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HS Code |
279748 |
| Cas Number | 14534-64-8 |
| Molecular Formula | C25H24O12 |
| Molecular Weight | 516.46 g/mol |
| Iupac Name | 3,5-bis(3,4-dihydroxycinnamoyl)quinic acid |
| Appearance | Yellowish powder |
| Solubility | Soluble in water, methanol, ethanol |
| Purity | Typically >98% (HPLC) |
| Storage | Store at -20°C, protected from light and moisture |
| Synonyms | 3,5-di-O-caffeoylquinic acid, 3,5-DCQA |
As an accredited 35-Dicaffeylquinic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 35-Dicaffeylquinic Acid, 100 mg, supplied in a sealed amber glass vial with tamper-evident cap, labeled with lot number. |
| Shipping | 35-Dicaffeylquinic Acid is shipped in secure, airtight containers to maintain stability and prevent contamination. It is handled according to standard chemical safety procedures, including temperature control if required. Detailed labeling and documentation are provided to ensure proper identification and compliance with international shipping regulations for laboratory and research use. |
| Storage | 35-Dicaffeoylquinic acid should be stored in a tightly sealed container, protected from light and moisture. Keep it in a cool, dry place, preferably at -20°C or lower. Ensure the storage area is free from incompatible substances and that the chemical is handled and labeled in accordance with standard laboratory safety protocols for chemical storage and use. |
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Purity 98%: 35-Dicaffeylquinic Acid with purity 98% is used in pharmaceutical formulations, where enhanced anti-inflammatory efficacy is achieved. Molecular weight 516.45 g/mol: 35-Dicaffeylquinic Acid at molecular weight 516.45 g/mol is used in nutraceutical supplements, where predictable bioavailability is ensured. Solubility in ethanol: 35-Dicaffeylquinic Acid with high solubility in ethanol is used in herbal extract preparations, where efficient active compound extraction is facilitated. Stability temperature 25°C: 35-Dicaffeylquinic Acid stable at 25°C is used in cosmetic serums, where prolonged shelf life and product efficacy are maintained. Melting point 270°C: 35-Dicaffeylquinic Acid with melting point 270°C is used in analytical reference standards, where accurate thermal analysis is supported. Particle size <10 μm: 35-Dicaffeylquinic Acid with particle size under 10 μm is used in micronized dietary powders, where rapid dissolution and absorption are improved. UV absorbance λmax 326 nm: 35-Dicaffeylquinic Acid with UV absorbance λmax 326 nm is used in analytical quantification, where precise detection in quality control is accomplished. Residual solvent <0.1%: 35-Dicaffeylquinic Acid with residual solvent below 0.1% is used in injectable formulations, where patient safety and regulatory compliance are ensured. Heavy metals <5 ppm: 35-Dicaffeylquinic Acid with heavy metals below 5 ppm is used in functional beverages, where toxicological safety is maintained. |
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Working with caffeoylquinic acids sparks a deep appreciation for both chemistry and patience. 35-Dicaffeylquinic acid stands out in our lab. Years back, most inquiries circled around simple chlorogenic acid or monocaffeoyl derivatives. Each year, demand for more complex and specific polyphenol compounds grows—and nowhere is that shift clearer than with 35-Dicaffeylquinic acid.
Scientists seek highly pure 35-Dicaffeylquinic acid for the cleanest readouts in their studies. Our experience refining this molecule has honed every step from extraction and purification to quality analytics. This isn’t a bulk commodity; it's a precise specialty product, and every batch shows the focus it takes. In our process, crude extraction yields a tangle of quinic acids and related polyphenol mixtures. Cutting through that complexity, then confirming structure and purity, has occupied much of our time and keen laboratory eyes.
The 35-Dicaffeylquinic acid we produce is typically requested at a purity over 98%, based on HPLC-UV analysis, with a faint yellow to off-white appearance. Most research teams prefer it in milligram or gram-scale orders, packed tightly in glass vials or inert containers, under nitrogen whenever possible. Moisture ruins the sharp, expected peak in a chromatogram, so we control for humidity with every move.
