Date published: 2026-5-5

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Tridemorph (CAS 24602-86-6)

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CAS Number:
24602-86-6
Molecular Weight:
297.52
Molecular Formula:
C19H39NO
Supplemental Information:
This is classified as a Dangerous Good for transport and may be subject to additional shipping charges.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Tridemorph, belongs to the phenylpyrrole family of fungicides, which includes trifloxystrobin and pyraclostrobin among others. With its wide-ranging effectiveness, Tridemorph has found utility in various agricultural, horticultural, and forestry applications for combating diverse fungal diseases. Extensive scientific research has been conducted on Tridemorph, exploring its diverse uses. It has proven effective in managing fungal diseases in plants, protecting seeds against fungal infections, and combating root diseases in soil. The mode of action of Tridemorph involves the disruption of fungal cell membranes, resulting in cell death. By binding to the cell membrane, it inhibits the activity of enzymes responsible for synthesizing essential components like proteins and lipids. This interference in cell membrane integrity leads to the demise of the fungal cells.


Tridemorph (CAS 24602-86-6) References

  1. Antimicrobial activity of o-carboranylalanine.  |  Oros, G., et al. 1999. Amino Acids. 17: 357-68. PMID: 10707765
  2. [Effect of tridemorph on Torulopsis candida Berlese].  |  Bergmann, H. 1979. Z Allg Mikrobiol. 19: 155-62. PMID: 117646
  3. Plasma Membrane Sterols Are Essential for Sensing Osmotic Changes in the Halotolerant Alga Dunaliella.  |  Zelazny, AM., et al. 1995. Plant Physiol. 109: 1395-1403. PMID: 12228675
  4. Determination of tridemorph and other fungicide residues in fruit samples by liquid chromatography-electrospray tandem mass spectrometry.  |  Zamora, T., et al. 2004. J Chromatogr A. 1045: 137-43. PMID: 15378888
  5. Manipulation by tridemorph, a systemic fungicide, of the sterol composition of maize leaves and roots.  |  Bladocha, M. and Benveniste, P. 1983. Plant Physiol. 71: 756-62. PMID: 16662902
  6. Stereochemical aspects of the biosynthesis of the side chain of 9beta, 19-cyclopropyl sterols in maize seedlings treated with tridemorph.  |  Bladocha, M. and Benveniste, P. 1985. Plant Physiol. 79: 1098-106. PMID: 16664538
  7. Effect of the fungicides tridemorph and vinclozolin on soil microorganisms and nitrogen metabolism.  |  Banerjee, A. and Banerjee, AK. 1991. Folia Microbiol (Praha). 36: 567-71. PMID: 1841872
  8. [The systemic fungicide tridermorph as an inhibitor of the respiratory chain of electron transfer particles from beef heart mitochondria].  |  Müller, W. and Schewe, T. 1976. Acta Biol Med Ger. 35: 693-707. PMID: 185865
  9. Physiological effects of fenpropimorph on wild-type Saccharomyces cerevisiae and fenpropimorph-resistant mutants.  |  Lorenz, RT. and Parks, LW. 1991. Antimicrob Agents Chemother. 35: 1532-7. PMID: 1929324
  10. Residual behavior and risk assessment of tridemorph in banana conditions.  |  Wang, S., et al. 2018. Food Chem. 244: 71-74. PMID: 29120807
  11. The action of the systemic fungicides tridemorph and fenpropimorph on sterol biosynthesis by the soil amoeba Acanthamoeba polyphaga.  |  Raederstorff, D. and Rohmer, M. 1987. Eur J Biochem. 164: 421-6. PMID: 3569273
  12. An embryotoxicity study of the fungicide tridemorph and its commercial formulation Calixin.  |  Merkle, J., et al. 1984. Teratology. 29: 259-69. PMID: 6740510
  13. Effects of the fungicide tridemorph on mitosis in Allium cepa.  |  Cortés, F., et al. 1982. Cytobios. 34: 181-90. PMID: 7172757

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Tridemorph, 100 mg

sc-229566
100 mg
$104.00