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HS Code |
589453 |
| Name | 4'-Methylsulfanyl-Biphenyl-4-Carbaldehyde |
| Molecular Formula | C14H12OS |
| Molecular Weight | 228.31 |
| Cas Number | 105357-94-4 |
| Appearance | White to off-white solid |
| Melting Point | 82-86°C |
| Purity | Typically >98% |
| Solubility | Soluble in organic solvents (e.g., DMSO, dichloromethane) |
| Smiles | CSC1=CC=C(C=C1)C2=CC=C(C=C2)C=O |
| Inchi | InChI=1S/C14H12OS/c1-16-14-8-6-12(7-9-14)13-4-2-11(10-15)3-5-13/h2-10H,1H3 |
| Storage Conditions | Store at room temperature, in a dry and well-ventilated place |
| Synonyms | 4'-Thiomethyl[1,1'-biphenyl]-4-carbaldehyde |
As an accredited 4'-Methylsulfanyl-Biphenyl-4-Carbaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 50g of 4'-Methylsulfanyl-Biphenyl-4-Carbaldehyde supplied in a sealed amber glass bottle with tamper-evident cap and safety labeling. |
| Shipping | 4'-Methylsulfanyl-Biphenyl-4-Carbaldehyde is shipped in tightly sealed chemical containers, protected from light and moisture. Packaging is compliant with international and local chemical transport regulations. The product is typically shipped at ambient temperature with appropriate hazard labeling, and accompanied by a Safety Data Sheet (SDS) for safe handling and regulatory compliance. |
| Storage | 4'-Methylsulfanyl-Biphenyl-4-Carbaldehyde should be stored in a tightly sealed container, away from light, moisture, and sources of ignition. Keep it in a cool, dry, and well-ventilated area, preferably in a dedicated chemical storage cabinet. Ensure compatibility with surrounding substances, and label the container clearly. Avoid exposure to strong oxidizers, acids, or bases to prevent degradation or hazardous reactions. |
Applications of 4'-Methylsulfanyl-Biphenyl-4-Carbaldehyde in Industrial ManufacturingAs a primary manufacturer specializing in 4'-Methylsulfanyl-Biphenyl-4-Carbaldehyde, we support industrial clients across specialized downstream sectors where this unique intermediate delivers targeted performance and functional value. The following use cases reflect verified end-market practices and current regulatory expectations, each highlighting our in-depth application expertise from batch formulation through end-product verification. 1. Advanced Liquid Crystal Materials for ElectronicsThis compound acts as a key aromatic aldehyde intermediate in custom syntheses of biphenyl-based mesogenic compounds used in advanced liquid crystal displays (LCDs) and devices requiring precise electro-optical performance. Producers utilize our material to control molecular orientation and thermal characteristics during proprietary liquid crystal component design, supporting innovation in smart displays, automotive panels, and specialty control panels. Industry compliance standards
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2. Pharmaceutical Intermediate in Selective Synthesis of Antihypertensive AgentsSeveral API manufacturers incorporate this aldehyde building block to prepare custom biphenyl derivatives for cardiovascular formulations, particularly within the angiotensin receptor antagonist (ARB) class. The defined aromatic structure allows for targeted functionalization, facilitating the creation of intermediates meeting both pharmacopoeial and ICH standards in regulated routes for drug substance manufacturing. Industry compliance standards
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3. Intermediate in High-Performance Organic SemiconductorsWithin the field of organic electronics, this raw material contributes to the tailored synthesis of functionalized biphenyl compounds and oligomers incorporated into organic semiconducting layers. Device manufacturers rely on it to control frontier orbital levels and electron transport efficiency for organic field-effect transistors (OFET) and related optoelectronic applications. Industry compliance standards
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4. Precursor for Custom Aromatic Polymers in Engineering PlasticsIn the realm of specialty engineering plastics, compounders use this aromatic aldehyde to tailor the backbone properties and thermal stability of custom aromatic polyesters and copolymers. The addition of methylsulfanyl functionality enhances processability and UV resistance, meeting end-user requirements in mass transit and high-durability applications. Industry compliance standards
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5. Building Block for Agrochemical Active Ingredient SynthesisChemical synthesis plants use this aromatic aldehyde for constructing sulfanyl-biphenyl moieties in select pre-emergent herbicide and fungicide agents. The core structure provides a platform for specific tailoring of biologically active groups, ensuring batch-to-batch consistency as demanded by regulated agrochemical manufacturing programs. Industry compliance standards
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In our years of experience as a chemical manufacturer, we have watched the landscape for specialty organic intermediates evolve. The emergence of 4'-Methylsulfanyl-Biphenyl-4-Carbaldehyde as a key building block in modern organic synthesis reflects a clear shift in what innovators demand from fine chemicals. This compound stands out not just because it fills a niche, but because it addresses real-world challenges in synthesis, scale-up, and downstream processing. At our plant, the journey with 4'-Methylsulfanyl-Biphenyl-4-Carbaldehyde has shaped both our production culture and how we think about purity, contaminant control, and consistency batch after batch.
