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CAS No 6577-41-9 , Oxapium iodideOxapium iodide

  • Name: Oxapium iodideOxapium iodide
  • Synonyms: Oxapium iodideOxapium iodide;1-[(2-Cyclohexyl-2-phenyl-1,3-dioxolan-4-yl)methyl]-1-methyl-3,4,5,6-tetrahydro-2H-pyridine iodide;
  • CAS Registry Number:
  • Safety Statements: Poison by subcutaneous, intravenous, and intraperitoneal routes. Moderately toxic by ingestion. Experimental reproductive effects. When heated to decomposition it emits toxic fumes of NOx and I−.
  • Molecular Weight: 471.42
  • InChI: InChI=1/C22H34NO2.HI/c1-23(15-9-4-10-16-23)17-21-18-24-22(25-21,19-11-5-2-6-12-19)20-13-7-3-8-14-20;/h2,5-6,11-12,20-21H,3-4,7-10,13-18H2,1H3;1H/q+1;/p-1
  • Molecular Formula: C22H34INO2
  • Molecular Structure:CAS No:6577-41-9 Oxapium iodideOxapium iodide
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6577-41-9 Oxapii iodidum

  • Denmark kemikalieimport [Manufacturers]
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6577-41-9 Oxapii iodidum

  • China innocechem-api [Manufacturers]
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6577-41-9 OXAPIUM IODIDE

  • China Nanjing Chemlin Chemical Industry Co.,Ltd. [Manufacturer]
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References of Oxapium iodideOxapium iodide
Title: Cyclonium Iodide
CAS Registry Number: 6577-41-9
CAS Name: 1-[(2-Cyclohexyl-2-phenyl-1,3-dioxolan-4-yl)methyl]-1-methylpiperidinium iodide
Synonyms: N-methyl-N-[(2-cyclohexyl-2-phenyl-1,3-dioxolan-4-yl)-methyl]piperidinium iodide; 1-(2-phenyl-2-cyclohexyl-1,3-dioxolan-4-yl)methyl-1-methylpiperidinium iodide; ciclonium iodide; oxapium iodide
Manufacturers' Codes: SH-100
Trademarks: Esperan (Toyama)
Molecular Formula: C22H34INO2
Molecular Weight: 471.42
Percent Composition: C 56.05%, H 7.27%, I 26.92%, N 2.97%, O 6.79%
Literature References: Prepn: M. Kimura et al., JP 66 6585 (1966 to Toyama), C.A. 65, 7191 (1966); and separation of isomers: I. Saikawa, JP 70 16475 (1970 to Toyama), C.A. 73, 45355t. Stability studies: Shiuchi, Miyazaki, Bunseki Kagaku 18, 455 (1969), C.A. 71, 74097z (1969). Incompatibility studies: Kunita et al., Yakuzaigaku 28, 84 (1968), C.A. 69, 99335x (1968). Anticholinergic activity and acute toxicity: J. Faff et al., Pol. J. Pharmacol. Pharm. 30, 493 (1978). Review: Jpn. Med. Gaz. 8(9), 11 (1971).
 
Derivative Type: a-Form
Properties: White crystals from monochlorobenzene or isopropyl alcohol, mp 195-197°. Insol in trichloroethylene.
Melting point: mp 195-197°
 
Derivative Type: b-Form
Properties: White crystals from monochlorobenzene, mp 150-152°. Sol in hot trichloroethylene. Both sol in methanol, ethanol, chloroform and tetrachlorethane. Hardly sol in benzene, toluene, xylene and water. LD50 i.p. in mice: 106 mg/kg (Faff).
Melting point: mp 150-152°
Toxicity data: LD50 i.p. in mice: 106 mg/kg (Faff)
 
Therap-Cat: Antispasmodic.
Keywords: Antispasmodic.