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HS Code |
837895 |
| Cas Number | 607-89-8 |
| Iupac Name | 2-Phenoxybenzaldehyde |
| Molecular Formula | C13H10O2 |
| Molecular Weight | 198.22 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Melting Point | 11-13 °C |
| Boiling Point | 168-170 °C at 4 mmHg |
| Density | 1.16 g/cm3 |
| Solubility In Water | Insoluble |
| Flash Point | 153 °C |
| Purity | Typically >98% |
| Smiles | C1=CC=C(C(=C1)C=O)OC2=CC=CC=C2 |
As an accredited 2-Phenoxybenzaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 100g bottle of 2-Phenoxybenzaldehyde arrives in a tightly sealed amber glass container with a clear hazard labeling and barcode. |
| Shipping | 2-Phenoxybenzaldehyde is shipped in tightly sealed containers, protected from moisture and light. It is handled as a hazardous chemical, requiring appropriate labeling and documentation. During transit, the package is cushioned to prevent leaks or spills, and handled according to local, national, and international chemical transportation regulations to ensure safety. |
| Storage | 2-Phenoxybenzaldehyde should be stored in a tightly sealed container, away from light, heat, and moisture, in a cool, well-ventilated area. Keep it separated from strong oxidizers, acids, and bases. Ensure all storage containers are clearly labeled. Use appropriate chemical storage cabinets, preferably flammable or hazardous materials storage, and avoid inhalation or direct contact when handling. |
Applications of 2-Phenoxybenzaldehyde in Industrial Manufacturing2-Phenoxybenzaldehyde supports specialized processes in fine chemicals, pharmaceuticals, agrochemicals, and specialty resins manufacturing. Below you will find detailed application scenarios, each addressing compliance, usage ratios, integration steps, and the corresponding finished products. 1. Pharmaceutical Intermediate SynthesisIn pharmaceutical manufacturing, this compound frequently serves as an essential intermediate in the synthesis of active pharmaceutical ingredients (APIs), particularly for molecules containing diaryl structural motifs. It functions as a key aldehyde donor in condensation or coupling steps, enabling precise control of molecular configuration and purity in non-aromatic and aromatic drug scaffolds. Application requires stringent handling to ensure conformity with medicinal-grade quality controls, batch-to-batch traceability, and impurity profiling tailored for regulated drug production facilities. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
2. Agrochemical Synthesis (Herbicide and Pesticide Intermediates)Fine chemical facilities employ 2-Phenoxybenzaldehyde in the production of agrochemical actives, notably as an intermediate in the assembly of selective herbicides and novel insecticidal agents. The grade used must conform to industrial standards for purity and trace-level contaminants to meet downstream regulatory registrations. Manufacturers adjust process flow depending on target molecule sensitivity and specific formulation requirements imposed by agricultural authorities. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Perfume and Aroma Chemical ManufacturingWithin the specialty fragrance sector, 2-Phenoxybenzaldehyde acts as a powerful building block for formulating luxury aldehydic notes and fine aroma molecules. Its reactivity profile enables selective modification to impart floral, powdery, or spicy tonality through acetalization or oxidation. The input material is subject to tight organoleptic evaluation and IFRA compliance to ensure safe use in personal care and household products. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Specialty Resin and Polymer AdditivesManufacturers in the polymer sector utilize this compound as a cross-linking aldehyde or precursor in the creation of advanced resins, including thermosetting and copolymer systems. The product typically enters as a functional monomer to control cure rates, flexibility, and adhesive properties. Its reactivity and compatibility with diverse resin chemistries require careful optimization based on target application, with full documentation provided for industrial safety and material performance. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
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Experience builds understanding. Over twenty years spent working in chemical manufacturing has taught us how nuances in compound structure open entirely new possibilities for downstream industries. Among many aromatic aldehydes we produce, 2-Phenoxybenzaldehyde often stands out in customer discussions—not just because of its unique molecular arrangement, but also due to the doors it opens in organic synthesis, especially across agrochemical and pharmaceutical sectors.
2-Phenoxybenzaldehyde’s backbone consists of a benzene ring carrying a phenoxy group at the ortho position relative to an aldehyde. This simple shift does more than chemistry textbooks would ever suggest. Newer colleagues sometimes ask us what makes this structure so desirable compared to other substituted benzaldehydes—such as the widely known 4-phenoxybenzaldehyde or plain benzaldehyde.
The answer starts with reactivity. The ortho-substituted ether linkage on the benzene ring modifies both electron density and steric properties near the reactive aldehyde group. That allows formulators to steer downstream reactions, tailoring nucleophilic additions or condensation steps with greater selectivity than with para- or meta-substituted analogues. In many cases, end-product developers can fine-tune functional group compatibility, especially in multi-step syntheses targeting active ingredients in crop protection or synthetic intermediates in medicinal chemistry.
