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Methyl 2,5-Dihydroxycinnamate

    • Product Name Methyl 2,5-Dihydroxycinnamate
    • Alias Methyl caffeate
    • Einecs 683-021-4
    • 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

    751927

    Name Methyl 2,5-Dihydroxycinnamate
    Cas Number 122800-51-5
    Molecular Formula C10H10O4
    Molecular Weight 194.18 g/mol
    Appearance White to off-white solid
    Melting Point 117-120°C
    Solubility Slightly soluble in water, soluble in organic solvents
    Purity Typically ≥98%
    Smiles COC(=O)C=CC1=CC(=C(C=C1)O)O
    Inchi InChI=1S/C10H10O4/c1-14-10(13)5-3-7-6-8(11)4-2-9(7)12/h2-6,11-12H,1H3

    As an accredited Methyl 2,5-Dihydroxycinnamate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The packaging is a 25g amber glass bottle, tightly sealed with a screw cap, labeled "Methyl 2,5-Dihydroxycinnamate."
    Shipping Methyl 2,5-Dihydroxycinnamate is shipped in tightly sealed containers to prevent contamination and moisture absorption. The packaging complies with chemical transport regulations, ensuring safety during transit. Labels indicating the chemical name and hazard information are provided. Shipments are handled with care, away from strong oxidizers and extreme temperatures.
    Storage Methyl 2,5-Dihydroxycinnamate should be stored in a tightly sealed container, away from light and moisture, in a cool, dry, and well-ventilated area. Keep it isolated from strong oxidizing agents and incompatible substances. Label the container clearly and store at room temperature, avoiding excessive heat. Follow local regulations and standard laboratory chemical storage guidelines for safe handling and storage.
    Application of Methyl 2,5-Dihydroxycinnamate

    Applications of Methyl 2,5-Dihydroxycinnamate in Industrial Manufacturing

    Methyl 2,5-Dihydroxycinnamate is a key building block in specialty chemical synthesis. Its hydroxyl groups and aromatic structure support specific applications in pharmaceutical, personal care, agrochemical, adhesive, and polymer industries. We supply to global manufacturers with validated, consistent quality for downstream integration into formulated products.

    1. Pharmaceutical Intermediates for Active Pharmaceutical Ingredients (APIs)

    This material plays a central role in synthesizing certain phenolic drug intermediates via esterification or amidation reactions. Its defined purity profile meets the stringent requirements for regulated drug synthesis, primarily used in the preparation of antioxidants and anti-inflammatory APIs. Formulators strictly control trace impurities and residual solvents, as downstream conversion requires high consistency for meeting clinical and registration standards.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for APIs
    • European Pharmacopoeia monographs (Ph. Eur.) involving related intermediates
    • US FDA 21 CFR Part 211 (finished pharmaceuticals manufacturing)
    • USP® regulations for related phenolic compounds

    Typical usage ratio

    • Batch input: 0.2–1.5 kg per kg of target intermediate, adjusted for stoichiometry in phenolic and ester group transformations
    • Excess reagent tailored for purity requirements and downstream yield optimization

    Downstream process integration

    • Fed into the early-stage reaction vessel for ester or amide synthesis
    • Removed after reaction via phase separation and followed by crystallization or distillation
    • Subject to multi-step purification to ensure pharmaceutical-grade quality
    • Trace analysis via HPLC or GC prior to API synthesis continuation

    Final product types

    • Antioxidant APIs for injectable and oral formulations
    • Topical anti-inflammatory actives
    • Specialty phenolic drug intermediates
    • Research-grade reference standards

    2. UV Stabilizers and Additives for High-Performance Polymers

    Manufacturers of advanced engineering plastics use this raw material as a precursor for synthesizing UV-absorbing additives. Its substituted cinnamate backbone enables high-efficiency stabilization against photodegradation, extending polymer service life in outdoor and high-heat applications. Stringent analytical testing ensures batch-to-batch consistency in absorption profile and compatibility with downstream copolymers.

