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448245-52-1

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448245-52-1 Usage

Description

1-Butyl-3-methylimidazolium dicyanamide is an ionic liquid that belongs to the imidazolium family. It is characterized by its cationic structure with a butyl group and a methyl group attached to the imidazolium ring, and an anionic dicyanamide group. This ionic liquid exhibits unique properties such as high thermal stability, low volatility, and good solubility, making it a versatile compound for various applications.

Uses

Used in Chemical Industry:
1-Butyl-3-methylimidazolium dicyanamide is used as a catalyst in the preparation method of Carbon-supported alkaline ionic liquid-metal catalysts. Its unique properties, such as high thermal stability and good solubility, make it an ideal candidate for catalytic applications.
Used in Textile Industry:
1-Butyl-3-methylimidazolium dicyanamide is used as a catalyst in the catalytic transfer hydrogenation of Azo intermediates to produce UV absorber Benzotriazole. This process is essential in the textile industry for the synthesis of dyes and pigments with improved properties, such as enhanced UV absorption and reduced environmental impact.

Check Digit Verification of cas no

The CAS Registry Mumber 448245-52-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,4,8,2,4 and 5 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 448245-52:
(8*4)+(7*4)+(6*8)+(5*2)+(4*4)+(3*5)+(2*5)+(1*2)=161
161 % 10 = 1
So 448245-52-1 is a valid CAS Registry Number.
InChI:InChI=1/C8H15N2.C2N3/c1-3-4-5-10-7-6-9(2)8-10;3-1-5-2-4/h6-8H,3-5H2,1-2H3;/q+1;-1

448245-52-1 Well-known Company Product Price

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  • (Code)Product description
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  • Alfa Aesar

  • (H59175)  1-n-Butyl-3-methylimidazolium dicyanamide, 97%   

  • 448245-52-1

  • 5g

  • 909.0CNY

  • Detail
  • Alfa Aesar

  • (H59175)  1-n-Butyl-3-methylimidazolium dicyanamide, 97%   

  • 448245-52-1

  • 50g

  • 5097.0CNY

  • Detail
  • Aldrich

  • (55220)  1-Butyl-3-methylimidazoliumdicyanamide  ≥97.0% (HPLC)

  • 448245-52-1

  • 55220-5G-F

  • 3,484.26CNY

  • Detail
  • Aldrich

  • (55220)  1-Butyl-3-methylimidazoliumdicyanamide  ≥97.0% (HPLC)

  • 448245-52-1

  • 55220-50G-F

  • 11,723.40CNY

  • Detail

448245-52-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-Butyl-3-methylimidazolium dicyanamide

1.2 Other means of identification

Product number -
Other names 1-Butyl-3-Methylimidazolium Dicyamide

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:448245-52-1 SDS

448245-52-1Relevant articles and documents

Electrodeposition of zinc coatings from the solutions of zinc oxide in imidazolium chloride/urea mixtures

Zheng, Yong,Dong, Kun,Wang, Qian,Zhang, Suo Jiang,Zhang, Qin Qin,Lu, Xing Mei

, p. 1587 - 1597 (2012)

To solve the inherent disadvantages in conventional processes for electrodeposition of zinc, it's necessary to develop more high-efficiency and environmentally friendly electrolytes. In this work, it was found that the dissolution of ZnO was remarkably enhanced in some imidazolium chloride by the addition of urea, and the solubility of ZnO in 1:1 [Amim]Cl/urea mixture was as high as 8.35 wt% at 373.2 K. Electrochemical measurements showed that zinc could be readily electrodeposited from the solutions of ZnO. Bright, dense and well adherent zinc coatings with good purity were obtained from 0.6 M solution of ZnO in 1:1 [Amim]Cl/urea at 323.2?343.2 K. It's expected that the solutions of ZnO in imidazolium chloride/urea mixtures have the potential to replace the traditional electrolytes, especially toxic zinc chloride-based ones for zinc electroplating, as well as preparation of zinc materials. Science China Press and Springer-Verlag Berlin Heidelberg 2012.

A Robust Fungal Allomelanin Mimic: An Antioxidant and Potent π-Electron Donor with Free-Radical Properties that can be Tuned by Ionic Liquids

Manini, Paola,Lino, Valeria,Franchi, Paola,Gentile, Gennaro,Sibillano, Teresa,Giannini, Cinzia,Picardi, Emanuela,Napolitano, Alessandra,Valgimigli, Luca,Chiappe, Cinzia,d'Ischia, Marco

, p. 1331 - 1337 (2019/06/24)

Developing effective strategies to increase the chemical stability and to fine-tune the physico-chemical properties of melanin biopolymers by rational control of π-electron conjugation is an important goal in materials science for biomedical and technological applications. Herein we report that poly-1,8-dihydroxynaphthalene (pDHN), a non-nitrogenous, catechol-free fungal melanin mimic, displays a high degree of structural integrity (from MALDI-MS and CP/MAS 13C NMR analysis), a strong radical scavenging capacity (DPPH and FRAP assays), and an unusually intense EPR signal (g=2.0030). Morphological and spectral characterization of pDHN, along with deassembly experiments in ionic liquids, indicated amorphous aggregates of small globular structures with an estimated stacking distance of 3.9 ? and broadband absorption throughout the visible range. These results indicate that DHN-based melanins exhibit a high structural integrity and enhanced antioxidant and free-radical properties of potentially greater biomedical and technological relevance than for typical indole-based eumelanins.

The effect of varying the anion of an ionic liquid on the solvent effects on a nucleophilic aromatic substitution reaction

Hawker, Rebecca R.,Haines, Ronald S.,Harper, Jason B.

supporting information, p. 3453 - 3463 (2018/05/23)

A variety of ionic liquids, each containing the same cation but a different anion, were examined as solvents for a nucleophilic aromatic substitution reaction. Varying the proportion of ionic liquid was found to increase the rate constant as the mole fraction of ionic liquid increased demonstrating that the reaction outcome could be controlled through varying the ionic liquid. The solvent effects were correlated with the hydrogen bond accepting ability (β) of the ionic liquid anion allowing for qualitative prediction of the effect of changing this component of the solute. To determine the microscopic origins of the solvent effects, activation parameters were determined through temperature-dependent kinetic analyses and shown to be consistent with previous studies. With the knowledge of the microscopic interactions in solution, an ionic liquid was rationally chosen to maximise rate enhancement demonstrating that an ionic solvent can be selected to control reaction outcome for this reaction type.

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