MilliporeSigma
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N11454

Chlorothalonil

analytical standard

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Synonym(s):
Tetrachloroisophthalodinitrile
Empirical Formula (Hill Notation):
C8Cl4N2
CAS Number:
1897-45-6
Molecular Weight:
265.91
Beilstein:
1978326
EC Number:
217-588-1
MDL number:
MFCD00045594
PubChem Substance ID:
329818504

grade

analytical standard

packaging

ampule of 250 mg

manufacturer/tradename

Chem Service, Inc. PS-1020

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

cleaning products
cosmetics
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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Christine Garron et al.
Pest management science, 68(1), 92-100 (2011-06-29)
Chlorothalonil is used extensively in Prince Edward Island for the control of blight on potatoes, and has been measured throughout summer months in ambient air monitoring studies. This study was designed to characterize near-field drift of chlorothalonil, and to evaluate
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.
C F Wilkinson et al.
Regulatory toxicology and pharmacology : RTP, 24(1 Pt 1), 69-84 (1996-08-01)
Chronic dietary treatment of rodents with the fungicide chlorothalonil causes an increased incidence of papillomas and carcinomas of the forestomach squamous epithelium (rats and mice, both sexes) and adenomas and carcinomas of the renal proximal tubule epithelium (rats, both sexes;
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
H S Rosenkranz
Mutation research, 423(1-2), 183-186 (1999-02-25)
Based upon analyses using a number of validated structure-activity relationship models, it is concluded that the carcinogenicity in rodents of chlorothalonil is not due to a genotoxic mechanism.
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