Tag: 200-300

Interfacial tension of crude oil-water system with imidazolium and lactam-based ionic liquids and their evaluation for enhanced oil recovery under high saline environment was written by Sakthivel, Sivabalan;Velusamy, Sugirtha;Nair, Vishnu Chandrasekharan;Sharma, Tushar;Sangwai, Jitendra S.. And the article was included in Fuel in 2017.Formula: C10H20N2O4S The following contents are mentioned in the article:

Matured reservoirs are being targeted for enhanced oil recovery (EOR) operations in the hope to recover the residual oil that remains trapped within the porous media. Chem. enhanced oil recovery is one of the successful oil recovery methods which is being employed for the recovery of the residual oil. Many of the conventional chems. fail to perform under high temperature and high saline reservoir conditions. These situations lead to the search for alternate flooding techniques which could efficiently produce the crude oil to the surface. The present work investigates a possible solution for the recovery of trapped crude oil using lactam and imidazolium based ionic liquids (ILs) specifically targeted towards recovery in high saline environment. Initially, the interfacial tension of the crude oil-water system has been investigated using various chem. agents, such as sodium dodecyl sulfate (SDS), and six different ILs at varying high saline concentrations as a function of temperature (283.15-353.15 K). Subsequently, flooding experiments with only polymer, only SDS, only IL, SDS + polymer and IL + polymer at zero and high saline conditions were performed. It was observed that the IL + polymer flood performed very well in both zero and high salinity conditions as compared to all other flooding systems. The present investigation also portrays an intuition on the evaluation of ILs based on their alkyl chain length. 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. 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.Formula: C10H20N2O4S

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

A series of hybrids with a framework constructed from {-SiW₁₁-Ln-SiW₁₁-}_n chains and {Cu/bimpy} ribbons was written by Zhou, Wanli;Zhang, Zheyu;Peng, Jun;Wang, Xiang;Shi, Zhenyu;Li, Guangzhe. And the article was included in CrystEngComm in 2014.Synthetic Route of C11H9N5 The following contents are mentioned in the article:

This paper reports the preparation and x-ray single crystal structures of five organic-inorganic hybrid compounds with 3D framework, [Cu_2.5(bimpy)₂(H₂O)₂][Ln(H₂O)₃(伪-SiW₁₁O₃₉)]路xH₂O [Ln = Eu^III and x = 3.5 for (1), Ln = Sm^III and x = 2.5 for (2), Ln = Ho^III and x = 3.5 for (3), Ln = Y^III and x = 3.5 for (4), Ln = Ce^III and x = 3 for (5)] (bimpy = 3,5-bis(1-imidazolyl)pyridine). Compounds 1–5 are isostructural, showing a 3D framework featured by {-SiW₁₁-Ln-SiW₁₁-}_n inorganic chains and {Cu/bimpy} metal-organic ribbons stemmed from Cu²⁺ ions and bimpy ligands. The adjacent {Cu/bimpy} ribbons are connected by two antiparallel {-SiW₁₁-Eu-SiW₁₁-}_n chains to create a 2D layer structure, which is extended to a (3,4,4,4,6)-connected 3D framework with (4路7²)(4路6路7³路8)(4²路5³路7)(4²路7²路9²)(4²路5²路6⁷路8³路10) topol. through the Cu-O covalent bonds. The magnetic and electrochem. properties of compounds 1 and 2 have been studied. This study involved multiple reactions and reactants, such as 3,5-Di(1H-imidazol-1-yl)pyridine (cas: 1374155-84-6Synthetic Route of C11H9N5).

3,5-Di(1H-imidazol-1-yl)pyridine (cas: 1374155-84-6) 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. Imidazole also acts as a microtubule destabilizing agents and inhibits topoisomerase and Cytochrome P450 Family 26 Subfamily A Member 1 (CYP26A1) enzymes.Synthetic Route of C11H9N5

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

A ‘two-in-one’ crystal having two different dimensionality in the extended structures: A series of cadmium(II) coordination polymers from V-shaped organic linkers was written by Ramathulasamma, Mukara;Bommakanti, Suresh;Das, Samar K.. And the article was included in Polyhedron in 2021.Application In Synthesis of 3,5-Di(1H-imidazol-1-yl)pyridine The following contents are mentioned in the article:

Three Cd(II) containing coordination polymers, formulated as {Cd(oba)(biip)}_n路nH₂O (1), {Cd(sdba)(biip)}_n路n5H₂O (2) and {[Cd_1.5(hfipbb)₂(biip)_1.5(H₂O)][Cd(hfipbb)(biip)]}_n路n2H₂O (3), were synthesized by using ditopic V-shaped ligands i.e., H₂oba (4,4′-oxydibenzoic acid), H₂sdba (4,4′-thiodibenzoic acid), H₂hfipbb {4,4′-(perfluoropropane-2,2-diyl)dibenzoic acid} and an auxiliary linker, biip [3,5-di(1H-imidazol-1-yl)pyridine] under solvothermal conditions. Compounds 1–3 are characterized by single crystal X-ray diffraction anal., IR spectroscopy, thermogravimetric (TG) and elemental analyses. Compound 1 contains a 3D framework, formed by the connectivity of {CdO₄N₂} secondary building unit (SBU) with the organic linkers, whereas compound 2 is a 2D coordination polymer. Interestingly, unlike to compounds 1 and 2, compound 3 possesses a distinctive structural feature having two crystallog. independent polymeric motifs (polymers, A and B) having two different dimensionality within the same crystal, i.e., coordination polymer A (CP-A) that forms a one-dimensional motif and coordination polymer B (CP-B), which has a two-dimensional structure. This study involved multiple reactions and reactants, such as 3,5-Di(1H-imidazol-1-yl)pyridine (cas: 1374155-84-6Application In Synthesis of 3,5-Di(1H-imidazol-1-yl)pyridine).

