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209215-55-4

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209215-55-4 Usage

General Description

2,6-Pyridinediacetic acid is a chemical compound with the molecular formula C8H7NO4. It is a white crystalline solid that is soluble in water. 2,6-Pyridinediacetic acid is commonly used as a chelating agent in chemical analysis and industrial processes. It has the ability to bind to metal ions and form stable complexes, making it useful in water treatment, pharmaceuticals, and as a dietary supplement. Additionally, 2,6-Pyridinediacetic acid has potential applications in the synthesis of organic compounds and coordination chemistry. It is also known for its potential as a pharmaceutical intermediate and for its anti-inflammatory and antioxidant properties.

Check Digit Verification of cas no

The CAS Registry Mumber 209215-55-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,9,2,1 and 5 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 209215-55:
(8*2)+(7*0)+(6*9)+(5*2)+(4*1)+(3*5)+(2*5)+(1*5)=114
114 % 10 = 4
So 209215-55-4 is a valid CAS Registry Number.

209215-55-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[6-(carboxymethyl)pyridin-2-yl]acetic acid

1.2 Other means of identification

Product number -
Other names 6-bromomethylpyridine-2-carboxylic acid ethylester

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:209215-55-4 SDS

209215-55-4Relevant articles and documents

VANADIUM INSULIN-MIMETICS, METHODS OF PREPARATION, AND METHODS FOR TREATMENT OF DIABETES

-

Paragraph 102; 103; 104, (2019/01/05)

Disclosed are vanadyl complexes of Formula 1, Formula 2, and Formula 3, wherein Ri, R2, and R are defined as in the description. The pharmaceutical compositions containing these complexes and uses of the complexes for treatment of Diabetes Mellitus, such as Diabetes Mellitus Type 2, are also disclosed.

Studies on the mechanism of chelate degradation in iron-based, liquid redox H2S removal processes

Chen, Dian,Martell, Arthur E.,McManus, Derek

, p. 264 - 274 (2007/10/02)

Available data on the oxidation of nitrilotriacetic acid (NTA), ethylenedinitrilotetraacetic acid (EDTA), N-hydroxyethylethylenediaminetriacetic acid (HEDTA), and other aminopolycarboxylate chelating agents are reviewed and the intermediates and products of the oxidative degradation of each chelating agent are described and compared.The oxidation of these chelating agents occurs during the reoxidation of the ferrous chelatre to the ferric chelate, during which a Fenton type side reaction occurs in which hydrogen peroxides is formed and which in turn generates the hydroxyl radical by reaction with ferrous ion.The site of oxidative attack by the hydroxyl radical on these ligands seems to be the -CH2- groups α to the carboxylate groups, as well as the -CH2- groups in the ethylene bridges between the nitrogens.The evidence for the implication of the hydroxyl radical as the active oxidant is discussed, and the use of phenyl-tert-butylnitrone (PBN) as the trapping agent for the hydroxyl radical is described.The use of chelating agents as Fe3+/Fe2+ redox catalysts for the oxidation of H2S to sulfur that are less reactive toward the hydroxyl radical is recommended. Key words: chelate degradation, H2S oxidation, nitrilotriacetic acid (NTA), ethylenedinitrilotetraacetic acid (EDTA), N-hydroxyethylethylenediaminetriacetic acid (HEDTA).

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