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2-Ethoxycinnamic Acid

    • Product Name 2-Ethoxycinnamic Acid
    • Alias Ethyl trans-cinnamate
    • Einecs 245-881-2
    • 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

    366129

    Product Name 2-Ethoxycinnamic Acid
    Cas Number 22071-66-7
    Molecular Formula C11H12O3
    Molecular Weight 192.21 g/mol
    Appearance White to off-white crystalline powder
    Melting Point 135-139°C
    Solubility Slightly soluble in water, soluble in ethanol and organic solvents
    Purity Typically ≥98%
    Smiles CCOC1=CC=CC=C1C=CC(=O)O
    Inchi InChI=1S/C11H12O3/c1-2-14-11-8-4-3-7-10(11)6-5-9(12)13/h3-8H,2H2,1H3,(H,12,13)
    Storage Conditions Store at room temperature, keep tightly sealed, protect from light

    As an accredited 2-Ethoxycinnamic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The packaging contains 100 grams of 2-Ethoxycinnamic Acid, sealed in a labeled amber glass bottle to ensure safe storage and handling.
    Shipping 2-Ethoxycinnamic Acid is shipped in tightly sealed containers to prevent moisture absorption and contamination. It should be transported and stored in a cool, dry, and well-ventilated area, away from incompatible substances. Proper labeling and adherence to regulations for handling organic chemicals are essential during shipping to ensure safety and product integrity.
    Storage 2-Ethoxycinnamic Acid should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from direct sunlight and moisture. Keep it separated from strong oxidizing agents and incompatible materials. Store at room temperature and avoid extremes of heat or cold. Ensure the storage area is clearly labeled and restricted to trained personnel to prevent accidental exposure.
    Application of 2-Ethoxycinnamic Acid

    Applications of 2-Ethoxycinnamic Acid in Industrial Manufacturing

    2-Ethoxycinnamic Acid serves as a key aromatic intermediate relied on by several specialized industries. Manufacturers consistently select this ingredient for its role in value-added synthesis and performance enhancement, driven by precise compliance demands and process parameters in downstream production lines. Below, we outline real-world application fields, each with technical considerations from formulation to end product assembly.

    1. UV Absorber Synthesis for Polymer Film Manufacturing

    Polymer film producers incorporate this compound during the synthesis of high-performance UV absorbers for transparent packaging and technical films. Its extended aromatic system and selective reactivity support the formation of efficient UV-blocking agents that withstand industrial extrusion and lamination cycles, maintaining optical clarity and product longevity. Utilization strictly follows polymer and food contact compliance, with batch-to-batch quality verification due to end-use sensitivity.

    Industry compliance standards

    • REACH Regulation (EC) No 1907/2006
    • FDA 21 CFR 177.1630 (Polyethylene phthalate polymers—food contact)
    • ISO 4892-3 (Plastics—Methods of exposure to laboratory light sources)
    • RoHS Directive (2011/65/EU, with amendments)

    Typical usage ratio

    • 0.1–0.5% by weight relative to the base polymer, adjusted based on film thickness and desired UV blocking spectrum

    Downstream process integration

    • Producers compound the ingredient with polymer pellets in a masterbatch during melt blending or extrusion processes, ensuring dispersion before film casting or blowing

    Final product types

    • Food packaging films
    • Agricultural mulch films
    • Photographic protective sheets
    • Outdoor signage laminates

    2. Intermediate for Pharmaceutical API Synthesis

    API manufacturers employ 2-Ethoxycinnamic Acid as a synthetic building block for specific pharmaceuticals, especially within the non-steroidal anti-inflammatory drugs (NSAIDs) and antispasmodic agent classes. Its ethoxy-substituted cinnamate structure facilitates regioselective transformations, amide coupling, or esterification steps requiring precise stoichiometry and GMP-grade documentation to guarantee active ingredient purity.

