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Diethylenetriamine





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Diethylenetriamine (abbreviated Dien or DETA) and also known as 2,2’-Iminodi(ethylamine)[2]) is an organic compound with the formula HN(CH2CH2NH2)2. This colourless hygroscopic liquid is soluble in water and polar organic solvents, but not simple hydrocarbons. Diethylenetriamine is structural analogue of diethylene glycol. Its chemical properties resemble those for ethylene diamine, and it has similar uses. It is a weak base and its aqueous solution is alkaline. DETA is a byproduct of the production of ethylenediamine from ethylene dichloride.[3]

Diethylenetriamine
Skeletal formula of diethylenetriamine
Ball and stick model of diethylenetriamine
Spacefill model of diethylenetriamine
Names
Preferred IUPAC name

N1-(2-Aminoethyl)ethane-1,2-diamine

Other names

N-(2-Aminoethyl)-1,2-ethanediamine; bis(2-Aminoethyl)amine; DETA; 2,2'-Diaminodiethylamine

Identifiers

CAS Number

3D model (JSmol)

Beilstein Reference

605314
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.003.515 Edit this at Wikidata
EC Number
  • 203-865-4

Gmelin Reference

2392
MeSH diethylenetriamine

PubChem CID

RTECS number
  • IE1225000
UNII
UN number 2079

CompTox Dashboard (EPA)

  • InChI=1S/C4H13N3/c5-1-3-7-4-2-6/h7H,1-6H2 checkY

    Key: RPNUMPOLZDHAAY-UHFFFAOYSA-N checkY

  • NCCNCCN

Properties

Chemical formula

C4H13N3
Molar mass 103.169 g·mol−1
Appearance Colourless liquid
Odor Ammoniacal
Density 955 mg mL−1
Melting point −39.00 °C; −38.20 °F; 234.15 K
Boiling point 204.1 °C; 399.3 °F; 477.2 K

Solubility in water

miscible[1]
log P −1.73
Vapor pressure 10 Pa (at 20 °C)

Refractive index (nD)

1.484
Thermochemistry

Heat capacity (C)

254 J K−1 mol−1 (at 40 °C)

Std enthalpy of
formation
fH298)

−65.7–−64.7 kJ mol−1

Std enthalpy of
combustion
cH298)

−3367.2–−3366.2 kJ mol−1
Hazards
GHS labelling:

Pictograms

GHS05: Corrosive GHS07: Exclamation mark

Signal word

Danger

Hazard statements

H302, H312, H314, H317

Precautionary statements

P280, P305+P351+P338, P310
Flash point 102 °C (216 °F; 375 K)

Autoignition
temperature

358 °C (676 °F; 631 K)
Explosive limits 2–6.7%
NIOSH (US health exposure limits):

PEL (Permissible)

none[1]

REL (Recommended)

TWA 1 ppm (4 mg/m3)[1]

IDLH (Immediate danger)

N.D.[1]
Related compounds

Related amines

  • Trimethylamine
  • N-Nitrosodimethylamine
  • Diethylamine
  • Triethylamine
  • Diisopropylamine
  • Dimethylaminopropylamine
  • N,N-Diisopropylethylamine
  • Triisopropylamine
  • Tris(2-aminoethyl)amine
  • Mechlorethamine
  • HN1 (nitrogen mustard)
  • HN3 (nitrogen mustard)
  • Related compounds

  • Biguanide
  • Dithiobiuret
  • Agmatine
  • 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

    Reactions and uses

    edit

    Diethylenetriamine is a common curing agent for epoxy resins in epoxy adhesives and other thermosets.[4] It is N-alkylated upon reaction with epoxide groups forming crosslinks.

     
    Structure of a triamine-cured epoxy glue. The resin's epoxide groups have all reacted with the hardener. The resulting highly crosslinked material contains many OH groups, which confer adhesive properties.

    Incoordination chemistry, it serves as a tridentate ligand forming complexes such as Co(dien)(NO2)3.[5]

    Like some related amines, it is used in oil industry for the extraction of acid gas.

    Like ethylenediamine, DETA can also be used to sensitize nitromethane, making a liquid explosive compound similar to PLX. This compound is cap sensitive with an explosive velocity of around 6200 m/s and is discussed in patent #3,713,915. Mixed with unsymmetrical dimethylhydrazine it was used as Hydyne, a propellent for liquid-fuel rockets.

    DETA has been evaluated for use in the Countermine System under development by the U.S. Office of Naval Research, where it would be used to ignite and consume the explosive fill of land mines in beach and surf zones.[6]

    See also

    edit

    References

    edit
    1. ^ a b c d NIOSH Pocket Guide to Chemical Hazards. "#0211". National Institute for Occupational Safety and Health (NIOSH).
  • ^ "Health Council of the Netherlands: Committee on Updating of Occupational Exposure Limits. 2,2'-Iminodi(ethylamine); Health-based Reassessment of Administrative Occupational Exposure Limits" (PDF). 2005.
  • ^ Eller, K.; Henkes, E.; Rossbacher, R.; Höke, H. "Amines, Aliphatic". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a02_001. ISBN 978-3527306732.
  • ^ Brydson, J. A. (1999). "Epoxide Resins". In J. A. Brydson (ed.). Plastics Materials (Seventh ed.). Oxford: Butterworth-Heinemann. pp. 744–777. doi:10.1016/B978-075064132-6/50067-X. ISBN 9780750641326.
  • ^ Crayton, P. H.; Zitomer, F.; Lambert, J. (1963). "Inner Complexes of Cobalt(III) with Diethylenetriamine". In Kleinberg, J. (ed.). Inorganic Syntheses. Vol. 7. pp. 207–213. doi:10.1002/9780470132388.ch56. ISBN 9780470132388.
  • ^ Hill, Brandon (January 25, 2007). "U.S. Navy Announces "Venom Penetrator" Countermine Projectile". DailyTech. Archived from the original on October 4, 2014. Retrieved July 16, 2013.
  • edit

    Retrieved from "https://en.wikipedia.org/w/index.php?title=Diethylenetriamine&oldid=1093987918"
     



    Last edited on 20 June 2022, at 02:49  





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    This page was last edited on 20 June 2022, at 02:49 (UTC).

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