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HS Code |
643483 |
| Iupac Name | Dibenzo[b,def]chrysene |
| Cas Number | 191-30-0 |
| Molecular Formula | C24H14 |
| Molar Mass | 302.37 g/mol |
| Appearance | Yellow crystals |
| Melting Point | 259-261 °C |
| Solubility In Water | Insoluble |
| Density | 1.32 g/cm³ |
| Synonyms | Dibenzchrysene, DBC, Dibenzochrysene |
| Structure Type | Polycyclic aromatic hydrocarbon (PAH) |
| Smiles | c1ccc2c(c1)c3ccc4cccc5ccc2c3c45 |
| Inchi | InChI=1S/C24H14/c1-2-7-17-15-10-6-14-12-16-11-8-3-4-9-13(11)18(14)20(15)22(17)24-21-19(5-1)23(8)24/h1-10H |
As an accredited Dibenzo[B,Def]Chrysene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Dibenzo[B,Def]Chrysene, 1g, supplied in a sealed amber glass vial with tamper-evident cap, labeled with hazard and identification information. |
| Shipping | Dibenzo[B,def]chrysene is shipped in tightly sealed containers to prevent exposure to air and moisture. The chemical is packaged in accordance with local and international regulations for hazardous substances, typically using inert packing material. It is labeled for laboratory use only and handled by trained personnel, ensuring safe and compliant transport. |
| Storage | Dibenzo[B,def]chrysene should be stored in a cool, dry, well-ventilated area, away from direct sunlight and sources of ignition. Keep the container tightly closed and clearly labeled. Store separately from strong oxidizing agents and acids. Use chemical-resistant containers, and avoid prolonged exposure. Ensure storage area has suitable spill containment and is accessible only to trained personnel due to its hazardous nature. |
Applications of Dibenzo[B,Def]Chrysene in Industrial ManufacturingAs a dedicated chemical manufacturer, we supply Dibenzo[B,Def]Chrysene for advanced industrial applications where its unique polycyclic aromatic structure meets strict regulatory and process requirements. Below, we outline verified downstream scenarios—including specialty electronic materials, reference standards, environmental monitoring, and advanced research—reflecting real-world industrial adoption, with details on compliance, formulation, operational integration, and resulting end products. 1. Electronic Organic Semiconductors for OFETsElectronic industry manufacturers employ this raw material as an aromatic building block during the synthesis of high-mobility organic field-effect transistor (OFET) layers. Owing to its extended π-conjugation, it serves as a critical precursor for developing stable organic semiconductor films required for thin-film electronics. The compound fits stringent requirements regarding purity and electronic properties to ensure consistent charge-transport performance in device fabrication. Industry compliance standards
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2. Analytical Reference Materials in Environmental Monitoring LaboratoriesAccredited environmental laboratories require polycyclic aromatic hydrocarbons (PAHs) as authentic reference standards for trace quantification and calibration procedures in water, soil, and air analysis. This compound, listed as a priority pollutant by several regulatory agencies, supports laboratories in achieving consistent QC, method validation, and reliable monitoring of environmental contamination, especially for regulatory compliance and pollution source tracing. Industry compliance standards
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3. Research-Grade Molecular Probes in PhotophysicsUniversity and industrial research institutes utilize this specific PAH as a molecular probe and model system in photonic materials studies, especially for investigation into excited state dynamics, singlet fission, and non-linear optical responses. Laboratories require gram-scale supplies with traceable purity documentation to structure, allowing precise experiments and scientific publications in the field of molecular electronics and photophysics. Industry compliance standards
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4. Forensic and Regulatory Quality Control for Industrial Compliance AuditsChemical manufacturers, compliance laboratories, and industrial auditors use this polycyclic aromatic compound as a marker substance for validation of clean production, workplace safety controls, and regulatory audits. It functions as a control sample to confirm absence of trace contamination in process streams governed by national or regional PAH restrictions, directly supporting compliance documentation and certification requirements. Industry compliance standards
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Dibenzochrysene stands out among polycyclic aromatic hydrocarbons for more than its striking molecular structure. While its name draws immediate attention in technical circles, its role in advanced research has only grown as analytical and industrial requirements become more demanding. Here on the production floor, understanding the ins and outs of this compound forms part of our everyday work. We don’t just see it as a chemical entity — for us, it’s a project spanning raw material control, precise reaction management, and real-world application.
