Category: 478935-29-4

Synthesis of palm acid polyol esters catalyzed by acidic ionic liquid was written by Niu, Yu-lian;Xing, Bao-mei;Lu, Yang;Li, Zai-jun;Liu, Jun-kang;Huang, Lu. And the article was included in Jiangnan Daxue Xuebao, Ziran Kexueban in 2011.Formula: C10H20N2O4S The following contents are mentioned in the article:

Five acidic ionic liquids were investigated to synthesize palmitoleic acid polyol esters, the results indicated triethylammonium sulfate offers best catalytic activity. Based on temperature-controlled characteristics of triethylammonium sulfate, we designed a novel method for preparation of palmitoleic acid polyol esters, in which the reaction under relatively high temperature combined with the separation of the ionic liquid under relatively low temperature The optimal conditions to produce palmitoleic acid pentaerythritol esters were obtained, and these include a 6:1 of palmitoleic acid/pentaerythritol, 5% of the ionic liquid, 210°C of the reaction temperature and 3.5 h of reaction time. Under corresponding optimal conditions, five palmitoleic acid pentaerythritol esters, which includes palmitoleic acid pentaerythritol ester, palmitoleic acid trimethylolpropane ester, palmitoleic acid dihydroxymethylneopentane ester, palmitoleic acid sorbitol ester and palmitoleic acid 1,3-butanediol ester, were synthesized in the laboratory, and their conversion rates were 94.6%, 94.5%, 97.0%, 98.5% and 99.2%, resp. After the completion of reaction, the triethylammonium sulfate precipitates and separates from the system with decreasing the temperature The ionic liquid obtained can be used to subsequent new synthesis of palmitoleic acid polyol ester. The physicochem. properties of five palmitoleic acid polyol esters were investigated, the results exhibited these are of excellent fluid and low temperature characteristics, their viscosity index and pour point were in the range of 184∼388 and -23∼-40°C resp., the data confirm palmitoleic acid polyol ester can be used as base oil of biodegradable lubricant. This study involved multiple reactions and reactants, such as 1-Hexyl-3-methyl-1H-imidazol-3-ium hydrogensulfate (cas: 478935-29-4Formula: C10H20N2O4S).

1-Hexyl-3-methyl-1H-imidazol-3-ium hydrogensulfate (cas: 478935-29-4) belongs to imidazole derivatives. 1H-imidazole is an imidazole tautomer which has the migrating hydrogen at position 1. It is a conjugate base of an imidazolium cation. It is a conjugate acid of an imidazolide. It is a tautomer of a 4H-imidazole. This ring system is present in important biological building blocks, such as histidine and the related hormone histamine.Formula: C10H20N2O4S

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Highly efficient separation of phenolic compounds from low-temperature coal tar by composite extractants with low viscosity was written by Liu, Qian;Zhang, Xianglan. And the article was included in Journal of Molecular Liquids in 2022.Application In Synthesis of 1-Hexyl-3-methyl-1H-imidazol-3-ium hydrogensulfate The following contents are mentioned in the article:

Highly efficient separation of phenolic compounds from low-temperature coal tar (LTCT) is significant in the industry. In this work, composite extractants composed of imidazolium-based ionic liquids (ILs) and solvents were used to sep. phenolic compounds from model oil and LTCT. First, the COSMO-RS model was used to screen composite extractants that combined the infinite dilution thermodn. indexes and liquid-liquid equilibrium (LLE) calculations Meanwhile, the separation mechanism was analyzed by σ-profile and σ-potential. Then, the reliability of the COSMO-RS model was validated by LLE experiments and FT-IR. The viscosity of composite extractants with high separation performance was further determined Among the composite extractants, 1-ethyl-3-methyl-imidazolium hydrogen sulfate ([emim][HSO4])/ethylene glycol (EG) was selected as the most suitable extractant in the separation process. The m-cresol extraction efficiency and cumene entrainment were 98.1% and 8.3%, resp., at a [emim][HSO₄]:EG molar ratio of 1:2, a temperature of 25 °C, and a composite extractant: model oil mass ratio of 1:1. Moreover, the viscosity of [emim][HSO₄]:EG (1:2) was only 51.8 cP at 25 °C and decreased by 95.6% compared with pure [emim][HSO₄], which enhanced the mass transfer in the separation process. The [emim][HSO₄]:EG (1:2) could be regenerated and reused without significant reduction in separation performance. Finally, [emim][HSO₄]:EG (1:2) was applied to sep. phenolic compounds from LTCT with a phenol extraction efficiency of more than 99.9% and a neutral oil entrainment of 8.3%, providing a promising prospect for the separation of phenolic compounds This study involved multiple reactions and reactants, such as 1-Hexyl-3-methyl-1H-imidazol-3-ium hydrogensulfate (cas: 478935-29-4Application In Synthesis of 1-Hexyl-3-methyl-1H-imidazol-3-ium hydrogensulfate).

