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Safety Information

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:
2054389
EC Number:
208-601-1
MDL number:
MFCD00007105
UNSPSC Code:
12000000
PubChem Substance ID:
24872086

grade

analytical standard

Quality Level

100

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 and environmental samples 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.

Signal Word

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

Supplementary Hazards

EUH044

Storage Class Code

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

Regulatory Information

新产品

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Certificates of Analysis (COA)

Lot/Batch Number
LC25844V
LC22071V
LC18040V
LC12394V
LC10853V

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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)
Determination of phenols in environmental samples by liquid chromatography-electrochemistry.
Cardellicchio N, et al.
Fresenius Journal of Analytical Chemistry, 358(6), 749-754 (1997)
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
Xia Zeng et al.
Journal of agricultural and food chemistry, 57(9), 3689-3694 (2009-03-31)
The Fenton degradation of 4,6-dinitro-o-cresol (DNOC) was studied under different experimental conditions using Amberlyst 15 ion-exchange resin containing ferrous ion. DNOC was found to be effectively degraded under most conditions, and it was observed that, with the addition of HCl
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
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