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HS Code |
854604 |
| chemical_name | Cinnamaldehyde Diethyl Acetal |
| cas_number | 2478-10-6 |
| molecular_formula | C13H18O2 |
| molar_mass | 206.28 g/mol |
| appearance | Colorless to pale yellow liquid |
| boiling_point | 140-142°C (at 13 mmHg) |
| density | 1.005 g/cm3 |
| refractive_index | 1.526-1.531 |
| solubility | Insoluble in water |
| flash_point | 102°C |
| smell | Characteristic, pleasant odor |
| purity | Typically ≥98% |
As an accredited Cinnamaldehyde Diethyl Acetal factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Cinnamaldehyde Diethyl Acetal, 100g, is packaged in a sealed amber glass bottle with a secure screw cap and clear labeling. |
| Shipping | Cinnamaldehyde Diethyl Acetal is shipped in tightly sealed containers, protected from light and moisture. It should be transported under cool, dry, and well-ventilated conditions, away from sources of ignition and incompatible substances. Ensure all containers are properly labelled, and handle according to standard chemical safety and regulatory guidelines during shipping. |
| Storage | Cinnamaldehyde Diethyl Acetal should be stored in a cool, dry, and well-ventilated area, tightly sealed in a suitable chemical-resistant container. Protect it from light, moisture, and sources of ignition. Keep it away from strong oxidizing agents and acids. Store at room temperature and ensure proper labeling. Follow all relevant safety and regulatory guidelines for safe chemical storage. |
Applications of Cinnamaldehyde Diethyl Acetal in Industrial ManufacturingCinnamaldehyde Diethyl Acetal supports specialized downstream workflows in multiple chemical sectors. As a chemical intermediate produced under stringent plant QC, our material integrates into precise process steps across diverse regulated industries. Below, we outline genuine B2B application scenarios based on customer requirements and ongoing market demand. 1. Flavor Formulations for Food and Beverage ConcentratesFood flavor manufacturers use Cinnamaldehyde Diethyl Acetal as a masking and rounding agent for complex spice notes in beverage syrups, preserved fruit bases, and confectionary pastes. Our industrial customers dose this acetal at calibrated points to capture the distinctive warm lift of cinnamon while controlling oxidized aldehyde sharpness. Its chemical profile delivers improved stability during pasteurization and retort processes, differentiating it from cinnamaldehyde in multi-step batch operations. The compound is added in strict accordance with flavor ingredient guidelines within the scope of global food safety requirements. Industry compliance standards
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2. Fragrance Compound ManufacturingFine fragrance and air care producers employ this acetal primarily for top-note modification in compositions requiring prolonged cinnamon diffusion without the degradation susceptibility of pure cinnamaldehyde. The ingredient provides a controlled, less reactive profile that enhances olfactive longevity in alcohol-based sprays and functional fragrance matrices. Formulators achieve consistent aroma profiles during high-solvent blending and multi-component co-distillation, addressing volatility and discoloration constraints specific to luxury and technical perfumery manufacturing environments. Industry compliance standards
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3. Pharmaceutical Intermediate in API SynthesisProcess chemists utilize Cinnamaldehyde Diethyl Acetal as a protected synthon during the large-scale synthesis of certain active pharmaceutical ingredients, especially those requiring selective introduction of a cinnamyl group while avoiding premature aldehyde reactivity. The acetal’s stability under common condensation, coupling, and downstream deprotection steps supports workflow yields during multi-stage frameworks for niche APIs, including selected antifungal and cardiovascular drug candidates. Industry compliance standards
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4. Agrochemical Synthesis for Pesticidal AgentsIn the crop protection sector, downstream formulators select Cinnamaldehyde Diethyl Acetal as a controlled-release precursor, facilitating the timed release of cinnamyl moieties in bioactive pesticide development. This approach allows sustained action in soil or foliar delivery systems while minimizing premature volatilization. Process teams value the acetal’s compatibility with standard inert carriers, and its chemical profile meets stringent residue and application safety benchmarks required by various agrochemical regulatory bodies. Industry compliance standards
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5. Chemical Intermediate in Polymer Modifier SynthesisProducers of specialty polymer additives use this acetal as an intermediate during the production of flexible plasticizers and molecular modifiers, especially when targeting anti-microbial or aroma-modified resins for packaging films. The acetal’s chemical structure enables sequential transformation to active aldehyde-bearing moieties during backbone modification or side-chain grafting steps, supporting production of custom-performance polymers for food-contact and household markets. Industry compliance standards
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Standing on the factory floor, we see Cinnamaldehyde Diethyl Acetal not as a distant molecule buried in some catalog, but as a steady performer involved in a wide sweep of chemical synthesis and fragrance preparation. At our facility, every batch we produce reflects a commitment to purity, accessibility, and process predictability. Over years of manufacturing experience, it’s become apparent how small structural tweaks—like the transformation from pure cinnamaldehyde into its diethyl acetal form—change both the handling and applications of a product. Chemistry is not just formulas; it changes the rhythm of scale-up reactions, the workflow of an R&D bench, and the quality of scents reaching global markets.
