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HS Code |
575298 |
| Iupac Name | 1,1-Diphenylhexane |
| Molecular Formula | C18H22 |
| Molar Mass | 238.37 g/mol |
| Cas Number | 1077-16-3 |
| Appearance | Colorless liquid |
| Boiling Point | 312-314 °C |
| Density | 0.948 g/cm³ at 25 °C |
| Solubility In Water | Insoluble |
| Flash Point | 129 °C |
| Refractive Index | 1.551 |
| Pubchem Cid | 11905513 |
As an accredited 1,1-Diphenylhexane factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 1,1-Diphenylhexane is packaged in a 100 mL amber glass bottle with a secure screw cap, labeled with hazard information. |
| Shipping | 1,1-Diphenylhexane is typically shipped in sealed, chemically resistant containers to prevent leaks or contamination. It should be stored and transported at ambient temperatures, away from heat, open flames, and incompatible substances. Ensure compliance with all relevant regulations regarding the labeling, documentation, and handling of organic chemicals during shipment. |
| Storage | 1,1-Diphenylhexane should be stored in a tightly closed container in a cool, dry, well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizing agents. Keep the storage area clearly labeled and protected from direct sunlight. Ensure the container is made of material compatible with organic chemicals, and avoid exposure to heat or moisture. |
Applications of 1,1-Diphenylhexane in Industrial Manufacturing1,1-Diphenylhexane serves as an important specialty aromatic hydrocarbon across several advanced manufacturing sectors. Its chemical stability, non-polarity, and solubility profile support specific downstream process requirements. As a direct manufacturer, we address real-world production scenarios with strict adherence to industrial benchmarks. 1. Fine Chemical Intermediates for Custom SynthesisThis material is commonly adopted as a building block or inert solvent for developing tailored organic intermediates. Research and scale-up laboratories often require precise aromatic substrates for Friedel–Crafts alkylation or Grignard reactions, where aromatic chain extension and hydrophobic modification are necessary. Reactors utilize 1,1-diphenylhexane for specialty coupling and protection of reactive benzene derivatives, ensuring reproducible yields and low residuals. Industry compliance standards
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2. Reference Standard and Internal Standard for Chromatographic AnalysisAnalytical laboratories utilize high-purity 1,1-diphenylhexane as a reliable internal standard for calibration in GC and HPLC methods. Its consistent retention time, chemical inertness, and non-interfering peaks enable accurate quantification of diverse hydrocarbon mixtures, especially in trace analysis for environmental monitoring, petrochemical analysis, and product QC release testing. Industry compliance standards
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3. Solvent Component in High-Performance Grease ManufacturingIndustrial lubricant formulators add this ingredient in high-performance grease base oils to enhance the solubility of functional additives and optimize low temperature flow. Its aromatic backbone provides good compatibility with lithium or calcium thickening systems. This allows for stable dispersion of anti-oxidants, anti-wear agents, and polymers required in demanding mechanical or automotive applications. Industry compliance standards
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4. Modifier and Hydrophobic Additive in Polymer CompoundingPolymer and elastomer manufacturers use this raw material as a hydrophobic modifier and flow enhancer in high-end thermoplastics. It is especially valued in polyolefin and styrenic resin blends to reduce viscosity and improve compatibility with other aromatic additives or fillers. Formulators specify its presence to tailor melt flow index and balance brittleness in engineering polymers used for demanding applications like automotive trims and consumer electronics housings. Industry compliance standards
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People working with specialty chemicals know the reliability and consistency of a product make all the difference. Over years of working in chemical synthesis and formulations, we've seen how meticulous attention to production details changes results in downstream applications. 1,1-Diphenylhexane stands out as one of those well-characterized building blocks for both research and industry, valued for its chemical stability, purity, and particular molecular design.
As a direct producer of 1,1-Diphenylhexane, we've spent a significant amount of time refining the reaction steps, purification techniques, and quality checks that it takes to deliver a material with low residuals and predictable behavior in use. From the earliest batches, we recognized chemists look for specific properties: ease of reaction, thermal and chemical stability, and a clear output in separation steps such as GC or HPLC.
