Difference between revisions of "Ortho-phenyl phenol"

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== Description ==
 
== Description ==
  
A [http://cameo.mfa.org/materials/fullrecord.asp?name=fungicide fungicide] and [http://cameo.mfa.org/materials/fullrecord.asp?name=bactericide bactericide]. Ortho-phenyl phenol (OPP) inhibits the growth of [http://cameo.mfa.org/materials/fullrecord.asp?name=fungus fungi] and bacteria. It is effective at concentrations as low as 0.05% by weight. OPP is an ingredient in [http://cameo.mfa.org/materials/fullrecord.asp?name=Lysol%C2%AE Lysol®] and has been used as a fungicides in [http://cameo.mfa.org/materials/fullrecord.asp?name=starch starch], [http://cameo.mfa.org/materials/fullrecord.asp?name=glue glue], and [http://cameo.mfa.org/materials/fullrecord.asp?name=polyvinyl%20acetate polyvinyl acetate] emulsions. Dilute solutions have also been used for removing [http://cameo.mfa.org/materials/fullrecord.asp?name=lichen lichens] from [http://cameo.mfa.org/materials/fullrecord.asp?name=granite granite]. OPPNa, the sodium salt of ortho-phenyl phenol, is more soluble.
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A [[fungicide|fungicide]] and [[bactericide|bactericide]]. Ortho-phenyl phenol (OPP) inhibits the growth of [[fungus|fungi]] and bacteria. It is effective at concentrations as low as 0.05% by weight. OPP is an ingredient in [[Lysol|Lysol®]] and has been used as a fungicides in [[starch|starch]], [[glue|glue]], and [[polyvinyl%20acetate|polyvinyl acetate]] emulsions. Dilute solutions have also been used for removing [[lichen|lichens]] from [[granite|granite]]. OPPNa, the sodium salt of ortho-phenyl phenol, is more soluble.
  
 
== Synonyms and Related Terms ==
 
== Synonyms and Related Terms ==
  
 
phenyl phenol; orthophenyl phenol; OPP; 2-phenylphenol; 2-biphenylol; 2-hydroxybiphenyl; Dowicide 1; Dowicide 1 [Dow Chemical]; Topane S [ICI]; Lysol® [Sterling]; Dowicide A (OPPNa) [Dow Chemical]; Topane WS (OPPNa) [ICI]; Mystox WFA (OPPNa) [Catomance]
 
phenyl phenol; orthophenyl phenol; OPP; 2-phenylphenol; 2-biphenylol; 2-hydroxybiphenyl; Dowicide 1; Dowicide 1 [Dow Chemical]; Topane S [ICI]; Lysol® [Sterling]; Dowicide A (OPPNa) [Dow Chemical]; Topane WS (OPPNa) [ICI]; Mystox WFA (OPPNa) [Catomance]
 
 
[[[SliderGallery rightalign|ortho-phenyl phenol.jpg~Chemical structure]]]
 
[[[SliderGallery rightalign|ortho-phenyl phenol.jpg~Chemical structure]]]
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== Risks ==
  
== Other Properties ==
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* Ingestion is toxic, especially to small mammals (e.g., cats) and aquatic organisms. LD50 = 2480 mg/kg 
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* Inhalation and contact may cause irritation and redness.
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*  Combustible.  Flash point = 124 C (255 F) 
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* May discolor textiles, especially silk. 
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* ThermoFisher [https://www.fishersci.com/store/msds?partNumber=AC110581000&productDescription=M-CRESOL%2C+99%25+100GR&vendorId=VN00032119&countryCode=US&language=en SDS]
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== Physical and Chemical Properties ==
  
 
Insoluble in water. Soluble in alcohols, glycols and sodium hydroxide solution..
 
Insoluble in water. Soluble in alcohols, glycols and sodium hydroxide solution..
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|-
 
|-
 
! scope="row"| Melting Point
 
! scope="row"| Melting Point
| 58-60
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| 58-60 C
 
|-
 
|-
 
! scope="row"| Density
 
! scope="row"| Density
| 1.217
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| 1.217 g/ml
 
|-
 
|-
 
! scope="row"| Molecular Weight
 
! scope="row"| Molecular Weight
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|-
 
|-
 
! scope="row"| Boiling Point
 
! scope="row"| Boiling Point
| 286
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| 286 C
 
|}
 
|}
  
== Hazards and Safety ==
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== Resources and Citations ==
 
 
Ingestion is toxic, expecially to small mammals (e.g., cats) and aquatic organisms. LD50 = 2480 mg/kg 
 
 
 
Inhalation and contact may cause irritation and redness. 
 
 
 
Combustible.  Flash point = 124 C (255 F) 
 
 
 
May discolor textiles, especially silk. 
 
 
 
[http://www.cdc.gov/niosh/ipcsneng/neng0669.html International Chemical Safety Card]
 
 
 
== Additional Information ==
 
 
 
J.Haines, S.Kohler "An Evaluation of Ortho-Phenyl Phenol as a Fungicidal Fumigant for Archives and Libraries" JAIC 25:49-55, 1986
 
  
== Sources Checked for Data in Record ==
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* J.Haines, S.Kohler "An Evaluation of Ortho-Phenyl Phenol as a Fungicidal Fumigant for Archives and Libraries" JAIC 25:49-55, 1986
  
 
* 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 14:40, 20 October 2022

Description

A Fungicide and Bactericide. Ortho-phenyl phenol (OPP) inhibits the growth of fungi and bacteria. It is effective at concentrations as low as 0.05% by weight. OPP is an ingredient in Lysol® and has been used as a fungicides in Starch, Glue, and Polyvinyl acetate emulsions. Dilute solutions have also been used for removing lichens from Granite. OPPNa, the sodium salt of ortho-phenyl phenol, is more soluble.

Synonyms and Related Terms

phenyl phenol; orthophenyl phenol; OPP; 2-phenylphenol; 2-biphenylol; 2-hydroxybiphenyl; Dowicide 1; Dowicide 1 [Dow Chemical]; Topane S [ICI]; Lysol® [Sterling]; Dowicide A (OPPNa) [Dow Chemical]; Topane WS (OPPNa) [ICI]; Mystox WFA (OPPNa) [Catomance]

Chemical structure

Ortho-phenyl phenol.jpg

Risks

  • Ingestion is toxic, especially to small mammals (e.g., cats) and aquatic organisms. LD50 = 2480 mg/kg
  • Inhalation and contact may cause irritation and redness.
  • Combustible. Flash point = 124 C (255 F)
  • May discolor textiles, especially silk.
  • ThermoFisher SDS

Physical and Chemical Properties

Insoluble in water. Soluble in alcohols, glycols and sodium hydroxide solution..

Composition C6H5C6H4OH
CAS 90-43-7
Melting Point 58-60 C
Density 1.217 g/ml
Molecular Weight mol. wt. = 170.2
Boiling Point 286 C

Resources and Citations

  • J.Haines, S.Kohler "An Evaluation of Ortho-Phenyl Phenol as a Fungicidal Fumigant for Archives and Libraries" JAIC 25:49-55, 1986
  • Richard S. Lewis, Hawley's Condensed Chemical Dictionary, Van Nostrand Reinhold, New York, 10th ed., 1993
  • Pam Hatchfield, Pollutants in the Museum Environment, Archetype Press, London, 2002
  • Marie Svoboda, Conservation Survey Index, unpublished, 1997
  • Conservation Materials Ltd., Catalog
  • A Glossary of Paper Conservation Terms, Margaret Ellis (ed.), Conservation Center of the Institute of Fine Arts, New York City, 1998

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