36677
三氯杀螨醇
PESTANAL®
别名:
2,2,2-三氯-1,1-双（4-氯苯基）乙醇
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关于此项目
经验公式（希尔记法）:
C14H9Cl5O
化学文摘社编号:
分子量:
370.49
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
EC Number:
204-082-0
Beilstein/REAXYS Number:
1886299
MDL number:
InChI key
UOAMTSKGCBMZTC-UHFFFAOYSA-N
InChI
1S/C14H9Cl5O/c15-11-5-1-9(2-6-11)13(20,14(17,18)19)10-3-7-12(16)8-4-10/h1-8,20H
SMILES string
OC(c1ccc(Cl)cc1)(c2ccc(Cl)cc2)C(Cl)(Cl)Cl
grade
analytical standard
product line
PESTANAL®
application(s)
agriculture
environmental
format
neat
storage temp.
2-8°C
Quality Level
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General description
Dicofol is a non-systemic insecticide used for a variety of crops. It can be synthesized from dichlorodiphenyltrichloroethane(DDT) via chlorination followed by hydrolysis.
Legal Information
PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany
signalword
Warning
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Skin Irrit. 2 - Skin Sens. 1
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
法规信息
有毒化学品
此项目有
"Estrogenic activity of dicofol with the human estrogen receptor: Isomer-and enantiomer-specific implications"
Hoekstra.FP, et al.
Chemosphere, 64(01), 174- 177 (2006)
"Contents and sources of DDT impurities in dicofol formulations in Turkey"
Turgut C, et al.
Environmental Science and Pollution Research International, 16(02), 214-217 (2009)
Shu-ying Han et al.
Chemosphere, 83(2), 131-136 (2011-02-09)
n-Octanol/water partition coefficients (P) for DDTs and dicofol were determined by reversed-phase high performance liquid chromatography (RP-HPLC) on a C(18) column using methanol-water mixture as mobile phase. A dual-point retention time correction (DP-RTC) was proposed to rectify chromatographic retention time
Juliana Elaine Perobelli et al.
Journal of toxicology and environmental health. Part A, 73(13-14), 991-1002 (2010-06-22)
The Brazilian Agency of Sanitary Vigilance (ANVISA) conducted a study that demonstrated the presence of residues of several pesticides in fresh fruits and vegetables that were available for purchase by the general populace. In order to evaluate potential adverse health
Cafer Turgut et al.
Environmental science and pollution research international, 16(2), 214-217 (2008-12-05)
Dicofol is widely used as a pesticide in agriculture applications. Since dicofol is mainly synthesized from dichlorodiphenyltrichlorethane (DDT), it contains DDT as an impurity. The European Community has forced Prohibition Directive 79/117/EEC to reduce DDT in dicofol formulations. Specifically, DDT
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