Date published: 2026-5-4

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Monolinuron (CAS 1746-81-2)

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CAS Number:
1746-81-2
Molecular Weight:
214.65
Molecular Formula:
C9H11ClN2O2
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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Monolinuron, belonging to the urea family, functions as a non-selective herbicide and has found diverse applications in agriculture, forestry, and horticulture. This versatile compound serves as a herbicide for weed control, a fungicide to combat fungal diseases, and an insecticide for insect control. Additionally, it plays a role in plant physiology research, enabling the study of plant responses to environmental stresses. Moreover, monolinuron contributes to investigations related to plant metabolism and the regulation of plant growth.


Monolinuron (CAS 1746-81-2) References

  1. Application of solid-phase extraction and micellar electrokinetic capillary chromatography to the study of hydrolytic and photolytic degradation of phenoxy acid and phenylurea herbicides.  |  Farran, A. and Ruiz, S. 2004. J Chromatogr A. 1024: 267-74. PMID: 14753728
  2. Analysis of phenylurea herbicides from plants by GC/MS.  |  Peña, F., et al. 2002. Talanta. 56: 727-34. PMID: 18968549
  3. Efficient biotransformation of herbicide diuron by bacterial strain Micrococcus sp. PS-1.  |  Sharma, P., et al. 2010. Biodegradation. 21: 979-87. PMID: 20401520
  4. Ultrasonic nebulization extraction coupled with headspace hollow fiber microextraction of pesticides from root of Panax ginseng C.A. Mey.  |  Li, X., et al. 2011. J Sep Sci. 34: 1582-9. PMID: 21626693
  5. Assessment of the leaching potential of 12 substituted phenylurea herbicides in two agricultural soils under laboratory conditions.  |  Navarro, S., et al. 2012. J Agric Food Chem. 60: 5279-86. PMID: 22578198
  6. Application of various methods to determine the lipophilicity parameters of the selected urea pesticides as predictors of their bioaccumulation.  |  Dołowy, M., et al. 2014. J Environ Sci Health B. 49: 730-7. PMID: 25065824
  7. Simultaneous determination of phenylurea herbicides in yam by capillary electrophoresis with electrochemiluminescence detection.  |  Hu, Y. 2015. J Chromatogr B Analyt Technol Biomed Life Sci. 986-987: 143-8. PMID: 25732033
  8. Preparation of a magnetic porous organic polymer for the efficient extraction of phenylurea herbicides.  |  Wang, J., et al. 2017. J Chromatogr A. 1519: 19-27. PMID: 28888678
  9. Use of a hypercrosslinked triphenylamine polymer as an efficient adsorbent for the enrichment of phenylurea herbicides.  |  Liang, X., et al. 2018. J Chromatogr A. 1538: 1-7. PMID: 29397984
  10. Solid phase extraction of pesticides from environmental waters using an MSU-1 mesoporous material and determination by UPLC-MS/MS.  |  Kharbouche, L., et al. 2019. Talanta. 199: 612-619. PMID: 30952305
  11. Facile synthesis of conjugated microporous polymer with spherical structure for solid phase extraction of phenyl urea herbicides.  |  Guo, Y., et al. 2020. J Chromatogr A. 1622: 461131. PMID: 32381301
  12. High sensitivity on-site early warning system monitoring of pesticides by photo-induced fluorescence.  |  Diop, NA., et al. 2023. Anal Chim Acta. 1250: 340969. PMID: 36898818
  13. Absorptiometric determination of monolinuron in herbicide formulations.  |  Yuen, SH. 1970. Analyst. 95: 408-10. PMID: 5440165
  14. Methemoglobinemia following ingestion of a monolinuron/paraquat herbicide (Gramonol).  |  Casey, PB., et al. 1994. J Toxicol Clin Toxicol. 32: 185-9. PMID: 8024655

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Monolinuron, 250 mg

sc-228613
250 mg
$43.00