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Merck
CN

917176

N-Butyl-1H-benzimidazole Solarpur®

Synonym(s):

1-Butyl- (7CI,8CI) benzimidazole, 1-Butyl-1H-1,3-benzodiazole, 1-Butyl-1H-benzimidazole, 1-Butylbenzimidazole, 1-Butylbenzoimidazole, N-Butyl-1H-benzimidazole, N-Butylbenzimidazole, NBB

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About This Item

Empirical Formula (Hill Notation):
C11H14N2
CAS Number:
4886-30-0
Molecular Weight:
174.24
UNSPSC Code:
12352202
MDL number:
MFCD00464045

Key Documents

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InChI

1S/C11H14N2/c1-2-3-8-13-9-12-10-6-4-5-7-11(10)13/h4-7,9H,2-3,8H2,1H3

InChI key

SHPPDRZENGVOOR-UHFFFAOYSA-N

assay

≥99% (HPLC)

form

liquid

impurities

≤100 ppm Halides, ≤1000 ppm Water

Application

N-Butyl-1H-benzimidazole Solarpur® is high-purity electronic grade electrolyte for various applications including synthesis of important chemicals and DSSCs.
Solarpur® electrolyte components for DSSC applications meet the highest purity standards regarding water and other impurities required for this technology.

Legal Information

Solarpur is a registered trademark of Merck KGaA, Darmstadt, Germany

pictograms

CorrosionExclamation mark
GHS05,GHS07

signalword

Danger

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

10 - Combustible liquids

wgk

WGK 3

flash_point_f

>230.0 °F

flash_point_c

> 110 °C

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
MKCN2892

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Iwona A Rutkowska et al.
ChemSusChem, 8(15), 2560-2568 (2015-06-30)
The ability of Pt nanostructures to induce the splitting of the II bond in iodine (triiodide) molecules is explored here to enhance electron transfer in the iodine/iodide redox couple. Following the dispersal of Pt nanoparticles at 2 % (weight) level, charge
The sensitization effect and microscopic essence of different additives on the electronic structure of nanocrystalline TiO2 in dye-sensitized solar cell
Wang X L, et al.
Journal of Solar Energy, 189, 372-384 (2019)
TEMPO-Mediated Synthesis of N-(Fluoroalkyl)imidazolones via Reaction of Imidazoles with Iodofluoroacetate.
Chen J H, et al.
Advanced Synthesis & Catalysis, 362(1), 269-276 (2020)

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