1,2-Dimorpholinoethane

Chemical compound From Wikipedia, the free encyclopedia

1,2-Dimorpholinoethane is an organic chemical and specifically a nitrogen-oxygen heterocyclic compound. At room temperature it is a solid with a melting point of 75 °C.[2] It has two tertiary amines in the same molecule meaning it is ideal for use as a polyurethane catalyst.[3] It has the CAS Registry Number 1723-94-0 and is TSCA and REACH registered and on EINECS with the number 217-026-5.[4] The IUPAC name is 4-(2-morpholin-4-ylethyl)morpholine and the chemical formula C10H20N2O2.[5]

Quick facts Names, Identifiers ...
1,2-Dimorpholinoethane
Names
Preferred IUPAC name
4,4′-(Ethane-1,2-diyl)dimorpholine
Identifiers
3D model (JSmol)
ChEMBL
ChemSpider
EC Number
  • 217-026-5
UNII
  • InChI=1S/C10H20N2O2/c1(11-3-7-13-8-4-11)2-12-5-9-14-10-6-12/h1-10H2
    Key: QRQKCMFVJWNKQI-UHFFFAOYSA-N
  • C1COCCN1CCN2CCOCC2
Properties
C10H20N2O2
Molar mass 200.282 g·mol−1
Hazards
GHS labelling:[1]
GHS05: CorrosiveGHS07: Exclamation mark
Danger
H315, H317, H318, H319, H335
P261, P264, P264+P265, P271, P272, P280, P302+P352, P304+P340, P305+P351+P338, P305+P354+P338, P317, P319, P321, P332+P317, P333+P313, P337+P317, P362+P364, P403+P233, P405, P501
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Synonyms

Section reference.[6]

  • 4,4'-Ethylenedimorpholine
  • 4,4'-(Ethane-1,2-diyl)bismorpholine
  • Morpholine, 4,4'-(1,2-ethanediyl)bis-
  • 1,2-Di-N-morpholinylethane
  • Morpholine,4,4'-(1,2-ethanediyl)bis-
  • Morpholine, 4,4'-ethylenedi-

Uses and synthesis

As the molecule has two tertiary nitrogen atoms in the molecule, the substance finds use as a catalyst for polyurethane[7] including PU foams.[8][9][10][11][12]

1,2-Dimorpholinoethane has been used to make transition metal complexes. As there are two nitrogen atoms in the molecule it acts as a bidentate ligand in these complexes.[13] These complexes have then be used in antibacterial applications.[14]

Toxicity

The toxicity of the compound and tertiary amines in general has been studied and published.[15]

References

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