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Phenylpropyl Aldehyde

    • Product Name Phenylpropyl Aldehyde
    • Alias 3-Phenylpropionaldehyde
    • Einecs 208-366-2
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
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    Specifications

    HS Code

    648073

    Chemicalname Phenylpropyl Aldehyde
    Iupacname 3-Phenylpropanal
    Molecularformula C9H10O
    Molecularweight 134.18 g/mol
    Casnumber 104-53-0
    Appearance Colorless to pale yellow liquid
    Boilingpoint 221-223 °C
    Meltingpoint -31 °C
    Density 1.006 g/cm³ at 25°C
    Flashpoint 94 °C
    Refractiveindex 1.522
    Solubilityinwater Slightly soluble
    Odor Floral, hyacinth-like
    Purity Typically ≥ 98%
    Vaporpressure 0.07 mmHg (20°C)

    As an accredited Phenylpropyl Aldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Phenylpropyl Aldehyde is supplied in a 100 mL amber glass bottle with a secure screw cap and tamper-evident seal.
    Shipping Phenylpropyl Aldehyde should be shipped in tightly sealed containers under cool, dry conditions and protected from light. Label containers according to regulatory guidelines, indicating flammability and health hazards. Use appropriate secondary containment and cushioning to prevent leaks or breakage during transport. Handle in compliance with all applicable local, national, and international shipping regulations.
    Storage Phenylpropyl aldehyde should be stored in a tightly sealed container, away from light and moisture, in a cool, well-ventilated area. Keep away from heat, ignition sources, and incompatible materials such as strong oxidizers. Properly label the container and store it in a designated flammable storage cabinet. Use secondary containment to prevent leaks or spills.
    Application of Phenylpropyl Aldehyde

    Applications of Phenylpropyl Aldehyde in Industrial Manufacturing

    As a primary producer of phenylpropyl aldehyde, we support industrial partners across specialized sectors that demand strict quality assurance, technical integration, and proven regulatory compliance. The following application scenarios represent established downstream uses where precise process knowledge, controlled formulation, and direct end-use documentation guide every shipment from our facility.

    1. Fine Fragrance Compound Formulation

    International fragrance compound manufacturers incorporate phenylpropyl aldehyde as a key top and heart note material due to its floral-green, hyacinth-like character and controlled volatility. Our product consistently meets the narrow odor specification and purity parameters required for the design of high-end perfumery bases and customized scent accords, especially in formulations targeting European and Asian consumer markets where compliance and batch traceability are paramount.

    Industry compliance standards

    • International Fragrance Association (IFRA) Standards & Amendments
    • EU Cosmetics Regulation (EC) No 1223/2009
    • REACH (EC) No 1907/2006 Registration & Safety Data Sheet
    • ISO 9235:2013 (Aromatic Natural Raw Materials)

    Typical usage ratio

    • 0.05% – 1.2% of total fragrance oil composition, varying by target application (eau de parfum, fine mist, or concentrated extract). Selection and adjustment depend on intensity, volatility profile, and finished product olfactory requirements.

    Downstream process integration

    • Added during the compounding phase of fragrance oil manufacture after solvent blend stabilization, before extended maturation and filtration
    • QC monitored for batch consistency and odor profile retention under blending and aging conditions

    Final product types

    • Luxury eau de parfum solutions
    • Fine mist body sprays
    • Scented personal care concentrates
    • High-performance accords for bespoke perfumery lines

    2. Flavors for Food and Non-Alcoholic Beverages

    Food ingredient manufacturers utilize phenylpropyl aldehyde in the development of floral and fruity top notes for use in flavor compositions for carbonated and still soft drinks, confectionary, and bakery applications. Because food products face extensive safety assessment, our facility provides detailed batch certificates and identity verification traceable down to approved food additive lists and migration guidelines relevant to every major market.

