Category: 478935-29-4

Reaction kinetics of trioxane synthesis from formaldehyde catalyzed by sulfuric acid/ionic liquid was written by Xie, Hui;Lv, Li;Zhang, Tao;Tang, Shengwei. And the article was included in Reaction Kinetics, Mechanisms and Catalysis in 2021.Electric Literature of C10H20N2O4S The following contents are mentioned in the article:

The composite catalyst composed of sulfuric acid and alkyl imidazole-based acidic ionic liquid was used to replace pure sulfuric acid as the catalyst for the synthesis of trioxane. 1-ethyl-3-methylimidazolium hydrosulfate ([EMIM][HSO₄]), 1-butyl-3-methylimidazolium hydrosulfate ([BMIM][HSO₄]), and 1-hexyl-3-methylimidazole hydrosulfate ([HMIM][HSO₄]) were chosen to form composite catalysts with sulfuric acid. The effects of ionic liquid types, formaldehyde concentration (35 鈭?55 wt%), and temperature (353 鈭?368 K) on the reaction were studied. When H₂SO₄ / [EMIM][HSO₄] was used as catalyst with a dosage of 0.6 mol/kg of formaldehyde solution, the optimal catalytic performance was obtained at 373 K with the 50 wt% formaldehyde solution as initial reactant. Compared to that with pure H₂SO₄ as the catalyst, the trioxane concentration in the reaction system was sharply increased with an increment of 17% by the synergy of ionic liquid [EMIM][HSO₄]. The equilibrium constant was increased from 3.08 x 10^-5 to 4.19 x 10^-5 by the addition of [EMIM][HSO₄]. The reaction was intensified by the inhibition of reverse reaction. It indicates that the addition of [EMIM][HSO₄] has complicated effects on the reaction. The research results provide a deep understand for the catalytic performance of mineral acid/ionic liquid composite catalysts. This study involved multiple reactions and reactants, such as 1-Hexyl-3-methyl-1H-imidazol-3-ium hydrogensulfate (cas: 478935-29-4Electric Literature of 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.Electric Literature of C10H20N2O4S

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

The efficient hydroxyalkylation of phenol with formaldehyde to bisphenol F over a thermoregulated phase-separable reaction system containing a water-soluble Bronsted acidic ionic liquid was written by Wang, Qing;Wu, Zhi Min;Li, Yongfei;Tan, Ying;Liu, Ning;Liu, Yuejin. And the article was included in RSC Advances in 2014.Product Details of 478935-29-4 The following contents are mentioned in the article:

The efficient hydroxyalkylation of phenol with formaldehyde to bisphenol F over a thermoregulated phase-separable reaction system containing a water-soluble Bronsted acidic ionic liquid(IL) was studied. The reaction system containing the water-soluble IL showed thermoregulated biphasic behavior with change of the alkyl chain length of IL, temperature and water amount. Four types of imidazolium-, ammonium-, phosphonium- and pyridinium-based water-soluble ionic liquids with different anions of dihydrogen phosphate [H₂PO₄]^–, acetate [CH₃COO]^– and hydrogen sulfate [HSO₄]^– were used as both Bronsted acidic catalysts and thermoregulated solvents. Among them, [C₆MIM][HSO₄] gave a high yield of 80.5% and a selectivity of 96.9% for bisphenol F, and the optimal reaction conditions were stirring speed 450 rpm, phenol-formaldehyde ratio 6 : 1, IL catalyst molar concentration 12.5%, reaction temperature 90 ° and reaction time 1 h. [C₆MIM][HSO₄] could be recovered by simple decantation and could retain its original activity even after six recycling-uses [C_nMIM][HSO₄] with the alkyl chain length n = 6 found to be the most suitable for the synthesis of bisphenol F because of both the formation of a thermoregulated monophasic reaction system at 90 °C to enhance the reaction efficiency and as a thermoregulated phase-transition solvent to facilitate its recovery from the reaction system. This study involved multiple reactions and reactants, such as 1-Hexyl-3-methyl-1H-imidazol-3-ium hydrogensulfate (cas: 478935-29-4Product Details of 478935-29-4).