Every batch we produce draws from a foundation of hands-on knowhow. The model we currently follow for synthesis has grown more efficient through years of incremental improvements. Our facilities use robust glass-lined reactors, inert gas handling, and refined phase-separation techniques, all tailored to maximize product yield while minimizing unwanted by-products. The key reaction—the selective formylation of methylsulfanyl-biphenyl—demands careful monitoring. We rely on well-calibrated instrumentation and staff experienced with aromatic chemistry. Our chemists stay close to reaction progress, verifying completion by both TLC and HPLC. From there, successive washes, rotary evaporation, and fine filtration play their part. We pioneered a crystallization protocol that consistently gives a crystalline solid with sharp melting characteristics, minimizing residual solvents and avoiding oiling out—a frequent headache for those unfamiliar with this family of aldehydes.
Anyone who spends time with this compound understands its sensitivity to oxygen and occasional air oxidation of the sulfanyl group, particularly if exposed for prolonged periods or stored under poor conditions. We recognized early on the need for nitrogen-blanketed storage, reduced headspace in containers, and proper labeling of manufacturing date and batch. Our staff checks IR and NMR spectra for each production lot—aromatic splitting patterns and aldehyde proton intensity make deviations easy to spot. Our internal standards for appearance, odour, and melting point serve as quick flags for handling mistakes or unreported degradation. Experience taught us that even trace peroxide or acid impurities can catalyze off-notes, so we go beyond the usual chromatography panels to confirm absence of these threats, particularly for pharma or electronics-grade shipments.
Chemists ask about purity with every order, and our labs routinely deliver material at or above 99% by HPLC, with controlled levels of moisture, non-volatile residue, and trace metals. Main analysis includes GC-MS and NMR authentication—molecular weight checks by mass spec, sulfur detection, and quantitative aldehyde titration ensure nothing unexpected remains. Over time, we optimized our purification train to balance throughput and solvent use. Key insights came from pilot campaigns, where incomplete washing led once to remnants of chlorinated phases. That episode prompted stricter phase separation checks and logs kept on equipment cleanouts to prevent run-to-run contamination. We meet internal criteria for color (off-white to pale yellow crystals), melting point, and solubility in common organic solvents such as dichloromethane, acetonitrile, and THF. While 4'-Methylsulfanyl-Biphenyl-4-Carbaldehyde dissolves well in most aromatic and polar aprotic solvents, our partners working with hydrogenation or metal-catalyzed reductions have given feedback on the need for trace metal control. Our team adopted in-line filtration rigs for handling transfer and packaging to reduce the risk of particulates.
Chemical manufacturers often group biphenylcarbaldehydes together, but their subtle differences matter in both research and industrial runs. The methylsulfanyl substituent at the two-position changes electronic properties and sterics, increasing nucleophilicity of the ring and shifting reactivity profile compared with unsubstituted biphenylcarbaldehyde or its methoxy analogs. In our own test reactions, formylation protocols optimized for 4'-Methylsulfanyl derivatives cut down on formation of undesired ortho side products. Other aldehydes in the biphenyl family often suffer from longer purification steps, lower isolated yields, or persistent color bodies unless careful control is maintained. We found that the sulfur moiety, while increasing overall functionality, requires targeted steps during purification—simple distillation rarely suffices in these cases.
