Welcome to LookChem.com Sign In|Join Free

CAS

  • or

262297-13-2

Post Buying Request

262297-13-2 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

262297-13-2 Usage

Uses

Different sources of media describe the Uses of 262297-13-2 differently. You can refer to the following data:
1. Basionic Ionic Liquids
2. [BMIM][HSO4] can be used as an additive to accelerate current efficiency, lower power consumption, and enhance the surface morphology during the electrodeposition of zinc from acidic sulfate solutions. The combination of sodium nitrate and [BMIM][HSO4] can be used as a nitrating agent for the selective nitration of phenols to afford its corresponding nitro derivatives. [BMIM][HSO4] can also be used as catalyst for the preparation of 1,8-dioxo-octahydroxanthenes.

General Description

1-Butyl-3-methylimidazolium hydrogen sulfate is an acidic ionic liquid.

Check Digit Verification of cas no

The CAS Registry Mumber 262297-13-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,6,2,2,9 and 7 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 262297-13:
(8*2)+(7*6)+(6*2)+(5*2)+(4*9)+(3*7)+(2*1)+(1*3)=142
142 % 10 = 2
So 262297-13-2 is a valid CAS Registry Number.
InChI:InChI=1/C8H15N2.H2O4S/c1-3-4-5-10-7-6-9(2)8-10;1-5(2,3)4/h6-8H,3-5H2,1-2H3;(H2,1,2,3,4)/q+1;/p-1

262297-13-2 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Aldrich

  • (57457)  1-Butyl-3-methylimidazoliumhydrogensulfate  ≥95% (HPLC)

  • 262297-13-2

  • 57457-100G-F

  • 1,737.45CNY

  • Detail
  • Aldrich

  • (57457)  1-Butyl-3-methylimidazoliumhydrogensulfate  ≥95% (HPLC)

  • 262297-13-2

  • 57457-1KG-F

  • 4,839.12CNY

  • Detail

262297-13-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-butyl-3-methylimidazol-3-ium,hydrogen sulfate

1.2 Other means of identification

Product number -
Other names 1-butyl-3-methylimidazolium hydrogen sulfate

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:262297-13-2 SDS

262297-13-2Synthetic route

1-methyl-3-(n-butyl)imidazolium iodide
65039-05-6

1-methyl-3-(n-butyl)imidazolium iodide

1-butyl-3-methylimidazolium hydrogen sulfate
262297-13-2

1-butyl-3-methylimidazolium hydrogen sulfate

Conditions
ConditionsYield
With Amberlyst A-26 (HSO4- form) In methanol100%
With Amberlist A-26 HSO4(-) form In methanol Ionic liquid;
1-butyl-3-methylimidazolium chloride
79917-90-1

1-butyl-3-methylimidazolium chloride

1-butyl-3-methylimidazolium hydrogen sulfate
262297-13-2

1-butyl-3-methylimidazolium hydrogen sulfate

Conditions
ConditionsYield
With sulfuric acid In dichloromethane for 48h; Reflux; Cooling with ice;99.4%
With sodium hydrogen sulfate In acetonitrile at 25℃; for 96h; Inert atmosphere;97%
With sulfuric acid In dichloromethane for 24h; Reflux;95%
1-butyl-3-methylimidazolium methylsulfate
401788-98-5

1-butyl-3-methylimidazolium methylsulfate

1-butyl-3-methylimidazolium hydrogen sulfate
262297-13-2

1-butyl-3-methylimidazolium hydrogen sulfate

Conditions
ConditionsYield
With water for 24h; Reagent/catalyst; Reflux;99%
With water at 149.84℃; for 18h; Autoclave; High pressure;
With sulfuric acid; water at 165℃;
C7H12N2*CH4O4S

C7H12N2*CH4O4S

1-butyl-3-methylimidazolium hydrogen sulfate
262297-13-2

1-butyl-3-methylimidazolium hydrogen sulfate

Conditions
ConditionsYield
In water at 170 - 215℃; for 4h; Inert atmosphere;98%
1-n-butyl-3-methylimidazolim bromide
85100-77-2