1,1-Diphenylhexane falls within the group of diarylalkanes, with two phenyl rings embracing a six-carbon linear backbone. The structure—hexane chain with phenyl groups at a single carbon—delivers that combination of rigidity and flexibility many lab teams want in synthesis planning. This backbone resists unwanted side reactions such as rearrangements or polymerization better than some related compounds like substituted benzenes or simple alkanes. Its melting point and boiling range facilitate purification, and over years, we've learned how this behavior helps users minimize cycle times in scale-up.
The consistency in our manufacturing starts with raw material selection and ongoing monitoring across each batch. We keep the product above 99% purity by employing fractional distillation and advanced filtration at critical points during the production process. Typical physical properties—density, boiling range, and UV absorbance—undergo regular checks in batch records, not just at final QC. We find frequent in-process controls deliver tighter results and fewer deviations between lots than just relying on endpoint tests.
To us, a reliable batch means more than just a CAS number—we log and report trace analyses for common side products so users can spot minute trends as they scale from grams to multi-kilogram runs. Having handled thousands of liters of 1,1-Diphenylhexane, we see that consistency in polarity, solubility, and volatility eases much of the troubleshooting teams otherwise encounter.
Of all diarylalkanes, 1,1-Diphenylhexane offers a balance rarely matched by more substituted cousins or linear alkylbenzenes. Its two aromatic rings confer resonance stabilization, so it resists oxidation more robustly than mono-phenyl hexanes or typical branched alkylbenzenes. This detail matters especially in manufacturing environments that require storage stability—no one wants to see an intermediate degrade prior to blending or further transformation.
We’ve supported several clients in the pharmaceutical intermediate sector who use 1,1-Diphenylhexane for coupling reactions where unwanted aromatic side reactions must be minimized. Over the years, they have relayed back to us how switching to our consistently manufactured product has cut down on rework, improved their batch yields, and reduced the need for extended purification. Some have found that even minor deviations in impurity profiles can lead to color or odor changes in downstream active compounds, negatively impacting regulatory documentation.
Applications for 1,1-Diphenylhexane stretch beyond lab chemistry. Certain polymer and additive manufacturers turn to this compound for creating plasticizers or chain extenders. Its aromatic content improves compatibility with thermoplastic systems—particularly where clarity, low volatility, and excellent aging resistance are vital. Knowing how aromatic content influences both flexibility and stiffness in materials, engineers in these sectors appreciate being able to rely on a batch that won’t introduce unpredictable variables into their production process.
Not every alkyl-substituted aromatic fits the same role as 1,1-Diphenylhexane. In many industrial syntheses, the small structural differences determine whether chemicals work harmoniously or create processing headaches. Hexylbenzene, for example, delivers just one aromatic ring so its polarity and electron distribution lack the complexity that two rings offer. We’ve tracked customer feedback indicating monofunctional alkylbenzenes are sometimes too volatile or react unpredictably under certain conditions.
Compared to isomeric diarylhexanes, the 1,1-variant places both rings on the same carbon along the hexane backbone. This placement influences not only spatial arrangement but also physical characteristics like melting behavior and refractive index. Our process intentionally suppresses the formation of 1,2- or 1,3-diaryl isomers as these often possess lower solubility or display distinct GC retention times that complicate purity analyses for users scaling up or validating methods.
Several of our recurring clients—especially those working in catalysis and advanced materials—have asked about using diphenylalkanes with different carbon skeletons. Experience tells us diarylpropane or diarylbutane derivatives just do not hit the same balance between processability and property enhancement. Changes in backbone length or substitution pattern tend to affect viscosity, volatility, and even color stability. Many engineers and formulators circle back to the hexane-based product after initial trials with shorter or longer chains, noting that 1,1-Diphenylhexane delivers the best synergy between aromatic content and aliphatic flexibility for their recipes.
