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Merck

559792

Sigma-Aldrich

[3-(3,5-Dichlorophenyl)-2,4-dioxoimidazolidinyl]-N-(methylethyl)carboxamide

97%

Sinónimos:

Iprodione

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About This Item

Fórmula lineal:
Cl2C6H3N2C3H2O2CONHCH(CH3)2
Número de CAS:
Peso molecular:
330.17
Beilstein/REAXYS Number:
895003
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

assay

97%

mp

130-134 °C (lit.)

functional group

amine
chloro

SMILES string

CC(C)NC(=O)N1CC(=O)N(C1=O)c2cc(Cl)cc(Cl)c2

InChI

1S/C13H13Cl2N3O3/c1-7(2)16-12(20)17-6-11(19)18(13(17)21)10-4-8(14)3-9(15)5-10/h3-5,7H,6H2,1-2H3,(H,16,20)

InChI key

ONUFESLQCSAYKA-UHFFFAOYSA-N

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pictograms

Health hazardEnvironment

signalword

Warning

hcodes

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 2

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type P3 (EN 143) respirator cartridges


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Renáta Húsková et al.
Journal of chromatography. A, 1216(35), 6326-6334 (2009-08-01)
A combination of fast GC with narrow-bore column and bench top quadrupole mass spectrometer (MS) detector in negative chemical ionization (NCI) mode (with methane as reagent gas) is set up and utilized for the ultratrace analysis of 25 selected pesticides.
Chad R Blystone et al.
Toxicology letters, 174(1-3), 74-81 (2007-10-13)
Iprodione (IPRO) is a dichlorophenyl dicarboximide fungicide similar to procymidone and vinclozolin. All three of these fungicides induce Leydig cell tumors in the rat testis in long-term studies and an endocrine mode of action has been hypothesized to mediate this
Chad R Blystone et al.
Toxicological sciences : an official journal of the Society of Toxicology, 111(1), 179-188 (2009-07-01)
Vinclozolin and iprodione are dicarboximide fungicides that display antiandrogenic effects in the male rat, which suggests that a mixture would lead to cumulative effects on androgen-sensitive end points. Iprodione is a steroid synthesis inhibitor, but androgen receptor antagonist activity, which
Abul K M Anisuzzaman et al.
Journal of agricultural and food chemistry, 56(2), 502-506 (2007-12-21)
Both primary and secondary alcohols degrade iprodione, 3-(3,5-dichlorophenyl)-N-(1-methylethyl)-2,4-dioxo-1-imidazolidine carboxamide. Steric hindrance has been found to have an inverse effect on the rate of its decomposition, and a fully substituted alcohol, such as tert-butanol, does not degrade iprodione due to extreme
Osamu Maeda et al.
Journal of agricultural and food chemistry, 58(3), 1416-1419 (2009-12-17)
Iprodione is an agricultural fungicide that is difficult to detect in foods by HPLC because it coelutes with natural compounds in the food. We previously showed that food matrix could be degraded with titanium dioxide powder (TP). Here we describe

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