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HS Code |
177144 |
| Productname | 4-(Phenylthio)Benzaldehyde |
| Casnumber | 3486-73-1 |
| Molecularformula | C13H10OS |
| Molecularweight | 214.28 g/mol |
| Appearance | Off-white to pale yellow solid |
| Meltingpoint | 73-77°C |
| Boilingpoint | 169-171°C at 4 mmHg |
| Purity | Typically ≥98% |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Smiles | C1=CC=C(C=C1)SC2=CC=C(C=C2)C=O |
| Inchikey | XMVUNVGEPIMSCR-UHFFFAOYSA-N |
As an accredited 4-(Phenylthio)Benzaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The packaging is a 25g amber glass bottle, tightly sealed, labeled "4-(Phenylthio)Benzaldehyde," with hazard warnings and product details. |
| Shipping | 4-(Phenylthio)benzaldehyde is shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. It is carefully packaged to prevent leaks or damage, and labeled according to regulatory standards. During transit, temperature and handling conditions are controlled to ensure product integrity and safety for both handlers and the environment. |
| Storage | 4-(Phenylthio)Benzaldehyde should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from incompatible substances like strong oxidizers. Protect it from light and moisture. Label the container clearly, and handle it with appropriate personal protective equipment. Store at room temperature and follow all relevant safety regulations and chemical hygiene practices. |
Applications of 4-(Phenylthio)Benzaldehyde in Industrial ManufacturingAs a direct manufacturer of 4-(Phenylthio)Benzaldehyde, we supply this fine chemical into specialized industrial processes where its structural attributes and reactivity offer significant downstream value. Below, we highlight the most established application segments, with detailed insights into compliance, operational dosage, integration points, and representative end-use products. 1. Advanced Organic Synthesis Intermediates for Pharmaceutical Chemical ProductionThis compound plays a critical role as a building block in multistep organic syntheses for pharmaceutical actives, especially in the assembly of sulfur-containing heterocyclic cores and benzaldehyde-functionalized scaffolds. Process chemists favor its reactivity for forming specific linkages required for API precursors, including selective condensation and cyclization routes. Industry compliance standards
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2. Specialty Ligand Manufacturing for Homogeneous CatalysisResearch and industrial catalyst developers use this molecule to synthesize S-aryl-containing ligand frameworks that coordinate transition metals for organic transformation processes. Its electron-rich aromatic sulfur bridge enables the fine-tuning of ligand geometry and electron density for improved selectivity and catalytic turnover in homogeneous systems. Industry compliance standards
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3. Electronic Materials: Organic Semiconductors Precursor SynthesisThe electronic materials industry leverages this molecule within the fabrication chain of organic semiconductors and conductive polymers. Its dual aromatic structure and sulfur bridge contribute to strong charge carrier mobility and tunable optoelectronic properties in advanced display and sensor applications. Industry compliance standards
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4. Synthesis of UV-Absorbing Monomers for Coatings and PolymersHigh-performance polymer and coating manufacturers utilize this specialty benzaldehyde as a starting monomer in the customized production of UV-absorbing and photostabilized coatings. Its structure facilitates the introduction of thioether functional groups into polymers, which enhances long-term resistance to UV-induced yellowing and degradation in specialty surface finishes. Industry compliance standards
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Within the evolving field of fine chemical manufacturing, 4-(Phenylthio)benzaldehyde continues to draw attention for its unique structure and versatile reactivity. Our team approaches the synthesis and refinement of this compound with a hands-on understanding that goes well beyond theoretical application. Our daily experience tells us its importance isn’t just written into its formula, but revealed in how reliably it enables targeted transformations across a range of advanced synthetic pathways.
Every batch of our 4-(Phenylthio)benzaldehyde follows careful procedures to lock in consistent color, purity, and performance. The material forms as a pale yellow to off-white crystalline solid. High-performance liquid chromatography confirms the purity, routinely exceeding 98%. We prepare each lot with an eye for further modification, anticipating the exacting demands of advanced organic synthesis. Chemists rely on its clean isolation and highly distinct odor—qualities that signal a clean product and discourage ambiguity during handling.
This compound fills a specific and valuable niche as an intermediate in the preparation of more complex molecules. In practice, our customers often use it as a starting building block for pharmaceuticals, organic functional materials, and specialty ligands. In our own work, we’ve employed it as a substrate in selective oxidation and reduction experiments. The aldehyde functional group sits adjacent to the phenylthio moiety, providing two highly reactive sites that open the door to wide chemistry—acylation, condensation, and coupling all become more controlled when this intermediate forms the backbone of the pathway.