In synthetic applications, the methylsulfanyl group serves as a synthetic handle. Our customers run cross-coupling reactions, Suzuki-Miyaura or Stille protocols, using the methylsulfanyl functionality for further derivatization before removing or substituting the group. In this context, 4'-Methylsulfanyl stands apart: the group directs reactivity selectively, and feedback from customers engaging in ligand development or specialty polymer synthesis credits the ease of manipulation with saving steps and raising productivities. Methoxy or hydroxy-substituted biphenylcarbaldehydes often require protective group manipulations or preactivation, adding to cost and time. We have routinely heard from users that the sulfur-containing variant minimizes extra reagents and workups.
Use cases for 4'-Methylsulfanyl-Biphenyl-4-Carbaldehyde extend beyond textbook transformations. In our discussions with users, applications in pharmaceutical starter units, OLED materials, and chiral ligand frameworks come up frequently. Our own pilot studies have involved its introduction as a late-stage functional group carrier in multi-step syntheses. The aldehyde moiety supports transformations like reductive aminations, Knoevenagel condensations, and Wittig reactions. We have tracked time savings in projects where the methylsulfanyl directs selectivity for cross-coupling reactions. In certain process routes, this advantage cuts back on isolation and purification costs, especially where high-throughput screening depends on compound libraries with narrow structural differences.
Some of our customers incorporate this compound in custom dye stuff preparations. In OLED research, the sulfur linker provides altered electron mobility compared to oxygenated biphenyl derivatives. Our feedback channels log distinct shifts in device performance metrics—charge balance, emission profile, stability—when comparing sulfur and oxygen variants. The success in these segments depends heavily on consistency, so we maintain package-out routines with argon sparging or vacuum-sealing for materials earmarked for optoelectronics. Pharmaceutical researchers appreciate reduced off-target reactivity when the methylsulfanyl moiety occupies activating positions, lowering risk of unwanted side reactions, especially oxidative dimerization or hydrolytic degradation, which plague similar aldehydes with less steric bulk.
As we work closely with developers scaling up from gram to kilogram runs, scale brings practical questions that too often get overlooked. Over years, we developed bulk dissolution and transfer methods that curb exposure to air and traces of water. Real-world handling differs greatly from benchtop runs—packaging large lots in moisture-proof containers, transport in climate-controlled vehicles, and detailed COAs that customers can trust. Our readiness to ship 4'-Methylsulfanyl-Biphenyl-4-Carbaldehyde with full spectral and analytical data spring from a culture where traceability and transparency are habits, not hoops to jump through.
Delivering specialty aldehydes goes beyond technical documentation. Scrutinizing raw material sources ranks high in importance: upstream impurities, such as halide or aromatic contaminants, can subtly alter end properties in advanced applications. Raw material batches undergo vetting with GC and NMR; staff in charge of supplier relations flag any deviation from agreed benchmarks. This diligence pays off downstream, with fewer process interruptions, less rework, and more reliable partnerships with buyers who expect practical assurances, not just datasheets and generic claims.
From an operational standpoint, reproducibility and on-time delivery require constant vigilance. Our production team faces routine challenges—solvent shortages, reactor downtime, purity drift from repeated use of filters or glassware, and the unpredictable nature of specialty chemical logistics. We invest in compatible processes and supplier networks, keeping enough inventory of precursor chemicals and solvents, and secure backup equipment for critical steps such as oxidation control. Every process change triggers a round of analytical comparison—spectral overlays, melting point checks, reaction yield retrospectives. This feedback cycle, built on direct lessons from earlier setbacks, forms the backbone of our continuous improvement ethos.
Every manufacturer in this industry must reckon with environmental responsibility. The aromatic and sulfur components in this product demand particular vigilance to air and water emissions. Our facility employs closed-circuit solvent recovery, efficient vent scrubbing, and targeted waste segregation. Sulfur-containing wastes often require separate handling to avoid deposition or overburdening centralized treatment plants. We regularly monitor stack emissions and effluents, making incremental upgrades when new best practices or government benchmarks arise. Staff training reinforces a zero-compromise culture regarding PPE and spill management. Our incident logs show that near misses have become rarer as we invested in better containment, handling protocols, and employee engagement.
