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
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
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
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 15:04:54 UTC 2023
by
admin
on
Fri Dec 15 15:04:54 UTC 2023
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Record UNII |
J2DF82JA7N
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Record Status |
Validated (UNII)
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Record Version |
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-
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Classification Tree | Code System | Code | ||
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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
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Code System | Code | Type | Description | ||
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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
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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
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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
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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
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PRIMARY | Merck Index | ||
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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
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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
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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
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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
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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
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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
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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
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PRIMARY | |||
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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
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PRIMARY | |||
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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
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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
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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
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PRIMARY |
Related Record | Type | Details | ||
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ACTIVE MOIETY |