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36677

Supelco

Dicofol

PESTANAL®

Synonym(s):

2,2,2-Trichloro-1,1-bis(4-chlorophenyl)ethanol

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100 MG
€89.50

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100 MG
€89.50

About This Item

Empirical Formula (Hill Notation):
C14H9Cl5O
CAS Number:
115-32-2
Molecular Weight:
370.49
Beilstein:
1886299
EC Number:
204-082-0
MDL number:
MFCD00055271
UNSPSC Code:
41116107
PubChem Substance ID:
329755445
NACRES:
NA.24

€89.50

Available to ship onApril 09, 2025Details

Request a Bulk Order

grade

analytical standard

product line

PESTANAL®

application(s)

agriculture
environmental

format

neat

storage temp.

2-8°C

SMILES string

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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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.[1][2]

Legal Information

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

Pictograms

Exclamation markEnvironment
GHS07,GHS09

Signal Word

Warning

Hazard Classifications

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

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCJ3199
BCBZ3113

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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)
Maher H Haeba et al.
Environmental science and pollution research international, 15(3), 222-227 (2008-05-28)
Pollution-induced endocrine disruption in vertebrates and invertebrates is a worldwide environmental problem, but relatively little is known about effects of endocrine disrupting compounds (EDCs) in planktonic crustaceans (including Daphnia magna). Aims of the present study were to investigate acute 48
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
View All Related Papers

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