Cas no 29812-79-1 (O-decylhydroxylamine)

O-Decylhydroxylamine is a hydroxylamine derivative featuring a decyl (C10) alkyl chain, offering a balance of lipophilicity and reactivity. This compound is commonly employed as a radical scavenger, polymerization inhibitor, and intermediate in organic synthesis. Its long alkyl chain enhances solubility in nonpolar media, making it suitable for applications in hydrocarbon-based systems. The hydroxylamine functional group provides effective antioxidant properties, inhibiting oxidative degradation in polymers, fuels, and lubricants. O-Decylhydroxylamine is also utilized in photoresist formulations and as a stabilizer in industrial processes where controlled radical reactions are critical. Its stability and selective reactivity make it a valuable tool in both research and industrial settings.
O-decylhydroxylamine structure
O-decylhydroxylamine structure
Product Name:O-decylhydroxylamine
CAS No:29812-79-1
MF:C10H23NO
MW:173.295723199844
MDL:MFCD21920915
CID:289659
PubChem ID:34704
Update Time:2025-06-08

O-decylhydroxylamine Chemical and Physical Properties

Names and Identifiers

    • Hydroxylamine, O-decyl-
    • O-Decylhydroxylamine
    • MQNAOOIFODUDES-UHFFFAOYSA-N
    • decyloxyamine
    • O-decyl-hydroxylamine
    • AT37841
    • NS00123549
    • AKOS017981930
    • MFCD21920915
    • SCHEMBL6725430
    • Q63409742
    • SY281732
    • A1-51525
    • EN300-1851870
    • 29812-79-1
    • DTXSID6074704
    • O-decylhydroxylamine
    • MDL: MFCD21920915
    • Inchi: 1S/C10H23NO/c1-2-3-4-5-6-7-8-9-10-12-11/h2-11H2,1H3
    • InChI Key: MQNAOOIFODUDES-UHFFFAOYSA-N
    • SMILES: O(CCCCCCCCCC)N

Computed Properties

  • Exact Mass: 173.17809
  • Monoisotopic Mass: 173.178
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 12
  • Rotatable Bond Count: 9
  • Complexity: 76.2
  • 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: 4.4
  • Topological Polar Surface Area: 35.2A^2

Experimental Properties

  • Density: 0.85
  • Boiling Point: 254.7°Cat760mmHg
  • Flash Point: 99.4°C
  • Refractive Index: 1.439
  • PSA: 35.25

O-decylhydroxylamine Pricemore >>

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Additional information on O-decylhydroxylamine

Professional Introduction to Compound with CAS No. 29812-79-1 and Product Name: O-decylhydroxylamine

Compound with the CAS number 29812-79-1 and the product name O-decylhydroxylamine represents a significant advancement in the field of specialty chemicals, particularly in pharmaceutical and biochemical applications. This compound, characterized by its unique molecular structure, has garnered considerable attention due to its versatile utility in synthetic chemistry and as an intermediate in the development of novel therapeutic agents.

The molecular formula of O-decylhydroxylamine is C??H??NO, reflecting its composition of a decyl group attached to a hydroxylamine moiety. This structural configuration imparts distinct chemical properties that make it invaluable in various industrial and research settings. The long hydrocarbon chain enhances solubility in organic solvents, while the hydroxylamine group provides reactivity suitable for nucleophilic substitution reactions, oxidation processes, and the synthesis of more complex molecules.

In recent years, O-decylhydroxylamine has been extensively studied for its potential applications in drug development. Its ability to act as a chiral auxiliary or a ligand in catalytic systems has opened new avenues for asymmetric synthesis, a critical aspect in producing enantiomerically pure pharmaceuticals. For instance, researchers have leveraged O-decylhydroxylamine to develop novel catalysts that facilitate the conversion of prochiral substrates into high-value chiral intermediates, thereby streamlining the synthesis of active pharmaceutical ingredients (APIs).

Moreover, the compound's role in biochemical research cannot be overstated. Its derivatives have been employed in studying enzyme mechanisms and developing inhibitors targeting specific metabolic pathways. A notable application involves its use as a precursor in synthesizing protease inhibitors, which are pivotal in treating chronic inflammatory diseases and viral infections. The long hydrocarbon tail of O-decylhydroxylamine allows for effective membrane penetration, making it an ideal candidate for designing membrane-targeting agents that can modulate cellular processes at the molecular level.

Recent advancements in green chemistry have also highlighted the importance of O-decylhydroxylamine as an environmentally friendly reagent. Its biodegradability and low toxicity profile make it an attractive alternative to traditional synthetic reagents that often require harsh conditions or generate hazardous byproducts. In one such study, researchers demonstrated the use of O-decylhydroxylamine in solvent-free reactions, reducing waste generation and energy consumption while maintaining high yields of desired products. This aligns with global efforts to promote sustainable chemical practices.

The compound's versatility extends to material science as well. Researchers have explored its potential in developing novel polymers and coatings with enhanced durability and functionality. The hydroxylamine group can participate in cross-linking reactions, creating polymers with improved thermal stability and mechanical strength. These materials find applications in automotive components, aerospace engineering, and protective coatings for electronics.

In conclusion, O-decylhydroxylamine (CAS No. 29812-79-1) stands as a testament to the ingenuity of modern chemical research. Its unique properties make it indispensable in pharmaceutical synthesis, biochemical studies, green chemistry initiatives, and material science applications. As scientific understanding progresses, it is anticipated that new uses for this compound will continue to emerge, further solidifying its role as a cornerstone molecule in industrial and academic research.

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