- Product Name
- CasNo
- MF
- MW
- Content
- Appearance
- Packing
- Apply
- Triethylene Diamine(TEDA)
- 280-57-9
- C6H12N2
- 112.175
- white crystalline powder
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Triethylenediamine is white crystalline powder, while it's Molecular Formula is C6H12N2. 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.
The CAS number of Triethylenediamine is 280-57-9.
More information of Triethylenediamine 280-57-9 are:
Synonyms |
Thancat TD 33A;Toral SM 2;Toyocat L 33;Toyocat TEDA L 33;Triethylenediamine;1,4-Ethylenepiperazine;33LV;A 33;AE 33;Activator 105E;Bicyclo[2.2.2]-1,4-diazaoctane;D 33LV;DABCO Crystal;Dabco;Dabco 33LV;Dabco 3LV;Dabco Crystalline;Dabco L 1202;Dabco S 25;Jeffcat TD 100;Kaolizer 31;L 33;L 33E;LC 96003;LV 33;Minico L1020;N,N'-endo-Ethylenepiperazine;NSC 56362;Niax A 33;PC CAT TD 33;PC-TD;Polycat 33LV;TD 100;TED;TEDA;Teda L 33;Tegamine 33;Tego Amine;Tegoamin33;Texacat TD 100;Texacat TD 33;Thancat TD 33; |
CAS Number |
280-57-9 |
Molecular Formula |
C6H12N2 |
Molecular Weight |
112.175 |
Density |
1.08 g/cm3 |
Melting Point |
156-159 °C(lit.) |
Boiling Point |
174 °C at 760 mmHg |
Flash Point |
62.2 °C |
HS CODE |
29335920 |
PSA |
6.48000 |
LogP |
-0.50660 |
Pka |
3.0, 8.7(at 25℃) |
Triethylenediamine, also known as DABCO or TEDA, is an organic heterobicylic compound with a highly symmetrical cage structure. It is a colorless, extremely hygroscopic substance that exists as crystals. As a highly nucleophilic tertiary amine base, it is commonly utilized as a catalyst and reagent in polymerization and organic synthesis. Triethylenediamine is characterized by its role as a catalyst, reagent, and antioxidant, and is classified as a bridged compound, a tertiary amino compound, a saturated organic heterobicyclic parent, and a diamine.
InChI:InChI=1/C6H12N2/c1-2-8-5-3-7(1)4-6-8/h1-6H2
Articles related to Triethylenediamine:
Article |
Source |
- |
Shishkin,G.V.,Anisimova,I.L. , (1978) |
CHARACTERIZATION OF TRANSIENT INTERMEDIATES ON LASER FLASH EXCITATION OF CYCLOHEXENONES IN THE PRESENCE OF AMINES |
Dunn, D. A.,Schuster, D. I.,Bonneau, R. , p. 2802 - 2804 (1985) |
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