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45374

Supelco

Chloranil

PESTANAL®, analytical standard

Synonym(s):

Tetrachloro-p-benzoquinone

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About This Item

Empirical Formula (Hill Notation):
C6Cl4O2
CAS Number:
118-75-2
Molecular Weight:
245.88
Beilstein:
393006
EC Number:
204-274-4
MDL number:
MFCD00001594
UNSPSC Code:
41116107
PubChem Substance ID:
329756682
NACRES:
NA.24

grade

analytical standard

Quality Level

100

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

agriculture
environmental

format

neat

SMILES string

ClC1=C(Cl)C(=O)C(Cl)=C(Cl)C1=O

InChI

1S/C6Cl4O2/c7-1-2(8)6(12)4(10)3(9)5(1)11

InChI key

UGNWTBMOAKPKBL-UHFFFAOYSA-N

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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

Signal Word

Danger

Hazard Statements

H315,H317,H318,H410

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1 - Skin Irrit. 2 - Skin Sens. 1

Storage Class Code

11 - Combustible Solids

WGK

WGK 2

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
BCCJ4884
BCBW8483
SZBD221XV
SZB8206XV
SZE8206X

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Ben-Zhan Zhu et al.
Proceedings of the National Academy of Sciences of the United States of America, 109(40), 16046-16051 (2012-09-19)
Most chemiluminescence (CL) reactions usually generate only one-step CL, which is rarely dependent on the highly reactive and biologically/environmentally important hydroxyl radicals ((•)OH). Here, we show that an unprecedented two-step CL can be produced by the carcinogenic tetrachloro-1,4-benzoquinone (also known
Ali A Ensafi et al.
Colloids and surfaces. B, Biointerfaces, 84(1), 148-154 (2011-01-25)
An electrochemical method is described for the voltammetric determination of isoproterenol in the presence of uric acid using p-chloranil-carbon nanotubes paste electrode. Cyclic voltammetric, chronoamperometric, and electrochemical impedance spectroscopic methods have used to investigate the suitability of p-chloranil as a
Prashant Singh et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 75(3), 983-991 (2010-01-19)
In the present work, we report the synthesis and characterization of novel charge-transfer complexes of thiazolidine-2,4-dione (TZD) with sigma acceptor (iodine) and pi acceptors (chloranil, dichlorodicyanoquinone, picric acid and duraquinone). We also evaluated their thermal and electrochemical properties and we
Suping Jia et al.
Analytical and bioanalytical chemistry, 397(6), 2395-2400 (2010-05-25)
Halogenated phenols are widely used as biocides and are considered to be possibly carcinogenic to humans. In this report, a previously developed photoelectrochemical DNA sensor was employed to investigate DNA damage induced by tetra-halogenated quinones, the in vivo metabolites of
C Balraj et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 79(5), 1137-1144 (2011-06-03)
The molecular complexes of the donors ketaconazole (KTZ) and oxatomide (OXA) drugs with 2,3,5,6-tetrachloro-1,4-benzoquinone (p-chloranil, p-CHL) have been investigated spectroscopically (UV-vis, FT-IR and 1H NMR) and spectrofluorimetrically in different solvents and temperatures. The stoichiometry of the complexes was found to
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