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Ethyl dichlorothiophosphate

Ethyl dichlorothiophosphate structure

Ethyl dichlorothiophosphate 

structure
  • CAS No:

    1498-64-2

  • Formula:

    C2H5Cl2OPS

  • Chemical Name:

    Ethyl dichlorothiophosphate

  • Synonyms:

    Phosphorodichloridothioic acid,O-ethyl ester;Phosphine sulfide,dichloroethoxy-;Ethyl dichlorothiophosphate;Ethyl phosphonodichloridothionate;Ethylphosphorothioic dichloride;O-Ethyl phosphorodichloridothioate;Ethyl thiophosphorodichloridate;O-Ethyl phosphorothiodichloridate;O-Ethylthiophosphoryl dichloride;Ethyl phosphorodichloridothionate;O-Ethyl dichlorothiophosphate;O-Ethyl phosphorodichlorothioate;(Dichloroethoxy)phosphine sulfide;NSC 91481

  • Categories:

    Agrochemicals  >  Pesticide Intermediates

Ethyl dichlorothiophosphate Basic Attributes

179.01

179.01

216-100-4

91481

DTXSID6061733

2931900090

Characteristics

41.3

3.37560

1.3968 g/cm3 @ Temp: 00 °C

52 °C @ Press: 10 Torr

>230 °F

n20/D 1.504(lit.)

10 mm Hg ( 55 °C)

Safety Information

II

6.1(a)

UN 3390 6.1/PG 1

3

23/24/25-34-23/24-22

22-26-36/37/39-45

TD4400000

T

P261-P280-P305 + P351 + P338-P310

H302-H311-H314-H331

|Danger|H302 (100%): Harmful if swallowed [Warning Acute toxicity, oral]|P260, P261, P264, P270, P271, P280, P301+P312, P301+P330+P331, P302+P352, P303+P361+P353, P304+P340, P305+P351+P338, P310, P311, P312, P321, P322, P330, P361, P363, P403+P233, P405, and P501|Aggregated GHS information provided by 38 companies from 1 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

Ethyl dichlorothiophosphate Use and Manufacturing

Methods of Manufacturing

The preparation method is to meter the fresh phosphorous trichloride into the reaction kettle, cool to -2°C, slowly add anhydrous ethanol dropwise, control the reaction temperature (0±2)°C, with negative pressure during the reaction, and extract the generated Hydrogen chloride, after the reaction is completed, move to the distillation pot, first distill the front fraction, and continue to distill to obtain the product.

Uses

O-ethyl thiophosphoryl dichloride is referred to as ethyl dichloride, which is used to synthesize the organophosphorus insecticide isopropylamine phosphorus (ethylisosphosphoryl) and the herbicides glufosinate and glufosinate.

Phosphorodichloridothioic acid, O-ethyl ester: INACTIVE

Computed Properties

Molecular Weight:179.00
XLogP3:3.1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:177.9175783
Monoisotopic Mass:177.9175783
Topological Polar Surface Area:41.3
Heavy Atom Count:7
Complexity:89.7
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

Material

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