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Merck
CN

49054

Methoxychlor

PESTANAL®, analytical standard

Synonym(s):

1,1,1-Trichloro-2,2-bis-(p-methoxyphenyl)ethane, 2,2-Bis(4-methoxyphenyl)-1,1,1-trichloroethane, DMDT

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About This Item

Empirical Formula (Hill Notation):
C16H15Cl3O2
CAS Number:
Molecular Weight:
345.65
EC Number:
200-779-9
UNSPSC Code:
41121813
PubChem Substance ID:
Beilstein/REAXYS Number:
2057367
MDL number:
Technical Service
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grade

analytical standard

Quality Level

product line

PESTANAL®

packaging

ampule of 1000 mg

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

mp

86-88 °C (lit.)

application(s)

agriculture
environmental

format

neat

storage temp.

room temp

SMILES string

COc1ccc(cc1)C(c2ccc(OC)cc2)C(Cl)(Cl)Cl

InChI

1S/C16H15Cl3O2/c1-20-13-7-3-11(4-8-13)15(16(17,18)19)12-5-9-14(21-2)10-6-12/h3-10,15H,1-2H3

InChI key

IAKOZHOLGAGEJT-UHFFFAOYSA-N

Gene Information

mouse ... Esr1(13982)

Application

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

Biochem/physiol Actions

Pesticide with estrogenic activity.

Legal Information

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


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Warning

Hazard Classifications

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

Storage Class

11 - Combustible Solids

wgk

WGK 3

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

Regulatory Information

农药列管产品

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Hye-Rim Lee et al.
International journal of molecular medicine, 29(5), 883-890 (2012-02-07)
Various endocrine disrupting chemicals (EDCs) are exogenous compounds found in the environment and have the potential to interfere with the endocrine system and hormonal regulation. Among EDCs, bisphenol A (BPA) and 1,1,1-trichloro-2,2-bis(4-methoxyphenol)-ethane [methoxychlor (MXC)] have estrogenic activity resulting in a variety
Minoru Masuda et al.
Bioscience, biotechnology, and biochemistry, 76(1), 73-77 (2012-01-11)
Agricultural waste water containing pesticides can reach the sea via rivers and estuaries, including brackish lakes. We studied the metabolic fate of methoxychlor [MXC; 1,1,1-trichloro-2,2-bis(4-methoxyphenyl)ethane] in a model system consisting of sediment and associated water collected from two sampling sites:
P Palanza et al.
Neurotoxicology and teratology, 24(1), 55-69 (2002-02-12)
There has been increasing interest, both at the scientific and regulatory level, in the use of ethological methods for evaluating neural effects of endocrine disrupters. We present a series of ethological studies on the effects of maternal exposure to low