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Merck
CN

40019

Supelco

2,4,6-三氯苯酚 溶液

certified reference material, 5000 μg/mL in methanol

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About This Item

CAS号:
UNSPSC代码:
41116105

等级

certified reference material
TraceCERT®

Agency

EPA 552

产品线

TraceCERT®

CofA

current certificate can be downloaded

特点

standard type calibration

包装

ampule of 1 mL

浓度

5000 μg/mL in methanol

技术

HPLC: suitable
gas chromatography (GC): suitable

应用

cleaning products
cosmetics
environmental
food and beverages
personal care

包装形式

single component solution

储存温度

2-8°C

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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应用

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

其他说明

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.

法律信息

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

警示用语:

Danger

危险分类

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

靶器官

Eyes,Central nervous system

储存分类代码

3 - Flammable liquids

WGK

WGK 3

闪点(°F)

51.8 °F - closed cup

闪点(°C)

11 °C - closed cup

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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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
Ting T Liao et al.
Journal of environmental science and health. Part A, Toxic/hazardous substances & environmental engineering, 46(14), 1769-1775 (2011-12-20)
In this article, the feasibility of propidium iodide (PI) staining based on cell membrane damage as a sensitive and quantitative method to test the cytotoxicity of typical lipophilic compounds including 2,4,6-trichlorophenol (TCP) and perfluorooctane sulfonate (PFOS) was examined. The sensitivity
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

实验方案

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

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