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1 References  





2 External links  














Bendiocarb






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From Wikipedia, the free encyclopedia
 


Bendiocarb
Skeletal formula of bendiocarb
Ball-and-stick model of the bendiocarb molecule
Names
Preferred IUPAC name

2,2-Dimethyl-2H-1,3-benzodioxol-4-yl methylcarbamate

Identifiers

CAS Number

3D model (JSmol)

ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.041.091 Edit this at Wikidata
KEGG

PubChem CID

UNII

CompTox Dashboard (EPA)

  • InChI=1S/C11H13NO4/c1-11(2)15-8-6-4-5-7(9(8)16-11)14-10(13)12-3/h4-6H,1-3H3,(H,12,13) checkY

    Key: XEGGRYVFLWGFHI-UHFFFAOYSA-N checkY

  • InChI=1/C11H13NO4/c1-11(2)15-8-6-4-5-7(9(8)16-11)14-10(13)12-3/h4-6H,1-3H3,(H,12,13)

    Key: XEGGRYVFLWGFHI-UHFFFAOYAG

  • CNC(=O)Oc1cccc2c1OC(C)(C)O2

Properties

Chemical formula

C11H13NO4
Molar mass 223.23 g/mol
Pharmacology

ATCvet code

QP53AE03 (WHO)

Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

☒N verify (what is checkY☒N ?)

Infobox references

Bendiocarb is an acutely toxic carbamate insecticide used in public health and agriculture and is effective against a wide range of nuisance and disease vector insects. Many bendiocarb products are or were sold under the tradenames "Ficam" and "Turcam."

All bendiocarb-containing products in the United States were recently[when?] cancelled, after its manufacturers voluntarily chose to pull their products off the market, rather than conduct additional safety studies required by the EPA.[1] In other countries, it is still used in homes, industrial plants, and food storage sites to control bedbugs, mosquitoes, flies, wasps, ants, fleas, cockroaches, silverfish, and ticks but can be used against a wide variety of insects as well as snails and slugs. It is one of 12 insecticides recommended by the World Health Organization for use in malaria control.[2]

Bendiocarb is not considered to be carcinogenic, but it is acutely toxic. Like other carbamates, it reversibly inhibits acetylcholinesterase, an enzyme required for normal transmission of nerve impulses. Bendiocarb binds to the active site of this enzyme leading to an accumulation of acetylcholine, which is required for the transmission of nerve impulses, at nerve muscle sites.[1]

Bendiocarb was invented in 1971 and was first introduced into the market by Fisons Ltd. It is currently marketed by Bayer CropScience and Kuo Ching under various trade names: Ficam, Dycarb, Garvox, Turcam, Niomil, Seedox, Tattoo

Bendiocarb is highly toxic to birds and fish. In addition, recently, a study in bone marrow cells of Calotes versicolor lizard demonstrated that chronic exposure to this contaminant increases the level of cytoxicity and genotoxicity (Anisha et al., 2019). In mammalian tissue, carbamates are generally excreted rapidly and do not accumulate.[1]

References

[edit]
  1. ^ a b c R.E.D. Facts: Bendiocarb Archived October 10, 2008, at the Wayback Machine U.S. EPA, September 1999.
  • ^ Sadasivaiah, Shobha; Tozan, Yesim; Breman, Joel G. (December 1, 2007), "Dichlorodiphenyltrichloroethane (DDT) for Indoor Residual Spraying in Africa: How Can It Be Used for Malaria Control?", Am. J. Trop. Med. Hyg., 77 (Suppl 6): 249–263, doi:10.4269/ajtmh.2007.77.249, PMID 18165500
  • Anisha, N.S.; Tumul, S., (2019). Evaluation of Genotoxic and Cytotoxic effects of BendioCarb in Bone Marrow cells of one Calotes Versicolor. Proceedings of the Zoological Society of India 18(1): 19-23

    [edit]
    Retrieved from "https://en.wikipedia.org/w/index.php?title=Bendiocarb&oldid=1222163492"

    Categories: 
    Acetylcholinesterase inhibitors
    Carbamate insecticides
    Benzodioxoles
    Phenol esters
    Aromatic carbamates
    Hidden categories: 
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    Short description is different from Wikidata
    Articles with changed CASNo identifier
    ECHA InfoCard ID from Wikidata
    Articles containing unverified chemical infoboxes
    Chembox image size set
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    All articles with vague or ambiguous time
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    This page was last edited on 4 May 2024, at 08:43 (UTC).

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