42104-58-5

Usage

Uses

Used in Water Treatment:
o-Xylylenediphosphonic Acid is used as a chelating agent for the sequestration of metal ions, which helps in preventing scale formation and corrosion in water treatment processes.
Used in Industrial Cleaning:
o-Xylylenediphosphonic Acid is utilized as a cleaning agent to remove metal deposits and scale, ensuring the efficiency of industrial equipment and processes.
Used in Oil and Gas Production:
o-Xylylenediphosphonic Acid is employed as a scale inhibitor to prevent the formation of mineral deposits that can hinder the flow of oil and gas through pipelines and production equipment.
Used in Environmentally Conscious Industries:
o-Xylylenediphosphonic Acid is used as a preferred chemical in various applications due to its low toxicity and reduced ecological impact, supporting industries in their efforts to minimize environmental footprints.

Upstream product

• 144052-38-0 [2-(Dimethoxy-phosphorylmethyl)-benzyl]-phosphonic acid dimethyl ester 
• 42092-05-7 tetraethyl [1,2-phenylene-bis-(methylene)]bis(phosphonate) 
• 91-13-4 α,α'-dibromo-o-xylene 
• 612-12-4 o-Xylylene dichloride 
• 122-52-1 triethyl phosphite 
• 612-14-6 phthalyl alcohol 

Downstream Products

• 42104-64-3 2-(2-methyl-benzyl)-2,3-dihydro-1H-isophosphindole 2-oxide 
• 1444154-33-9 [Cu(1,10-phenanthroline)(o-xylenediphosphonic acid(-2H))] 
• 1564243-81-7 [Cd(o-phen)(1,2-HO₃PC₈H₈PO₃H)] 
• 1564243-79-3 [Zn(tpyprz)(1,2-HO₃PC₈H₈PO₃H)] 
• 1564243-73-7 [Zn(o-phen)(1,2-HO₃PC₈H₈PO₃H)] 
• 1564243-65-7 [Zn(H₂O)(bpy)(1,2-HO₃PC₈H₈PO₃H)] 
• 20148-17-8 2-hydroxyisophosphindoline-2-oxide 

Relevant academic research and scientific papers

Nanomolar inhibitors of the transcription factor STAT5b with high selectivity over STAT5a

Src homology 2 (SH2) domains play a central role in signal transduction. Although many SH2 domains have been validated as drug targets, their structural similarity makes development of specific inhibitors difficult. The cancer-relevant transcription facto

Rapid one-pot synthesis of alkane-α ω, diylbisphosphonic acids from dihalogenoalkanes under microwave irradiation

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.

Phosphonic acid derivatives useful as anti-inflammatory agents

Novel 1,2-oxaphosphepins are useful as antiinflammatory and antiarthritic agents. A representative oxaphosphepin is 3,4-dihydro-3-methoxy-7-(phenylmethoxy)-1H-naphth[1,8de][1,2]oxaphosphepin-3-oxide.

(o-Hydroxyphenyl)methylphosphonic acids: Synthesis and Potentiometric Determinations of their pKa Values

(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