1-Hexyl-3-methyl-1H-imidazol-3-ium hydrogensulfate (cas: 478935-29-4) belongs to imidazole derivatives. Many natural products, especially alkaloids, contain the imidazole ring. These imidazoles share the 1,3-C3N2 ring but feature varied substituents. Imidazole has been usedin the lysis, wash and elution buffer for the purification of histidine tagged Sonic Hedgehog(shh-N) protein, in elution buffer in stepwise gradient for the purification of histidine tagged aldo keto reductases using nickel affinity chromatography, as a component of homogenization buffer for the purification of phagosomal compartments from dendritic cells.Application In Synthesis of 1-Hexyl-3-methyl-1H-imidazol-3-ium hydrogensulfate

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Effect of Imidazolium-Based Ionic Liquids on the Interfacial Tension of the Alkane-Water System and Its Influence on the Wettability Alteration of Quartz under Saline Conditions through Contact Angle Measurements was written by Velusamy, Sugirtha;Sakthivel, Sivabalan;Sangwai, Jitendra S.. And the article was included in Industrial & Engineering Chemistry Research in 2017.Safety of 1-Hexyl-3-methyl-1H-imidazol-3-ium hydrogensulfate The following contents are mentioned in the article:

Depleted matured reservoirs contain almost two-thirds trapped oil, which remains unrecovered even after primary and secondary oil recovery methods. Chem. enhanced oil recovery (EOR) methods involve the usage of chem. agents that improve the mobility of the residual oil by mechanisms involving alteration of wettability, viscous fingering reduction within the pay zone, and interfacial tension (IFT) between interfaces of fluids (oil/water) and rock, followed by reduced capillary forces during flooding. Chem. EOR methods need more research for high saline reservoir conditions. In this work, the effect of six imidazolium ionic liquids (ILs) on the IFT of alkane-water systems and alteration of wettability of quartz surface was investigated as a function of IL concentration (0-10000 ppm) and temperature (288.15, 298.15, 308.15, and 318.15 K). Initially, the effect of the various ILs on the IFT of the alkane-aqueous IL system was studied and compared with the neat alkane-water system. Subsequently, synergistic behavior of the ILs + NaCl (0-200000 ppm NaCl) on the system of alkane-aqueous IL + NaCl was performed and compared with the alkane-aqueous IL system at zero salinity. Thereafter, the wettability alteration of quartz-alkane-aqueous IL and quartz-crude oil-aqueous IL systems, under both zero and high salinity conditions at 298.15 K at atm. pressure, was studied using contact angle measurements. The systems with IL showed an increase of contact angle exhibiting an alteration in the wettability from water wet to oil wet, whereas the systems under saline conditions showed a wettability from oil wet to water wet. A synergistic effect of ILs with salt on IFT reduction and wettability alteration has been detected. It is suggested that longer ILs could be a better option for EOR application. This study involved multiple reactions and reactants, such as 1-Hexyl-3-methyl-1H-imidazol-3-ium hydrogensulfate (cas: 478935-29-4Safety of 1-Hexyl-3-methyl-1H-imidazol-3-ium hydrogensulfate).

