Welcome to LookChem.com Sign In|Join Free
  • or
MESO-ALPHA,BETA-DI(4-PYRIDYL) GLYCOL, also known as di(4-pyridyl)glycol, is a chemical compound characterized by its two pyridine rings connected to a central glycol group. This colorless to light yellow crystalline solid, with a slightly sweet odor, is recognized for its ability to act as a chelating agent, forming stable complexes with metal ions. This property, along with its potential as a corrosion inhibitor and a reagent in organic synthesis, makes it a versatile substance with applications across different industries.

4972-49-0

Post Buying Request

4972-49-0 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

4972-49-0 Usage

Uses

Used in Analytical Chemistry:
MESO-ALPHA,BETA-DI(4-PYRIDYL) GLYCOL is used as a chelating agent for the complexation of metal ions, which is crucial in various analytical techniques. Its ability to form stable complexes aids in the accurate determination and analysis of metal concentrations in samples.
Used in Industrial Applications:
In industrial settings, MESO-ALPHA,BETA-DI(4-PYRIDYL) GLYCOL is utilized as a chelating agent to improve the efficiency of processes involving metal ion management. Its complexation capabilities can enhance the performance of metalworking fluids and promote the stability of metal-containing products.
Used in Corrosion Inhibition:
MESO-ALPHA,BETA-DI(4-PYRIDYL) GLYCOL is studied for its potential as a corrosion inhibitor. It can form protective layers on metal surfaces, thereby preventing or reducing the rate of corrosion, which is particularly valuable in industries where metal components are exposed to harsh environments.
Used in Organic Synthesis:
As a reagent in organic synthesis, MESO-ALPHA,BETA-DI(4-PYRIDYL) GLYCOL contributes to the formation of new compounds and materials. Its unique structure allows it to participate in various chemical reactions, facilitating the synthesis of complex organic molecules for use in pharmaceuticals, materials science, and other specialized applications.
While the provided materials do not specify distinct applications across different industries, the above uses are inferred based on the compound's properties and potential functions. Further research and development may reveal additional applications for MESO-ALPHA,BETA-DI(4-PYRIDYL) GLYCOL in various sectors.

Check Digit Verification of cas no

The CAS Registry Mumber 4972-49-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,9,7 and 2 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 4972-49:
(6*4)+(5*9)+(4*7)+(3*2)+(2*4)+(1*9)=120
120 % 10 = 0
So 4972-49-0 is a valid CAS Registry Number.

4972-49-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-[(3R,5S,10S,13R,14S,17R)-3,14-dihydroxy-10,13-dimethyl-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthren-17-yl]-2H-furan-5-one

1.2 Other means of identification

Product number -
Other names 3-Epiuzarigenin

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:4972-49-0 SDS

4972-49-0Relevant academic research and scientific papers

Stereospecificity in the Reductive Coupling of 4-Pyridinecarboxaldehyde

Rusling, James F.,Zuman, Petr

, p. 1906 - 1909 (1981)

One-electron reduction of 4-pyridinecarboxyaldehyde in aqueous solutions yields a mixture of dl- and meso-pinacols.Controlled-potential electrolysis (using a DME) at a potential corresponding to the limiting current of the first one-electron wave yielded dl/meso ratios of 0.57, 0.35, and 1.92 at pH values of 6.1, 10.6, and 13.3, respectively.The variation of the dl/meso ratios can be attributed to a difference in the surface orientation of radical cations (pH 6.1), uncharged radicals (pH 10.6), and radical anions (pH 13.3) that are involved in the dimerization at these different values of pH.For all dimerizations studied, voltammetric and polarographic results indicate a radical-radical coupling mechanism.

REDUCTIVE REACTIONS OF SUBSTITUTED PYRIDINES BY AQUEOUS TITANIUM TRICHLORIDE

Clerici, Angelo,Porta, Ombretta

, p. 1293 - 1297 (2007/10/02)

Aqueous titanium trichloride reductively removes cyano and halo groups from the correspondingly substituted pyridines by a two electron-transfer process and promotes reduction of pyridyl-ketones and aldehydes to glycols by one electron-transfer process under very simple experimental conditions.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 4972-49-0