Cas no 3046-94-4 (N-Butyl-N-2-hydroxyethylaniline)

N-Butyl-N-2-hydroxyethylaniline is an aromatic amine derivative featuring both butyl and hydroxyethyl substituents on the nitrogen atom. This compound is valued for its dual functionality, combining the reactivity of an aniline derivative with the solubility and polarity imparted by the hydroxyethyl group. It serves as a versatile intermediate in organic synthesis, particularly in the production of dyes, pigments, and specialty chemicals. The hydroxyl group enhances its compatibility with polar solvents, while the butyl chain contributes to lipophilic character, making it useful in formulations requiring balanced hydrophilicity-lipophilicity. Its structural features also make it a candidate for applications in polymer chemistry and as a corrosion inhibitor.
N-Butyl-N-2-hydroxyethylaniline structure
3046-94-4 structure
Product Name:N-Butyl-N-2-hydroxyethylaniline
CAS No:3046-94-4
MF:C12H19NO
MW:193.285363435745
CID:43736
PubChem ID:18271
Update Time:2025-11-02

N-Butyl-N-2-hydroxyethylaniline Chemical and Physical Properties

Names and Identifiers

    • 2-(Butyl(phenyl)amino)ethanol
    • N-butyl-N-2-hydroxyethylaniline
    • N-butyl-N-phenylethanolamine
    • 2-(N-BUTYLANILINO)ETHANOL
    • N-Butyl-N-<2-hydroxy-ethyl>-anilin
    • Ethanol, 2-(N-butylanilino)-
    • NS00028928
    • DTXSID3062811
    • N-Hydroxyethyl-N-butylaniline
    • AKOS006242954
    • 2-(Butylanilino)ethanol #
    • N-Butyl-N-hydroxyethylaniline
    • PMRRSCWLXKOMSK-UHFFFAOYSA-N
    • SCHEMBL1674608
    • 2-(butyl(phenyl)amino)ethan-1-ol
    • EINECS 221-253-5
    • Ethanol, 2-(butylphenylamino)-
    • 3046-94-4
    • DTXCID0038203
    • N-Butyl-N-2-hydroxyethylaniline
    • Inchi: 1S/C12H19NO/c1-2-3-9-13(10-11-14)12-7-5-4-6-8-12/h4-8,14H,2-3,9-11H2,1H3
    • InChI Key: PMRRSCWLXKOMSK-UHFFFAOYSA-N
    • SMILES: OCCN(C1C=CC=CC=1)CCCC

Computed Properties

  • Exact Mass: 193.14700
  • Monoisotopic Mass: 193.147
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 14
  • Rotatable Bond Count: 6
  • Complexity: 132
  • 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: 3
  • Topological Polar Surface Area: 23.5A^2

Experimental Properties

  • Density: 1.012
  • Boiling Point: 310.6°Cat760mmHg
  • Flash Point: 140.5°C
  • Refractive Index: 1.547
  • PSA: 23.47000
  • LogP: 2.28540

N-Butyl-N-2-hydroxyethylaniline Customs Data

  • HS CODE:2922199090
  • Customs Data:

    China Customs Code:

    2922199090

    Overview:

    2922199090. Other amino alcohols and their ethers,Esters and their salts(Except those containing more than one oxygen-containing group). VAT:17.0%. Tax refund rate:13.0%. Regulatory conditions:nothing. MFN tariff:6.5%. general tariff:30.0%

    Declaration elements:

    Product Name, component content, use to, The color of ethanolamine and its salt should be reported, The package of ethanolamine and its salt shall be declared

    Summary:

    2922199090. other amino-alcohols, other than those containing more than one kind of oxygen function, their ethers and esters; salts thereof. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

N-Butyl-N-2-hydroxyethylaniline Pricemore >>

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Additional information on N-Butyl-N-2-hydroxyethylaniline

Recent Advances in the Study of N-Butyl-N-2-hydroxyethylaniline (CAS: 3046-94-4) in Chemical and Biomedical Applications

N-Butyl-N-2-hydroxyethylaniline (CAS: 3046-94-4) is an important chemical compound with diverse applications in the fields of organic synthesis, pharmaceuticals, and materials science. Recent studies have explored its potential as a key intermediate in the synthesis of novel bioactive molecules and its role in advanced material development. This research brief aims to provide an overview of the latest findings related to this compound, highlighting its significance in current chemical and biomedical research.

One of the most notable advancements in the study of N-Butyl-N-2-hydroxyethylaniline is its application in the development of new pharmaceutical agents. Researchers have identified its utility as a precursor in the synthesis of compounds with potential therapeutic effects, particularly in the areas of anti-inflammatory and antimicrobial agents. Recent publications have demonstrated that modifications to the hydroxyethyl and butyl groups can significantly alter the biological activity of the resulting derivatives, opening new avenues for drug discovery.

In addition to its pharmaceutical applications, N-Butyl-N-2-hydroxyethylaniline has been investigated for its role in material science. Studies have shown that this compound can be used as a building block for the synthesis of advanced polymers and coatings with unique properties, such as enhanced durability and biocompatibility. These materials have potential applications in medical devices, drug delivery systems, and other biomedical technologies.

The chemical properties of N-Butyl-N-2-hydroxyethylaniline, including its solubility, reactivity, and stability, have been the subject of recent investigations. Advanced spectroscopic and computational techniques have been employed to elucidate its molecular structure and interactions, providing valuable insights for its optimization in various applications. These studies have also highlighted the importance of controlling reaction conditions to achieve high yields and purity of the desired products.

Despite the promising findings, challenges remain in the large-scale production and application of N-Butyl-N-2-hydroxyethylaniline. Issues such as cost-effectiveness, environmental impact, and scalability need to be addressed to fully realize its potential. Ongoing research is focused on developing greener synthesis methods and exploring novel applications that leverage its unique chemical properties.

In conclusion, N-Butyl-N-2-hydroxyethylaniline (CAS: 3046-94-4) continues to be a compound of significant interest in chemical and biomedical research. Its versatility as an intermediate and its potential in drug discovery and material science make it a valuable subject for further study. Future research should aim to overcome existing challenges and expand its applications in innovative ways.

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