1-Hexyl-3-methyl-1H-imidazol-3-ium hydrogensulfate (cas: 478935-29-4) belongs to imidazole derivatives. Among the different heterocyclic compounds, imidazole is better known due to its broad range of chemical and biological properties. Imidazole has become an important synthon in the development of new drugs. Imidazole derivatives have antibacterial, antifungal and anticancer functionality. It interacts with DNA and also binds to protein and stops cell division.Safety of 1-Hexyl-3-methyl-1H-imidazol-3-ium hydrogensulfate

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Contact angles and wettability of ionic liquids on polar and non-polar surfaces was written by Pereira, Matheus M.;Kurnia, Kiki A.;Sousa, Filipa L.;Silva, Nuno J. O.;Lopes-da-Silva, Jose A.;Coutinho, Joao A. P.;Freire, Mara G.. And the article was included in Physical Chemistry Chemical Physics in 2015.Related Products of 478935-29-4 The following contents are mentioned in the article:

Many applications involving ionic liquids (ILs) require the knowledge of their interfacial behavior, such as wettability and adhesion. In this context, herein, two approaches were combined aiming at understanding the impact of the IL chem. structures on their wettability on both polar and non-polar surfaces, namely: (i) the exptl. determination of the contact angles of a broad range of ILs (covering a wide number of anions of variable polarity, cations, and cation alkyl side chain lengths) on polar and non-polar solid substrates (glass, Al-plate, and poly-(tetrafluoroethylene) (PTFE)); and (ii) the correlation of the exptl. contact angles with the cation-anion pair interaction energies generated by the Conductor-like Screening Model for Real Solvents (COSMO-RS). The combined results reveal that the hydrogen-bond basicity of ILs, and thus the IL anion, plays a major role through their wettability on both polar and non-polar surfaces. The increase of the IL hydrogen-bond accepting ability leads to an improved wettability of more polar surfaces (lower contact angles) while the opposite trend is observed on non-polar surfaces. The cation nature and alkyl side chain lengths have however a smaller impact on the wetting ability of ILs. Linear correlations were found between the exptl. contact angles and the cation-anion hydrogen-bonding and cation ring energies, estimated using COSMO-RS, suggesting that these features primarily control the wetting ability of ILs. Furthermore, two-descriptor correlations are proposed here to predict the contact angles of a wide variety of ILs on glass, Al-plate, and PTFE surfaces. A new extended list is provided for the contact angles of ILs on three surfaces, which can be used as a priori information to choose appropriate ILs before a given application. This study involved multiple reactions and reactants, such as 1-Hexyl-3-methyl-1H-imidazol-3-ium hydrogensulfate (cas: 478935-29-4Related Products of 478935-29-4).

1-Hexyl-3-methyl-1H-imidazol-3-ium hydrogensulfate (cas: 478935-29-4) belongs to imidazole derivatives. 1H-imidazole is an imidazole tautomer which has the migrating hydrogen at position 1. It is a conjugate base of an imidazolium cation. It is a conjugate acid of an imidazolide. It is a tautomer of a 4H-imidazole. Many drugs contain an imidazole ring, such as certain antifungal drugs, the nitroimidazole series of antibiotics, and the sedative midazolam.Related Products of 478935-29-4

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Effectiveness of various solvents in the microwave-assisted extraction of cellulose from oil palm mesocarp fiber was written by Azlan, Nadiah Syafiqah Mohd;Yap, Chiew Lin;Gan, Suyin;Rahman, Mohd Basyaruddin Abdul. And the article was included in Materials Today: Proceedings in 2022.Application In Synthesis of 1-Hexyl-3-methyl-1H-imidazol-3-ium hydrogensulfate The following contents are mentioned in the article:

