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Phosalone
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Welcome to the community hub built on top of the Phosalone Wikipedia article. Here, you can discuss, collect, and organize anything related to Phosalone. The purpose of the hub is to connect people, foste...
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Phosalone
Phosalone
Names
Preferred IUPAC name
S-[(6-Chloro-2-oxo-1,3-benzoxazol-3(2H)-yl)methyl] O,O-diethyl phosphorodithioate
Other names
Zolone
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.017.270 Edit this at Wikidata
KEGG
UNII
  • InChI=1S/C12H15ClNO4PS2/c1-3-16-19(20,17-4-2)21-8-14-10-6-5-9(13)7-11(10)18-12(14)15/h5-7H,3-4,8H2,1-2H3 checkY
    Key: IOUNQDKNJZEDEP-UHFFFAOYSA-N checkY
  • InChI=1/C12H15ClNO4PS2/c1-3-16-19(20,17-4-2)21-8-14-10-6-5-9(13)7-11(10)18-12(14)15/h5-7H,3-4,8H2,1-2H3
    Key: IOUNQDKNJZEDEP-UHFFFAOYAA
  • Clc2ccc1c(OC(=O)N1CSP(=S)(OCC)OCC)c2
Properties
C12H15ClNO4PS2
Molar mass 367.80 g·mol−1
Appearance Colorless crystalline
Odor garlic
Density 1.39 g cm−3
Melting point 47.5 to 48 °C (117.5 to 118.4 °F; 320.6 to 321.1 K)
3.05 mg/L
Solubility many organic solvents
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)

Phosalone is an organophosphate chemical commonly used as an insecticide and acaricide. It is developed by Rhône-Poulenc in France but EU eliminated it from pesticide registration in December 2006.

The median lethal dose of oral exposure in rat is 85 mg/kg and that of dermal is 390 mg/kg.[1]。It is a weak acetylcholinesterase inhibitor.[2] It is taken by not only oral and inhalation but skin and it causes toxic symptoms peculiar to organophosphorus compounds such as miosis, hypersalivation, hyperhidrosis, chest pressure, pulmonary edema and fecal incontinence.[3] It is flammable and decomposes to toxic gases such as phosphorus oxides, sulfur oxides and nitrogen oxides.[2] It is harmful especially to water creatures.

References

[edit]
  1. ^ 製品安全データシート(安全衛生情報センター) Archived 2014-10-25 at the Wayback Machine
  2. ^ a b "国際化学物質安全性カード". Archived from the original on 2012-12-11. Retrieved 2012-09-06.
  3. ^ 植村振作・河村宏・辻万千子・冨田重行・前田静夫著 (2002). 農薬毒性の事典 改訂版. 三省堂. ISBN 978-4385356044.
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