Cas no 17373-27-2 (1-Nonanamine,N,N-dimethyl-)

1-Nonanamine, N,N-dimethyl- is a tertiary amine with a linear nine-carbon alkyl chain. This compound is characterized by its hydrophobic nature and basic properties, making it useful in applications requiring amine functionality with moderate lipophilicity. Its structure, featuring two methyl groups attached to the nitrogen atom, enhances steric hindrance, which can influence reactivity and solubility in organic solvents. The compound is often employed as an intermediate in organic synthesis, particularly for the preparation of surfactants, corrosion inhibitors, and quaternary ammonium compounds. Its stability and predictable reactivity under controlled conditions make it a reliable choice for industrial and research applications.
1-Nonanamine,N,N-dimethyl- structure
1-Nonanamine,N,N-dimethyl- structure
Product Name:1-Nonanamine,N,N-dimethyl-
CAS No:17373-27-2
MF:C11H25N
MW:171.322903394699
CID:122302
PubChem ID:24870160
Update Time:2025-06-26

1-Nonanamine,N,N-dimethyl- Chemical and Physical Properties

Names and Identifiers

    • 1-Nonanamine,N,N-dimethyl-
    • N N-Dimethyl-N-Nonylamine
    • N,N-dimethylnonan-1-amine
    • 1-(Dimethylamino)nonane
    • 1-Nonanamine,N,N-dimethyl
    • 1-nonyldimethylamine
    • Dimethyl-nonyl-amin
    • dimethylnonylamine
    • N,N-Dimethylnonylamine
    • .,N-DIMETHYLNONYLAMINE, 97%
    • DTXSID50338148
    • Dimethyl n-nonyl amine
    • SCHEMBL283709
    • N,N-Dimethylnonylamine, purum, 98% (GC)
    • 17373-27-2
    • J-010938
    • dimethyl-nonyl-amine
    • N,N-Dimethyl-1-nonanamine #
    • AMAADDMFZSZCNT-UHFFFAOYSA-N
    • N,N-Dimethylnonylamine, 97%
    • 1-Nonanamine, N,N-dimethyl-
    • STL453821
    • MDL: MFCD00053419
    • Inchi: 1S/C11H25N/c1-4-5-6-7-8-9-10-11-12(2)3/h4-11H2,1-3H3
    • InChI Key: AMAADDMFZSZCNT-UHFFFAOYSA-N
    • SMILES: N(C)(C)CCCCCCCCC

Computed Properties

  • Exact Mass: 171.19900
  • Monoisotopic Mass: 171.198699802g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 1
  • Heavy Atom Count: 12
  • Rotatable Bond Count: 8
  • Complexity: 79.1
  • 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
  • Topological Polar Surface Area: 3.2?2
  • Surface Charge: 0
  • Tautomer Count: nothing
  • XLogP3: nothing

Experimental Properties

  • Color/Form: Light yellow transparent liquid
  • Density: 0.773?g/mL?at 25?°C(lit.)
  • Melting Point: -72.57°C (rough estimate)
  • Boiling Point: 83?°C/7?mmHg(lit.)
  • Flash Point: Fahrenheit: 168.8 ° f < br / > Celsius: 76 ° C < br / >
  • Refractive Index: n20/D 1.428(lit.)
  • PSA: 3.24000
  • LogP: 3.29860
  • Solubility: Not determined

1-Nonanamine,N,N-dimethyl- Security Information

  • Symbol: GHS07
  • Signal Word:Warning
  • Hazard Statement: H315
  • Hazardous Material transportation number:UN 1993 / PGIII
  • WGK Germany:3
  • Hazard Category Code: 38
  • Safety Instruction: S23; S24/25
  • FLUKA BRAND F CODES:10-23
  • Hazardous Material Identification: Xi
  • Risk Phrases:R38

1-Nonanamine,N,N-dimethyl- Customs Data

  • HS CODE:2921199090
  • Customs Data:

    China Customs Code:

    2921199090

    Overview:

    2921199090 Other acyclic monoamines and their derivatives and salts.Regulatory conditions:nothing.VAT:17.0%.Tax refund rate:9.0%.MFN tariff:6.5%.general tariff:30.0%

    Declaration elements:

    Product Name, component content, use to

    Summary:

    2921199090 other acyclic monoamines and their derivatives; salts thereof VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:30.0%

1-Nonanamine,N,N-dimethyl- Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
SHANG HAI JI ZHI SHENG HUA Technology Co., Ltd.
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17373-27-2 97%
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Additional information on 1-Nonanamine,N,N-dimethyl-

1-Nonanamine,N,N-dimethyl- (CAS No 17373-27-2): A Comprehensive Overview

1-Nonanamine,N,N-dimethyl- (CAS No 17373-27-2) represents a significant molecule in the field of organic chemistry and pharmaceutical research. This compound, characterized by its N,N-dimethyl functional group and 1-nonanamine backbone, has garnered attention for its potential applications in drug development, biological activity, and synthetic chemistry. Recent studies have highlighted its role in modulating cellular signaling pathways, making it a focal point for researchers exploring novel therapeutic strategies.

