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Merck
CN

76547

Supelco

稻瘟灵

PESTANAL®, analytical standard

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别名:
Diisopropyl 2-(1,3-dithiolan-2-ylidene)malonate
经验公式(希尔记法):
C12H18O4S2
CAS号:
分子量:
290.40
Beilstein:
2128528
MDL编号:
UNSPSC代码:
41116107
PubChem化学物质编号:
NACRES:
NA.24

等级

analytical standard

质量水平

产品线

PESTANAL®

检测方案

≥98.0% (HPLC)

保质期

limited shelf life, expiry date on the label

技术

HPLC: suitable
gas chromatography (GC): suitable

应用

agriculture
environmental

格式

neat

储存温度

2-8°C

SMILES字符串

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

InChI key

UFHLMYOGRXOCSL-UHFFFAOYSA-N

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相关类别

一般描述

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.

应用

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.

包装

Bottomless glass bottle. Contents are inside inserted fused cone.

法律信息

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

象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Acute Tox. 4 Oral

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

法规信息

农药列管产品

分析证书(COA)

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Y Matsui et al.
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
Metabolic Pathways of Agrochemicals: Insecticides and fungicides (1998)
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
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
H Katamoto et al.
Nihon juigaku zasshi. The Japanese journal of veterinary science, 52(6), 1189-1197 (1990-12-01)
To study effects of isoprothiolane and phytosterol on dietary fat necrosis, 3 groups of rats were fed hardened-tallow (HT) diet. Two groups of rats received either isoprothiolane (50 mg/kg) or phytosterol (20 mg/kg) orally once a day consecutively for 10

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