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CAS No 55285-14-8 , (2,2-dimethyl-3H-1-benzofuran-7-yl)
N-(dibutylamino)sulfanyl-N-methylcarbamate Search by region : China

  • Name: (2,2-dimethyl-3H-1-benzofuran-7-yl)
    N-(dibutylamino)sulfanyl-N-methylcarbamate
  • Synonyms: RCRA waste no. P189; Caswell No. 463C; FMC 35001; Dibutylaminosulfenylcarbofuran; Advantage; Posse;(2,2-dimethyl-3H-1-benzofuran-7-yl)
    N-(dibutylamino)sulfanyl-N-methylcarbamate; Marshall;Marshal;
  • CAS Registry Number:
  • Transport: UN 2810
  • Density: 1.099 g/cm3
  • Refractive index: 1.536
  • Safety Statements: R23/25;R43;R50/53
  • Hazard Symbols: N: Dangerous for the environment;T: Toxic;
  • EINECS: 259-565-9
  • Molecular Weight: 380.54468
  • InchiKey: JLQUFIHWVLZVTJ-UHFFFAOYSA-N
  • InChI: InChI=1S/C20H32N2O3S/c1-6-8-13-22(14-9-7-2)26-21(5)19(23)24-17-12-10-11-
    16-15-20(3,4)25-18(16)17/h10-12H,6-9,13-15H2,1-5H3
  • Risk Statements: S24;S37;S38;S45;S60;S61
  • Molecular Formula: C20H32N2O3S
  • Molecular Structure:CAS No:55285-14-8 (2,2-dimethyl-3H-1-benzofuran-7-yl)<br />N-(dibutylamino)sulfanyl-N-methylcarbamate

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References of (2,2-dimethyl-3H-1-benzofuran-7-yl)
N-(dibutylamino)sulfanyl-N-methylcarbamate
Title: Carbosulfan
CAS Registry Number: 55285-14-8
CAS Name: [(Dibutylamino)thio]methylcarbamic acid 2,3-dihydro-2,2-dimethyl-7-benzofuranyl ester
Manufacturers' Codes: FMC-35001
Trademarks: Marshal (FMC); Posse (FMC)
Molecular Formula: C20H32N2O3S
Molecular Weight: 380.54
Percent Composition: C 63.12%, H 8.48%, N 7.36%, O 12.61%, S 8.43%
Literature References: Carbamate cholinesterase inhibitor which is hydrolyzed to carbofuran in soil. Prepn: A. L. Black, T. R. Fukuto, BE 817517; eidem, US 4006231 (1975, 1977 both to Regents Univ. Calif.). Metabolism in orange tree leaves and fruit: V. E. Clay, T. R. Fukuto, Arch. Environ. Contam. Toxicol. 13, 53 (1984). Degradation and persistence in soil: A. Sahoo et al., Bull. Environ. Contam. Toxicol. 50, 29 (1993). HPLC determn in oranges: M.W. Brooks, A. Barros, Analyst 120, 2479 (1995). Spectrophotometric determn in formulations and water samples: K. R. Mohan et al., Asian J. Chem. 10, 457 (1998). Review of physical properties and field trials: E. G. Maitlen, N. A. Sladen, Proc. Br. Crop Prot. Conf. - Pests Dis. 1979, 557-564.
Properties: Viscous, brown liquid. Soly in water at 25°: 0.3 ppm. Soly in organic solvents: > 50%. Vapor pressure: 0.31 ′ 10-6 mmHg. LD50 in male, female rats (mg/kg): 250, 185 orally; in male, female rabbits (mg/kg): >2000, >2000 dermally; in pheasant, mallard, quail (ppm): 26.2, 8.1, 81.6 orally. LC50 (96 hr) in bluegill, trout (ppb): 14.9, 42.4 (Maitlen).
Toxicity data: LD50 in male, female rats (mg/kg): 250, 185 orally; in male, female rabbits (mg/kg): >2000, >2000 dermally; in pheasant, mallard, quail (ppm): 26.2, 8.1, 81.6 orally. LC50 (96 hr) in bluegill, trout (ppb): 14.9, 42.4 (Maitlen).
Use: Insecticide.