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Merck
CN

36543

2,4,6-Trichlorophenol

PESTANAL®, analytical standard

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About This Item

Linear Formula:
Cl3C6H2OH
CAS Number:
88-06-2
Molecular Weight:
197.45
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
329755386
EC Number:
201-795-9
Beilstein/REAXYS Number:
776729
MDL number:
MFCD00002172

Key Documents

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Product Name

2,4,6-Trichlorophenol, PESTANAL®, analytical standard

InChI key

LINPIYWFGCPVIE-UHFFFAOYSA-N

InChI

1S/C6H3Cl3O/c7-3-1-4(8)6(10)5(9)2-3/h1-2,10H

SMILES string

Oc1c(Cl)cc(Cl)cc1Cl

grade

analytical standard

vapor pressure

1 mmHg ( 76.5 °C)

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

bp

246 °C (lit.)

mp

64-66 °C (lit.)

application(s)

agriculture
cleaning products
cosmetics
environmental
food and beverages
personal care

format

neat

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Application

2,4,6-Trichlorophenol may be used as an analytical reference standard for the determination of the analyte in environmental samples using gas chromatography coupled to mass spectrometry (GC-MS).
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

General description

2,4,6-Trichlorophenol belongs to the class of chlorophenols, which occur as industrial wastes and direct environmental pollutants.

Other Notes

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

Legal Information

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

signalword

Danger

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 2 - Eye Dam. 1 - Skin Irrit. 2

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

210.2 °F - closed cup

flash_point_c

99 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

Regulatory Information

危险化学品
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Certificates of Analysis (COA)

Lot/Batch Number
BCCH5170
BCCC7820
BCBS5703V

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Jijun Gao et al.
Chemosphere, 71(6), 1181-1187 (2007-11-27)
The chlorophenol pollutants (CPs) have been reported to occur at relatively high concentrations in some Chinese waters. To map the distribution of CPs in the surface water throughout China, samples were collected from over 600 sites in the seven major
Nadavala Siva Kumar et al.
Colloids and surfaces. B, Biointerfaces, 94, 125-132 (2012-03-01)
Biosorption of 2,4,6-trichlorophenol (2,4,6-TCP) from aqueous solution by biomass prepared from Acacia leucocephala bark, an agricultural solid waste has been investigated in the present study. All the experiments are carried out by batch mode technique. The resulting biosorbent was characterized
Meiqin Hu et al.
Environmental science & technology, 46(16), 9005-9011 (2012-07-26)
Molecular iodine has been studied, for the first time, as a sensitizer for the degradation of 2,4,6-trichlorophenol (TCP) in aqueous solution under visible light (λ ≥ 450 nm). TCP was degraded in the presence of commercial I(2), but the reaction
Stefan Franzen et al.
The journal of physical chemistry. B, 116(5), 1666-1676 (2011-12-14)
Kinetic and structural studies have shown that peroxidases are capable of the oxidation of 2,4,6-trichlorophenol (2,4,6-TCP) to 2,6-dichloro-1,4-benzoquinone (2,6-DCQ). Further reactions of 2,6-DCQ in the presence of H(2)O(2) and OH(-) yield 2,6-dichloro-3-hydroxy-1,4-benzoquinone (2,6-DCQOH). The reactions of 2,6-DCQ have been monitored
Aki Sinkkonen et al.
Environmental science and pollution research international, 20(3), 1737-1745 (2012-07-04)
Chlorophenols, like many other synthetic compounds, are persistent problem in industrial areas. These compounds are easily degraded in certain natural environments where the top soil is organic. Some studies suggest that mineral soil contaminated with organic compounds is rapidly remediated
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