Cas no 22078-09-7 ((7-aminoheptyl)dimethylamine)

(7-Aminoheptyl)dimethylamine is a bifunctional organic compound featuring a primary amine and a tertiary amine group separated by a seven-carbon alkyl chain. This structure imparts versatility in applications such as polymer modification, surfactant synthesis, and as a building block for pharmaceuticals or chelating agents. The primary amine enables covalent bonding with electrophiles, while the tertiary amine offers coordination or catalytic potential. Its linear hydrocarbon spacer enhances solubility in organic media while maintaining compatibility with aqueous systems. The compound's dual functionality allows for tailored reactivity in crosslinking or surface modification processes. Careful handling is advised due to the amine groups' sensitivity to air and moisture. Storage under inert atmosphere is recommended to preserve stability.
(7-aminoheptyl)dimethylamine structure
(7-aminoheptyl)dimethylamine structure
Product Name:(7-aminoheptyl)dimethylamine
CAS No:22078-09-7
MF:C9H22N2
MW:158.284382343292
CID:1410134
PubChem ID:3822076
Update Time:2025-10-29

(7-aminoheptyl)dimethylamine Chemical and Physical Properties

Names and Identifiers

    • 1,7-Heptanediamine, N,N-dimethyl-
    • N',N'-dimethylheptane-1,7-diamine
    • AKOS000262688
    • 7-DIMETHYLAMINOHEPTYLAMINE
    • OXAUQAUWLUANLY-UHFFFAOYSA-N
    • N1,N1-Dimethylheptane-1,7-diamine
    • EN300-56229
    • DTXSID70396886
    • 7-dimethyl-aminoheptylamine
    • SCHEMBL527111
    • DB-109857
    • G44614
    • 22078-09-7
    • A1-61608
    • (7-aminoheptyl)dimethylamine
    • Inchi: 1S/C9H22N2/c1-11(2)9-7-5-3-4-6-8-10/h3-10H2,1-2H3
    • InChI Key: OXAUQAUWLUANLY-UHFFFAOYSA-N
    • SMILES: N(C)(C)CCCCCCCN

Computed Properties

  • Exact Mass: 158.17846
  • Monoisotopic Mass: 158.178298710g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 11
  • Rotatable Bond Count: 7
  • Complexity: 72
  • 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: 1.3
  • Topological Polar Surface Area: 29.3?2

Experimental Properties

  • PSA: 29.26

(7-aminoheptyl)dimethylamine Pricemore >>

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Additional information on (7-aminoheptyl)dimethylamine

Comprehensive Analysis of (7-aminoheptyl)dimethylamine (CAS No. 22078-09-7): Properties, Applications, and Industry Trends

(7-aminoheptyl)dimethylamine (CAS No. 22078-09-7) is a versatile aliphatic amine compound with a unique molecular structure, featuring a seven-carbon chain terminated by a primary amine group and a dimethylamine moiety. This bifunctional characteristic makes it valuable in organic synthesis, particularly in the production of specialty polymers, surfactants, and pharmaceutical intermediates. The compound's aminoheptyl backbone provides flexibility in chemical modifications, while the dimethylamino group enhances its reactivity in nucleophilic substitution reactions.

Recent advancements in green chemistry have increased interest in 22078-09-7 as a potential building block for biodegradable materials. Researchers are exploring its use in water treatment chemicals and corrosion inhibitors, addressing growing environmental concerns. The compound's amphiphilic nature allows it to function as a cationic surfactant, making it relevant to formulations in personal care products and industrial cleaners where mildness and efficiency are prioritized.

From a technical perspective, (7-aminoheptyl)dimethylamine demonstrates excellent solubility in polar solvents including water, ethanol, and acetone, with a typical purity grade of ≥95%. Its molecular weight of 158.28 g/mol and boiling point range of 210-215°C make it suitable for various high-temperature applications. The compound's Hansen solubility parameters have been extensively studied for compatibility with epoxy resins and polyurethane systems, reflecting its importance in advanced material science.

The pharmaceutical industry utilizes CAS 22078-09-7 as a precursor for drug delivery systems, particularly in creating pH-sensitive carriers that respond to biological environments. Its amine functionality enables conjugation with active pharmaceutical ingredients (APIs), while the hydrocarbon spacer provides optimal molecular spacing for enhanced bioavailability. Current research focuses on its potential in targeted cancer therapies and neurological drug development, aligning with the healthcare sector's emphasis on precision medicine.

In material sciences, (7-aminoheptyl)dimethylamine serves as a crucial modifier for surface coatings and adhesive formulations. Its ability to improve substrate wetting and interfacial adhesion has been leveraged in automotive and aerospace composites. The compound's crosslinking potential enhances the mechanical properties of epoxy networks, making it valuable for high-performance composites in extreme environments. Recent patents highlight innovative applications in smart packaging materials with antimicrobial properties.

Quality control protocols for 22078-09-7 typically involve gas chromatography (GC) analysis and titration methods to verify amine content. Storage recommendations emphasize protection from moisture and oxidation, with optimal conditions in nitrogen-purged containers at temperatures below 30°C. The compound's shelf stability and handling considerations are frequently discussed in technical forums, reflecting industry demand for safe handling guidelines of amine compounds.

Emerging applications in nanotechnology utilize (7-aminoheptyl)dimethylamine as a surface functionalization agent for quantum dots and metallic nanoparticles. Its molecular length provides precise control over interparticle spacing in self-assembled monolayers, crucial for optoelectronic devices and sensor technologies. This aligns with the growing Internet of Things (IoT) market, where advanced materials enable next-generation wearable electronics and environmental sensors.

From a commercial perspective, the global market for specialty amines like 22078-09-7 is projected to grow at 5.8% CAGR through 2030, driven by demand from Asia-Pacific manufacturing hubs. Suppliers increasingly emphasize sustainable production methods, including catalytic amination processes that reduce energy consumption. Current price trends reflect fluctuations in raw material costs, particularly for heptylene derivatives used in synthesis.

Regulatory compliance for (7-aminoheptyl)dimethylamine varies by region, with most jurisdictions requiring standard SDS documentation and proper transport classification. The compound is not currently listed under major chemical restriction programs, though users should monitor evolving REACH regulations and TSCA updates. Industry best practices recommend exposure monitoring in workplace settings and proper waste management procedures for unused material.

Future research directions for CAS 22078-09-7 include development of enzyme-catalyzed synthesis routes and exploration of its bioconjugation potential in biopharmaceuticals. The compound's versatility continues to attract interest across multiple disciplines, from advanced materials to life sciences, ensuring its ongoing relevance in industrial chemistry. As innovation drives new applications, (7-aminoheptyl)dimethylamine remains a compound of significant scientific and commercial interest.

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