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1-BUTYL-3-METHYLIMIDAZOLIUM (L)-LACTATE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 878132-20-8 Structure
  • Basic information

    1. Product Name: 1-BUTYL-3-METHYLIMIDAZOLIUM (L)-LACTATE
    2. Synonyms: 1-BUTYL-3-METHYLIMIDAZOLIUM (L)-LACTATE;1-Butyl-3-methylimidazolium (L)-lactate, 95+%;1-Butyl-3-MethyliMidazoliuM (L)-lactate, 95+% 5GR;1-Butyl-3-MethyliMidazoliuM (L)-LaCLate;[C4MIm]L-Lac;1-Butyl-3-methyl-1H-imidazol-3-ium 2-hydroxypropanoate
    3. CAS NO:878132-20-8
    4. Molecular Formula: C11H20N2O3
    5. Molecular Weight: 228.29
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 878132-20-8.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: Clear yellow to brown/Viscous Liquid
    5. Density: N/A
    6. Refractive Index: 1.491-1.493
    7. Storage Temp.: Inert atmosphere,Room Temperature
    8. Solubility: N/A
    9. CAS DataBase Reference: 1-BUTYL-3-METHYLIMIDAZOLIUM (L)-LACTATE(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-BUTYL-3-METHYLIMIDAZOLIUM (L)-LACTATE(878132-20-8)
    11. EPA Substance Registry System: 1-BUTYL-3-METHYLIMIDAZOLIUM (L)-LACTATE(878132-20-8)
  • Safety Data

    1. Hazard Codes: Xi
    2. Statements: 36/37/38
    3. Safety Statements: 37/39-26
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 878132-20-8(Hazardous Substances Data)

878132-20-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 878132-20-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,8,1,3 and 2 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 878132-20:
(8*8)+(7*7)+(6*8)+(5*1)+(4*3)+(3*2)+(2*2)+(1*0)=188
188 % 10 = 8
So 878132-20-8 is a valid CAS Registry Number.

878132-20-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-Butyl-3-Methylimidazolium (L)-Lactate

1.2 Other means of identification

Product number -
Other names 1-BUTYL-3-METHYLIMIDAZOLIUM (L)-LACTATE

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:878132-20-8 SDS

878132-20-8Downstream Products

878132-20-8Relevant articles and documents

Water sorption by ionic liquids: Evidence of a diffusion-controlled sorption process derived from the case study of [BMIm][OAc]

Spie?, Alex,Brandt, Philipp,Schmitz, Alexa,Janiak, Christoph

, (2021/11/24)

The hydrophilicity of ionic liquids (ILs) could be exploited as desiccants or in sorption-driven heat transformation, yet reports of water sorption isotherms of pure ionic liquids are still scarce. Here, water sorption studies for the six pure hydrophilic ionic liquids with 1-ethyl-3-methylimidazolium [EMIm]+ or 1-butyl-3-methylimidazolium [BMIm]+ cations and acetate [OAc]?, formate [HCOO]? or lactate [Lac]? anions show a steady and high water uptake with a small hysteresis between absorption and desorption over the relative pressure range of p/p0 = 0 – 0.9 for the first time. Repeated static volumetric sorption measurements with different amounts or different surface area of the example IL [BMIm][OAc] reveal a slow and strongly diffusion-driven sorption process stemming from the absorption of surface-adsorbed water into the bulk IL. Extrapolation of the water uptake to very small IL amounts with negligible kinetic hindrance gives an equilibrium water uptake capacity of over 2100 mg/g(IL) at p/p0 = 0.9. Gravimetric control experiments at a relative humidity of 75.5 % confirm the time-dependence with the IL surface area at the gas–liquid-interface and the amount of the IL to reach the equilibrium uptake of 1040 mg/g at p/p0 = 0.75.

A simple halide-to-anion exchange method for heteroaromatic salts and ionic liquids

Alcalde, Ermitas,Dinares, Immaculada,Ibanez, Anna,Mesquida, Neus

experimental part, p. 4007 - 4027 (2012/07/28)

A broad and simple method permitted halide ions in quaternary heteroaromatic and ammonium salts to be exchanged for a variety of anions using an anion exchange resin (A- form) in non-aqueous media. The anion loading of the AER (OH- form) was examined using two different anion sources, acids or ammonium salts, and changing the polarity of the solvents. The AER (A- form) method in organic solvents was then applied to several quaternary heteroaromatic salts and ILs, and the anion exchange proceeded in excellent to quantitative yields, concomitantly removing halide impurities. Relying on the hydrophobicity of the targeted ion pair for the counteranion swap, organic solvents with variable polarity were used, such as CH3OH, CH3CN and the dipolar nonhydroxylic solvent mixture CH3CN:CH2Cl 2 (3:7) and the anion exchange was equally successful with both lipophilic cations and anions.

Imidazolium ionic liquids: A simple anion exchange protocol

Dinares, Immaculada,Garcia De Miguel, Cristina,Ibanez, Anna,Mesquida, Neus,Alcalde, Ermitas

supporting information; experimental part, p. 1507 - 1510 (2010/06/11)

An efficient and simple protocol was developed to obtain quantitative iodide or bromide exchange for a broad range of anions in imidazolium ionic liquids. Selected anions were loaded in an anion exchange resin using two different procedures and were then used to provide a pure convenient ion pair. The Royal Society of Chemistry 2009.

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