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Ethyl metaphosphate, also known as EMPA, is an organophosphorus compound with the chemical formula C2H7O3P. It is a colorless, oily liquid that is soluble in water and organic solvents. Ethyl metaphosphate is primarily used as an intermediate in the synthesis of various organophosphorus compounds, including pesticides, flame retardants, and plasticizers. It is also used as a chemical warfare agent, where it acts as a nerve agent, inhibiting the enzyme acetylcholinesterase and disrupting the nervous system. Due to its potential toxicity and environmental impact, the production and use of ethyl metaphosphate are strictly regulated in many countries.

4697-37-4

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4697-37-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4697-37-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,6,9 and 7 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 4697-37:
(6*4)+(5*6)+(4*9)+(3*7)+(2*3)+(1*7)=124
124 % 10 = 4
So 4697-37-4 is a valid CAS Registry Number.

4697-37-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl metaphosphate

1.2 Other means of identification

Product number -
Other names Aethylmetaphosphat

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:4697-37-4 SDS

4697-37-4Relevant academic research and scientific papers

Fragmentation-Rearrangement of 2-Acyloxyalkylphosphonates - a Novel Route to Alkyl Metaphosphate Extrusion

Jongh, Connie P. de,Modro, Tomasz A.

, p. 1003 - 1004 (2007/10/02)

Thermolysis of dialkyl 2-acyloxyalkylphosphonates, resulting in the fragmentation to an alkene, ester and alkyl metaphosphate, represents the first example of a reaction in which alkyl group migration has to occur before the metaphosphate species can be extruded from the system.

The mechanism of fragmentation of alky α-(oxyimino)benzylphosphonates; use of silica gel as a novel hydroxylic trapping reactant for an intermediate alkyl metaphosphate

Quin, Louis D.,Wu, Xiao-Ping,Breuer, Eli,Mahajna, Mahmoud

, p. 6281 - 6282 (2007/10/02)

Silica gel was employed to react with the suspected metaphosphate intermediate of the acid-promoted cleavage of monoalkyl α-(oxyimino)benzylphosphonates. The silica gels displayed CP-MAS 31P NMR signals at about δ-8. A similar value was obtained for silica gel phosphorylated with ethyl metaphosphate from a different source (thermolysis of a P-ethoxy 2,3-oxaphosphabicyclo[2.2.2]octene derivative.

GENERATION OF ESTER AND AMIDE DERIVATIVES OF METHAPHOSPHORIC ACID BY PHOTOLYSIS OF 2,3-OXAPHOSPHABICYCLOOCT-5-ENE DERIVATIVES

Quin, Louis D.,Pete, Bela,Szewczik, Jerzy,Hughes, Alan N.

, p. 2627 - 2630 (2007/10/02)

Irradiation at 254 nm of P-NMe2 and P-OEt derivatives of phosphonates where P is incorporated into the 2,3-oxabicyclooct-ene framework results in fragmentation of the molecules to release N,N-dimethylamino metaphosphoramidate and ethyl metaphophate, respectively.Both species polymerize rapidly, but are effectively trapped as phosphate derivatives when alcohols are included in the reaction mixtures.

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