16610-63-2 Usage
Description
LAURYL ALCOHOL DIPHOSPHONIC ACID is a phosphonic acid derivative characterized by a long hydrophobic chain, which serves as a corrosion inhibitor and chelating agent in various industrial applications. Its unique structure allows it to effectively prevent and control scale deposits and corrosion in water systems, making it a valuable component in maintaining clean and protected equipment.
Uses
Used in Industrial Water Treatment:
LAURYL ALCOHOL DIPHOSPHONIC ACID is used as a corrosion inhibitor and chelating agent for preventing and controlling scale deposits and corrosion in water systems. Its hydrophobic chain and phosphonic acid properties make it highly effective in this application.
Used in Oilfield Applications:
In the oilfield industry, LAURYL ALCOHOL DIPHOSPHONIC ACID is utilized as a corrosion inhibitor and scale control agent to protect equipment and infrastructure from the damaging effects of scale buildup and corrosion.
Used in Cleaning and Personal Care Products:
LAURYL ALCOHOL DIPHOSPHONIC ACID is used as a surfactant and detergent in various cleaning and personal care products. Its ability to form micelles and emulsify oils makes it an effective ingredient for creating foam and removing dirt and grease.
Used in Water Treatment for Equipment Protection:
LAURYL ALCOHOL DIPHOSPHONIC ACID is employed as a component in water treatment systems to keep equipment clean and protected against scale and corrosion. Its properties help maintain the efficiency and longevity of water systems and associated equipment.
Check Digit Verification of cas no
The CAS Registry Mumber 16610-63-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,6,1 and 0 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 16610-63:
(7*1)+(6*6)+(5*6)+(4*1)+(3*0)+(2*6)+(1*3)=92
92 % 10 = 2
So 16610-63-2 is a valid CAS Registry Number.
16610-63-2Relevant articles and documents
A mild and efficient one-pot synthesis of 1-hydroxymethylene-1,1-bisphosphonic acids. Preparation of new tripod ligands
Lecouvey, Marc,Mallard, Isabelle,Bailly, Théodorine,Burgada, Ramon,Leroux, Yves
, p. 8475 - 8478 (2001)
A simple and efficient one-pot procedure for synthesis of 1-hydroxymethylene-1,1-bisphosphonic acids by reaction of acyl chlorides and tris(trimethylsilyl)phosphite is described. This method was applied to the synthesis of new phosphonated chelating tripod ligands.
Cyclodextrins: A promising drug delivery vehicle for bisphosphonate
Monteil, Maelle,Lecouvey, Marc,Landy, David,Ruellan, Steven,Mallard, Isabelle
, p. 285 - 293 (2016/09/23)
Bisphosphonates are well established pharmaceutical drugs with wide applications in medicine. Nevertheless, the side chain and the nature of phosphorous groups could induce a poor aqueous solubility and act on their bioavailability. At the same time, cyclodextrins are cage molecules that facilitate transport of hydrophobic molecules to enhance the intestinal drug absorption of these molecules by forming inclusion complexes. Here we demonstrate that cyclodextrins could be used as a bisphosphonate carrier. The formation of cyclodextrins-bisphosphonate complexes was characterized by 1D and 2D NMR spectroscopy, Isothermal Titration Calorimetry and UV–vis spectroscopy. The results revealed that only the side chain of bisphosphonate was involved in the inclusion phenomenon and its length was a crucial parameter in the control of affinity. Findings from this study suggest that cyclodextrin will be a useful carrier for bisphosphonates.
Bisphosphonates as inhibitors of acid sphingomyelinase
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Page/Page column 8-10, (2011/04/14)
The present invention refers to bisphosphonate and phosphonate/phosphate compounds of Formulae I and II and its use as inhibitors of aSMase enzyme activity.
