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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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产品名称

绿麦隆, PESTANAL®, analytical standard

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

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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.

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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Bin Xu et al.
Chemosphere, 83(7), 909-916 (2011-03-26)
Chlortoluron chlorination is studied in the pH range of 3-10 at 25 ± 1°C. The chlorination kinetics can be well described by a second-order kinetics model, first-order in chlorine and first-order in chlortoluron. The apparent rate constants were determined and
Edgar Hiller et al.
Bulletin of environmental contamination and toxicology, 80(5), 412-416 (2008-04-11)
Sorption of the herbicides (acetochlor, atrazine, 2,4-D: , chlorotoluron, MCPA and trifluralin) in their commercially available formulations was characterized on six agricultural soils from Slovakia. Weak acid herbicides (2,4-D: and MCPA) were the least sorbed, whereas weak base such as
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
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.
Environmental pollution (Barking, Essex : 1987), 158(3), 906-912 (2009-10-13)
Chlorotoluron (Chl) is a phenylurea herbicide and is widely used for controlling weeds. While it has brought great benefits to crop production, it has also resulted in contamination to ecosystem. In this study, we investigated accumulation of chlorotoluron (Chl) and

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