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Merck
CN

35835

Supelco

2,5-二氯苯酚

PESTANAL®, analytical standard

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线性分子式:
Cl2C6H3OH
CAS号:
分子量:
163.00
Beilstein:
1907692
EC 号:
MDL编号:
UNSPSC代码:
41116107
PubChem化学物质编号:
NACRES:
NA.24

等级

analytical standard

质量水平

产品线

PESTANAL®

保质期

limited shelf life, expiry date on the label

技术

HPLC: suitable
gas chromatography (GC): suitable

bp

211 °C (lit.)

mp

54-57 °C (lit.)

应用

agriculture
environmental

格式

neat

SMILES字符串

Oc1cc(Cl)ccc1Cl

InChI

1S/C6H4Cl2O/c7-4-1-2-5(8)6(9)3-4/h1-3,9H

InChI key

RANCECPPZPIPNO-UHFFFAOYSA-N

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相关类别

应用

2,5-Dichlorophenol may be used as an analytical reference standard for the determination of the analyte in water, and wood, paper, cardboard, fruits, and fruit juices using simultaneous dispersive liquid-liquid microextraction and derivatization followed by gas chromatography-electron-capture detection (GC-ECD) and gas chromatography-mass spectrometry (GC-MS), respectively.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

法律信息

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

象形图

Exclamation markEnvironment

警示用语:

Warning

危险分类

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

WGK

WGK 2

个人防护装备

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

法规信息

危险化学品

分析证书(COA)

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N Díaz-Alejo et al.
Journal of chromatography, 622(2), 179-186 (1993-12-22)
O-Hexyl O-2,5-dichlorophenyl phosphoramidate (HDCP) is a chiral organophosphorus compound that undergoes enzymatic hydrolysis in the rat and hen. Studies of the stereospecificity of its biodegradation are necessary to establish HDCP toxicity. To this effect, methods have been developed for the
M A Sogorb et al.
Chemico-biological interactions, 87(1-3), 117-125 (1993-06-01)
The organophosphorus (OP) compound O-hexyl-O-2,5-dichlorophenyl phosphoramidate (H-DCP) is hydrolysed in the plasma, liver and brain of hens and rats. We study in hen plasma the effect of tissue and substrate concentrations and of pH on the hydrolysing activity of H-DCP.
T Yoshida et al.
Archives of environmental contamination and toxicology, 43(4), 481-485 (2002-10-26)
The relationship between exposure to p-dichlorobenzene (p-DCB) and urinary excretion of 2,5-dichlorophenol (2,5-DCP), the major metabolite of p-DCB, was examined to evaluate the usefulness of the metabolite as a biological index for low-level exposure of p-DCB in the general population.
R H Hill et al.
Archives of environmental health, 50(4), 277-280 (1995-07-01)
p-Dichlorobenzene is used widely in the United States as a room deodorizer, a moth repellent, and a precursor for a polymer. In a previous study of selected children in Arkansas, we found that 96% of the children had detectable urinary
Xiaoyun Ye et al.
Environment international, 35(8), 1160-1163 (2009-08-12)
In humans, the metabolism of environmental phenols may include the formation of conjugated species (e.g., glucuronides and sulfates), but the free species-not the conjugated forms-are considered biologically active. Therefore, information on the concentration of these free species in blood or

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