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Contents

   



(Top)
 


1 Toxicology  





2 References  





3 External links  














Acephate






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From Wikipedia, the free encyclopedia
 


Acephate
Skeletal formula of acephate
Ball-and-stick model of the acephate molecule
Names
Preferred IUPAC name

Dimethyl N-acetylphosphoramidothioate

Identifiers

CAS Number

3D model (JSmol)

ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.045.659 Edit this at Wikidata
KEGG

PubChem CID

RTECS number
  • TB4760000
UNII

CompTox Dashboard (EPA)

  • InChI=1S/C4H10NO3PS/c1-4(6)5-9(7,8-2)10-3/h1-3H3,(H,5,6,7) checkY

    Key: YASYVMFAVPKPKE-UHFFFAOYSA-N checkY

  • InChI=1/C4H10NO3PS/c1-4(6)5-9(7,8-2)10-3/h1-3H3,(H,5,6,7)

    Key: YASYVMFAVPKPKE-UHFFFAOYAG

  • O=C(NP(=O)(OC)SC)C

Properties

Chemical formula

C4H10NO3PS
Molar mass 183.16 g·mol−1
Appearance colourless to white solid
Density 1.35 g/cm3
Melting point 88–90 °C (190–194 °F; 361–363 K)

Solubility in water

79 g/100 mL
Solubility very soluble in acetone
soluble in ethanol
Vapor pressure 2x10−6 mmHg
Pharmacology
Legal status
  • AU: S6 (Poison)
Hazards
GHS labelling:[1]

Pictograms

GHS07: Exclamation mark

Signal word

Warning

Hazard statements

H302

Precautionary statements

P264, P270, P301+P312, P330, P501

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

Acephate is an organophosphate foliar and soil insecticide of moderate persistence with residual systemic activity of about 10–15 days at the recommended use rate. It is used primarily for control of aphids, including resistant species, in vegetables (e.g. potatoes, carrots, greenhouse tomatoes, and lettuce) and in horticulture (e.g. on roses and greenhouse ornamentals). It also controls leaf miners, caterpillars, sawflies, thrips, and spider mites in the previously stated crops as well as turf, and forestry. By direct application to mounds, it is effective in destroying imported fire ants.

Acephate is sold as a soluble powder, as emulsifiable concentrates, as pressurized aerosol, and in tree injection systems and granular formulations.

As of 2012, the EPA no longer allows the usage of acephate on green beans grown in the United States.[2]

Toxicology[edit]

It is considered non-phytotoxic on many crop plants. Acephate and its primary metabolite, methamidophos, are toxic to Heliothis spp. that are considered resistant to other organophosphate insecticides. Acephate emits toxic fumes of various oxidesofphosphorus, nitrogen, and sulfur when heated to decomposition. Symptoms of exposure to acephate include a slight irritation of eyes and skin.

The U.S. annually uses 4–5 million pounds of acephate.[3]

The EU classifies Acephate as an Annex III substance, meaning that it meets the requirements to be considered a health and environmental hazard. [4]

References[edit]

  1. ^ "Acephate". PubChem. Archived from the original on 2021-03-07. Retrieved 2021-03-17.
  • ^ "Food and Pesticides". 21 February 2013. Archived from the original on 28 May 2023. Retrieved 28 May 2023.
  • ^ "Acephate Facts" (PDF). Retrieved 2024-07-03.
  • ^ "Substance Information - ECHA". echa.europa.eu. Retrieved 2023-10-31.
  • External links[edit]


    Retrieved from "https://en.wikipedia.org/w/index.php?title=Acephate&oldid=1232327703"

    Categories: 
    Acetylcholinesterase inhibitors
    Pesticides
    Phosphoramidothioates
    Leaf miners
    Hidden categories: 
    Articles with changed EBI identifier
    ECHA InfoCard ID from Wikidata
    Chembox having GHS data
    Articles containing unverified chemical infoboxes
    Chembox image size set
    Articles with short description
    Short description matches Wikidata
     



    This page was last edited on 3 July 2024, at 05:16 (UTC).

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