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词条 Dichlorophen
释义

  1. References

{{Drugbox
| Verifiedfields = changed
| Watchedfields = changed
| verifiedrevid = 446639999
| IUPAC_name = 4-Chloro-2-[(5-chloro-2-hydroxyphenyl)methyl]phenol
| image = Dichlorophen.svg
| image2 = Dichlorophen molecule ball.png
| width2 = 200
| alt2 = Ball-and-stick mode of the dichlorophen molecule
| tradename =
| Drugs.com = {{drugs.com|international|dichlorophen}}
| pregnancy_AU =
| pregnancy_US =
| pregnancy_category =
| legal_AU =
| legal_CA =
| legal_UK =
| legal_US =
| legal_status =
| routes_of_administration =
| bioavailability =
| protein_bound =
| metabolism =
| elimination_half-life =
| excretion =
| CAS_number_Ref = {{cascite|correct|??}}
| CAS_number = 97-23-4
| ATC_prefix = P02
| ATC_suffix = DX02
| DrugBank_Ref = {{drugbankcite|correct|drugbank}}
| DrugBank =
| PubChem = 3037
| ChemSpiderID_Ref = {{chemspidercite|changed|chemspider}}
| ChemSpiderID = 2929
| UNII_Ref = {{fdacite|correct|FDA}}
| UNII = T1J0JOU64O
| KEGG_Ref = {{keggcite|correct|kegg}}
| KEGG = C14292
| ChEMBL_Ref = {{ebicite|changed|EBI}}
| ChEMBL = 33845


| C=13 | H=10 | Cl=2 | O=2
| molecular_weight = 269.12 g/mol
| smiles = C1=CC(=C(C=C1Cl)CC2=C(C=CC(=C2)Cl)O)O
| StdInChI_Ref = {{stdinchicite|changed|chemspider}}
| StdInChI = 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
| StdInChIKey_Ref = {{stdinchicite|changed|chemspider}}
| StdInChIKey = MDNWOSOZYLHTCG-UHFFFAOYSA-N
| density = 1.42 g/cm3
| melting_point = 177.5
| solubility = 0.003 g/100 mL[1]


}}Dichlorophen is an anticestodal agent, fungicide, germicide, and antimicrobial agent.[3] It is used in combination with toluene for the removal of parasites such as ascarids, hookworms, and tapeworms from dogs and cats.[4]

References

1. ^{{Citation| last = Lide| first = David R.| author-link =| last2 =| first2 =| author2-link =| publication-date =| date =| year = 1998| title = Handbook of Chemistry and Physics| edition = 87| volume =| series =| publication-place = Boca Raton, Florida| place =| publisher = CRC Press| id =| isbn = 0-8493-0594-2| doi =| oclc =| pages = 8–118| url =| accessdate =}}
2. ^{{Citation| last = Lide| first = David R.| author-link =| last2 =| first2 =| author2-link =| publication-date =| date =| year = 1998| title = Handbook of Chemistry and Physics| edition = 87| volume =| series =| publication-place = Boca Raton, Florida| place =| publisher = CRC Press| id =| isbn = 0-8493-0594-2| doi =| oclc =| pages = 3–174| url =| accessdate =}}
3. ^Milne, G.W.A. (Ed.). (2005). Gardner's commercially important chemicals: Synonyms, trade names, and properties. Hoboken, N.J.: Wiley-Interscience. [https://books.google.com/books?id=oWdc2qcb3QsC&pg=PA201 Google Books]
4. ^{{Citation | title=Code of Federal Regulations | url= http://frwebgate1.access.gpo.gov/cgi-bin/TEXTgate.cgi?WAISdocID=220114194717+2+1+0&WAISaction=retrieve| work= Code of Federal Regulations, Title 21, Volume 6| publisher=U.S. Government Printing Office | date= 2005-04-01| accessdate=2009-05-01}}
{{Anthelmintics}}{{antiinfective-drug-stub}}

4 : Antiparasitic agents|Chloroarenes|Phenols|Veterinary drugs

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