Pyrazothion

Base Information

Chemical Name:Pyrazothion
CAS No.:108-35-0
Molecular Formula:C₈H₁₅N₂O₃PS
Molecular Weight:250.258
Hs Code.:2933199011
UNII:L0HUM41IX2
DSSTox Substance ID:DTXSID8057932
Nikkaji Number:J5.075J
Wikidata:Q27282546

Synonyms:PYRAZOTHION;BRN 0019355;Geigy G-24027;Methylpyrazolyl diethylthiophosphate;ENT 25,557-X;108-35-0;UNII-L0HUM41IX2;L0HUM41IX2;Diethyl 3-methyl-5-pyrazolyl thionophosphate;G-24027;O,O-Diethyl O-(3-methyl-5-pyrazolyl) phosphorothionate;Phosphorothioic acid, O,O-diethyl O-(3-methyl-1H-pyrazol-5-yl) ester;4-23-00-02424 (Beilstein Handbook Reference);Phosphorothioic acid, O,O-diethyl-O-(5-methyl-3-pyrazolyl) ester;C8H15N2O3PS;SCHEMBL2689311;DTXSID8057932;C8-H15-N2-O3-P-S;LS-108676;G-23027;Q27282546;O,O-DIETHYL O-3-METHYLPYRAZOL-5-YL PHOSPHOROTHIOATE;O,O-DIETHYL O-(3-METHYL-1H-PYRAZOL-5-YL) PHOSPHOROTHIOATE

Suppliers and Price of Pyrazothion

Supply Marketing:

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

Total 4 raw suppliers

Chemical Property of Pyrazothion

Chemical Property:

Boiling Point:350.5°Cat760mmHg
Flash Point:165.8°C
PSA：98.27000
Density:1.279g/cm³
LogP:3.04500
XLogP3:2.8
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:6
Exact Mass:250.05410052
Heavy Atom Count:15
Complexity:232

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCOP(=S)(OCC)OC1=NNC(=C1)C

Technology Process of Pyrazothion

There total 1 articles about Pyrazothion 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:

Reference yield: