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165638

Sigma-Aldrich

2-(Aminomethyl)benzimidazole dihydrochloride

98%

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About This Item

Empirical Formula (Hill Notation):
C8H9N3 · 2HCl
CAS Number:
5993-91-9
Molecular Weight:
220.10
EC Number:
227-820-3
MDL number:
MFCD00012677
UNSPSC Code:
12352100
eCl@ss:
32151902
PubChem Substance ID:
24850141
NACRES:
NA.22

Quality Level

100

Assay

98%

form

solid

mp

264 °C (dec.) (lit.)

SMILES string

Cl.Cl.NCc1nc2ccccc2[nH]1

InChI

1S/C8H9N3.2ClH/c9-5-8-10-6-3-1-2-4-7(6)11-8;;/h1-4H,5,9H2,(H,10,11);2*1H

InChI key

HAEYZZSSSUIZAN-UHFFFAOYSA-N

Related Categories

Application

2-(Aminomethyl)benzimidazole dihydrochloride was used in the synthesis of N-(benzimidazol-2-ylmethyl)iminodiacetic acid.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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Six-co-ordinated vanadium-(IV) and-(V) complexes of benzimidazole and pyridyl containing ligands.
Crans DC, et al.
J. Chem. Soc., Dalton Trans., 16, 1799-1812 (1997)
Ganesan Kumaravel et al.
International journal of biological macromolecules, 126, 1303-1317 (2018-09-24)
This work deals with a series of biologically important novel transition metal(II) Schiff base chelates containing terpyridine. Benzimidazole, a moiety found in broad spectrum of drugs is espoused in a Schiff base ligand system. Eight such metal(II) complexes are designed
Bin Qian et al.
Molecules (Basel, Switzerland), 24(19) (2019-10-05)
A series of fluorescent coumarin derivatives 2a-e were systematically designed, synthesized and studied for their Cu2+ sensing performance in aqueous media. The sensitivities and selectivities of the on-to-off fluorescent Cu2+ sensing signal were in direct correlation with the relative arrangements

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