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1,2-Benzenediol, 5-(2-aminoethyl)-3-methoxy- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

16032-86-3

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16032-86-3 Usage

Type of compound

Organic compound

Derivative of

Catechol

Benzene ring

A six-carbon ring with alternating single and double bonds

Two hydroxyl groups

Two -OH groups attached to the benzene ring

Methoxy group

An -OCH3 group attached to the benzene ring

Aminoethyl group

A -NH2CH2CH2group attached to the benzene ring

Biological activity

Potential pharmacological applications

Field of interest

Medicine and pharmaceuticals

Check Digit Verification of cas no

The CAS Registry Mumber 16032-86-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,0,3 and 2 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 16032-86:
(7*1)+(6*6)+(5*0)+(4*3)+(3*2)+(2*8)+(1*6)=83
83 % 10 = 3
So 16032-86-3 is a valid CAS Registry Number.

16032-86-3SDS

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-(2-amino-ethyl)-3-methoxy-pyrocatechol

1.2 Other means of identification

Product number -
Other names 5-(2-Amino-aethyl)-3-methoxy-brenzcatechin

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:16032-86-3 SDS

16032-86-3Downstream Products

16032-86-3Relevant academic research and scientific papers

Methoxy group substitution on catechol ring of dopamine facilitates its polymerization and formation of surface coatings

Zhang, Jieyu,Cheah, Yong Shung,Santhanakrishnan, Sridhar,Neoh, Koon Gee,Chai, Christina L.L.

, p. 5 - 15 (2017/03/31)

Deposition of polydopamine on substrates is a facile and effective method of surface modification and the deposited polydopamine can reduce silver ions to form silver nanoparticles (AgNPs) for antibacterial applications. However, polydopamine deposition is a time-consuming process that usually requires 24?h to produce a dense surface coating. Since oxidation of dopamine is critical for its polymerization, we hypothesize herein that substitution of an electron-donating group on the catechol ring of dopamine can enhance its oxidation potential and subsequently accelerate its polymerization. In this work, dopamine substituted with a 5-methoxy group (OMeDA) was prepared. OMeDA polymerized faster than dopamine under similar reaction conditions, resulting in a polymer coating of 13?nm thickness on a silicon surface after 8?h, compared to the 24?h required for dopamine to form a coating of similar thickness. A polymer layer with AgNPs can be directly formed on the silicon substrate after exposure to a solution containing OMeDA and silver nitrate. After 2?h exposure, the silver content on the modified surfaces prepared with OMeDA was 187% higher than that obtained with dopamine, and the antibacterial efficacy of the former against Staphylococcus aureus was correspondingly higher than that of the latter. This study demonstrates that OMeDA with an electron-donating group in the catechol ring offers improvements over dopamine for surface modification applications.

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