Cas no 14703-69-6 (3-(Methylamino)phenol)

3-(Methylamino)phenol is an organic compound with the molecular formula C?H?NO, featuring a phenolic hydroxyl group and a methylamino substituent. This compound serves as a versatile intermediate in organic synthesis, particularly in the production of dyes, pharmaceuticals, and specialty chemicals. Its reactive functional groups enable selective modifications, making it valuable for constructing complex molecular architectures. The methylamino group enhances solubility in polar solvents, facilitating its use in aqueous or mixed-phase reactions. With a well-defined structure and consistent purity, 3-(Methylamino)phenol is suitable for applications requiring precise chemical functionality. Proper handling is advised due to potential sensitivity to oxidation and reactivity under acidic or basic conditions.
3-(Methylamino)phenol structure
3-(Methylamino)phenol structure
Product Name:3-(Methylamino)phenol
CAS No:14703-69-6
MF:C7H9NO
MW:123.152461767197
MDL:MFCD16998628
CID:96559
PubChem ID:10820513
Update Time:2025-11-02

3-(Methylamino)phenol Chemical and Physical Properties

Names and Identifiers

    • 3-(Methylamino)phenol
    • 3-?(Methylamino)?phenol
    • Phenol, 3-(methylamino)-
    • N-Methyl-m-aminophenol
    • N-Methyl-m-hydroxyaniline
    • m-(Methylamino)phenol
    • m-Hydroxy-N-methylaniline
    • 3-Methylamino-phenol
    • 3-(N-methylamino)phenol
    • 3 -(methylamino)phenol
    • KLLOEOPUXBJSOW-UHFFFAOYSA-N
    • SCHEMBL54893
    • DTXSID70445267
    • 14703-69-6
    • C72795
    • MFCD16998628
    • MB25493
    • DS-18349
    • Z1082872246
    • 3-methylaminophenol
    • A911449
    • 3- (N-methylamino) phenol
    • EN300-79043
    • AKOS012390550
    • CS-0151034
    • XH1336
    • DB-330834
    • MDL: MFCD16998628
    • Inchi: 1S/C7H9NO/c1-8-6-3-2-4-7(9)5-6/h2-5,8-9H,1H3
    • InChI Key: KLLOEOPUXBJSOW-UHFFFAOYSA-N
    • SMILES: OC1=CC=CC(=C1)NC

Computed Properties

  • Exact Mass: 123.06847
  • Monoisotopic Mass: 123.068413911g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 9
  • Rotatable Bond Count: 1
  • Complexity: 85
  • 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: 1.6
  • Topological Polar Surface Area: 32.3?2

Experimental Properties

  • Density: 1.147±0.06 g/cm3 (20 oC 760 Torr),
  • Solubility: Slightly soluble (7.6 g/l) (25 o C),
  • PSA: 32.26

3-(Methylamino)phenol Security Information

3-(Methylamino)phenol Pricemore >>

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3-(Methylamino)phenol Related Literature

Additional information on 3-(Methylamino)phenol

Comprehensive Guide to 3-(Methylamino)phenol (CAS No. 14703-69-6): Properties, Applications, and Industry Insights

3-(Methylamino)phenol (CAS No. 14703-69-6), also known as m-Methylaminophenol, is an organic compound widely used in various industrial and research applications. This aromatic amine derivative has gained significant attention due to its unique chemical properties and versatility. With the growing interest in specialty chemicals and fine intermediates, 3-(Methylamino)phenol has become a subject of increasing research and commercial importance.

The molecular structure of 3-(Methylamino)phenol features both hydroxyl and methylamino functional groups on a benzene ring, making it particularly valuable for synthetic applications. This compound typically appears as a white to light brown crystalline powder with a molecular weight of 123.15 g/mol. Its solubility profile includes good solubility in water and common organic solvents, which enhances its utility in various formulations.

One of the primary applications of 3-(Methylamino)phenol is in the field of hair dye formulations, where it serves as an important intermediate for oxidative hair coloring products. Recent trends in the personal care industry show growing demand for more stable and safer dye intermediates, positioning 3-(Methylamino)phenol as a valuable component in modern cosmetic chemistry. The compound's ability to form stable color complexes when oxidized makes it particularly useful in permanent hair color systems.

Beyond cosmetic applications, 3-(Methylamino)phenol finds use in pharmaceutical synthesis as a building block for various active pharmaceutical ingredients (APIs). Researchers have explored its potential in developing novel therapeutic agents, particularly in neurological and cardiovascular drug development. The compound's structural features make it suitable for creating molecules with specific biological activities.

In the field of material science, 3-(Methylamino)phenol serves as a monomer or modifier for specialty polymers. Its incorporation into polymer chains can impart specific properties such as enhanced thermal stability or modified solubility characteristics. Recent advancements in polymer chemistry have highlighted the potential of amine-containing phenols like 3-(Methylamino)phenol in creating advanced materials for electronics and coatings.

The global market for 3-(Methylamino)phenol has shown steady growth, driven by increasing demand from end-use industries. Market analysis indicates particular growth in Asia-Pacific regions, where the personal care and pharmaceutical sectors are expanding rapidly. Quality standards for 3-(Methylamino)phenol typically require high purity levels (often >98%), with strict control over impurities that might affect downstream applications.

From a safety perspective, proper handling procedures should be followed when working with 3-(Methylamino)phenol. While not classified as highly hazardous, standard laboratory precautions including proper ventilation and personal protective equipment are recommended. The compound's Material Safety Data Sheet (MSDS) provides detailed information about handling, storage, and disposal requirements.

Recent research has explored green chemistry approaches to the synthesis of 3-(Methylamino)phenol, aiming to reduce environmental impact and improve process efficiency. These developments align with broader industry trends toward sustainable chemical production. Novel catalytic methods and alternative reaction media are being investigated to optimize the manufacturing process for this valuable intermediate.

Analytical characterization of 3-(Methylamino)phenol typically involves techniques such as HPLC, GC-MS, and NMR spectroscopy. Quality control protocols emphasize the importance of verifying purity and identifying potential byproducts or degradation products. These analytical methods ensure that the material meets the stringent requirements of various application sectors.

The future outlook for 3-(Methylamino)phenol appears promising, with potential new applications emerging in areas such as advanced materials and specialty chemicals. Ongoing research continues to uncover novel uses for this versatile compound, while process optimization efforts aim to make its production more economical and environmentally friendly. As industries continue to demand high-performance intermediates, 3-(Methylamino)phenol (CAS No. 14703-69-6) is well-positioned to maintain its importance in chemical synthesis and product formulation.

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