Our chemists often mention the fused aromatic rings in Dibenzochrysene. Its structure, built from six rings fused in a specific pattern, creates a rigid and planar configuration, making it both chemically stable and resistant to breakdown under standard storage. We watch for impurities, primarily smaller polyaromatic siblings during synthesis. We rely on high-performance liquid chromatography and tailored recrystallization steps, tuning our process to achieve a purity exceeding 98 percent based on our latest lot analyses. Many laboratories view this purity as a baseline, not just for integrity in their work, but also to minimize background signals during advanced testing.
Our final product appears as a yellow crystalline powder. Color shifts in this material indicate oxidation or contamination—signs we catch thanks to regular color spectrophotometry and vigilant operators. Melting point determination gives us a reliable check: any deviation outside the narrow range of 278°C to 281°C signals us to re-examine process parameters or raw materials. Water content presents another challenge since trace moisture changes the way this compound behaves, especially during weighing or transfer. Routine Karl Fischer titration and controlled atmosphere packaging keep moisture below 0.1 percent for outgoing lots.
Academic laboratories first drew our attention to Dibenzochrysene’s ability to serve as a model carcinogen for toxicology. When our early customers came from environmental monitoring, we refined our handling process to guarantee ultra-trace quantities in matrix-matched standards. Chromatography reference standards must not introduce signal drift, so purity and packaging matter as much as the molecular backbone. Research shifted as universities and industry teams explored its utility as a component in organic semiconductors, photovoltaics, and as an intermediate for high-end dyes. We manufacture in small, well-defined batches to support this diversity — there’s little room for a ‘one-size-fits-all’ mentality here.
People sometimes ask us what distinguishes Dibenzochrysene from molecules like benzo[a]pyrene or chrysene. Experience showed us the difference lies in both risk and utility. Its higher number of aromatic rings leads to increased chemical stability reflected in both environmental persistence and handling precautions. Routine tests confirm that our finished material resists atmospheric photodegradation better than its less-complex cousins. Users working in optoelectronics prize the extended π-conjugation, which offers different absorption and emission characteristics when compared to other PAHs, and we supply custom documentation for these specialists on request.
Long before Dibenzochrysene reaches the shipping dock, hands-on checks and multi-point analysis shape its journey. Our batch records don’t just detail synthesis steps, but also environmental monitoring for dust and vapor, given the recognized toxicology of even trace polycyclic aromatic hydrocarbons. Cross-contamination risk can’t be left to chance, so we dedicate equipment for each group of structurally-related compounds. Internal reference spectra for FTIR and NMR give us fast feedback; deviation from baseline means rework, not release.
Customers count on us to deliver Dibenzochrysene in a condition ready for precise work. We favor amber glass vials for light exclusion and use nitrogen backfill to keep air sensitive lots protected during transit and storage. The powder clings to container surfaces, so we calibrate filling equipment for static reduction and work with antistatic tools; staff training makes an impact when every milligram counts. Temperature excursions during transport shorten shelf life, so we log and review every data point from shipment sensors.
As organic electronics and environmental analysis programs expand, users demand even tighter control over trace residuals and cross-reactants. Production must stay ahead. We review synthesis catalysts annually and benchmark our process yields against both published literature and customer feedback. Sometimes, improvements come from technician suggestions — swapping out a drying agent or adjusting dissolution timing. Customer returns dropped once we raised the bar on these manual checks, a point our team takes pride in.
Our staff know firsthand that producing Dibenzochrysene requires more than standard gloves and lab coats. Handling powdered PAHs means we invest in high-volume HEPA local exhaust and run regular air monitoring in weighing stations. This effort aligns with published findings linking exposure to polycyclic aromatics to potential health risks. While some operations can be run on a closed batch reactor, analysts and operators remain proactive in full decontamination routines at each stage. Training programs draw on both international guidelines and what we've learned from years of hands-on work.