Cinnamaldehyde Diethyl Acetal brings clear advantages in reactivity and stability compared to straight cinnamaldehyde. Structurally, it shields the reactive aldehyde site by acetalization, resulting in improved resistance to oxidation and polymerization during storage and transport. This feature alone explains why clients working in sensitive synthesis frequently come back for this derivative. In our own practice, shifts in ambient temperature and humidity are less likely to compromise the chemical’s shelf quality. Acetal derivatives consistently deliver on both yield and reproducibility in reactions where excessive self-condensation of the bare aldehyde might cause problems.
During production, we prioritize analytical verification to keep each consignment within narrow impurity profiles. Typical purity for Cinnamaldehyde Diethyl Acetal from our reactors exceeds 98%, confirmed by GC and NMR analysis. Even though analytical chemistry seldom makes headlines, trust starts by removing unexpected contaminants that could jeopardize a high-value synthesis downstream or leave an off-note in a fine fragrance blend.
Our customers use Cinnamaldehyde Diethyl Acetal in both classic organics labs and industrial fragrance assembly. Acetals have a long tradition as protective groups in synthetic organic chemistry. We have seen this molecule steadily preferred for multi-step syntheses involving Grignard reagents, strong base conditions, or routes prone to atmospheric oxidation. Labs gain more control this way because the acetal withstands tough reaction conditions, enabling smooth deprotection only when necessary, often with mild acids.
The impact goes beyond chemical benchwork. Feedback from formulators in the fragrance and flavor sectors highlights its unique role. In perfume design, the diethyl acetal imparts a light, slightly floral nuance, lacking the sharp and sometimes overpowering character of pure cinnamaldehyde. Scent stability improves in complex blends since the acetal form delays, or sometimes prevents, unwanted secondary reactions. Our partners working on long-lasting diffusers and specialty home scents point out a reduced tendency for yellowing or formation of off-smelling byproducts over time. The applications continue to expand as manufacturers push for cleaner product labels and more stable scent delivery in both personal care and ambient environments.
Experience shows that “model” is more than a label here. What we supply generally conforms to the laboratory-grade Cinnamaldehyde Diethyl Acetal, with molecular formula C13H18O2, CAS registration as part of our traceability, and batch reports available upon request. Chemists in procurement or R&D know that the finer details—such as whether ethanol or another alcohol was used in the acetalization process—can impact both process byproducts and regulatory acceptability. Our focus stays on diethyl acetals, matching regulatory confidence and analytical clarity needed for scale-up and commercialization.
Consistent specifications mean low water and low peroxide content. Moisture-control is especially critical in applications involving water-sensitive downstream chemistry. Each shipping drum or canister is double-sealed with desiccant inserts to maintain this standard, which we learned keeps complaints—and spoiled reaction runs—to a minimum. Many manufacturers simply repackage or relay intermediates; in contrast, we have direct input into process parameters, reducing the “telephone game” effect that causes variations when outsourcing production.
