Molecular structure of Fenbutatin oxide, CAS Number: 13356-08-6
Fenbutatin oxide (CAS 13356-08-6)
Alternate Names:
Bis[tris-(2-methyl-2-phenylpropyl)tin] oxide
Application:
Fenbutatin oxide is an organotin pesticide
CAS Number:
13356-08-6
Molecular Weight:
1052.68
Molecular Formula:
C60H78OSn2
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
Fenbutatin Oxide is an organotin pesticide. Fenbutatin Oxide is widely used as an aracacide in the control of mites, in particular spider mites. Fenbutatin oxide, also known as Hexakis(2-methyl-2-phenylpropyl)distannoxane, is a white crystalline solid with a mild odor. It functions as an organotin acaricide, specifically classified as a phenylpropane compound. Phenylpropanes are organic substances featuring a phenylpropane moiety, and in the case of Hexakis(2-methyl-2-phenylpropyl)distannoxane, it is regarded as a practically insoluble compound in water.
Fenbutatin oxide (CAS 13356-08-6) References
- Differential sensitivity of three cyanobacterial and five green algal species to organotins and pyrethroids pesticides. | Ma, J. 2005. Sci Total Environ. 341: 109-17. PMID: 15833245
- Lethal and sub-lethal selectivity of fenbutatin oxide and sulfur to the predator Iphiseiodes zuluagai (Acari: Phytoseiidae) and its prey, Oligonychus ilicis (Acari: Tetranychidae), in Brazilian coffee plantations. | Teodoro, AV., et al. 2005. Exp Appl Acarol. 36: 61-70. PMID: 16082924
- Reduction of spermatogenesis and steroidogenesis in mice after fentin and fenbutatin administration. | Reddy, PS., et al. 2006. Toxicol Lett. 166: 53-9. PMID: 16806747
- Sub-lethal effects of fenbutatin oxide on prey location by the predatory mite Iphiseiodes zuluagai (Acari: Phytoseiidae). | Teodoro, AV., et al. 2009. Exp Appl Acarol. 47: 293-9. PMID: 19009359
- Matrix solid-phase dispersion and solid-phase microextraction applied to study the distribution of fenbutatin oxide in grapes and white wine. | Montes, R., et al. 2009. Anal Bioanal Chem. 395: 2601-10. PMID: 19806346
- Disruptive effects of two organotin pesticides on the thyroid signaling pathway in Xenopus laevis during metamorphosis. | Li, S., et al. 2019. Sci Total Environ. 697: 134140. PMID: 31476497
- Review of the existing maximum residue levels for fenbutatin oxide according to Article 12 of Regulation (EC) No 396/2005. | , ., et al. 2017. EFSA J. 15: e05091. PMID: 32625377
- Acaricide resistance status and identification of resistance mutations in populations of the two-spotted spider mite Tetranychus urticae from Ethiopia. | Simma, EA., et al. 2020. Exp Appl Acarol. 82: 475-491. PMID: 33174613
- Trace Analysis of Fenbutatin Oxide in Soil and Plant- and Animal-Derived Foods Using Modified QuEChERS Coupled with HPLC-MS/MS. | Lin, Z., et al. 2021. ACS Omega. 6: 10260-10265. PMID: 34056180
- Assessment of pesticide residues in citrus fruit on the Czech market. | Drábová, L., et al. 2022. Food Addit Contam Part A Chem Anal Control Expo Risk Assess. 39: 311-319. PMID: 34871518
- QTL mapping suggests that both cytochrome P450-mediated detoxification and target-site resistance are involved in fenbutatin oxide resistance in Tetranychus urticae. | De Beer, B., et al. 2022. Insect Biochem Mol Biol. 145: 103757. PMID: 35301092
- Fenbutatin oxide and chlorfenvinphos effects on the entomophagous arthropod fauna of citrus. | Inglesfield, C. 1987. Bull Environ Contam Toxicol. 38: 813-9. PMID: 3580598
- Determination of the pesticide fenbutatin oxide in tomatoes, cucumbers and bananas by high performance liquid chromatographic/atmospheric pressure chemical ionization-mass spectrometry. | Barnes, KA., et al. 1997. Rapid Commun Mass Spectrom. 11: 159-64. PMID: 9050264
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Fenbutatin oxide, 250 mg | sc-239986 | 250 mg | $46.00 |