Production Method 1

5911-04-6

17301-94-9

871-83-0

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

5911-04-6

15869-85-9

17301-94-9

871-83-0

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

5911-04-6

15869-85-9

17301-94-9

871-83-0

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

3-Methylnonane Preparation Products

• Nonane, 5-methyl- (15869-85-9)
• 4-Methylnonane (17301-94-9)
• 3-Methylnonane (5911-04-6)
• 2-Methylnonane (871-83-0)

• 1. Evolution of important glucosinolates in three common Brassica vegetables during their processing into vegetable powder and in vitro gastric digestion
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• 3. Evolution of calcium phosphate precipitation in hanging drop vapor diffusion by in situRaman microspectroscopy
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• 4. Establishment and implications of a characterization method for magnetic nanoparticle using cell tracking velocimetry and magnetic susceptibility modified solutions
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• 5. Evolution in surface coverage of CH3NH3PbI3?XClXvia heat assisted solvent vapour treatment and their effects on photovoltaic performance of devices
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• Solvents and Organic Chemicals Organic Compounds Hydrocarbons Saturated hydrocarbons Branched alkanes
• Solvents and Organic Chemicals Organic Compounds Hydrocarbons Saturated hydrocarbons Alkanes Branched alkanes
• Solvents and Organic Chemicals Organic Compounds Hydrocarbons
• Other Chemical Reagents

Introduction to 3-Methylnonane (CAS No. 5911-04-6)

3-Methylnonane, also known by its chemical name 3-methylnonane, is an organic compound belonging to the alkane family. With the CAS number 5911-04-6, this molecule is characterized by a straight-chain hydrocarbon structure containing nine carbon atoms and eighteen hydrogen atoms, with a methyl group attached to the third carbon. This specific arrangement imparts unique chemical and physical properties that make it of significant interest in various industrial and research applications.

The molecular formula of 3-methylnonane is C?H??, reflecting its aliphatic nature. As a saturated hydrocarbon, it exhibits low reactivity under normal conditions, which is typical for alkanes. However, its structural versatility allows for diverse functionalization, making it a valuable intermediate in synthetic chemistry. The presence of the methyl group at the third carbon position influences its boiling point, density, and solubility characteristics compared to its isomers.

In recent years, 3-methylnonane has garnered attention in the field of polymer science and material engineering. Its linear structure and moderate molecular weight make it an excellent candidate for blending with other monomers to enhance the properties of polymers used in coatings, adhesives, and lubricants. Research has demonstrated that incorporating 3-methylnonane into polymer matrices can improve thermal stability and mechanical strength, which are critical factors in high-performance materials.

Moreover, the compound has found applications in the fragrance and flavor industry due to its contribution to the aroma profile of certain synthetic scents. Its relatively simple structure allows for easy modification, enabling chemists to tailor its olfactory characteristics for use in perfumes, soaps, and other consumer products. The growing demand for natural-looking fragrances has spurred interest in synthesizing compounds like 3-methylnonane that mimic organic notes found in essential oils.

From an environmental perspective, 3-methylnonane is being explored as a potential biofuel additive. Its compatibility with existing petroleum-based fuel infrastructure makes it a promising candidate for blending with gasoline or diesel to improve combustion efficiency and reduce emissions. Studies have shown that additives like 3-methylnonane can enhance the octane rating of fuels while maintaining low toxicity profiles, aligning with global efforts to develop cleaner energy solutions.

The synthesis of 3-methylnonane typically involves catalytic cracking or fractional distillation of larger hydrocarbon fractions derived from crude oil refining. Advances in catalytic processes have enabled more efficient production methods, reducing waste and energy consumption. Researchers are also investigating biotechnological routes to produce alkanes like 3-methylnonane through microbial fermentation using renewable feedstocks, which could further reduce reliance on fossil fuels.

In academic research, 3-methylnonane serves as a model compound for studying reaction mechanisms and spectroscopic techniques. Its well-defined structure allows chemists to probe interactions between molecules at a molecular level, providing insights into fundamental processes in organic chemistry. For instance, computational studies have utilized 3-methylnonane as a reference point to predict the behavior of more complex hydrocarbons under various conditions.

The safety profile of 3-methylnonane is another area of active investigation. While it is generally considered non-toxic at low concentrations, prolonged exposure or improper handling may pose health risks typical of hydrocarbons. Industrial guidelines recommend proper ventilation and personal protective equipment when working with this compound to minimize inhalation or dermal exposure. Regulatory bodies continue to monitor its use to ensure compliance with occupational health standards.

Future research directions for 3-methylnonane include exploring its role in nanotechnology and advanced material design. Its ability to form stable self-assembled structures makes it a candidate for use in nanocarriers or as a solvent in high-performance liquid chromatography (HPLC) systems. By leveraging its unique properties, scientists aim to develop innovative solutions for drug delivery systems and analytical chemistry applications.

In conclusion,3-Methylnonane (CAS No. 5911-04-6) is a versatile hydrocarbon with broad applicability across multiple industries. From enhancing polymer performance to contributing to sustainable energy solutions,3-Methylnonane continues to be a subject of interest in both industrial and academic research. As technology advances,3-Methylnonane is poised to play an even greater role in shaping future innovations in chemistry and materials science.

• 62108-21-8(Decane,6-ethyl-2-methyl-)
• 76275-83-7(Tetracosane, 4-methyl-)
• 62016-34-6(Octane,2,3,7-trimethyl-)
• 65431-89-2(Octadecane,7,11-dimethyl-)
• 76535-46-1(Tetratriacontane, 13,17-dimethyl-)
• 76535-35-8(Tetratriacontane, 13-methyl-)
• 76535-45-0(Tetratriacontane, 11,15-dimethyl-)
• 76535-41-6(Hentetracontane, 13,17-dimethyl-)
• 76535-33-6(Nonacosane, 7-methyl-)
• 3074-77-9(Hexane,3-ethyl-4-methyl-)