A question that reaches our technical team repeatedly centers on why someone would choose the acetal over the parent aldehyde, or how it stacks up against benzaldehyde and its acetals. There’s no single answer, but practical experience always trumps theory. In routine storage, acetal forms possess superior oxidative stamina, so they last longer and perform more predictably in both lab and plant environments. If you run into trouble with instability or darkening of aldehyde-based stocks, converting to the diethyl acetal is usually a direct remedy.
On the reaction front, acetals deliver site-selectivity and functional group compatibility. For example, standard cinnamaldehyde will rapidly participate in Michael additions or self-condensation under mild base conditions; swapping to the diethyl acetal blocks this pathway, letting chemists build up more complex molecules without structural scrambling. In comparison, benzaldehyde diethyl acetal serves similar stability advantages for aryl-based synthesis, but the cinnamaldehyde backbone grants further possibilities—such as in flavoring or where a longer-chain aromatic base tailors volatility and olfactory impact.
From an inside vantage, the production of Cinnamaldehyde Diethyl Acetal demands unflagging attention to processing steps. Acetal interchange reactions need precise control over temperature, catalyst loading, solvent choice, and water removal by azeotropic distillation. Our workflow draws on continuous improvements, inspired by years of scaling up small-batch reactions to industrial output. Small deviations, like incomplete distillation or trace acid presence, risk forming mixed acetals or leaving behind unreacted cinnamaldehyde, which could poison a downstream process or generate off-notes in a perfume blend.
We discovered that maintaining batch-to-batch uniformity depends on disciplined raw material procurement. Ethanol for acetalization must pass both chemical and organoleptic screening, as inferior grades produce solvent-like undertones detectable in finished fragrances. Cinnamaldehyde sourced from poor runs harms both yield and purity; for this reason, all inputs are tagged and audited starting from farm-level feedstock, since much cinnamon-derived oil in the market fluctuates in trans/cis isomerism and unwanted coumarin content.
Equipment maintenance and operator experience also weigh heavily on final product reliability. Small leaks, cross-contamination between product runs, or even variance in filter handling can cause subtle, but commercially significant, problems down the supply line. Accepting responsibility from synthesis to packing has taught us how minor process lapses snowball, especially as acetal derivatives have little forgiveness for out-of-specification handling.
Several regulatory regimes scrutinize both raw materials and derivatives that enter personal care, food, and home fragrance markets. Through robust documentation and analytical transparency, our batches clear not just REACH and TSCA gates but also pass muster for flavor and fragrance standards set by groups like IFRA and FEMA. Any chemical supplier could recount headaches from shifting compliance targets; as manufacturers, our response is not to take shortcuts but to design process audits, cross-check impurity profiles, and work with third-party labs to verify what’s inside every drum that leaves the dock.
A surprising recent trend is the ever-increasing attention to traceability, not only for safety but also for consumer trust. Many clients now demand documented provenance extending from the original cinnamon bark sourcing, through processing, to final acetal packaging. This movement, once viewed as bureaucracy, now actively shapes how we approach documentation, as traceable supply chains curb the risk of adulteration and accidental mixing with banned or restricted substances.
Sustainability further complicates decisions. Cinnamaldehyde and its acetals are, in principle, renewable when cinnamon production is responsibly managed. We work with agricultural partners to tighten sustainability verification, supporting biodiversity, and labor standards from the base of the supply chain. Customers in the fragrance sector, especially, want to ensure that “natural” and “renewable” claims withstand technical scrutiny—not just marketing soundbites. For us, chemical transparency and ecological mindfulness hang together in real day-to-day trading and supplier agreements. Responsible stewardship is more than paperwork: it is a daily discipline around solvent recycling, waste management, and reducing the carbon footprint of each finished kilogram.