A research chemist will sometimes call or email, pointing out that our current batch suits a new thin film application or runs clean in a specific mass spectrometry assay. Requests like these push us to review our synthetic route and downstream steps, seeking ways to expand the range of guaranteed specifications. No single production run remains static for long. If a partner needs microgram accuracy or adjusted batch size, we collaborate directly rather than hand off to a middleman.
Aromatic ring closure reactions, as used in dibenzochrysene synthesis, introduce unique obstacles unseen in simpler PAHs. Byproducts tend to arise from minor variances in reagent concentration, heating rate, or solvent purity. Our team tracks these variables closely through digital batch logs and routine small-scale trials. Even with years of experience, surprises occur — a one-degree shift in oil bath temperature once proved enough to raise a secondary impurity by nearly 1 percent. We use this feedback to adjust technical protocol and shorten troubleshooting cycles.
It’s no secret that polycyclic aromatic hydrocarbons face close environmental scrutiny. Waste management here goes beyond basic filtration. We incinerate all process residues in a dedicated unit with real-time emissions monitoring. Local regulators review our procedures, but internal standards usually go further. We host annual review meetings and update our documentation according to the latest research about PAH toxicity, supporting efforts to minimize accidental environmental release.
We keep reserve samples from each Dibenzochrysene batch for over a decade as part of our traceability commitment. Outside laboratories occasionally request archival samples to audit batch continuity or explore aging behavior in long-term storage. Documentation includes identity confirmation from both NMR and GC-MS, with access provided for major research partners. This approach builds trust with long-term clients and supports regulatory compliance for critical projects.
Producing Dibenzochrysene at a scale that meets modern demand requires more than reactor size-up. Exothermic steps pose risks, especially where small deviations in addition rate magnify byproduct buildup. To address this, we engineered a semi-batch addition protocol, paired with real-time calorimetry, which trims side reactions and delivers more consistent yields. Our learning curve involved many production trials, support from team chemists, and lessons drawn from field failures.
Quality in finished Dibenzochrysene links back to where we find our raw inputs. We source aromatics from vetted suppliers, with full traceability down to lot number and storage condition. Routine FTIR and NMR on each input prevent contamination or mistaken identity, long before batch synthesis starts. Materials flow through controlled storage, with temperature and humidity limits observed from receiving dock to final packaging. Routinely, we audit storage areas for compliance and train staff on best practices.
In our early years, collaboration with university groups provided insight we couldn’t have gained in isolation. Today, industrial partners share analytical results, technical needs, and new applications, allowing us to expand our process and troubleshoot issues ahead of release. Field data from optoelectronic development groups, for example, informed a process tweak removing a persistent trace contaminant. Win-win outcomes come from sharing information and maintaining transparent technical correspondence.
Confidence in Dibenzochrysene doesn’t begin and end at purity data. Researchers often request extended certificates, stability data, or insight into atypical lot observations. We document spectral signatures, batch records, and full storage logs, enabling partners to review the product’s journey from start to finish. When issues arise, such as a rare tone variation or solubility comment, we dig into the records, provide findings, and resolve concerns through open communication, not runaround responses.
Emerging uses for Dibenzochrysene increasingly shape how we refine our material specifications. Demand from electronics researchers for ultra-high purity prompts us to invest further in enhanced purification equipment and more sensitive analytical techniques. Growth in environmental screening work means we continue to expand our standard mixes and cross-train analysts in trace analysis workflows. These investments pay off not just in fewer product complaints, but stronger relationships built on confidence in our production.
Making Dibenzochrysene is about more than just combining chemicals — it’s a steady challenge that calls on both science and real-world experience. We see every lot as a new chance to improve, drawing lessons from customers, staff, and research partners. Delivering this material to scientists and engineers around the world keeps us sharp: each request, question, or observation makes tomorrow’s production better than yesterday’s.