1-n-butyl-3-methylimidazolim bromide

1-butyl-3-methylimidazolium hydrogen sulfate
262297-13-2

1-butyl-3-methylimidazolium hydrogen sulfate

Conditions
ConditionsYield
With 1-hexene; sulfuric acid; dihydrogen peroxide at 25℃; for 3h;97%
With sulfuric acid; silver sulfate In ethanol at 50℃; for 2h;75%
With sulfuric acid; silver sulfate In ethanol; water at 50℃; for 2h;75%
1-methyl-1H-imidazole
616-47-7

1-methyl-1H-imidazole

n-Butyl chloride
109-69-3

n-Butyl chloride

1-butyl-3-methylimidazolium hydrogen sulfate
262297-13-2

1-butyl-3-methylimidazolium hydrogen sulfate

Conditions
ConditionsYield
Stage #1: 1-methyl-1H-imidazole; n-Butyl chloride In toluene for 48h; Reflux;
Stage #2: With potassium hydrogensulfate In toluene
94%
Stage #1: 1-methyl-1H-imidazole; n-Butyl chloride In dichloromethane at 49.84 - 59.84℃;
Stage #2: With potassium hydrogensulfate In dichloromethane at 69.84℃;
1-Butylimidazole
4316-42-1

1-Butylimidazole

1-butyl-3-methylimidazolium hydrogen sulfate
262297-13-2

1-butyl-3-methylimidazolium hydrogen sulfate

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: toluene / 4 h / 20 °C / Inert atmosphere; Cooling with ice
2: water / 18 h / 149.84 °C / Autoclave; High pressure
View Scheme
sulfuric acid
7664-93-9

sulfuric acid

sodium sulfate
7757-82-6

sodium sulfate

1-butyl-3-methylimidazolium chloride
79917-90-1

1-butyl-3-methylimidazolium chloride

1-butyl-3-methylimidazolium hydrogen sulfate
262297-13-2

1-butyl-3-methylimidazolium hydrogen sulfate

Conditions
ConditionsYield
Ionic liquid; Inert atmosphere;
1-methyl-1H-imidazole
616-47-7

1-methyl-1H-imidazole

1-butyl-3-methylimidazolium hydrogen sulfate
262297-13-2

1-butyl-3-methylimidazolium hydrogen sulfate

Conditions
ConditionsYield
Stage #1: 1-methyl-1H-imidazole at 69.84℃; for 12h;
Stage #2: With sulfuric acid In acetonitrile at 69.84℃;
1-methyl-1H-imidazole
616-47-7

1-methyl-1H-imidazole

1-bromo-butane
109-65-9

1-bromo-butane

1-butyl-3-methylimidazolium hydrogen sulfate
262297-13-2

1-butyl-3-methylimidazolium hydrogen sulfate

Conditions
ConditionsYield
Stage #1: 1-methyl-1H-imidazole; 1-bromo-butane for 48h;
Stage #2: With sulfuric acid In ethyl acetate at 70℃; for 48h;
1-butyl-3-methylimidazolium hydroxide

1-butyl-3-methylimidazolium hydroxide

1-butyl-3-methylimidazolium hydrogen sulfate
262297-13-2

1-butyl-3-methylimidazolium hydrogen sulfate

Conditions
ConditionsYield
With sulfuric acid In water
1-butyl-3-methylimidazolium hydrogen sulfate
262297-13-2

1-butyl-3-methylimidazolium hydrogen sulfate

sodium tungstate

sodium tungstate

O32W10(4-)*4C8H15N2(1+)

O32W10(4-)*4C8H15N2(1+)

Conditions
ConditionsYield
at 83℃; for 8h; Ionic liquid;83.5%
1-butyl-3-methylimidazolium hydrogen sulfate
262297-13-2

1-butyl-3-methylimidazolium hydrogen sulfate

1-butyl-3-methylimidazolium propioanate
914497-10-2

1-butyl-3-methylimidazolium propioanate

Conditions
ConditionsYield
With barium dihydroxide; acetic acid In water at 20 - 76℃; for 14.5h;
1-butyl-3-methylimidazolium hydrogen sulfate
262297-13-2