Cellulose is a valuable resource for organic synthesis owing to its low cost, abundance, and sustainability. However, crystalline cellulose in lignocellulosic biomass is frequently smothered by the recalcitrant amorphous layers of lignin and hemicellulose that limit its extractability. Therefore, this study aimed to find the best solvent to combine with a microwave-assisted method for fast and efficient extraction of cellulose from oil palm mesocarp fiber. Results showed that γ-valerolactone gave the highest average cellulose yield (64.0%), followed by protic solvents viz. 2-butoxyethanol (62.8%) and Et lactate (57.3%), however, there was no statistical difference (p > 0.05) between the three solvents. Crystalline cellulose in biomass seems to interact with aprotic solvent via dipole-dipole interactions slightly more efficiently than with protic solvent via hydrogen bonds. However, as an aprotic solvent, Et acetate showed an exception low cellulose yield (50.7%), presumably due to its b.p. which is lower than the operating temperature Among all, ILs ([BMIM][Cl], [HMIM][HSO₄] and [EMIM][Ac]) performed the poorest giving only 36.0% to 52.0% of cellulose yields. The mixture of [HMIM][HSO₄]/γ-valerolactone (1:1, volume/volume) performed similar to the sole [HMIM][HSO₄]. Overall, the combination of γ-valerolactone and microwave extraction allowed a high yield of cellulose to be achieved within a short period of 2 min, at a relatively low temperature of 140°C, although faint hydrolysis into glucose was detected. The cellulose extracted from γ-valerolactone showed a higher crystallinity index (46.81%) than raw biomass (24.06%), indicating a high purity product and the removal of amorphous portion. This study involved multiple reactions and reactants, such as 1-Hexyl-3-methyl-1H-imidazol-3-ium hydrogensulfate (cas: 478935-29-4Application In Synthesis of 1-Hexyl-3-methyl-1H-imidazol-3-ium hydrogensulfate).

1-Hexyl-3-methyl-1H-imidazol-3-ium hydrogensulfate (cas: 478935-29-4) belongs to imidazole derivatives. Imidazole is the basic core of some natural products such as histidine, purine, histamine and DNA based structures, etc. Among the different heterocyclic compounds, imidazole is better known due to its broad range of chemical and biological properties. The pharmacophore of imidazole exists in bioactive compounds including amino acids, plant growth regulators and therapeutic agents.n increase of the alkyl chain length of the alcohols. Application In Synthesis of 1-Hexyl-3-methyl-1H-imidazol-3-ium hydrogensulfate

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

A quantum-chemical-based guide to analyze/quantify the cytotoxicity of ionic liquids was written by Torrecilla, J. S.;Palomar, J.;Lemus, J.;Rodriguez, F.. And the article was included in Green Chemistry in 2010.Quality Control of 1-Hexyl-3-methyl-1H-imidazol-3-ium hydrogensulfate The following contents are mentioned in the article:

A COSMO-RS descriptor (S_σ-profile) has been used in quant. structure-activity relationship studies (QSARs) based on a neural network for the prediction of the toxicol. effect of ionic liquids (ILs) on a leukemia rat cell line (Log EC₅₀ IPC-81) for a wide variety of compounds including imidazolium, pyridinium, ammonium, phosphonium, pyrrolidinium and quinolinium ILs. S_σ-profile is a two-dimensional quantum-chem. parameter capable of characterizing the electronic structure and mol. size of cations and anions. By using a COSMO-RS descriptor for a training set of 105 compounds (96 ILs and 9 closely related salts) with known biol. activities (exptl. Log EC₅₀ IPC-81 values), a reliable neural network was designed for the systematic anal. of the influence of structural IL elements (cation side chain, head group, anion type and the presence of functional groups) on the cytotoxicity of ∼450 IL compounds The Quant. Structure-Activity Map (QSAM), a new concept developed here, was proposed as a valuable tool for (i) the mol. understanding of IL toxicity, by relating Log EC₅₀ IPC-81 parameters to the electronic structure of compounds given by quantum-chem. calculations; and (ii) the sustainable design of IL products with low toxicity, by linking the chem. structure of counterions to the predictions of IL cytotoxicity in handy contour plots. As a principal contribution, quantum-chem.-based QSAM guides allow the anal./quantification of the non-linear mixture effects of the toxicophores constituting the IL structures. Based on these favorable results, the QSAR model was applied to estimate IL cytotoxicities in order to screen com. available compounds with comparatively low toxicities. This study involved multiple reactions and reactants, such as 1-Hexyl-3-methyl-1H-imidazol-3-ium hydrogensulfate (cas: 478935-29-4Quality Control of 1-Hexyl-3-methyl-1H-imidazol-3-ium hydrogensulfate).