    Industry compliance standards

    • US Pharmacopeia (USP)
    • European Pharmacopoeia (Ph. Eur.)
    • ICH Q7 GMP for APIs
    • Drug Master File (DMF) submission standards

    Typical usage ratio

    • Stoichiometric ratios based on target molecule; generally ranges from 0.25–0.9 molar equivalents, as defined by synthetic route and batch size

    Downstream process integration

    • Introduced at the condensation or coupling step, followed by purification, crystallization, and analytical verification of the pharmaceutical intermediate or API

    Final product types

    • Cinnamate-derivative antispasmodics (e.g., specific muscle relaxants)
    • NSAIDs developed from cinnamic acid platforms
    • Clinical research compounds with substituted phenylpropanoic acid motifs

    3. Fragrance Ingredient in Fine Chemical Blending

    Aromatic chemical manufacturers utilize this ingredient for the synthesis of ester-based fragrance molecules, which find further use as blenders in personal care and household fragrance formulations. Its structure supports precise esterification to generate esters known for green, balsamic, and sweet notes in perfumery. Strict quality and purity standards apply because of the material’s trace level influence on finished scent performance.

    Industry compliance standards

    • International Fragrance Association (IFRA) Standards
    • Cosmetic Ingredient Review (CIR) safety guidelines
    • EU Regulation (EC) No 1223/2009 (Cosmetics Regulation)
    • IFRA allergen labeling requirements

    Typical usage ratio

    • 0.01–1.0% in compounded fragrances; adjusted based on olfactory intensity and regulatory thresholds per region

    Downstream process integration

    • Subjected to acid-catalyzed esterification, typically with branched or linear alcohols, then fractionally distilled and blended into base fragrance compounds

    Final product types

    • Perfume concentrates
    • Personal care blends (eau de toilette, creams)
    • Household air care formulations (diffusers, sprays)
    • Scented personal hygiene products

    4. Photoinitiator Precursor for Specialty Coatings

    Specialty chemical suppliers in the UV-cured coatings sector use 2-Ethoxycinnamic Acid as an advanced intermediate to generate cinnamate-based photoinitiators. Structural features contribute to specific absorption maxima and high quantum efficiency during coating polymerization on wood, plastics, and metal surfaces. Raw material lots undergo extensive photophysical and impurity screening in line with coating industry protocols.

    Industry compliance standards

    • ISO 9001 Quality Management for chemical manufacturing
    • ASTM D7767 (Standard Test Method for UV-Curable Materials)
    • EU Regulation (EC) No 1272/2008 (CLP for hazardous mixtures)
    • China GB/T 20631.2-2006 (Light-curing coatings safety)

    Typical usage ratio

    • 0.2–1.5% of paint or ink formulation; ratio depends on desired cure speed, film thickness, and lamp intensity used in end-user application

    Downstream process integration

    • Incorporated during pre-polymer blending, followed by in situ photoinitiator formation; integrated into the UV-curable base before application by spraying, rolling, or curtain coating methods

    Final product types

    • UV-cured wood coatings
    • Plastic surface finishes
    • Metallic coating systems
    • Printed electronics ink formulations

    5. Light Stabilizer Intermediate for Cosmetic Sunscreen Ingredients

    Personal care raw material fabricators leverage 2-Ethoxycinnamic Acid as an intermediate in synthesizing UVB blocking agents for sunscreen products. The ethoxy group enhances oil solubility and compatibility with multiple emollients, supporting stable emulsions in cream or lotion matrices. Quality control programs emphasize photostability and impurity profiling to meet strict personal care regulatory frameworks worldwide.

    Industry compliance standards

    • EU Cosmetics Regulation (EC) No 1223/2009 and Annex VI
    • US FDA OTC Monograph for Sunscreen Drug Products
    • ISO 24443 (Determination of sunscreen UVA protection)
    • ASEAN Cosmetic Directive (ACD) requirements

    Typical usage ratio

    • Converted to sunscreen agents used at 2–8% in finished SPF formulations, selection based on broad-spectrum coverage and local legal maximums

    Downstream process integration

    • Transformed in-house through condensation with alkoxy benzyl groups, then micronized as a powder or solubilized before being dispersed in the oil phase of emulsified sunscreen creams and sprays

    Final product types

    • SPF creams and lotions
    • Sunblock sprays
    • Makeup with integrated UVB protection
    • Daily-use cosmetic emulsions with photoprotection claims
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    Certification & Compliance
    More Introduction

