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Chlorothalonil

PESTANAL®, analytical standard

Synonym(s):

Tetrachloroisophthalodinitrile

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About This Item

Empirical Formula (Hill Notation):
C8Cl4N2
CAS Number:
1897-45-6
Molecular Weight:
265.91
Beilstein:
1978326
EC Number:
217-588-1
MDL number:
MFCD00045594
UNSPSC Code:
41116107
PubChem Substance ID:
329755511
NACRES:
NA.24

grade

analytical standard

Quality Level

100

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

SMILES string

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

InChI key

CRQQGFGUEAVUIL-UHFFFAOYSA-N

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General description

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.

Legal Information

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

Signal Word

Danger

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

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

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCL6035
BCCK6258
BCCG8356
BCCC8347
BCBZ8713

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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
Y L Phyu et al.
Chemosphere, 85(10), 1568-1573 (2011-09-20)
Pesticides predominantly occur in aquatic ecosystems as mixtures of varying complexity, yet relatively few studies have examined the toxicity of pesticide mixtures. Atrazine, chlorothalonil and permethrin are widely used pesticides that have different modes of action. This study examined the
Bin Liang et al.
Applied and environmental microbiology, 77(12), 4268-4272 (2011-04-19)
Horizontal transfer of the chlorothalonil hydrolytic dehalogenase gene (chd) is proposed based on the high conservation of the chd gene and its close association with a novel insertion sequence, ISOcsp1, in 16 isolated chlorothalonil-dechlorinating strains belonging to eight different genera.
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