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Sigma-Aldrich T0886 Triethylamine ≥99% CAS No.: 121-44-8 1 L
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LB.SA.T0886-1L
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Synonym(s): TEA, N,N-Diethylethanamine Linear Formula: (C2H5)3N CAS Number: 121-44-8 Molecular Weight: 101.19 Beilstein: 605283 EC Number: 204-469-4 MDL number: MFCD00009051 UNSPSC Code: 12352116 PubChem Substance ID: 24899917 NACRES: NA.21 Assay: ≥99% Bp: 88.8 °C (lit.) Vapor pressure: 51.75 mmHg ( 20 °C)
| Sigma-Aldrich T0886 Triethylamine ≥99% CAS No.: 121-44-8 |
| Synonym(s): TEA, N,N-Diethylethanamine Linear Formula: (C2H5)3N CAS Number: 121-44-8 Molecular Weight: 101.19 Beilstein: 605283 EC Number: 204-469-4 MDL number: MFCD00009051 UNSPSC Code: 12352116 PubChem Substance ID: 24899917 NACRES: NA.21 Assay: ≥99% Bp: 88.8 °C (lit.) Vapor pressure: 51.75 mmHg ( 20 °C) |
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PROPERTIES
vapor density 3.5 (vs air)
Quality Level 200 vapor pressure 51.75 mmHg ( 20 °C) Assay ≥99% autoignition temp. 593 °F shelf life 3 yr expl. lim. 8 % impurities ≤0.5% water (Karl Fischer) refractive index n20/D 1.401 (lit.) bp 88.8 °C (lit.) mp −115 °C (lit.) density 0.726 g/mL at 25 °C (lit.) functional group amine SMILES string CCN(CC)CC InChI 1S/C6H15N/c1-4-7(5-2)6-3/h4-6H2,1-3H3 InChI key ZMANZCXQSJIPKH-UHFFFAOYSA-N DESCRIPTION Application Triethylamine has been used: - as a hydrogen donor for the polymerization of various monomers[1] - to catalyze silanization[2] - in the synthesis of the Cy3-Alexa647 heterodimer[3] - in the synthesis of methacrylated solubilized decellularized cartilage[4] Biochem/physiol Actions Triethylamine is known to drive polymerization reaction. It acts as a source of carbon and nitrogen for bacterial cultures. Triethylamine is used in pesticides.[5] Triethylamine can serve as an organic solvent.[6] |
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