Years in production have shown us that the cleanest route to 1,1-Diphenylhexane involves careful monitoring during alkylation and crystallization steps. Unmonitored conditions can prompt over-alkylation, oligomerization, or unwanted isomers that are tough to remove later on. We have incorporated multi-stage purification, which includes targeted distillation and adsorption steps tailored to this specific chemistry, allowing us to pull out the narrowest boiling ranges and color bodies. Our investment in high-sensitivity analytics, including GC-MS and FTIR at each stage, has paid off in batches that pass downstream customer's requirements with few hiccups.
We often participate in conversations with technical teams interested in integrating 1,1-Diphenylhexane into R&D or production lines. Many voice concern about reproducibility or batch-to-batch color drift they’ve experienced with resellers or off-spec sources. Drawing on our own production data, we share full batch histories, including the details on reagent suppliers, temperature curves, and even equipment cleaning protocols. Being transparent about process variability builds trust with partners who need a reliable product whether scales run from pilot to annual forecasts in metric tons.
Chemists and engineers who request special packaging or certifications regarding trace metals or VOCs routinely cite difficulties encountered buying from intermediaries who can’t trace batches past the final filled drums. We have made it a priority to maintain both full production logs and retained samples for several years so recurring partners can pull historical comparisons, supporting both quality systems and regulatory filings.
Pharmaceutical and chemical synthesis remain the core areas using 1,1-Diphenylhexane. Its solid solubility profile enables dissolution both in non-polar solvents and certain chlorinated media, making it a key stepping stone for organic syntheses that require bench-scale predictability and straightforward scaling. Numerous process chemists highlight the product’s role in Friedel–Crafts alkylation reactions or as a reference compound in aromatic substitution studies. The predictability of molecular weight and spectral features allows for robust NMR calibration and purity checks.
In plastics and polymers, the role shifts from chemical synthesis to performance enhancement. The presence of two phenyl rings in the structure reduces migration and volatility in plasticizer applications. This feature translates to less plasticizer loss during heating and aging, which manufacturers report leads to more reliable long-term properties in finished materials. We see the chemical’s appeal particularly in polyvinyl chloride (PVC) applications where regulatory guidelines restrict certain low molecular weight additives. The predictable boiling range and low impurities profile align well with both safety regulations and target performance properties.
A subset of customers working in specialty coatings and lubricants value the ability of 1,1-Diphenylhexane to weather oxidative stress better than mono-alkylated aromatics. Lube formulators face constant challenges around deposit formation and oil breakdown. Over several product cycles, we've seen solid results in reducing varnish formation—a clear signal the phenyl-hexane structure provides both lubricity and resistance to unwanted chemical changes during use.
We regularly supply research teams piloting new catalytic materials. In these fields, subtle changes in the structure of backbone compounds play an outsized role in tuning catalyst support behavior or ligand fields. The symmetry and electron-donating/withdrawing nature of 1,1-Diphenylhexane enables predictable integration with transition metals, providing a stable platform for fine-tuning catalytic activity. Teams report good recovery and reuse profiles compared to less robust diarylalkanes.
Reliable performance in the field comes not just from chemical structure, but also from practical handling lessons earned in real-world manufacturing. 1,1-Diphenylhexane resists oxidation and photodegradation more effectively than many similar chemicals, as long as containers remain well-sealed and light exposure stays restricted. In our warehouses, we use nitro-sealed drums where long-term aging tests consistently return unchanged GC and color values across multiple seasons. Customers with experience storing other diaryl compounds often share stories about color drift or aroma changes after a few weeks—issues we rarely encounter due to robust packaging and logistics.
Flexible packaging options, including high-barrier drums and custom tote sizes, allow our partners to match usage volumes without excessive waste. In high-throughput operations, packaging integrity makes a difference between a batch that runs all the way without incident and one plagued by partial loss due to poorly controlled evaporation or contamination.
