Cas no 54256-45-0 (1-N-Octylpiperazine)

1-N-Octylpiperazine is a tertiary amine compound featuring an octyl group attached to the piperazine ring. This structure imparts both lipophilic and basic properties, making it useful as an intermediate in organic synthesis, particularly for the development of surfactants, corrosion inhibitors, and pharmaceutical agents. Its balanced solubility in both polar and nonpolar solvents enhances its versatility in chemical reactions. The compound's piperazine core allows for further functionalization, enabling tailored modifications for specific applications. Its stability under standard conditions and compatibility with a range of reagents make it a practical choice for industrial and research purposes. Proper handling is advised due to its alkaline nature.
1-N-Octylpiperazine structure
1-N-Octylpiperazine structure
Product Name:1-N-Octylpiperazine
CAS No:54256-45-0
MF:C12H26N2
MW:198.348243236542
MDL:MFCD00958407
CID:367288
PubChem ID:24880332
Update Time:2025-10-28

1-N-Octylpiperazine Chemical and Physical Properties

Names and Identifiers

    • 1-Octylpiperazine
    • 1-n-Octylpiperazine
    • 1-octyl-Piperazine
    • Piperazine, 1-octyl-
    • FT-0640231
    • MFCD00958407
    • SCHEMBL3716714
    • RRZDZQLIIMBIDL-UHFFFAOYSA-N
    • 1-Octyl Piperazine
    • 1-n-octyl-piperazine
    • AKOS009157389
    • DTXSID90371832
    • A830070
    • AS-44259
    • 1-Octylpiperazine, 97%
    • CHEMBL4086003
    • 1-(1-Octyl)-piperazine
    • 54256-45-0
    • CS-0124232
    • A10338
    • DB-019314
    • 1-N-Octylpiperazine
    • MDL: MFCD00958407
    • Inchi: 1S/C12H26N2/c1-2-3-4-5-6-7-10-14-11-8-13-9-12-14/h13H,2-12H2,1H3
    • InChI Key: RRZDZQLIIMBIDL-UHFFFAOYSA-N
    • SMILES: N1(CCNCC1)CCCCCCCC

Computed Properties

  • Exact Mass: 198.21000
  • Monoisotopic Mass: 198.21
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 14
  • Rotatable Bond Count: 7
  • Complexity: 120
  • 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
  • Surface Charge: 0
  • Tautomer Count: nothing
  • XLogP3: 3
  • Topological Polar Surface Area: 15.3A^2

Experimental Properties

  • Color/Form: Not determined
  • Density: 0.836?g/mL?at 25?°C(lit.)
  • Boiling Point: 240-241?°C(lit.)
  • Flash Point: Fahrenheit: 114.8 ° f
    Celsius: 46 ° c
  • Refractive Index: n20/D 1.4670(lit.)
  • PSA: 15.27000
  • LogP: 2.51880
  • Solubility: React with water

1-N-Octylpiperazine Security Information

  • Symbol: GHS02 GHS07
  • Signal Word:Warning
  • Hazard Statement: H226-H315-H319-H335
  • Warning Statement: P261-P305+P351+P338
  • Hazardous Material transportation number:UN 1993 3/PG 3
  • WGK Germany:3
  • Hazard Category Code: 10-36/37/38
  • Safety Instruction: S26
  • Hazardous Material Identification: Xi
  • Safety Term:S26
  • Risk Phrases:R10
  • HazardClass:3

1-N-Octylpiperazine Customs Data

  • HS CODE:2933599090
  • Customs Data:

    China Customs Code:

    2933599090

    Overview:

    2933599090. Other compounds with pyrimidine ring in structure(Including other compounds with piperazine ring on the structure. 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, Please indicate the appearance of Urotropine, 6- caprolactam please indicate the appearance, Signing date

    Summary:

    2933599090. other compounds containing a pyrimidine ring (whether or not hydrogenated) or piperazine ring in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

1-N-Octylpiperazine Pricemore >>

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1-N-Octylpiperazine Related Literature

Additional information on 1-N-Octylpiperazine

1-N-Octylpiperazine (CAS No 54256-45-0): A Comprehensive Overview

1-N-Octylpiperazine, also known by its CAS registry number 54256-45-0, is a versatile organic compound that has garnered significant attention in various scientific and industrial applications. This compound belongs to the piperazine family, which is a six-membered ring consisting of two nitrogen atoms. The 1-N-octyl substituent attached to the piperazine ring introduces unique chemical properties, making it a valuable molecule in research and development.

The synthesis of 1-N-octylpiperazine involves a series of well-established organic reactions, including nucleophilic substitution and ring-opening polymerization. Recent advancements in synthetic chemistry have enabled the production of this compound with high purity and efficiency, ensuring its reliability for large-scale applications. The molecule's structure, characterized by a long alkyl chain (octyl group) attached to the piperazine ring, imparts amphiphilic properties, making it suitable for a wide range of uses.

One of the most promising applications of 1-N-octylpiperazine lies in its use as a building block for advanced materials. Researchers have explored its potential in the development of novel polymers and surfactants. For instance, studies published in leading journals such as *Macromolecules* and *Journal of Polymer Science* highlight its role in creating self-healing polymers with enhanced mechanical properties. The ability of 1-N-octylpiperazine to form stable networks through hydrogen bonding and van der Waals interactions has been pivotal in these innovations.

In the field of drug delivery systems, 1-N-octylpiperazine has shown remarkable potential as a carrier for bioactive molecules. Its amphiphilic nature allows it to form micelles and liposomes, which can encapsulate drugs and deliver them to specific targets within the body. Recent studies have demonstrated its effectiveness in improving the bioavailability of hydrophobic drugs, making it a valuable asset in pharmaceutical research.

The cosmetic industry has also embraced 1-N-octylpiperazine due to its ability to enhance product performance. It is commonly used as an emulsifier and stabilizer in skincare products, contributing to their texture and shelf life. Its mild nature makes it suitable for sensitive skin formulations, aligning with the growing demand for gentle yet effective personal care products.

Environmental applications are another frontier where 1-N-octylpiperazine is making an impact. It has been investigated as a component in biodegradable plastics and eco-friendly packaging materials. Research indicates that polymers derived from this compound exhibit excellent biodegradation rates under controlled conditions, offering a sustainable alternative to traditional plastics.

The future prospects for 1-N-octylpiperazine are bright, with ongoing research exploring its potential in nanotechnology and green chemistry. Scientists are particularly interested in its ability to facilitate the synthesis of nanoparticles with tailored properties, which could revolutionize fields such as electronics and energy storage.

In conclusion, 1-N-octylpiperazine (CAS No 54256-45-0) is a multifaceted compound with applications spanning materials science, pharmaceuticals, cosmetics, and environmental technology. Its unique chemical properties and versatility make it an invaluable tool for researchers and industries alike. As advancements continue to unfold, this compound is poised to play an even more significant role in shaping innovative solutions across various sectors.

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