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1,5-Pentanebisphosphonic acid is a chemical compound with the formula C5H12O6P2. It is an organic compound that belongs to the class of bisphosphonic acids, which are characterized by the presence of two phosphonic acid groups. This particular compound is used in various industrial applications, including as a scale inhibitor in water treatment processes, where it helps to prevent the formation of calcium carbonate and other mineral deposits. It is also used in the oil and gas industry to control scale formation in pipelines and drilling fluids. Due to its ability to chelate metal ions, 1,5-pentanebisphosphonic acid can be effective in managing scale and corrosion in industrial systems.

4672-25-7

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4672-25-7 Usage

Chemical Category

Organophosphorus compounds

Physical State

White crystalline solid

Primary Use

Scale and corrosion inhibitor in water treatment processes

Pharmaceutical Industry Application

Chelating agent

Metal Ion Binding

Effectively binds to metal ions

Insoluble Precipitate Prevention

Prevents formation of insoluble precipitates

Affinity for Calcium Ions

High affinity for calcium ions

Industrial Process Use

Stabilizer and sequestrant

Check Digit Verification of cas no

The CAS Registry Mumber 4672-25-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,6,7 and 2 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 4672-25:
(6*4)+(5*6)+(4*7)+(3*2)+(2*2)+(1*5)=97
97 % 10 = 7
So 4672-25-7 is a valid CAS Registry Number.

4672-25-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-phosphonopentylphosphonic acid

1.2 Other means of identification

Product number -
Other names 1,5-pentylenediphosphonic acid

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:4672-25-7 SDS

4672-25-7Downstream Products

4672-25-7Relevant academic research and scientific papers

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

experimental part, p. 1583 - 1586 (2010/10/01)

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.

Highly potent bisphosphonate ligands for phosphoglycerate kinase

Jakeman, David L.,Ivory, Andrew J.,Williamson, Michael P.,Blackburn, G. Michael

, p. 4439 - 4452 (2007/10/03)

We have synthesized a series of novel analogs of 1,3-bisphospho-D- glyceric acid, 1,3-BPG, and evaluated their binding to phosphoglycerate kinase, PGK (EC 2.7.2.3). Nonscissile methanephosphonic acids replace the two phosphate monoesters of 1,3-BPG and lead to several stable, tight-binding mimics of this intermediate species in glycolysis. Multiple fluorine substitution for hydrogen in the α-methylene groups of the phosphonic acid 1,3-BPG analogs markedly improves their binding to PGK as determined by NMR analysis. The best ligands bind some 50-100 times more strongly than does the substrate 3-phospho-D-glyceric acid and show a requirement for pK(a)3 to be generally below 6.0, while the presence of a β-carbonyl group seems to be of secondary importance.

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