Production Method 1

94259-20-8

Reaction Conditions

1.1 Reagents: Potassium carbonate Solvents: Dimethylformamide ;  rt → 70 °C
1.2 70 °C; 15 h, 80 °C

Reference

Preparation of phenylethylamine derivatives as antimicrobials for treatment of surfaces

, World Intellectual Property Organization, , ,

Production Method 2

94259-20-8

Reaction Conditions

1.1 Reagents: Potassium carbonate Catalysts: Potassium iodide Solvents: Ethanol ;  60 h, 85 °C

Reference

Method for synthesizing discotic liquid crystal material of triphenylene decaneoxy bridged perylene tetracarboxylic butyl ester

, China, , ,

Production Method 3

94259-20-8

Reaction Conditions

1.1 Reagents: Potassium carbonate Catalysts: Potassium iodide Solvents: Ethanol ;  60 h, 85 °C

Reference

Preparation of triphenylene hexyloxy bridging isooctane oxy phenyl porphyrin ternary compound as discotic liquid crystal material

, China, , ,

Production Method 4

94259-20-8

Reaction Conditions

1.1 Reagents: Potassium carbonate Solvents: Dimethylformamide ;  2 h, 110 °C

Reference

Tetrabenzotetracenes, their preparation method, and their use for organic semiconductor films and elements and transistors

, Japan, , ,

Production Method 5

94259-20-8

Reaction Conditions

1.1 Reagents: Potassium carbonate Solvents: Acetone ;  rt; 48 h, reflux

Reference

A new family of bent-core C2-symmetric liquid crystals

Hope-Ross, Kyle A.; Heiney, Paul A.; Kadla, John F., Canadian Journal of Chemistry, 2010, 88(7), 639-645

Production Method 6

94259-20-8

Reaction Conditions

1.1 Reagents: Potassium carbonate Catalysts: Potassium iodide Solvents: Ethanol ;  24 h, reflux

Reference

Perylene monoimide dicarboxylic acid diester-flexible bridge-benzophenanthrene dendrimer, and preparation method thereof

, China, , ,

Production Method 7

94259-20-8

Reaction Conditions

1.1 Reagents: Potassium carbonate Catalysts: Potassium iodide Solvents: Ethanol ,  Hexane ;  1 h, rt; rt → reflux; 24 h, reflux

Reference

Synthesis method of dodecyloxyphenylporphyrin benzamide octane imine-perylene-decane imine hexyloxybenzophenanthrene ternary compound applied in organic solar cell and organic light emitting diode

, China, , ,

Production Method 8

94259-20-8

Reaction Conditions

1.1 Reagents: Potassium carbonate Catalysts: Potassium iodide Solvents: Ethanol ;  60 h, 85 °C

Reference

Synthesis of benzophenanthrene dodecyl bridged ethyl perylene tetraformate binary discotic liquid crystals

, China, , ,

Production Method 9

94259-20-8

Reaction Conditions

1.1 Reagents: Potassium carbonate Catalysts: Potassium iodide Solvents: Ethanol ;  60 h, 85 °C

Reference

Synthesis of triphenylene decyl bridged ethyl perylene-tetracarboxylate binary discotic liquid crystal material

, China, , ,

Production Method 10

94259-20-8

Reaction Conditions

1.1 Reagents: Potassium carbonate Catalysts: Potassium iodide Solvents: Ethanol ;  60 h, 85 °C

Reference

Synthetic method of hexyloxy benzophenanthrene-bridged isooctyloxyphenyl porphyrin metal zinc complex

, China, , ,

Production Method 11

94259-20-8

Reaction Conditions

1.1 Reagents: Potassium carbonate Catalysts: Potassium iodide Solvents: Ethanol ;  60 h, 85 °C

Reference

Synthesis method of benzophenanthrene dodecyloxy bridged isooctyloxyphenyl porphyrin metal zinc complex