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. This ring system is present in important biological building blocks, such as histidine and the related hormone histamine.Product Details of 478935-29-4

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Study on mechanism of ionic liquid for methane plasma conversion using spectra method was written by Zhang, Xiu-ling;Zhou, Qian;Di, Lan-bo;Yu, Miao. And the article was included in Guangpuxue Yu Guangpu Fenxi in 2012.Recommanded Product: 1-Hexyl-3-methyl-1H-imidazol-3-ium hydrogensulfate The following contents are mentioned in the article:

C₆MIMBF₄, C₆MIMCF₃COO and C₆MIMHSO₄ were introduced into a d.c. discharge plasma system resp. for methane conversion. The kinds of active species and relative intensity of spectral peaks were detected through online spectrum diagnosis technique of optical emission spectroscopy. Mechanism of ionic liquid for methane conversion in gas-liquid plasma was investigated. The results showed that a spatially and temporally stable gas-liquid interface was obtained in ionic liquid incorporated plasma system. With introduction of ionic liquid, methane conversion and C₂ hydrocarbons yields increased. The C₂ hydrocarbon selectivity greatly increased when C₆MIMCF₃COO and C₆MIMBF₄ were introduced to the plasma, and decreased when C₆MIMHSO₄ was used. Active species like C, C₂, C₃, CH and H were detected in gas-liquid plasma system of methane discharge. Compared with the absence of ionic liquid in the plasma system, the relative intensity of spectral peaks of most active species increased when ionic liquid was introduced into the plasma system. ¹H NMR results showed that the structure of ionic liquid kept stable during plasma discharge progress. Those indicated that ionic liquid could improve the plasma discharge intensity. At the same time, ionic liquid showed good catalytic activity in gas-liquid surface reaction. 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. 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. Recommanded Product: 1-Hexyl-3-methyl-1H-imidazol-3-ium hydrogensulfate

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Nitrolysis of hexamethylenetetramine in presence of ionic liquids was written by Wang, Nai;Shi, Yu;Yang, Hong-wei;Chen, Guang-bin;Lu, Chun-xu. And the article was included in Hanneng Cailiao in 2011.Safety of 1-Hexyl-3-methyl-1H-imidazol-3-ium hydrogensulfate The following contents are mentioned in the article:

Direct nitrolysis of hexamethylenetetramine catalyzed by ionic liquids was studied. The effects of dosage of ionic liquid and different ionic liquids on the nitrolysis were investigated in the systems of 95% nitric acid and nitrogen pentoxide/nitric acid. In the system of 95% nitric acid, [Hmim]NO₃ shows the best catalytic activity in all of ionic liquids screened. The optimal reaction condition is 1.5mol% ionic liquid loading, 12 : 1 of quality ratio of 95% nitric acid to hexamethylenetetramine and 90 min of reaction time at -5-0 °C. 1,3,5-Tri-nitroperhydro-1,3,5-triazine can be obtained in yield of 75.9% using ionic liquid as catalyst under optimized condition, while 1,3,5-tri-nitroperhydro-1,3,5-triazine can be generated in lower yield of 68.3% without adding ionic liquid In the system of nitrogen pentoxide/nitric acid, [Bmim]BF₄ shows the best catalytic activity. The optimal reaction conditions are 5mol% ionic liquid loading, 9 : 1 of mass ratio of 100% nitric acid to hexamethylenetetramine, 2 : 1 of quality ratio of 100% hexamethylenetetramine to nitrogen pentoxide and 60 min of reaction time at -5-0 °C. Under optimized conditions, 77.6% yield of 1,3,5-tri-nitroperhydro-1,3,5-triazine can be obtained without adding ionic liquid, while yield of 1,3,5-tri-nitroperhydro-1,3,5-triazine can be improved to 85.4% using ionic liquid as catalyst. It indicates that ionic liquids have observably catalytic activity on the direct nitrolysis of hexamethylenetetramine. 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 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).Safety of 1-Hexyl-3-methyl-1H-imidazol-3-ium hydrogensulfate