    Industry compliance standards

    • REACH Regulation (EC) No 1907/2006 registration for chemical safety
    • UL 746C (Polymeric materials—Use in electrical equipment evaluations)
    • ASTM D5208 Accelerated Weathering of Plastics
    • ISO 4892-2:2013 (Plastics — Methods of exposure to laboratory light sources)

    Typical usage ratio

    • 0.1–0.5% w/w in finished masterbatch or compounded formulation
    • Concentration adjusted based on polymer matrix and projected weathering exposure

    Downstream process integration

    • Blended during compounding of polymer resins, ideally introduced at pelletizing or melt-extrusion stage
    • Subject to high-shear mixing for uniform additive dispersion
    • Tested for thermal stability prior to molding or extrusion of final parts

    Final product types

    • Polycarbonate and acrylic panels with enhanced UV resistance
    • Automotive trim and exterior polymer components
    • Consumer electronics housings subject to sunlight exposure
    • Outdoor construction plastics and agricultural films

    3. Cosmetic Ingredient for Whitening and Protective Formulations

    The compound is incorporated into cosmetic actives through multi-step reactions, often resulting in derivatives for skin-lightening or UV-protective applications. Cosmetic ingredient manufacturers rely on its mild profile and controlled impurities to produce high-purity, non-irritant substances. Finished ingredient lots undergo trace contaminant screening and stability tests according to industry-specific cosmetic regulations.

    Industry compliance standards

    • EU Cosmetics Regulation (EC) No 1223/2009
    • Cosmetics Ingredient Review (CIR) safety assessments
    • China National Medical Products Administration (NMPA) cosmetic raw material filing
    • ISO 22716:2007 (Cosmetics — Good Manufacturing Practices)

    Typical usage ratio

    • 0.01–0.2% w/w in formulated bulk ingredient, tailored to solubility and efficacy of the end product
    • Subject to maximum authorized dosages stipulated by local regulatory approvals

    Downstream process integration

    • Undergoes esterification or etherification prior to addition to bulk actives
    • Pre-blended with solvents and surfactants for homogeneous cream-formulation bases
    • Microbial quality and residual solvent validation before shipment to formulators

    Final product types

    • Skin whitening serums and lotions
    • Broad-spectrum sunscreen agents (ingredient derivatives)
    • Facial care emulsions and gels targeting photoprotection
    • Anti-spot cosmetic actives for premium skincare lines

    4. Agrochemical Synthesis for Fungicides and Plant Growth Regulators

    Agrochemical producers process this aromatic ester as a starting material for phenolic-based fungicide synthesis. Process controls focus on maintaining regulated levels of residual precursors and by-products to comply with crop safety and environmental policies. Advanced chemical analytics provide assurance in conversion efficiency and waste minimization during large-scale batch reactions.

    Industry compliance standards

    • FAO/WHO specifications for pesticide products
    • OECD Guidelines for the Testing of Chemicals / Crop Protection Products registration
    • ISO 9001:2015 for agrochemical production QA/QC
    • China GB 2763 Maximum Residue Limits for Pesticides in Food

    Typical usage ratio

    • Active ingredient loading: 0.5–2.0 molar equivalents per batch, customized for synthesis route and end-use regulation ceilings
    • Fine-tuned for impurity control and yield efficiency

    Downstream process integration

    • Processed via condensation or coupling in early-stage fungicide intermediates
    • Integrated into stirred tank or flow reactors on kilogram to ton scale
    • Final batch subjected to multi-stage purification for safe crop application

    Final product types

    • Registered phenolic fungicides for fruit and vegetable crops
    • Plant anti-stress regulator actives
    • Seed treatment formulations targeting pre-emergence pathogens
    • Specialty biocide solutions for integrated pest management

    5. High-Temperature Resistant Adhesive Components

    Manufacturers of specialty adhesives incorporate this compound in synthesis steps for making aromatic ether monomers. Its phenolic characteristics provide high thermal stability after polymerization, allowing production of adhesives for electronics and automotive industries. Processing requires control of reaction temperature, moisture, and batch timing to avoid premature cross-linking or hydrolysis during resin formation.

