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48551

Supelco

2-Methyl-4,6-dinitrophenol

analytical standard

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Synonym(s):
3,5-Dinitro-2-hydroxytoluene, 4,6-Dinitro-2-methylphenol, 4,6-Dinitro-o-cresol, DNOC
Empirical Formula (Hill Notation):
C7H6N2O5
CAS Number:
Molecular Weight:
198.13
Beilstein:
2054389
EC Number:
MDL number:
UNSPSC Code:
12000000
PubChem Substance ID:

grade

analytical standard

Quality Level

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

WGK

WGK 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Regulatory Information

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Certificates of Analysis (COA)

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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)
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
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

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