Many labs working with standard benzaldehyde derivatives run into problems with selectivity or reactivity. The difference with 4-(Phenylthio)benzaldehyde lies in the impact of the phenylthio substitution at the para position. The sulfur atom increases electron density, shifting the reactivity profile of the aromatic ring. We’ve seen this adjustment produce better outcomes in nucleophilic substitution and cross-coupling reactions that often stall when basic benzaldehydes fall short. The sulfur bridge does more than tweak electronics; it also provides a handle for future elaboration, letting researchers extend their molecular targets without costly protection and deprotection steps. Our colleagues in medicinal chemistry report that this property streamlines their workflow, especially during combinatorial library expansion.
Manufacturers face plenty of risk when handling sensitive or complex intermediates. Over the years, we’ve optimized our supply chain to minimize those risks, drawing on reliable sources for raw thioanisole and precision-reactor environments for each phase of synthesis. We utilize glass-lined vessels and inert atmospheres at key points to curb side reaction rates—a lesson learned from early efforts where sulfur compounds sometimes surprised us with unpredictability. This reliability proves valuable not only to our downstream partners with their just-in-time inventory needs, but also to early-stage researchers whose projects depend on a fresh batch at a moment’s notice.
In the day-to-day of manufacturing and laboratory support, we prioritize manageable handling and storage logistics. Short-term storage at cool room temperature suffices for most applications, and we package the material in sealed, light-blocking containers to prevent premature oxidation. The aldehyde and thioether groups each need respect, as aldehydes in general trend towards polymerization or self-condensation if left uncapped; our stability testing, run over years, directs us to include small amounts of stabilizer only where necessary, steering clear of unnecessary additives. Material transfer—especially for scale-ups—uses equipment chosen to minimize both operator contact and exposure to air or moisture. Safe handling protocols emerge from repeated use, not from theory, and our supervisors highlight small changes such as antistatic procedures and personal protective gear as habits proven to protect staff over the long haul.
4-(Phenylthio)benzaldehyde offers an aromatic aldehyde structure with a para-phenylthio substitution. This structural twist lets chemists access cross-coupling, condensation, and rearrangement chemistry that ordinary 4-substituted benzaldehydes struggle to support. In production, we’ve noticed how its melting point and solubility profile cater well to both traditional organic reactions and newer methodologies involving C-H activation or photoredox catalysis. Many customers exploit the enhanced reactivity for Suzuki, Stille, or Heck-type couplings, which harness the thioether as a leaving group or anchoring site. Our hands-on experience also validates the compound’s superior resistance to uncontrolled side reactions compared to unsubstituted isomers—which often degrade more rapidly or lose definition in large-scale heating steps.
Our product serves those looking to customize small molecules in medicinal and material science research. During process optimization, partners reported a marked drop in byproduct formation because the sulfur linkage provides steric shielding, which reduces adventitious reactions at the aldehyde group. Others take advantage of the para-position thioether for downstream oxidation, making sulfoxides or sulfones as core fragments in heterocyclic ring formation. We’ve collaborated with teams investigating new photovoltaic materials, and their synthetic work uses this intermediate as a bridge between aromatic layers, showing improved electronic transmission and stability in the finished devices. These shared successes emphasize the compound’s flexibility—a feature we witness not as a catchphrase, but as demonstrated performance over time.
In our facility, every lot passes through rigorous quality and traceability checks before shipment. Batch numbers, manufacturing logs, and retention samples provide a clear audit trail, supporting transparency and accountability. Our packaging scale ranges from grams for research applications up to multi-kilogram drums for process development and commercial runs. Customers value this adaptability, since procurement often demands reliable supply at both pilot and production levels. All documentation—COAs, MSDS, impurity profiles—comes compiled through routine, not as a reluctant afterthought, reflecting our role as both manufacturer and long-term partner in the supply chain.
New synthetic targets rarely cooperate with straightforward paths. In our own campaigns and through feedback from synthetic chemists worldwide, the addition of a phenylthio group at the para-position frequently resolves selectivity bottlenecks. For example, in trials comparing 4-hydroxybenzaldehyde and 4-(phenylthio)benzaldehyde as starting materials, yields for sensitive coupling reactions increased by over 25%, and purification steps simplified, thanks to improved solubility differences between product and byproducts. The extra lever that this sulfur substituent provides lets project teams pivot chemistry mid-course, switching easily between reduction, oxidation, or cross-coupling as ideas evolve. We track each change in method, learn from outcomes, and implement solutions in the next manufacturing cycle, constantly improving both quality and versatility.