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Probing interfacial behaviors of Bronsted acidic ionic liquids improved isobutane alkylation with C4 olefin catalyzed by sulfuric acid was written by Sun, Weizhen;Zheng, Weizhong;Cao, Piao;Zhao, Ling. And the article was included in Chemical Engineering Journal (Amsterdam, Netherlands) in 2019.Related Products of 478935-29-4 The following contents are mentioned in the article:

The interfacial microenvironments between catalysts and C4 hydrocarbons for the isobutane alkylation is of vital importance to producing high-quality alkylate. In the present work, the interfacial properties between Bronsted acidic ionic liquids (BILs)/H₂SO₄ and C4 mixtures, as well as between the cationic and anionic surfactants/H₂SO₄ and C4 mixtures were investigated using mol. dynamic (MD) simulations, in which BILs share different alkyl chain length on cations with or without a sulfonic acid group. It indicated both BILs and surfactants can enhance the H₂SO₄/C4 reactants interfacial properties and facilitate C4 reactants dissolution, contributing to a better catalytic performance. The enhancement of the interfacial properties can be ascribed into the stronger d. enrichment and perpendicular behaviors of the longer alkyl chains at the interface. Compared to non-SFILs, sulfonic-acid-functionalized Bronsted acidic ionic liquids (SFILs) can facilitate a higher dissolution of isobutane in both bulk and interfacial regions, but result in a lower interfacial diffusion. In addition, the much stronger interfacial enrichment of surfactants without mixing with H₂SO₄ leads to a worse catalytic performance than BILs. However, the better mixing between BILs and H₂SO₄ leading to better catalytic performance suggests the important role of the BILs acting as phase transfer catalyst for the H₂SO₄-catalyzed alkylation. 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. 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 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. Related Products of 478935-29-4

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Optimization and kinetic study of biodiesel production through esterification of oleic acid applying ionic liquids as catalysts was written by Roman, Fernanda F.;Ribeiro, Antonio E.;Queiroz, Ana;Lenzi, Giane G.;Chaves, Eduardo S.;Brito, Paulo. And the article was included in Fuel in 2019.Safety of 1-Hexyl-3-methyl-1H-imidazol-3-ium hydrogensulfate The following contents are mentioned in the article:

In this study, 1-methylimidazolium hydrogen sulfate, [HMIM]HSO₄, ionic liquid, was successfully applied as a catalyst in the biodiesel production through the esterification reaction of oleic acid with methanol. A response surface methodol. (RSM) known as Box-Behnken Design (BBD) was applied to optimize the main exptl. reaction conditions, using a set of 27 experiments This optimization was based on the maximization of both the conversion of oleic acid and the Fatty Acid Me Esters (FAME) content of the obtained biodiesel samples. It was concluded that the two most relevant parameters for both the conversion and the FAME content were the molar ratio between oleic acid and methanol and the catalyst dosage. Accordingly to the model, the optimum condition for the maximum conversion was determined as being 8 h, 110 ± 2 °C, 15:1 M ratio methanol/oleic acid and a catalyst dosage of 15 wt%, resulting in a 95% conversion and for the maximum FAME content were 8 h, 110 ± 2 °C, 14:1 M ratio and a catalyst dosage of 14 wt%, leading to a FAME content of 90%. The kinetics of the esterification reaction was also evaluated, and the exptl. results were well described using a third-order reaction model. The kinetic parameters were exptl. determined, and the value of the activation energy was 6.8 kJ/mol and the pre-exponential factor was 0.0765 L².mol^-2.min^-1 confirming that the ionic liquid, [HMIM]HSO₄, is a good alternative for replacing traditional catalysts for biodiesel production through esterification reaction. 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. Imidazole is a heterocyclic compound with a five-membered planar ring. It is amphoteric and highly polar. 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).Safety of 1-Hexyl-3-methyl-1H-imidazol-3-ium hydrogensulfate

