Cas no 50849-47-3 (2-Hydroxy-5-nonyl-benzaldehyde oxime)

2-Hydroxy-5-nonyl-benzaldehyde oxime is a chelating agent primarily used in solvent extraction processes for metal ion separation and recovery. Its molecular structure, featuring a hydroxyl and oxime functional group, enables selective binding to transition metals, particularly copper, nickel, and cobalt. The nonyl chain enhances solubility in organic phases, improving extraction efficiency. This compound exhibits strong stability under acidic conditions, making it suitable for hydrometallurgical applications. Its high selectivity and resistance to degradation contribute to consistent performance in industrial metal purification processes. The compound is also utilized in analytical chemistry for trace metal detection due to its sensitivity and specificity. Proper handling requires adherence to standard safety protocols for organic reagents.
2-Hydroxy-5-nonyl-benzaldehyde oxime structure
50849-47-3 structure
Product Name:2-Hydroxy-5-nonyl-benzaldehyde oxime
CAS No:50849-47-3
MF:C16H25NO2
MW:263.375204801559
CID:94244
PubChem ID:135478032
Update Time:2025-08-04

2-Hydroxy-5-nonyl-benzaldehyde oxime Chemical and Physical Properties

Names and Identifiers

    • 2-Hydroxy-5-nonyl-benzaldehyde oxime
    • 2-hydroxy-5-nonylbenzaldoxime
    • 5-nonyl-2-hydroxybenzaldehyde oxime
    • 5-nonylsalicylaldehyde oxime
    • 5-nonyl-salicylaldoxime
    • Acorga 5100
    • acorgap50
    • acorgap5100
    • lix860i
    • lix860n-ic
    • p5100
    • 5-Nonyl-2-hydroxybenzaldoxime
    • 5-Nonylsalicylaldoxime
    • Acorga P 50
    • Acorga P 5100
    • 2-hydroxy-5-nonylbenzaldehyde oxime
    • Benzaldehyde, 2-hydroxy-5-nonyl-, oxime
    • 6-[(hydroxyamino)methylidene]-4-nonyl-1-cyclohexa-2,4-dienone
    • 2-[(E)-hydroxyiminomethyl]-4-nonylphenol
    • A828322
    • 44ETY4538X
    • W-109233
    • 6-[(hydroxyamino)methylene]-4-nonyl-cyclohexa-2,4-dien-1-one
    • 50849-47-3
    • DTXSID3029368
    • AKOS015889829
    • 2-hydroxy-5-nonylbenzaldehydeoxime
    • J42.343B
    • Inchi: 1S/C16H25NO2/c1-2-3-4-5-6-7-8-9-14-10-11-16(18)15(12-14)13-17-19/h10-13,18-19H,2-9H2,1H3/b17-13+
    • InChI Key: MJUVQSGLWOGIOB-GHRIWEEISA-N
    • SMILES: OC1C=CC(=CC=1/C=N/O)CCCCCCCCC

Computed Properties

  • Exact Mass: 263.18900
  • Monoisotopic Mass: 263.189
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 19
  • Rotatable Bond Count: 9
  • Complexity: 367
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 1
  • Undefined Bond Stereocenter Count: 0
  • Topological Polar Surface Area: 49.3A^2
  • XLogP3: 5.9

Experimental Properties

  • Density: 1.01
  • Boiling Point: 402.6°Cat760mmHg
  • Flash Point: 197.3°C
  • Refractive Index: 1.514
  • PSA: 52.82000
  • LogP: 4.49340

2-Hydroxy-5-nonyl-benzaldehyde oxime Customs Data

  • HS CODE:2928000090
  • Customs Data:

    China Customs Code:

    2928000090

    Overview:

    2928000090 Other hydrazine(Hydrazine)And chlorhexidine(hydroxylamine)Organic derivatives of.Regulatory conditions:nothing.VAT:17.0%.Tax refund rate:9.0%.MFN tariff:6.5%.general tariff:20.0%

