3,8-Diamino-ethyl-6-phenylphenanthridinium bromide - Synonyme de

Numéro CAS : 1239-45-8

  • Fiche complète
  • PMSD
  • SIMDUT
  • Résumé

Identification

Description


Formule moléculaire brute : C21H20BrN3

Principaux synonymes

Noms français :

  • Bromure d'homidium
  • Bromure d'éthidium
  • Bromure de diamino-3,8 éthyl-5 phényl-6 phénanthridinium
  • Éthidium, bromure de

Noms anglais :

  • 2,7-Diamino-10-ehtyl-9-phenylphenanthridinium bromide
  • 2,7-Diamino-9-phenyl-10-ethylphenanthridinium bromide
  • 2,7-Diamino-9-phenylphenanthridine ethobromide
  • 3,8-Diamino-ethyl-6-phenylphenanthridinium bromide
  • Ethidium bromide
  • Homidium bromide
Utilisation et sources d'émission

Médicament pour usage vétérinaire

Références

  • ▲1.  O’Neil, M.J., Smith, A. et Heckelman, P.E., The Merck index : an encyclopedia of chemicals, drugs, and biologicals. 13th ed. Cambridge, MA : Cambridge Soft; Merck & CO. (2001). [RM-403001]
  • ▲2.  France. Institut national de recherche et de sécurité, Fiche toxicologique no 236 : Bromure d'éthidium. Cahiers de notes documentaires. Paris : INRS. (2010). [RE-005509]   http://www.inrs.fr/publications/bdd/fichetox.html
    http://www.inrs.fr/publications/bdd/fichetox/fiche.html?refINRS=FICHETOX_236
  • ▲3.  Joint WHO/FAO Expert Committee on Food Additives (JECFA ), «Isometamidium (20438-03-3).» In: WHO food additives series. Vol. 25. Genève : World Health Organization ; International Programme on Chemical Safety. (1990).   http://www.inchem.org/documents/jecfa/jecmono/v25je10.htm
  • ▲4.  National Toxicology Program, Nomination Background: Ethidium bromide (CASRN: 1239-45-8). (1994).   https://ntp.niehs.nih.gov/ntp/htdocs/chem_background/exsumpdf/ethidiumbromide_508.pdf
  • ▲5.  Gupta R.S. et Singh B., «Mutagenic Responses of Five Independent Genetic Loci in CHO Cells to a Variety of Mutagens.» Mutation Research. Vol. 94, p. 449-466. (1982). [AP-035725]
  • ▲6.  Oberly T.J., Bewsey B.J. et Probst G.S., «An Evaluation of the L5178Y TK +/- Mouse Lymphoma Forward Mutation Assay Using 42 Chemicals.» Mutation Research. Vol. 125, p. 291-306. (1984). [AP-034388]
  • ▲7.  Rogers A.M. et Back K.C., «Comparative Mutagenicity of 4 DNA-Intercalating Agents in L5178Y Mouse Lymphoma Cells.» Mutation Research. Vol. 102, p. 447-455. (1982).
  • ▲8.  Belyaev, I.Y. et al., «Effets of ethidium bromide on DNA loop organisation in human lymphocyte measured by anomalous viscosity time dependance and single cell gel electrophoresis.» Biochimica et Biocphysica Acta (BBA)-General Subjects. Vol. 1428, no. 2-3, p. 348-356. (1999).   https://www.sciencedirect.com/science/article/pii/S0304416599000768
  • ▲9.  Shubber, E.K., Kram, D. et Williams, J., «In vitro assay of cytogenetic damage induced in bone marrow cells in vivo by chemical carcinogens.» Japanese journal of medical science and biology. Vol. 38, no. 5-6, p. 207-216. (Oct.-Dec. 1985). [AP-001153]   https://www.jstage.jst.go.jp/article/yoken1952/38/5-6/38_5-6_207/_pdf/-char/ja
  • ▲10.  National Library of Medicine, The Hazardous Substances Data Bank (HSDB). Hamilton (Ont.) : Canadian Centre for Occupational Health and Safety.   http://www.ccohs.ca/

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