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1-Dodecyl-3-methylimidazolium iodide is an ionic liquid crystal that exhibits high conductivity and forms a self-assembled smectic A phase with an interdigitated bilayer structure, making it effective as a hole transport layer in dye-sensitized solar cells. Its mesogenic properties, including mesophase temperature range and anisotropic ionic conductivity, can be enhanced when combined with other components like 1-dodecyl-3-methylimidazolium tetrafluoroborate, forming binary or multi-component systems. The ability to regulate its properties through compositional adjustments highlights its versatility in applications requiring tailored ionic conductivity and phase behavior.

81995-09-7

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81995-09-7 Usage

Cation

1-Dodecyl-3-methylimidazolium The cationic part of the compound, consisting of a dodecyl chain (12 carbon atoms) and a methylimidazolium ring.

Anion

Iodide The iodide anion provides the negative charge to balance the positive charge of the cation.

Physical state

Liquid at or near room temperature The compound is in a liquid state, which is a characteristic feature of ionic liquids.

Hydrophobicity

Due to the dodecyl chain and methylimidazolium cation The compound is hydrophobic, meaning it repels water and can dissolve nonpolar compounds.

Uses

Solvent or catalyst in chemical reactions The compound is often used as a solvent or catalyst in various chemical reactions due to its ability to dissolve a wide range of compounds.

Thermal stability

High The compound is resistant to decomposition at high temperatures, making it suitable for use in various industrial and scientific applications.

Industrial and scientific applications

Production of pharmaceuticals, organic synthesis The compound is used in the production of pharmaceuticals and as a solvent in organic synthesis.

Electrochemical properties

Potential applications in energy storage and conversion devices The compound has been studied for its potential use in energy storage and conversion devices, such as batteries and fuel cells, due to its electrochemical properties.

Check Digit Verification of cas no

The CAS Registry Mumber 81995-09-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,9,9 and 5 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 81995-09:
(7*8)+(6*1)+(5*9)+(4*9)+(3*5)+(2*0)+(1*9)=167
167 % 10 = 7
So 81995-09-7 is a valid CAS Registry Number.
InChI:InChI=1/C16H31N2.HI/c1-3-4-5-6-7-8-9-10-11-12-13-18-15-14-17(2)16-18;/h14-16H,3-13H2,1-2H3;1H/q+1;/p-1

81995-09-7 Well-known Company Product Price

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  • Aldrich

  • (18289)  1-Dodecyl-3-methylimidazoliumiodide  ≥95.0%

  • 81995-09-7

  • 18289-5G-F

  • 2,627.82CNY

  • Detail
  • Aldrich

  • (18289)  1-Dodecyl-3-methylimidazoliumiodide  ≥95.0%

  • 81995-09-7

  • 18289-50G-F

  • 10,301.85CNY

  • Detail

81995-09-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-dodecyl-3-methylimidazol-3-ium,iodide

1.2 Other means of identification

Product number -
Other names 1-Dodecyl-3-methylimidazolium iodide

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:81995-09-7 SDS

81995-09-7Downstream Products

81995-09-7Relevant academic research and scientific papers

Ionic liquid crystal as a hole transport layer of dye-sensitized solar cells

Yamanaka, Noriyo,Kawano, Ryuji,Kubo, Wataru,Kitamura, Takayuki,Wada, Yuji,Watanabe, Masayoshi,Yanagida, Shozo

, p. 740 - 742 (2005)

Use of a new ionic liquid crystal, 1-dodecyl-3-methylimidazolium iodide, and iodine as an electrolyte of dye-sensitized solar cells leads to a high short circuit photocurrent density and a high light-to-electricity conversion efficiency, due to a self-assembled structure of the imidazolium cations, resulting in high conductivity of the electrolyte. The Royal Society of Chemistry 2005.

Regulating mesogenic properties of ionic liquid crystals by preparing binary or multi-component systems

Wang, Meng,Pan, Xu,Xiao, Shangfeng,Zhang, Changneng,Li, Wenxin,Dai, Songyuan

, p. 2299 - 2305 (2012)

In this study, a series of binary systems based ionic liquid crystals (ILCs) C12MIm(BF4)yIx (x + y = 1) are prepared by mixing ILCs 1-dodecyl-3-methylimidazolium iodide (C 12MImI) and 1-dodecyl-3-methylimidazolium tetrafluoroborate (C 12MImBF4), aiming to combine the properties of both C 12MImBF4 and C12MImI. Their mesogenic properties are characterized by thermal analysis, polarized optical microscopy, X-ray diffraction as well as anisotropic ionic conductivity measurements. It is found that the smectic A phase with interdigitated bilayer structure is observed in the C12MIm(BF4)yIx series. The binary system C12MIm(BF4)yIx has a larger mesophase temperature range and interdigitated layer spacing than pure C12MImBF4. And the anisotropic ionic conductivity of the binary system, including parallel and perpendicular to smectic layer, is higher than pure C12MImI. Moreover, in binary system C 12MIm(BF4)yIx, with the increasing content of C12MImI the ability of the anion to form three dimensional hydrogen bonds increases, resulting in the increase of the mesophase temperature range, interdigitated layer spacing and the decrease of anisotropic ionic conductivity. Furthermore, multi-component system based ILCs are obtained by introducing iodine to the binary system, and the mesophase temperature range is lowered, which is associated with the weak ability of I3 - to form hydrogen bond with cations. All these results suggest that we can regulate the mesogenic properties of ILCs as we need by making binary or even multi-component systems.

Ready Access to Anhydrous Anionic Lanthanide Acetates by Using Imidazolium Acetate Ionic Liquids as the Reaction Medium

Bousrez, Guillaume,Renier, Olivier,Kelley, Steven P.,Adranno, Brando,Tahavori, Elnaz,Titi, Hatem M.,Smetana, Volodymyr,Tang, Si-Fu,Mudring, Anja-Verena,Rogers, Robin D.

supporting information, p. 13181 - 13189 (2021/08/16)

Access to lanthanide acetate coordination compounds is challenged by the tendency of lanthanides to coordinate water and the plethora of acetate coordination modes. A straightforward, reproducible synthetic procedure by treating lanthanide chloride hydrates with defined ratios of the ionic liquid (IL) 1-ethyl-3-methylimidazolium acetate ([C2mim][OAc]) has been developed. This reaction pathway leads to two isostructural crystalline anhydrous coordination complexes, the polymeric [C2mim]n[{Ln2(OAc)7}n] and the dimeric [C2mim]2[Ln2(OAc)8], based on the ion size and the ratio of IL used. A reaction with an IL : Ln-salt ratio of 5 : 1, where Ln=Nd, Sm, and Gd, led exclusively to the polymer, whilst for the heaviest lanthanides (Dy?Lu) the dimer was observed. Reaction with Eu and Tb resulted in a mixture of both polymeric and dimeric forms. When the amount of IL and/or the size of the cation was increased, the reaction led to only the dimeric compound for all the lanthanide series. Crystallographic analyses of the resulting salts revealed three different types of metal-acetate coordination modes where η2μκ2 is the most represented in both structure types.

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