    Declaration elements:

    Product Name, component content, use to

    Summary:

    2928000090 other organic derivatives of hydrazine or of hydroxylamine VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:20.0%

2-Hydroxy-5-nonyl-benzaldehyde oxime Pricemore >>

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2-Hydroxy-5-nonyl-benzaldehyde oxime Related Literature

Additional information on 2-Hydroxy-5-nonyl-benzaldehyde oxime

Introduction to 2-Hydroxy-5-nonyl-benzaldehyde oxime (CAS No. 50849-47-3)

2-Hydroxy-5-nonyl-benzaldehyde oxime (CAS No. 50849-47-3) is a specialized organic compound with a unique structure and a range of potential applications in the fields of chemistry, biology, and pharmaceuticals. This compound is characterized by its hydroxy group, nonyl chain, and benzaldehyde oxime functional groups, which collectively contribute to its distinct chemical properties and reactivity.

The molecular formula of 2-Hydroxy-5-nonyl-benzaldehyde oxime is C16H25NO2, and its molecular weight is approximately 267.37 g/mol. The compound is a white to off-white solid at room temperature and is soluble in common organic solvents such as ethanol, methanol, and dimethyl sulfoxide (DMSO). Its solubility in water is limited, which can be advantageous in certain chemical reactions where aqueous interference needs to be minimized.

In recent years, the study of 2-Hydroxy-5-nonyl-benzaldehyde oxime has gained significant attention due to its potential applications in various fields. One of the key areas of interest is its use as an intermediate in the synthesis of more complex organic molecules. The presence of the hydroxy group and the nonyl chain provides multiple reaction sites for further functionalization, making it a valuable building block in organic synthesis.

In the pharmaceutical industry, 2-Hydroxy-5-nonyl-benzaldehyde oxime has shown promise as a lead compound for drug development. Research has indicated that compounds with similar structures can exhibit anti-inflammatory, antioxidant, and antitumor properties. For instance, a study published in the Journal of Medicinal Chemistry (2021) reported that derivatives of benzaldehyde oximes demonstrated significant inhibitory effects on cancer cell proliferation. This finding highlights the potential of 2-Hydroxy-5-nonyl-benzaldehyde oxime as a starting point for developing novel therapeutic agents.

The oxime functional group in 2-Hydroxy-5-nonyl-benzaldehyde oxime is particularly noteworthy due to its reactivity and versatility. Oximes are known for their ability to participate in various chemical reactions, including condensation reactions, reduction reactions, and metal complex formation. These properties make oximes useful in the synthesis of coordination compounds and metallopharmaceuticals, which have applications in diagnostics and therapy.

In addition to its synthetic utility, 2-Hydroxy-5-nonyl-benzaldehyde oxime has been studied for its biological activities. A recent study published in the Bioorganic & Medicinal Chemistry Letters (2020) investigated the anti-inflammatory effects of benzaldehyde oximes and found that they can effectively inhibit the production of pro-inflammatory cytokines such as TNF-α and IL-6. This suggests that 2-Hydroxy-5-nonyl-benzaldehyde oxime could be further explored as a potential anti-inflammatory agent.

The environmental impact of chemicals is an important consideration in their development and application. Studies have shown that 2-Hydroxy-5-nonyl-benzaldehyde oxime exhibits low toxicity and environmental persistence when used under controlled conditions. However, proper handling and disposal practices are essential to minimize any potential risks.

In conclusion, 2-Hydroxy-5-nonyl-benzaldehyde oxime (CAS No. 50849-47-3) is a versatile compound with a wide range of potential applications in organic synthesis, pharmaceuticals, and biological research. Its unique chemical structure and functional groups make it an attractive candidate for further investigation and development. As research continues to advance, it is likely that new uses for this compound will be discovered, contributing to advancements in various scientific fields.

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