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线性分子式:
CH2[C6H3(Cl)OH]2
化学文摘社编号:
分子量:
269.12
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
EC Number:
202-567-1
Beilstein/REAXYS Number:
1884514
MDL number:
InChI key
MDNWOSOZYLHTCG-UHFFFAOYSA-N
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
SMILES string
Oc1ccc(Cl)cc1Cc2cc(Cl)ccc2O
grade
analytical standard
product line
PESTANAL®
shelf life
limited shelf life, expiry date on the label
technique(s)
HPLC: suitable, gas chromatography (GC): suitable
mp
168-172 °C (lit.)
application(s)
agriculture
cleaning products
cosmetics
environmental
food and beverages
personal care
format
neat
Quality Level
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General description
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.
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
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.
Legal Information
PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Irrit. 2
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
法规信息
农药列管产品
此项目有
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
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
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
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