3,5-Di(1H-imidazol-1-yl)pyridine (cas: 1374155-84-6) 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. 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 3,5-Di(1H-imidazol-1-yl)pyridine

Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem

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

Rational design of three bifunctional MOFs for photocatalysis degradation and selective adsorption of wastewater organic dyes removal was written by Zhang, Xiaoyin;Zong, Ziao;Zhang, Xia;Zhang, Dongmei;Luo, Qingdan;Bi, Caifeng;Fan, Yuhua. And the article was included in Polyhedron in 2020.Application of 1374155-84-6 The following contents are mentioned in the article:

Three metal-organic frameworks (MOFs) based on transition metals, namely {[Cd(HL)(tib)(H₂O)]·1.5H₂O}_n (1), {[Co₃(L)₂(tib)₂]·4H₂O}_n (2), [Cu(L)(3,5-bibp)]_n (3) (H₃L = 4-(3,5-dicarboxylatobenzyloxy)benzoic, tib = 1,3,5-tris(1-imidazolyl)benzene and 4,4′-bibp = 4,4′-bis(imidazol-1-yl)biphenyl) were designed and successfully synthesized under solvothermal conditions. These three compounds were characterized by single crystal X-ray diffraction, elemental anal., IR spectra, powder X-ray diffraction (PXRD), TGA(TGA) and electrochem. studies. Single crystal X-ray diffraction anal. reveals that compound 1 possesses a 2-nodal (3,5)-connected hms topol. framework with the point symbol (6³·6^9.8), compound 2 unprecedented 3-nodal (8,8,11)-connected 3D framework with a (3⁷·4¹²·5⁹) (3⁸·4¹³·5⁷) (3⁹·4¹⁹·5²³·6⁴) topol., while compound 3 displays a 3D 4-connected sql topol. The electrochem. studies for compound 2 and 3 are discussed. Photocatalytic degradation and adsorption for organic dyes removal from wastewater using three compounds were studied. Significantly, all of the three compounds show good photocatalytic activities for MB and selective adsorption capacity for CR. This study involved multiple reactions and reactants, such as 3,5-Di(1H-imidazol-1-yl)pyridine (cas: 1374155-84-6Application of 1374155-84-6).

3,5-Di(1H-imidazol-1-yl)pyridine (cas: 1374155-84-6) 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.Application of 1374155-84-6

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

Experimental and theoretical study of bifunctional electro-catalysts constructed from different Polyoxometalates and Ag-bimpy segments was written by Zheng, Yanping;Zhou, Wanli;Liu, Xuekun;Yuan, Gang;Peng, Jun. And the article was included in Electrochimica Acta in 2021.Application of 1374155-84-6 The following contents are mentioned in the article:

In this work, upon subtle POMs variation, we reported on the assembly and performances of three new bimetallic component organic-inorganic hybrids, [Ag₂(bimpy)(V^V₂O₆)](1), [Ag₃(bimpy)₂(β-Mo^VI₈O₂₆)](2), [Ag₄(bimpy)₂(H₂O)₂(α-SiW^VI₁₂O₄₀)]â€?H₂O (3) (bimpy = 3,5-bis(1-imidazoly) pyridine). Compound 1 with 3D framework structure is featured by {-V-O-V-}n helical chains, {Ag₃} clusters and {bimpy-Ag-bimpy} units. Compound 2 has a 3,3,6,6-connected 3D architecture with the (4³)(4³)(4²â€?⁹â€?â€?³)(4⁶â€?²â€?⁴â€?â€?²) topol. Compound 3 has a 3,3,4-connected 2D layer with (6²â€?)(6²â€?)(6⁶) topol. The electrochem. and bifunctional electro-catalytic activities of three compounds have been conducted. The exptl. results show that β-[Mo₈O₂₆]^4- hybrid displays better electrocatalytic performance than [V₂O₆]^2- and Keggin-type hybrids for reduction of nitrite, while [V₂O₆]^2- hybrid exhibits better electrocatalytic activity than β-[Mo₈O₂₆]^4- and Keggin hybrids towards oxidations of ascorbic acid. Furthermore, the mol. electrostatic potential and frontier MO were performed. This study involved multiple reactions and reactants, such as 3,5-Di(1H-imidazol-1-yl)pyridine (cas: 1374155-84-6Application of 1374155-84-6).

3,5-Di(1H-imidazol-1-yl)pyridine (cas: 1374155-84-6) 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. 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 of 1374155-84-6

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