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1,4-Diazabicyclo[2.2.2]octane

Base Information Edit
  • Chemical Name:1,4-Diazabicyclo[2.2.2]octane
  • CAS No.:280-57-9
  • Deprecated CAS:101484-19-9,150605-01-9,203072-11-1,23790-33-2,88935-43-7,309955-09-7,165724-47-0,903524-95-8,746642-46-6,1357848-51-1,682335-96-2,2260745-52-4,150605-01-9,165724-47-0,203072-11-1,23790-33-2,309955-09-7,746642-46-6,88935-43-7
  • Molecular Formula:C6H12N2
  • Molecular Weight:112.175
  • Hs Code.:29335920
  • European Community (EC) Number:205-999-9
  • NSC Number:56362
  • UNII:X8M57R0JS5
  • DSSTox Substance ID:DTXSID0022016
  • Nikkaji Number:J5.451H
  • Wikipedia:DABCO
  • Wikidata:Q423673
  • Pharos Ligand ID:DLRGNCAASW1Z
  • Metabolomics Workbench ID:130613
  • ChEMBL ID:CHEMBL3183414
  • Mol file:280-57-9.mol
1,4-Diazabicyclo[2.2.2]octane

Synonyms:1,4-diazabicyclo(2.2.2)octane;1,4-diazabicyclo-octane;DABCO;DABCO cpd;triethylenediamine;triethylenediamine diacetate

Suppliers and Price of 1,4-Diazabicyclo[2.2.2]octane
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • TRC
  • 1,4-Diazabicyclo[2.2.2]octane
  • 2.5g
  • $ 110.00
  • TCI Chemical
  • 1,4-Diazabicyclo[2.2.2]octane >98.0%(GC)(T)
  • 500g
  • $ 125.00
  • TCI Chemical
  • 1,4-Diazabicyclo[2.2.2]octane >98.0%(GC)(T)
  • 100g
  • $ 47.00
  • TCI Chemical
  • 1,4-Diazabicyclo[2.2.2]octane >98.0%(GC)(T)
  • 25g
  • $ 21.00
  • SynQuest Laboratories
  • 1,4-Diazabicyclo[2.2.2]octane(DABCO)
  • 500 g
  • $ 36.00
  • SynQuest Laboratories
  • 1,4-Diazabicyclo[2.2.2]octane(DABCO)
  • 100 g
  • $ 21.00
  • SynQuest Laboratories
  • 1,4-Diazabicyclo[2.2.2]octane(DABCO)
  • 1 kg
  • $ 61.00
  • Sigma-Aldrich
  • Dabco? 33-LV
  • 100ml
  • $ 67.70
  • Sigma-Aldrich
  • 1,4-Diazabicyclo[2.2.2]octane ReagentPlus , ≥99%
  • 100g
  • $ 66.20
  • Sigma-Aldrich
  • 1,4-Diazabicyclo[2.2.2]octane for synthesis. CAS 280-57-9, pH (H O, 20 °C) alkaline,Aqueous solution., for synthesis
  • 8034560100
  • $ 58.30
Total 167 raw suppliers
Chemical Property of 1,4-Diazabicyclo[2.2.2]octane Edit
Chemical Property:
  • Appearance/Colour:white crystalline powder 
  • Vapor Pressure:2.9 mm Hg ( 50 °C) 
  • Melting Point:156-159 °C(lit.) 
  • Refractive Index:n20/D 1.4634(lit.)  
  • Boiling Point:174 °C at 760 mmHg 
  • PKA:3.0, 8.7(at 25℃) 
  • Flash Point:62.2 °C 
  • PSA:6.48000 
  • Density:1.08 g/cm3 
  • LogP:-0.50660 
  • Storage Temp.:2-8°C 
  • Sensitive.:Hygroscopic 
  • Solubility.:400g/l 
  • Water Solubility.:46 g/100 mL (26 ºC) 
  • XLogP3:-0.2
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:0
  • Exact Mass:112.100048391
  • Heavy Atom Count:8
  • Complexity:61.5
Purity/Quality:

99% *data from raw suppliers

1,4-Diazabicyclo[2.2.2]octane *data from reagent suppliers

Safty Information:
  • Pictogram(s): HarmfulXn, Flammable
  • Hazard Codes:Xn,F 
  • Statements: 22-36/37/38-52/53-41-36/38-11 
  • Safety Statements: 26-60-37/39-3-16-36/37-61 
MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:
  • Chemical Classes:Nitrogen Compounds -> Amines, Cyclic
  • Canonical SMILES:C1CN2CCN1CC2
  • Recent ClinicalTrials:Long-term Safety and Efficacy Study of Teduglutide in Pediatric Participants With Short Bowel Syndrome (SBS)
  • Uses An anti-fade reagent shown to scavenge free-radicals due to flurochrome excitation. 1,4-Diazabicyclo[2.2.2]octane is used as polyurethane catalyst, Balis-Hillman reaction catalyst complexing ligand and lewis base. It finds use in dye lasers and in mounting samples for fluorescence microscopy and as anti-fade reagent shown to scavenge free radicals due to flurochrome excitation of fluorochromes. Further, it is an oxidation and polymerization catalyst.
Technology Process of 1,4-Diazabicyclo[2.2.2]octane

There total 64 articles about 1,4-Diazabicyclo[2.2.2]octane which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With Rh/Al2O3; hydrogen; In tetrahydrofuran; at 175 ℃; under 37503.8 Torr; Reagent/catalyst; Temperature; Solvent; Sealed tube;
Guidance literature:
With aluminum phosphate molded body; In water; at 380 ℃;
Guidance literature:
With H type zeolite(ZSM-5); In water; at 380 ℃;
Refernces Edit
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