, China, , ,

Production Method 12

94259-20-8

Reaction Conditions

1.1 Reagents: Potassium carbonate Catalysts: Potassium iodide Solvents: Ethanol ;  60 h, 85 °C

Reference

Synthetic method of benzophenanthrene dodecyl bridged butyl perylenetetracarboxylate binary compound discotic liquid crystal material

, China, , ,

Production Method 13

94259-20-8

Reaction Conditions

1.1 Reagents: Potassium carbonate Catalysts: Potassium iodide Solvents: Ethanol ;  60 h, 85 °C

Reference

Synthesis method of benzophenanthrene decyloxy-bridged isooctoxyphenylporphyrin-zinc coordination compound

, China, , ,

Production Method 14

94259-20-8

Reaction Conditions

1.1 Reagents: Potassium carbonate Catalysts: Potassium iodide Solvents: Ethanol ;  60 h, 85 °C

Reference

Synthetic method of benzophenanthrene decylalkoxy bridged methoxycarbonyl phenyl porphyrin metal Zn complex

, China, , ,

Production Method 15

94259-20-8

Reaction Conditions

1.1 Reagents: Potassium carbonate Catalysts: Potassium iodide Solvents: Ethanol ;  60 h, 85 °C

Reference

Preparation of benzophenanthrene dodecyloxy-bridged methoxycarbonyl phenyl porphyrin-Zn complex

, China, , ,

Production Method 16

94259-20-8

Reaction Conditions

1.1 Reagents: Potassium carbonate Catalysts: Potassium iodide Solvents: Ethanol ;  60 h, 85 °C

Reference

Preparation of triphenylene dodecyloxy bridging isooctane oxy phenyl porphyrin ternary compound as discotic liquid crystal material

, China, , ,

Production Method 17

94259-20-8

Reaction Conditions

1.1 Reagents: Potassium carbonate Catalysts: Potassium iodide Solvents: Ethanol ;  60 h, 85 °C; 85 °C → rt

Reference

Preparation of benzophenanthrene decyloxy bridging tetraphenyl porphyrin ternary compound as discotic liquid crystal material

, China, , ,

Production Method 18

94259-20-8

Reaction Conditions

1.1 Reagents: Potassium carbonate Catalysts: Potassium iodide Solvents: Ethanol ;  60 h, 85 °C

Reference

Preparation of benzophenanthrene dodecyloxy bridging tetraphenylporphyrin ternary compound as discotic liquid crystal material

, China, , ,

Production Method 19

94259-20-8

Reaction Conditions

1.1 Reagents: Potassium carbonate Catalysts: Potassium iodide Solvents: Ethanol ;  1 h, rt; rt → 80 °C; 24 h, 80 °C

Reference

Method for synthesizing dodecyloxy phenyl porphyrin benzamido hexyl-perylene diimide-decyloxy hexyloxy benzophenanthrene ternary compound

, China, , ,

Production Method 20

94259-20-8

Reaction Conditions

1.1 Reagents: Potassium carbonate Catalysts: Potassium iodide Solvents: Ethanol ,  Hexane ;  1 h, rt; rt → 80 °C; 24 h, 80 °C

Reference

Synthesis method of dodecyloxyphenyl porphyrin benzamide decane imine perylene decane imine hexyloxy benzophenanthrene ternary compound used in organic photovoltaic field

, China, , ,

1 2-DIHEXYLOXYBENZENE 98 Preparation Products

• 1 2-DIHEXYLOXYBENZENE 98 (94259-20-8)

• 1. Excimer–monomer switch: a reaction-based approach for selective detection of fluoride?
  Qiao Song,Angela Bamesberger,Lingyun Yang,Haley Houtwed,Haishi Cao Analyst, 2014,139, 3588-3592
• 2. Fast-Track to Research Data Management in Experimental Material Science-Setting the Ground for Research Group Level Materials Digitalization.
  LarsBanko,AlfredLudwig
• 3. Empowering microfluidics by micro-3D printing and solution-based mineral coating?
  Hongxia Li,Aikifa Raza,Qiaoyu Ge,Jin-You Lu,TieJun Zhang Soft Matter, 2020,16, 6841-6849
• 4. Enabling chloride salts for thermal energy storage: implications of salt purity?
  J. Matthew Kurley,Phillip W. Halstenberg,Abbey McAlister,Stephen Raiman,Richard T. Mayes RSC Adv., 2019,9, 25602-25608
• 5. Evidence of rutile-to-anatase photo-induced electron transfer in mixed-phase TiO2 by solid-state NMR spectroscopy?
  Weili Dai,Guangjun Wu,Michael Hunger Chem. Commun., 2015,51, 13779-13782

