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Details

Stereochemistry ACHIRAL
Molecular Formula C9H24N2O.2Cl
Molecular Weight 247.206
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PROLONIUM CHLORIDE

SMILES

[Cl-].[Cl-].C[N+](C)(C)CC(O)C[N+](C)(C)C

InChI

InChIKey=UIYQPSXVBLBPQP-UHFFFAOYSA-L
InChI=1S/C9H24N2O.2ClH/c1-10(2,3)7-9(12)8-11(4,5)6;;/h9,12H,7-8H2,1-6H3;2*1H/q+2;;/p-2

HIDE SMILES / InChI

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

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

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 Sat Dec 16 07:59:37 GMT 2023
Edited
by admin
on Sat Dec 16 07:59:37 GMT 2023
Record UNII
4IBH37ORJM
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
PROLONIUM CHLORIDE
Common Name English
1,3-PROPANEDIAMINIUM, 2-HYDROXY-N1,N1,N1,N3,N3,N3-HEXAMETHYL-, CHLORIDE (1:2)
Systematic Name English
4-HYDROXY-2,2,6,6-TETRAMETHYL-2,6-DIAZONIAHEPTANE DICHLORIDE
Systematic Name English
1,3-PROPANEDIAMINIUM, 2-HYDROXY-N,N,N,N',N',N'-HEXAMETHYL-, DICHLORIDE
Systematic Name English
(2-HYDROXYTRIMETHYLENE)BIS(TRIMETHYLAMMONIUM CHLORIDE)
Common Name English
Code System Code Type Description
CAS
55636-09-4
Created by admin on Sat Dec 16 07:59:37 GMT 2023 , Edited by admin on Sat Dec 16 07:59:37 GMT 2023
PRIMARY
PUBCHEM
6453216
Created by admin on Sat Dec 16 07:59:37 GMT 2023 , Edited by admin on Sat Dec 16 07:59:37 GMT 2023
PRIMARY
FDA UNII
4IBH37ORJM
Created by admin on Sat Dec 16 07:59:37 GMT 2023 , Edited by admin on Sat Dec 16 07:59:37 GMT 2023
PRIMARY
EPA CompTox
DTXSID00970976
Created by admin on Sat Dec 16 07:59:37 GMT 2023 , Edited by admin on Sat Dec 16 07:59:37 GMT 2023
PRIMARY
ECHA (EC/EINECS)
259-734-7
Created by admin on Sat Dec 16 07:59:37 GMT 2023 , Edited by admin on Sat Dec 16 07:59:37 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY