Description

2-Diethylaminoethyl hexanoate (CAS No. 10369-83-2) is a high-purity organic compound with the molecular formula C₁₂H₂₅NO₂. This ester derivative of hexanoic acid and diethylaminoethanol is widely utilized in pharmaceutical, agrochemical, and specialty chemical research. The compound features a hexanoate ester group linked to a diethylaminoethyl moiety, offering unique solubility and reactivity properties. Available in >98% purity by GC, this product is supplied as a clear, colorless to pale yellow liquid with a characteristic amine-like odor. Suitable for use as an intermediate in organic synthesis, it is packaged under inert gas to ensure stability and shipped with comprehensive analytical data (GC, NMR, MS). Store in a cool, dry place away from strong oxidizing agents.

Properties

• CAS Number: 10369-83-2
• Complexity: 156
• IUPAC Name: 2-(diethylamino)ethyl hexanoate
• InChI: InChI=1S/C12H25NO2/c1-4-7-8-9-12(14)15-11-10-13(5-2)6-3/h4-11H2,1-3H3
• InChI Key: AEIJVYPRKAWFPN-UHFFFAOYSA-N
• Exact Mass: 215.188529040
• Molecular Formula: C12H25NO2
• Molecular Weight: 215.33
• SMILES: CCCCCC(=O)OCCN(CC)CC
• Topological: 29.5
• Monoisotopic Mass: 215.188529040
• Synonyms: 2-DIETHYLAMINOETHYL HEXANOATE, 10369-83-2, 2-(Diethylamino)ethyl hexanoate, Diethly aminoethyl hexanoate, Hexanoic acid, 2-(diethylamino)ethyl ester, DA-6;2-(Diethylamino)ethyl hexanoate, Anxianzhi, 2-(Diethylamino)ethyl caproate, DA-6, Hexanoic acid, 2-(diethylamino)ethyl ester; 2-(Diethylamino)ethyl caproate; 2-Diethylaminoethyl hexanoate; DA 6; Diethyl aminoethyl hexanoate; HKL 4, MFCD12827534, HKL4, Q3S9KHG9EY, HKL-4, SCHEMBL7940412, DTXSID40564151, AEIJVYPRKAWFPN-UHFFFAOYSA-N, 2-Diethylaminoethyl Hexanoate 100 microg/mL in Acetonitrile, AKOS015904405, FD15528, Hexanoic acid, 2-diethylaminoethyl ester, AS-20014, hexanoic acid 2-(diethylamino) ethyl ester, CS-0043355, E79222, 2-Diethylaminoethyl Hexanoate 1000 microg/mL in Acetone

Application

2-Diethylaminoethyl hexanoate serves as a versatile intermediate in the synthesis of pharmaceutical compounds, particularly those requiring amine-functionalized ester groups. It finds application in the development of local anesthetics and other bioactive molecules due to its balanced lipophilic/hydrophilic properties. Researchers also employ this compound in catalyst systems and as a building block for specialty surfactants. Its ester functionality makes it useful for prodrug formulations where controlled release is desired.

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