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

Description
Curator's Comment: Description was created based on several sources, including http://icm-eg.com/AgriculturalSector/PDF/DIFETHIALONE%20Wheat.pdf and http://sitem.herts.ac.uk/aeru/iupac/Reports/233.htm

Difethialone is an anticoagulant used as a rodenticide. Difethialone is not approved for use in Europe but is still used elsewhere. It is relatively volatile, has low potential to leach to groundwater but is highly persistent in soils. It is highly toxic to humans and considered to produce adverse effects on the reproduction system. In May 2008, the United States Environmental Protection Agency banned the use of difethialone in consumer-use rodenticide products and also for exterior use by commercial applicators.

Approval Year

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
PubMed

PubMed

TitleDatePubMed
Response of predominant rodent borne diseases to difethialone anticoagulant rodenticide under laboratory conditions.
2010-12
Analysis of multiple anticoagulant rodenticides in animal blood and liver tissue using principles of QuEChERS method.
2010-06
Validation of a new liquid chromatography- tandem mass spectrometry ion-trap technique for the simultaneous determination of thirteen anticoagulant rodenticides, drugs, or natural products.
2010-03
Anticoagulant rodenticides in three owl species from Western Canada, 1988-2003.
2010-02
Consequences of the Y139F Vkorc1 mutation on resistance to AVKs: in-vivo investigation in a 7th generation of congenic Y139F strain of rats.
2009-10
Simultaneous bleeding and thrombosis in superwarfarin poisoning.
2009-02
Pharmacokinetics of eight anticoagulant rodenticides in mice after single oral administration.
2008-10
Intoxication with three different superwarfarin compounds in an adult woman.
2008-07
Multi-residue analysis of eight anticoagulant rodenticides in animal plasma and liver using liquid chromatography combined with heated electrospray ionization tandem mass spectrometry.
2008-06-15
Acute bromadiolone intoxication.
2006-05
Evaluation of secondary poisoning of difethialone, a new second-generation anticoagulant rodenticide to barn owl, Tyto alba Hartert under captivity.
2004-10
Effect of supplementary feeding of vitamin K1 on difethialone treated Indian gerbil, Tatera indica Hardwicke in laboratory.
2004-03
Field evaluation of difethialone, a new second generation anticoagulant rodenticide in the rice fields.
2003-06
A scheme for the placement of rodenticide baits for rat eradication on confinement livestock farms.
2003-05-15
[Plague control in Madagascar: evaluation of the efficacy of Kartman baitboxes in urban areas].
2003
Patents

Sample Use Guides

In Vivo Use Guide
Unknown
Route of Administration: Unknown
In Vitro Use Guide
Unknown
Substance Class Mixture
Created
by admin
on Mon Mar 31 21:33:49 GMT 2025
Edited
by admin
on Mon Mar 31 21:33:49 GMT 2025
Record UNII
KOL4VXI5O0
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
DIFETHIALONE
ISO   MI  
Common Name English
DIFETHIAROL
JAN  
Preferred Name English
DIFETHIAROL [JAN]
Common Name English
LM-2219
Code English
BARAKI
Brand Name English
2H-1-BENZOTHIOPYRAN-2-ONE, 3-(3-(4'-BROMO(1,1'-BIPHENYL)-4-YL)-1,2,3,4-TETRAHYDRO-1-NAPHTHALENYL)-4-HYDROXY-
Common Name English
DIFETHIALONE [MI]
Common Name English
DIFETHIALONE [ISO]
Code English
LM 2219
Code English
Classification Tree Code System Code
EPA PESTICIDE CODE 128967
Created by admin on Mon Mar 31 21:33:49 GMT 2025 , Edited by admin on Mon Mar 31 21:33:49 GMT 2025
Code System Code Type Description
SMS_ID
100000125992
Created by admin on Mon Mar 31 21:33:49 GMT 2025 , Edited by admin on Mon Mar 31 21:33:49 GMT 2025
PRIMARY
WIKIPEDIA
DIFETHIALONE
Created by admin on Mon Mar 31 21:33:49 GMT 2025 , Edited by admin on Mon Mar 31 21:33:49 GMT 2025
PRIMARY
HSDB
7119
Created by admin on Mon Mar 31 21:33:49 GMT 2025 , Edited by admin on Mon Mar 31 21:33:49 GMT 2025
PRIMARY
ALANWOOD
difethialone
Created by admin on Mon Mar 31 21:33:49 GMT 2025 , Edited by admin on Mon Mar 31 21:33:49 GMT 2025
PRIMARY
MESH
C060340
Created by admin on Mon Mar 31 21:33:49 GMT 2025 , Edited by admin on Mon Mar 31 21:33:49 GMT 2025
PRIMARY
MERCK INDEX
m4428
Created by admin on Mon Mar 31 21:33:49 GMT 2025 , Edited by admin on Mon Mar 31 21:33:49 GMT 2025
PRIMARY Merck Index
EVMPD
SUB33152
Created by admin on Mon Mar 31 21:33:49 GMT 2025 , Edited by admin on Mon Mar 31 21:33:49 GMT 2025
PRIMARY
EPA CompTox
DTXSID4032374
Created by admin on Mon Mar 31 21:33:49 GMT 2025 , Edited by admin on Mon Mar 31 21:33:49 GMT 2025
PRIMARY
FDA UNII
KOL4VXI5O0
Created by admin on Mon Mar 31 21:33:49 GMT 2025 , Edited by admin on Mon Mar 31 21:33:49 GMT 2025
PRIMARY
CAS
104653-34-1
Created by admin on Mon Mar 31 21:33:49 GMT 2025 , Edited by admin on Mon Mar 31 21:33:49 GMT 2025
PRIMARY
PUBCHEM
91771
Created by admin on Mon Mar 31 21:33:49 GMT 2025 , Edited by admin on Mon Mar 31 21:33:49 GMT 2025
PRIMARY
All of the following components must be present:
Definition References