Diethylhydroxylamine
Appearance
| |||
Names | |||
---|---|---|---|
IUPAC name
N,N-Diethylhydroxylamine[1]
| |||
Other names
N-Ethyl-N-hydroxyethanamine
| |||
Identifiers | |||
3D model (JSmol)
|
|||
1731349 | |||
ChemSpider | |||
ECHA InfoCard | 100.020.960 | ||
EC Number |
| ||
MeSH | N,N-diethylhydroxylamine | ||
PubChem CID
|
|||
RTECS number |
| ||
UNII | |||
UN number | 1993 | ||
CompTox Dashboard (EPA)
|
|||
| |||
| |||
Properties | |||
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 | ||
Miscible | |||
Vapor pressure | 500 Pa (at 0 °C) | ||
Acidity (pKa) | 5.67 (est) [2] | ||
Thermochemistry | |||
Heat capacity (C)
|
370.8 J K−1 mol−1 | ||
Std enthalpy of
formation (ΔfH⦵298) |
−175.47–−174.03 kJ mol−1 | ||
Std enthalpy of
combustion (ΔcH⦵298) |
−2.97201–−2.97069 MJ mol−1 | ||
Hazards | |||
GHS labelling: | |||
Warning | |||
H226, H312, H315, H319, H332 | |||
P280, P305+P351+P338 | |||
Explosive limits | 1.9–10% | ||
Lethal dose or concentration (LD, LC): | |||
LD50 (median dose)
|
| ||
Related compounds | |||
Related alkanols
|
|||
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
|
Diethylhydroxylamine (DEHA) is an organic compound with the formula (C2H5)2NOH. It is a colorless liquid, although it is usually encountered as a solution. It is mainly used as an oxygen scavenger in water treatment.
It is a volatile oxygen scavenger 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.
It has these other uses:
- Polymerization inhibitor
- Color stabilizer (photographics)
- Corrosion inhibitor
- Discoloration inhibitor (phenolics)
References
- ^ "N,N-diethylhydroxylamine - Compound Summary". PubChem Compound. USA: National Center for Biotechnology Information. 27 March 2005. Identification. Retrieved 17 March 2012.
- ^ 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/