Ethoprophos

Base Information

• Chemical Name: Ethoprophos
• CAS No.: 13194-48-4
• Molecular Formula: C8H19O2PS2
• Molecular Weight: 242.343
• Hs Code.: 29309090
• European Community (EC) Number: 236-152-1
• ICSC Number: 1660
• UN Number: 3018
• UNII: 765Y5683OQ
• DSSTox Substance ID: DTXSID4032611
• Nikkaji Number: J8.092F
• Wikipedia: Ethoprophos
• Wikidata: Q411754
• Metabolomics Workbench ID: 55958
• ChEMBL ID: CHEMBL1894994
• Mol file: 13194-48-4.mol

Synonyms:ethoprop;ethoprophos;Mocap;O-ethyl S,S-diprophyl phosphorodithioate

Chemical Property of Ethoprophos

Chemical Property:

• Vapor Pressure: 0.00111mmHg at 25°C
• Melting Point: -13oC
• Refractive Index: 1.493
• Boiling Point: 310.2 °C at 760 mmHg
• Flash Point: 141.4 °C
• PSA: 86.71000
• Density: 1.106 g/cm³
• LogP: 4.41740
• Storage Temp.: APPROX 4°C
• Water Solubility.: 700 mg l-1 (20 °C)
• XLogP3: 3.6
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 8
• Exact Mass: 242.05640919
• Heavy Atom Count: 13
• Complexity: 152
• Transport DOT Label: Poison

Purity/Quality:

90%, ^*data from raw suppliers

Ethoprophos(~90%) ^*data from reagent suppliers

Safty Information:

• Pictogram(s): T+,N
• Hazard Codes: T+;N,N,T+
• Statements: 25-26/27-43-50/53
• Safety Statements: 27-28-36/37/39-45-60-61-27/28

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Chemical Classes: Pesticides -> Organophosphate Insecticides
• Canonical SMILES: CCCSP(=O)(OCC)SCCC
• Inhalation Risk: Evaporation at 20 °C is negligible; a harmful concentration of airborne particles can, however, be reached quickly when dispersed.
• Effects of Short Term Exposure: Cholinesterase inhibition. The substance may cause effects on the nervous system. This may result in convulsions and respiratory depression. Exposure could cause death. The effects may be delayed. Medical observation is indicated.
• Effects of Long Term Exposure: Cholinesterase inhibition. Cumulative effects are possible. See Acute Hazards/Symptoms.
• Description: Introduced in the 1960s, ethoprop is a nonsystemic insecticide/nematicide. The mobility of ethoprop in soil and its half-life are strongly dependent on soil organic matter (21). It is not known to be carcinogenic and is available as granules or emulsifiable concentrates.
• Uses: Nonsystemic, nonfumigant nematocide and soil insecticide for control of insects in ornamentals, potatoes, sweet potatoes, tomatoes, strawberries, bananas, pineapples, sugar cane, turf and many other crops. Ethoprophos is used to control plant parasitic nematodes and soil insects. Ethoprophos is an organophosphate non-systemic nematicide and soil insecticide. Ethoprophos is an acetylcholinesterase (AChE) inhibitor. Insecticide; nematocide.

Technology Process of Ethoprophos

There total 1 articles about Ethoprophos 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:

→ Ethoprophos (13194-48-4)

Guidance literature:

Reference yield:

Ethoprophos (13194-48-4) → 1-thiopropane (107-03-9)

Guidance literature:

With methanol; 5,5'-dithiobis-(2-nitrobenzoic acid); Sphingobium sp. TCM₁ phosphotriesterase; manganese(ll) chloride; In aq. buffer; at 30 ℃; pH=8; Enzymatic reaction;

DOI:10.1021/acs.biochem.5b01144

Downstream raw materials:

1-thiopropane

Refernces

• 1、 -. "Protection of trees". . . Retrieved 2008/06/13.
• 2、 -. "Pesticide compositions and method". . . Retrieved 2008/06/13.