One aspect of Cinnamaldehyde Diethyl Acetal often overlooked outside the factory is its sensitivity to acid, moisture, and heat once unpacked. As manufacturers, we emphasize training, not just for our staff, but for clients receiving shipments, because care in transfer and storage goes a long way toward keeping the material in spec for its ultimate application. We always store in cool, dry locations, sealed under nitrogen or dry air, with clear date-of-manufacture labeling to prevent accidental use of expired stock.
Clients in flavor or fragrance blending sometimes introduce Cinnamaldehyde Diethyl Acetal directly to alcohol or oil carriers. Practice here shows that pre-dissolving in a small test batch reveals both stability and olfactory compatibility before full-size blending. Where large-scale chemical synthesis uses the acetal as a protected intermediate, pilot-scale trials at modestly raised temperatures confirm it performs as predicted under the designed deprotection or conversion steps. Consistent outcomes depend on up-front communication about the starting materials and intended use.
Disposal and waste streams are handled in accordance with both local regulations and internal protocols honed through years of experience. Unlike some low-molecular-weight acetals, Cinnamaldehyde Diethyl Acetal carries a relatively low volatility, which simplifies solvent capture and atmospheric emissions control during both production and downstream handling. Our on-site safety teams conduct regular drills for accidental spills or leaks. Each protocol builds on lessons learned from past incidents; we do not just copy regulatory folders, but adjust to the idiosyncrasies picked up from our own and our clients' workspaces.
Over the past decade, Cinnamaldehyde Diethyl Acetal’s role has grown along with demand for safer, more stable scent ingredients, and multi-step specialty chemical building blocks. As manufacturers, we watch R&D teams in both academic and industrial labs using acetals to develop greener or milder transformation protocols—cutting down inorganic byproduct loads or moving away from hazardous metal catalysts. The acetal’s protective abilities under both acidic and basic conditions have been central to routes generating value-added aromatics or natural product derivatives with improved atom economy.
Interest from materials science is another area where we see developing applications. The cinnamyl backbone, protected by the diethyl acetal group, serves as a precursor to specialty polymers or functionalized aromatic systems in electronics or novel coating technologies. Researchers ask for repeatable, high-purity batches as the building blocks for new materials where minute impurities can disturb performance or consistency.
We have seen inquiries from green chemistry developers aiming to replace less benign preservatives or enhance the shelf-life of bio-derived fragrances using Cinnamaldehyde Diethyl Acetal. The naturally derived character of the parent cinnamaldehyde, combined with the non-reactivity of the acetal group under standard conditions, positions this molecule as a bridge between classic organic chemistry and the next generation of “clean” chemical technologies.
For those involved in either niche chemical synthesis or bulk blending, direct relationships with the actual producer make a difference. Industrial buyers and lab chemists alike reduce risk when they rely on a manufacturer who conducts the synthesis, performs the purification, and controls the packing. We welcome technical discussions, whether about reaction troubleshooting, custom purity grades, or tailored batch sizes, because the real-world use of Cinnamaldehyde Diethyl Acetal often depends on details that never appear in a specification sheet.
Trust in our product comes from practical transparency: analytic certificates linked to each production run, open dialogue about starting material origins, and a willingness to investigate or replicate reaction inquiries from clients. This approach means less time spent on problem-solving unexpected off-odors or instability, and more time on advancing R&D, launching new products, or filling orders that demand on-time, in-spec supply.
Cinnamaldehyde Diethyl Acetal, to us, isn’t simply a code or a stock item. It’s the product of disciplined chemistry, detailed tracking, rigorous analytical verification, and years of patient troubleshooting. The acetal structure represents more than a chemical transformation—it’s a practical answer to challenges faced by everyone from the synthetic chemist at the bench, to the industrial-scale fragrance blender, to the sustainability-focused product developer launching tomorrow’s best-sellers. Real-world performance, accountability in quality, and straightforward communication let this molecule support innovation, stability, and trust across global chemical markets. We continue to refine our methods so that each drum bearing our label stands for reliability, transparency, and the accumulated know-how of hands-on manufacturing.