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| density = 1.5 g/cm<sup>3</sup>
| density = 1.5 g/cm<sup>3</sup>
| melting_point = 177.5
| melting_point = 177.5
| solubility = 0.003 g/100 mL<ref name="hand2">{{cite book | vauthors = Lide DR | year = 1998 | title = Handbook of Chemistry and Physics | edition = 87 | location = Boca Raton, Florida | publisher = CRC Press | isbn = 0-8493-0594-2 | pages = 8–118 }}</ref>
| solubility = 0.003 g/100 mL<ref name="hand2">
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| year = 1998
| title = Handbook of Chemistry and Physics
| edition = 87
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| place =
| publisher = CRC Press
| id =
| isbn = 0-8493-0594-2
| doi =
| oclc =
| pages = 8–118
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| SolubleOther = 53 g/100 mL in [[ethanol]], 80 g/100 mL in [[acetone]]<ref name="hand">
| SolubleOther = 53 g/100 mL in [[ethanol]], 80 g/100 mL in [[acetone]]<ref name="hand">{{cite book | vauthors = Lide DR | year = 1998 | title = Handbook of Chemistry and Physics | edition = 87 | location = Boca Raton, Florida | publisher = CRC Press | isbn = 0-8493-0594-2 | pages = 3–174 }}</ref>
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| LD50 = 1000 mg/kg (mouse, oral)<ref name="gard"/>
| LD50 = 1000 mg/kg (mouse, oral)<ref name="gard"/>
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==Safety and regulation==
==Safety and regulation==
[[LD50]] (oral, mouse) is 3300 mg/kg.<ref name="a">{{Ullmann| author1=Helmut Fiege | author2=Heinz-Werner Voges | author3=Toshikazu Hamamoto | author4=Sumio Umemura | author5=Tadao Iwata | author6=Hisaya Miki | author7=Yasuhiro Fujita | author8=Hans-Josef Buysch | author9=Dorothea Garbe | author10=Wilfried Paulus | contribution=Phenol Derivatives | year=2007 | doi=10.1002/14356007.a19_313}}</ref>
[[LD50]] (oral, mouse) is 3300 mg/kg.<ref name="a">{{Ullmann| vauthors = Fiege H, Voges HW, Hamamoto T, Umemura S, Iwata T, Miki H, Fujita Y, Buysch HJ, Garbe D, Paulus W | contribution=Phenol Derivatives | year=2007 | doi=10.1002/14356007.a19_313}}</ref>
==References==
==References==
{{reflist}}
{{reflist}}

Revision as of 18:53, 4 December 2020

Dichlorophen
Ball-and-stick mode of the dichlorophen molecule
Clinical data
AHFS/Drugs.comInternational 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 InfoCard100.002.335 Edit this at Wikidata
Chemical and physical data
FormulaC13H10Cl2O2
Molar mass269.12 g·mol−1
3D model (JSmol)
Density1.5 g/cm3 g/cm3
Melting point177.5 °C (351.5 °F)
Solubility in water0.003 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 ☒N
  • Key:MDNWOSOZYLHTCG-UHFFFAOYSA-N ☒N
 ☒NcheckY (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]

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. ISBN 978-3527306732.