Date published: 2025-10-16

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Tepraloxydim (CAS 149979-41-9)

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Alternate Names:
trans-2-[1-(3-Chloroallyloxyimino)propyl]-3-hydroxy-5-(tetrahydro-2H-pyran-4-yl)-2-cyclohexen-1-one
CAS Number:
149979-41-9
Molecular Weight:
341.83
Molecular Formula:
C17H24ClNO4
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Tepraloxydim, an herbicide belonging to the cycloxydim family, is widely utilized to effectively control annual and perennial grasses as well as broadleaf weeds in various crops. The broad spectrum of grasses and broadleaf weeds that can be controlled by tepraloxydim has led to its application in both pre- and post-emergence scenarios. Researchers have also investigated its impact on crop yields and its ability to reduce weed populations in diverse cropping systems. Tepraloxydim exerts several biochemical and physiological effects on weeds, such as inhibiting photosynthesis, disrupting cell division, and impeding respiration. Moreover, it has been observed to decrease the production of chlorophyll and other pigments, resulting in leaf yellowing and eventual death. The mode of action of tepraloxydim involves the inhibition of acetolactate synthase (ALS), an enzyme critical for the synthesis of branched-chain amino acids. By disrupting the growth and development of weeds, tepraloxydim effectively leads to their demise.


Tepraloxydim (CAS 149979-41-9) References

  1. Cross-resistance to ACCase inhibitors of Lolium multiflorum, Lolium perenne and Lolium rigidum found in Chile.  |  Michitte, P., et al. 2003. Commun Agric Appl Biol Sci. 68: 397-402. PMID: 15149135
  2. A different mechanism for the inhibition of the carboxyltransferase domain of acetyl-coenzyme A carboxylase by tepraloxydim.  |  Xiang, S., et al. 2009. Proc Natl Acad Sci U S A. 106: 20723-7. PMID: 19926852
  3. Mechanism for the inhibition of the carboxyltransferase domain of acetyl-coenzyme A carboxylase by pinoxaden.  |  Yu, LP., et al. 2010. Proc Natl Acad Sci U S A. 107: 22072-7. PMID: 21135213
  4. A novel W1999S mutation and non-target site resistance impact on acetyl-CoA carboxylase inhibiting herbicides to varying degrees in a UK Lolium multiflorum population.  |  Kaundun, SS., et al. 2013. PLoS One. 8: e58012. PMID: 23469130
  5. Role of a novel I1781T mutation and other mechanisms in conferring resistance to acetyl-CoA carboxylase inhibiting herbicides in a black-grass population.  |  Kaundun, SS., et al. 2013. PLoS One. 8: e69568. PMID: 23936046
  6. Monitoring and risk assessment of tepraloxydim in banana (Musa paradisiaca) and sweet orange (Citrus sinensis).  |  Lim, SJ., et al. 2020. Environ Sci Pollut Res Int. 27: 33882-33889. PMID: 32535830
  7. High-throughput identification of oxidative stress-inducing environmental chemicals in the C. elegans system.  |  Huynh, D. and Wu, CW. 2022. Free Radic Biol Med. 191: 59-65. PMID: 36031165
  8. Determination of herbicide tepraloxydim and main metabolites in drinking water by solid-phase extraction and liquid chromatography with UV detection  |   and P. Sandín-España, J. J. González-Blázquez, J. O. Magrans & J. M. García-Baudín. 2002. Chromatographia. 55: 681–686.
  9. Mechanism of herbicidal activity of a new cyclohexane-1,3-dione, tepraloxydim to Poa annua L.  |   and Akihiro Takahashi, Sigeo Yamada, Katsunori Tanaka. 2002. Weed Biology and Management. 2, 2: 84-91.
  10. Optimization of hydroponic bioassay for herbicide tepraloxydim by using water free from chlorine  |   and P Sandín-España, S Llanos, J O Magrans, J L Alonso-Prados, J M García-Baudín. 2003. Weed Research. 43(6): 451-457.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Tepraloxydim, 100 mg

sc-229357
100 mg
$134.00