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Poly(oxy-1,2-ethanediyl), .alpha.-(2-methyl-1-oxo-2-propenyl)-.omega.-(phosphonooxy)is a polymeric chemical compound composed of ethylene oxide units connected by alpha-(2-methyl-1-oxo-2-propenyl)and omega-(phosphonooxy)groups. Poly(oxy-1,2-ethanediyl), .alpha.-(2-methyl-1-oxo-2-propenyl)-.omega.-(phosphonooxy)is recognized for its surfactant and dispersing properties, which are instrumental in reducing surface tension and enhancing the solubility and dispersion of various substances in water.

35705-94-3

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35705-94-3 Usage

Uses

Used in Detergent Industry:
Poly(oxy-1,2-ethanediyl), .alpha.-(2-methyl-1-oxo-2-propenyl)-.omega.-(phosphonooxy)is utilized as a surfactant and dispersing agent in detergents to improve their cleaning efficiency. Its ability to lower surface tension and increase the solubility of dirt and grease in water makes it an effective component in detergent formulations.
Used in Emulsifier Industry:
In the production of emulsifiers, Poly(oxy-1,2-ethanediyl), .alpha.-(2-methyl-1-oxo-2-propenyl)-.omega.-(phosphonooxy)- serves as a key ingredient that helps in stabilizing mixtures of immiscible liquids, such as oil and water. Its surfactant properties allow for the formation of stable emulsions, which are essential in various applications, including food products and cosmetic formulations.
Used in Cleaning Agents:
Poly(oxy-1,2-ethanediyl), .alpha.-(2-methyl-1-oxo-2-propenyl)-.omega.-(phosphonooxy)is also used in cleaning agents to enhance their effectiveness in removing dirt, stains, and other contaminants. Its capacity to improve the solubility and dispersion of substances in water contributes to the overall performance of cleaning products.
Used in Water Treatment:
The presence of phosphonooxy groups in Poly(oxy-1,2-ethanediyl), .alpha.-(2-methyl-1-oxo-2-propenyl)-.omega.-(phosphonooxy)- makes it useful in water treatment applications, particularly in preventing the buildup of mineral deposits and scale formation in water systems. This property is valuable in maintaining the efficiency and longevity of water treatment equipment and systems.

Check Digit Verification of cas no

The CAS Registry Mumber 35705-94-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,7,0 and 5 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 35705-94:
(7*3)+(6*5)+(5*7)+(4*0)+(3*5)+(2*9)+(1*4)=123
123 % 10 = 3
So 35705-94-3 is a valid CAS Registry Number.

35705-94-3Downstream Products

35705-94-3Relevant academic research and scientific papers

Hyperbranched polyphosphoesters with reactive end groups synthesized via acyclic diene metathesis polymerization and their transformation to crosslinked nanoparticles

Ding, Liang,Qiu, Jun,Lu, Rong,Zheng, Xueqin,An, Jing

, p. 4331 - 4340 (2013)

A novel hyperbranched polyphosphoester (HBPPE) was prepared by acyclic diene metathesis (ADMET) polymerization of an AB2 monomer using the second-generation Hoveyda-Grubbs catalyst. IR analysis, gel permeation chromatography with multiangle laser light scattering, and NMR spectroscopy confirmed their controlled synthesis. The effect of the ADMET polymerization time in the thermal properties of HBPPEs was studied and their thermal degradation and flame-retardant properties were evaluated. These reactive HBPPEs were used to synthesize polyphosphoesters nanoparticles by intramolecular crosslinking of the end acrylate groups in dilute solution. The successful preparation of this new type of polymer nanoparticles was proven by NMR spectroscopy and gel permeation chromatography. The morphologies of nanostructures were investigated via dynamic light scattering, atom force microscopy, and transmission electron microscopy. The results revealed that the crosslinked nanoparticles, which have a comparatively uniform size, were stable and reproducible in organic solvents.

Cyclic polyphosphoesters synthesized by acyclic diene metathesis polymerization and ring closing metathesis

Ding, Liang,Lu, Rong,An, Jing,Zheng, Xueqin,Qiu, Jun

, p. 1242 - 1248 (2013)

This article describes the synthesis of cyclic polyphosphoester (PPE) by the ring-closing metathesis (RCM) of different difunctional linear PPEs. Linear PPE precursors were prepared through a selective head-to-tail acyclic diene metathesis polymerization of phenyl dienephosphate monomer using 2-hydroxyethyl acrylate as a selective chain terminator, followed by the transformation of the terminal acrylate functional group into a hydroxyl group utilizing a thiol-Michael addition click reaction. These products were then reacted with the corresponding acyl chloride containing a vinyl end group. The subsequent end-to-end intramolecular coupling reaction was performed under highly dilute conditions. The successful transformation of the linear PPE precursors to cyclic PPE was confirmed by NMR spectroscopy and gel permeation chromatography. The thermal and flame retardant properties of linear and cyclic PPEs were investigated, and their thermal degradation and flame retardance were evaluated, as these are important features for future applications.

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