Every product has its pain points, and 1,1-Diphenylhexane presents its own set of technical challenges during scale-up. Maintaining tight purity specs as batch sizes climb demands continuous attention to distillation parameters and cooling rates. Early on, we tackled several persistent side reaction pathways by refining our catalysts—life in chemical plants rarely follows textbook directions, so direct feedback from process operators remains crucial for tweaks and improvements.
Occasionally, requests arise for product with particular trace characteristics—such as ultra-low sulfur or halide levels—that require custom purification runs or specialty adsorbents. Our production teams have built the flexibility to handle such custom runs without disrupting base product supply, marking a key differentiator compared with bulk traders or contract blending operations.
Shipping regulations for aromatic chemicals keep evolving, especially as authorities seek to tighten guidelines around VOC emissions and environmental impacts. We collaborate with compliance specialists and logistic partners to monitor the latest regulatory pronouncements, adapting labeling, documentation, and container specs as needed. By keeping full product dossiers and collaborating with auditing bodies, we've avoided delays for both domestic and export customers.
With the uptick in global regulatory scrutiny, traceability and transparency matter to clients running analytical and formulation development programs. Batch traceability down to source materials, instrument calibration records, and detailed impurity profiles support regulatory filings and customer audits. Several quality-conscious customers have shared with us that switching from generic suppliers to direct manufacturer relationships reduced time spent on quality investigations and allowed for more reliable, repeatable innovation cycles.
Our own lab teams often field requests for spectral data packages—NMR, mass spec, FTIR, UV-vis—and maintain archives covering multiple years of production runs. This back-catalog assists anyone re-validating methods or benchmarking new batch performance. We frequently participate in joint troubleshooting sessions with customer labs, sharing raw data and real-use experience to identify potential sources of inconsistencies or unexpected test results. By removing ambiguity at the analytical level, chemists and product developers gain the confidence to push forward on tighter timelines.
Long-standing relationships with R&D teams allow us to add more value than simply delivering a chemical. Several partners work with us to design next-generation diarylalkane derivatives, leveraging our synthetic know-how to streamline their own lead compound synthesis. Our close ties with academic groups and technical centers have led to pilot studies exploring new uses for 1,1-Diphenylhexane in advanced electronics and energy storage sectors. By staying hands-on in both bench-scale and production settings, we put practical chemistry to work for customers, helping bridge the perennial gap between laboratory scale and commercial viability.
As a direct producer, we support method validation, supply chain security audits, and the tailoring of delivery formats to fit particular manufacturing protocols. Collaboration often takes the form of reciprocal lab visits, cross-validation of test protocols, and knowledge transfer around process controls—areas where direct producer-partner teams find efficiencies unavailable to those sourcing through intermediaries. These hands-on exchanges anchor stronger supplier relationships and equip all parties to anticipate and solve real-world problems as market and technical needs evolve.
Real feedback from users shapes every refinement we make to the production process. Over the years, customers have pointed out minor changes in product tonality, subtle differences in odor, or shifts in GC retention behavior. Each instance led to targeted investigations, revealing subtle process deviations or new analytical needs we had overlooked. This ongoing dialogue invites honest input and spurs us toward proactive troubleshooting—challenges become opportunities when both sides share their experience and knowledge.
Our technical and sales teams bridge the lab and factory floor, regularly meeting with customers both onsite and remotely to understand current demands and future trends. By merging first-hand user experience with production capability, we close the loop that leads to a higher performing, more trusted product engineered to meet the needs of formulating chemists, process engineers, and technical managers.
Direct manufacturing of 1,1-Diphenylhexane is not just about chemical synthesis; it’s about building sustained trust through every layer of the process. From selecting high-grade starting materials to customizing purification regimes and supporting regulatory documentation, our entire workflow focuses on delivering a product that does not let customers down. Constantly tuning methods based on feedback and hands-on operating experience keeps us at the forefront of chemical production, preparedness for regulatory environments, and technical support. For applications where purity, consistency, and performance anchor success, 1,1-Diphenylhexane represents a compound forged by experience and tailored through real-world use.