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Merck
CN

45851

Supelco

Diuron solution

100 μg/mL in acetonitrile, PESTANAL®, analytical standard

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About This Item

Empirical Formula (Hill Notation):
C9H10Cl2N2O
CAS Number:
330-54-1
Molecular Weight:
233.09
Beilstein:
2215168
EC Number:
200-835-2
MDL number:
MFCD00018136
UNSPSC Code:
41116107
PubChem Substance ID:
329756987
NACRES:
NA.24

Key Documents

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grade

analytical standard

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

concentration

100 μg/mL in acetonitrile

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

agriculture
cleaning products
cosmetics
environmental
food and beverages
personal care

format

single component solution

storage temp.

2-8°C

SMILES string

CN(C)C(=O)Nc1ccc(Cl)c(Cl)c1

InChI

1S/C9H10Cl2N2O/c1-13(2)9(14)12-6-3-4-7(10)8(11)5-6/h3-5H,1-2H3,(H,12,14)

InChI key

XMTQQYYKAHVGBJ-UHFFFAOYSA-N

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

Pictograms

FlameExclamation mark
GHS02,GHS07

Signal Word

Danger

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Flam. Liq. 2

Storage Class Code

3 - Flammable liquids

WGK

WGK 2

Flash Point(F)

35.6 °F - closed cup

Flash Point(C)

2 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

危险化学品
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Certificates of Analysis (COA)

Lot/Batch Number
BCBS0783V

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Geneviève Bricheux et al.
Ecotoxicology and environmental safety, 88, 126-134 (2012-12-04)
River biofilms are assemblies of autotrophic and heterotrophic microorganisms that can be affected by pollutants such as those found in watersheds and wastewater treatment plants. In the laboratory, experimental biofilms were formed from river water, and their overall composition was
Bernard Lepetit et al.
Plant physiology, 161(2), 853-865 (2012-12-05)
In diatoms, the process of energy-dependent chlorophyll fluorescence quenching (qE) has an important role in photoprotection. Three components are essential for qE: (1) the light-dependent generation of a transthylakoidal proton gradient; (2) the deepoxidation of the xanthophyll diadinoxanthin (Dd) into
Perry J Mitchell et al.
Environmental science & technology, 47(1), 412-419 (2012-12-05)
Reported correlations between organic contaminant sorption affinity and soil organic matter (OM) structure vary widely, suggesting the importance of OM physical conformation and accessibility. Batch equilibration experiments were used to examine the sorption affinity of bisphenol A, atrazine, and diuron
Priyanka Sharma et al.
Biosensors & bioelectronics, 39(1), 99-105 (2012-08-14)
We report a novel in-situ electrochemical synthesis approach for the formation of functionalized graphene-graphene oxide (fG-GO) nanocomposite on screen-printed electrodes (SPE). Electrochemically controlled nanocomposite film formation was studied by transmission electron microscopy (TEM) and Raman spectroscopy. Further insight into the
Mitscheli S Da Rocha et al.
Toxicological sciences : an official journal of the Society of Toxicology, 130(2), 281-288 (2012-08-28)
Diuron, a substituted urea herbicide, is carcinogenic to the rat urinary bladder at high dietary levels (2500 ppm). To further elucidate the mode of action, this study aimed to determine the time course and sequence of bladder cytotoxic and proliferative
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