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46273-39-6

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46273-39-6 Usage

General Description

1-(carboxymethyl)quinolinium is a chemical compound with the molecular formula C12H11NO2. It is a quinoline derivative that contains a carboxymethyl group attached to the quinoline ring. 1-(carboxymethyl)quinolinium has potential applications in pharmaceutical and medical research, as well as in the development of new materials and chemical intermediates. It's also been studied for its antimicrobial and anticancer properties. 1-(carboxymethyl)quinolinium is a versatile molecule that exhibits a range of interesting chemical and biological properties, making it an intriguing subject for further study and potential applications in various fields.

Check Digit Verification of cas no

The CAS Registry Mumber 46273-39-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,6,2,7 and 3 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 46273-39:
(7*4)+(6*6)+(5*2)+(4*7)+(3*3)+(2*3)+(1*9)=126
126 % 10 = 6
So 46273-39-6 is a valid CAS Registry Number.

46273-39-6SDS

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 1-Carboxymethyl-5-joduracil

1.2 Other means of identification

Product number -
Other names 1-Carboxymethyl-chinolinium,Chlorid

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:46273-39-6 SDS

46273-39-6Downstream Products

46273-39-6Relevant articles and documents

Indolizine quaternary ammonium salt inhibitors, part III: Insights into the highly effective low-toxicity acid corrosion inhibitor-synthesis and protection performance

Yang, Zhen,Wang, Yefei,Zhan, Fengtao,Chen, Wuhua,Ding, Mingchen,Qian, Cheng,Wang, Renzhuo,Hou, Baofeng

, p. 18461 - 18475 (2019/12/09)

Three indolizine derivatives (Di-BQC, QM-DiBQC, and PyM-DiBQC), which were prepared facilely in high yield via a 1,3-dipolar cycloaddition reaction, were found to exhibit good corrosion inhibition for steel in concentrated acid without the synergism of propargyl alcohol (PA). The inhibitive derivatives exhibit high protection efficiency and have eco-friendly advantages over the highly toxic PA. The accurate formulas and structures of the three compounds are characterized by high resolution mass spectrometry (HRMS) and nuclear magnetic resonance (NMR) spectroscopy. The corrosion inhibition performance of the indolizine derivatives toward N80 steel was investigated in 15 wt% HCl and 20 wt% HCl by weight loss measurements, electrochemical tests (Tafel and EIS), SEM/EDX analysis and theoretical calculations. The biological toxicity was investigated by using the Microtox toxicity test. At 90 °C, a dosage of 0.1 wt% indolizine derivatives in 15 wt% HCl would decrease the corrosion rate of N80 steel dramatically to less than 10 g m-2 h-1. While for PA, a much higher corrosion rate was observed under the same conditions, indicating that the indolizine derivatives are more effective inhibitors in contrast with PA. Results from gravimetric analysis as well as the electrochemical studies and DFT methods are in good agreement, verifying the fine corrosion prevention of the three compounds. The results of biotoxicity tests confirmed the relatively low-toxicity properties of the indolizine derivatives and the suggested inhibition mechanism was also discussed. All the conclusions above indicate that the new indolizine derivatives could be presented as highly effective acidizing inhibitors and the derivatives may offer a new enlightening strategy for corrosion protection under acidizing conditions.

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