We offer this compound either as a fine powder or, on rare occasions, dissolved in methanol for select partners. Solubility features prominently in many questions we answer every week: it dissolves slowly in methanol, ethanol, and DMSO, and barely mixes with water unless heated or treated with base. For test settings, most rely on fresh solutions before each assay.
Researchers working with this molecule investigate antioxidant capacity, anti-inflammatory effects, and cellular signaling pathways. Some probe polyphenol metabolism, using 35-Dicaffeylquinic acid as a standard or reference marker. In comparative phytochemistry, this standard helps distinguish coffee bean and chicory profiles. Nutraceutical teams look at its potential for bioactive compound enrichment. Analytical chemists keep it on hand to identify and quantify similar structures in plant extracts or to calibrate precision equipment.
Demand from pharmacology and cosmetics has intensified. Formula development today wants detailed insight into multi-caffeoyl scaffolding. Funding bodies expect rigorous purity and clear identities, which cannot come from rough extracts or partially defined standards. Delivering the consistent, clean substance they require takes a manufacturing flow rooted in detail and adjustment, not automation alone.
The most common query after, “How much can I order?” is, “How does this compare to 5-CQA or 3,5-DCQA?” Ours is a clear answer: structure and downstream effect both set 35-Dicaffeylquinic acid apart. The key differences start with the number and position of caffeoyl groups on the quinic backbone. Monocaffeoylquinic acids (like 5-CQA, or chlorogenic acid) appear in common foods, represent lower antioxidant potential, and are everywhere—cheap, easy, and almost bland for a seasoned chemist.
Dicaffeylquinic acids, particularly the 35- isomer, reflect higher biological activities. The structure affects both radical scavenging properties and how the compound is absorbed, metabolized, and excreted in animals or humans. These differences are not just footnotes in journal articles. Prematurely switching a project from monocaffeoyl to dicaffeoyl derivatives has, in several customer projects, shifted the outcome from null to significant effect. Some plant physiologists specifically look for 35-Dicaffeylquinic acid to trace plant cell wall modifications, while others use it as a marker of coffee bean maturity and post-harvest fermentation. Oils and extracts with unclear 3,4- or 3,5- substitutions lack the research reproducibility teams always need.
Our own HPLC systems easily resolve these isomers. The methodology and standards we've established give cleaner, more reliable retention times and spectra than any available commercial mix. Trading companies often claim all dicaffeoylquinic acids are interchangeable; seasoned scientists know otherwise and have set their protocols around real-world, batch-to-batch performance.
From raw material selection to crystallization, every step in making 35-Dicaffeylquinic acid tests patience and precision. Extraction starts with freeze-dried source material specifically chosen for its polyphenol content, no matter how small the yield. The process requires a firm sense of timing—leave plant matter in the solvent too long and unwanted hydrolysates or artifacts take over; cut extraction short, and yield drops. Early mistakes in timing, solvent ratio, or temperature reveal themselves as streaks and shadows on chromatograms hours or days later. These setbacks have inspired us to redesign both the extraction equipment and the workflow, not once but several times.
Post-extraction, the greatest complication comes during separation of structurally similar dicaffeoylquinic isomers. Some batches fly through, while others demand fractional crystallization against a tight temperature window, then repeated column re-purifications. Trace cross-contamination between 3,4- and 3,5- isomers can throw off entire research projects. Experience has led us to cross-check each batch using both HPLC and high-resolution mass spectrometry, double-confirming the absence of unwanted isomers. Even after years of production, every lot exposes new angles: trace oxidized byproducts, persistent solvent residues, or splittings in the UV spectrum when glassware is not fully dry. Fixes require close feedback between bench chemists and QC managers, leaving no detail to drift.
