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 Applications  





2 References  














Diethylhydroxylamine






تۆرکجه
Deutsch
فارسی
Français
Русский
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
 


Diethylhydroxylamine
Skeletal formula of diethylhydroxylamine
Ball-and-stick model of the diethylhydroxylamine molecule
Names
Preferred IUPAC name

N-Ethyl-N-hydroxyethanamine

Identifiers

CAS Number

3D model (JSmol)

Beilstein Reference

1731349
ChemSpider
ECHA InfoCard 100.020.960 Edit this at Wikidata
EC Number
  • 223-055-4
MeSH N,N-diethylhydroxylamine

PubChem CID

RTECS number
  • NC3500000
UNII
UN number 1993

CompTox Dashboard (EPA)

  • InChI=1S/C4H11NO/c1-3-5(6)4-2/h6H,3-4H2,1-2H3 checkY

    Key: FVCOIAYSJZGECG-UHFFFAOYSA-N checkY

  • CCN(O)CC

Properties

Chemical formula

C4H11NO
Molar mass 89.138 g·mol−1
Appearance Colorless liquid
Odor Ammoniacal
Density 867 mg mL−1
Melting point −26 to −25 °C (−15 to −13 °F; 247 to 248 K)
Boiling point 127.6 °C; 261.6 °F; 400.7 K

Solubility in water

Miscible
Vapor pressure 500 Pa (at 0 °C)
Acidity (pKa) 5.67 (est) [1]
Thermochemistry

Heat capacity (C)

370.8 J K−1 mol−1

Std enthalpy of
formation
fH298)

−175.47–−174.03 kJ mol−1

Std enthalpy of
combustion
cH298)

−2.97201–−2.97069 MJ mol−1
Hazards
GHS labelling:

Pictograms

GHS02: Flammable GHS07: Exclamation mark

Signal word

Warning

Hazard statements

H226, H312, H315, H319, H332

Precautionary statements

P280, P305+P351+P338
Explosive limits 1.9–10%
Lethal dose or concentration (LD, LC):

LD50 (median dose)

  • 1.3 g kg−1 (dermal, rabbit)
  • 2.19 g kg−1 (oral, rat)
  • Related compounds

    Related alkanols

  • Dimethylethanolamine
  • Diethylethanolamine
  • Diethanolamine
  • N,N-Diisopropylaminoethanol
  • Methyl diethanolamine
  • Triethanolamine
  • Bis-tris methane
  • Meglumine
  • Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

    checkY verify (what is checkY☒N ?)

    Infobox references

    Diethylhydroxylamine (DEHA) is an organic compound with the formula (C2H5)2NOH. Strictly, this is N,N-diethylhydroxylamine. It has an isomer, N,O-diethylhydroxylamine with the formula EtNHOEt. Pure N,N-diethylhydroxylamine is a colorless liquid, although it is usually encountered as a colourless-to-yellow solution in water with an amine-like odor.

    DEHA can be synthesised from a reaction between triethylamine and a peroxide.

    Applications[edit]

    DEHA is largely used as an oxygen scavengerinwater treatment.

    It is a volatile oxygen scavenger[2][3] and reacts in a ratio of 2.8/1 DEHA/O2. It is employed in high pressure (>70 bar) boiler systems due to a very low rate of reaction at low temperatures and pressures. Due to its volatility, it acts as an oxygen scavenger throughout the entire boiler system due to steam carryover.

    DEHA also reacts with ferrous metals to form a passivized film of magnetite throughout the boiler system. The reduction of toxic heavy metals, such as hexavalent chromium to their more environmentally-friendly counterparts like trivalent chromium, is also performed using aqueous solutions containing DEHA.

    Several other applications include its use as:

    1. Polymerisation inhibitor
    2. Color stabilizer (photographics)
    3. Corrosion inhibitor
    4. Discoloration inhibitor (phenolics)
    5. Antiozonant
    6. Radical scavenger[4]

    References[edit]

    1. ^ Hilal SH et al; pp. 291-353 in Quantitative Treatments of Solute/Solvent Interactions: Theoretical and Computational Chemistry Vol. 1 NY, NY: Elsevier (1994). SPARC (Software Process Automation Reaction Chemistry) Available from, as of Dec 7, 2007: http://ibmlc2.chem.uga.edu/sparc/
  • ^ Cáceres, T.; Lissi, E. A.; Sanhueza, E. (November 1978). "Autooxidation of diethyl hydroxylamine". International Journal of Chemical Kinetics. 10 (11): 1167–1182. doi:10.1002/kin.550101107.
  • ^ Shaffer, Dean; Heicklen, Julian (August 1986). "Oxidation of diethylhydroxylamine in water solution at 25-80.degree". The Journal of Physical Chemistry. 90 (18): 4408–4413. doi:10.1021/j100409a039.
  • ^ Abuin, E.; Encina, M. V.; Diaz, S.; Lissi, E. A. (July 1978). "On the reactivity of diethyl hydroxyl amine toward free radicals". International Journal of Chemical Kinetics. 10 (7): 677–686. doi:10.1002/kin.550100704.

  • Retrieved from "https://en.wikipedia.org/w/index.php?title=Diethylhydroxylamine&oldid=1221501845"

    Categories: 
    Hydroxylamines
    Corrosion inhibitors
    Hidden categories: 
    Articles without InChI source
    Articles without EBI source
    Articles without KEGG source
    ECHA InfoCard ID from Wikidata
    Chembox having GHS data
    Articles containing unverified chemical infoboxes
    Chembox image size set
    Articles with short description
    Short description matches Wikidata
     



    This page was last edited on 30 April 2024, at 09:26 (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