Cas no 17301-94-9 (4-Methylnonane)

4-Methylnonane is a branched-chain alkane with the molecular formula C??H??, characterized by a methyl group substitution at the fourth carbon of a nonane backbone. This structural feature imparts distinct physicochemical properties, including a lower boiling point and reduced viscosity compared to its linear isomer, n-nonane. It is commonly utilized as a reference standard in chromatography and as a solvent in specialized industrial applications due to its moderate volatility and hydrophobic nature. The compound's branched structure also enhances its stability under thermal and oxidative conditions, making it suitable for use in high-performance fuel formulations and lubricant research. Its well-defined isomer purity ensures reproducibility in analytical and experimental settings.
4-Methylnonane structure
4-Methylnonane structure
Product Name:4-Methylnonane
CAS No:17301-94-9
MF:C10H22
MW:142.281683444977
MDL:MFCD00027289
CID:212385
Update Time:2025-06-10

4-Methylnonane Chemical and Physical Properties

Names and Identifiers

    • Nonane, 4-methyl-
    • 4-Methylnonane
    • 4-Methylnonane1000μg
    • p-Methylnonane
    • (±)-nonane,4-methyl-
    • n-C3H7CH(CH3)(CH2)4CH3
    • 4-METHYLNONANE 98%
    • MDL: MFCD00027289
    • Inchi: 1S/C10H22/c1-4-6-7-9-10(3)8-5-2/h10H,4-9H2,1-3H3
    • InChI Key: IALRSQMWHFKJJA-UHFFFAOYSA-N
    • SMILES: C(C)(CCC)CCCCC

Computed Properties

  • Exact Mass: 142.17200
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 0
  • Heavy Atom Count: 10
  • Rotatable Bond Count: 6
  • Complexity: 57.1
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 1
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Surface Charge: 0
  • Tautomer Count: nothing
  • XLogP3: 5.3

Experimental Properties

  • Color/Form: Uncertain
  • Density: 0.73?g/mL?at 20?°C(lit.)
  • Melting Point: -98.7°C
  • Boiling Point: 165°C
  • Flash Point: Fahrenheit: 111.2 ° f
    Celsius: 44 ° c
  • Refractive Index: n20/D 1.413
  • PSA: 0.00000
  • LogP: 4.00290
  • Solubility: Uncertain

4-Methylnonane Security Information

4-Methylnonane Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
SHANG HAI A LA DING SHENG HUA KE JI GU FEN Co., Ltd.
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TI XI AI ( SHANG HAI ) HUA CHENG GONG YE FA ZHAN Co., Ltd.
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abcr
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4-Methylnonane Production Method

Production Method 1

Reaction Conditions
1.1 Reagents: Hydrogen Catalysts: Alumina ,  Platinum ,  Silica ,  Phosphoric acid ;  60 min, 1 atm, 330 °C
Reference
Microwave synthesis of SAPO-11 materials for long chain n-alkanes hydroisomerization: Effect of physical parameters and chemical gel composition
Bertolo, R.; et al, Applied Catalysis, 2017, 542, 28-37

Production Method 2

Reaction Conditions
1.1 Reagents: Hydrogen Catalysts: Alumina ,  Platinum ,  Silica ,  Phosphoric acid ;  60 min, 1 atm, 330 °C
Reference
Microwave synthesis of SAPO-11 materials for long chain n-alkanes hydroisomerization: Effect of physical parameters and chemical gel composition
Bertolo, R.; et al, Applied Catalysis, 2017, 542, 28-37

Production Method 3

Reaction Conditions
1.1 Catalysts: Sodium oxide ,  Palladium ,  Silica ,  1H-Imidazolium, 1,3-dicyclohexyl-, hydroxide (1:1) Solvents: Water ;  3 h, 482 °C
Reference
Synthesis, Physicochemical Characterization, and Catalytic Evaluation of Fe3+-Containing SSZ-70 Zeolite
Lew, Christopher M. ; et al, ACS Catalysis, 2022, 12(11), 6464-6477

4-Methylnonane Preparation Products

4-Methylnonane Related Literature

Additional information on 4-Methylnonane

Research Brief on 17301-94-9 and 4-Methylnonane: Latest Advances in Chemical and Biomedical Applications

The chemical compound with the CAS number 17301-94-9 and the product name 4-Methylnonane has recently garnered significant attention in the fields of chemical synthesis and biomedical research. This research brief aims to provide an overview of the latest findings related to these substances, focusing on their synthesis, properties, and potential applications in drug development and other biomedical areas.

Recent studies have explored the synthesis and characterization of 4-Methylnonane, a branched alkane with potential applications as a solvent or intermediate in pharmaceutical manufacturing. Researchers have investigated its physicochemical properties, including boiling point, solubility, and stability, which are critical for its use in various chemical processes. Additionally, the compound's low toxicity profile makes it a candidate for further exploration in drug delivery systems.

In the context of CAS 17301-94-9, recent literature highlights its role as a key intermediate in the synthesis of more complex organic molecules. Its unique structural features have been leveraged in the development of novel catalysts and ligands, which are essential for asymmetric synthesis and other advanced chemical transformations. These advancements have implications for the production of enantiomerically pure pharmaceuticals, a growing area of interest in the industry.

One notable study published in 2023 demonstrated the use of 4-Methylnonane as a reaction medium in the synthesis of bioactive compounds. The research showed that the compound's inert nature and ability to dissolve a wide range of organic molecules make it an excellent candidate for green chemistry applications. This aligns with the broader industry trend toward sustainable and environmentally friendly chemical processes.

Further investigations into the biomedical applications of these compounds are ongoing. Preliminary data suggest that derivatives of 17301-94-9 may exhibit antimicrobial or anti-inflammatory properties, though more in vitro and in vivo studies are needed to confirm these effects. The potential for these compounds to serve as scaffolds for new drug candidates is an exciting avenue for future research.

In conclusion, the latest research on 17301-94-9 and 4-Methylnonane underscores their versatility and potential in both chemical and biomedical fields. Continued exploration of their properties and applications could lead to significant advancements in drug development and sustainable chemistry. Researchers are encouraged to further investigate these compounds to unlock their full potential.

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