Dioxacarb (CAS 6988-21-2)
Alternate Names:
2-(1,3-Dioxolan-2-yl)phenol 1-(N-Methylcarbamate); Methylcarbamic Acid o-1,3-Dioxolan-2-ylphenyl Ester; 2-(1,3-Dioxolan-2-yl)phenol Methylcarbamate; 2-(1,3-Dioxolan-2-yl)phenyl N-Methylcarbamate; 2-(1,3-Dioxolan-2-yl)phenyl Methylcarbamate; 2-(1,3-Dioxolane-2-yl)-phenyl N-Methylcarbamate; C 8353; CIBA 8353; CIBA C 8353; Du Pont 1519; Elocron; Elocron 50WP; Elocron 8353; Famid; MCDP; Rovlinka; o-(1,3-Dioxolan-2-yl)phenyl Methylcarbamate
CAS Number:
6988-21-2
Molecular Weight:
223.23
Molecular Formula:
C11H13NO4
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
Dioxacarb, an organophosphorus pesticide, finds wide application in agriculture, horticulture, and public health. Its versatility extends to various commercial products, encompassing insecticides, herbicides, fungicides, and rodenticides. Additionally, it serves as an insect repellent and a wood preservative. The mechanism of action of dioxacarb revolves around the inhibition of acetylcholinesterase, an enzyme responsible for the breakdown of acetylcholine. Acetylcholine, a neurotransmitter involved in nerve impulse transmission, becomes accumulated in the nervous system due to the enzyme inhibition caused by dioxacarb. Consequently, this buildup induces paralysis and eventual demise of the targeted pests.
Dioxacarb (CAS 6988-21-2) References
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- Competitive degradation and detoxification of carbamate insecticides by membrane anodic Fenton treatment. | Wang, Q. and Lemley, AT. 2003. J Agric Food Chem. 51: 5382-90. PMID: 12926887
- [Experimental studies of the control of mosquitoes of the genus Anopheles using selected insecticides]. | Wegner, Z., et al. 1991. Wiad Parazytol. 37: 179-83. PMID: 1823486
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- Cytotoxic and genotoxic effects of dioxacarb by human peripheral blood lymphocytes CAs and Allium test. | Eren, Y., et al. 2015. Cytotechnology. 67: 1023-30. PMID: 24848210
- The potential environmental risks of the utilization of composts from household food waste. | Růžičková, J., et al. 2021. Environ Sci Pollut Res Int. 28: 24663-24679. PMID: 32705551
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- Study of modeling and optimization for predicting the acute toxicity of carbamate pesticides using the binding information with carrier protein. | Hou, C., et al. 2022. Spectrochim Acta A Mol Biomol Spectrosc. 273: 121038. PMID: 35189491
- An assessment of health risks posed by consumption of pesticide residues in fruits and vegetables among residents in the Kampala Metropolitan Area in Uganda. | Ssemugabo, C., et al. 2022. Int J Food Contam. 9: 4. PMID: 35535174
- Liquid chromatographic determination of N-methylcarbamate insecticides and metabolites in crops. II. Analytical characteristics and residue findings. | Krause, RT. 1985. J Assoc Off Anal Chem. 68: 734-41. PMID: 4030646
- Residual toxicity of wall-sprayed organophosphates, carbamates and pyrethroids to mosquito Culex pipiens molestus Forskal. | Rettich, F. 1980. J Hyg Epidemiol Microbiol Immunol. 24: 110-7. PMID: 7190586
- Analyte stability study of N-methylcarbamate pesticides in beef and poultry liver tissues by liquid chromatography. | Ali, MS., et al. 1993. J AOAC Int. 76: 1309-16. PMID: 8286970
- Resistance of the German cockroach Blattella germanica (L.) to dioxacarb in Bulgaria. | Gecheva, G. 1993. Appl Parasitol. 34: 295-8. PMID: 8298663
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Dioxacarb, 50 mg | sc-497474 | 50 mg | $380.00 |