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Encyclopedia

Phosmet

Base Information Edit
  • Chemical Name:Phosmet
  • CAS No.:732-11-6
  • Molecular Formula:C11H12 N O4 P S2
  • Molecular Weight:317.326
  • Hs Code.:
  • European Community (EC) Number:211-987-4
  • ICSC Number:0543
  • UN Number:3077,2783
  • UNII:VN04LI540Y
  • DSSTox Substance ID:DTXSID5024261
  • Nikkaji Number:J2.108C
  • Wikipedia:Phosmet
  • Wikidata:Q421379
  • NCI Thesaurus Code:C76877
  • Metabolomics Workbench ID:56001
  • ChEMBL ID:CHEMBL1481873
  • Mol file:732-11-6.mol
Phosmet

Synonyms:Imidan;N-(Mercaptomethyl)phthalimide S-(O,O-dimethyl phosphorothionate);Phosmet;Phthalophos;Prolate

Suppliers and Price of Phosmet
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • Sigma-Aldrich
  • Phosmet PESTANAL
  • 100mg
  • $ 77.60
  • Medical Isotopes, Inc.
  • Phosmet
  • 1 g
  • $ 2400.00
  • Cayman Chemical
  • Phosmet ≥95%
  • 100mg
  • $ 65.00
  • Cayman Chemical
  • Phosmet ≥95%
  • 50mg
  • $ 50.00
  • Cayman Chemical
  • Phosmet ≥95%
  • 25mg
  • $ 33.00
  • American Custom Chemicals Corporation
  • PHOSMET 95.00%
  • 200MG
  • $ 660.36
  • AK Scientific
  • Phosmet
  • 100mg
  • $ 181.00
  • AHH
  • Phosmet 98%
  • 10g
  • $ 420.00
Total 17 raw suppliers
Chemical Property of Phosmet Edit
Chemical Property:
  • Vapor Pressure:5.11E-07mmHg at 25°C 
  • Melting Point:72.5 ºC 
  • Boiling Point:412.6oC at 760 mmHg 
  • PKA:-2.63±0.20(Predicted) 
  • Flash Point:>100°C 
  • PSA:123.04000 
  • Density:1.473g/cm3 
  • LogP:3.07910 
  • Storage Temp.:0-6°C 
  • Water Solubility.:25 mg l-1 (25°C) 
  • XLogP3:2.8
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:6
  • Rotatable Bond Count:5
  • Exact Mass:316.99453721
  • Heavy Atom Count:19
  • Complexity:399
  • Transport DOT Label:Class 9
Purity/Quality:

95% *data from raw suppliers

Phosmet PESTANAL *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes:Xn;N,N,Xn 
  • Statements: 21/22-50/53 
  • Safety Statements: 22-36/37-60-61 
MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:
  • Chemical Classes:Pesticides -> Organophosphate Insecticides
  • Canonical SMILES:COP(=S)(OC)SCN1C(=O)C2=CC=CC=C2C1=O
  • Inhalation Risk:A harmful concentration of airborne particles can be reached quickly on spraying or when dispersed, especially if powdered.
  • Effects of Short Term Exposure:The substance may cause effects on the nervous system. This may result in convulsions and respiratory depression. Cholinesterase inhibition. The effects may be delayed. Medical observation is indicated.
  • Effects of Long Term Exposure:The substance may have effects on the nervous system. This may result in weakness. Cholinesterase inhibition. Cumulative effects are possible. See Acute Hazards/Symptoms.
  • Description Phosmet is an organophosphate insecticide and acaricide. It reduces apple damage by a large variety of insects, including apple maggots, codling moths, and obliquebanded leafrollers when used as either a border or cover spray at a concentration of 1.9 kg AI/hectare. Phosmet is effective in controlling S. scabiei in pigs when applied as a 20% pour-on solution. It is toxic to rats via oral administration (LC50 = 230 mg/kg). Formulations containing phosmet have been used in the control of insects and mites in agriculture.
  • Uses Nonsystemic acaricide and insecticide used on citrus, fruit, grape and potato crop Phosmet is used to control a wide range of insects and mites in fruit, potatoes, sweet potatoes, vines, cotton and many other crops. It is also used as a veterinary ectoparasiticide. Phosmet is used as a pesticide to protect crops and vegetation. Insecticide. Insecticide, acaricide.
Technology Process of Phosmet

There total 2 articles about Phosmet which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With water; acetone;

Reference yield:

Guidance literature:
entspr. Thioverb.-K-Salz, N-Hydroxymethylphthalimid;
DOI:10.1002/hlca.19740570619
Guidance literature:
With sodium carbonate; at 25 ℃; for 170h;
Refernces Edit
Post RFQ for Price