76547
Isoprothiolane
PESTANAL®, analytical standard
Sinónimos:
Diisopropyl 2-(1,3-dithiolan-2-ylidene)malonate
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About This Item
Fórmula empírica (notación de Hill):
C12H18O4S2
Número de CAS:
Peso molecular:
290.40
Beilstein:
2128528
Número MDL:
Código UNSPSC:
41116107
ID de la sustancia en PubChem:
NACRES:
NA.24
Productos recomendados
grado
analytical standard
Nivel de calidad
Línea del producto
PESTANAL®
Ensayo
≥98.0% (HPLC)
caducidad
limited shelf life, expiry date on the label
técnicas
HPLC: suitable
gas chromatography (GC): suitable
aplicaciones
agriculture
environmental
Formato
neat
temp. de almacenamiento
2-8°C
cadena SMILES
CC(C)OC(=O)\C(C(=O)OC(C)C)=C1/SCCS1
InChI
1S/C12H18O4S2/c1-7(2)15-10(13)9(11(14)16-8(3)4)12-17-5-6-18-12/h7-8H,5-6H2,1-4H3
Clave InChI
UFHLMYOGRXOCSL-UHFFFAOYSA-N
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Descripción general
Isoprothiolane is a systemic fungicide, which is used in controlling diseases rice stem rot, rice blast and Fusarium leaf spot on rice. Its mode of action basically involves the inhibition of penetration and elongation of infecting hyphae via inhibiting the formation of infecting peg or cellulose secretion.
Aplicación
Isoprothiolane may be used as a reference standard in the determination of isoprothiolane in food samples using gas chromatography coupled with mass spectrometry (GC-MS).
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Envase
Bottomless glass bottle. Contents are inside inserted fused cone.
Información legal
PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany
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Water science and technology : a journal of the International Association on Water Pollution Research, 56(1), 71-80 (2007-08-23)
Verification of a diffuse pollution model involves comparing results actually observed with those predicted by precise model inputs. Acquisition of precise model inputs is, however, problematic. In particular, when the target catchment is large and substantial estimation uncertainty exists, not
S Nagasawa et al.
Nihon juigaku zasshi. The Japanese journal of veterinary science, 51(2), 284-293 (1989-04-01)
Isoprothiolane was administered continuously of various doses to heifers with liver lesions induced by carbon tetrachloride, to determine the effect of the drug on blood components, enzymatic activities, and liver microsome functions. After injection of carbon tetrachloride, a decrease in
Metabolic Pathways of Agrochemicals: Insecticides and fungicides (1998)
S S Chou et al.
Journal of environmental science and health. Part. B, Pesticides, food contaminants, and agricultural wastes, 15(2), 135-146 (1980-01-01)
The fungicide isoprothiolane (diisopropyl 1,3-dithiolan-2-ylidenemalonate) decomposed slowly in deionized water under ultraviolet light or sunlight irradiation. Rice-paddy water greatly accelerated the photodegradation. This photosensitizing effect was comparable to that of 2% acetone. Soil extracts, rice-plant extracts, and chlorophylls showed little
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