1-butyl-3-methylimidazolium hydrogen sulfate

potassium sulfate

potassium sulfate

sulfur trioxide
7446-11-9

sulfur trioxide

2K(1+)*O7S2(2-)*H2O4S

2K(1+)*O7S2(2-)*H2O4S

Conditions
ConditionsYield
at 60℃; for 96h; Schlenk technique;
1-butyl-3-methylimidazolium hydrogen sulfate
262297-13-2

1-butyl-3-methylimidazolium hydrogen sulfate

1-butyl-3-methylimidazolium peroxymonosulphate
1505450-88-3

1-butyl-3-methylimidazolium peroxymonosulphate

Conditions
ConditionsYield
With Oxone; oxone In acetone for 2h; Sonication; Inert atmosphere;
1-butyl-3-methylimidazolium hydrogen sulfate
262297-13-2

1-butyl-3-methylimidazolium hydrogen sulfate

sulfur trioxide pyridine complex
26412-87-3

sulfur trioxide pyridine complex

C8H15N2(1+)*C5H5N*HO7S2(1-)

C8H15N2(1+)*C5H5N*HO7S2(1-)

Conditions
ConditionsYield
With germaniumtetrachloride at 50℃; for 24h; Sealed tube;
1-butyl-3-methylimidazolium hydrogen sulfate
262297-13-2

1-butyl-3-methylimidazolium hydrogen sulfate

pyridine
110-86-1

pyridine

sulfur trioxide pyridine complex
26412-87-3

sulfur trioxide pyridine complex

2C5H5N*H2O7S2

2C5H5N*H2O7S2

Conditions
ConditionsYield
With europium(III) oxide at 25 - 60℃; for 168h; Sealed tube;
1-butyl-3-methylimidazolium hydrogen sulfate
262297-13-2

1-butyl-3-methylimidazolium hydrogen sulfate

zinc(II) chloride
7646-85-7

zinc(II) chloride

C8H15N2(1+)*HO4S(1-)*ZnCl2

C8H15N2(1+)*HO4S(1-)*ZnCl2

Conditions
ConditionsYield
at 26.84℃; for 5h;
1-butyl-3-methylimidazolium hydrogen sulfate
262297-13-2

1-butyl-3-methylimidazolium hydrogen sulfate

molybdenum dichloride

molybdenum dichloride

C8H15N2(1+)*HO4S(1-)*MoCl2

C8H15N2(1+)*HO4S(1-)*MoCl2

Conditions
ConditionsYield
at 26.84℃; for 5h;
1-butyl-3-methylimidazolium hydrogen sulfate
262297-13-2

1-butyl-3-methylimidazolium hydrogen sulfate

manganese(ll) chloride

manganese(ll) chloride

C8H15N2(1+)*HO4S(1-)*MnCl2

C8H15N2(1+)*HO4S(1-)*MnCl2

Conditions
ConditionsYield
at 26.84℃; for 5h;
1-butyl-3-methylimidazolium hydrogen sulfate
262297-13-2

1-butyl-3-methylimidazolium hydrogen sulfate

iron(III) chloride

iron(III) chloride

C8H15N2(1+)*HO4S(1-)*FeCl3

C8H15N2(1+)*HO4S(1-)*FeCl3

Conditions
ConditionsYield
at 26.84℃; for 5h;
1-butyl-3-methylimidazolium hydrogen sulfate
262297-13-2

1-butyl-3-methylimidazolium hydrogen sulfate

copper dichloride

copper dichloride

C8H15N2(1+)*HO4S(1-)*CuCl2

C8H15N2(1+)*HO4S(1-)*CuCl2

Conditions
ConditionsYield
at 26.84℃; for 5h;
1-butyl-3-methylimidazolium hydrogen sulfate
262297-13-2

1-butyl-3-methylimidazolium hydrogen sulfate

cobalt(II) chloride
7646-79-9

cobalt(II) chloride

C8H15N2(1+)*HO4S(1-)*CoCl2

C8H15N2(1+)*HO4S(1-)*CoCl2

Conditions
ConditionsYield
at 26.84℃; for 5h;
1-butyl-3-methylimidazolium hydrogen sulfate
262297-13-2