We maintain in-house archives of every batch, and revisit old methods when a process improvement shows unexpected side-effects. Quality never leapfrogs experience; cumulative detection limits, subtle spectral artifacts, and shifting impurity baselines stay top of mind. Most competitors trade simple purity data sheets or basic HPLC traces, but seasoned chemists and purchasing agents visit our lab just to see the consistency in person.
Phytochemical research in the last five years has shifted from rough botanical extracts to compounds with clear, referenced identities. Researchers cite failed projects where heterogeneous "dicaffeoylquinic acid" mixes created irreproducible results. Our goal remains ongoing dialogue with the research community, learning what works and what wastes time. Many university researchers ask for custom packaging, or direct delivery into pre-weighed vials for blinded assays. In response, we have retooled some packaging lines for these custom requests and can scale up or down depending on trial progress.
Some customers request new documentation—full COAs with UV, NMR, and MS overlays—not just boilerplate testing. Through long partnerships with quality teams at universities and clinical research organizations, we provide method validation files, contamination risk assessments, and full documentation at each step. We keep an open file of customer feedback, both on the compound itself and how its performance syncs with their ongoing projects.
Researchers sometimes ask about regulatory status or food additive acceptance for 35-Dicaffeylquinic acid. This compound is not listed as a GRAS food additive or cosmetic ingredient in any major database. Its use sits squarely in research, analytical validation, and product development—often preceding regulatory filings or scaled-up application trials by years. Safety data comes from animal and cellular experiments and should not be confused with final toxicology or safety standards for consumer products.
In our own handling, we use laboratory PPE, maintain negative pressure spaces, and regularly audit both inventory and waste streams. Every shipment leaves the factory with a full analytical profile, detailed material data, and guidance for protected laboratory handling. Bulk shipments trigger a separate series of checks, and we revisit safety protocols whenever scale increases.
Requests for this compound range from university graduate projects to established analytical laboratories and formulation houses. An emerging group of nutraceutical developers have rebuilt their R&D programs around defined caffeoylquinic standards, rejecting old modes based on poorly characterized plant extracts. We have partnered with several teams working at the intersection of basic biology and product innovation—addressing both precise scientific questions and the ambitions of brands seeking new functional compounds.
Consistent supply runs deeper than filling orders. We update customers on improvements, alert them to global crop shifts, and advise on best storage practices for both short and long-term use. Unexpected supply interruptions in recent years (drought, export restrictions, shipping slowdowns) taught us hard lessons about forward planning and honest communication. These events re-shaped our procurement and batch scheduling priorities, keeping both science and logistics aligned.
For industrial clients, scale-up presents a different challenge than research batches. Quality controls expand to cover larger volumes, new testing points, and the possible presence of additional trace impurities. We have built extra cleanroom capacity and diversified raw material suppliers to meet these larger, more demanding orders, all while keeping test criteria as tight as the research-scale runs.
Several years ago, only a handful of labs worldwide chased specialty dicaffeoylquinic acids. Now, their applications cover not just antioxidant studies or botanical fingerprinting, but high-precision bioactive development, cell signaling, and nutritional chemistry. Keeping pace with customer needs, we draw on a mixture of best-in-class instrumentation, custom chemical knowhow, and the relentless improvement that comes from facing down failed batches, refining steps, and learning from every anomaly.
Continuous technical learning is part of our culture. Our team keeps close tabs on published research, incorporating new information on reactivity, degradation, and applications of 35-Dicaffeylquinic acid. If a new publication hints at better separation, or a patent reveals a new derivative, we bring that knowledge to both R&D and routine production. Recurring customer audits and invited research projects keep external standards high, sparking both trust and a willingness to try bolder approaches.
We see clear separation between high-end research compounds and the bulk-diluted offerings moving through trading channels. Researchers want answers, not just milligrams. Direct dialogue, transparent records, and a rigorous approach to every gram define our daily work and our promise to continue meeting the technical challenges of next-generation polyphenol research.