Dichlorophen
Chemical compound
- P02DX02 (WHO)
- 4-Chloro-2-[(5-chloro-2-hydroxyphenyl)methyl]phenol
- 97-23-4 Y
- 3037
- 2929 N
- T1J0JOU64O
- C14292 Y
- ChEMBL33845 N
- DTXSID6021824
- Interactive image
- C1=CC(=C(C=C1Cl)CC2=C(C=CC(=C2)Cl)O)O
InChI
- 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 N
- Key:MDNWOSOZYLHTCG-UHFFFAOYSA-N N
Dichlorophen is an anticestodal agent, fungicide, germicide, and antimicrobial agent.[2] It is used in combination with toluene for the removal of parasites such as ascarids, hookworms, and tapeworms from dogs and cats.[3]
Safety and regulation
LD50 (oral, mouse) is 3300 mg/kg.[4]
References
- ^ Lide DR (1998). Handbook of Chemistry and Physics (87 ed.). Boca Raton, Florida: CRC Press. pp. 8–118. ISBN 0-8493-0594-2.
- ^ Milne, G.W.A. (Ed.). (2005). Gardner's commercially important chemicals: Synonyms, trade names, and properties. Hoboken, N.J.: Wiley-Interscience. Google Books
- ^ "Code of Federal Regulations", Code of Federal Regulations, Title 21, Volume 6, U.S. Government Printing Office, 2005-04-01, retrieved 2009-05-01
- ^ Fiege H, Voges HW, Hamamoto T, Umemura S, Iwata T, Miki H, Fujita Y, Buysch HJ, Garbe D, Paulus W (2007). "Phenol Derivatives". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a19_313. ISBN 978-3527306732.
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Antitrematodals (schistosomicides) |
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Anticestodals (taeniacides) |
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(including
macrofilaricides)
Binds tubulin | |
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Glutamate-gated chloride channel, GABA receptor | |
NMDA |
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Other/unknown |
- #WHO-EM
- ‡Withdrawn from market
- Clinical trials:
- †Phase III
- §Never to phase III
This antiinfective drug article is a stub. You can help Wikipedia by expanding it. |
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