1-Hexyl-3-methyl-1H-imidazol-3-ium hydrogensulfate (cas: 478935-29-4) belongs to imidazole derivatives. Imidazole derivatives generally have good solubility in protic solvents. Simple imidazole derivatives, such as 1H-imidazole, 2-methyl-1H-imidazole, and 1,2-dimethylimidazole, have very high solubility in water. The pharmacophore of imidazole exists in bioactive compounds including amino acids, plant growth regulators and therapeutic agents.n increase of the alkyl chain length of the alcohols. Quality Control of 1-Hexyl-3-methyl-1H-imidazol-3-ium hydrogensulfate

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Optimization on the conversion of bamboo shoot shell to levulinic acid with environmentally benign acidic ionic liquid and response surface analysis was written by Zhou, Cunshan;Yu, Xiaojie;Ma, Haile;He, Ronghai;Vittayapadung, Saritporn. And the article was included in Chinese Journal of Chemical Engineering in 2013.Recommanded Product: 1-Hexyl-3-methyl-1H-imidazol-3-ium hydrogensulfate The following contents are mentioned in the article:

Levulinic acid (LA) has been identified as a promising green, biomass derived platform chem. Response surface anal. (RSA) with a four-factor-five-level central composite design (CCD) was applied to optimize the hydrolysis conditions for the conversion of bamboo (Phyllostachys Praecox f. preveynalis) shoot shell (BSS) to LA catalyzed with ionic liquid[C₄min]HSO₄. The effects of four main reaction parameters including temperature, time, C_[C4min]HSO4 (initial [C₄mim]HSO₄ concentration) and X_BSS (initial BSS intake) on the hydrolysis reaction for yield of LA were analyzed. A quadratic equation model for yield of LA was established and fitted to the data with an R² of 0.9868, and effects of main factors and their corresponding relationships were obtained with RSA. Model validation and results of CCD showed good correspondence between actual and predicted values. The anal. of variance (ANOVA) of the results indicated that the yield of LA in the range studied was significantly (P < 0.05) affected by the four factors. The optimized reaction conditions were as follows: temperature of 145°C, time of 103.8 min, C_[C4min]HSO4 of 0.9 mol · L^-1 and X_BSS of 2.04% (by mass), resp. A high yield [(71 ± 0.41)% (by mol), triplicate experiment] was obtained at the optimum conditions of temperature of 145°C, time of 104 min, C_[C4min]HSO4 of 0.9 mol · L^-1 and X_BSS of 2% (by mass), which obtained from the real experiments, concurred with the model prediction [73.8% (by mol) based on available C₆ sugars in BSS or 17.9% (by mass) based on the mass of BSS], indicating that the model was adequate for the hydrolysis process. This study involved multiple reactions and reactants, such as 1-Hexyl-3-methyl-1H-imidazol-3-ium hydrogensulfate (cas: 478935-29-4Recommanded Product: 1-Hexyl-3-methyl-1H-imidazol-3-ium hydrogensulfate).

1-Hexyl-3-methyl-1H-imidazol-3-ium hydrogensulfate (cas: 478935-29-4) belongs to imidazole derivatives. Many natural products, especially alkaloids, contain the imidazole ring. These imidazoles share the 1,3-C3N2 ring but feature varied substituents. Imidazole based anticancer drug find applications in cancer chemotherapy. It is used as buffer component for purification of the histidine tagged recombinant proteins in immobilized metal-affinity chromatography (IMAC).Recommanded Product: 1-Hexyl-3-methyl-1H-imidazol-3-ium hydrogensulfate

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Eco-efficient and green method for the enhanced dissolution of aromatic crude oil sludge using ionic liquids was written by Sakthivel, Sivabalan;Velusamy, Sugirtha;Gardas, Ramesh L.;Sangwai, Jitendra S.. And the article was included in RSC Advances in 2014.Application of 478935-29-4 The following contents are mentioned in the article:

