Molecular structure of Cycloate, CAS Number: 1134-23-2
Cycloate (CAS 1134-23-2)
Alternate Names:
S-Ethyl N-cyclohexyl-N-ethylthiocarbamate
CAS Number:
1134-23-2
Molecular Weight:
215.36
Molecular Formula:
C11H21NOS
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
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Cycloate, a thiocarbamate herbicide, acts as a lipid biosynthesis inhibitor, making it effective in managing annual grass weeds, perennial grasses, and annual broad-leaved weeds in crops such as spinach, sugar beet, fodder beet, and beetroot. It serves as the active ingredient in several herbicide formulations. Notably, unlike some other herbicides, cycloate has been classified by the United States Environmental Protection Agency as "not likely to be a carcinogen to humans."
Cycloate (CAS 1134-23-2) References
- Neuropathological studies on cycloate-induced neuronal cell death in the rat brain. | Simpson, MG., et al. 2005. Neurotoxicology. 26: 125-32. PMID: 15527880
- Effects of cycloate on development of Heterodera schachtii and growth of three Beta species. | Abivardi, C. and Altman, J. 1978. J Nematol. 10: 90-4. PMID: 19305818
- Cycloate, an inhibitor of fatty acid elongase, modulates the metabolism of very-long-side-chain alkylresorcinols in rye seedlings. | Magnucka, EG., et al. 2009. Pest Manag Sci. 65: 1065-70. PMID: 19479950
- Community air monitoring for pesticides-part 2: multiresidue determination of pesticides in air by gas chromatography, gas chromatography-mass spectrometry, and liquid chromatography-mass spectrometry. | Hengel, M. and Lee, P. 2014. Environ Monit Assess. 186: 1343-53. PMID: 24370860
- Cis-vaccenic acid induces differentiation and up-regulates gamma globin synthesis in K562, JK1 and transgenic mice erythroid progenitor stem cells. | Aimola, IA., et al. 2016. Eur J Pharmacol. 776: 9-18. PMID: 26879870
- The impairment of mobility and development in freshwater snails (Physa fontinalis and Lymnaea stagnalis) caused by herbicides. | Kosanke, GJ., et al. 1988. Comp Biochem Physiol C Comp Pharmacol Toxicol. 90: 373-9. PMID: 2902998
- Effects of Industrial Processing on Pesticide Multiresidues Transfer from Raw Tomatoes to Processed Products. | Corrias, F., et al. 2020. Foods. 9: PMID: 33086739
- Determination of more than 500 Pesticide Residues in Hen Eggs by Liquid Chromatography-Tandem Mass Spectrometry (LC-MS/MS) and Gas Chromatography-Tandem Mass Spectrometry (GC/MS/MS). | Golge, O., et al. 2021. Food Sci Anim Resour. 41: 816-825. PMID: 34632401
- Pesticides in ambient air, influenced by surrounding land use and weather, pose a potential threat to biodiversity and humans. | Zaller, JG., et al. 2022. Sci Total Environ. 838: 156012. PMID: 35597361
- Rapid Screening of 352 Pesticide Residues in Chrysanthemum Flower by Gas Chromatography Coupled to Quadrupole-Orbitrap Mass Spectrometry with Sin-QuEChERS Nanocolumn Extraction. | Wang, Y., et al. 2022. J Anal Methods Chem. 2022: 7684432. PMID: 35757318
- Ocean current redistributed the currently using Organoamine Pesticides in Arctic summer water. | Ding, Y., et al. 2023. Sci Total Environ. 886: 163979. PMID: 37164088
- Cometabolism of low concentrations of propachlor, alachlor, and cycloate in sewage and lake water. | Novick, NJ. and Alexander, M. 1985. Appl Environ Microbiol. 49: 737-43. PMID: 4004208
- Residues of cycloate and influence of herbicides on some of nutritional factors in spinach. | Czapski, J., et al. 1983. J Environ Sci Health B. 18: 497-503. PMID: 6630897
- Aldehyde dehydrogenase of mice inhibited by thiocarbamate herbicides. | Quistad, GB., et al. 1994. Life Sci. 55: 1537-44. PMID: 7968224
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Cycloate, 250 mg | sc-239601 | 250 mg | $67.00 |