U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C3H6I2O
Molecular Weight 311.8881
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of DIIODOHYDROXYPROPANE

SMILES

OC(CI)CI

InChI

InChIKey=DNKPFCQEGBJJTE-UHFFFAOYSA-N
InChI=1S/C3H6I2O/c4-1-3(6)2-5/h3,6H,1-2H2

HIDE SMILES / InChI
Molecular Formula C3H6I2O
Molecular Weight 311.8881
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Description

Diiodohydroxypropane was once used as an antiseptic and disinfectant. Diiodohydroxypropane was investigated in the therapy of gingival bacteroiditis.

Approval Year

Unknown
139594
PubMed

PubMed

TitleDatePubMed
[Efficacy of diiodo-propanol in the control of bacterial plaque].
1982 May-Jun
[Disinfecting mechanism of jothion (1,3-diiodo-2-hydroxypropane)].
1983 Mar
[Assay of 1,3-diiodo-2-propanol (Iothion) in various pharmaceutical preparations].
1985 Aug
Patents

Patents

20100136617
1
6284449
1
6319659
1
6403279
2
6420354
1
6479498
1
6761952
1
6770432
1
WO2009106211A1
1
Substance Class Chemical
Created
by admin
on Fri Dec 15 17:50:55 GMT 2023
Edited
by admin
on Fri Dec 15 17:50:55 GMT 2023
Record UNII
1Z11279H67
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
DIIODOHYDROXYPROPANE
Systematic Name English
IOTONE
Common Name English
DIJODAN
Common Name English
IOTHION [MI]
Common Name English
AGOJODO
Common Name English
1,3-DIIODOISOPROPYL ALCOHOL
Common Name English
DIIODO-2-PROPANOL, 1,3-
Systematic Name English
2-PROPANOL, 1,3-DIIODO-
Systematic Name English
IOPROPANE
Common Name English
IOTHION
MI  
Common Name English
1,3-DIIODO-2-PROPANOL
Systematic Name English
JOTHION
Common Name English
GLYCEROL-.ALPHA.,.GAMMA.-DIIODOHYDRIN
Common Name English
Classification Tree Code System Code
WHO-VATC QD08AG04
Created by admin on Fri Dec 15 17:50:55 GMT 2023 , Edited by admin on Fri Dec 15 17:50:55 GMT 2023
WHO-ATC D08AG04
Created by admin on Fri Dec 15 17:50:55 GMT 2023 , Edited by admin on Fri Dec 15 17:50:55 GMT 2023
Code System Code Type Description
MERCK INDEX
m775
Created by admin on Fri Dec 15 17:50:55 GMT 2023 , Edited by admin on Fri Dec 15 17:50:55 GMT 2023
PRIMARY Merck Index
WIKIPEDIA
DIIODOHYDROXYPROPANE
Created by admin on Fri Dec 15 17:50:55 GMT 2023 , Edited by admin on Fri Dec 15 17:50:55 GMT 2023
PRIMARY
DRUG BANK
DB13383
Created by admin on Fri Dec 15 17:50:55 GMT 2023 , Edited by admin on Fri Dec 15 17:50:55 GMT 2023
PRIMARY
ChEMBL
CHEMBL3707258
Created by admin on Fri Dec 15 17:50:55 GMT 2023 , Edited by admin on Fri Dec 15 17:50:55 GMT 2023
PRIMARY
EPA CompTox
DTXSID8074992
Created by admin on Fri Dec 15 17:50:55 GMT 2023 , Edited by admin on Fri Dec 15 17:50:55 GMT 2023
PRIMARY
DRUG CENTRAL
4421
Created by admin on Fri Dec 15 17:50:55 GMT 2023 , Edited by admin on Fri Dec 15 17:50:55 GMT 2023
PRIMARY
PUBCHEM
68295
Created by admin on Fri Dec 15 17:50:55 GMT 2023 , Edited by admin on Fri Dec 15 17:50:55 GMT 2023
PRIMARY
ECHA (EC/EINECS)
208-586-1
Created by admin on Fri Dec 15 17:50:55 GMT 2023 , Edited by admin on Fri Dec 15 17:50:55 GMT 2023
PRIMARY
FDA UNII
1Z11279H67
Created by admin on Fri Dec 15 17:50:55 GMT 2023 , Edited by admin on Fri Dec 15 17:50:55 GMT 2023
PRIMARY
CAS
534-08-7
Created by admin on Fri Dec 15 17:50:55 GMT 2023 , Edited by admin on Fri Dec 15 17:50:55 GMT 2023
PRIMARY
Related Record Type Details
Structure of DIIODOHYDROXYPROPANE
ACTIVE MOIETY
NIH
NCATS
PRIVACY ACT
ACCESSIBILITY
DISCLAIMER
HHS VULNERABILITY DISCLOSURE
For language access assistance, contact the NCATS Public Information Officer
National Center for Advancing Translational Sciences (NCATS),
6701 Democracy Boulevard, Bethesda MD 20892-4874 • 301-594-8966