    Industry compliance standards

    • RoHS Directive 2011/65/EU (restriction of hazardous substances)
    • UL 94 Standard for flammability of adhesive components
    • ISO 9001 Certified QC procedures in adhesive manufacturing
    • ASTM D1002-10 Standard Test for Lap Shear Adhesive Bonds

    Typical usage ratio

    • 1.0–3.0% of total monomer feed by weight, determined by targeted thermal resistance and mechanical strength
    • Manufacturer adjusts ratio based on processability in mixing and curing stages

    Downstream process integration

    • Introduced during pre-polymer reactor charge for aromatic ether synthesis
    • Polymerized through controlled heat and vacuum processing
    • Integrated into two-component or hot-melt adhesive systems following QC validation

    Final product types

    • High-temperature solder mask adhesives for PCBs
    • Structural automotive sealants
    • Industrial thermal cycling resistant assembly glues
    • Chemically resistant packaging adhesives
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    Certification & Compliance
    More Introduction

    Methyl 2,5-Dihydroxycinnamate: An Insider’s Perspective from the Manufacturing Floor

    Understanding Methyl 2,5-Dihydroxycinnamate

    On a busy shift at our chemical plant, we see plenty of substances come and go, but Methyl 2,5-Dihydroxycinnamate holds a particular place in our production lineup. Our hands have turned raw materials into this finished powder or crystalline solid countless times, and we’ve watched it become a staple for customers in pharmaceuticals, fine chemicals, and scientific research. As manufacturers, we pay attention to every aspect of its development because tiny differences in process or purification can shift the outcome.

    We know Methyl 2,5-Dihydroxycinnamate as a derivative of cinnamic acid, carrying two hydroxyl groups on the aromatic ring at the 2 and 5 positions. These traits matter. Placement of those hydroxyl groups changes how the molecule interacts with other chemicals and with biological systems. R&D teams searching for new compounds in drug development, cosmetics, or agrochemical testing often specify our product by its exact structure, knowing even a small change produces starkly different results.

    Specifications We Deliver

    Consistency starts on our shop floor. In the end, we provide a colorless to slightly off-white solid, with purity levels regularly at 98% or above. We run HPLC and NMR analyses every batch. Low levels of impurities mean less noise in the results for researchers and a cleaner profile for industrial syntheses. Our drying processes keep moisture minimal, measured routinely below 0.5%. These are not just numbers. Over years of feedback, we’ve seen how residual solvents or water content can undermine entire experimental batches. Many of our staff have backgrounds in analytical chemistry and know how reliable results depend on reliable inputs. We record every adjustment, every deviation, and keep production logs stretching back years. Auditors from outside labs have reviewed our processes and signed off more times than I can count.

    Form-wise, we most often supply Methyl 2,5-Dihydroxycinnamate as a fine powder between 40 and 100 microns, though larger crystals are available for certain applications. Granularity changes reactivity, and we’ve seen clients in catalytic testing prefer the finer powder for faster uptake, while intermediates production may lean toward crystals for easier isolation after synthesis. All material comes in sealed, inert-lined bags to avoid oxidation and moisture pickup. From hands-on experience, we’ve learned the effect of improper packaging on quality; even a short exposure can degrade color and, ultimately, composition.

    Usage in Applied Science and Industry

    Most inquiries we field about Methyl 2,5-Dihydroxycinnamate relate to research on enzyme inhibition, antioxidant effects, and new molecule development. Many scientists care about sourcing from a manufacturer over a third-party warehouse, and there’s a reason for that: traceability and customizability. We receive calls weekly for slight tweaks in specification. One research team may request ultra-low metal content, whereas a startup in photovoltaic research wants an untouched, standard batch to establish baselines. We are well set up for both scenarios.

    In pharmaceutical research, the compound gets tested for biological activity, particularly as a lead structure for designing enzyme modulators or anti-inflammatory agents. Its precise hydroxyl placements mean it binds differently than simple methyl cinnamates. We’ve sat in on discussions with partners testing our batches on receptor assays. Sometimes the difference between success and failure comes down to a couple tenths of a percent in impurity content or crystal habit. Because we usually deliver directly from production, every researcher knows the full chain of custody.

