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

Details

Stereochemistry MIXED
Molecular Formula C12H26O6P2S4
Molecular Weight 456.539
Optical Activity UNSPECIFIED
Defined Stereocenters 0 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of DIOXATION

SMILES

CCOP(=S)(OCC)SC1OCCOC1SP(=S)(OCC)OCC

InChI

InChIKey=VBKKVDGJXVOLNE-UHFFFAOYSA-N
InChI=1S/C12H26O6P2S4/c1-5-15-19(21,16-6-2)23-11-12(14-10-9-13-11)24-20(22,17-7-3)18-8-4/h11-12H,5-10H2,1-4H3

HIDE SMILES / InChI

Molecular Formula C12H26O6P2S4
Molecular Weight 456.539
Charge 0
Count
Stereochemistry MIXED
Additional Stereochemistry No
Defined Stereocenters 0 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

Dioxation is an organophosphorous insecticide. It is a narrow-spectrum insecticide and acaricide with long residual effectiveness. The technical product is a mixture of cis and trans isomers and the oxygen analog of dioxation is relatively unstable. Dioxation is used as a spray to control mites on cotton, grapes, citrus, ornamentals, and certain other fruits including apples, pears, and quinces; and as a spray or dip on cattle, goats, sheep, and hogs for control of ticks, lice, horn flies, and sheep ked. Dietary administration of dioxation was not carcinogenic in Osborne-Mendel rats or B6C3F1 mice. Dioxation has moderate to extreme acute toxicity in mammal species tested and is moderately toxic to birds.

Approval Year

PubMed

PubMed

TitleDatePubMed
Susceptibility of Amblyomma variegatum ticks to acaricides in Ghana.
2005
Longitudinal trends in organophosphate incidents reported to the National Pesticide Information Center, 1995-2007.
2009 Apr 20
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:04:54 UTC 2023
Edited
by admin
on Fri Dec 15 15:04:54 UTC 2023
Record UNII
J2DF82JA7N
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
DIOXATION
HSDB   INN   MART.  
INN  
Official Name English
S,S'-(1,4-DIOXANE-2,3-DIYL) O,O,O',O'-TETRAETHYL BIS(PHOSPHORODITHIOATE)
Common Name English
DIOXATION [MART.]
Common Name English
DIOXATION [HSDB]
Common Name English
AC-528
Code English
DIOXATHION
ISO   MI  
Common Name English
S,S'-1,4-DIOXANE-2,3-DIYL BIS(O,O-DIETHYL PHOSPHORODITHIOATE)
Common Name English
DIOXATHION [MI]
Common Name English
DIOXATHION [ISO]
Common Name English
dioxation [INN]
Common Name English
Classification Tree Code System Code
EPA PESTICIDE CODE 37801
Created by admin on Fri Dec 15 15:04:54 UTC 2023 , Edited by admin on Fri Dec 15 15:04:54 UTC 2023
Code System Code Type Description
SMS_ID
100000082894
Created by admin on Fri Dec 15 15:04:54 UTC 2023 , Edited by admin on Fri Dec 15 15:04:54 UTC 2023
PRIMARY
WIKIPEDIA
DIOXATHION
Created by admin on Fri Dec 15 15:04:54 UTC 2023 , Edited by admin on Fri Dec 15 15:04:54 UTC 2023
PRIMARY
PUBCHEM
6531
Created by admin on Fri Dec 15 15:04:54 UTC 2023 , Edited by admin on Fri Dec 15 15:04:54 UTC 2023
PRIMARY
MERCK INDEX
m4600
Created by admin on Fri Dec 15 15:04:54 UTC 2023 , Edited by admin on Fri Dec 15 15:04:54 UTC 2023
PRIMARY Merck Index
NCI_THESAURUS
C169914
Created by admin on Fri Dec 15 15:04:54 UTC 2023 , Edited by admin on Fri Dec 15 15:04:54 UTC 2023
PRIMARY
INN
2101
Created by admin on Fri Dec 15 15:04:54 UTC 2023 , Edited by admin on Fri Dec 15 15:04:54 UTC 2023
PRIMARY
EPA CompTox
DTXSID9020534
Created by admin on Fri Dec 15 15:04:54 UTC 2023 , Edited by admin on Fri Dec 15 15:04:54 UTC 2023
PRIMARY
EVMPD
SUB07203MIG
Created by admin on Fri Dec 15 15:04:54 UTC 2023 , Edited by admin on Fri Dec 15 15:04:54 UTC 2023
PRIMARY
ECHA (EC/EINECS)
201-107-7
Created by admin on Fri Dec 15 15:04:54 UTC 2023 , Edited by admin on Fri Dec 15 15:04:54 UTC 2023
PRIMARY
ALANWOOD
dioxathion
Created by admin on Fri Dec 15 15:04:54 UTC 2023 , Edited by admin on Fri Dec 15 15:04:54 UTC 2023
PRIMARY
FDA UNII
J2DF82JA7N
Created by admin on Fri Dec 15 15:04:54 UTC 2023 , Edited by admin on Fri Dec 15 15:04:54 UTC 2023
PRIMARY
CAS
78-34-2
Created by admin on Fri Dec 15 15:04:54 UTC 2023 , Edited by admin on Fri Dec 15 15:04:54 UTC 2023
PRIMARY
MESH
C004838
Created by admin on Fri Dec 15 15:04:54 UTC 2023 , Edited by admin on Fri Dec 15 15:04:54 UTC 2023
PRIMARY
ChEMBL
CHEMBL2106286
Created by admin on Fri Dec 15 15:04:54 UTC 2023 , Edited by admin on Fri Dec 15 15:04:54 UTC 2023
PRIMARY
HSDB
1599
Created by admin on Fri Dec 15 15:04:54 UTC 2023 , Edited by admin on Fri Dec 15 15:04:54 UTC 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY