CC(O)C[N+](C)(C)C

InChI

InChIKey=SEOAESNTVSJYIF-UHFFFAOYSA-N
InChI=1S/C9H24N2O/c1-10(2,3)7-9(12)8-11(4,5)6/h9,12H,7-8H2,1-6H3/q+2

HIDE SMILES / InChI

Molecular Formula C9H23N2O
Molecular Weight 175.2917
Charge 1
Count
Stereochemistry MIXED
Additional Stereochemistry No
Defined Stereocenters 0 / 2
E/Z Centers 0
Optical Activity NONE

Prolonium is a quartenary amine derivative. Prolonium iodide has been given by injection as a source of iodine as part of the treatment of thyroid storm and for the pre-operative management of hyperthyroidism. It is marketed in Italy for veterinary use for the treatment of infectious granulomas, in the various forms of actinomycosis actinobacillosis of the tongue, larynx, pharynx, skin and subcutaneous connective tissue.

Approval Year

Substance Class Chemical
Created
by admin
on Mon Mar 31 21:25:56 GMT 2025
Edited
by admin
on Mon Mar 31 21:25:56 GMT 2025
Record UNII
B7I54M7Z12
Record Status Validated (UNII)
Record Version
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Name Type Language
PROLONIUM CATION
Preferred Name English
PROLONIUM
WHO-DD  
Common Name English
PROLONIUM ION
Common Name English
2-HYDROXY-N,N,N,N',N',N'-HEXAMETHYL-1,3-PROPANEDIAMINIUM
Systematic Name English
1,3-PROPANEDIAMINIUM, 2-HYDROXY-N1,N1,N1,N3,N3,N3-HEXAMETHYL-
Systematic Name English
Prolonium [WHO-DD]
Common Name English
1,3-PROPANEDIAMINIUM, 2-HYDROXY-N1,N1,N1,N3,N3,N3-HEXAMETHYL-, CHLORIDE
Systematic Name English
1,3-PROPANEDIAMINIUM, 2-HYDROXY-N,N,N,N',N',N'-HEXAMETHYL-
Systematic Name English
Code System Code Type Description
EPA CompTox
DTXSID70861761
Created by admin on Mon Mar 31 21:25:56 GMT 2025 , Edited by admin on Mon Mar 31 21:25:56 GMT 2025
PRIMARY
PUBCHEM
67159
Created by admin on Mon Mar 31 21:25:56 GMT 2025 , Edited by admin on Mon Mar 31 21:25:56 GMT 2025
PRIMARY
SMS_ID
100000085086
Created by admin on Mon Mar 31 21:25:56 GMT 2025 , Edited by admin on Mon Mar 31 21:25:56 GMT 2025
PRIMARY
FDA UNII
B7I54M7Z12
Created by admin on Mon Mar 31 21:25:56 GMT 2025 , Edited by admin on Mon Mar 31 21:25:56 GMT 2025
PRIMARY
CAS
45021-15-6
Created by admin on Mon Mar 31 21:25:56 GMT 2025 , Edited by admin on Mon Mar 31 21:25:56 GMT 2025
PRIMARY
EVMPD
SUB04065MIG
Created by admin on Mon Mar 31 21:25:56 GMT 2025 , Edited by admin on Mon Mar 31 21:25:56 GMT 2025
PRIMARY
Related Record Type Details
ACTIVE MOIETY