Difference between revisions of "Hexachlorophene"

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2,2'-methylenebis[3,4,6-trichlorphenol]; AT-7; G-11; Bilevon; Dermadex; Exofene; Gamophen; Hexosan; pHisohex; Surgi-Cen; Surofene; Acigena; Almederm; AT17; Fostril; G-11; Germa-Medica; Septisol
 
2,2'-methylenebis[3,4,6-trichlorphenol]; AT-7; G-11; Bilevon; Dermadex; Exofene; Gamophen; Hexosan; pHisohex; Surgi-Cen; Surofene; Acigena; Almederm; AT17; Fostril; G-11; Germa-Medica; Septisol
  
== Other Properties ==
+
== Risks ==
 +
 
 +
* Excessive dosage causes neurotoxicity. 
 +
* Usage regulated in U.S. by FDA in 1972. 
 +
* Cayman Chemical: [https://www.caymanchem.com/msdss/23948m.pdf SDS]
 +
 
 +
== Physical and Chemical Properties ==
  
 
Soluble in alcohol, acetone, ether, chloroform, propylene glycol, olive oil, cottonseed oil, benzene. Insoluble in water.
 
Soluble in alcohol, acetone, ether, chloroform, propylene glycol, olive oil, cottonseed oil, benzene. Insoluble in water.
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! scope="row"| Melting Point
 
! scope="row"| Melting Point
| 164-165
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| 164-165 C
 
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! scope="row"| Molecular Weight
 
! scope="row"| Molecular Weight
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== Hazards and Safety ==
+
== Resources and Citations ==
 
 
Excessive dosage causes neurotoxicity.  Usage regulated in U.S. by FDA in 1972. 
 
 
 
LINK: [http://www.cdc.gov/niosh/ipcsneng/neng0161.html International Chemical Safety Card]
 
 
 
== Authority ==
 
  
 
* Richard S. Lewis, ''Hawley's Condensed Chemical Dictionary'', Van Nostrand Reinhold, New York, 10th ed., 1993
 
* Richard S. Lewis, ''Hawley's Condensed Chemical Dictionary'', Van Nostrand Reinhold, New York, 10th ed., 1993

Latest revision as of 13:33, 31 August 2022

Description

A topical disinfectant formerly used as a major component in disinfectant soaps, such as pHisohex. Hexachlorophene, first patented in 1941, was restricted for use in 1972.

Synonyms and Related Terms

2,2'-methylenebis[3,4,6-trichlorphenol]; AT-7; G-11; Bilevon; Dermadex; Exofene; Gamophen; Hexosan; pHisohex; Surgi-Cen; Surofene; Acigena; Almederm; AT17; Fostril; G-11; Germa-Medica; Septisol

Risks

  • Excessive dosage causes neurotoxicity.
  • Usage regulated in U.S. by FDA in 1972.
  • Cayman Chemical: SDS

Physical and Chemical Properties

Soluble in alcohol, acetone, ether, chloroform, propylene glycol, olive oil, cottonseed oil, benzene. Insoluble in water.

Composition C13H6Cl6O2
CAS 70-30-4
Melting Point 164-165 C
Molecular Weight mol. wt. = 406.92

Resources and Citations

  • Richard S. Lewis, Hawley's Condensed Chemical Dictionary, Van Nostrand Reinhold, New York, 10th ed., 1993
  • Random House, Webster's Encyclopedic Unabridged Dictionary of the English Language, Grammercy Book, New York, 1997
  • The Merck Index, Martha Windholz (ed.), Merck Research Labs, Rahway NJ, 10th edition, 1983 Comment: entry 4716