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About This Item
Empirical Formula (Hill Notation):
C12H10N2O2
CAS Number:
Molecular Weight:
214.22
Beilstein:
170877
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Assay
98%
form
crystals
mp
69-71 °C (lit.)
SMILES string
[O-][N+](=O)c1ccc(Cc2ccncc2)cc1
InChI
1S/C12H10N2O2/c15-14(16)12-3-1-10(2-4-12)9-11-5-7-13-8-6-11/h1-8H,9H2
InChI key
MNHKUCBXXMFQDM-UHFFFAOYSA-N
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Application
Used in tests for alkylating agents and in a spectroscopic method for phosgene determination.
Storage Class Code
13 - Non 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
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S K Dangwal
Industrial health, 32(1), 41-47 (1994-01-01)
A reagent consisting of 0.4% of nitrobenzyl pyridine and 0.5% of sodium acetate in ethanol was found to be applicable as a sampling and coloring solution to a sensitive and relatively specific spectrophotometric determination of phosgene. This method is a
Use of 4-(nitrobenzyl)pyridine (4-NBP) to test mutagenic potential of slow-reacting epoxides, their corresponding olefins, and other alkylating agents.
J H Kim et al.
Bulletin of environmental contamination and toxicology, 49(6), 879-885 (1992-12-01)
Marcio Fronza et al.
Phytochemistry, 78, 107-119 (2012-03-23)
Abietane diterpenes, especially those containing quinone moieties, are often reported to have cytotoxic effects on cancer cell lines. They deserve greater attention because several cancer chemotherapeutic agents also possess the quinone structural feature. To date, very little is known about
Rafael Gómez-Bombarelli et al.
Chemical research in toxicology, 25(6), 1176-1191 (2012-04-07)
Alkylating agents are considered to be archetypal carcinogens. One suitable technique to evaluate the activity of alkylating compounds is the NBP assay. This method is based on the formation of a chromophore in the reaction between the alkylating agent and
Rafael Gómez-Bombarelli et al.
Environmental science & technology, 45(20), 9009-9016 (2011-09-14)
Hydroxyhalofuranones form a group of genotoxic disinfection byproduct (DBP) of increasing interest. Among them, mucohalic acids (3,4-dihalo-5-hydroxyfuran-2(5H)-one, MXA) are known mutagens that react with nucleotides, affording etheno, oxaloetheno, and halopropenal derivatives. Mucohalic acids have also found use in organic synthesis
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