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Merck
CN

H19859

2-Hydroxybenzimidazole

97%

Synonym(s):

2(1H)-Benzimidazolone, 2-Hydroxy-benzimidazol

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About This Item

Empirical Formula (Hill Notation):
C7H6N2O
CAS Number:
Molecular Weight:
134.14
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
210-412-4
Beilstein/REAXYS Number:
119866
MDL number:
Assay:
97%
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Quality Level

assay

97%

mp

>300 °C (lit.)

SMILES string

O=C1Nc2ccccc2N1

InChI

1S/C7H6N2O/c10-7-8-5-3-1-2-4-6(5)9-7/h1-4H,(H2,8,9,10)

InChI key

SILNNFMWIMZVEQ-UHFFFAOYSA-N

Gene Information

human ... EPHX2(2053)
mouse ... Ephx2(13850)



pictograms

Exclamation mark

signalword

Warning

hcodes

Hazard Classifications

Acute Tox. 4 Oral

Storage Class

11 - Combustible Solids

wgk

WGK 1

ppe

Eyeshields, Gloves, type N95 (US)



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Xinjian Zhang et al.
PloS one, 8(10), e74810-e74810 (2013-10-08)
Carbendazim (methyl 1H-benzimidazol-2-yl carbamate) is one of the most widely used fungicides in agriculture worldwide, but has been reported to have adverse effects on animal health and ecosystem function. A highly efficient carbendazim-degrading bacterium (strain dj1-11) was isolated from carbendazim-contaminated
A Bojanowska-Czajka et al.
Journal of radioanalytical and nuclear chemistry, 289(2), 303-314 (2011-01-01)
The radiolytic degradation of widely used fungicide, carbendazim, in synthetic aqueous solutions and industrial wastewater was investigated employing γ-irradiation. The effect of the absorbed dose, initial concentration and pH of irradiated solution on the effectiveness of carbendazim decomposition were investigated.
Vangelis Agouridas et al.
Chemical reviews, 119(12), 7328-7443 (2019-05-06)
The native chemical ligation reaction (NCL) involves reacting a C-terminal peptide thioester with an N-terminal cysteinyl peptide to produce a native peptide bond between the two fragments. This reaction has considerably extended the size of polypeptides and proteins that can



Global Trade Item Number

SKUGTIN
H19859-5G04061833350577
H19859-25G04061833317761