We have spent years refining purification protocols, learning from each production run about the critical impact of even trace side products. In our experience, color stability under ambient conditions served as an early indicator of meaningful product quality. By the time GC and HPLC became daily tools in our labs, we knew what impurity profiles to watch for—the appearance of 2-hydroxybenzaldehyde, dimers, or unreacted phenol trace back to the nuances of oxidative conditions during synthesis or subtle control of temperature gradients in the final batch distillation.
For 2-Phenoxybenzaldehyde (often sold under the “OPB” model label, derived from ortho-phenoxybenzaldehyde), the norm is to target a colorless to pale yellow oily liquid, with purity routinely exceeding 99% by area (GC). Boiling point under atmospheric pressure hovers around 150°C at reduced pressures, such as 1 mmHg, while the true decomposition temperature lies well above typical lab glassware tolerances, reducing handling risk during scale-up.
Water content remains critical. We invest in Karl Fischer titration and constant nitrogen blanketing during decant for this very reason—a wet batch can tank downstream reactions, especially where moisture-sensitive reactants or catalysts are involved, such as in the formation of benzimidazoles or imines.
The best way to step beyond marketing hype is to discuss practical use. The bulk of commercial 2-Phenoxybenzaldehyde demand lands in pesticide intermediate synthesis, particularly for those seeking a route to compounds like fungicidal benzimidazoles. By comparison, other isomers (like para-phenoxybenzaldehyde) often find their way into dyes or specialty fragrance chemistry, where steric hindrance and ring activation differ. Having supplied both, we regularly see the ortho form requested for projects where intermediate reactivity—the ease with which an imine forms, or coupling to an amine—is key to process efficiency.
Unlike basic benzaldehyde derivatives that oxidize quickly in open air, our 2-Phenoxybenzaldehyde batches maintain stability on the shelf, resisting the slow resinification or darkening that frustrates research teams who need weeks or months for process optimization. Regular feedback from our pilot customers, ranging from regional agrochemical labs to global synthesis plants, helped shape our internal stability tests. This ongoing feedback cycle influences our purification decisions and the way we package bulk shipments, avoiding plasticizers and volatile contaminants that would otherwise seep into supposedly “pure” stocks.
Comparing 2-Phenoxybenzaldehyde directly to other common aromatic aldehydes, the distinctions never ring clearer than during actual production campaigns. For example, chemists pursuing 4-phenoxybenzaldehyde will notice that critical step conditions—like reaction pH, temperature, and solvent chapel—shift when moving to the ortho isomer. This can mean re-tooling reactor setups or adjusting feedstock timings during scale-up, time that can quickly add up unless you have experienced staff on hand. In our plant, cross-training for those moving between product campaigns proved essential, and we now recommend similar approaches for customer facilities working with a mix of isomers.
Some buyers prefer to discuss 2-Phenoxybenzaldehyde’s odor—a matter that rarely appears in technical sheets, but in reality, the mild but distinct almond-like smell can serve as an in-process check on material purity. Our blending operators use the sensory cues as backup confirmation, especially when rapid batch checks need to support inline HPLC.
Aldehyde chemistry gets tricky for unprepared hands. Over the years, stories circulated through the industry about unexpected side reactions triggered by residual peroxides in aged solvents or by metal-catalyzed oxidation lurking in recycled glassware. Several years back, a skip in routine cleaning led us to a stubborn contamination issue—a costly lesson, but one we share with any partner scaling up their own handling protocol for 2-Phenoxybenzaldehyde.
We observed that ortho-substituted phenoxy structures resist self-condensation under mild storage conditions, meaning our product ships and stores more cleanly than highly reactive, less substituted isomers. But even with increased stability, an aldehyde’s reactivity never fully disappears. We train our operators to manage short exposures and stress good airflow—safety goggles and gloves are a must, and after one misadventure with overloaded vapors, we refined our use of local extraction and regular air monitoring. These aren’t just regulatory requirements; they protect your crew and prevent workplace interruptions.
Chemistry is nothing if not iterative. We began searching for greener synthesis routes to 2-Phenoxybenzaldehyde years ago—long before “green chemistry” became a conference buzzword. Classical methods once used higher quantities of chlorinated solvents and generated byproduct salt loads difficult to treat. Our team experimented with phase-transfer catalysts and recyclable base systems, eventually slashing wastewater loads by a measurable margin. The real test comes from regulatory visits—sampling wastewater at the fence line, not just in the laboratory. It changes your view on process yields and motivates further recycling and heat integration.
Our ongoing pursuit of minimized solvent use, waste acid neutralization, and energy efficiency has become part of the daily production cycle. We monitor solvent loss and vapor emissions, not simply to meet limits, but to shave down production costs and reduce impact on neighboring communities. This hands-on approach to sustainable production can’t be captured by a technical data sheet, but partners who tour the plant quickly pick up on the changes we’ve put into practice.
Every manufacturer faces a defining moment—what to do when a batch fails on spec. We keep detailed production logs reaching back over a decade, mapping not just average batch values but outlier incidents, strange GC spike patterns, or customer returns linked to downstream isolation failures. That record-keeping builds institutional memory. One of our more striking findings was the influence of minor solvent residues left after vacuum stripping, which led to subtle side reactions in a few high-value pharma projects. Today’s process incorporates extra steps in in-line degassing and product hold-out tests, directly responding to those gigabytes of actual plant data.
