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(2-Pyridinylmethyl)phosphonic acid is a phosphonic acid derivative that features a pyridine ring connected to a phosphonic acid group via a methyl bridge. This unique structure endows it with strong metal ion binding properties, making it a versatile chemical for various applications in science and industry.

80241-45-8

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80241-45-8 Usage

Uses

Used in Industrial Applications:
(2-Pyridinylmethyl)phosphonic acid is used as a chelating agent for metal ion sequestration, which is crucial in various industrial processes. Its ability to bind with metal ions effectively helps in controlling and removing these ions from aqueous solutions, thereby preventing issues such as scale formation and corrosion.
Used in Water Treatment:
In the water treatment industry, (2-Pyridinylmethyl)phosphonic acid is utilized as a chelating agent to manage metal ions in water systems. This application is essential for maintaining water quality and preventing the adverse effects of metal ion contamination, such as the promotion of microbial growth and the corrosion of pipes and equipment.
Used in Corrosion Inhibition:
(2-Pyridinylmethyl)phosphonic acid serves as a corrosion inhibitor in industrial settings, where it helps to protect metal surfaces from degradation. Its chelating properties allow it to form stable complexes with metal ions, thereby reducing the corrosive effects of these ions on metal surfaces.
Used in Research Applications:
(2-Pyridinylmethyl)phosphonic acid is used as a research chemical, where its strong metal ion binding properties are leveraged to study and understand the interactions between metal ions and various chemical species. This research can lead to the development of new technologies and methods for metal ion management.
Used in Pharmaceutical Synthesis:
As a precursor for the synthesis of other phosphonic acid-based compounds, (2-Pyridinylmethyl)phosphonic acid is used in the pharmaceutical industry. Its unique structure can be employed to create new drug candidates with potential therapeutic applications.
Used in Agrochemicals:
(2-Pyridinylmethyl)phosphonic acid also has potential applications in the agrochemical industry, where it may be used to develop new compounds for crop protection and enhancement of agricultural productivity.
Used in Material Science:
In the field of material science, (2-Pyridinylmethyl)phosphonic acid can be used to develop new materials with specific properties, such as improved metal binding capabilities or enhanced resistance to corrosion. Its unique structure and properties make it a valuable component in the creation of advanced materials for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 80241-45-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,2,4 and 1 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 80241-45:
(7*8)+(6*0)+(5*2)+(4*4)+(3*1)+(2*4)+(1*5)=98
98 % 10 = 8
So 80241-45-8 is a valid CAS Registry Number.

80241-45-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name pyridin-2-ylmethylphosphonic acid

1.2 Other means of identification

Product number -
Other names SYC

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:80241-45-8 SDS

80241-45-8Upstream product

80241-45-8Downstream Products

80241-45-8Relevant academic research and scientific papers

Photolysis of Pyridylmethyl- and Pyridiniomethylphosphonic Acids

Okamoto, Yoshiki,Kokubo, Ichiro,Takamuku, Setsuo

, p. 2438 - 2440 (2007/10/02)

Upon UV-irradiation, the C-P bond of (4-pyridylmethyl)phosphonic acid cleaved only near the isoelectronic point to give 4-methylpyridinium phophate, while (1-benzyl-4-pyridiniomethyl)phosphonic acid underwent C-P bond cleavage above pH 4 to give 1-benzyl-4-methylpyridinium phosphate.On the other hand, the C-P bond of (2-pyridylmethyl)phosphonic acid cleaved under pH region of about 1 to 2, while (1-benzyl-2-pyridiniomethyl)phosphonic acid underwent C-P bond cleavage above pH4.

Carbon-Phosphorus Bond Formation by Reaction of Pyridine and its Monomethyl-substituted Derivatives with Tetraphosphorus Decasulphide

Bunel, Emilio,Manzur, Jorge,Retuert, Jaime

, p. 3438 - 3445 (2007/10/02)

The reactions of pyridine and 2-, 3-, and 4-methylpyridines with tetraphosphorus decasulfide have been investigated.With the exception of 3-methylpyridine the reactions lead to compounds with a carbon-phosphorus bond. 3-Methylpyridine gives only an adduct with an internal salt structure.

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