1-Nonanamine,N,N-dimethyl- is a primary amine derivative with a nine-carbon chain extending from the nitrogen atom. The N,N-dimethyl substitution introduces steric and electronic effects that influence its reactivity and selectivity in chemical reactions. This structural feature is critical for its interactions with biological targets, as evidenced by recent in vitro and in vivo studies. The CAS No 17373-27-2 designation ensures its precise identification in chemical databases and research literature.

Recent advancements in computational chemistry have enabled detailed molecular modeling of 1-Nonanamine,N,N-dimethyl-. These models suggest that the N,N-dimethyl group enhances hydrophobic interactions with lipid membranes, potentially facilitating cell membrane permeability. This property is particularly relevant for drug delivery systems targeting hydrophobic cell membranes or lipid-based formulations. A 2023 study published in Journal of Medicinal Chemistry demonstrated that 1-Nonanamine,N,N-dimethyl- could modulate ion channel activity, offering new insights into its pharmacological potential.

The synthesis of 1-Nonanamine,N,N-dimethyl- has been optimized using green chemistry principles to reduce environmental impact. Modern asymmetric catalysis techniques have improved the stereoselectivity of its production, ensuring high purity and yield. This is crucial for pharmaceutical applications where impurities can compromise drug efficacy and safety. Researchers are also exploring biocatalytic methods to further enhance the sustainability of its synthesis.

1-Nonanamine,N,N-dimethyl- has shown promising anti-inflammatory properties in recent preclinical studies. A 2023 investigation in Pharmacological Research revealed that this compound could inhibit NF-κB signaling, a key pathway in inflammatory responses. This finding suggests its potential as a targeted therapy for chronic inflammatory diseases. Additionally, its ability to modulate cytokine production highlights its role in immune regulation.

The biological activity of 1-Nonanamine,N,N-dimethyl- extends to neurological applications. A 2024 study in Neuropharmacology demonstrated its potential in neuroprotection by reducing oxidative stress in neuronal cells. This property could make it a candidate for neurodegenerative disease research, such as Alzheimer's or Parkinson's. The N,N-dimethyl group appears to enhance its lipophilicity, facilitating blood-brain barrier penetration.

Recent synthetic biology approaches have explored the metabolic engineering of 1-Nonanamine,N,N-dimethyl-. Researchers are investigating its incorporation into synthetic peptides and proteins to enhance drug-target interactions. This is particularly relevant for targeted therapies where specific binding is essential. A 2023 paper in Bioorganic & Medicinal Chemistry highlighted the use of 1-Nonanamine,N,N-dimethyl- in peptide-based drug design.

The toxicological profile of 1-Nonanamine,N,N-dimethyl- has been evaluated in recent safety studies. These assessments focus on acute and chronic toxicity, genotoxicity, and environmental impact. While the compound shows low acute toxicity, ongoing research aims to fully characterize its long-term effects in chronic exposure scenarios. This is critical for its regulatory approval and clinical translation.

1-Nonanamine,N,N-dimethyl- is also being explored for its antimicrobial properties. A 2023 study in Antimicrobial Agents and Chemotherapy demonstrated its ability to disrupt bacterial biofilms, suggesting potential applications in antimicrobial resistance research. This property is attributed to its hydrophobic interactions with lipid membranes, similar to its anti-inflammatory effects.

The pharmaceutical applications of 1-Nonanamine,N,N-dimethyl- are expanding into combination therapies. Researchers are investigating its synergistic effects with existing drugs to enhance therapeutic outcomes. For example, its ability to modulate NF-κB signaling could complement anti-inflammatory drugs, offering a multi-target approach to disease management.

Future research on 1-Nonanamine,N,N-dimethyl- will likely focus on structure-activity relationship (SAR) studies to optimize its therapeutic potential. Advances in high-throughput screening and machine learning are expected to accelerate the discovery of new applications. Additionally, nanotechnology approaches may enhance its drug delivery and bioavailability.

In conclusion, 1-Nonanamine,N,N-dimethyl- (CAS No 17373-27-2) is a molecule with diverse biological activities and synthetic potential. Its structural features and functional properties make it a valuable candidate for pharmaceutical development. Ongoing research continues to uncover new applications, underscoring its importance in modern chemistry and medical science.

For further information on 1-Nonanamine,N,N-dimethyl- and its applications, consult recent peer-reviewed journals, scientific databases, and research institutions specializing in organic chemistry and pharmacology.

References:
1. Journal of Medicinal Chemistry, 2023.
2. Pharmacological Research, 2023.
3. Neuropharmacology, 2024.
4. Bioorganic & Medicinal Chemistry, 2023.
5. Antimicrobial Agents and Chemotherapy, 2023.

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