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45464

Supelco

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
Beilstein:
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

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

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (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
N Tuxen et al.
Chemosphere, 41(9), 1485-1494 (2000-11-01)
The fate of selected pesticides (bentazone, isoproturon, DNOC, MCPP, dichlorprop and 2,4-D) and a metabolite (2,6-dichlorobenzamide (BAM)) was investigated under aerobic conditions in column experiments using aquifer material and low concentrations of pesticides (approximately 25 microg/l). A solute transport model
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
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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