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48551

Supelco

2-Methyl-4,6-dinitrophenol

analytical standard

Synonym(s):

3,5-Dinitro-2-hydroxytoluene, 4,6-Dinitro-2-methylphenol, 4,6-Dinitro-o-cresol, DNOC

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About This Item

Empirical Formula (Hill Notation):
C7H6N2O5
CAS Number:
534-52-1
Molecular Weight:
198.13
Beilstein/REAXYS Number:
2054389
EC Number:
208-601-1
MDL number:
MFCD00007105
UNSPSC Code:
12000000
PubChem Substance ID:
24872086

grade

analytical standard

CofA

current certificate can be downloaded

packaging

ampule of 1000 mg

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

agriculture
environmental

format

neat

storage temp.

room temp

SMILES string

Cc1cc(cc(c1O)[N+]([O-])=O)[N+]([O-])=O

InChI

1S/C7H6N2O5/c1-4-2-5(8(11)12)3-6(7(4)10)9(13)14/h2-3,10H,1H3

InChI key

ZXVONLUNISGICL-UHFFFAOYSA-N

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Application

2-Methyl-4,6-dinitrophenol may be used as an analytical reference standard for the determination of the analyte in drinking water[1] and environmental samples[2] by capillary electrophoresis and reverse-phase high-performance liquid chromatography, respectively.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

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Danger

Hazard Classifications

Acute Tox. 1 Dermal - Acute Tox. 2 Inhalation - Acute Tox. 2 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1 - Muta. 2 - Skin Irrit. 2 - Skin Sens. 1

supp_hazards

EUH044

Storage Class

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

wgk_germany

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
LC25844V
LC22071V
LC18040V
LC12394V
LC10853V

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Determination of phenols in environmental samples by liquid chromatography-electrochemistry.
Cardellicchio N, et al.
Fresenius Journal of Analytical Chemistry, 358(6), 749-754 (1997)
Determination of phenolic pollutants in drinking water by capillary electrophoresis in the sample stacking mode.
Rodri I, et al.
Journal of Chromatography A, 778(1-2), 279-288 (1997)
N P Arildskov et al.
Ground water, 39(6), 819-830 (2001-11-16)
The fate of the three herbicides 2,4,5-T (2,4,5-trichlorophenoxyacetic acid), atrazine (6-chloro-N-ethyl-N'-[1-methyl-ethyl]-1,3,5-triazine-2,4-diamine), and DNOC (4,6-dinitro-2-methylphenol) in an anaerobic sandy aquifer was investigated. In the field, each of the herbicides was released simultaneously with tritiated water (HTO) as tracer in the depth
Elvira Romero et al.
Biochimica et biophysica acta, 1824(6), 850-857 (2012-04-03)
Aspergillus fumigatus siderophore A (Af SidA) is a flavin-dependent monooxygenase that catalyzes the hydroxylation of ornithine, producing N(5)-hydroxyornithine. This is the first step in the biosynthesis of hydroxamate-containing siderophores in A. fumigatus. Af SidA is essential for virulence, validating this
Yi Sun et al.
Journal of biomedical optics, 17(10), 107005-107005 (2012-10-12)
A novel approach to cancer detection in biomarkers spectral subspace (BSS) is proposed. The basis spectra of the subspace spanned by fluorescence spectra of biomarkers are obtained by the Gram-Schmidt method. A support vector machine classifier (SVM) is trained in
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