    Industry compliance standards

    • Food Chemicals Codex (FCC)
    • Regulation (EU) No 1334/2008 (Flavourings and Food Ingredients With Flavouring Properties)
    • US FDA 21 CFR Part 172.515 (Synthetic Flavoring Substances)
    • ISO 22000:2018/FSCC 22000 Food Safety Management

    Typical usage ratio

    • 2–12 ppm in finished beverage or food matrices; adjusted based on product type, base acidity, and shelf life requirements determined by sensory panels and regulatory maximums

    Downstream process integration

    • Incorporated in the final flavor oil or water-soluble flavor base preparation, post thermal processing to preserve aromatic integrity
    • Compatibility tests performed to evaluate heat and light stability before final blending

    Final product types

    • Flavored sparkling beverages (e.g., floral sodas, botanical mixers)
    • Chewing gums and sugar confectionery
    • Ready-to-drink teas and functional drinks
    • Baked fruit bars with floral notes

    3. Pharmaceutical Intermediate in Cardiovascular APIs

    The pharmaceutical sector employs phenylpropyl aldehyde for the controlled synthesis of certain cardioactive active pharmaceutical ingredients (APIs) and their intermediates, especially within aromatic drug family production. Analytical batch documentation, strict impurity profiles, and qualification for multi-stage synthesis ensure customers receive materials suitable for high-purity downstream transformation under GMP guidelines.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.) monographs for intermediates
    • US Pharmacopeia (USP) <493> Residual Solvents
    • Chinese GMP (2010, revised 2020)

    Typical usage ratio

    • 10–20% molar equivalent as a coupling partner in selective aromatic substitutions or reductive amination reactions; ratio determined by targeted synthetic route and required final API purity

    Downstream process integration

    • Fed into staged reactor setups directly after the completion of precursor reduction step, typically under N2 atmosphere
    • Subjected to rigorous in-process controls for residual aldehyde and impurity quantification during subsequent reaction and isolation

    Final product types

    • Aromatic cardiovascular drug intermediates (proprietary structures)
    • Bespoke custom synthesis building blocks for further scale-up
    • cGMP-certified pharmaceutical actives subject to full regulatory submission

    4. Aroma Chemicals for Air Care and Home Fragrance

    High-volume aroma chemical formulators draw on the pronounced green floral facets of phenylpropyl aldehyde to provide both top-load and lasting background notes in a wide spectrum of air care and home fragrance bases, including engineered gels and polymer-embedded scent systems. Strict evaluation protocols govern its admission into such products, given the open-system volatility and consumer sensory exposure profiles.

    Industry compliance standards

    • IFRA Air Freshener Standard (Annex I, III)
    • OECD Guidelines on Volatile Organic Compounds in Consumer Products
    • California Air Resources Board (CARB) VOC regulations for Air Fresheners
    • EU CLP Regulation (EC) No 1272/2008 for labeling/classification

    Typical usage ratio

    • 0.1% – 1.5% in aroma oil or air care base, determined by end dispersion method (aerosol spray vs. gel or reed diffuser) and target longevity/evaporation rate

    Downstream process integration

    • Blended into specialized carrier matrices before emulsification or polymer casting stage; compatibility screening with fixatives and stabilizers for consistent volatilization
    • Performance tests executed for continuous-release and consumer panel feedback prior to final filling

    Final product types

    • Aerosol and non-aerosol air fresheners
    • Reed diffusers with floral-green accord
    • Polymer scent beads, engineered gels
    • Plug-in fragrance refills

    5. Scented Detergent and Fabric Care Applications

    Industrial detergent and fabric care formulators employ phenylpropyl aldehyde to impart complex floral-green notes in high-temperature or high-alkaline environments, where classic perfumery aldehydes may lack heat or base stability. We guarantee material performance through dedicated application trials and supply raw material tailored for large-scale blending and end-user validation studies under realistic wash conditions.

