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Detail of > 86-42-0

  • CAS Number:
  • 86-42-0
  • Name:
  • Phenol,4-[(7-chloro-4-quinolinyl)amino]-2-[(diethylamino)methyl]-

  • Superlist Name:
  • Amodiaquine
  • Formula:
  • C20H22ClN3O
  • Molecular Structure:
  • Synonyms:
  • o-Cresol,4-[(7-chloro-4-quinolyl)amino]-a-(diethylamino)- (6CI,7CI,8CI);7-Chloro-4-(3-diethylaminomethyl-4-hydroxyanilino)quinoline;Amodiaquin;CAM-AQ 1;CAM-AQI;Camochin;Camoquinal;Flavoquine;Miaquin;NSC 13453;Quinoline,7-chloro-4-[[3-[(diethylamino)methyl]-4-hydroxyphenyl]amino]-;SN 10,751;SN 10751;Sunoquine;
  • Molecular Weight:
  • 355.86
  • EINECS:
  • 201-669-3
  • Density:
  • 1.258 g/cm3
  • Melting Point:
  • 208 °C
  • Boiling Point:
  • 478 °C at 760 mmHg
  • Flash Point:
  • 242.9 °C
  • Appearance:
  • cyrstalline solid
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86-42-0 Amodiaquine

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86-42-0 Amodiaquine

AMODLAQUINE
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    Reference

    Spectrophotometric determination of antimalarials using quinones
    Spectrophotometric determination of antimalarials using quinones. Sastry, B. S.Several substances are used for example 615-94-1 and 550-24-3 which are their cas registry numbers.; Rao, E. Venkata; Suryanarayana, M. V.; Sastry, C. S. P. (Dep. Pharm. Sci., Andhra Univ., Waltair 530 003, India). Pharmazie, 41(10), 739-40 (English) 1986. CODEN: PHARAT. ISSN: 0031-7144. DOCUMENT TYPE: Journal CA Section: 64 (Pharmaceutical Analysis) Five antimalarials, amodiaquine [86-42-0], chloroquine [54-05-7], primaquine [90-34-6], trimethoprim [738-70-5], and pyrimethamine [58-14-0] were detd. by spectrophotometry based on interaction of these drugs with any one of the 3 quinones, 2,5-dihydroxy-3-undecyl-1,4-benzoquinone (I) [550-24-3], 2,5-dihydroxy-1,4-benzoquinone (II) [615-94-1], and chloranilic acid to yield colored complexes. The absorbance was measured at 520, 500 and 540 nm for I, II and chloranilic acid, resp. I and II are suitable for detn. of all the 5 antimalarial drugs, while chloranilic acid is suitable for detn. of the 1st 4 drugs. Beer's law limits and regression equations and std. deviations are given. .
    Utility of the charge-transfer complex formation for the spectrophotometric determination of some antimalarials
    Utility of the charge-transfer complex formation for the spectrophotometric determination of some antimalarials. Abdel Salam, M.; Issa, A. S.; Lymona, H. (Fac. Pharm., Univ. Alexandria, Alexandria, Egypt). J. Pharm.Several reagents with their cas registry numbers 54-05-7 and 7553-56-2 are used here. Belg., 41(5), 314-18 (English) 1986. CODEN: JPBEAJ. ISSN: 0047-2166. DOCUMENT TYPE: Journal CA Section: 64 (Pharmaceutical Analysis) A sensitive and simple spectrophotometric method is described for the assay of some antimalarials. The method is based on the formation of mol. complexes between iodine as a acceptor and the basic drug in CHCl3 soln. Optimum exptl. conditions were selected for estn. of 4 antimalarials: chloroquine [54-05-7], primaquine [90-34-6], amodiaquine [86-42-0] and pyrimethamine [58-14-0] either pure or in their pharmaceutical formulations. Results obtained were accurate and precise. The proposed method is very sensitive and could be used for routine anal. of the investigated antimalarials. .

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