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1-tetradecylquinolinium bromide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

77101-52-1

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77101-52-1 Usage

Common Uses

Surfactant, antimicrobial agent

Chemical Class

Quaternary ammonium compound

Structure

Long hydrophobic tail, positively charged nitrogen atom

Effectiveness

Disrupts cell membranes, kills bacteria and microorganisms

Applications

Household and personal care products, industrial and agricultural uses

Antimicrobial Properties

Strong ability to inhibit harmful bacteria and fungi growth

Potential Medical Use

Inhibition of harmful bacteria and fungi growth

Safety Precautions

Handle with care due to potential hazards and toxicity

Check Digit Verification of cas no

The CAS Registry Mumber 77101-52-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,1,0 and 1 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 77101-52:
(7*7)+(6*7)+(5*1)+(4*0)+(3*1)+(2*5)+(1*2)=111
111 % 10 = 1
So 77101-52-1 is a valid CAS Registry Number.
InChI:InChI=1/C23H36N.BrH/c1-2-3-4-5-6-7-8-9-10-11-12-15-20-24-21-16-18-22-17-13-14-19-23(22)24;/h13-14,16-19,21H,2-12,15,20H2,1H3;1H/q+1;/p-1

77101-52-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-tetradecylquinolin-1-ium,bromide

1.2 Other means of identification

Product number -
Other names tetradecyloquinolinium bromide

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:77101-52-1 SDS

77101-52-1Downstream Products

77101-52-1Relevant academic research and scientific papers

Preparation of quinolinium salts differing in the length of the alkyl side chain

Marek, Jan,Buchta, Vladimir,Soukup, Ondrej,Stodulka, Petr,Cabal, Jiri,Ghosh, Kallol K.,Musilek, Kamil,Kuca, Kamil

experimental part, p. 6386 - 6394 (2012/09/07)

Quaternary quinolinium salts differing in alkyl chain length are members of a widespread group of cationic surfactants. These compounds have numerous applications in various branches of industry and research. In this work, the preparation of quinoline-derived cationic surface active agents differing in the length of the side alkyl chains (from C8 to C20) is described. An HPLC method was successfully developed for distinction of all members of the series of prepared long-chain quinolinium derivatives. In conclusion, some possibilities of intended tests or usage have been summarized. In vitro testing using a microdilution broth method showed good activity of a substance with a C12 chain length against Gram-positive cocci and Candida species.

Antimicrobial and antibiofilm activities of 1-alkylquinolinium bromide ionic liquids

Busetti, Alessandro,Crawford, Deborah E.,Earle, Martyn J.,Gilea, Manuela A.,Gilmore, Brendan F.,Gorman, Sean P.,Laverty, Garry,Lowry, Andrew F.,McLaughlin, Martin,Seddon, Kenneth R.

experimental part, p. 420 - 425 (2010/08/04)

Quinoline derivatives are known to possess a range of bioactive and medicinal activities, which have been exploited in the design of antibacterial, antifungal and antimalarial compounds. In this study, we report on the microbiological toxicity of a series of 1-alkylquinolinium bromides against a range of clinically relevant microorganisms, in both planktonic and sessile (biofilm) cultures. A comparison of antimicrobial activity against planktonic bacteria and established biofilms is presented. In general, 1-alkylquinolinium ionic liquids possess excellent, broad spectrum antimicrobial activity against microorganisms grown in both the planktonic and sessile, or biofilm, mode of growth. Importantly, these compounds are potent against Gram positive and Gram negative bacteria, as well as fungi, with a clear dependency on length of the alkyl substituent for activity, with compounds containing twelve and fourteen carbons in the alkyl group exhibiting highest antimicrobial and antibiofilm activity.

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