    2-Ethoxycinnamic Acid: Insights from the Manufacturer’s Perspective

    Meeting Industry Challenges with 2-Ethoxycinnamic Acid

    Over the years, the chemical industry has kept pushing for specialty compounds that serve a range of applications with reliability and consistency. Our journey with 2-Ethoxycinnamic Acid reflects the story of an increasing need for precision and adaptability, especially across pharmaceuticals, fragrances, UV absorbers, and advanced materials. On our production floor, we experience firsthand the importance of controlling not just purity, but particle size, color, and reaction profiles. Our engineers learned early that a small deviation in feedstock or process temperature can introduce detectable impurities, undermining subsequent performance for downstream formulators.

    Working directly with customers in pharmaceuticals and personal care, we see a clear demand for transparency. Clients ask not just for material but the reassurance that every metric has been tracked — from trace metal content to moisture control in final packaging. There’s little appetite for shortcuts. This is why, for our 2-Ethoxycinnamic Acid model, we set specifications that go beyond the basics. Content typically runs above 99% by HPLC, but real usability comes from careful handling during crystallization and drying. Off-white to light-yellow crystalline powder signals clean production and careful process management, and we refuse to ship any lot with visible agglomerate or discoloration.

    The Unique Profile of Ethoxylated Cinnamic Structures

    Our team is sometimes asked what distinguishes 2-Ethoxycinnamic Acid from similar compounds, such as cinnamic acid itself, 4-methoxycinnamic acid, or other substituted aromatics. Differences begin in the basic chemistry. The ethoxy substitution at the 2-position alters solubility and reactivity compared with other isomers. For example, clients working in organic synthesis or API intermediate manufacture report less tarry byproduct formation, smoother filtration, and better reaction yield with 2-ethoxy compared to unsubstituted variants.

    In fragrance work, the ethoxy group softens the base note while maintaining the characteristic cinnamon-spice of the cinnamic backbone. Flavor researchers tend to favor this variant as a non-coumarin alternative, since regulatory pressures keep rising on potential sensitizers and phototoxic molecules. UV formulation scientists, by contrast, exploit the ethoxy group for increased oil solubility, which assists with even distribution when blending into sunscreen matrices or polymer films. Through feedback loops with our partner labs, we iterate on these qualities, tweaking process controls to accommodate new specifications as research trends evolve.

    Production Choices Shape Functionality

    Behind every lot of 2-Ethoxycinnamic Acid lies a long series of technical choices. We use a modified Perkin condensation to guarantee reproducibility. By sourcing cinnamaldehyde and ethyl alcohol directly and purifying on-site, our chemists avoid the most common feedstock contaminants that plague less controlled operations. Reaction monitoring includes in-process GC to check for over-reaction and byproducts like diethoxy derivatives, which can complicate downstream formulations. We insist on jacketed glass-lined reactors to prevent trace iron pickup, as even minor metal contamination can produce stubborn yellow tint or haze downstream, risking product rejection for cosmetic or pharmaceutical applications.

    It sounds simple: a batch comes off, then it’s crystallized, washed, filtered, vacuum dried and milled. But every physical detail matters. Crystal habit and particle morphology determine not just filterability, but how easily the powder wets when added to organic phases. Over-milling turns a good batch into a dusting hazard, so our operators are trained to check bulk density and flow properties at every critical stage. In past years, we’ve responded to customer findings that certain particle ranges performed better in microencapsulation. Now, we tailor our crushing and sieving steps for batches destined for those clients, skipping unnecessary processing steps and improving throughput.

    Specifying Quality: Why Each Parameter Matters

    Lab reports list metric after metric, but factory life teaches which numbers really matter. Purity, measured by HPLC, remains the main benchmark — higher purity means fewer headaches for both our team and our end users. Yet actual benefit comes from managing residual moisture, ash, heavy metals, and specific single impurities. Trace iron, copper, and lead levels can spell the difference between a lot that passes or fails EU or US pharmacopeia standards. Ash content uncovers lingering inorganic residues, often from filtration aids or aged gaskets on processing equipment.