On-site handling focuses on minimizing dust and fume potential. We favor packaging formats that align with workplace safety. Our chosen drums and liners prevent offgassing and accidental puncture—our warehouse layout and racking design evolved from first-hand experience, using lessons from early spills and overfills. We take pride in chemical stewardship, not just compliance: outreach with customers includes tailored advice on in-lab handling and waste disposal, especially for those new to this class of compounds. Our incident response draws on actual accident investigations, not just playbook procedures, and has directly shaped our advice on storage, shelf life, and expiration monitoring.
The landscape for sourcing and logistics in specialty chemicals has become more complex over the last decade. Global logistics slowdowns, evolving environmental regulations, and geopolitical uncertainties all impact the steady availability of raw materials. We maintain multiple approved sources for precursors and work with partners in various regions to reduce exposure to bottlenecks. Our supply network builds on trust and shared standards. Any upstream event—a port closure, policy change, price spike in solvents—triggers a process review and a contingency plan for customers relying on consistent supply.
Looking ahead, we consider both the product and the process. Innovators require better, cleaner, and more sustainable chemicals. Our R&D group tests greener syntheses for this and related aromatic aldehydes, evaluating catalytic rather than stoichiometric approaches, and reducing chlorinated byproduct streams. Progress comes in steps. Running small-scale demonstrations, collecting real emission data, and making incremental upgrades compound into a culture of continuous, not occasional, improvement. We build sustainability into our client conversations and regularly solicit feedback on packaging, delivery, and recyclability options.
End users in cutting-edge materials science and pharmaceutical discovery deserve confidence in what they receive. Our approach to traceability grew out of industry requirements as well as direct client feedback. Each lot receives a unique identifier, batch record, and full analytical report. That transparency does more than reassure inspectors—it serves chemists who might need to trace issues back to source. We maintain sample retention and chain-of-custody logs for years, and frequently assist customers troubleshooting syntheses, drawing from our own batch records.
The analytical journey for this compound—IR, NMR, HPLC, GC-MS, sometimes elemental microanalysis—satisfies both regulatory and user needs. Our philosophy holds that the data belongs to those who trust us with their projects. When questions or inconsistencies arise, our technical support team investigates in-house, referencing archived spectral files and supplier COAs, not generic boilerplates. Lessons from real-world problem-solving—brown coloration from micro-oxidation during storage, unexpected odor changes traced to packaging glue interaction, or variability in crystallization from batch-to-batch—clarify why consistency, feedback, and verification matter more than ever before.
Knowledge empowers both the producers and the users of specialty chemicals. Our staff participates in worksite training, external symposia, and day-to-day troubleshooting. Lessons from each run, each scale-up, every feedback call contribute to collective experience. We pass along best practices to customers for in-house handling, using concrete case studies rather than generic warnings—how improved ventilation addressed off-odour concerns, how trace water led to aldehyde hydration, how packaging design change resolved clumping in humid shipment routes.
Through open dialogue with academic and industrial partners, we refine our approach. Internally, every improvement made in the plant—better cleaning routines, machine upgrades, more robust analytical checks—leads directly to outcomes in quality and reliability. The discipline of sharing both successes and stumbles has built trust in our ability to deliver high-purity specialty intermediates to even the most exacting users.
As real manufacturers, our perspective grows from daily involvement, not just catalog curation. 4'-Methylsulfanyl-Biphenyl-4-Carbaldehyde earned its importance through the demands created by new synthetic routes, uncompromising researchers, and more challenging performance targets in end-use industries. The way it responds to careful process design, its impact on reaction outcomes, and the specific demands it places on safety, traceability, and environmental stewardship have made it a focus for our teams. Each challenge we solved—whether purity, stability, or scale—built confidence in our methods and understanding. We see the story of this chemical as a reflection of broader changes in specialty manufacturing, where informed practice and open collaboration shape not just what gets made, but how safely, sustainably, and reliably we deliver it to those pushing the boundaries of science and technology.