Every machine operator and chemist at our plant recognizes the expectations that come when shipping fine chemicals to research and manufacturing customers. Missed shipments or drifts in quality disrupt research schedules, wasting weeks or even months of effort. We focus on stable process control—temperature, pressure, and in-process analytics—using automated feeds and in-line sensors for instant checks. Staff training, rigorous cleaning protocols, and immediate supervisor reviews keep material contamination close to zero. During times of supply chain stress, these habits matter. Our stockroom keeps buffer inventory on hand, isolating critical supply from raw material delays.
Our team learned early that waste generated from aldehyde and thioether chemistry can pose environmental risks if left unmanaged. We invested in on-site scrubbers and closed-loop handling systems to minimize fugitive emissions of sulfur compounds, which often present as pungent, lingering odors or corrosive vapors. The spent organic solvents from purification receive careful disposal or recycling, protecting both worker health and ambient air quality in our neighborhood. Industry leadership on sustainability does not materialize from slogans; it emerges from repeated scrutiny and steady process recalibration.
4-(Phenylthio)benzaldehyde does not stop at the research bench. Tech-transfer and process teams rely on access to consistent, high-quality batches as they move from experimental validation to commercial run rates. Early-stage discovery projects often need just a few grams, while process chemists request tens of kilograms, occasionally more. Seamless communication and rigorous order tracking lets us adjust rapidly to sudden upscaling, providing the bridge from promising invention to market-ready reality. We observe how specification drift or process mishaps during scale-up can derail otherwise successful research; the lessons learned from each ramp-up feed improvements into the next cycle, avoiding repetition of common pitfalls.
Each batch runs through multi-stage analytical testing calibrated by years of real-world experience. Our investment in GC-MS, HPLC, and titrations prevents ambiguity or drift in composition. Internal reference standards and blind trials weed out systemic error long before material leaves the warehouse. Operators who supervise dozens of product runs know the signature odor and behavior changes signaling a problem: these are not just numbers, but lived knowledge, amplifying early warnings and preventing costly mishaps. The balance between speedy delivery and uncompromising testing follows not from policy, but practice developed side-by-side with our customers.
The international market now demands greater regulatory focus, precision, and documentation than in the last decade. From REACH compliance in Europe to local environmental monitoring, we adapt our in-house protocols to anticipate these shifts. Reagents and auxiliary materials used in the process comply with relevant industry standards, and we review hazard communications and labeling after any process change. We neither understate hazards nor drown buyers in unnecessary warnings, preferring clarity and honest communication. As experienced operators, we respect that our job includes both sharp technical expertise and clear, open lines of dialogue with every customer or auditor walking our floor.
Compared to related benzaldehyde derivatives, 4-(Phenylthio)benzaldehyde consistently generates less process waste due to its enhanced selectivity and higher yields. Chain-of-custody records demonstrate fewer failed reactions, fewer returns, and higher downstream product acceptance rates from our customers. Coupling partners, functionalized resins, and high-performance polymers all benefit from the unique sulfur handle—phenomena that do not surface so predictably with 4-alkoxy or 4-halogenated analogs. Its nuanced aromaticity and modular reactivity guarantee it remains the preferred choice in scenarios demanding both a tough aldehyde and a transformable sulfide group.
We devote considerable attention to sharing practical knowledge gained during production and application. Our technical support engineers consult on reaction design, workup, and purification strategies, offering insights born of years handling this exact compound. Customers routinely tap into this knowledge bank, bridging gaps between new lab discoveries and established best practices. We keep detailed records not only on process conditions but also on recurring troubleshooting advice, passing along wisdom from dozens of process improvement cycles. Continuity in personnel further bolsters this network, ensuring that field guidance draws on lived experience, not recycled abstractions.
As demand for highly functionalized aromatic intermediates continues to climb, 4-(Phenylthio)benzaldehyde stands ready for new roles in greener chemistry, advanced electronics, and streamlined pharmaceutical synthesis. Our process chemists and operators keep their eyes open for next-generation applications—photochemical switches, chiral auxiliaries, novel monomers—constantly updating techniques and documentation with every validated experiment. We embrace a feedback culture that prizes openness, letting each unexpected result shape future syntheses and factory policy. In this way, every drum and shipment sent out the door contains not just molecules but a living record of teamwork, technical persistence, and customer dialogue.
Forged through teamwork, tested during batch trials, and relied upon by researchers from bench to reactor hall, 4-(Phenylthio)benzaldehyde stands out for more than just the sum of its atoms. Our commitment runs through every stage of its journey, shaped not by marketing language but by stubborn dedication to outcomes that hold up under real-world pressures. The lessons we gather—about sulfur chemistry, aromatic reactivity, or simply how to keep a batch stable during transit—fuel our ongoing work and connect our daily routines with the needs of scientists and engineers around the globe.