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Merck

35992

Supelco

双氯酚

PESTANAL®, analytical standard

别名:

双氯酚, 二氯芬, 双(5-氯-2-羟苯基)甲烷

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About This Item

线性分子式:
CH2[C6H3(Cl)OH]2
CAS号:
分子量:
269.12
Beilstein:
1884514
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

mp

168-172 °C (lit.)

应用

agriculture
cleaning products
cosmetics
environmental
food and beverages
personal care

包装形式

neat

SMILES字符串

Oc1ccc(Cl)cc1Cc2cc(Cl)ccc2O

InChI

1S/C13H10Cl2O2/c14-10-1-3-12(16)8(6-10)5-9-7-11(15)2-4-13(9)17/h1-4,6-7,16-17H,5H2

InChI key

MDNWOSOZYLHTCG-UHFFFAOYSA-N

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一般描述

Dichlorophene is a halogenated phenolic compound, which can basically play the role of a fungicide and bacteriocide in the cosmetic industry. It can also act like an antiprotozoan agent.
This substance is listed on the positive list of the EU regulation 10/2011 for plastics intended to come into contact with food.

应用

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

象形图

Exclamation markEnvironment

警示用语:

Warning

危险声明

危险分类

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

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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访问文档库

Safety assessment of dichlorophene and chlorophene
Yamarik AT
International Journal of Toxicology, 23, 1-27 (2004)
Toxicogenetic evaluation of dichlorophene in peripheral blood and in the cells of the immune system using molecular and flow cytometric approaches
Lone IM, et al.
Chemosphere, 167, 520-529 (2017)
Antoine Ghauch et al.
Journal of hazardous materials, 164(2-3), 665-674 (2008-09-30)
Palladium, ruthenium and silver were investigated as catalysts for the dechlorination of dichlorophen (DCP, 2,2'-methylenebis(4-chlorophenol)), an antimicrobial and anthelmintic agent largely used as algicide, fungicide and bactericide. Experiments were undertaken under oxic and anoxic conditions for experimental durations up to
Kenichi Onda et al.
Bioorganic & medicinal chemistry, 16(18), 8627-8634 (2008-08-30)
During our research using a high-throughput screening system for discovery of a new class of human liver glycogen phosphorylase a (hLGPa) inhibitors, a series of 3-(3,4-dichlorophenyl)acrylamide derivatives were synthesized, and their inhibitory activities toward hLGPa were evaluated. Among the derivatives
J Langrand et al.
Clinical toxicology (Philadelphia, Pa.), 51(3), 178-181 (2013-03-12)
Human dichlorophen poisoning is rare. We aim to report a case of dichlorophen poisoning resulting in complete recovery despite life-threatening multiorgan failure and huge serum dichlorophen concentrations. Description of features and management in one dichlorophen-poisoned patient. After liquid-liquid extraction, dichlorophen

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