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Benthiocarb

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Benthiocarb
Names
Preferred IUPAC name
S-[(4-Chlorophenyl)methyl] diethylcarbamothioate
Other names
Thiobencarb, Saturn, Bolero
Identifiers
3D model (JSmol)
ChEMBL
ChemSpider
ECHA InfoCard 100.044.461 Edit this at Wikidata
KEGG
UNII
  • InChI=1S/C12H16ClNOS/c1-3-14(4-2)12(15)16-9-10-5-7-11(13)8-6-10/h5-8H,3-4,9H2,1-2H3 checkY
    Key: QHTQREMOGMZHJV-UHFFFAOYSA-N checkY
  • InChI=1S/C12H16ClNOS/c1-3-14(4-2)12(15)16-9-10-5-7-11(13)8-6-10/h5-8H,3-4,9H2,1-2H3
  • Clc1ccc(cc1)CSC(=O)N(CC)CC
Properties
C12H16ClNOS
Molar mass 257.78 g·mol−1
Appearance Pale yellow to brownish-yellow liquid
Density 1.145-1.180 g cm−3 at 20 °C
Melting point 3.3 °C (37.9 °F; 276.4 K)
Boiling point 126 to 129 °C (259 to 264 °F; 399 to 402 K) at 0.008 Torr
28.0 mg/L at 25 °C
Solubility Readily soluble in: acetone, ethanol, xylene, methanol, benzene, n-hexane, and acetonitrile
log P 3.42 (octanol/water)[1]
Hazards
NFPA 704 (fire diamond)
NFPA 704 four-colored diamondHealth 4: Very short exposure could cause death or major residual injury. E.g. VX gasFlammability 1: Must be pre-heated before ignition can occur. Flash point over 93 °C (200 °F). E.g. canola oilInstability 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g. liquid nitrogenSpecial hazards (white): no code
4
1
0
Flash point 165.8 °C (330.4 °F; 438.9 K)
Lethal dose or concentration (LD, LC):
Rat, oral 1300 mg/kg

Mouse, oral 560 mg/kg [2]

Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
checkY verify (what is checkY☒N ?)

Benthiocarb is a thiocarbamate cholinesterase inhibitor used as an herbicide. Benthiocarb is almost always used to control the weeds around rice crops, but its effectiveness is not specific to just rice crops.[3] The benthiocarb molecule is an organic molecule containing a phenol bonded to a chlorine atom.

Benthiocarb is a major herbicide for rice crops

See also

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References

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  1. ^ Tomlin, C.D.S., ed. (1997). The Pesticide Manual - World Compendium (11th ed.). Surrey, England: British Crop Protection Council. p. 1192.
  2. ^ Worthing, C.R. and S.B. Walker, ed. (1987). The Pesticide Manual - A World Compendium (8th ed.). Thornton Heath, UK: The British Crop Protection Council. p. 796.
  3. ^ United States Environmental Protection Agency (September 1997). "R.E.D. FACTS Thiobencarb" (PDF). Retrieved September 26, 2022.
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