The upstream petroleum industry faces operational and tech. problems due to increased deposition of waxes, aromatics and asphaltene from crude oil sludge in oil storage tanks in the form of tank-bottom sludge (TBS). This results in huge production losses, and threatens environmentally safe operation; therefore, safer solutions are needed. In this work, nine aromatic ionic liquids (ILs) are synthesized and tested for the dissolution of TBS with the aid of five solvents, namely, toluene, heptane, decane, Et acetate and hexane. The UV absorbance values of the standard solutions (TBS in solvent) are compared with the sample solutions (TBS in solvent + ILs). It is observed that ILs significantly improve the dissolution of TBS in solvents compared with neat solvent alone. Different weight ratios of TBS : ILs (1 : 1, 1 : 0.5 and 1 : 0.1) are considered in this study. Ionic liquids (ILs) based on an imidazolium cation and various anions, such as [Cl]^–, [Br]^–, [BF₄]^–, [H₂PO₄]^–, [HSO₄]^–, and [PF₆]^–, are considered in this investigation. It is observed that the dissolution of TBS in heptane in the presence of [HMIM]⁺[Br]^– is efficient to a maximum extent of 66% with other solvents showing similar increased solubility effect with various ILs. In the case of hexane, it should be noted that the efficiency of dissolution of TBS goes on decreasing with increasing concentration of TBS in hexane. A hold-time study is also performed with heptane containing ILs and heptanes without ILs to determine the maximum time required for efficient dissolution of TBS. It is observed that the efficiency is increased beyond 66% in the presence of ILs for the dissolution of TBS in heptane, provided that the mixture of solvent and ILs are in contact with the TBS for a prolonged period of 30 days, or even longer as required. FT-IR and ¹³C-NMR spectral analyses are also performed so as to understand the efficiency of the ILs in the dissolution of TBS in various solvents, and it was observed that there is a decrease in the intensity of the peaks in the spectra of treated TBS with solvents, which is further enhanced by the addition of ILs. This study involved multiple reactions and reactants, such as 1-Hexyl-3-methyl-1H-imidazol-3-ium hydrogensulfate (cas: 478935-29-4Application of 478935-29-4).

1-Hexyl-3-methyl-1H-imidazol-3-ium hydrogensulfate (cas: 478935-29-4) belongs to imidazole derivatives. Imidazole derivatives generally have good solubility in protic solvents. Simple imidazole derivatives, such as 1H-imidazole, 2-methyl-1H-imidazole, and 1,2-dimethylimidazole, have very high solubility in water. This ring system is present in important biological building blocks, such as histidine and the related hormone histamine.Application of 478935-29-4

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Use of Aromatic Ionic Liquids in the Reduction of Surface Phenomena of Crude Oil-Water System and their Synergism with Brine was written by Sakthivel, Sivabalan;Velusamy, Sugirtha;Gardas, Ramesh L.;Sangwai, Jitendra S.. And the article was included in Industrial & Engineering Chemistry Research in 2015.HPLC of Formula: 478935-29-4 The following contents are mentioned in the article:

Enhanced oil recovery is governed primarily by the role of interfacial tension between crude oil and water. Interfacial tension (IFT) of the crude oil-water system is one of the vital factors in the anal. of the capillary forces affecting trapped oil within the reservoir rocks. High salinity and temperature of the reservoirs tend to make researchers search for new surfactants to lower the interfacial tension in crude oil-water systems. The current study hopes to create a move toward solving the above problem through the use of aromatic ionic liquids (ILs) based on imidazolium as the cation and various anions such as [Cl]^–, [Br]^–, [BF₄]^–, [H₂PO₄]^–, [HSO₄]^–, and [PF₆]^– in different concentrations This work involves the study of the effect of concentration, temperature, time, and brine on the fate of surface tension (SFT) of water and interfacial tension of crude oil-water systems. The present study also addresses the trend in the elec. conductivity of ILs in water along with the effect of temperature and concentration of ILs. The study reveals that these ILs are effective in reducing the SFT and IFT of water and crude oil-water systems at high salinity and temperature conditions. In the IFT measurements, a linear decrement with increase in temperature is observed for crude oil-water in the presence of ILs. The interfacial tension of the various imidazolium-based ionic liquids with the crude oil-water system has been measured as a function of temperature by means of the Wilhelmy plate method. The influence of the nature of cation and anion of ionic liquids and of the chain length on the cationic head of the ILs on interfacial tension is also discussed in detail. At increased salinity conditions, unlike classical surfactants, these ILs are found to be more successful. Enhanced efficiency of the drop in IFT using NaCl and IL mixture has been confirmed by measuring the IFT between crude oil and the aqueous solution of IL. The synergism of salt and IL mixture on the reduction of IFT has been observed This study involved multiple reactions and reactants, such as 1-Hexyl-3-methyl-1H-imidazol-3-ium hydrogensulfate (cas: 478935-29-4HPLC of Formula: 478935-29-4).

