Jump to content
 







Main menu
   


Navigation  



Main page
Contents
Current events
Random article
About Wikipedia
Contact us
Donate
 




Contribute  



Help
Learn to edit
Community portal
Recent changes
Upload file
 








Search  

































Create account

Log in
 









Create account
 Log in
 




Pages for logged out editors learn more  



Contributions
Talk
 



















Contents

   



(Top)
 


1 References  














Amidol






تۆرکجه
Čeština
فارسی
Հայերեն
Ido
Polski
Português
Русский
Slovenčina
Српски / srpski
Srpskohrvatski / српскохрватски
 

Edit links
 









Article
Talk
 

















Read
Edit
View history
 








Tools
   


Actions  



Read
Edit
View history
 




General  



What links here
Related changes
Upload file
Special pages
Permanent link
Page information
Cite this page
Get shortened URL
Download QR code
Wikidata item
 




Print/export  



Download as PDF
Printable version
 




In other projects  



Wikimedia Commons
 
















Appearance
   

 






From Wikipedia, the free encyclopedia
 


Amidol[1]
Names
Preferred IUPAC name

2,4-Diaminophenol

Identifiers

CAS Number

  • 137-09-7 (dihydrochloride) ☒N
  • 3D model (JSmol)

  • Interactive image
  • ChEMBL
    ChemSpider
    ECHA InfoCard 100.002.237 Edit this at Wikidata
    EC Number
    • 202-459-4

    PubChem CID

    UNII

    CompTox Dashboard (EPA)

    • InChI=1S/C6H8N2O/c7-4-1-2-6(9)5(8)3-4/h1-3,9H,7-8H2 checkY

      Key: XIWMTQIUUWJNRP-UHFFFAOYSA-N checkY

    • InChI=1/C6H8N2O/c7-4-1-2-6(9)5(8)3-4/h1-3,9H,7-8H2

      Key: XIWMTQIUUWJNRP-UHFFFAOYAD

    • NC1=CC(N)=C(O)C=C1

    • Oc1ccc(N)cc1N

    Properties

    Chemical formula

    C6H8N2O
    Molar mass 124.14 g/mol
    Appearance Colorless solid
    Melting point 78 to 80 °C (172 to 176 °F; 351 to 353 K)

    Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

    ☒N verify (what is checkY☒N ?)

    Infobox references

    Amidol is a colorless crystalline compound with the molecular structure C6H3(NH2)2OH. It is a dihydrogen chloride salt and is used as a photographic developer. It was introduced as a developing agent for photographic papers in 1892. It is unusual amongst developing agents as it works most effectively in slightly acid conditions rather than the strongly alkaline conditions required for most other developers. As amidol ages it changes color to a dark red-brown. Developing dishes and equipment used to prepare amidol solutions are also frequently stained brown, a stain that is very persistent.

    Prints developed in amidol are typically a very warm brown-black color, but overdevelopment can quickly lead to chemical fogging.

    Amidol's color change upon oxidation is used to advantage as a convenient colorimetric method for measuring the dissolved oxygen concentration in water supplies, rivers, etc.[2]

    References

    [edit]
    1. ^ Merck Index, 11th Edition, 2961.
  • ^ Westfall and Ellis (1848). "Determination of Water Quality". U.S. Govt. Printing Office. p. 21.

  • Retrieved from "https://en.wikipedia.org/w/index.php?title=Amidol&oldid=1177071109"

    Categories: 
    Photographic chemicals
    Anilines
    Phenols
    Hidden categories: 
    Chemical articles with multiple compound IDs
    Multiple chemicals in an infobox that need indexing
    Chemical articles with multiple CAS registry numbers
    Articles without KEGG source
    Articles with changed CASNo identifier
    ECHA InfoCard ID from Wikidata
    Articles containing unverified chemical infoboxes
    Chembox image size set
    Articles with short description
    Short description matches Wikidata
     



    This page was last edited on 25 September 2023, at 19:37 (UTC).

    Text is available under the Creative Commons Attribution-ShareAlike License 4.0; additional terms may apply. By using this site, you agree to the Terms of Use and Privacy Policy. Wikipedia® is a registered trademark of the Wikimedia Foundation, Inc., a non-profit organization.



    Privacy policy

    About Wikipedia

    Disclaimers

    Contact Wikipedia

    Code of Conduct

    Developers

    Statistics

    Cookie statement

    Mobile view



    Wikimedia Foundation
    Powered by MediaWiki