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CAS No 112410-23-8 , N-tert-butyl-N'-(4-ethylbenzoyl)-3,5-dimethylbenzohydrazide Search by region : China

  • Name: N-tert-butyl-N'-(4-ethylbenzoyl)-3,5-dimethylbenzohydrazide
  • Synonyms: RH 5992;112410-23-8; HSDB 7050; N-tert-Butyl-N'-(4-ethylbenzoyl)-3,5-dimethylbenzohydrazide; Tebufenozide [ISO];N-tert-butyl-N'-(4-ethylbenzoyl)-3,5-dimethylbenzohydrazide; CHEBI:38452; RH-5992;
  • CAS Registry Number:
  • Transport: UN 3077
  • Melting Point: 191 deg C
  • Flash Point: °C
  • Boiling Point: °Cat760mmHg
  • Density: 1.074 g/cm3
  • Refractive index: 1.561
  • Safety Statements: R51/53
  • Hazard Symbols: N: Dangerous for the environment;
  • Flash Point: °C
  • EINECS: 412-850-3
  • Molecular Weight: 352.46992
  • InchiKey: QYPNKSZPJQQLRK-UHFFFAOYSA-N
  • InChI: InChI=1S/C22H28N2O2/c1-7-17-8-10-18(11-9-17)20(25)23-24(22(4,
    5)6)21(26)19-13-15(2)12-16(3)14-19/h8-14H,7H2,1-6H3,(H,23,25)
  • Risk Statements: S61
  • Molecular Formula: C22H28N2O2
  • Molecular Structure:CAS No:112410-23-8 N-tert-butyl-N'-(4-ethylbenzoyl)-3,5-dimethylbenzohydrazide

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References of N-tert-butyl-N'-(4-ethylbenzoyl)-3,5-dimethylbenzohydrazide
Title: Tebufenozide
CAS Registry Number: 112410-23-8
CAS Name: 3,5-Dimethylbenzoic acid 1-(1,1-dimethylethyl)-2-(4-ethylbenzoyl)hydrazide
Synonyms: N-tert-butyl-N￠-(4-ethylbenzoyl)-3,5-dimethylbenzoylhydrazide
Manufacturers' Codes: RH-5992
Trademarks: Confirm (Dow AgroSci.); Mimic (Dow AgroSci.)
Molecular Formula: C22H28N2O2
Molecular Weight: 352.47
Percent Composition: C 74.97%, H 8.01%, N 7.95%, O 9.08%
Literature References: Synthetic nonsteroidal ecdysone agonist causing premature molting; novel insect growth regulator specific to lepidopteran species. Prepn: A. C. Hsu, H. E. Aller, AU 64289; eidem, US 4985461 (1986, 1991 both to Rohm & Haas). Properties and field evaluation: J. J. Heller et al., Brighton Crop Prot. Conf. - Pests Dis. 1992, 59. Determn by LC in environmental samples: K. M. S. Sundaram et al., J. AOAC Int. 76, 668 (1993); by GC and LC in formulations: idem, et al., J. Chromatogr. A 687, 323 (1994). Soil adsorption: idem, J. Environ. Sci. Health B29, 415 (1994). Insecticidal activity: G. Smagghe, D. Degheele, Pestic. Sci. 42, 85 (1994). Mechanism of action: A. Retnakaran et al., Insect Biochem. Mol. Biol. 25, 109 (1995). Aquatic toxicology: D. P. Kreutzweiser et al., Ecotoxicol. Environ. Saf. 28, 14 (1994). Review of biological activity and use: H. Oberlander et al., Arch. Insect Biochem. Physiol. 28, 209-223 (1995).
Properties: mp 191°. Also reported as mp 186-188° (Sundaram, 1081). Vapor pressure (25°): 3 ′ 10-8 mm Hg. Also reported as vapor pressure (25°): 1.7 ′ 10-6 mm Hg (Sundaram, 415). Soly (25°): 0.83 mg/ml water. Partition coefficient (octanol/water): 32000. LD50 orally in rats, mice: >5000 mg/kg; dermally in rats: >5000 mg/kg; LD50 in honey bees (96 hr, contact): >234 mg/bee; LC50 in mallard duck (8-day dietary): >5000 mg/kg; LC50 in rainbow trout (96 hr): 5.7 mg/l (Heller).
Melting point: mp 191°; mp 186-188° (Sundaram, 1081)
Log P: Partition coefficient (octanol/water): 32000
Toxicity data: LD50 orally in rats, mice: >5000 mg/kg; dermally in rats: >5000 mg/kg; LD50 in honey bees (96 hr, contact): >234 mg/bee; LC50 in mallard duck (8-day dietary): >5000 mg/kg; LC50 in rainbow trout (96 hr): 5.7 mg/l (Heller)
Use: Insecticide.