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
存储类别
3 - Flammable liquids
flash_point_f
51.8 °F - closed cup
flash_point_c
11 °C - closed cup
wgk
WGK 2
法规信息
危险化学品
此项目有
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
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
James Huff
Chemosphere, 89(5), 521-525 (2012-07-04)
Carcinogenesis bioassays were conducted by giving 2,4,6-trichlorophenol [2,4,6-TCP] in feed to groups of 50 male and female Fischer rats and male B6C3F1 mice for two years. Dietary concentrations were 0 [20/group], 5000 [0.5%], or 10,000 [1%] ppm. Female mice began
Ning Yan et al.
Huan jing ke xue= Huanjing kexue, 32(10), 3059-3066 (2012-01-28)
Photolytic circulating-bed biofilm reactor (PCBBR) and internal loop photolytic-biological reactor (ILPBR) were respectively used for degradation of phenol, 2, 4, 6-trichlorophenol (TCP) and sulfamethoxazole (SMX). Experimental results indicated that the rates of phenol, TCP and SMX removal by coupled photolysis
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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