1-butyl-3-methylimidazolium hydrogen sulfate

1-butyl-3-methylimidazolium hydroxide

1-butyl-3-methylimidazolium hydroxide

Conditions
ConditionsYield
With strontium(II) hydroxide octahydrate; water Large scale;

262297-13-2Downstream Products

262297-13-2Relevant articles and documents

Concentration-dependent apparent partition coefficients of ionic liquids possessing ethyl- and bi-sulphate anions

Jain, Preeti,Kumar, Anil

, p. 1105 - 1113 (2016)

This study deals with the concentration dependent apparent partition coefficients log P of the ethyl and bisulfate-based ionic liquids. It is observed that the bisulfate-based ionic liquids show different behaviour with respect to concentration as compared to ethyl sulphate-based ionic liquids. It is significant and useful analysis for the further implementation of alkyl sulfate based ionic liquids as solvents in extraction processes. The log P values of the ethyl sulphate-based ionic liquids were noted to vary linearly with the concentration of the ionic liquid, whereas a flip-flop trend with the concentration for the log P values of the bisulphate-based ionic liquids was observed due to the difference in hydrogen bond accepting basicity and possibility of aggregate formation of these anions. The π-π interactions between the imidazolium and pyridinium rings were seen to affect the log P values. The alkyl chain length of anions was also observed to influence the log P values. The hydrophobicity of ionic liquid changes with the alkyl chain in the anion in the order; [HSO4]- 4]- 4]-.

Choline chloride-thiourea, a deep eutectic solvent for the production of chitin nanofibers

Mukesh, Chandrakant,Mondal, Dibyendu,Sharma, Mukesh,Prasad, Kamalesh

, p. 466 - 471 (2014)

Deep eutectic solvents (DESs) consisting of the mixtures of choline halide (chloride/bromide)-urea and choline chloride-thiourea were used as solvents to prepare α-chitin nanofibers (CNFs). CNFs of diameter 20-30 nm could be obtained using the DESs comprising of the mixture of choline chloride and thiourea (CCT 1:2); however, NFs could not be obtained using the DESs having urea (CCU 1:2) as hydrogen bond donor. The physicochemical properties of thus obtained NFs were compared with those obtained using a couple of imidazolium based ionic liquids namely, 1-butyl-3-methylimidazolium hydrogen sulphate [(Bmim)HSO4] and 1-methylimidazolium hydrogen sulphate [(Hmim)HSO4] as well as choline based bio-ILs namely, choline hydrogen sulphate [(Chol)HSO4] and choline acrylate. The CNFs obtained using the DES as a solvent were used to prepare calcium alginate bio-nanocomposite gel beads having enhanced elasticity in comparison to Ca-alginate beads. The bio-nanocomposite gel beads thus obtained were used to study slow release of 5-fluorouracil, an anticancer drug.

A quick, simple, robust method to measure the acidity of ionic liquids

Gr?svik, John,Hallett, Jason P.,To, Trang Quynh,Welton, Tom

, p. 7258 - 7261 (2014)

Introduced here is a quick, simple, robust method to measure acidity in ionic liquid (IL) systems by the use of the NMR-probe mesityl oxide. Acidity corresponding to a Hammett acidity of -1 to -9 can be measured reliably using this technique, a range that vastly exceeds that of any single UV-vis probe.

Efficient combination of recyclable task specific ionic liquid and microwave dielectric heating for the synthesis of lipophilic esters

Arfan, Atef,Bazureau, Jean Pierre

, p. 743 - 748 (2005)

Mild and efficient esterification reactions of carboxylic acids with neo-pentanol were carried out using task-specific ionic liquids with hydrogen sulphate counteranion under microwave irradiation. The latent acidity of the ionic liquid was introduced by

Development of Acidic Imidazolium Ionic Liquids for Activation of Kraft Lignin by Controlled Oxidation: Comprehensive Evaluation and Practical Utility

Klapiszewski, ?ukasz,Szalaty, Tadeusz J.,Kurc, Beata,Stanisz, Ma?gorzata,Zawadzki, Bartosz,Skrzypczak, Andrzej,Jesionowski, Teofil

