Phorate

Source: Wikipedia, the free encyclopedia.
Phorate
Names
Preferred IUPAC name
O,O-Diethyl S-[(ethylsulfanyl)methyl] phosphorodithioate
Other names
Thimet (trademark)
3911 (trademark)
Identifiers
3D model (
JSmol
)
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard
100.005.503 Edit this at Wikidata
UNII
  • InChI=1S/C7H17O2PS3/c1-4-8-10(11,9-5-2)13-7-12-6-3/h4-7H2,1-3H3 checkY
    Key: BULVZWIRKLYCBC-UHFFFAOYSA-N checkY
  • InChI=1/C7H17O2PS3/c1-4-8-10(11,9-5-2)13-7-12-6-3/h4-7H2,1-3H3
    Key: BULVZWIRKLYCBC-UHFFFAOYAA
  • S=P(OCC)(SCSCC)OCC
Properties
C7H17O2PS3
Molar mass 260.36 g·mol−1
Appearance Colorless liquid
Odor Skunk-like[1]
Density 1.16 g/mL
Melting point −43 °C; −45 °F; 230 K[1]
Boiling point 118-120°C (2.0 mm Hg)[2]
0.005% (20°C)[1]
Vapor pressure 0.0008 mmHg (20°C)[1]
Hazards
Flash point 160 °C; 320 °F; 433 K (open cup)[1]
NIOSH (US health exposure limits):
PEL (Permissible)
none[1]
REL (Recommended)
TWA 0.05 mg/m3 ST 0.2 mg/m3 [skin][1]
IDLH
(Immediate danger)
N.D.[1]
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 ?)

Phorate is an organophosphate used as an insecticide and acaricide.

Overview

At normal conditions, it is a pale yellow mobile liquid poorly

mammals including human. It inhibits acetylcholinesterase and butyrylcholinesterase.[3]

Phorate is most commonly applied in

granular form. It is non-biocumulative and has no residual action. But some metabolites may persist in soil. It also damages some seeds.[3]

Toxicity

Phorate (Thimate) is absorbed readily through all ways. Its

References

  1. ^ a b c d e f g h NIOSH Pocket Guide to Chemical Hazards. "#0502". National Institute for Occupational Safety and Health (NIOSH).
  2. ^ Farm Chemicals Handbook, Meister Publishing Co., Willoughby, OH (1991)
  3. ^ a b c "Data sheets on pesticides No. 75 – Phorate". Archived from the original on 2014-07-02. Retrieved 2011-07-31.

External links

  • Phorate in the Pesticide Properties DataBase (PPDB)