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Merck
CN

45400

绿麦隆

PESTANAL®, analytical standard

别名:

N′-(3-氯-4-甲基苯基)-N,N-二甲基脲

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关于此项目

经验公式(希尔记法):
C10H13ClN2O
化学文摘社编号:
分子量:
212.68
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
EC Number:
239-592-2
Beilstein/REAXYS Number:
2647688
MDL number:
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InChI key

JXCGFZXSOMJFOA-UHFFFAOYSA-N

InChI

1S/C10H13ClN2O/c1-7-4-5-8(6-9(7)11)12-10(14)13(2)3/h4-6H,1-3H3,(H,12,14)

SMILES string

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

grade

analytical standard

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

Quality Level

Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Other Notes

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

Legal Information

PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany

pictograms

Health hazardEnvironment

signalword

Warning

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 2 - Repr. 2

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

法规信息

农药列管产品
此项目有

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Yaron Drori et al.
Journal of environmental quality, 35(6), 2154-2161 (2006-10-31)
The soil lipid fraction can play an important role in the sorption of organic compounds. In this study, the impact of the lipid fraction of freshwater- and wastewater-irrigated soils on the sorption of non- and relatively polar compounds was assessed.
Malik M Haque et al.
Environmental science & technology, 40(15), 4765-4770 (2006-08-18)
The photocatalytic degradation of a herbicide derivative, chlorotoluron [3-(3-chloro-4-methylphenyl)-1,1-dimethylurea, 1], has been investigated in aqueous suspensions of titanium dioxide (TiO2) under a variety of conditions. The degradation was studied by monitoring the change in substrate concentration employing UV spectroscopic analysis
Ning Hui Song et al.
Chemosphere, 68(9), 1779-1787 (2007-04-28)
Chlorotoluron is a phenylurea herbicide that is widely used for controlling grass weeds in the land of cereal, cotton and fruit production. However, extensive use of this herbicide may lead to its accumulation in ecosystems, thus inducing the toxicity to
J Villaverde et al.
Environmental science & technology, 43(21), 8227-8232 (2009-11-21)
This study investigates time-dependent sorption of pesticides in soil aggregates. We tested if the sorption kinetics of pesticides in soil aggregates can be described by modeling diffusion into aggregates for a range of soils and pesticides. Our hypothesis is that
Robin G Oliver et al.
Pest management science, 69(1), 120-125 (2012-08-29)
It is important to understand the degradation of organic molecules in surface waters to ensure that risk assessments, intended to prevent adverse effects on human health and the environment, are robust. One important degradation mechanism in surface waters is photodegradation.

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