External audits matter too. We regularly host process walk-throughs for clients and third-party quality specialists, opening up yields, formaldehyde emission logs, raw material traceability, and batch-to-batch reproducibility studies. Experience has shown that an open-book approach not only builds customer trust but also spurs improvements straight from user feedback. Clean reports sometimes give way to collaborative troubleshooting, which has steadily improved our product’s standing in both domestic and export markets.
Nothing deflates a supplier relationship quite like logistics gone wrong. We learned the hard way years ago that 2-Phenoxybenzaldehyde can react with some plastics, even those regarded as industrial-grade. Direct-to-metal drums with certified liners now make up the bulk of our shipments, and pre-shipment QC pulls random samples for odor, tint, and water content—all actual order-winning criteria for global pharma customers.
Storage brings its own set of considerations. We’ve seen slow product darkening in drums exposed to fluctuating warehouse temperatures, which correlates with polymerization triggers in other aldehydes as well. Shaded storage, stable temperatures, and periodic opening for off-gassing combine for the best shelf-life outcomes, a lesson learned from a failed early shipment to a tropical partner. We archive shelf samples from every batch and track them for a minimum of eighteen months, releasing stability data to any end user who requests it for regulatory or internal qualification.
Open lines of communication became our best safeguard against field complaints. Our support teams—not sales departments—field calls about product clouding or unexpected residuals after months in a drum. Sometimes, an issue boils down to storage at ambient humidity, or to incomplete cleaning of customer tanks. We offer troubleshooting rooted in years of field visits, including sampling techniques, glassware cycling, and cross-contamination fixes that have saved users whole batches of sensitive intermediates.
We invite critical feedback to spot trends—rising impurity bands in targeted applications or unwelcome reactivity during custom syntheses—allowing for more rapid production adjustments than top-down management would ever consider. That level of responsiveness often means more to repeat customers than marginal pricing tweaks, especially for those seeking a reliable partner over extended procurement cycles.
It’s easy to focus on raw numbers or theoretical meta-analyses of performance. The lived reality runs deeper. In our labs, we produce gram-scale pilot runs alongside every commercial batch, linking bench-top findings with actual factory output. Analytical protocols—titrations, GC, NMR—underpin every lot released, but so do lived partnerships between research chemists and plant operators who have experienced firsthand the challenges of scale-up, sudden supply chain breakdowns, or equipment upgrades that shift yield curves.
We keep open records of batch data, letting those seeking ISO or GMP pathways review process history for their own audits. That transparency ties directly to the real-world reliability and consistency demanded by regulatory authorities in pharmaceuticals, as well as agricultural product compliance inspectors.
Industrial chemistry rewards discipline, but it also values adaptability. Every time a production hiccup brings a new lesson, the feedback integrates into not just plant documentation, but team training. We incorporate lessons from near-misses and best practices, training operators on not only the technical steps involved in 2-Phenoxybenzaldehyde manufacture but the judgment calls that keep output predictable and safe. Actual experience with daily plant conditions—temperature fluctuations, raw material deviations, or even power interruptions—often proves more valuable than the theoretical optimal. Regular refresher sessions ensure lessons stick, not just on paper but out on the plant floor.
There’s no substitute for direct head-to-head comparison. Engineers asking about switching from 2-Phenoxybenzaldehyde to simpler benzaldehydes quickly learn that reaction route selection impacts more than yield. Each benzaldehyde isomer brings a slightly different set of reactivity and separation challenges. Where bulk para-phenoxybenzaldehyde or unsubstituted benzaldehyde offer easier access or lower price, the ortho compound delivers gains in selectivity and process safety at several downstream steps. Customers who evaluate total lifecycle costs—including process optimization, stability, and rework rates—frequently return to the ortho isomer for these reasons, pushing us to stay vigilant on production quality and supply guarantees.
Adaptation never ends. As new regulatory pressures build and market shifts prompt formulation changes, we stay in close dialogue with users, tweaking product specifications and shipping options to suit evolving needs. Whether that means implementing additional filtration, testing lower-odor batches, or offering technical guidance on solvent compatibility, our daily hands-on experience with the chemistry ensures that support runs deeper than a product code or technical bulletin.
We built our reputation not just on in-spec production, but on shared problem-solving with labs, process engineers, and logistics teams navigating the messy realities of chemical manufacturing. There’s no magic bullet for each challenge, but open dialogue, proven expertise, and constant improvement drive the industry forward.
Every shipment of 2-Phenoxybenzaldehyde goes out backed by years of accumulated practical wisdom, careful record-keeping, and the sometimes hard-earned lessons that come from operating at commercial scale. Customers don’t just buy a compound—they trust that our experience will catch mistakes before they matter, support troubleshooting when surprises arise, and reflect a proven track record of responsiveness. That’s what turns a niche product into a business-critical link in diverse supply chains—agricultural, pharmaceutical, or otherwise—bound together by real-world reliability.