Alloxan tetrahydrate

For research use only. Not for therapeutic Use.

  • CAT Number: I021793
  • CAS Number: 6010-91-9
  • Molecular Formula: C4H10N2O8
  • Molecular Weight: 214.13
  • Purity: 98%
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Alloxan tetrahydrate (CAT: I021793) is an acidic compound resulting from the oxidation of uric acid. This compound is known for its ability to induce diabetes in experimental animals by damaging insulin-producing pancreatic beta cells. Alloxan selectively targets these cells due to their high sensitivity to oxidative stress, resulting in a reduction in insulin secretion and the development of diabetes-like symptoms. Its application in inducing diabetes in research models underscores its importance in the study of diabetes pathogenesis and potential therapeutic interventions.


Catalog Number I021793
CAS Number 6010-91-9
Synonyms

Alloxan tetrahydrate; Mesoxalylurea tetrahydrate

Molecular Formula C4H10N2O8
Purity 98%
Solubility To be determined
Appearance Solid powder
Storage Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years).
IUPAC Name 2,4,6(1H,3H,5H)-Pyrimidinetrione, 5,5-dihydroxy-, hydrate (1:3)
InChI InChI=1S/C4H4N2O5.3H2O/c7-1-4(10,11)2(8)6-3(9)5-1;;;/h10-11H,(H2,5,6,7,8,9);3*1H2
InChIKey PBPLAJFENFYAFN-UHFFFAOYSA-N
SMILES O.O.O.OC1(O)C(=O)NC(=O)NC1=O
Reference

1: Lin H, Zheng M, Mao X, Feng X, Li J, Rao G, Lin F. Oxytocin treatment prevents marrow adiposity observed in alloxan-induced diabetic rabbits using proton MR spectroscopy. Endokrynol Pol. 2018 Jun 28. doi: 10.5603/EP.a2018.0040. [Epub ahead of print] PubMed PMID: 29952410.
2: Kato Y, Masago Y, Kondo C, Yogo E, Torii M, Hishikawa A, Izawa T, Kuwamura M, Yamate J. Comparison of Acute Gene Expression Profiles of Islet Cells Obtained via Laser Capture Microdissection between Alloxan- and Streptozotocin-treated Rats. Toxicol Pathol. 2018 Jan 1:192623318783957. doi: 10.1177/0192623318783957. [Epub ahead of print] PubMed PMID: 29929439.

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