Merck
CN

36677

Supelco

三氯杀螨醇

PESTANAL®

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别名:
2,2,2-三氯-1,1-双(4-氯苯基)乙醇
经验公式(希尔记法):
C14H9Cl5O
CAS号:
分子量:
370.49
Beilstein:
1886299
EC 号:
MDL编号:
PubChem化学物质编号:
NACRES:
NA.24

等级

analytical standard

质量水平

产品线

PESTANAL®

应用

agriculture
environmental

格式

neat

储存温度

2-8°C

SMILES字符串

OC(c1ccc(Cl)cc1)(c2ccc(Cl)cc2)C(Cl)(Cl)Cl

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

InChI key

UOAMTSKGCBMZTC-UHFFFAOYSA-N

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一般描述

Dicofol is a non-systemic insecticide used for a variety of crops. It can be synthesized from dichlorodiphenyltrichloroethane(DDT) via chlorination followed by hydrolysis.

法律信息

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

象形图

Exclamation markEnvironment

警示用语:

Warning

危险分类

Acute Tox. 4 Dermal - Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Skin Irrit. 2 - Skin Sens. 1

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

法规信息

监管及禁止进口产品

分析证书(COA)

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示例

T1503
货号
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25G
包装规格/数量

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705578-5MG-PW

PL860-CGA/SHF-1EA

MMYOMAG-74K-13

1000309185

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"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
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
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

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