Dichlorophen: Difference between revisions
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| density = 1.5 g/cm<sup>3</sup> |
| density = 1.5 g/cm<sup>3</sup> |
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| melting_point = 177.5 |
| melting_point = 177.5 |
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| 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> |
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| solubility = 0.003 g/100 mL<ref name="hand2"> |
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| title = Handbook of Chemistry and Physics |
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| edition = 87 |
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| pages = 8–118 |
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}}</ref> |
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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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| title = Handbook of Chemistry and Physics |
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}}</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== |
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[[LD50]] (oral, mouse) is 3300 mg/kg.<ref name="a">{{Ullmann| |
[[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> |
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==References== |
==References== |
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{{reflist}} |
{{reflist}} |
Revision as of 18:53, 4 December 2020
Clinical data | |
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AHFS/Drugs.com | International Drug Names |
ATC code | |
Identifiers | |
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CAS Number | |
PubChem CID | |
ChemSpider | |
UNII | |
KEGG | |
ChEMBL | |
CompTox Dashboard (EPA) | |
ECHA InfoCard | 100.002.335 |
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) |
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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 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.