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Chlorothalonil

PESTANAL®, analytical standard

Synonyme(s) :

Tetrachloroisophthalodinitrile

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About This Item

Formule empirique (notation de Hill):
C8Cl4N2
Numéro CAS:
Poids moléculaire :
265.91
Numéro Beilstein :
1978326
Numéro CE :
Numéro MDL:
Code UNSPSC :
41116107
ID de substance PubChem :
Nomenclature NACRES :
NA.24

Qualité

analytical standard

Niveau de qualité

Gamme de produits

PESTANAL®

Durée de conservation

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

Chaîne SMILES 

Clc1c(Cl)c(C#N)c(Cl)c(C#N)c1Cl

InChI

1S/C8Cl4N2/c9-5-3(1-13)6(10)8(12)7(11)4(5)2-14

Clé InChI

CRQQGFGUEAVUIL-UHFFFAOYSA-N

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Description générale

Chlorothalonil is a an organochlorine, broad-spectrum and non-systemic fungicide, which can be widely used in agriculture, in order to have a control on foliar pathogens.

Application

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

Informations légales

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

Mention d'avertissement

Danger

Classification des risques

Acute Tox. 2 Inhalation - Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 2 - Eye Dam. 1 - Skin Sens. 1 - STOT SE 3

Organes cibles

Respiratory system

Code de la classe de stockage

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

dust mask type N95 (US), Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges


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Certificats d'analyse (COA)

Lot/Batch Number

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Retrouvez la documentation relative aux produits que vous avez récemment achetés dans la Bibliothèque de documents.

Consulter la Bibliothèque de documents

Study of chlorothalonil photodegradation in natural waters and in the presence of humic substances
Sakkas.AV, et al.
Chemosphere, 48, 939-945 (2002)
Transformation pathways of 14C-chlorothalonil in tropical soils
Regitano.B.J, et al.
Archives of Environmental Contamination and Toxicology, 40, 295-302 (2001)
Xing-Hai Liu et al.
European journal of medicinal chemistry, 44(7), 2782-2786 (2009-02-28)
A series of cyclopropanecarboxamide were prepared and tested for antifungal activity in vivo. The preliminary bioassays indicated that some compounds are comparable to the commercial fungicides. To further explore the comprehensive structure-activity relationship on the basis of fungicidal activity data
Zining Cui et al.
Bioorganic & medicinal chemistry letters, 21(23), 7193-7196 (2011-10-19)
Assuming that the water solubility of our previous hydrazone derivatives would improve after modification with sugars while keeping or modulating their notable biological activities, we designed and synthesized some glycosyl hydrazine and hydrazone derivatives. Bioassay results indicated that the antitumor
Taegan A McMahon et al.
Ecology letters, 15(7), 714-722 (2012-05-17)
Although studies on biodiversity and ecosystem function are often framed within the context of anthropogenic change, a central question that remains is how important are direct vs. indirect (via changes in biodiversity) effects of anthropogenic stressors on ecosystem functions in

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GC Analysis of Agricultural Pesticides (Standard) on SLB®-5ms

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