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399353

Sigma-Aldrich

1-Methylbenzimidazole

99%

Synonym(s):

1-Methyl-1H-benzimidazole, 1-Methyl-1H-benzo[d]imidazole, 3-Methylbenzimidazole, N-Methylbenzimidazole

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About This Item

Empirical Formula (Hill Notation):
C8H8N2
CAS Number:
1632-83-3
Molecular Weight:
132.16
MDL number:
MFCD00192275
UNSPSC Code:
12352100
eCl@ss:
32151902
PubChem Substance ID:
24864808
NACRES:
NA.22

assay

99%

form

solid

bp

154 °C/12 mmHg (lit.)

mp

59-62 °C (lit.)

SMILES string

Cn1cnc2ccccc12

InChI

1S/C8H8N2/c1-10-6-9-7-4-2-3-5-8(7)10/h2-6H,1H3

InChI key

FGYADSCZTQOAFK-UHFFFAOYSA-N

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General description

1-Methylbenzimidazole is a heterocyclic building block. Effect of the interaction between 1-methylbenzimidazole (MBI) with Li+ and TiO2 on the performance of dye-sensitized solar cells has been investigated.

Application

1-Methylbenzimidazole is the suitable reagent used as electrolyte additive for the dye-sensitized solar cells and solid-state dye-sensitized solar cells.

pictograms

CorrosionExclamation mark
GHS05,GHS07

signalword

Danger

Hazard Classifications

Acute Tox. 4 Oral - Eye Dam. 1 - Skin Irrit. 2 - STOT SE 3

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
0000399223
0000399246
0000361571
0000361571
0000399223

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Sigma-Aldrich

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Benzothiazole

1-Hexyl-3-methylimidazolium iodide ≥98% (HPLC)

Sigma-Aldrich

713058

1-Hexyl-3-methylimidazolium iodide

Yanyan Fang et al.
Chemistry, an Asian journal, 14(23), 4201-4206 (2019-10-10)
Two types of ionic liquids (ILs), 1-(3-hexenyl)-3-methyl imidazolium iodide and 1-(3-butenyl)-3-methyl imidazolium iodide, are synthesized by introducing an unsaturated bond into the side alkyl chain of the imidazolium cation. These new ionic liquids exhibit high thermal stability and low viscosity
Influence of 1-methylbenzimidazole interactions with Li+ and TiO 2 on the performance of dye-sensitized solar cells.
Zhang C, et al.
Electrochimica Acta, 53(17), 5503-5508 (2008)
Kelvin K H Tong et al.
Molecules (Basel, Switzerland), 25(16) (2020-08-17)
Thiones have been investigated as ligands in metal complexes with catalytic and biological activity. We report the synthesis, characterization, and biological evaluation of a series of MII/III complexes of the general formulae [MII(cym)(L)Cl]X (cym = η6-p-cymene) or [MIII(Cp*)(L)Cl]X (Cp* =
Solid-state dye-sensitized solar cells made of multilayer nanocrystalline titania and poly (3-hexylthiophene).
Balis N, et al.
Journal of Photochemistry and Photobiology A: Chemistry, 214(1), 69-73 (2010)
Optimization of dye-sensitized solar cells prepared by compression method.
Boschloo G, et al.
Journal of Photochemistry and Photobiology A: Chemistry, 148(1), 11-15 (2002)
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