97-23-4
Chemical Structure
Dichlorophen
Synonym(s): DDM
- CAS No.: 97-23-4
- Formula:C13H10Cl2O2
- Molecular Weight:269.12
IUPAC Name: 2,2'-methylenebis(4-chlorophenol)
InChIKey: MDNWOSOZYLHTCG-UHFFFAOYSA-N
SMILES: OC1=CC=C(Cl)C=C1CC2=CC(Cl)=CC=C2O
Biological Activity: Dichlorophen is a chlorophenol antimicrobial agent that can destroy the integrity of microbial cell membranes and interfere with the activity of metabolic enzymes. Dichlorophen can covalently bind to the thiol groups of microbial proteins and has broad-spectrum antibacterial, antifungal and anthelmintic activity. Dichlorophen can be used as an antimicrobial agent in the study of drug-resistant bacterial infections[1][2].
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Dichlorophen | 98.55% | Dichlorophen is a chlorophenol antimicrobial agent that can destroy the integrity of microbial cell membranes and interfere with the activity of metabolic enzymes. Dichlorophen can covalently bind to the thiol groups of microbial proteins and has broad-spectrum antibacterial, antifungal and anthelmintic activity. Dichlorophen can be used as an antimicrobial agent in the study of drug-resistant bacterial infections. | ||||||||||||||||||||
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Dichlorophen (Standard) | ≥98% | Dichlorophen (Standard) is the analytical standard of Dichlorophen (HY-12638). This product is intended for research and analytical applications. Dichlorophen is a chlorophenol antimicrobial agent that can destroy the integrity of microbial cell membranes and interfere with the activity of metabolic enzymes. Dichlorophen can covalently bind to the thiol groups of microbial proteins and has broad-spectrum antibacterial, antifungal and anthelmintic activity. Dichlorophen can be used as an antimicrobial agent in the study of drug-resistant bacterial infections. | ||||||||||||||||||||
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- [1]. Kintz P, et al. Acute fatal poisoning with dichlorophen. Int J Legal Med. 1997;110(2):95-6. [Content Brief]
- [2]. Khaw TH, et al. Identification of Bithionol, Dichlorophen, and Miconazole as Antibacterial Agents against Acinetobacter calcoaceticus. ACS Omega. 2020 Sep 8;5(37):23951-23959. [Content Brief]
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