Cas no 6321-07-9 (4-Morpholin-4-ylbutan-1-amine)

4-Morpholin-4-ylbutan-1-amine is a versatile organic compound featuring both a morpholine ring and a primary amine functional group. This structure imparts favorable properties for applications in pharmaceutical synthesis, agrochemical development, and specialty chemical manufacturing. The morpholine moiety enhances solubility and stability, while the amine group provides reactivity for further derivatization, such as amide formation or Schiff base reactions. Its balanced polarity makes it suitable for use as an intermediate in heterocyclic chemistry and ligand design. The compound’s well-defined reactivity profile and compatibility with common synthetic protocols contribute to its utility in research and industrial processes requiring precise molecular modifications.
4-Morpholin-4-ylbutan-1-amine structure
4-Morpholin-4-ylbutan-1-amine structure
Product Name:4-Morpholin-4-ylbutan-1-amine
CAS No:6321-07-9
MF:C8H18N2O
MW:158.241322040558
MDL:MFCD03161271
CID:517137
PubChem ID:233611
Update Time:2025-05-27

4-Morpholin-4-ylbutan-1-amine Chemical and Physical Properties

Names and Identifiers

    • 4-Morpholin-4-ylbutan-1-amine
    • 4-(4-AMINO-1-BUTYL)-MORPHOLINE
    • 4-(morpholin-4-yl)butan-1-amine
    • 4-morpholinobutan-1-amine
    • 4-(4-aminobutyl)morpholine
    • 4-(4-morpholino)butylamine
    • 4-morpholin-4-yl-butylamine
    • 4-morpholinebutanamine
    • 4-morpholino-butylamine
    • N-(4-aminobutyl)morpholine
    • N-aminobutylmorpholine
    • 4-(4-Morpholinyl)butylamine
    • 4-Morpholinobutylamine
    • NSC 32425
    • DUYYFMPMGYATPO-UHFFFAOYSA-N
    • AKOS000163217
    • EN300-41484
    • 4-Morpholino-1-butanamine
    • NSC-32425
    • G78589
    • [4-(4-Morpholinyl)butyl]amine
    • MFCD03161271
    • SCHEMBL179978
    • 6321-07-9
    • NSC32425
    • DA-04188
    • BS-13448
    • CS-0248810
    • DTXSID30283607
    • Z285162580
    • 4-morpholinylbutylamine
    • F2187-2315
    • 4-(4-Amino-1-butyl)morpholine
    • AR-527/41149362
    • MDL： MFCD03161271
    • Inchi： 1S/C8H18N2O/c9-3-1-2-4-10-5-7-11-8-6-10/h1-9H2
    • InChI Key： DUYYFMPMGYATPO-UHFFFAOYSA-N
    • SMILES： O1CCN(CC1)CCCCN

Computed Properties

  • Exact Mass: 158.14200
  • Monoisotopic Mass: 158.142
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 11
  • Rotatable Bond Count: 4
  • Complexity: 92.1
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: -0.3
  • Topological Polar Surface Area: 38.5?2

Experimental Properties

  • Density: 0.9804 g/cm3
  • Boiling Point: 123-125 oC (15 Torr)
  • Flash Point: 101.7±23.2 oC,
  • Refractive Index: 1.5052 (589.3 nm 25 oC)
  • Solubility: Soluble (465 g/l) (25 o C),
  • PSA: 38.49000
  • LogP: 0.69570
  • Vapor Pressure: 0.0±0.5 mmHg at 25°C

4-Morpholin-4-ylbutan-1-amine Security Information

4-Morpholin-4-ylbutan-1-amine 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%

4-Morpholin-4-ylbutan-1-amine Pricemore >>

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4-Morpholin-4-ylbutan-1-amine Related Literature

Related Categories

Additional information on 4-Morpholin-4-ylbutan-1-amine

Comprehensive Overview of 4-Morpholin-4-ylbutan-1-amine (CAS No. 6321-07-9): Properties, Applications, and Innovations

4-Morpholin-4-ylbutan-1-amine (CAS No. 6321-07-9) is a versatile organic compound with a molecular structure that combines a morpholine ring and a butylamine chain. This unique configuration grants it a wide range of applications in pharmaceuticals, agrochemicals, and material science. The compound's CAS number 6321-07-9 is frequently searched in scientific databases, reflecting its relevance in research and industrial processes. Its amine functional group and morpholine moiety make it a valuable intermediate in synthetic chemistry, particularly in the development of bioactive molecules.

In recent years, the demand for 4-Morpholin-4-ylbutan-1-amine has surged due to its role in the synthesis of drug candidates and specialty chemicals. Researchers are particularly interested in its potential applications in cancer therapeutics and neuropharmacology, as its structure can be modified to target specific biological pathways. The compound's solubility and stability under various conditions also make it a preferred choice for formulation scientists. Online searches for "6321-07-9 supplier" or "4-Morpholin-4-ylbutan-1-amine synthesis" highlight its commercial and academic significance.

The morpholine ring in 4-Morpholin-4-ylbutan-1-amine contributes to its electron-donating properties, which are critical in catalysis and polymer chemistry. This feature has led to its use in the development of advanced materials, such as conductive polymers and coatings. Additionally, its amine group allows for facile derivatization, enabling the creation of custom-tailored molecules for niche applications. Queries like "morpholine derivatives in material science" or "amine-functionalized compounds" often lead to discussions about this compound's utility.

From an environmental perspective, 4-Morpholin-4-ylbutan-1-amine is being studied for its biodegradability and low toxicity profile, aligning with the growing emphasis on green chemistry. Innovations in sustainable synthesis methods, such as microwave-assisted reactions or enzymatic catalysis, are further enhancing its appeal. These advancements address common search terms like "eco-friendly amine synthesis" and "green morpholine derivatives," showcasing the compound's alignment with modern scientific trends.

In summary, 4-Morpholin-4-ylbutan-1-amine (CAS No. 6321-07-9) is a multifaceted compound with expanding applications across industries. Its structural features, combined with evolving synthetic techniques, position it as a key player in the future of organic chemistry and applied sciences. As research continues, its role in addressing challenges like drug discovery and sustainable manufacturing will likely grow, making it a compound worth watching in the coming years.

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