1,2-Dimorpholinoethane

Dimorpholinoethane.svg 200px 4,4′-(Ethane-1,2-diyl)dimorpholine 1723-94-0 correct CAS 3408516 65720 217-026-5 72888 FX7MP8BZX9 1S/C10H20N2O2/c1(11-3-7-13-8-4-11)2-12-5-9-14-10-6-12/h1-10H2 QRQKCMFVJWNKQI-UHFFFAOYSA-N C1COCCN1CCN2CCOCC2 10 20 2 2 1,2-Dimorpholinoethane https://pubchem.ncbi.nlm.nih.gov/compound/72888#section=Safety-and-Hazards pubchem.ncbi.nlm.nih.gov en 05 07 Danger 315 317 318 319 335 261 264 264+265 271 272 280 302+352 304+340 305+351+338 305+354+338 317 319 321 332+317 333+313 337+317 362+364 403+233 405 501 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.CAS Common Chemistry https://commonchemistry.cas.org/detail?cas_rn=1723-94-0 2023-06-23 commonchemistry.cas.org It has two tertiary amines in the same molecule meaning it is ideal for use as a polyurethane catalyst.1,2-Dimorpholinoethane C10H20N2O2 ChemSpider http://www.chemspider.com/Chemical-Structure.65720.html 2023-06-23 www.chemspider.com It has the CAS Registry Number 1723-94-0 and is TSCA and REACH registered and on EINECS with the number 217-026-5.Substance Information - ECHA https://echa.europa.eu/substance-information/-/substanceinfo/100.015.478 2023-06-23 echa.europa.eu en-GB The IUPAC name is 4-(2-morpholin-4-ylethyl)morpholine and the chemical formula C10H20N2O2.4,4'-(ethane-1,2-diyl)bismorpholine CAS#: 1723-94-0 https://www.chemicalbook.com/ProductChemicalPropertiesCB8925275_EN.htm 2023-06-23 www.chemicalbook.com en Synonyms Section reference.PubChem 1,2-Dimorpholinoethane https://pubchem.ncbi.nlm.nih.gov/compound/72888 2023-06-23 pubchem.ncbi.nlm.nih.gov en 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 polyurethaneVan Maris Roger Tamano Yutaka Yoshimura Hiroyuki Gay Kenneth M. July 2005 Polyurethane Catalysis by Tertiary Amines http://journals.sagepub.com/doi/10.1177/0021955X05055113 Journal of Cellular Plastics en 41 4 305–322 10.1177/0021955X05055113 98546778 0021-955X subscription including PU foams.Bacaloglu R. Cotarcâ L. Marcu N. Tölgyi St 1988 Kinetics and mechanism of isocyanate reactions. II. Reactions of Aryl Isocyanates with Alcohols in the presence ob tertiary amines https://onlinelibrary.wiley.com/doi/10.1002/prac.19883300406 Journal für Praktische Chemie en 330 4 530–540 10.1002/prac.19883300406 subscription 10.1002/14356007.a21_665.pub2 Polyurethanes 2005 Adam Norbert Avar Geza Blankenheim Herbert Friederichs Wolfgang Giersig Manfred Weigand Eckehard Halfmann Michael Wittbecker Friedrich-Wilhelm Larimer Donald-Richard Maier Udo Meyer-Ahrens Sven Noble Karl-Ludwig Wussow Hans-Georg 978-3-527-30673-2 Jeffcat Amine Catalysts for the Polyurethane Industry 2006 http://www.huntsman.com/performance_products/Media/JEFFCAT_Catalyst_Trifold_bulletin.pdf 2007-10-23 https://web.archive.org/web/20071129082418/http://www.huntsman.com/performance_products/Media/JEFFCAT_Catalyst_Trifold_bulletin.pdf 2007-11-29Muuronen Mikko Deglmann Peter Tomović Željko 2019-06-21 Design Principles for Rational Polyurethane Catalyst Development https://pubs.acs.org/doi/10.1021/acs.joc.9b01319 The Journal of Organic Chemistry en 84 12 8202–8209 10.1021/acs.joc.9b01319 31125228 164217639 0022-3263 subscription Marsella John A. February 1987 Homogeneously catalyzed synthesis of .beta.-amino alcohols and vicinal diamines from ethylene glycol and 1,2-propanediol https://pubs.acs.org/doi/abs/10.1021/jo00379a035 The Journal of Organic Chemistry en 52 3 467–468 10.1021/jo00379a035 0022-3263 subscription 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.Mazhar-Ul-Haque Sakhawat Hussain M. Ahmed Jamil 1992-02-01 Tetrahedral complexes of 1,2-dimorpholinoethane and 1,3-dimorpholinopropane: Crystal and molecular structure of dichloro(1,2-dimorpholinoethane)cobalt(II) https://doi.org/10.1007/BF01161361 Journal of Crystallographic and Spectroscopic Research en 22 1 37–41 10.1007/BF01161361 1992JCCry..22...37M 98169856 1572-8854 subscription These complexes have then be used in antibacterial applications.Goudarziafshar Hamid Rezaeivala Majid Khosravi Fayezeh Abbasityula Yunes Yousefi Somaieh Özbek Neslihan Eigner Václav Dušek Michal 2015-01-01 Synthesis, characterization and crystal structures of new Zinc(II) and Nickel(II) complexes containing morpholine moiety and their antibacterial studies https://doi.org/10.1007/s13738-014-0462-2 Journal of the Iranian Chemical Society en 12 1 113–119 10.1007/s13738-014-0462-2 94843521 1735-2428 subscription Toxicity The toxicity of the compound and tertiary amines in general has been studied and published.Albrecht William N Stephenson Richard L 1988 Health hazards of tertiary amine catalysts Scandinavian Journal of Work, Environment & Health 14 4 209–219 10.5271/sjweh.1930 40965565 3051334 7451672 0355-3140 free References Category:Catalysis Category:Heterocyclic compounds with 2 rings Category:Tertiary amines Category:4-Morpholinyl compounds