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2,3-BIS(4-PYRIDYL)BUTANE, also known as BPB, is a versatile chemical compound with the molecular formula C16H16N2. It is a derivative of pyridine and is recognized for its role as a chelating agent in coordination chemistry. BPB's unique structure allows it to form stable and selective metal complexes, making it a valuable ligand in the synthesis of metal-organic frameworks and coordination polymers. Its potential applications span across catalysis, sensing, drug delivery, and the treatment of metal poisoning, highlighting its significance in various scientific and industrial fields.

655-47-0

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655-47-0 Usage

Uses

Used in Coordination Chemistry:
2,3-BIS(4-PYRIDYL)BUTANE is used as a chelating agent for forming stable and selective metal complexes, which is crucial in the synthesis of metal-organic frameworks and coordination polymers. Its ability to chelate metals contributes to the development of advanced materials with tailored properties for specific applications.
Used in Catalysis:
In the field of catalysis, 2,3-BIS(4-PYRIDYL)BUTANE is utilized as a ligand to create catalytically active metal complexes. These complexes can enhance the efficiency and selectivity of various chemical reactions, making BPB an important component in the design of new catalysts.
Used in Sensing Applications:
2,3-BIS(4-PYRIDYL)BUTANE is employed as a sensing agent due to its ability to interact with metal ions. This interaction can lead to changes in the compound's properties, such as fluorescence or color, which can be used to detect and quantify the presence of specific metal ions in a sample.
Used in Drug Delivery Systems:
In pharmaceutical applications, 2,3-BIS(4-PYRIDYL)BUTANE is used as a component in drug delivery systems. Its chelating properties allow for the development of metal-based drug carriers that can improve the bioavailability and targeting of therapeutic agents, potentially enhancing the efficacy and reducing the side effects of certain treatments.
Used in Metal Poisoning Treatment:
2,3-BIS(4-PYRIDYL)BUTANE is used as a potential therapeutic agent for the treatment of metal poisoning. Its ability to chelate heavy metals, such as lead and cadmium, can help in reducing their toxic effects on the body and facilitate their removal from the system.

Check Digit Verification of cas no

The CAS Registry Mumber 655-47-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,5 and 5 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 655-47:
(5*6)+(4*5)+(3*5)+(2*4)+(1*7)=80
80 % 10 = 0
So 655-47-0 is a valid CAS Registry Number.

655-47-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3-bis(4-pyridyl)butane

1.2 Other means of identification

Product number -
Other names meso-2,3-Bis-(4-pyridyl)butan

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:655-47-0 SDS

655-47-0Upstream product

655-47-0Downstream Products

655-47-0Relevant academic research and scientific papers

Elemental selenium reactions with 4-ethylpyridine

Gleich, Edward,Warnke, Zygmunt

, p. 13 - 28 (2007/10/03)

A reaction of elemental selenium with 4-ethylpyridine has been studied. The process was run in sealed ampuls, within 205 - 240°C, under nitrogen. The reaction products were indentified by GC-MS and 1H NMR. The following products have been identified: (4-pyridyl)hydroxymethyl ketone, (4-pyridyl)methyl ketone, (4-pyridyl)-hydroselenomethyl ketone, 2,3-di(4-pyridyl)butane, 1,3-di(4-pyridyl)butane, 1-(4-pyridyl)-1-[2-(4-ethyl)pyridyl]-ethane, 1-(4-pyridyl)-1-[2-(4-ethenyl)pyridyl]ethane.

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