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36543

Supelco

2,4,6-Trichlorophenol

PESTANAL®, analytical standard

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About This Item

Fórmula lineal:
Cl3C6H2OH
Número de CAS:
88-06-2
Peso molecular:
197.45
Beilstein/REAXYS Number:
776729
EC Number:
201-795-9
MDL number:
MFCD00002172
UNSPSC Code:
41116107
PubChem Substance ID:
329755386
NACRES:
NA.24

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

SMILES string

Oc1c(Cl)cc(Cl)cc1Cl

InChI

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

InChI key

LINPIYWFGCPVIE-UHFFFAOYSA-N

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General description

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

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.

Recommended products

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_germany

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

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Certificados de análisis (COA)

Lot/Batch Number
BCCH5170
BCCC7820
BCBS5703V
SZBF232XV
SZBB294XV

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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
Minhee Kim et al.
Chemosphere, 89(3), 262-268 (2012-05-17)
The well-known cosolvency-induced sorption model is not applicable to predict the sorption of carboxylic acids in cosolvent system. To investigate the phenomenon, sorption and solubility of chlorinated phenols (2,4-dichlorophenol (2,4-DCP) and 2,4,6-trichlorophenol (2,4,6-TCP)) and carboxylic acids (benzoic acid and 2,4-dichlorophenoxyacetic
Supreet S Bahga et al.
Electrophoresis, 33(6), 1048-1059 (2012-04-25)
We present a novel method of creating concentration cascade of leading electrolyte (LE) in isotachophoresis (ITP) by using bidirectional ITP. ITP establishes ion-concentration shock waves between high-mobility LE and low-mobility trailing electrolyte (TE) ions. In bidirectional ITP, we set up
Yabo Wang et al.
ACS applied materials & interfaces, 4(8), 3965-3972 (2012-07-12)
Cu(2)O/TiO(2) heterojunction photocatalyst is built on carbon aerogel (CA) substrate with good adsorption properties by sol impregnation and seed-mediated synthesis approach. The Cu(2)O/TiO(2)/CA electrode has excellent electrosorptive and high efficient photocatalytic properties. Its morphology and surface chemical composition are characterized
Chunxue Wang et al.
Biochemistry, 52(36), 6203-6210 (2013-08-21)
The hemoglobin of sea worm Amphitrite ornata, which for historical reasons is abbreviated as DHP for dehaloperoxidase, has two physiological functions: it binds dioxygen in the ferrous state and dehalogenates halophenols, such as 2,4,6-trichlorophenol (TCP), using hydrogen peroxide as the
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