, p. 361 - 374 (2018)

A novel, eco-friendly method for the activation of lignin by controlled oxidation was studied. The results obtained for six acidic imidazolium ionic liquids containing the hydrogen sulfate anion were compared. The key goal of this research was to increase the content of carbonyl groups in the lignin structure because these may play the main role in the transport of protons and electrons in active materials for electrochemical applications. By means of a variety of analytical techniques (FTIR, 13C CP/MAS NMR, and X-ray photoelectron spectroscopy; selected reactions to determine the presence of carbonyl groups; SEM; zeta-potential analysis; thermogravimetric analysis/differential thermogravimetric analysis; and porous structure analysis), it was determined that the product obtained after treatment with 3-cyclohexyloxymethy-1-methylimidazolium hydrogen sulfate had favorable properties, in terms of the target application. Electrochemical tests proved that the obtained materials could be used as anodes in lithium batteries. The results show that the activation of lignin with ionic liquids can increase its capacity and maintain stability.

Kinetics and quantum chemical study for cyclotrimerization of propanal catalyzed by Br?nsted acidic ionic liquids

Wu, Li,Li, Zhen,Wang, Fang,Lei, Min,Chen, Jing

, p. 86 - 93 (2013)

Several Br?nsted acidic ionic liquids (BAILs) were synthesized and used as catalysts for the cyclotrimerization of propanal. The acidity of different BAILs was explored and a preliminarily study of the relationship between catalytic activity and acidity was performed. The kinetics for the BAILs-catalyzed cyclotrimerization of propanal was studied systemically to determine the kinetic model and the kinetic parameters by taking [BSTMG][HSO4] as the representative catalyst. The effects of various parameters such as catalyst loading, reaction temperature on the kinetics were examined in detail. Besides, the structures of three representative BAILs and the interactions between propanal molecule and ionic pairs of BAILs were studied by means of quantum chemistry calculations.

Insights on the catalytic behaviour of sulfonic acid-functionalized ionic liquids (ILs) in transesterification reactions - voltammetric characterization of sulfonic task-specific ILs with bisulfate anions

Martini, María B.,Fernández, José L.,Adam, Claudia G.

, p. 2731 - 2741 (2021/02/12)

This work shows for the first time the link between the amount of free sulfuric acid (as detected by cyclic voltammetry) and the activity of sulfonic-acid-functionalized ionic liquids (ILs) as acid catalysts for a transesterification reaction, and demonstrates that sulfonic acid groups, while are not directly involved in the catalysis, release the free acid during the reaction. Two imidazolic ILs with bisulfate as the counterion and their corresponding task-specific ILs (TSILs) that resulted from the addition of a sulfonic acid group inside the imidazolic-base structure were studied. The outstanding catalytic activity at room temperature of the TSILs 1-(4-sulfonic acid)-butyl-3-methylimidazolium bisulfate ([bsmim]HSO4) and 1-(4-sulfonic acid)-butyl-imidazolium bisulfate ([bsHim]HSO4) for the transesterification ofp-nitrophenyl acetate with methanol was associated to the significant amounts of free sulfuric acid in equilibria with the ionic pairs. It was concluded that these TSILs function as reservoirs for releasing the free acid, which is the actual acid catalyst. In contrast, the corresponding non-sulfonic ILs supply very little amounts of free acid and consequently present low catalytic activities at room temperature, which in fact can be improved by increasing the reaction temperature up to 100 °C.

Preparation method of low-molecular olefin polymer

-

Paragraph 0053, (2018/06/26)

The invention provides a preparation method of a low-molecular olefin polymer. The preparation method comprises the following steps: low-molecular olefin is subjected to a polymerization reaction under the action of a catalyst, and a product is collected; the catalyst is prepared from ionic liquid, polyphosphoric acid and heteropolyacid by mixing at 30-100 DEG C for 1-12 h. The preparation methodhas the advantages of mild reaction conditions, high conversion rate and good selectivity, and the catalyst is easy to recover and can be recycled; the preparation method is green and pollution-free.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 262297-13-2