144052-40-4 Usage
Description
m-Xylylenediphosphonic Acid, with the chemical formula C8H10O6P2, is a phosphonic acid-based compound known for its chelating properties. It is recognized for its effectiveness in binding to metal ions, which makes it a versatile agent in a range of industrial applications.
Uses
Used in Water Treatment:
m-Xylylenediphosphonic Acid is used as a chelating agent to prevent metal ions from precipitating. This enhances the efficiency of water treatment processes by keeping the water free from unwanted metal deposits.
Used in Metal Cleaning:
In the metal cleaning industry, m-Xylylenediphosphonic Acid serves as a chelating agent, aiding in the removal of metal ions and ensuring a thorough and effective cleaning process.
Used in Metal Surface Treatment:
m-Xylylenediphosphonic Acid is utilized as a chelating agent in metal surface treatment processes, where it helps in the prevention of metal ion precipitation, thus improving the quality and longevity of the treated surfaces.
Used as a Corrosion Inhibitor in Cooling Water Systems:
m-Xylylenediphosphonic Acid is employed as a corrosion inhibitor, leveraging its ability to form stable complexes with metal ions to protect cooling water systems from corrosion, thereby extending their service life and reducing maintenance costs.
Used as a Scale Inhibitor in Oilfield Applications:
In the oil and gas industry, m-Xylylenediphosphonic Acid is used as a scale inhibitor to prevent the formation of mineral deposits that can hinder oil extraction and refinery processes. Its chelating properties help maintain the efficiency of oilfield operations.
Check Digit Verification of cas no
The CAS Registry Mumber 144052-40-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,4,0,5 and 2 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 144052-40:
(8*1)+(7*4)+(6*4)+(5*0)+(4*5)+(3*2)+(2*4)+(1*0)=94
94 % 10 = 4
So 144052-40-4 is a valid CAS Registry Number.
144052-40-4Relevant articles and documents
Rapid one-pot synthesis of alkane-α ω, diylbisphosphonic acids from dihalogenoalkanes under microwave irradiation
Villemin, Didier,Moreau, Bernard,Kaid, M'Hamed,Didi, Mohamed Amine
, p. 1583 - 1586 (2010)
A one-pot, two-step synthesis of alkylenebisphosphonic acids from dihalogenoalkanes was performed under microwave irradiation. The reaction is very rapid and convenient for the synthesis of small samples of alkylenebisphosphonic acids. Copyright Taylor & Francis Group, LLC.
The synthesis of novel bisphosphonates as inhibitors of phosphoglycerate kinase (3-PGK)
Caplan, Neil A.,Pogson, Christopher I.,Hayes, David J.,Blackburn, G. Michael
, p. 421 - 437 (2007/10/03)
A series of conformationally-restrained analogues of 1,3-bisphospho-D-glyceric acid (1,3-BPG) 1 has been synthesised for use as inhibitors of 3-PGK (E.C. 2.7.2.3). These compounds have non-scissile phosphonate linkages and also incorporate α-halogen substituents to make them isopolar and isosteric mimics of the natural substrate. A monocyclic aryl core between the two phosphoryl centres provides both a rigid framework linking these moieties and loci for further substitution. The compounds were tested against human 3-PGK and found to be good competitive inhibitors. α-Fluorination of the phosphonic acids increased the affinity for the enzyme into the submicromolar range. Correlation of IC50 data with pKa. and pKa, values indicates that the acidity of the phosphoryl group exerts a strong influence on protein binding. The Royal Society of Chemistry 2000.
(o-Hydroxyphenyl)methylphosphonic acids: Synthesis and Potentiometric Determinations of their pKa Values
Boehmer, Volker,Vogt, Walter,Chafaa, Salah,Meullemeestre, Jean,Schwing, Marie-Jose,Vierling, Francois
, p. 139 - 149 (2007/10/02)
(o-Hydroxyphenyl)methylphosphonic acids are readily obtained from o-(bromomethyl)- or o-(hydroxymethyl)phenols and trialkyl phosphites.Subsequent hydrolysis leads to the corresponding phosphonic acids.For a series of such compounds, the pKa val
