Cas no 55265-24-2 (3-ethylmorpholine)

3-Ethylmorpholine is a versatile heterocyclic amine with the molecular formula C6H13NO, featuring a morpholine ring substituted with an ethyl group at the 3-position. This compound is widely utilized as an intermediate in organic synthesis, particularly in pharmaceuticals, agrochemicals, and specialty chemicals. Its polar aprotic nature and moderate basicity make it suitable for use as a catalyst or solvent in various reactions, including polymerizations and condensations. The ethyl group enhances its lipophilicity, improving solubility in organic matrices. 3-Ethylmorpholine is valued for its stability, low volatility, and efficient reactivity under controlled conditions, making it a reliable choice for industrial and laboratory applications.
3-ethylmorpholine structure
3-ethylmorpholine structure
Product Name:3-ethylmorpholine
CAS No:55265-24-2
MF:C6H13NO
MW:115.173521757126
MDL:MFCD09054774
CID:1026808
PubChem ID:14267782
Update Time:2025-05-20

3-ethylmorpholine Chemical and Physical Properties

Names and Identifiers

    • 3-Ethylmorpholine hydrochloride
    • 3-ethyl-Morpholine
    • 3-Aethyl-morpholin
    • 3-ethylMorpholine
    • 3-ethylmorpholine(SALTDATA: FREE)
    • AX8212750
    • 3-Ethylmorpholine--hydrogen chloride (1/1)
    • A830560
    • SB12763
    • m-ethylmorpholine
    • AB49617
    • BS-12880
    • F2148-0111
    • Z405749950
    • F17622
    • SCHEMBL16953
    • R-(-)-3-ethyl-morpholine
    • 55265-24-2
    • EN300-43359
    • CS-0059261
    • AB89232
    • SY173807
    • AKOS009386508
    • MFCD09054774
    • JBQWQBSRIAGTJT-UHFFFAOYSA-N
    • 3-ethylmorpholine
    • MDL: MFCD09054774
    • Inchi: 1S/C6H13NO/c1-2-6-5-8-4-3-7-6/h6-7H,2-5H2,1H3
    • InChI Key: JBQWQBSRIAGTJT-UHFFFAOYSA-N
    • SMILES: O1CCNC(CC)C1

Computed Properties

  • Exact Mass: 115.10000
  • Monoisotopic Mass: 115.099714038g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 9
  • Rotatable Bond Count: 1
  • Complexity: 65.5
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 1
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Topological Polar Surface Area: 21.3
  • XLogP3: 0.4

Experimental Properties

  • Density: 0.878±0.06 g/cm3 (20 oC 760 Torr),
  • Boiling Point: 156.5-157.5 oC
  • Flash Point: 54.2±9.8 oC,
  • Refractive Index: 1.4519 (589.3 nm 20 oC)
  • Solubility: Soluble (149 g/l) (25 o C),
  • PSA: 21.26000
  • LogP: 0.71360

3-ethylmorpholine Customs Data

  • HS CODE:2934999090
  • Customs Data:

    China Customs Code:

    2934999090

    Overview:

    2934999090. Other heterocyclic compounds. VAT:17.0%. Tax refund rate:13.0%. Regulatory conditions:nothing. MFN tariff:6.5%. general tariff:20.0%

    Declaration elements:

    Product Name, component content, use to

    Summary:

    2934999090. other heterocyclic compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

3-ethylmorpholine Pricemore >>

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Additional information on 3-ethylmorpholine

Professional Introduction to Compound with CAS No. 55265-24-2 and Product Name: 3-Ethylmorpholine

3-Ethylmorpholine, identified by the Chemical Abstracts Service Number (CAS No.) 55265-24-2, is a significant compound in the field of chemical and pharmaceutical research. This bicyclic amine derivative has garnered considerable attention due to its versatile applications and structural properties. As a derivative of morpholine, 3-Ethylmorpholine exhibits unique chemical characteristics that make it a valuable intermediate in synthesizing various pharmaceuticals, agrochemicals, and specialty chemicals.

The molecular structure of 3-Ethylmorpholine consists of a morpholine ring substituted with an ethyl group at the 3-position. This substitution imparts distinct reactivity and solubility properties, making it particularly useful in organic synthesis. The compound’s ability to act as a ligand in coordination chemistry has been explored in recent years, particularly in the development of catalytic systems for asymmetric synthesis. Researchers have leveraged the chiral environment provided by 3-Ethylmorpholine to enhance the enantioselectivity of catalytic reactions, which is crucial for producing optically active pharmaceuticals.

In the realm of pharmaceutical applications, 3-Ethylmorpholine has been investigated as a potential precursor for antihistamines and anticholinergic drugs. Its structural motif is reminiscent of several bioactive molecules, suggesting its utility in drug discovery programs. Recent studies have highlighted its role in modulating neurotransmitter receptors, which could have implications for treating neurological disorders. The compound’s ability to interact with biological targets without excessive toxicity makes it an attractive candidate for further pharmacological exploration.

From an industrial perspective, 3-Ethylmorpholine finds use as a solvent and additive in various chemical processes. Its high boiling point and relatively low toxicity make it suitable for applications where thermal stability and environmental compatibility are desired. In agrochemical formulations, it has been tested as a component in pesticide formulations due to its ability to enhance the solubility and bioavailability of active ingredients. This application aligns with the growing demand for more efficient and sustainable agricultural practices.

The synthesis of 3-Ethylmorpholine typically involves the reaction of morpholine with ethylating agents under controlled conditions. Advances in catalytic methods have improved the efficiency and yield of these reactions, reducing the environmental footprint of production processes. Green chemistry principles have guided researchers to develop solvent-free or aqueous-phase synthesis routes, minimizing waste generation and energy consumption. Such innovations underscore the compound’s relevance in modern chemical manufacturing.

Recent breakthroughs in computational chemistry have also contributed to our understanding of 3-Ethylmorpholine’s reactivity. Molecular modeling studies have predicted new synthetic pathways and revealed insights into its interaction with biological molecules. These computational approaches complement experimental work, accelerating the discovery process by allowing researchers to screen numerous possibilities before conducting wet-lab experiments.

The regulatory landscape for 3-Ethylmorpholine is another area of interest. As regulations evolve to address environmental concerns, manufacturers must ensure compliance with safety standards while maintaining cost-effectiveness. Documentation of its safe handling practices and disposal methods is essential for industrial applications. Industry stakeholders collaborate with regulatory bodies to establish guidelines that balance innovation with responsibility.

In conclusion, 3-Ethylmorpholine (CAS No. 55265-24-2) represents a compound with multifaceted applications across pharmaceuticals, agrochemicals, and industrial chemistry. Its unique structural features and functional properties continue to drive research into new uses and improved synthesis methods. As scientific understanding advances, so too will the applications of this versatile chemical building block.

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