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Atomfair 2-Diethylaminoethyl hexanoate C12H25NO2

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,…

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Description

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.

  • CAS No: 10369-83-2
  • Molecular Formula: C12H25NO2
  • Molecular Weight: 215.33
  • Exact Mass: 215.188529040
  • Monoisotopic Mass: 215.188529040
  • IUPAC Name: 2-(diethylamino)ethyl hexanoate
  • SMILES: CCCCCC(=O)OCCN(CC)CC
  • Synonyms: 2-DIETHYLAMINOETHYL HEXANOATE, 10369-83-2, 2-(Diethylamino)ethyl hexanoate, Diethly aminoethyl hexanoate, Hexanoic acid, 2-(diethylamino)ethyl ester

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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