Molecular structure of Fosthiazate, CAS Number: 98886-44-3
Fosthiazate (CAS 98886-44-3)
Alternate Names:
O-Ethyl S-(1-methylpropyl) 2-oxo-3-thiazolidinylphosphonothioate; S-sec-Butyl O-ethyl 2-oxo-3-thiazolidinylphosphonothioate
Application:
Fosthiazate is used for chemical synthesis
CAS Number:
98886-44-3
Molecular Weight:
283.35
Molecular Formula:
C9H18NO3PS2
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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SDS & Certificate of Analysis
Fosthiazate is used for chemical synthesis. Fosthiazate is an analytical method utilized to detect the presence of pesticides and other organic compounds in water. Furthermore, it exhibits a synergistic effect when combined with pesticides like chlorpyrifos, dichlorvos, or fumigants. Fosthiazate has demonstrated its efficacy as both a nematicide and a fatty acid inhibitor of plant growth. As a non-fumigant, organophosphate nematicide, it displays a broad-spectrum activity against various plant parasitic nematodes, including Meloidogyne spp., Globodera spp., and Pratylenchus spp.
Fosthiazate (CAS 98886-44-3) References
- Degradation and adsorption of fosthiazate in soil. | Qin, S., et al. 2004. J Agric Food Chem. 52: 6239-42. PMID: 15453693
- Influence of soil physicochemical and biological properties on the degradation and adsorption of the nematicide fosthiazate. | Pantelelis, I., et al. 2006. J Agric Food Chem. 54: 6783-9. PMID: 16939340
- Leaching of the organophosphorus nematicide fosthiazate. | Karpouzas, DG., et al. 2007. Chemosphere. 68: 1359-64. PMID: 17316750
- Stereoisomeric separation and toxicity of the nematicide fosthiazate. | Lin, K., et al. 2007. Environ Toxicol Chem. 26: 2339-44. PMID: 17941748
- Fosthiazate Controls Meloidogyne arenaria and M. incognita in Flue-Cured Tobacco. | Pullen, MP. and Fortnum, BA. 1999. J Nematol. 31: 694-9. PMID: 19270938
- Residues and dissipation dynamics of fosthiazate in tomato and soil. | Wu, J., et al. 2012. Bull Environ Contam Toxicol. 89: 664-8. PMID: 22801926
- Effective removal of nemacide fosthiazate from an aqueous solution using zero-valent iron. | Wu, J., et al. 2015. J Environ Manage. 161: 11-20. PMID: 26143081
- Isolation and characterization of soil bacteria able to rapidly degrade the organophosphorus nematicide fosthiazate. | Lagos, S., et al. 2019. Lett Appl Microbiol. 68: 149-155. PMID: 30444532
- Nematicidal Activity of Fosthiazate Against Soybean Cyst Nematode Heterodera glycines. | Wu, HY., et al. 2019. J Nematol. 51: 1-9. PMID: 31088033
- Cocktail Therapy of Fosthiazate and Cupric-Ammoniun Complex for Citrus Huanglongbing. | Duan, J., et al. 2021. Front Plant Sci. 12: 643971. PMID: 33868341
- Dissipation and residue of fosthiazate in tomato and cherry tomato and a risk assessment of dietary intake. | Lin, S., et al. 2022. Environ Sci Pollut Res Int. 29: 9248-9256. PMID: 34505248
- Fosthiazate exposure induces oxidative stress, nerve damage, and reproductive disorders in nontarget nematodes. | Liu, S., et al. 2023. Environ Sci Pollut Res Int. 30: 12522-12531. PMID: 36112285
- Fosthiazate inhibits root-knot disease and alters rhizosphere microbiome of Cucumis melo var. saccharinus. | Wang, H., et al. 2022. Front Microbiol. 13: 1084010. PMID: 36687623
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Fosthiazate, 50 mg | sc-228230 | 50 mg | $375.00 |