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Tris(2-aminoethyl)amine, 97%, Thermo Scientific Chemicals
Catalog number: B21789.22
100 g, Each
Thermo Scientific Chemicals
Tris(2-aminoethyl)amine, 97%, Thermo Scientific Chemicals
Catalog number: B21789.22
100 g, Each
Quantity
Catalog number: B21789.22
also known as B21789-22
Price (USD)
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172.65 203.00 Save 30.35 (14%)
Ends: 15-Oct-2024
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Chemical Identifiers
CAS
4097-89-6
IUPAC Name
tris(2-aminoethyl)amine
Molecular Formula
C6H18N4
InChI Key
MBYLVOKEDDQJDY-UHFFFAOYSA-N
SMILES
NCCN(CCN)CCN
Specifications
Specification SheetIdentification (FTIR)
Conforms
Appearance (Color)
Clear colorless to yellow
Refractive Index
1.4945 - 1.4995 @ 20?C
Form
Liquid
Assay (GC)
≥96.0%
Description
Tris(2-aminoethyl)amine is a tetradentate chelating ligand and forms stable complexes with transition metals. It is also used as a carbon dioxide absorbent. Further, it acts as a reagent for cleavage of the fluorenylmethyloxycarbonyl (Fmoc) group in peptide synthesis. It reacts with aryl isocyanates and isothiocyanates to give tris-urea and -thiourea derivatives.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
Tris(2-aminoethyl)amine is a tetradentate chelating ligand and forms stable complexes with transition metals. It is also used as a carbon dioxide absorbent. Further, it acts as a reagent for cleavage of the fluorenylmethyloxycarbonyl (Fmoc) group in peptide synthesis. It reacts with aryl isocyanates and isothiocyanates to give tris-urea and -thiourea derivatives.
Solubility
Miscible with water.
Notes
Air sensitive and hygroscopic. Store in a cool place. Incompatible with strong acids and strong oxidizing agents.
Tris(2-aminoethyl)amine is a tetradentate chelating ligand and forms stable complexes with transition metals. It is also used as a carbon dioxide absorbent. Further, it acts as a reagent for cleavage of the fluorenylmethyloxycarbonyl (Fmoc) group in peptide synthesis. It reacts with aryl isocyanates and isothiocyanates to give tris-urea and -thiourea derivatives.
Solubility
Miscible with water.
Notes
Air sensitive and hygroscopic. Store in a cool place. Incompatible with strong acids and strong oxidizing agents.
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