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Merck
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Key Documents

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45464

Supelco

DNOC

PESTANAL®, analytical standard

Sinónimos:

2-Methyl-4,6-dinitrophenol

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About This Item

Fórmula empírica (notación de Hill):
C7H6N2O5
Número de CAS:
534-52-1
Peso molecular:
198.13
Beilstein/REAXYS Number:
2054389
EC Number:
208-601-1
MDL number:
MFCD00007105
UNSPSC Code:
41116107
PubChem Substance ID:
329756757
NACRES:
NA.24

grade

analytical standard

Quality Level

100

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

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

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_germany

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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Certificados de análisis (COA)

Lot/Batch Number
BCCJ7293
BCBX5762
SZBD326XV
SZBA330XV
SZB6159XV

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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
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
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
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
Ken L Takahashi et al.
Reproductive toxicology (Elmsford, N.Y.), 22(3), 501-507 (2006-05-23)
In order to elucidate the pathogenesis of tailless sperm, 4,6-dinitro-o-cresol (DNOC) was administered to Jcl:SD male rats at daily oral doses of 0, 10 or 15mg/kg for 5 days. Sperm were collected from the caput, corpus, and cauda epididymides on
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