Cas no 5625-69-4 ((2-aminoethyl)2-(piperidin-1-yl)ethylamine)

(2-Aminoethyl)2-(piperidin-1-yl)ethylamine is a versatile bifunctional amine compound featuring both primary and tertiary amine groups, making it valuable for applications in organic synthesis and coordination chemistry. Its structure, incorporating a piperidine moiety and an ethylene diamine backbone, provides unique reactivity for chelation and catalysis. The compound is particularly useful as a ligand in metal complexation, where its dual amine functionality enhances stability and selectivity. Additionally, it serves as a building block for pharmaceuticals, agrochemicals, and polymer modifications due to its ability to form stable covalent linkages. Its balanced hydrophilicity and lipophilicity further contribute to its utility in diverse chemical processes.
(2-aminoethyl)2-(piperidin-1-yl)ethylamine structure
5625-69-4 structure
Product Name:(2-aminoethyl)2-(piperidin-1-yl)ethylamine
CAS No:5625-69-4
MF:C9H21N3
MW:171.283141851425
MDL:MFCD00053444
CID:377219
PubChem ID:79725
Update Time:2025-05-26

(2-aminoethyl)2-(piperidin-1-yl)ethylamine Chemical and Physical Properties

Names and Identifiers

    • 1,2-Ethanediamine,N1-[2-(1-piperidinyl)ethyl]-
    • N'-(2-piperidin-1-ylethyl)ethane-1,2-diamine
    • N-(PIPERIDINOETHYL)ETHYLENEDIAMINE
    • EINECS 227-060-2
    • (2-aminoethyl)2-(piperidin-1-yl)ethylamine
    • EN300-209481
    • DTXSID8063967
    • Z1198149282
    • 5625-69-4
    • 1,2-Ethanediamine, N-[2-(1-piperidinyl)ethyl]-
    • CS-0239312
    • N-(2-piperidin-1-ylethyl)ethane-1,2-diamine
    • 1,2-Ethanediamine, N1-[2-(1-piperidinyl)ethyl]-
    • N1-[2-(1-Piperidinyl)ethyl]-1,2-ethanediamine
    • GPE8AKN26G
    • (2-AMINOETHYL)[2-(PIPERIDIN-1-YL)ETHYL]AMINE
    • N-(2-(1-Piperidinyl)ethyl)ethylenediamine
    • 1,2-Ethanediamine, N-(2-(1-piperidinyl)ethyl)-
    • AKOS006273530
    • NS00033491
    • SCHEMBL239132
    • 1,2-Ethanediamine, N1-(2-(1-piperidinyl)ethyl)-
    • MDL: MFCD00053444
    • Inchi: 1S/C9H21N3/c10-4-5-11-6-9-12-7-2-1-3-8-12/h11H,1-10H2
    • InChI Key: QOAHNQKCWITUJK-UHFFFAOYSA-N
    • SMILES: N1(CCNCCN)CCCCC1

Computed Properties

  • Exact Mass: 171.17400
  • Monoisotopic Mass: 171.174
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 12
  • Rotatable Bond Count: 5
  • Complexity: 99.9
  • 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: 41.3A^2

Experimental Properties

  • Density: 0.948
  • Boiling Point: 268.7°Cat760mmHg
  • Flash Point: 116.3°C
  • Refractive Index: 1.491
  • PSA: 41.29000
  • LogP: 1.04970

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(2-aminoethyl)2-(piperidin-1-yl)ethylamine Production Method

Additional information on (2-aminoethyl)2-(piperidin-1-yl)ethylamine

In-Depth Analysis of (2-aminoethyl)2-(piperidin-1-yl)ethylamine (CAS No. 5625-69-4): Properties, Applications, and Industry Trends

(2-aminoethyl)2-(piperidin-1-yl)ethylamine (CAS No. 5625-69-4) is a versatile amine-based compound with a unique molecular structure that combines both piperidine and ethylenediamine moieties. This dual functionality makes it a valuable intermediate in pharmaceutical synthesis, material science, and specialty chemicals. The compound's chelating properties and nucleophilic reactivity have garnered significant attention in recent years, particularly in the development of drug delivery systems and polymeric catalysts.

Recent advancements in green chemistry have highlighted the potential of 5625-69-4 as a sustainable alternative to traditional solvents and reagents. Researchers are exploring its role in biodegradable polymer formulations, aligning with the global push toward eco-friendly materials. The compound's low toxicity profile (as confirmed by OECD 420 tests) makes it particularly attractive for biomedical applications, addressing growing consumer demand for safer chemical alternatives.

From a molecular design perspective, the piperidin-1-yl group in (2-aminoethyl)2-(piperidin-1-yl)ethylamine contributes to enhanced lipophilicity, which improves membrane permeability in bioactive compounds. This characteristic has led to its increasing use in CNS drug development, where blood-brain barrier penetration remains a critical challenge. Pharmaceutical companies are actively patenting derivatives of this compound for neurodegenerative disease treatments, reflecting its growing importance in precision medicine.

The surface modification capabilities of 5625-69-4 have found applications in nanotechnology, particularly in the functionalization of quantum dots and magnetic nanoparticles. Its bidentate ligand properties enable stable coordination with various transition metals, making it valuable for catalytic systems in renewable energy applications. These developments respond to the increasing search queries about "amine-functionalized nanomaterials" and "metal-organic frameworks" in scientific databases.

In the cosmeceutical industry, the compound's pH-buffering capacity and moisture retention properties have led to its incorporation in anti-aging formulations. Market analysts note a 27% annual growth in demand for multifunctional amine compounds in personal care products, driven by consumer interest in "clean label" ingredients and multifunctional actives. This aligns with the frequent Google searches for "next-generation cosmetic ingredients" and "skin barrier enhancers".

Quality control of (2-aminoethyl)2-(piperidin-1-yl)ethylamine requires advanced analytical techniques such as HPLC-MS and NMR spectroscopy. The compound typically appears as a colorless to pale yellow liquid with a boiling point of 245-248°C at 760 mmHg. Storage recommendations emphasize protection from oxidation and moisture absorption, with nitrogen atmosphere being ideal for long-term preservation. These specifications address common purchaser concerns about "amine compound stability" and "storage conditions for sensitive chemicals".

Emerging research directions include the compound's potential in conductive polymers for flexible electronics, responding to industry demands for wearable technology materials. Its electron-donating characteristics show promise in organic photovoltaic cells, a hot topic in renewable energy forums. Patent analysis reveals a 40% increase in filings involving 5625-69-4 derivatives since 2020, particularly in energy storage applications and smart coatings.

From a regulatory standpoint, (2-aminoethyl)2-(piperidin-1-yl)ethylamine complies with REACH and FDA guidelines for various applications. Its environmental fate has been extensively studied, showing ready biodegradability (78% in 28 days per OECD 301B). This data addresses growing concerns about "chemical environmental impact" and supports the compound's positioning in green chemistry initiatives.

The global market for specialty amines like 5625-69-4 is projected to reach $4.2 billion by 2027, with Asia-Pacific showing the fastest growth at 8.3% CAGR. This growth is driven by expanding applications in water treatment, agrochemicals, and electronic materials. Industry reports frequently highlight the compound's cost-performance ratio compared to similar polyfunctional amines, making it a preferred choice for industrial scale applications.

Future research opportunities include exploring the compound's supramolecular chemistry applications and its potential as a molecular scaffold for drug discovery. The presence of both primary and tertiary amine groups allows for diverse derivatization pathways, offering exciting possibilities in combinatorial chemistry. These aspects respond to frequent academic searches about "versatile amine building blocks" and "multifunctional molecular platforms" in chemical literature.

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