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Performance and Mechanism of Alkylimidazolium Ionic Liquids as Corrosion Inhibitors for Copper in Sulfuric Acid Solution was written by Tian, Guocai;Yuan, Kaitao. And the article was included in Molecules in 2021.SDS of cas: 478935-29-4 The following contents are mentioned in the article:

The addition of corrosion inhibitors is an economic and environmental protection method to prevent the corrosion of copper. The adsorption, performance, and mechanism of three 1-alkyl-3-methylimidazolium hydrogen sulfate ([BMIM]HSO4, [HMIM]HSO4, and [OMIM]HSO4) ionic liquids (ILs) on the copper surface in 0.5 M H₂SO₄ solutions were studied by quantum chem. calculation, quant. structure-activity relationship (QSAR), and mol. dynamics simulation. It is found that the main reactive site is located on the imidazolium ring (especially the C2, N4, and N7 groups). When the alkyl chain of the imidazolium ring is increasing, the mol. reactivity of the ILs and the interaction between the ILs inhibitor and copper surface are enhanced. The imidazole ring of the ILs tends to be adsorbed on Cu (111) surface in parallel through phys. adsorption. The order of adsorption energy is [Bmim]HSO4 < [Hmim]HSO4 < [OMIM]HSO4, which is in agreement with the exptl. order of corrosion efficiency. On the imidazole ring, the interaction between the copper surface and the C atom is greater than that between the copper surface and the N atom. It is found that ILs addition can hinder the diffusion of corrosion particles, reduce the number d. of corrosion particles and slow down the corrosion rate. The order of inhibition ability of three ILs is [Bmim]HSO4 < [Hmim]HSO4 < [OMIM]HSO4,which agree well with exptl. results. A reliable QSAR correlation between the inhibition corrosion efficiency and mol. reactivity parameters of the ILs was established. This study involved multiple reactions and reactants, such as 1-Hexyl-3-methyl-1H-imidazol-3-ium hydrogensulfate (cas: 478935-29-4SDS of cas: 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 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.SDS of cas: 478935-29-4

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

Probing the solute-solvent interactions in the binary mixtures of ionic liquids with water and alcohols by conductance, viscosity and IR spectroscopy was written by Jain, Preeti;Kumar, Anil. And the article was included in Journal of Molecular Liquids in 2017.Formula: C10H20N2O4S The following contents are mentioned in the article:

The molar conductance and viscosities of the bisulfate ([HSO₄]^–) and ethylsulfate ([EtSO₄]^–)-based imidazolium ionic liquids in various mol. solvents have been measured at 298.15 K as a function of concentration of ionic liquids (1 × 10^– 4 to 0.1 mol L^– 1). It is shown that the anions have considerable effect on the molar conductance and association constant of the [HSO₄]^– and [EtSO₄]^–-based imidazolium ionic liquids Higher molar conductance of the [HSO₄]^–-based imidazolium ionic liquids in polar protic solvents (water and methanol) is noted as compared to the [EtSO₄]^–-based imidazolium ionic liquids, though the [HSO₄]^–-based imidazolium ionic liquids possess higher association constant in water than in methanol. The intermol. interactions in the pure and binary mixture of [HSO₄]^– and [EtSO₄]^–-based imidazolium ionic liquids have been investigated by IR spectroscopy. The C₂-H stretching vibration frequency of the imidazolium ring reveals the H-bonding between cations and anions of pure ionic liquids and their solutions The transport properties (limiting molar conductance, transport number, ionic mobility and diffusion coefficient) of cations and anions correlate well with the hydrodynamic radius in their aqueous solutions The study shows that the energy barrier for charge transfer is minimal as compared to the fluidity of the aqueous solution of the studied ionic liquids obtained from the Arrhenius equation. 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. 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. 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

Effect of alkylimidazolium ionic liquids on the corrosion inhibition of copper in sulfuric acid solution was written by Zhang, Qi-Bo;Hua, Yi-Xin. And the article was included in Wuli Huaxue Xuebao in 2011.Synthetic Route of C10H20N2O4S The following contents are mentioned in the article:

