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Merck
CN

N12707

2,4′-DDE

analytical standard

Synonym(s):

2-(2-Chlorophenyl)-2-(4-chlorophenyl)-1,1-dichloroethene, o,p′-DDE

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About This Item

Empirical Formula (Hill Notation):
C14H8Cl4
CAS Number:
Molecular Weight:
318.03
UNSPSC Code:
41116107
EC Number:
222-318-0
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InChI key

ZDYJWDIWLRZXDB-UHFFFAOYSA-N

InChI

1S/C14H8Cl4/c15-10-7-5-9(6-8-10)13(14(17)18)11-3-1-2-4-12(11)16/h1-8H

grade

analytical standard

packaging

ampule of 50 mg

manufacturer/tradename

Chem Service, Inc. N-12707-50MG

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

format

neat

Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

signalword

Warning

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 2

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


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Anna A Kasperlik-Zaluska et al.
Journal of experimental therapeutics & oncology, 5(2), 125-132 (2006-02-14)
Our study aimed at evaluation of the relations between the plasma levels of mitotane (o,p'-DDD) and its metabolites, o,p'-DDA and o,p'-DDE, and the efficacy of Mitotane therapy during a long-term follow-up. Eighteen patients, aged 11 to 70 years, were included
D B Carlson et al.
Environmental health perspectives, 108(3), 249-255 (2000-03-08)
Fish sexual development is sensitive to exogenous hormone manipulation, and salmonids have been used extensively as environmental sentinels and models for biomedical research. We simulated maternal transfer of contaminants by microinjecting rainbow trout (Oncorhynchus mykiss) and chinook salmon (Oncorhynchus tshawytscha)
R Benecke et al.
European journal of clinical pharmacology, 41(3), 259-261 (1991-01-01)
Mitotane (o,p'-DDD) can be used for the treatment of various adrenocortical diseases such as Cushing's syndrome, but the usual doses of 6-8 g per day are often associated with severe adverse effects. This paper reports the results of much lower
P Balaguer et al.
The Science of the total environment, 233(1-3), 47-56 (1999-09-24)
In order to characterize the estrogenic activity of chemicals, we established complementary in vitro recombinant receptor-reporter gene assays in stably transfected MCF-7 and HeLa cells. MCF-7 cells which express the endogenous estrogen receptor alpha (ER alpha) were stably transfected with
W Foster et al.
The Journal of clinical endocrinology and metabolism, 85(8), 2954-2957 (2000-08-18)
Man-made chemicals that have been shown to modulate endocrine function in animal models, so-called "endocrine disrupters", are suspected to play a role in the development of male reproductive tract abnormalities and neurobehaviroal deficits in children. However in utero exposure to

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