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Merck
CN

36543

Supelco

2,4,6-三氯苯酚

PESTANAL®, analytical standard

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About This Item

线性分子式:
Cl3C6H2OH
CAS号:
分子量:
197.45
Beilstein:
776729
EC 号:
MDL编号:
UNSPSC代码:
41116107
PubChem化学物质编号:
NACRES:
NA.24

等级

analytical standard

蒸汽压

1 mmHg ( 76.5 °C)

产品线

PESTANAL®

保质期

limited shelf life, expiry date on the label

技术

HPLC: suitable
gas chromatography (GC): suitable

沸点

246 °C (lit.)

mp

64-66 °C (lit.)

应用

agriculture
cleaning products
cosmetics
environmental
food and beverages
personal care

包装形式

neat

SMILES字符串

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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一般描述

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

应用

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.

推荐产品

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.

法律信息

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

警示用语:

Danger

危险分类

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

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

210.2 °F - closed cup

闪点(°C)

99 °C - closed cup

个人防护装备

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

法规信息

危险化学品

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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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
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
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
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

实验方案

Analytical standard separation of various phenols for research and industrial applications.

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