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Merck
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Documenti fondamentali

45400

Supelco

Chlortoluron

PESTANAL®, analytical standard

Sinonimo/i:

3-(3-Chloro-4-methyl)-1,1-dimethylurea

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About This Item

Formula empirica (notazione di Hill):
C10H13ClN2O
Numero CAS:
Peso molecolare:
212.68
Beilstein:
2647688
Numero CE:
Numero MDL:
Codice UNSPSC:
41116107
ID PubChem:
NACRES:
NA.24

Grado

analytical standard

Livello qualitativo

Nome Commerciale

PESTANAL®

Durata

limited shelf life, expiry date on the label

tecniche

HPLC: suitable
gas chromatography (GC): suitable

applicazioni

agriculture
cleaning products
cosmetics
environmental
food and beverages
personal care

Formato

neat

Stringa SMILE

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

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)
JXCGFZXSOMJFOA-UHFFFAOYSA-N

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Applicazioni

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

Prodotti consigliati

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.

Note legali

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

Pittogrammi

Health hazardEnvironment

Avvertenze

Warning

Indicazioni di pericolo

Classi di pericolo

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

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable


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Certificati d'analisi (COA)

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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.
N Baran et al.
Environmental pollution (Barking, Essex : 1987), 148(3), 729-738 (2007-05-26)
The monitoring of a spring and seven piezometers in the 3km(2) Brévilles agricultural catchment (France) over five and a half years revealed considerable spatial and temporal variability in the concentrations of atrazine and its metabolite deethylatrazine (both systematically quantified at
Nora Badawi et al.
Environmental pollution (Barking, Essex : 1987), 157(10), 2806-2812 (2009-05-26)
Phenylurea herbicides are used worldwide, and often pollute surface- and groundwater in concentrations exceeding the limit value for drinking water (0.1 microg l(-1)). Bacteria degrade phenylurea herbicides by successive N-dealkylation to substituted aniline products. Little is known about the corresponding
Sylvie Nélieu et al.
Environmental toxicology and chemistry, 29(12), 2644-2652 (2010-10-12)
The ecotoxicological impact of nitrate-induced photodegradation products of diuron and chlorotoluron was studied through monospecific biotests conducted in conjunction with experiments in outdoor aquatic mesocosms. Organisms representing three trophic levels were used: two heterotrophic microorganisms, the luminescent bacterium Vibrio fischeri
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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