1-Hexyl-3-methyl-1H-imidazol-3-ium hydrogensulfate (cas: 478935-29-4) belongs to imidazole derivatives. The solubility of imidazoles in ethers is lower than that in alcohols and decreases with increasing chain length of the ethers . In contrast, the solubility of benzimidazoles in alcohols (C3–C6) is higher than in water and generally decreases with a This ring system is present in important biological building blocks, such as histidine and the related hormone histamine.HPLC of Formula: 478935-29-4

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Influence of the calcination temperature and ionic liquid used during synthesis procedure on the physical and electrochemical properties of Ti/(RuO₂)_0.8-(Sb₂O₄)_0.2 anodes was written by Santos, Marcel O.;Santos, Gessica V.;Mattedi, Silvana;Griza, Sandro;Eguiluz, Katlin I. B.;Salazar-Banda, Giancarlo R.. And the article was included in Journal of Electroanalytical Chemistry in 2018.Formula: C10H20N2O4S The following contents are mentioned in the article:

The development of synthesis methods to produce efficient anodes for wastewater treatment systems is an important industrial issue. Here, we describe the synthesis and the phys. and electrochem. characterization of Ti/(RuO₂)_0.8-(Sb₂O₄)_0.2 anodes prepared by thermal decomposition The electrodes were prepared using three calcination temperatures (500, 550 and 600 °C) and using 2-hydroxyethylammonium acetate (2HEAA) and methyl-imidazolium hydrogensulfate ((HMIM)HSO₄) ionic liquids (IL) as solvents for the precursors solutions Both ionic liquids used were characterized in terms of water content and viscosity. The 2HEAA IL is almost 10 times more viscous than the (HMIM)HSO₄ IL. The anodes developed were electrochem. characterized by cyclic voltammetry, morphol. factor, electrochem. impedance spectroscopy and accelerated service lifetime tests. The electrodes synthesized using the 2HEAA IL have superior electrocatalytic properties and electrochem. stability than those made using the (HMIM)HSO₄ IL. In addition, the anodes made using the 2HEAA IL as solvent have more homogenous surfaces and higher crystallinity degree than those made using the (HMIM)HSO₄ IL. Among the studied calcination temperatures, combining 550 °C and the 2HEAA IL results in more compact and rough electrode surfaces with the highest electroactive areas and electrochem. stability. Thus, the temperature of 550 °C is suitable for the synthesis of mixed metal oxide (MMO) anodes. The electrodes synthesized using the 2HEAA IL are more efficient in the electrochem. oxidation of the Reactive Yellow 186 dye than those made using the (HMIM)HSO₄ IL. Consequently, the viscosity of the IL used has great influence on the performance of the synthesized anodes. In addition, the high viscosity of the 2HEAA IL results in a lower number of calcinations steps to produce the anodes and, hence, lower production cost. Viscous ionic liquids are therefore promising for the production of MMO anodes via thermal decomposition methods. This study involved multiple reactions and reactants, such as 1-Hexyl-3-methyl-1H-imidazol-3-ium hydrogensulfate (cas: 478935-29-4Formula: C10H20N2O4S).

1-Hexyl-3-methyl-1H-imidazol-3-ium hydrogensulfate (cas: 478935-29-4) belongs to imidazole derivatives. Among the different heterocyclic compounds, imidazole is better known due to its broad range of chemical and biological properties. Imidazole has become an important synthon in the development of new drugs. Imidazole also acts as a microtubule destabilizing agents and inhibits topoisomerase and Cytochrome P450 Family 26 Subfamily A Member 1 (CYP26A1) enzymes.Formula: C10H20N2O4S

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem