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Merck
CN

442298

2,4,5,6-Tetrachloro-m-xylene

PESTANAL®, analytical standard

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About This Item

Empirical Formula (Hill Notation):
C8H6Cl4
CAS Number:
Molecular Weight:
243.95
UNSPSC Code:
41121813
PubChem Substance ID:
EC Number:
212-886-8
MDL number:
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InChI key

NTUBJKOTTSFEEV-UHFFFAOYSA-N

InChI

1S/C8H6Cl4/c1-3-5(9)4(2)7(11)8(12)6(3)10/h1-2H3

SMILES string

Cc1c(Cl)c(C)c(Cl)c(Cl)c1Cl

grade

analytical standard

product line

PESTANAL®

packaging

ampule of 1000 mg

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

application(s)

agriculture
environmental

format

neat

storage temp.

room temp

Quality Level

Application

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

Legal Information

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

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


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Ochan Otim
Environmental science. Processes & impacts, 21(9), 1580-1595 (2019-08-15)
Assessing the extent of ocean bed contamination by anthropogenic organic chemicals requires collecting and preserving the native state of sediments. The latter is particularly important since most sediment analyses are performed away from the sites of samples collection. Preservation, however
Xiang Wu et al.
Environmental pollution (Barking, Essex : 1987), 246, 124-130 (2018-12-12)
Predicting the translocation of organic contaminants to plants is crucial to ensure the quality of agricultural goods and assess the risk of human exposure through the food web. In this study, the performance of a modified plant uptake model was
Shanshan Yin et al.
Environment international, 130, 104939-104939 (2019-06-30)
Currently, there is limited information about the mechanism of the human transplacental transfer for organochlorine pesticides (OCPs). This study aimed to evaluate the transplacental transfer of OCPs to better understand the influencing factors of exposure and transplacental efficiency. The study
Swatantra Pratap Singh et al.
The journal of physical chemistry. A, 121(27), 5156-5163 (2017-06-20)
The objective of this study was to elucidate the mechanism of abiotic hydrolysis of ES isomers, i.e., Endosulfan-1 (ES-1) and Endosulfan-2 (ES-2), using a combination of experiments and density functional theory (DFT) calculations. Hydrolysis of both ES-1 and ES-2 resulted
Meiqing Jin et al.
Environmental pollution (Barking, Essex : 1987), 222, 109-117 (2017-01-11)
The spatial distribution, compositional profiles, and enantiomer fractions (EFs) of organochlorine pesticides (OCPs), including hexachlorocyclohexanes (HCHs), dichlorodiphenyltrichloroethanes (DDTs), and chlordanes (CHLs), in the surface sediments in the Bering Sea, Chukchi Sea and adjacent areas were investigated. The total concentrations of

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