Comprehensive Overview of 1,2-Dihexyloxybenzene 98% (CAS No. 94259-20-8): Properties, Applications, and Industry Relevance

1,2-Dihexyloxybenzene 98% (CAS No. 94259-20-8) is a high-purity organic compound widely recognized for its unique chemical structure and versatile applications. As a derivative of benzene, this compound features two hexyloxy groups attached to adjacent carbon atoms, enhancing its solubility in non-polar solvents and thermal stability. With a purity of 98%, it is a preferred choice for researchers and industries seeking reliable performance in advanced material synthesis and specialty chemical formulations.

The growing demand for high-performance additives and liquid crystal materials has positioned 1,2-Dihexyloxybenzene as a critical component in cutting-edge technologies. Its molecular design aligns with trends in green chemistry and sustainable manufacturing, addressing concerns about environmental impact and energy efficiency. Researchers frequently explore its role in organic electronics, such as OLEDs and photovoltaic devices, where its electron-donating properties improve device efficiency.

In the pharmaceutical sector, CAS No. 94259-20-8 is investigated as an intermediate for drug development due to its stable aromatic backbone. Its compatibility with lipid-based systems also makes it valuable in cosmetic formulations, particularly in emollients and UV stabilizers. Recent studies highlight its potential in nanotechnology, where it serves as a building block for self-assembling monolayers (SAMs) and molecular sensors.

From an industrial perspective, 1,2-Dihexyloxybenzene 98% meets stringent quality standards required for batch-to-batch consistency, a key concern for manufacturers. Analytical techniques like HPLC and GC-MS ensure its purity aligns with specifications. Storage recommendations typically emphasize protection from light and moisture to maintain stability, reflecting broader industry practices for oxygen-sensitive compounds.

The compound’s relevance extends to academic research, where it is utilized to study supramolecular interactions and solvent effects in organic reactions. FAQs from scientific communities often focus on its synthesis scalability and reaction kinetics, underscoring its role in method development. As industries prioritize bio-based alternatives, derivatives of 94259-20-8 are being evaluated for reduced ecological footprints.

With advancements in computational chemistry, molecular modeling of 1,2-Dihexyloxybenzene provides insights into its conformational flexibility and intermolecular forces. This data-driven approach supports innovation in material science, particularly for designing thermally resistant polymers. Regulatory compliance with REACH and other global frameworks further ensures its safe utilization across markets.

In summary, 1,2-Dihexyloxybenzene 98% (CAS No. 94259-20-8) exemplifies the intersection of chemistry and technology, offering solutions for modern challenges in sustainability and performance optimization. Its multidisciplinary applications reinforce its significance in both industrial and research settings.

• 51241-37-3(Benzene, 1-methoxy-2-(pentyloxy)-)
• 42244-53-1(1,2-(Didodecyloxy)benzene)
• 921938-30-9(1-Methoxy-2-(undecyloxy)benzene)
• 906663-75-0(Benzene, 1-(heptyloxy)-2-methoxy-)
• 25934-47-8(Benzene,1,2-bis(decyloxy)-)
• 151237-06-8(Benzene,1,2-bis(hexadecyloxy)-)
• 86955-51-3(Phenol, 2,2'-[1,6-hexanediylbis(oxy)]bis-)
• 123934-38-3(1-Undecanol,11,11'-[1,2-phenylenebis(oxy)]bis- (9CI))
• 105849-26-1(Phenol, (octadecyloxy)-)
• 89290-75-5(Benzene, 1,2-bis(octadecyloxy)-)