Triethylenediamine

Triethylenediamine Basic information
Product Name:Triethylenediamine
Synonyms:Bicyclo(2,2,2)-1,4-diazaoctane;Dabco(rg~TEDA~Triethylenediamine;TRIETHLENE DIAMINE;1,4-DIAZABICYCLO(2.2.2)OCTAN;1,4-Diazabicyclo(2.2.2)octane, 97+%;1,4-diazabicyclo[2.2.2]octane solution;teda, dabco;TRIETHYLENEDIAMINE=1,4-DIAZABICYCLO(2,2,2)OCTANE
CAS:280-57-9
MF:C6H12N2
MW:112.17
EINECS:205-999-9
Product Categories:Polyamines;API intermediates;Biochemistry;Reagents for Oligosaccharide Synthesis;pharmacetical;280-57-9
Mol File:280-57-9.mol
Triethylenediamine Structure
Triethylenediamine Chemical Properties
Melting point 156-159 °C(lit.)
Boiling point 174 °C
density 1.02 g/mL
vapor pressure 2.9 mm Hg ( 50 °C)
refractive index n20/D 1.4634(lit.)
Fp 198 °F
storage temp. Store below +30°C.
solubility 400g/l
form Hygroscopic Crystals
pka3.0, 8.7(at 25℃)
color White to pale yellow
Water Solubility 46 g/100 mL (26 ºC)
Sensitive Hygroscopic
Merck 14,9669
BRN 103618
Stability:Stable, but very hygroscopic. Incompatible with strong oxidizing agents, strong acids. Highly flammable.
LogP-0.49 at 20℃
CAS DataBase Reference280-57-9(CAS DataBase Reference)
NIST Chemistry ReferenceTriethylenediamine(280-57-9)
EPA Substance Registry System1,4-Diazabicyclo[2.2.2]octane (280-57-9)
Safety Information
Hazard Codes Xn,F
Risk Statements 22-36/37/38-52/53-41-36/38-11
Safety Statements 26-60-37/39-3-16-36/37-61
RIDADR UN 1325 4.1/PG 2
WGK Germany 1
RTECS HM0354200
3
Autoignition Temperature350 °C
TSCA Yes
HazardClass 8
PackingGroup III
HS Code 29335920
Hazardous Substances Data280-57-9(Hazardous Substances Data)
ToxicityLD50 orally in Rabbit: 700 mg/kg
MSDS Information
ProviderLanguage
1,4-Diazabicyclo[2.2.2]octane English
SigmaAldrich English
ACROS English
ALFA English
Triethylenediamine Usage And Synthesis
Chemical PropertiesTriethylenediamine also known as DABCO or TEDA, is a highly symmetrical molecule with a cage structure. The colorless extremely hygroscopic crystals is a highly nucleophilic tertiary amine base, which is used as a catalyst and reagent in polymerization and organic synthesis.
Uses1,4-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.
UsesAn anti-fade reagent shown to scavenge free-radicals due to flurochrome excitation.
DefinitionChEBI: Triethylenediamine is an organic heterobicylic compound that is piperazine with an ethane-1,2-diyl group forming a bridge between N1 and N4. It is typically used as a catalyst in polymerization reactions. It has a role as a catalyst, a reagent and an antioxidant. It is a bridged compound, a tertiary amino compound, a saturated organic heterobicyclic parent and a diamine.
PreparationTriethylenediamine can be produced from ethylenediamine or ethanolamine, diethanolamine, or diethylenetriamine with a variety of different catalysts.
ReactionsTriethylenediamine reacts virtually quantitatively with bromine to give a 1/1 adduct. With alkyl halides it forms quaternary salts, even in nonpolar solvents. Apart from its highly nucleophilic nature, triethylenediamine exhibits catalytic activity in base-catalyzed reactions.
General DescriptionDabco?33-LV (Db) is a gelling catalyst and a bidentate ligand that forms a self-assembled monolayer (SAM) on a variety of substrates. It functionalizes the surface and immobilizes the surface atoms.
HazardSkin irritant.
Flammability and ExplosibilityFlammable
Purification MethodsDABCO crystallises from 95% EtOH, pet ether or MeOH/diethyl ether (1:1). Dry it under vacuum over CaCl2 and BaO. It can be sublimed in vacuo, and readily at room temperature. It has also been purified by removal of water during azeotropic distillation of a *benzene solution. It is then recrystallised twice from anhydrous diethyl ether under argon, and stored under argon [Blackstock et al. J Org Chem 52 1451 1987]. [Beilstein 23/3 V 487.]
vinylamine (1,4-Diazabicyclo[2.2.2]octane)copper(I)chloride complex 1-CHLOROMETHYL-4-FLUORO-1,4-DIAZONIABICYCLO[2.2.2]OCTANE BIS(TRIFLUOROMETHANESULFONATE) (1R,4R)-1-Hydroxymethyl-5,7-dimethyl-4-phenylmethyl-2,3-dithia-5,7-diazabicyclo[2.2.2]octane-6,8-dione TRIETHYLENE DIAMINE COBALTINITRATE 1,4-Diazabicyclo[2.2.2]octane-2-carboxylic acid methyl ester,METHYL 1,4-DIAZABICYCLO[2.2.2]OCTANE-2-CARBOXYLATE SALOR-INT L124389-1EA AURORA 15199 SALOR-INT L123951-1EA TRIETHYLENEDIAMINE, 1,4-BUTANEDIOL 2,3-DITHIA-5,7-DIAZABICYCLO[2.2.2]OCTANE-6,8-DIONE 1,4-Diazabicyclo[2.2.2]octane-2,3-dicarboxylic acid dimethyl ester SALOR-INT L146706-1EA 1,1'-(DECANE-1,10-DIYL)BIS[4-AZA-1-AZONIABICYCLO[2.2.2]OCTANE] DIBROMIDE 1,4-diazabicyclo(2.2.2)octane N,N'-distearyldiammonium 1,4-DIAZABICYCLO [2.2.2] OCTANE, [2,3-14C] 2,5-Dimethyl-1,4-diazabicyclo[2.2.2]octane (3-OXO-1,4-DIAZA-BICYCLO[2.2.2]OCT-2-YL)-ACETIC ACID METHYL ESTER

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