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Key Documents

H48409

Sigma-Aldrich

3-Hydroxy-4-nitrobenzoic acid

95%

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About This Item

Linear Formula:
HOC6H3(NO2)CO2H
CAS Number:
Molecular Weight:
183.12
Beilstein:
2107564
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

95%

mp

229-231 °C (lit.)

SMILES string

OC(=O)c1ccc(c(O)c1)[N+]([O-])=O

InChI

1S/C7H5NO5/c9-6-3-4(7(10)11)1-2-5(6)8(12)13/h1-3,9H,(H,10,11)

InChI key

XLDLRRGZWIEEHT-UHFFFAOYSA-N

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Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2

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

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Daiki Asakawa
Journal of the American Society for Mass Spectrometry, 30(8), 1491-1502 (2019-05-31)
Nitrogen-centered and β-carbon-centered hydrogen-deficient peptide radicals are considered to be intermediates in the matrix-assisted laser desorption/ionization in-source decay (MALDI-ISD)-induced Cα-C bond cleavage of peptide backbones when using an oxidizing matrix. To understand the general mechanism of Cα-C bond cleavage by
Midori Natsume et al.
Journal of clinical biochemistry and nutrition, 42, 50-53 (2008-01-31)
Previously, we identified four metabolites of (-)-epicatechin in blood and urine: (-)-epicatechin-3'-O-glucuronide (E3'G), 4'-O-methyl-(-)-epicatechin-3'-O-glucuronide (4'ME3'G), (-)-epicatechin-7-O-glucuronide (E7G), and 3'-O-methyl-(-)-epicatechin-7-O-glucuronide (3'ME7G) (Natsume et al. Free Radical Biol. Med. 34, 840-849, 2003). The aim of the current study was to compare the
Yuko Fukuyama et al.
Journal of the American Society for Mass Spectrometry, 29(11), 2227-2236 (2018-08-01)
In in-source decay (ISD) in matrix-assisted laser desorption/ionization (MALDI)-mass spectrometry (MS), 1,5-diaminonaphthalene (1,5-DAN) is a most frequently used matrix probably due to the highly sensitive detection of fragment ions. 1,5-DAN is a reducing matrix generating c- and z-series ions by
Cosima Damiana Calvano et al.
Analytical and bioanalytical chemistry, 410(17), 4015-4038 (2018-04-24)
Since its introduction in the 1980s, matrix-assisted laser desorption/ionization mass spectrometry (MALDI MS) has gained a prominent role in the analysis of high molecular weight biomolecules such as proteins, peptides, oligonucleotides, and polysaccharides. Its application to low molecular weight compounds

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