Molecular structure of Sulprofos, CAS Number: 35400-43-2
Sulprofos (CAS 35400-43-2)
Alternate Names:
Mercaprofos
CAS Number:
35400-43-2
Molecular Weight:
322.45
Molecular Formula:
C12H19O2PS3
Supplemental Information:
This is 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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Sulprofos is an extensively utilized organophosphate insecticide. It has played a role in various scientific research endeavors. It has been employed to investigate the impact of insecticides on diverse pest populations. Additionally, it has been utilized to examine the effects of insecticides on both plants and animals. Furthermore, its environmental effects have been subjects of scientific inquiry. The mechanism of action of Sulprofos centers around the inhibition of the enzyme acetylcholinesterase, responsible for the breakdown of the neurotransmitter acetylcholine. By impeding this enzymatic activity, Sulprofos interferes with the normal transmission of nerve impulses, resulting in the accumulation of acetylcholine within the nervous system.
Sulprofos (CAS 35400-43-2) References
- Evaluation of peracid activated organophosphates in studies of insecticide resistance conferred by insensitive acetylcholinesterases. | Byrne, FJ. and Toscano, NC. 2002. J Econ Entomol. 95: 425-9. PMID: 12020023
- In vitro sulfoxidation of thioether compounds by human cytochrome P450 and flavin-containing monooxygenase isoforms with particular reference to the CYP2C subfamily. | Usmani, KA., et al. 2004. Drug Metab Dispos. 32: 333-9. PMID: 14977868
- The stability of organophosphorus insecticides in fresh blood. | Ageda, S., et al. 2006. Leg Med (Tokyo). 8: 144-9. PMID: 16517205
- Nonaqueous and aqueous-organic media for the enantiomeric separations of neutral organophosphorus pesticides by CE. | Huang, L., et al. 2007. Electrophoresis. 28: 2758-64. PMID: 17592615
- Separation of organophosphorus pesticides by using nano-liquid chromatography. | Buonasera, K., et al. 2009. J Chromatogr A. 1216: 3970-6. PMID: 19321170
- Dislodgable insecticide residues on cotton foliage: permethrin, curacron, fenvalarate, sulprofos, decis, and endosulfan. | Estesen, BJ., et al. 1979. Bull Environ Contam Toxicol. 22: 245-8. PMID: 465782
- Dislodgable insecticide residues on cotton foliage: fenvalarate, permethrin, sulprofos, chlorpyrifos, methyl parathion, EPN, oxamyl, and profenofos. | Buck, NA., et al. 1980. Bull Environ Contam Toxicol. 24: 283-8. PMID: 6153915
- Characterization of the purified microsomal FAD-containing monooxygenase from mouse and pig liver. | Sabourin, PJ. and Hodgson, E. 1984. Chem Biol Interact. 51: 125-39. PMID: 6432350
- Effects of molasses, summer emulsifiable oil concentrate, crude cotton seed oil, and glycerin on the residual life of sulprofos on cotton. | Ware, GW., et al. 1982. Bull Environ Contam Toxicol. 28: 624-7. PMID: 6896466
- Effects of sulprofos and its sulfoxide and sulfone metabolites on laying hens fed the compounds in the diet. | Clark, DE., et al. 1979. J Agric Food Chem. 27: 103-7. PMID: 762315
- Subchronic neurotoxicity screening studies with six organophosphate insecticides: an assessment of behavior and morphology relative to cholinesterase inhibition. | Sheets, LP., et al. 1997. Fundam Appl Toxicol. 35: 101-19. PMID: 9024678
- Pesticide interactions: effects of organophosphorus pesticides on the metabolism, toxicity, and persistence of selected pyrethroid insecticides | Gaughan, L. C., Engel, J. L., & Casida, J. E. 1980. Pesticide biochemistry and physiology. 14(1): 81-85.
- Resistance to pyrethroid, carbamate, and organophosphate insecticides in field populations of tobacco budworm (Lepidoptera: Noctuidae) in 1990 | Elzen, G. W., Leonard, B. R., Graves, J. B., Burris, E., & Micinski, S. 1992. Journal of economic entomology. 85(6): 2064-2072.
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Sulprofos, 100 mg | sc-251098 | 100 mg | $56.00 |