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Merck

32007

Supelco

Imazalil

PESTANAL®, analytical standard

Sinónimos:

1-[2-(Allyloxy)-2-(2,4-dichlorophenyl)ethyl]imidazole

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About This Item

Fórmula empírica (notación de Hill):
C14H14Cl2N2O
Número de CAS:
Peso molecular:
297.18
Beilstein/REAXYS Number:
545683
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard

Quality Level

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

agriculture
environmental

format

neat

SMILES string

Clc1ccc(C(Cn2ccnc2)OCC=C)c(Cl)c1

InChI

1S/C14H14Cl2N2O/c1-2-7-19-14(9-18-6-5-17-10-18)12-4-3-11(15)8-13(12)16/h2-6,8,10,14H,1,7,9H2

InChI key

PZBPKYOVPCNPJY-UHFFFAOYSA-N

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General description

Imazalil is a fungicide mostly used to avoid decay during postharvest. It is mostly used for fruits, vegetables and ornamental plants to control fungi growth.

Application

Imazalil has been used as reference standard in direct analysis in real time mass spectrometry (DART-MS) technique for determination of xenobiotics from fruit samples. It may have been used as reference standard in Flow injection photoinduced chemiluminescence method for determination of Imazalil concentration from water samples.
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

signalword

Danger

Hazard Classifications

Acute Tox. 3 Oral - Acute Tox. 4 Inhalation - Aquatic Chronic 1 - Carc. 2 - Eye Dam. 1

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves


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Flow injection photoinduced chemiluminescence determination of imazalil in water samples.
Meseguer-Lloret S, Torres-Cartas S, Gomez-Benito MC.
Analytical and Bioanalytical Chemistry, 398(7-8), 3175-3182 (2010)
Direct peel monitoring of xenobiotics in fruit by direct analysis in real time coupled to a linear quadrupole ion trap-orbitrap mass spectrometer.
Farre M, Pico Y, Barcelo D.
Analytical Chemistry, 85(5), 2638-2644 (2013)
E J Keeble et al.
The Veterinary record, 167(22), 862-864 (2011-01-26)
An outbreak of Trichophyton dermatophytosis was diagnosed in a group of four L'Hoest's monkeys (Cercopithecus lhoesti) housed in the primate section at a zoological collection. The affected animals presented with areas of non-pruritic alopecia, scaling and crusting. The diagnosis was
M Sharman et al.
The Journal of small animal practice, 53(3), 161-167 (2012-02-04)
Multiple topical treatments are often required for clinical cure of mycotic rhinosinusitis in dogs. The objective of this study was to describe the distribution and retention of enilconazole and clotrimazole solutions using a temporary trephination protocol. Nine client-owned dogs diagnosed
Didier Noël Carlotti et al.
Veterinary dermatology, 21(3), 259-266 (2009-08-27)
Enzootic dermatophytosis in a shelter with approximately 140 cats was treated according to a protocol combining identification, isolation and treatment of subclinical carrier and affected animals in accordance with a three-area system: healthy animals (no lesions and negative cultures), subclinical

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