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23381-52-4

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23381-52-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 23381-52-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,3,8 and 1 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 23381-52:
(7*2)+(6*3)+(5*3)+(4*8)+(3*1)+(2*5)+(1*2)=94
94 % 10 = 4
So 23381-52-4 is a valid CAS Registry Number.

23381-52-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name didecyl(dimethyl)azanium,hydroxide

1.2 Other means of identification

Product number -
Other names -

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:23381-52-4 SDS

23381-52-4Relevant articles and documents

Ammonium ionic liquids with anions of natural origin

Pernak, Juliusz,Lgosz, Bartosz,Walkiewicz, Filip,Klejdysz, Tomasz,Borkowski, Andrzej,Chrzanowski, Lukasz

, p. 65471 - 65480 (2015)

This study was focused on presenting a new class of ionic liquids (ILs) with anions of natural origin. The salts were obtained by hydrolysis of defined triglycerides or edible vegetable oils (coconut oil and canola oil) by quaternary ammonium hydroxides. The basic physicochemical properties of the obtained products were studied and their microbial and deterrent activity was determined. Additionally, their susceptibility to biodegradation was evaluated. The described synthesis pathway utilizes vegetable oils and quaternary ammonium hydroxides as reactants in order to obtain ILs with anions of natural origin, which are characterized by specific biological activity. The majority of the prepared ILs exhibited excellent feeding deterrent properties and could be classified as readily biodegradable compounds. The employed method is characterized by low cost of substrates, high yields and high purity of the obtained products. It might potentially find application as a tool to synthesize environmentally friendly ILs with attractive properties for a wide range of applications.

Epoxy resins cured with ionic liquids as novel supports for metal complex catalysts

Ostrowska, Sylwia,Markiewicz, Bartosz,Wa?sikowska, Karolina,Ba?czek, Natalia,Pernak, Juliusz,Strzelec, Krzysztof

, p. 752 - 760 (2013)

In this work, the application of an epoxy resin cured with ammonium ionic liquids as a support for palladium complex catalyst is reported. Supports based on epoxy resin were obtained as a result of the use of ionic liquids: didecyldimethylammonium tetrafluoroborate [d2m2am][BF 4], 1-methyltheobromine tetrafluoroborate [mthb][BF4], didecyldimethylammonium theobrominate [d2m2am][thb], didecyldimethylammonium theophyllinate [d2m2am][thp] as cross-linking agents. The characterization of polymeric supports and heterogenized palladium catalysts has involved research methods like time-of-flight secondary ion mass spectrometry (TOF-SIMS), infrared spectroscopy (IR), scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS). The activity and stability during long-term use of the investigated catalytic systems were tested in a model Heck reaction. The influence of the type of ILs used as epoxy hardeners on the catalytic properties of epoxy-supported palladium catalysts is discussed.

Synthesis method of amino acid quaternary amino carboxylate

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Paragraph 0059; 0061-0063, (2017/10/07)

The invention relates to a synthesis method of an amino acid quaternary amino carboxylate, and belongs to the technical field of compound synthesis. The synthesis method comprises: dissolving 1 mole of an alkali metal hydroxide in a volatile organic solvent with a temperature of 20-30 DEG C to obtain a solution A; dissolving 1 mole of double chain quaternary amino ammonium halide or single chain quaternary amino ammonium halide into a volatile organic solvent to obtain a solution B; mixing A and B, and removing insoluble substances to obtain a solution C; dissolving acetylated amino acid in a volatile organic solvent until the obtained solution contains 1 mole of the acetylated amino acid anions so as to obtain a solution D; and mixing C and D, and removing insoluble substances and the volatile organic solvents to obtain the product. According to the present invention, the synthesis steps are simplified, the organic reagents with characteristics of low toxicity, easy recovery and easy treatment are used, and the purity of the amino acid quaternary amino carboxylate is improved.

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