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Merck

45464

DNOC

PESTANAL®, analytical standard

Synonym(s):

2-Methyl-4,6-dinitrophenol, 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
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
329756757
EC Number:
208-601-1
Beilstein/REAXYS Number:
2054389
MDL number:
MFCD00007105

Key Documents

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Product Name

DNOC, PESTANAL®, analytical standard

InChI key

ZXVONLUNISGICL-UHFFFAOYSA-N

InChI

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

SMILES string

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

grade

analytical standard

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

agriculture
cleaning products
cosmetics
environmental
food and beverages
personal care

format

neat

Quality Level

100

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Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Legal Information

PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany

signalword

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

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges

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Certificates of Analysis (COA)

Lot/Batch Number
BCBX5762

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Hanh Nguyen-Ngoc et al.
Ecotoxicology and environmental safety, 72(2), 316-320 (2008-06-17)
Synchronous-scan spectrofluorometry was applied to Chlorella vulgaris cells to assess the toxicity of heavy metals and herbicides in water. Simultaneous scan of both the excitation and emission spectra was done at a constant wavelength difference Deltalambda (20-140 nm) between the
Fanny Marlin et al.
Chembiochem : a European journal of chemical biology, 13(17), 2593-2598 (2012-11-07)
Oligonucleotides and their analogues, such as peptide nucleic acids (PNAs), can be used in chemical strategies to artificially control gene expression. Inefficient cellular uptake and inappropriate cellular localization still remain obstacles in biological applications, however, especially for PNAs. Here we
Peng Ye et al.
Water research, 43(5), 1303-1312 (2009-01-27)
The adsorption and degradation of 4,6-o-dinitrocresol (DNOC) and p-nitrophenol (PNP) in SWy-2 montmorillonite clay slurry were investigated. The pH and type of cation of the slurry were varied. Results showed that adsorption of DNOC and PNP increased at lower pH
Jolanta Bieganska
Environmental science & technology, 39(4), 1190-1196 (2005-03-19)
Neutralization of 4,6-dinitro-o-cresol, of which the best-before date had expired and which could not be used any longer, was carried out by means of the detonative combustion method. The pesticide comprises two nitro groups and is called DNOC. Composition of
Nicholas J Kotloski et al.
mBio, 4(1), doi:10-doi:10 (2013-01-17)
Shewanella oneidensis strain MR-1 is widely studied for its ability to respire a diverse array of soluble and insoluble electron acceptors. The ability to breathe insoluble substrates is defined as extracellular electron transfer and can occur via direct contact or
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