    Industry compliance standards

    • A.I.S.E. Charter for Sustainable Cleaning (Europe)
    • IFRA Guidance for Detergent Applications
    • REACH Annex XVII Restrictions for Home Care Chemicals
    • ISO 9001:2015 Quality Management

    Typical usage ratio

    • 0.02% – 0.5% of total perfume accord added to the detergent or fabric softener matrix, modulated according to base composition and wash process conditions (liquid, powder, capsule)

    Downstream process integration

    • Integrated after base surfactant formulation and pre-encapsulation if used with controlled-release mechanisms
    • Ensured odor hold and performance in simulated thermal cycling and wet-dry fabric tests

    Final product types

    • High-performance laundry detergents
    • Premium fabric softeners
    • Liquid and sheet-based fabric freshening products
    • Heavy-duty powder cleaners for commercial use
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    Competitive Phenylpropyl Aldehyde prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    Phenylpropyl Aldehyde: Taking Clarity and Reliability to Craft Chemical Work

    A Manufacturer’s Perspective on Phenylpropyl Aldehyde

    Over the years, few specialty chemicals have proven themselves as versatile as Phenylpropyl Aldehyde. In our operations, each batch stands as both a technical product and the result of careful, hands-on chemical management. Quality at this level isn’t just about purity — it builds on process controls, real-world supplier relationships, and user feedback from industries facing tight regulatory and performance targets.

    What Sets Phenylpropyl Aldehyde Apart?

    Known among chemists by its molecular formula, C9H10O, Phenylpropyl Aldehyde’s main draw lies in its reactivity and aromatic structure. Our experience shows that making this compound requires tight control from raw feedstock selection straight through distillation and purification. By focusing on trace contaminant removal and maintaining a colorless, low-odor product, our team has helped fine fragrance blenders, pharma intermediates producers, and advanced material labs work without unexpected off-notes or reactivity issues.

    We’ve answered many technical questions about aldehyde impurities. Structurally, phenylpropionaldehyde differs from related aldehydes such as benzaldehyde or cinnamaldehyde by its unique side chain: a phenyl ring tethered to a three-carbon aldehyde group. This structure changes how the molecule behaves not just in lab glassware, but in high-throughput manufacturing lines. Benzaldehyde brings a sharper, almond-like aroma and a different reactivity profile; cinnamaldehyde leans spicy and works better in food flavoring and antimicrobial formulations. Phenylpropyl Aldehyde, by contrast, lands with a subtler, more rounded aroma, valued for both masking unwanted notes and building layered scent profiles.

    Product Models, Purity, and Consistency

    We’ve tailored our Phenylpropyl Aldehyde output to meet the real demands of industrial users. Common specifications include assay values exceeding 98%, water content below 0.1% by Karl Fischer titration, and carefully managed peroxide and acid numbers. These figures aren’t pulled from theoretical tables, but measured batch after batch with the same attention a craftsman brings to handmade goods.

    Applications keep expanding. In perfumery, users need high-purity material that won’t muddy floral, woody, or citrus compositions, nor introduce harsh metallic notes after blending. For pharmaceutical synthesis, controlling for trace metals and side-reaction byproducts becomes non-negotiable. Some end users request lower color indexes for optical material synthesis. Our production lines flex to produce multiple grades — but always with one eye on long-term customer partnerships and real use feedback.

    Besides purity, physical properties matter for handling and processing. Operators benefit from a liquid state at room temperature, without solidification or phase separation. Flash point, boiling range, and density are confirmed using ASTM or EN methods. Every specification draws from extensive dialogues with process engineers, perfumers, and downstream quality teams.

    Manufacturing Know-How and Experience Matters

    Controlling batch quality starts long before the reaction even begins. We start with bulk aromatic feedstocks chosen for historical reliability, not just price. Our reactors run under nitrogen to avoid unwanted oxidations, and analytical QC checks begin even before distillation. Repeatable, reproducible color, odor, and assay outcomes follow naturally.

    Several times each year, a customer will troubleshoot a batch’s performance. In one case, a perfumer in Europe traced back an off-note to a trace impurity at the ppm level — something only someone who works with real volumes and real processes notices. That’s where experience counts: we pulled past batch records, re-examined all spectrograms, and discovered the source came from a feedstock change at one supplier. Switching to our historically tested supplier line restored the quality and client trust.

    Handling waste and byproducts means keeping an eye on environmental compliance. Over time, we’ve improved process yields and reduced residuals. Residual aromatics move to solvent recovery rather than waste, and neutralization reactions send byproducts safely for disposal by licensed firms. Keeping a shop floor clean and a compliance file up-to-date doesn’t just tick regulatory boxes; it keeps lines running and customers supplied without supply chain interruptions.

