Dichlorophen

Dichlorophen
Clinical data
AHFS/Drugs.com	International Drug Names
ATC code	P02DX02 (WHO) ;
Identifiers
	IUPAC name 4-Chloro-2-[(5-chloro-2-hydroxyphenyl)methyl]phenol;
CAS Number	97-23-4 ;
PubChem CID	3037;
ChemSpider	2929 ;
UNII	T1J0JOU64O;
KEGG	C14292 ;
ChEMBL	ChEMBL33845 ;
CompTox Dashboard (EPA)	DTXSID6021824 ;
ECHA InfoCard	100.002.335
Chemical and physical data
Formula	C13H10Cl2O2
Molar mass	269.12 g/mol g·mol−1
3D model (JSmol)	Interactive image;
Density	1.5 g/cm3 g/cm3
Melting point	177.5 °C (351.5 °F)
Solubility in water	0.003 g/100 mL[1] mg/mL (20 °C)
	SMILES 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 ; Key:MDNWOSOZYLHTCG-UHFFFAOYSA-N ;
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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, David R. (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
Helmut Fiege; Heinz-Werner Voges; Toshikazu Hamamoto; Sumio Umemura; Tadao Iwata; Hisaya Miki; Yasuhiro Fujita; Hans-Josef Buysch; Dorothea Garbe (2007). "Phenol Derivatives". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a19_313.

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[hand2-1] Lide, David R. (1998), Handbook of Chemistry and Physics (87 ed.), Boca Raton, Florida: CRC Press, pp. 8–118, ISBN 0-8493-0594-2

[gard-2] Milne, G.W.A. (Ed.). (2005). Gardner's commercially important chemicals: Synonyms, trade names, and properties. Hoboken, N.J.: Wiley-Interscience. Google Books

[cfr-3] "Code of Federal Regulations", Code of Federal Regulations, Title 21, Volume 6, U.S. Government Printing Office, 2005-04-01, retrieved 2009-05-01

[a-4] Helmut Fiege; Heinz-Werner Voges; Toshikazu Hamamoto; Sumio Umemura; Tadao Iwata; Hisaya Miki; Yasuhiro Fujita; Hans-Josef Buysch; Dorothea Garbe (2007). "Phenol Derivatives". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a19_313.