Oryzalin

In this article, we will explore in depth the topic of Oryzalin and its impact on contemporary society. Oryzalin has generated a debate between experts and citizens, generating conflicting opinions and questions about its relevance today. Throughout history, Oryzalin has played a fundamental role in different areas, from politics to popular culture, and its influence continues to be palpable on a daily basis. In this sense, it is crucial to analyze in detail the implications of Oryzalin and how its evolution has shaped our way of understanding the world around us. From its origins to its current situation, this article seeks to provide a comprehensive perspective on Oryzalin and its importance in contemporary society.

Oryzalin
Clinical data
ATC code
  • none
Identifiers
  • 4-(Dipropylamino)-3,5-dinitrobenzenesulfonamide
CAS Number
PubChem CID
ChemSpider
UNII
KEGG
CompTox Dashboard (EPA)
ECHA InfoCard100.038.873 Edit this at Wikidata
Chemical and physical data
FormulaC12H18N4O6S
Molar mass346.36 g·mol−1
3D model (JSmol)
Melting point137 to 139 °C (279 to 282 °F)
  • CCCN(CCC)c1c((=O))cc(S(N)(=O)=O)cc1(=O)
  • InChI=1S/C12H18N4O6S/c1-3-5-14(6-4-2)12-10(15(17)18)7-9(23(13,21)22)8-11(12)16(19)20/h7-8H,3-6H2,1-2H3,(H2,13,21,22) ☒N
  • Key:UNAHYJYOSSSJHH-UHFFFAOYSA-N ☒N
 ☒NcheckY (what is this?)  (verify)

Oryzalin is a herbicide of the dinitroaniline class. It acts through the disruption (depolymerization) of microtubules, thus blocking anisotropic growth of plant cells.[1] It can also be used to induce polyploidy in plants as an alternative to colchicine.[2]

References

  1. ^ Taiz L, Zeiger E (2010). Plant Physiology (5th ed.). Sinauer Associates. pp. 433–434. ISBN 978-0-87893-866-7.
  2. ^ Klíma M, Vyvadilová M, Kucera V (January 2008). "Chromosome doubling effects of selected antimitotic agents in Brassica napus microspore culture" (PDF). Czech Journal of Genetics and Plant Breeding. 44 (1): 30–36. doi:10.17221/1328-CJGPB.
  • Oryzalin in the Pesticide Properties DataBase (PPDB)
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