    Real-World Usage: Why Industry Relies on Genuine Manufacturer Support

    Users in perfumery, flavor manufacturing, and intermediate chemical synthesis all require something different from their Phenylpropyl Aldehyde supplier. For a fragrance firm, odor stability with minimal drift under storage means finished fragrances remain true over months or years on store shelves. Multiple small batch trials, spot odor checks, and aging trials guide our production standards just as much as gas chromatography does.

    For pharmaceutical users, reactivity and process compatibility matter most. Batch-to-batch certainty lets process chemists hit target yields while keeping qualification paperwork manageable. That’s why we run not only typical purity tests, but also impurity profiling to single-digit ppm levels for identified aldehyde and alcohol by-products.

    Flavor formulators look for the balance between performance and regulatory clearance. Phenylpropyl Aldehyde brings a soft, honey-floral impression that can enhance fruit and floral notes, blending in where more aggressive aldehydes would overwhelm the matrix or introduce safety concerns. The FIEMA and JECFA clearance status of our product comes after detailed composition and residue testing.

    Other users—those making advanced polymers or specialty resins—value both reactivity and physical handling. At our site, we developed protocols for drums and iso tanks to avoid contamination, water ingress, or solvent carryover. Precise bulk transfer, dedicated hoses, and nitrogen blanketing became standard operating practice after feedback from the field showed how even minor cross-contamination could affect end properties of high-value resins and coatings.

    Comparing Phenylpropyl Aldehyde with Other Aromatic Aldehydes

    Benzaldehyde, cinnamaldehyde, and vanillin come up often as comparison points during formulation development. Each brings distinct profiles and limitations. Benzaldehyde works in applications needing bright, high-volatility top notes, but it also introduces risks around polymer yellowing and regulatory restrictions in ingestible products. Cinnamaldehyde, with its characteristic cinnamon bite, is preferred in oral care and culinary contexts, but often causes skin sensitivity and performance trade-offs in complex formulations.

    Our experience shows Phenylpropyl Aldehyde addresses a gap between these alternatives. Its milder, delicate note enables broader formula compatibility, with fewer odor clashes and regulatory barriers in personal care, fine chemical, and art restoration uses. At a technical level, the more extended alkyl side chain softens volatility, delivering a more subtle release profile in fragranced consumer products. We’ve even seen research labs experimenting with unique cross-linking patterns in material sciences, taking advantage of the compound’s moderate aldehyde reactivity rate.

    Process Reliability from Lab to Loading Dock

    With each production run, our lab team documents sample retention, chromatogram libraries, and stability records. Real learnings come from what happens after the drums leave our site: feedback from process upsets, fine-tuning of storage instructions, or adjustments to stabilization additives. By keeping technical and commercial teams close, we track lot performance over time. We routinely review logistics and packaging practices — from drum linings that resist solvent attack to supply chains built on local and global redundancy — based on what actually delivers value in the hands of plant operators.

    Regular site audits and ever-tightening international standards drive improvements. We act on reports of material settling, pumpability changes at low temperatures, or clouding under temperature swings. One customer in North America reported gumming after a spell of winter transport; we adjusted drum warming protocols and internal product testing to replicate the cold-chain effect, preventing similar problems three winters running.

    Upstream Sourcing and Downstream Impact

    Sourcing transparency anchors our entire workflow. Feedstock quality shapes every batch’s cost, yield, risk profile, and customer satisfaction level. We maintain direct ties to a network of vetted raw material suppliers, drawing on more than a decade of collective purchase histories and analytical data. A shift in source purity or byproduct spectrum triggers immediate trial batches, documentation, and customer notification where relevant.

    Downstream, we see Phenylpropyl Aldehyde show up in surprising places. In European plant extract refineries, the compound’s gentle aromatic boost refines essential oil blends for luxury perfumery. Small-scale electronics assemblers request it for surface cleaning and resin curing work. Specialty agrochemical developers reach for it as a reactive intermediate for targeted crop protection synthesis. Each of these users faces their own cost pressures, regulatory hurdles, and product integrity demands.