The effects of three newly synthesized alkylimidazolium based ionic liquids: 1-butyl-3- methylimidazolium hydrogen sulfate ([BMIM]HSO₄), 1-hexyl-3-methylimidazolium hydrogen sulfate ([HMIM]HSO₄), and 1-octyl-3-methylimidazolium hydrogen sulfate ([OMIM]HSO₄), on the corrosion inhibition of Cu in 0.5 mol/L^-1 H₂SO₄ solution were investigated using potentiodynamic polarization and electrochem. impedance spectroscopy. All the measurements show that these alkylimidazolium ionic liquids are excellent inhibitors for Cu in H₂SO₄ media and the effectiveness of these inhibitors decreases as follows: [OMIM]HSO₄ > [HMIM]HSO₄ > [BMIM]HSO₄ at the same concentration Potentiodynamic polarization studies indicate that the three inhibitors are mixed type inhibitors and that both the cathodic and anodic processes of Cu corrosion are suppressed. The electrochem. impedance results were evaluated using an equivalent circuit in which two constant phase elements (CPE) were offered for these systems with 2 time constants Changes in impedance parameters (charge transfer resistance and double layer capacitance) with the addition of the inhibitors also suggest that these imidazolium based mols. act by adsorbing at the Cu/solution interface. The adsorption of these imidazolium based compounds on the Cu surface in an acidic solution is found to fit the Langmuir adsorption isotherm. Thermodn. calculations reveal that the adsorption of inhibitors on the metal surface occurs by a physisorption-based mechanism involving a spontaneous process. This study involved multiple reactions and reactants, such as 1-Hexyl-3-methyl-1H-imidazol-3-ium hydrogensulfate (cas: 478935-29-4Synthetic Route of C10H20N2O4S).

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.Synthetic Route of C10H20N2O4S

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

A thermodynamic framework for determination of gas hydrate stability conditions and water activity in ionic liquid aqueous solution was written by Rasoolzadeh, Ali;Bakhtyari, Ali;Sedghamiz, Mohammad Reza;Javanmardi, Jafar;Nasrifar, Khashayar;Mohammadi, Amir H.. And the article was included in Journal of Molecular Liquids in 2022.Synthetic Route of C10H20N2O4S The following contents are mentioned in the article:

The formation of gas hydrates in pipelines and plugging of the gas flow path are a major cause of operating expenses, safety issues, pressure drop, and fatal accidents. Therefore, the inhibition of gas hydrate formation is of paramount importance. The utilization of a new class of inhibitors such as ionic liquids (ILs) is currently of great interest. In this regard, adjusting water activity in the inhibitor blend (water + IL) is a vital factor. Several models have been developed to calculate the activity of water in the presence of IL(s). The major disadvantage of these models is their correlative basis. This study aimed to propose a rigorous predictive model for the calculation of water activity in the presence of IL(s), which would then be applied in the prediction of the gas hydrate stability conditions. The model is made up of a mol. term (the short-range interactions from Free-Volume-Flory-Huggins (FVFH) activity model) as well as a contribution from ionic interactions as a result of IL(s) dissociation in water (the long-range electrostatic interactions from the extended Debye-Huckel (EDH) model). The overall absolute temperature deviation and the average absolute relative deviation percent in the calculated gas (methane and carbon dioxide) hydrate dissociation temperatures for the whole databank (500 data points including 37 ILs) were found to be 0.61 K and 0.22%, resp. This proves the superiority of the model over the previous correlative-basis ones. Finally, it is concluded that the higher temperature, the higher the IL(s) concentration, and the lower IL(s) mol. weight(s) result in larger model deviations. This study involved multiple reactions and reactants, such as 1-Hexyl-3-methyl-1H-imidazol-3-ium hydrogensulfate (cas: 478935-29-4Synthetic Route of C10H20N2O4S).

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.Synthetic Route of C10H20N2O4S

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem