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CAS No 63-25-2 , naphthalen-1-yl N-methylcarbamate

  • Name: naphthalen-1-yl N-methylcarbamate
  • Synonyms: methylcarbamate; Carylderm; Carbavur; Caprolin;naphthalen-1-yl N-methylcarbamate; 1-Naphthyl N-methylcarbamate; 1-Naphthalenol;Carbaril; Carbatox; Sevin;
  • CAS Registry Number:
  • Transport: UN 2757
  • Melting Point: 142 ºC
  • Flash Point: 202.7 ºC
  • Boiling Point: 315 ºC
  • Density: 1.183 g/cm3
  • Safety Statements: R22;R40;R50
  • Hazard Symbols: Xn: Harmful;N: Dangerous for the environment;
  • Flash Point: 202.7 ºC
  • EINECS: 200-555-0
  • Molecular Weight: 201.22124
  • InchiKey: CVXBEEMKQHEXEN-UHFFFAOYSA-N
  • InChI: InChI=1S/C12H11NO2/c1-13-12(14)15-11-8-4-6-9-5-2-3-7-10(9)11/h2-8H,1H3,
    (H,13,14)
  • Risk Statements: S2;S22;S24;S36/37;S46;S61
  • Molecular Formula: C12H11NO2
  • Molecular Structure:CAS No:63-25-2 naphthalen-1-yl N-methylcarbamate

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63-25-2 CARBARYL

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63-25-2 carbaryl

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63-25-2 Carbaryl

  • IUPAC NAME-1-naphthyl methylcarbamate MOLECULAR FORMULA-C12H11NO2 MOLAR MASS-201.22 g mol?1 Carbaryl is a chemical in the carbamate family used chiefly as an insecticideThe development of the carbamate insecticides has been called a major breakthroug...
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63-25-2 3329.12-100 CARBARYL

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63-25-2 Carbaryl

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References of naphthalen-1-yl N-methylcarbamate
Title: Carbaryl
CAS Registry Number: 63-25-2
CAS Name: 1-Naphthalenol methylcarbamate
Synonyms: methyl carbamic acid 1-naphthyl ester; 1-naphthyl N-methylcarbamate
Manufacturers' Codes: ENT-23969; OMS-29; UC-7744
Trademarks: Carylderm (Mundipharma); Derbac (Mundipharma); Ravyon (Bayer CropSci.); Sevin (Bayer CropSci.)
Molecular Formula: C12H11NO2
Molecular Weight: 201.22
Percent Composition: C 71.63%, H 5.51%, N 6.96%, O 15.90%
Literature References: Cholinesterase inhibitor. Prepn and description: Haynes et al., Contrib. Boyce Thompson Inst. 18, 507 (1957); Lambrech, US 2903478 (1959 to Union Carbide). Metabolism: W. E. Whitehurst et al., J. Agric. Food Chem. 11, 167 (1963); J. B. Houston et al., Xenobiotica 5, 637 (1975). Degradation: D. G. Crosby et al., J. Agric. Food Chem. 13, 204 (1965); D. L. Heywood, Environ. Qual. Saf. 4, 128 (1975). Toxicology: I. Nisbet, D. Miner, Environment 13, 10 (1971). Toxicity: M. Vandekar et al., Bull. WHO 44, 241 (1971). Clinical trial in pediculosis: J. W. Maunder, Clin. Exp. Dermatol. 6, 605 (1981). Review: Carbamate Insecticides: Chemistry, Biochemistry and Toxicology, R. J. Kuhr, H. W. Dorough, Eds. (CRC Press, Cleveland, 1976) 301 pp.
Properties: Crystals, mp 142°. d2020 1.232. Moderately sol in DMF, acetone, isophorone, cyclohexanone. Soly in water at 30°: 120 mg/l. Vapor pressure at 25°: <4 ′ 10-5 mm Hg. Stable to heat, light, acids; hydrolyzed in alkalies; noncorrosive. LD50 orally in rats: 250 mg/kg (Vandekar).
Melting point: mp 142°
Density: d2020 1.232
Toxicity data: LD50 orally in rats: 250 mg/kg (Vandekar)
CAUTION: Potential symptoms of overexposure are skin irritation; miosis, blurred vision, tearing; rhinorrhea, excessive salivation, sweating; abdominal cramps, nausea, vomiting, diarrhea; tremor, muscle twitching, slurred speech; cyanosis, convulsions; coma, respiratory failure; possible reproductive effects. See NIOSH Pocket Guide to Chemical Hazards (DHHS/NIOSH 97-140, 1997) p 50; Clinical Toxicology of Commercial Products, R. E. Gosselin et al., Eds. (Williams & Wilkins, Baltimore, 5th ed., 1984) Section II p 305, Section III, pp 86-90.
Use: Contact insecticide.
Therap-Cat: Ectoparasiticide.
Therap-Cat-Vet: Ectoparasiticide.
Keywords: Ectoparasiticide.