Dichlorophen

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Dichlorophen
Dichlorophen.svg
Dichlorophen molecule ball.png
Clinical data
AHFS/Drugs.com International Drug Names
ATC code
Identifiers
  • 4-Chloro-2-[(5-chloro-2-hydroxyphenyl)methyl]phenol
CAS Number
PubChem CID
ChemSpider
UNII
KEGG
ChEMBL
CompTox Dashboard (EPA)
ECHA InfoCard 100.002.335 OOjs UI icon edit-ltr-progressive.svg
Chemical and physical data
Formula C13H10Cl2O2
Molar mass 269.12 g·mol−1
3D model (JSmol)
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)
  • C1=CC(=C(C=C1Cl)CC2=C(C=CC(=C2)Cl)O)O
  • 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 X mark.svgN
  • Key:MDNWOSOZYLHTCG-UHFFFAOYSA-N X mark.svgN
 X mark.svgNYes check.svgY  (what is this?)    (verify)

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]

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References

  1. Lide DR (1998). Handbook of Chemistry and Physics (87 ed.). Boca Raton, Florida: CRC Press. pp. 8–118. ISBN   0-8493-0594-2.
  2. Milne, G.W.A. (Ed.). (2005). Gardner's commercially important chemicals: Synonyms, trade names, and properties. Hoboken, N.J.: Wiley-Interscience. Google Books
  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
  4. 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.