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143-09-9

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143-09-9 Usage

General Description

Decan-1-aminium chloride, also known as decylamine hydrochloride, is a chemical compound with the molecular formula C10H23ClN. It is a quaternary ammonium salt that is commonly used as a surfactant and a corrosion inhibitor in various industrial applications. Decan-1-aminium chloride is highly soluble in water and is often used as an emulsifier in the production of cosmetics, pharmaceuticals, and cleaning products. It is also used as a phase-transfer catalyst in organic synthesis reactions. Due to its ability to lower the surface tension of liquids and its corrosion inhibiting properties, decan-1-aminium chloride is widely used in the manufacturing of industrial cleaning agents and antistatic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 143-09-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,4 and 3 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 143-09:
(5*1)+(4*4)+(3*3)+(2*0)+(1*9)=39
39 % 10 = 9
So 143-09-9 is a valid CAS Registry Number.

143-09-9SDS

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 n-Decylammonium chloride

1.2 Other means of identification

Product number -
Other names NDA hydrochloride

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:143-09-9 SDS

143-09-9Relevant articles and documents

Synthesis, Characterization, Surface, and Thermodynamic Studies of Alkyl Tetrachloroferrates: Performance Evaluation of Their Nanostructures as Biocides

El-Shamy, Omnia A. A.,Habib, Amr O.,Mohamed, Dalia E.,Badawi, Abdelfattah M.

, p. 215 - 223 (2020)

Decyl and dodecylamino tetrachloroferrates were synthesized and characterized using Fourier-transform infrared spectroscopy (FTIR), elemental analysis, X-ray diffraction (XRD), nuclear magnetic resonance (1H-NMR), and atomic absorption spectroscopy (AAS). The surface properties of the cationic surfactants including critical micelle concentration, effectiveness, minimum surface area, and maximum surface excess were determined using surface tension measurements. The effectiveness of surface tension reduction (πcmc) was found to increase as the hydrophobic chain length increases with values of 30 and 34 mN m?1 for C10 and C12, respectively. Moreover, the effect of temperature on micellization was determined over the range of 35–55?°C. Thermodynamic parameters (ΔG°, ΔS°, and ΔH°) were calculated and the results indicate a spontaneous process for both micellization and adsorption. The nanoparticles (NC10 and NC12) of the prepared surfactants were obtained using the ball mill technique. The particle size and morphology of the nanoparticles were determined using transmission electron microscope measurements. The antibacterial study of the nanoparticle surfactants revealed their strong efficiency against fungi and different pathogenic bacteria compared with the original surfactants.

Synthesis of Molybdenum Pincer Complexes and Their Application in the Catalytic Hydrogenation of Nitriles

Leischner, Thomas,Spannenberg, Anke,Junge, Kathrin,Beller, Matthias

, p. 4543 - 4549 (2020/07/13)

A series of molybdenum(0), (I) and (II) complexes ligated by different PNP and NNN pincer ligands were synthesized and structurally characterized. Along with previously described Mo?PNP complexes Mo-1 and Mo-2, all prepared compounds were tested in the catalytic hydrogenation of aromatic nitriles to primary amines. Among the applied catalysts, Mo-1 is particularly well suited for the hydrogenation of electron-rich benzonitriles. Additionally, two aliphatic nitriles were transformed into the desired products in 80 and 86 percent, respectively. Moreover, catalytic intermediate Mo-1a was isolated and its role in the catalytic cycle was subsequently demonstrated.

Designing Simple Lipidated Lysines: Bifurcation Imparts Selective Antibacterial Activity

Ghosh, Chandradhish,Konai, Mohini Mohan,Sarkar, Paramita,Samaddar, Sandip,Haldar, Jayanta

supporting information, p. 2367 - 2371 (2016/11/13)

In the global effort to thwart antimicrobial resistance, lipopeptides are an important class of antimicrobial agents, especially against Gram-negative infections. In an attempt to circumvent their synthetic complexities, we designed simple membrane-active agents involving only one amino acid and two lipid tails. Herein we show that the use of two short lipid tails instead of a single long one significantly increases selective antibacterial activity. This study yielded several selective antibacterial compounds, and investigations into the properties of this compound class were conducted with the most active compound. Fluorescence spectroscopic studies revealed the capacity of the representative compound to cause depolarization and permeabilization of bacterial cell membranes. This membrane-active nature of the compound imparts superior activity against persister cells, biofilms, and planktonic cells. Topical application of the compound decreased bacterial burden in mice inflicted with burn-infections caused by Acinetobacter baumannii. We anticipate that the design principles described herein will direct the development of several antimicrobial agents of clinical importance.

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