    Moisture sits at the center of long-term storage stability. Most clients want moisture under 0.5%, since higher water can spoil product shelf life, introduce clumping, or support unwanted hydrolysis over time. In-house, our focus stays on quick sealed transfer from dryer to packaging under inert gas. Desiccant and triple-sealing protocols practically eliminate reabsorption in transit, an adjustment we made following reports of caking in humid seasons.

    Applications in Real-World Context

    Pharmaceutical companies depend on precise chemistry for their intermediates. For them, a compound that deviates from standard melting point or shows haze in solution triggers immediate rejection. Through years in the field, we’ve become used to the high stakes: a single bad lot can shut down a production line or cascade into extensive recalls. One client, focused on non-steroidal anti-inflammatory compounds, relies on our material because it maintains a tight melting point window and never introduces phosphate or sulfide residues. Their reactions tolerate even mild oxidative impurities poorly, so we built our process to minimize exposure to air and light at every phase.

    Cosmetics and UV protection formulators come with a different set of requirements. Here, trace color and odor decide product suitability as much as technical data. Slight notes of aldehyde or an oily feel can spoil sensory qualities in a sunscreen or fragrance blend. Several years back, we invested in improved filtration and deodorization steps, lowering residual volatiles and granting cleaner, more reproducible scented bases for customer labs. As global regulations ban more UV filters and demand for safer alternatives grows, our team leverages feedback from personal care clients to continually update our exclusion criteria and reporting on extractables.

    Navigating Global Standards and Compliance

    No chemical manufacturer works in isolation. With 2-Ethoxycinnamic Acid, we regularly review shifts in Asian, European, and North American safety, purity, and reporting rules. REACH in Europe and the US FDA both maintain evolving lists of allowed processing aids and classify trace impurities. We see more clients requesting full documentation on solvents, residual metals, and even trace process chemicals, such as cleaning and anti-foam agents. Our documentation package routinely includes heavy metal screening down to the parts-per-billion range in support of both regulatory and high-sensitivity downstream uses.

    Batch traceability can slow down production, but the alternative — lack of transparency — invites recalls and trust issues. By logging every input lot and step, we make it possible for users to satisfy audits or track down root causes if a downstream process stalls. Pharma and cosmetic customers face intense scrutiny over allergen labeling and banned substance lists, so we avoid cross-contamination by physical separation and equipment cleaning protocols. In industries where supply interruptions can destabilize ROI for years, stable compliance reassures our customers and protects our own reputation.

    Considering Alternatives: A Comparison to Related Molecules

    Labs and formulators ask why we invest so much into this ethoxy-substituted variant, given the existence of dozens of similar aromatic acids. Simple cinnamic acid or its para-methoxy cousin cost less to synthesize, and other alkoxy-cinnamic acids sometimes appear as byproducts or research leads. Over time, direct experience taught us that the ortho-ethoxy group strikes the right balance for many users. It lowers melting point and increases solubility in both alcohols and aromatic solvents, essential for some applications in coatings and inks where rapid, even dissolution overrides pure economics.

    The bulk of competing products deliver wider melting points or slightly higher residue, leading to risks in precise downstream reactions. 2-Ethoxycinnamic Acid’s reactivity, thanks to both the activated side chain and electron-donating ethoxy, allows selective couplings or cyclizations without many side reactions common to less-symmetrical analogs. Decades of field feedback drove our commitment to mastering this chemistry. Reports from adhesive and polymer manufacturers confirm that slight adjustments in the aromatic substituent pattern can shift UV absorption maxima or flexibility in end-use materials.

    Scaling Production to Match Demand

    Manufacturing at moderate scale means every change in global or local demand flows directly to our production scheduling. In periods of high interest, such as after a publication on new materials or successful patent applications, we work overtime to retool reactors and hold extra raw material inventory. Too often, companies depend on traders or third-party stockpiles and then encounter aged, degraded stock that performs erratically in modern processes. By maintaining regular capacity checks and direct communication with major users, we minimize old inventory, reduce waste, and ship fresher, more consistent lots.

