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Home > Chemical Reagents > Organic Reagents > N-(3-dimethylaminopropyl)-2-ethyl-hexanamide for Sale > pure N-(3-dimethylaminopropyl)-2-ethyl-hexanamide
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pure N-(3-dimethylaminopropyl)-2-ethyl-hexanamide

2 Inquiries

Unit Price: Get Latest Price
CAS No.:

6325-18-4

Grade:

Industrial Grade

Port:

rotterdam

Packaging:

bags

Price valid (until):

2025-01-18

Company Type:
Distributor
Location:
Netherlands
Qualification:
Main Products:

ethanol,ascorbic acid,acetone,Poly(ethylene) LDPE,Polypropylene,sodium carbonate

  • Product Description

  • Seller Information

  • Inquiry History

  • Description


     

    N-(3-Dimethylaminopropyl)-2-ethylhexanamide is a chemical compound that contains both an amide group and a dimethylamino group, typically used in various industrial and chemical applications. This compound can be classified as an amide due to the presence of the -C=O-N group, with the structure incorporating a dimethylamino group attached to a propyl chain.

    Chemical Structure:

    The structure of N-(3-dimethylaminopropyl)-2-ethylhexanamide can be described as follows:

    • Amide Group: The central feature of the molecule is the amide group (-C=O-N), which consists of a carbonyl group (C=O) bonded to a nitrogen atom (N) that is also bonded to a 3-dimethylaminopropyl group.
    • Dimethylaminopropyl Group: The nitrogen of the amide group is connected to a 3-dimethylaminopropyl group, which consists of a three-carbon chain with a dimethylamino group (-N(CH₃)₂) on the third carbon.
    • 2-Ethylhexane Backbone: The rest of the structure is based on a 2-ethylhexane chain (a branched six-carbon chain with an ethyl group attached to the second carbon).

    The chemical formula for this compound is C₁₀H₂₁NO₂.

    Key Functional Groups:

    1. Amide Group (-C=O-N): The amide linkage is a carbonyl group bonded to a nitrogen, which is typical of many biologically active molecules and industrial chemicals.
    2. Dimethylamino Group (-N(CH₃)₂): A nitrogen atom bonded to two methyl groups (CH₃), which is characteristic of compounds that can act as tertiary amines. This group often imparts basicity and can be involved in various types of chemical reactivity or interactions.
    3. Ethylhexane Backbone: The 2-ethylhexane portion provides hydrophobic characteristics, making the compound potentially useful in applications where solubility in non-polar solvents or oils is needed.

    Potential Applications:

    1. Cosmetic and Personal Care Products:

      • Amides with Dimethylamino Groups: Compounds like N-(3-dimethylaminopropyl)-2-ethylhexanamide are often used as surfactants, emulsifiers, or conditioning agents in cosmetic formulations. The dimethylamino group can contribute to the compound's ability to interact with skin or hair, making it useful in products like shampoos, conditioners, and skin care formulations.
    2. Chemical Intermediate:

      • As an amide with a dimethylamino group, this compound may be used as an intermediate in the production of other chemicals, including pharmaceuticals, agrochemicals, or polymers.
    3. Surfactants and Detergents:

      • The structure suggests that it could be used as a surfactant in cleaning or industrial applications. Surfactants with both hydrophilic and hydrophobic groups (such as this compound) are effective at reducing surface tension and facilitating emulsification.
    4. Polymer and Coating Industry:

      • The presence of both the amide and the hydrophobic 2-ethylhexane group could make this compound useful in the production of specialty coatings, adhesives, or polymeric materials where a balance of solubility and reactivity is needed.
    5. Potential Biological Activity:

      • The dimethylamino group is often found in compounds that exhibit biological activity due to its ability to interact with biological membranes or enzymes. Therefore, compounds like N-(3-dimethylaminopropyl)-2-ethylhexanamide might have potential as a pharmaceutical agent, though this would require more specific research into its biological properties.

