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18186-71-5

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18186-71-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 18186-71-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,1,8 and 6 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 18186-71:
(7*1)+(6*8)+(5*1)+(4*8)+(3*6)+(2*7)+(1*1)=125
125 % 10 = 5
So 18186-71-5 is a valid CAS Registry Number.

18186-71-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name dodecyl(triethyl)azanium,bromide

1.2 Other means of identification

Product number -
Other names triethyllaurylammonium 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:18186-71-5 SDS

18186-71-5Downstream Products

18186-71-5Relevant articles and documents

Micelle-to-vesicle transition induced by organic additives in catanionic surfactant systems

Yin, Haiqing,Lei, Sheng,Zhu, Shengbao,Huang, Jianbin,Ye, Jianpin

, p. 2825 - 2835 (2006)

A micelle-to-vesicle transition (MVT) induced by the addition of a series of apolar hydrocarbons (n-butylbenzene, n-hexane, n-octane, and n-dodecane) to the catanionic surfactant system n-dodecyltriethylammonium bromide/sodium n-dodecylsulfate (DTEAB/SDS) has been investigated for the first time by means of rheology and turbidity measurements, dynamic light scattering (DLS), and transmission electron microscopy (TEM). Interestingly, a MVT can take place within certain micellar regions, which are dependent on the structure and chain length of the hydrocarbon. However, these hydrocarbons are unable to induce a MVT in another catanionic surfactant system, namely, n-dodecyltriethylammonium bromide/sodium n-dodecylsulfonate (DTEAB/SDSO3), in which the molecular interactions are weaker than in the DTEAB/SDS system. On the other hand, polar additives, such as n-octanol and n-octylamine, exhibit much higher efficiency and activity in inducing MVT than hydrocarbons in both DETAB/SDS and DTEAB/SDSO3. Moreover, DLS, TEM, and time-resolved fluorescence quenching (TRFQ) results demonstrate that the ratio of vesicles to micelles in the system can be actively controlled by addition of polar additives. Possible mechanisms for the above phenomena are presented, and the potential application of controllable micelle/vesicle systems in the synthesis of tailored bimodal mesoporous materials is discussed.

Highly ordered supermicroporous aluminosilicates with cubic Pm3n symmetry fabricated in weakly acidic solution

Fu, Wen Hua,Wang, Yi Meng,He, Ming Yuan

, p. 18519 - 18528 (2013)

Highly ordered supermicroporous aluminosilicates with cubic Pm3n symmetry were prepared for the first time in weakly acidic solutions of succinic acid and malonic acid using dodecyltriethylammonium bromide as a template. The polycarboxylic acids acted as auxiliaries for fabricating the cubic Pm3n structure as well as weak acids. Thermally stable aluminosilicates with a high utilization ratio of Al could be obtained in the presence of succinic acid by either facilely adding aluminum source into the initial synthesis gel or by grinding the as-made silica-surfactant composite with aluminum nitrate. In contrast, thermally stable aluminosilicates could only be prepared via a post-synthesis approach in the presence of malonic acid, probably because of the powerful coordination tendency between malonic acid and Al cations. The thermal stability of the aluminosilicates was enhanced because of the incorporation of Al into the framework or grafting of Al onto the pore walls. Aluminosilicates prepared via the post-synthesis approach preserved the cubic Pm3n structure better than the directly-synthesized ones. In spite of the kind of polycarboxylic acids or the preparation methods, Al was predominantly tetrahedrally coordinated. The aluminosilicates showed a high specific area and pore volume, especially for the post-synthesized ones. The pore size was in the supermicroporous range evidenced by N2 physisorption, though that of the aluminosilicates prepared via the post-synthesis approach was larger. TEM images verified the Pm3n symmetry of the materials herein. The cubic Pm3n aluminosilicates prepared in our research exhibited equal reactivity but a much pronounced deactivation resistance property in the acetalization of cyclohexanone with pentaerythritol.

New chemical family of [n-CxH(2X+1)Net3][BeT3Me] showing ionic plastic-crystal (x = 4, 5), rotator-crystal (x = 6, 7) and liquid-crystal phases (X = 816)

Yamada, Yudai,Kashimoto, Erina,Honda, Hisashi

, p. 1289 - 1298 (2019/09/18)

New ionic liquid crystals of [n-CxH(2x+1)NEt3][BEt3Me] (abbreviated to [CxNEt3][BEt3Me]) were detected for species with even numbers of 8 ˉ x ˉ 16. In contrast, plastic- and rota

Investigation of cationic surfactants and sulfonamides and their nanoparticles as biocides against sulfur reducing bacteria in the petroleum industry

Morsy, Salwa M. I.,Ibrahim, Mohamed M.

, p. 530 - 536 (2014/01/06)

A series of cationic ammonium surfactants (1-3) and sulfonamides (4-5) were synthesized and characterized using elemental analysis and FT-IR spectroscopy. The nanostructures of the synthesized surfactants and sulfonamides as silver and zinc nanoparticles

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