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Detail of > 117-96-4

  • MSDS Download
  • CAS Number:
  • 117-96-4
  • Name:
  • Benzoic acid,3,5-bis(acetylamino)-2,4,6-triiodo-

  • Superlist Name:
  • Amidotrizoic acid
  • Formula:
  • C11H9I3N2O4
  • Molecular Structure:
  • Synonyms:
  • Benzoicacid, 3,5-diacetamido-2,4,6-triiodo- (6CI,8CI);2,4,6-Triiodo-3,5-diacetamidobenzoic acid;3,5-Bis(acetylamino)-2,4,6-triiodobenzoicacid;3,5-Diacetamido-2,4,6-triiodobenzoic acid;Diatrizoate;Diatrizoic acid;NSC 262168;Odiston;Urografin acid;Urogranoicacid;Urotrast;
  • Molecular Weight:
  • 613.92
  • EINECS:
  • 204-223-6
  • Density:
  • 2.619 g/cm3
  • Melting Point:
  • >300 °C
  • Boiling Point:
  • 614.1 °C at 760 mmHg
  • Flash Point:
  • 325.2 °C
  • Appearance:
  • White solid
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117-96-4 Amidotrizoic acid

2,4,6-triiodo-3,5-diacetamidobenzoicacid;3,5-bis(acetylamino)-2,4,6-triiodo-benzoicaci;3,5-diacetamido-2,4,6-triiodo-benzoicaci;amidotrizoate;diat;diatriazoate;diatrizoate;diatrizoesaure;odiston;triombrin;urografinacid;urogranoicacid;urotrast;3,5-BIS(ACET
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117-96-4 366J YC
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    Reference

    Alanine aminopeptidase excretion in urine after amidotrizoate administration in diabetics
    Alanine aminopeptidase excretion in urine after amidotrizoate administration in diabetics. Stammberger, K.; Thulin, H.; Schanzenbach, H. (Kliniksanatorium Schielo, Schielo, E. Ger.). Dtsch. Gesundheitswes., 32(12), 542-3 (German) 1977. CODEN: DEGEA3. DOCUMENT TYPE: Journal CA Section: 1 (Pharmacodynamics) Injection of the renal contrast medium amidotrizoate (I) [117-96-4] into patients with diabetic nephropathy caused a greater increase in alanine aminopeptidase [54465-38-2] activity in the urine than in healthy subjects or diabetics without nephropathy.
    Some organic acids attenuate the effects of furosemide on the endocochlear potential
    Some organic acids attenuate the effects of furosemide on the endocochlear potential. Rybak, Leonard P.; Whitworth, Craig (Sch. Med., SIU, Springfield, IL 62708, USA). Hear. Res., 26(1), 89-93 (English) 1987. CODEN: HERED3. ISSN: 0378-5955. DOCUMENT TYPE: Journal CA Section: 1 (Pharmacology) A series of org. acid transport inhibitors reduced the endocochlear potential (EP) decline produced by furosemide [54-31-9] in the chinchilla. Probenecid [57-66-9], salicylate [69-72-7] and penicillin G [61-33-6] were much more effective than novobiocin [303-81-1], meclofenamate [644-62-2], or diatrizoate [117-96-4]. Inhibitors of org.There are some commonly used reagents with their cas registry numbers 114-33-0 and 644-62-2 in this article. base transport, choline [62-49-7], and N-Me nicotinamide [114-33-0] had no effect on the furosemide-induced drop of the EP. These findings suggest that at least part of furosemide ototoxicity may be mediated by org. acid transport. .

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