Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C14H13O3.Na |
| Molecular Weight | 252.241 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
[Na+].CC(C)(C)C(=O)[C-]1C(=O)C2=C(C=CC=C2)C1=O
InChI
InChIKey=PPRNMFDWJLACKG-UHFFFAOYSA-N
InChI=1S/C14H13O3.Na/c1-14(2,3)13(17)10-11(15)8-6-4-5-7-9(8)12(10)16;/h4-7H,1-3H3;/q-1;+1
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Analysis of multiple anticoagulant rodenticides in animal blood and liver tissue using principles of QuEChERS method. | 2010-06 |
|
| Simultaneous measurement of indandione-type rodenticides in human serum by liquid chromatography-electrospray ionization- tandem mass spectrometry. | 2009-08-06 |
|
| Analysis of indandione anticoagulant rodenticides in animal liver by eluent generator reagent free ion chromatography coupled with electrospray mass spectrometry. | 2008-12-05 |
|
| Multiresidue analysis of seven anticoagulant rodenticides by high-performance liquid chromatography/electrospray/mass spectrometry. | 2007-02-07 |
|
| Effect of the anticoagulant, pindone, on the breeding performance and survival of merino sheep, Ovis aries. | 2005-03 |
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EPA PESTICIDE CODE |
67704
Created by
admin on Mon Mar 31 23:00:13 GMT 2025 , Edited by admin on Mon Mar 31 23:00:13 GMT 2025
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DTXSID9058440
Created by
admin on Mon Mar 31 23:00:13 GMT 2025 , Edited by admin on Mon Mar 31 23:00:13 GMT 2025
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6120-20-3
Created by
admin on Mon Mar 31 23:00:13 GMT 2025 , Edited by admin on Mon Mar 31 23:00:13 GMT 2025
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5E8BW66VY3
Created by
admin on Mon Mar 31 23:00:13 GMT 2025 , Edited by admin on Mon Mar 31 23:00:13 GMT 2025
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pindone-sodium
Created by
admin on Mon Mar 31 23:00:13 GMT 2025 , Edited by admin on Mon Mar 31 23:00:13 GMT 2025
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23707501
Created by
admin on Mon Mar 31 23:00:13 GMT 2025 , Edited by admin on Mon Mar 31 23:00:13 GMT 2025
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PRIMARY |
SUBSTANCE RECORD
