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CAS No 40596-69-8 , Methoprene

  • Name: Methoprene
  • Synonyms: ALTOSID(R); altosidigr; 2,4-dodecadienoicacid,11-methoxy-3,7,11-trimethyl-,1-methylethylester,(e,e; dianex; kabat; ent70460; METHOPRENE (TM); manta; ISOPROPYL (2E,4E)-11-METHOXY-3,7,11-TRIMETHYL-2,4-DODECADIENOATE;Methoprene; METHOPRENE; diacon; minex; 11-METHOXY-3,7,11-TRIMETHYL-2E,4E-DODECADIENOIC ACID, ISOPROPYL ESTER; oms1697; PRECOR; ZR-515; altosidsr10; altosid; pharoid; apex;
  • CAS Registry Number:
  • Transport: UN3082 9/PG 3
  • Melting Point: 164
  • Flash Point: 56
  • Boiling Point: 135 - 136 at 0.06 mm Hg
  • Density: 0.9261
  • Refractive index: 1.462
  • Water Solubility: Miscible
  • Safety Statements: Moderately toxic by skin contact. Mildly toxic by ingestion. Mutation data reported. When heated to decomposition it emits acrid smoke and fumes.
  • Hazard Symbols: Xi: Irritant;N: Dangerous for the environment;
  • Flash Point: 56
  • EINECS: 254-993-2
  • Molecular Weight: 310.47
  • InChI: InChI=1/C19H34O3/c1-15(2)22-18(20)14-17(4)11-8-10-16(3)12-9-13-19(5,6)21-7/h8,11,14-16H,9-10,12-13H2,1-7H3/b11-8+,17-14+
  • Risk Statements: 36/37/38-51/53
  • Molecular Formula: C19H34O3
  • Molecular Structure:CAS No:40596-69-8 Methoprene

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40596-69-8 11-METHOXY-3,7-11-TRIMETHYL-2,4-DODECADIENOIC ACID ISOPROPYL ESTER

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40596-69-8 Methoprene

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40596-69-8 Methoprene

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40596-69-8 METHOPRENE

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40596-69-8 Methoprene

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References of Methoprene
Title: Methoprene
CAS Registry Number: 40596-69-8
CAS Name: (2E,4E)-11-Methoxy-3,7,11-trimethyl-2,4-dodecadienoic acid 1-methylethyl ester
Synonyms: isopropyl (2E,4E,7RS)-11-methoxy-3,7,11-trimethyl-2,4-dodecadienoate
Manufacturers' Codes: ZR-515
Molecular Formula: C19H34O3
Molecular Weight: 310.47
Percent Composition: C 73.50%, H 11.04%, O 15.46%
Literature References: Juvenile hormone mimic. Prepn: BE 778242; see also C. A. Henrick, US 3818047 (1972, 1974 both to Zoecon); idem et al., J. Org. Chem. 40, 1 (1975); L. Novák et al., Ann. 1982, 1173. Effect on mustard aphid: P. J. Rup, R. K. Gill, Insect Sci. Applic. 14, 173 (1993). Field trial in a saltwater marsh against mosquitoes: V. L. Kramer et al., J. Am. Mosq. Control Assoc. 9, 127 (1993). Mechanism of action study: E. M. Berger et al., Dev. Biol. 151, 410 (1992). HPLC determn in tobacco: S. S. Yang, Chromatographia 33, 309 (1992). GC determn in aquatic microcosms: D. H. Ross et al., J. Am. Mosq. Control Assoc. 10, 202 (1994). Impact on the fathead minnow: idem et al., ibid. 211. Review of properties, metabolism, toxicology, and use: J. B. Siddall, Environ. Health Perspect. 14, 119-126 (1976). Review of analytical methods: L. L. Dunham, W. W. Miller in Analytical Methods for Pesticides and Plant Growth Regulators vol. X, G. Zweig, Ed. (Academic Press, New York, 1978) pp 95-109.
Properties: Amber liquid, bp0.06 135-136°. d20 0.9261 g/ml. Vapor pressure at 25°: 2.37 ′ 10-5 mm Hg. Soly in water at 25°: 1.39 ppm. Sol in org solvents. Temperature stable up to at least 42° for 24 months. Stable in water, org solvents, and in the presence of dil alkali and acid. LD50 orally in rats: >34500 mg/kg (Siddall).
Boiling point: bp0.06 135-136°
Density: d20 0.9261 g/ml
Toxicity data: LD50 orally in rats: >34500 mg/kg (Siddall)
 
Derivative Type: (7S)-Form
CAS Registry Number: 65733-16-6
Synonyms: S-Methoprene
Manufacturers' Codes: ZR-2458
Trademarks: Altosid (Wellmark); Precor (Wellmark); Extinguish (Wellmark); Pharorid (Wellmark)
 
Use: Insecticide; insect growth regulator.
Therap-Cat-Vet: Ectoparasiticide.