Date published: 2025-9-5

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Diethylamine (CAS 109-89-7)

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Alternate Names:
N-Ethylethanamine
CAS Number:
109-89-7
Purity:
≥99%
Molecular Weight:
73.14
Molecular Formula:
C4H11N
Supplemental Information:
This is classified as a Dangerous Good for transport and may be subject to additional shipping charges.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Diethylamine (DEA), recognized by its chemical formula (C2H5)2NH, is classified as an organic base and a weak σ-donor ligand. Its primary function involves serving as a bond-breaking agent in a novel Enzyme-Linked Immunosorbent Assay (ELISA) designed to measure the avidity index (AI) of Immunoglobulin G-anti-pertussis toxin (IgG-anti-PT) antibodies.Physically, diethylamine presents as a clear, colorless liquid that emits an odor reminiscent of ammonia. Its vapors tend to be denser than the surrounding air, and during combustion, it produces toxic oxides of nitrogen.Diethylamine falls under the category of dialkylamines, which are organic compounds featuring a dialkylamine group characterized by two alkyl groups attached to the amino nitrogen. This compound is predominantly liquid, soluble in water, and exhibits strong basic properties, as evidenced by its low pKa value. Additionally, diethylamine can be chemically transformed into N-(trimethylsilyl)diethylamine. Diethylamine is a secondary aliphatic amine with two ethyl substituents on its nitrogen atoms, and it functions as the conjugate base of diethylammonium. Its diverse properties and chemical characteristics make it a valuable component in various scientific applications, including ELISA assays.


Diethylamine (CAS 109-89-7) References

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  3. Diethylamine extraction of proteins and peptides isolated with a mono-phasic solution of phenol and guanidine isothiocyanate.  |  Nolan, RL. and Teller, JK. 2006. J Biochem Biophys Methods. 68: 127-31. PMID: 16750859
  4. Assessment of chronic inhalation non-cancer toxicity for diethylamine.  |  Grant, RL., et al. 2015. Inhal Toxicol. 27: 778-86. PMID: 26671196
  5. Muscle-Type Nicotinic Receptor Blockade by Diethylamine, the Hydrophilic Moiety of Lidocaine.  |  Alberola-Die, A., et al. 2016. Front Mol Neurosci. 9: 12. PMID: 26912995
  6. Supercritical diethylamine facilitated loading of ultrafine Ru particles on few-layer graphene for solvent-free hydrogenation of levulinic acid to γ-valerolactone.  |  Tao, H., et al. 2018. Nanotechnology. 29: 075708. PMID: 29148984
  7. The simplest supramolecular helix.  |  Hanke, F., et al. 2018. Chem Commun (Camb). 54: 6012-6015. PMID: 29796532
  8. Diethylamine fluorescence sensor based on silica hollow sphere photonic crystals.  |  Li, L., et al. 2021. Anal Methods. 13: 2189-2195. PMID: 33899837
  9. Formation of diethylamine thermal ionization mass spectrum on NaAux intermetallide.  |  Knatko, MV. and Lapushkin, MN. 2021. Rapid Commun Mass Spectrom. 35: e9144. PMID: 34125499
  10. Peak shape enhancement using diethylamine in hydrophilic liquid interaction chromatography: Application in simultaneous determination of methionine and paracetamol.  |  Binh, VN., et al. 2021. J Pharm Biomed Anal. 203: 114214. PMID: 34153937
  11. An improved method for detection of urinary diethylamine to monitor disulfiram compliance in alcohol dependent subjects.  |  Jain, R., et al. 2021. Asian J Psychiatr. 64: 102756. PMID: 34311433
  12. Non-adiabatic dynamics of Rydberg-excited diethylamine.  |  Qiu, Z., et al. 2022. Spectrochim Acta A Mol Biomol Spectrosc. 274: 121065. PMID: 35245801
  13. Lysergic acid diethylamine: mutagenic effects in Drosophila.  |  Browning, LS. 1968. Science. 161: 1022-3. PMID: 5671478

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Diethylamine, 5 ml

sc-214887
5 ml
$33.00

Diethylamine, 100 ml

sc-214887A
100 ml
$42.00