    Chemical Properties:

    • Basicity: The dimethylamino group imparts a basic nature to the compound, meaning it could accept protons and form salts with acids.
    • Reactivity: The compound may participate in typical reactions of amides and amines, such as nucleophilic substitution, hydrolysis, or reactions with electrophiles.
    • Solubility: It is likely to be soluble in polar organic solvents due to the presence of the amide and amine groups, while the 2-ethylhexane part may make it somewhat soluble in non-polar solvents as well.

    Safety and Handling:

    • Toxicity: As with many chemical compounds containing amine and amide groups, proper handling is necessary. Exposure to amines can cause irritation to the skin, eyes, or respiratory system, and amides may also have varying degrees of toxicity depending on their structure.
    • Safety: Personal protective equipment (PPE) like gloves and goggles should be used when handling this compound, especially in industrial or laboratory settings.

    Summary:

    N-(3-dimethylaminopropyl)-2-ethylhexanamide is a versatile compound with a dimethylamino group attached to a propyl chain and an amide group. It has potential applications in cosmetics, surfactants, polymers, and chemical synthesis, as well as possibly having biological activity. The presence of both hydrophobic (2-ethylhexane) and hydrophilic (amide and dimethylamino) groups makes it a candidate for use in formulations requiring surface-active or emulsifying properties. However, handling should be done with care due to its chemical reactivity and potential toxicity.

     


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    Items Specifications






    Basic Info
    Product Name:

    N-(3-dimethylaminopropyl)-2-ethyl-hexanamide

    Other Name:

    n-[3-(dimethylamino)propyl]-2-ethylhexanamide;NSC29722;N-(3-DIMETHYLAMINOPROPYL)-2-ETHYL-HEXANAMIDE;SCHEMBL4601722;CTK2F8900;DTXSID70283106;NSC-29722;AKOS003798293

    CAS No.:

    6325-18-4

    Molecular Formula:

    C13H28N2O

    InChIKeys:

    YHKAXGJQOPRDPZ-UHFFFAOYSA-N

    Molecular Weight:

    228.37

    Exact Mass:

    228.220163521

    NSC Number:

    29722

    DSSTox ID:

    DTXSID70283106

    Categories:

    Organic Reagents

    Characteristics

    Hazard Identification

    Classification of the substance or mixture

    no data available

    GHS label elements, including precautionary statements

    Pictogram(s) no data available
    Signal word

    no data available

    Hazard statement(s)

    no data available

    Precautionary statement(s)
    Prevention

    no data available

    Response

    no data available

    Storage

    no data available

    Disposal

    no data available

    Other hazards which do not result in classification

    no data available

    Handling and Storage

    Precautions for safe handling

    Handling in a well ventilated place. Wear suitable protective clothing. Avoid contact with skin and eyes. Avoid formation of dust and aerosols. Use non-sparking tools. Prevent fire caused by electrostatic discharge steam.

    Conditions for safe storage, including any incompatibilities

    Store the container tightly closed in a dry, cool and well-ventilated place. Store apart from foodstuff containers or incompatible materials.

  • Seller Information
    Business Type:

    Distributor

    Main Products:

    ethanol,ascorbic acid,acetone,Poly(ethylene) LDPE,Polypropylene,sodium carbonate

    Location:

    Admiraal Banckertweg 12 2315 SR, Leiden, Zuid-Holland

    Payment Terms:

    TT against copy of documents,L/C,TT against B/L draft before shipment

    Average lead Time:

    45

    Total Annual Revenue:

    $1 million-$2.5 million

    Total Employees:

    11-50

    Year of Establishment:

    2010

    Certifications:

    business

  • Inquiry History
    2 Inquiries
    Country Product Purchase Quantity Date Posted
    Argentina

    N-(3-dimethylaminopropyl)-2-ethyl-hexanamide TECHNICAL GRADE

    10 MT Dec 23, 2024
    Argentina

    N-(3-dimethylaminopropyl)-2-ethyl-hexanamide

    20 MT Dec 17, 2024
    Post an enquiry for this product
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