所有图片(2)
About This Item
经验公式（希尔记法）:
C14H15O2PS2
CAS号:
分子量:
310.37
Beilstein:
1988797
EC 号:
MDL编号:
UNSPSC代码:
41116107
PubChem化学物质编号:
NACRES:
NA.24
推荐产品
等级
analytical standard
质量水平
产品线
PESTANAL®
保质期
limited shelf life, expiry date on the label
技术
HPLC: suitable
gas chromatography (GC): suitable
应用
agriculture
environmental
包装形式
neat
储存温度
2-8°C
SMILES字符串
CCOP(=O)(Sc1ccccc1)Sc2ccccc2
InChI
1S/C14H15O2PS2/c1-2-16-17(15,18-13-9-5-3-6-10-13)19-14-11-7-4-8-12-14/h3-12H,2H2,1H3
InChI key
AWZOLILCOUMRDG-UHFFFAOYSA-N
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相关类别
一般描述
Edifenphos is a selective and protective, organophosphorus foliar fungicide, used in controlling rice diseases such as blast caused by Pyricularia oryzae, sheath blight caused by Rhizoctonia solani and brown spot by Cochliobolus miyabeanus.
应用
Edifenphos may be used as a reference standard in the analysis of the analyte in rice using gold nanoparticle (AuNP)-based colorimetric multi-aptasensor.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
法律信息
PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany
警示用语：
Danger
危险分类
Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Skin Sens. 1
储存分类代码
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
农药列管产品
危险化学品
Biochemistry of Cell Walls and Membranes in Fungi (2012)
The Pesticide Encyclopedia (2014)
Detection of Iprobenfos and Edifenphos using a new Multi-aptasensor.
Agricultural and Biological Chemistry, 868(5), 60-66 (2015)
Edifenphos, Inhibitor of Phosphatidylcholine Biosynthesis in Pyricularia oryzae.
Kodama O, et al.
Agricultural and Biological Chemistry, 44(5), 1015-1021 (1980)
B E Causier et al.
Microbiology (Reading, England), 140 ( Pt 9), 2199-2205 (1994-09-01)
Chitin synthase in a microsomal preparation from Botrytis cinerea had an apparent Km for UDP-N-acetylglucosamine of 2.0 mM while nikkomycin Z and polyoxin D inhibited enzyme activity competitively with apparent Ki values of approximately 0.1 microM and 6 microM respectively.
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