    As a manufacturer, we embrace the need for open technical feedback. We set up direct lines from quality teams to end-user technical managers, aiming for quick resolution and data sharing. One advantage of making a product instead of moving it as a trader: deep technical archives, in-house analytical gear, and dedicated batch records that help solve a wide range of after-sale questions.

    Troubleshooting and Ongoing Improvement

    Even with mature processes, challenges arise. On occasion, a customer line will see inconsistent curing rates or off-spec odor drift. Our team reviews historical lot data, current batch test results, and process logs, chasing root causes down to possible storage environment swings, equipment fouling, or operator process changes. In one recent instance, a minor storage tank coating incompatibility led to increased metallic trace content; we swapped tank linings and retested the outgoing lots, restoring baseline performance.

    We invest steadily in new analytical tools — NMR, GC-MS, trace water detectors — but never overlook hands-on inspections. Many issues come to light only through direct odor or visual checks. Repeat sampling, manual drum inspections, and open-door policy for customer site audits reflect our belief that durable supply relationships depend on mutual trust and shared technical knowledge.

    Regulatory changes and customer-driven initiatives push us toward continuous process improvement. When a global flavor house moved to restrict minor impurities flagged by evolving European Union rules, our site adjusted purification sequences and tightened documentation, then worked with their lab to validate suitability over months of joint trials.

    Supporting Application Development

    Real-world chemical supply means more than just filling orders. Many of our users—working in fields from hair-care bases to specialty inks—innovate rapidly, looking for unique olfactory signatures, improved chemical compatibility, or even novel medical delivery platforms. Our technical service group fields countless questions about process integration, compatibility with complex matrices, or targeted removal of co-impurities. Each new user trial brings insights for the next round of improvement.

    Collaboration between process engineers, in-house QC, and external application scientists often triggers small but meaningful adjustments, whether to stabilize color, minimize migration in final products, or simplify downstream analysis. For a recent start-up in the fine fragrances sector, we supplied sample lots in multiple grades, held joint odor panel testing, and cycled testing through accelerated light-aging environments to fine-tune their blending protocol.

    Innovation sometimes plays out at the micro-scale—gram quantities for pharmaceutical reference standard synthesis or advanced material research. Here, scalable consistency, prompt batch release, and full traceability define service almost as much as bulk supply security. Our centralized data management and real-time batch release processes support these tight, time-sensitive customer needs.

    Meeting Challenges in the Future of Phenylpropyl Aldehyde

    Even as global markets shift and new technologies reshape chemical production, core user needs — clean, consistent, traceable material — remain constant. Customers count on traceability not only for regulatory review but also for internal recall power and product improvement cycles. Our ability to keep detailed batch genealogy, certificate-of-analysis archives, and real-time logistics tracking draws directly from manufacturing site investment and a problem-solving mindset.

    Sustainability and responsible manufacturing continue to rise as focal points. We have implemented energy recovery from our process with solvent recycling, reduced water consumption per ton of output, and adopted stricter emission controls across the site. In response to partner requests, we supply expanded lifecycle impact documentation and third-party audit access. Each year, more partners ask for REACH, IFRA, or Kosher compliance documentation; we prepare for these with robust documentation rather than backfilling after requests come in.

    Shifting raw material costs present cost and supply planning challenges. We manage price instability with buffer stock strategies, local warehousing near key trade hubs, and flexible packaging formats — drums, IBCs, ISO tanks — matching volume needs from pilot trials to full-scale plant runs. This logistics flexibility ensures that the opportunity to innovate or recover from unforeseen supply hiccups remains open to both new and long-term users.

    The Path Forward

    Our work with Phenylpropyl Aldehyde is built on knowing both the molecule and the people who rely on it. By staying focused on technical dialogue, hands-on quality control, and a willingness to adapt production based on hard-won experience, we help customers keep final product integrity high and their compliance headaches low. Each improvement, each technical support request, and each batch shipped confirms that consistency, clarity, and technical partnership matter as much as the chemistry itself.