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Merck
CN

40019

2,4,6-Trichlorophenol solution

certified reference material, 5000 μg/mL in methanol

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About This Item

CAS Number:
88-06-2
UNSPSC Code:
41116105

Key Documents

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InChI key

LINPIYWFGCPVIE-UHFFFAOYSA-N

InChI

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

grade

certified reference material, TraceCERT®

agency

EPA 552

product line

TraceCERT®

CofA

current certificate can be downloaded

feature

standard type calibration

packaging

ampule of 1 mL

concentration

5000 μg/mL in methanol

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

application(s)

cleaning products
cosmetics
environmental
food and beverages
personal care

format

single component solution

storage temp.

2-8°C

Application

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

Other Notes

This Certified Reference Material (CRM) is produced and certified in accordance with ISO 17034 and ISO/IEC 17025. All information regarding the use of this CRM can be found on the certificate of analysis.

Legal Information

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

signalword

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Chronic 3 - Flam. Liq. 2 - STOT SE 1

target_organs

Eyes,Central nervous system

Storage Class

3 - Flammable liquids

flash_point_f

51.8 °F - closed cup

flash_point_c

11 °C - closed cup

wgk

WGK 2

Regulatory Information

危险化学品
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Certificates of Analysis (COA)

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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
L S Iaguzhinskiĭ et al.
Biofizika, 58(1), 117-125 (2013-05-09)
In the process of mitochondrial respiratory H(+)-pumps functioning, the fraction membrane-bound protons (R-protons), which have an excess of free energy is formed. According to R.J. Williams this fraction is included as energy source in the reaction of ATP synthesis. Previously
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
Junjie Zhao et al.
The journal of physical chemistry. B, 116(40), 12065-12077 (2012-08-30)
The distal histidine mutations of dehaloperoxidase-hemoglobin A (DHP A) to aspartate (H55D) and asparagine (H55N) have been prepared to study the role played by the distal histidine in both activation and protection against oxidation by radicals in heme proteins. The
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
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