    Unlike large-volume commodity chemicals, specialty organic acids like this require agility. If a pharmaceutical customer needs tighter control over isomer content, we can reprogram screening and purification to match. If an aroma or cosmetic company wants absence of any mineral oil or plasticizers, we document new cleaning regimes between batches. These efforts translate into higher material costs, but they also reduce waste and rework. Experience tells us that even small efficiency gains during filtration or crystallization can save thousands of dollars downstream by cutting re-blending due to offcolor or under-performing batches.

    The Ongoing Evolution of Customization

    Modern product development depends on dialogue. Pharmaceutical and advanced material manufacturers almost always want options for particle size, bulk density, or blending aids. We started offering non-standard mesh sizes for microencapsulation after research partners showed us better encapsulation yields and cleaner cuts between batch fractions. Cosmetic and sun care formulators sometimes ask for added stability agents during storage; our technical team works alongside their researchers to validate compatibility without introducing foreign residues. The need for flexibility and responsiveness only increases with time, propelling us to invest in new sieving, blending, and screening equipment every year.

    In high-value applications, users increasingly insist on real-time analytics. Our investment in near-infrared spectroscopy and high-throughput chromatography speeds up both release times and early identification of contamination. Rapid feedback shortens the cycle from raw feedstock to refined batch, supporting those customers for whom every day lost in processing surfaces as lost opportunity in the market. Instead of holding to fixed spec sheets, we find that routine back-and-forth between our lab staff and client chemists trims the time between research trial and scaled adoption.

    Traceability and Sustainability Commitments

    Supply chains constantly evolve, and sustainability pressures grow ever stronger. Each kilogram of 2-Ethoxycinnamic Acid carries an environmental footprint — both in raw materials and process energy. Over years, we cut solvent and energy use, preferring greener condensation methods where possible and upgrading to closed-loop solvent recovery. Bulk handling improvements lowered fugitive emissions, and waste minimization drives remain ongoing.

    Downstream users increasingly request renewable or recyclable packaging, carbon accounting, and process documentation. For those exporting to regions with stringent green chemistry requirements, we supply statements on material origin, recycled content, and emission controls as part of our routine technical package. Adapting plant operations to these trends presents real cost and logistical hurdles, but also builds resilience as global regulatory and consumer preferences shift toward stronger sustainability profiles.

    Continuous Improvement Based on Real-World Feedback

    No process ever stands still in specialty manufacturing. Over years, customer feedback, batch failures, and regulatory curveballs all force change. One season, excess static during powder transfer led to airborne dust and spill risk; engineers responded by installing grounded transfer lines and improved PPE protocols, quickly dropping incidents. In another case, a rise in out-of-spec color correlated with incoming raw material variability — so we introduced a second round of feedstock validation.

    Mistakes can be expensive but invaluable. In years past, early shipment of slightly over-milled product led to customer mixing problems and denials. Today, every batch runs through laser diffraction sizing and hands-on flowability trials before release. Visiting our clients’ manufacturing lines taught us more than any spec sheet ever could — it highlighted where slight agglomeration clogs feeding hoppers, or where a trace impurity disrupts a $20,000 pilot run. That sort of practical, face-to-face problem solving forms the core of how we operate.

    Building Future Value from Today’s Product Experience

    In the field of fine organics, reputation and repeatability win business. We view each lot of 2-Ethoxycinnamic Acid as both a product and a promise to deliver value beyond technical compliance. Our staff invest in building production know-how, laboratory skill, and customer relationships that stand up to scrutiny from regulators, researchers, and production engineers alike. Specialty materials never stand still — one decade’s novel compound turns into the next decade’s staple, shaped by tighter rules and new functionalities.

    As the world pushes toward safer, greener, and more functional molecules, our work with 2-Ethoxycinnamic Acid serves as a snapshot of this ongoing shift. Production methods grow smarter, real-time analytics shave variation from every batch, and direct conversations with front-line users uncover problems and solutions faster than any top-down mandate ever could. The compound itself may sit quietly in inventory, but its history traces constant improvement, adaptation, and hands-on learning — a hallmark of the chemical manufacturing industry’s past, present, and future.