Ethyl dichlorophosphate

95%

Reagent Code: #180995
label
Alias Ethylphosphoryldichloride; O-ethylphosphoryldichloride
fingerprint
CAS Number 1498-51-7

science Other reagents with same CAS 1498-51-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 162.94 g/mol
Formula C₂H₅Cl₂O₂P
badge Registry Numbers
EC Number 216-099-0
MDL Number MFCD00002069
thermostat Physical Properties
Boiling Point 60-65 °C10 mm Hg(lit.)
inventory_2 Storage & Handling
Density 1.373 g/mL at 25 °C(lit.)
Storage Room temperature, inert gas storage

description Product Description

Used primarily as an intermediate in the synthesis of organophosphorus compounds, including pesticides and flame retardants. It plays a key role in phosphorylation reactions, enabling the formation of phosphate esters and related derivatives. Due to its reactivity, it is also employed in the preparation of chemical warfare agent simulants for research and detection purposes. Its high reactivity with alcohols and amines makes it valuable in organic synthesis for introducing phosphoryl groups. Requires careful handling due to its corrosive and moisture-sensitive nature.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿1,770.00
inventory 100g
10-20 days ฿6,740.00
inventory 500g
10-20 days ฿32,530.00

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Ethyl dichlorophosphate
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Used primarily as an intermediate in the synthesis of organophosphorus compounds, including pesticides and flame retardants. It plays a key role in phosphorylation reactions, enabling the formation of phosphate esters and related derivatives. Due to its reactivity, it is also employed in the preparation of chemical warfare agent simulants for research and detection purposes. Its high reactivity with alcohols and amines makes it valuable in organic synthesis for introducing phosphoryl groups. Requires car

Used primarily as an intermediate in the synthesis of organophosphorus compounds, including pesticides and flame retardants. It plays a key role in phosphorylation reactions, enabling the formation of phosphate esters and related derivatives. Due to its reactivity, it is also employed in the preparation of chemical warfare agent simulants for research and detection purposes. Its high reactivity with alcohols and amines makes it valuable in organic synthesis for introducing phosphoryl groups. Requires careful handling due to its corrosive and moisture-sensitive nature.

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