    Beyond pharma, Methyl 2,5-Dihydroxycinnamate serves as a building block for specialty polymers and performance materials. The dual hydroxyl structure means it can undergo polymerization or act as a crosslinker, and we supply specific melting point data at shipment to give process engineers the information they need. Our plant team has worked with formulation scientists to tweak melt and grind processes, making sure our product folds smoothly into their workflows. Feedback from coating manufacturers has even led us to prototype modified forms and blend ratios.

    Perfume and flavor chemists have tested our product for unique aromatic properties. Few compounds combine phenolic and ester notes as cleanly as Methyl 2,5-Dihydroxycinnamate. This unique profile, shaped by the precise position of those hydroxyl groups, confers subtlety and complexity that the more typical methyl cinnamates can’t match. We’ve provided gram to kilogram quantities for preliminary assessments and seen the uptake grow as formulators discover where it fits a broader aromatic palette.

    Distinguishing Features: What Sets This Molecule Apart

    Many of our customers have worked with methyl cinnamates before. Yet when they first use Methyl 2,5-Dihydroxycinnamate, the shift is often dramatic. Conventional methyl cinnamate lacks the hydrogen-bonding potential or altered solubility profile we provide here. We regularly field requests to compare our product with ortho- or para-hydroxy analogs, but the difference in polarity, intermolecular interaction, and downstream reactivity is hard to overstate. We’ve collaborated on comparative dissolution and stability testing, and lab results consistently confirm what our chemists see on the production floor—placement of functional groups changes everything, from storage to final application.

    For process chemists, our product dissolves more readily in polar solvents, thanks to extra hydroxyl substituents. Formulators in aqueous systems notice fewer clumping issues, especially when we freshly mill the batch to order. On the production side, we monitor this closely, revising both solvent and temperature conditions batch by batch. Over years of manufacturing, we’ve learned that one-size-fits-all doesn’t work when functional group chemistry moves to the center of product performance.

    Pharmaceutical developers seek improved receptor binding or bioavailability, and Methyl 2,5-Dihydroxycinnamate delivers a targeted alternative to more basic esters or mono-hydroxy forms. We see fewer metabolic byproducts during biotransformation studies, and customer labs report lower batch-to-batch variation. Every year, we run in-house trials to ensure our newly synthesized lots mirror reference standards, a practice rooted in dozens of validation projects and customer audits.

    Quality, Reliability, and Transparency: The Manufacturer’s Experience

    Factory knowledge accumulates in ways you can’t find in the literature. We’ve noticed how atmospheric humidity affects crystallization, how even minor catalyst inconsistencies can introduce trace impurities, and how storage temperature can preserve appearance and reactivity. These are lessons rooted in late-night adjustments and multi-day troubleshooting stretches. Every batch of Methyl 2,5-Dihydroxycinnamate moves through a workflow shaped by these hard-won insights.

    We follow international quality standards but don’t just tick boxes. Years of hands-on experience taught us to go beyond basic compliance. Operators check every piece of incoming raw material, and our small-batch approach lets us catch anomalies early. We have had times where a single out-of-profile reading flagged a filtration problem upstream, sparing both us and the client costly disruption. Those episodes turned into revised SOPs, where real experience, not just documentation, shaped our manufacturing scripts.

    Some clients request site visits or want video footage of their batches as part of onboarding. Having worked directly with these partners, we encourage transparency because we understand why it matters. Many of our clients operate in regulated industries and can’t risk uncertainty in raw material supply. In sharing our own data, we build the kind of trust you only get from seeing the process up close.

    Practical Challenges and the Ways Forward

    Manufacturing Methyl 2,5-Dihydroxycinnamate means confronting evolving demands and new technical rows. Global supply chain disruptions or policy shifts in chemical hazards reporting can abruptly change input prices or delivery timelines. We’ve diversified our supplier base, maintaining backup vendors for all raw materials. Sometimes, we have to reformulate or adapt our pre-treatment steps when regional standards phase out a particular solvent or reagent. In-house technical staff routinely pilot alternative synthesis routes or run accelerated stability testing on new packaging types, adapting as the regulatory environment changes.

