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M50850

Sigma-Aldrich

2-Methylimidazole

99%

Synonym(s):

2-Methylglyoxaline

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About This Item

Empirical Formula (Hill Notation):
C4H6N2
CAS Number:
693-98-1
Molecular Weight:
82.10
Beilstein:
1368
EC Number:
211-765-7
MDL number:
MFCD00005190
UNSPSC Code:
12352005
PubChem Substance ID:
24896976
NACRES:
NA.22

vapor pressure

<1 mmHg ( 0 °C)

Quality Level

200

Assay

99%

bp

267-268 °C (lit.)

mp

142-143 °C (lit.)

SMILES string

Cc1ncc[nH]1

InChI

1S/C4H6N2/c1-4-5-2-3-6-4/h2-3H,1H3,(H,5,6)

InChI key

LXBGSDVWAMZHDD-UHFFFAOYSA-N

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Application

2-Methylimidazole can be used as:      
  • A coordination regulator to fabricate 2D metal-organic framework-5 (MOF-5) nanosheet, which is used as an efficient catalyst for Knoevenagel condensation reaction.      
  • An alkaline inducer in the synthesis of amorphous FeCoNi ternary hydroxide nanosheets applicable as an active electrocatalyst for oxygen evolution reaction.      
  • A solvent system in combination with water to synthesize zeolitic imidazolate frameworks-8 (ZIF-8) membrane for the potential application in gas separation.

Signal Word

Danger

Hazard Statements

H302,H314,H351,H360Df

Hazard Classifications

Acute Tox. 4 Oral - Carc. 2 - Eye Dam. 1 - Repr. 1B - Skin Corr. 1C

Storage Class Code

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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2-CHLORO-N-P-TOLYL-ACETAMIDE AldrichCPR

S278947

2-CHLORO-N-P-TOLYL-ACETAMIDE

Trimesic acid 95%

Sigma-Aldrich

482749

Trimesic acid

Kyo Sung Park et al.
Proceedings of the National Academy of Sciences of the United States of America, 103(27), 10186-10191 (2006-06-27)
Twelve zeolitic imidazolate frameworks (ZIFs; termed ZIF-1 to -12) have been synthesized as crystals by copolymerization of either Zn(II) (ZIF-1 to -4, -6 to -8, and -10 to -11) or Co(II) (ZIF-9 and -12) with imidazolate-type links. The ZIF crystal
Reda M Abdelhameed et al.
Journal of colloid and interface science, 552, 494-505 (2019-06-04)
Removal of naphthols, as one of the most common pharmaceutical intermediates which released in the wastewater, is in the top priority for the time being. In the current study, zeolitic imidazole frameworks (ZIF-8, Zn & ZIF-67, Co) were directly prepared
Janosch Cravillon et al.
Angewandte Chemie (International ed. in English), 50(35), 8067-8071 (2011-07-13)
Prenucleation clusters: in situ synchrotron X-ray scattering with a one-second time resolution revealed the occurrence of nano-sized clusters during the nucleation and early growth of nanocrystals of a zeolitic imidazolate framework (ZIF). The complex crystallization process exhibits similarities with crystallization processes
Saleh A Ahmed et al.
Scientific reports, 9(1), 19372-19372 (2019-12-20)
In this work, we have successfully synthesized a bimetallic (Zinc and Cobalt) Zeolitic Imidazolate Framework (Zn50Co50-ZIF), a class in a wider microporous Metal-Organic Framework (MOF) family. The synthesized nanostructures maintain both water stability like ZIF-8 (solely Zn containing) and charge
Po-Hsun Huang et al.
Advanced science (Weinheim, Baden-Wurttemberg, Germany), 6(19), 1900913-1900913 (2019-10-09)
Synthesis of nanoparticles and particulate nanomaterials with tailored properties is a central step toward many applications ranging from energy conversion and imaging/display to biosensing and nanomedicine. While existing microfluidics-based synthesis methods offer precise control over the synthesis process, most of
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