    We have worked through ramp-ups for pilot production to meet sudden spikes in demand, especially when a promising research breakthrough boosts global interest in Methyl 2,5-Dihydroxycinnamate. Expanding capacity isn’t just about adding reactors or doubling shifts; we train staff continually, focusing on maintaining safety and precision as complexity increases. Feedback loops with customers help stabilize forecasting, but we’ve also had to learn from mistaken estimates and scramble to catch up.

    Logistics matter as much as chemistry. Poorly sealed containers or delays at customs can mean returned batches or, worse, irretrievable spoilage. We’ve improved our export SOPs, invested in better traceable shipping, and moved to more robust liners for temperature-sensitive shipments. Even the best product on paper loses value if quality degrades in transit. Regular dialogue with transport partners and dynamic internal audits help maintain the integrity our clients expect.

    Addressing Safety and Environmental Responsibility

    Sustainable manufacturing sits at the core of how we approach production. Every synthesis run produces waste streams requiring care. Operators have worked alongside EHS specialists to improve solvent recovery, update filtration, and shift to greener reagents wherever possible. Years ago, we expanded our on-site monitoring and treatment capabilities, helping ensure that we’re not just meeting, but outpacing, environmental requirements.

    We train every team member on best practices for handling all reagents and intermediates, especially since hydroxylated aromatics call for adequate care during both large-scale manufacture and small-scale packaging. We track emissions and water use as part of integrated reporting. Insurance audits highlight our lower incident rates, which stem in large part from these attention-driven practices. In several cases, feedback from our own operators led directly to engineered solutions—better venting, improved PPE protocols, and modular storage for more rapid cleanup and containment.

    Ultimately, we aim for a transparent relationship with labs and traders alike, divulging all composition, impurity, and safety data generated along the way. We know that our clients’ own ESG disclosures depend on reliable input from suppliers, and we take that responsibility seriously.

    Customer Collaboration Drives Product Evolution

    Experience tells us that shared progress comes out of conversation, not just contracts. Communication with formulation scientists, synthetic chemists, and engineers has driven major improvements in our materials. One customer’s desire for a particular particle size distribution prompted a review of our milling and sieving process, which we optimized after several rounds of feedback. After another needed tighter control of metallic contaminants, our staff reviewed every supply chain touchpoint, identifying a source of trace copper from a gasket and resolving the issue with a simple equipment swap.

    We invite input and create tailored feedback reports for every significant batch. This is not just for regulatory compliance. Over the years, we have learned that even minor adjustments—drying protocol, analytical standardization, post-synthesis purification—can mean the difference between routine supply and scientific breakthrough. These hands-on relationships with customers help us zero in on the details that matter most in diverse and rapidly changing fields of application.

    Looking Ahead: The Future for Methyl 2,5-Dihydroxycinnamate

    Every chemist and plant worker who has contributed to the production of Methyl 2,5-Dihydroxycinnamate knows there is more to explore. Continuing advances in pharmaceutical research, new material science, and custom-tailored biotechnologies point to both broader and deeper use cases. Because molecular structure dictates performance, our teams keep refining both upstream synthesis and downstream handling techniques. Demand for transparency, safety, and sustainability only intensifies, and we’re evolving our practices to keep pace with what research and regulatory partners expect.

    We plan to continue investing in both capacity and analytical technology. Enhanced purification machinery and full-spectrum analysis capability allow us to deliver ever higher purity and stability, supporting the needs of innovators in both academia and industry. Sharing technical know-how, supplying documentation as thick as an encyclopedia, and standing ready to adapt to each partner’s requirements has drawn customers back year after year.

    Anyone handling Methyl 2,5-Dihydroxycinnamate in the lab or on the plant floor will recognize both its opportunity and its demands. Most substances pass through our hands and into the world with little fanfare, but when it comes to this one, attention to detail creates opportunities—from the tiniest tweak in molecular structure to far-reaching changes in product performance. As the original manufacturer, we recognize our unique position. We channel our expertise, listen to our partners, and stand ready to continue turning this specialized compound into the reliable, precisely tailored input that so many vital innovations demand.