|
HS Code |
367943 |
| Chemicalname | Shikimic Acid |
| Chemicalformula | C7H10O5 |
| Molecularweight | 174.15 g/mol |
| Casnumber | 138-59-0 |
| Appearance | White to off-white crystalline powder |
| Solubilityinwater | Soluble |
| Meltingpoint | 188–191 °C |
| Ph | 2.4 (0.1% solution) |
| Boilingpoint | Decomposes before boiling |
| Odor | Odorless |
| Storagetemperature | 2-8 °C |
| Purity | Typically ≥98% |
As an accredited Shikimic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Shikimic Acid is packaged in a sealed, amber glass bottle containing 100 grams, with a tamper-evident cap and safety labeling. |
| Shipping | Shikimic Acid is typically shipped in sealed, airtight containers to prevent moisture absorption and contamination. It should be stored and transported in a cool, dry place, away from direct sunlight and incompatible substances. Proper labeling and documentation are required to comply with regulations, ensuring safe and secure delivery during transit. |
| Storage | Shikimic Acid should be stored in a tightly sealed container, protected from light and moisture. Keep it in a cool, dry, and well-ventilated area, ideally at temperatures between 2–8°C (refrigerated conditions). Avoid exposure to incompatible materials such as strong oxidizing agents. Properly label the container and ensure it is only accessible to trained personnel to maintain safety and stability. |
Competitive Shikimic Acid prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please contact us at +8615365186327 or mail to sales3@ascent-chem.com.
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Tel: +8615365186327
Email: sales3@ascent-chem.com
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On the production floor, nothing ever goes exactly as the lab predicts. This is especially true with Shikimic Acid, a compound extracted and refined through many careful steps. At our facility, it isn’t harvested from wild plants or sourced from brokers who source from brokers; it’s the end product of precision fermentation and extraction managed on site. That’s important. Every chemist, technician, and operator here watches the process from the moment the substrate enters the bioreactor until we bottle the crystalline powder. It’s quality that’s built by hands and eyes, not just signed off on paper.
Plenty of suppliers tout high purity, but from our side of the industry, purity is more than a number. After repeated crystallization, our Shikimic Acid regularly exceeds 98% assay as determined by HPLC—tested every batch. Loss on drying remains low, under 0.5%. Handling matters, too. Clumping and discoloration can happen if you cheat on the drying times or use mixed-source plant material. Here, we learned early on that patience and process discipline cut down impurities. This avoids issues in downstream applications, whether our clients are using it in synthetic antivirals (like oseltamivir) or as a fine chemical in flavor and fragrance segments.
Shikimic Acid holds its reputation in pharmaceuticals, especially as the key starting point in the synthesis of neuraminidase inhibitors. Because so much of the world’s supply once depended on star anise pods, shortages and price spikes hit hard any time crop yields fell. We built our process for stability, relying now on controlled biotransformation instead of wild harvests. Our customers come back not because of a brochure’s promises, but because the product behaves batch-to-batch the way their processes expect. Even subtle shifts in isomer balance or residual moisture can ruin a synthesis route or cause scale-up headaches. By handling every variable ourselves, we take away that uncertainty.
Broader chemical catalogs list Shikimic Acid with similar stats—purity, physical form, sometimes even pricing. The reality inside a full-scale plant, though, is messier. Shikimic Acid derived from star anise extract still dominates certain markets. It’s worked for decades, and the right supply chain can give consistent output, but trace pesticide residues and heavy metals sometimes exceed specifications placed by pharma developers. Synthetic routes, often based on quinic acid conversions, appeal on paper. Yet catalysts and solvent residues can linger in the product stream. Over dozens of cycles, we honed our in-house route to skirt those pitfalls. Repetitive in-process checks weed out contaminant issues, and feedback from customers—especially those in regulated sectors—has kept us honest about how the product performs outside QC labs.
Formulating teams look beyond raw specifications, and they have good reason. Shikimic Acid delivers value as either a chiral building block or an intermediate, depending on the synthesis. Where you source it changes how it fits into the flow of manufacturing, especially under quality-driven regimes. We’ve watched clients scale up batches only to face inconsistencies when switching to third-party material. Through those experiences, we learned that controlling particle size, moisture, and isomeric purity doesn’t only affect reaction yields but lowers the risk of rework and regulatory headaches. In real medical chemistry applications, each deviation risks an entire batch.
Ten years ago, anyone in the business still felt the effects of star anise crop failures in China. Prices of Shikimic Acid whiplashed; so did delivery times. Hard plants supplied by nature can’t always meet huge global demand for antiviral raw materials, especially in crisis seasons. As manufacturers, we took matters out of the field and into fermentation. Setting up the bioreactors and purification trains wasn’t rapid or cheap, but it broke the pattern of volatility. Now, clients aren’t left waiting for the whims of rainfall or pests. We watch every reaction, every kilo, every filtration step, so that the product isn’t only available—it meets pharmaceutical-grade rigor every single day.
Some non-manufacturers frame Shikimic Acid as just another chemical. In practice, every kilo represents months of upstream planning. The utility in bulk chemistry, such as in flavor modification or fragrance building, rests on its predictable reactivity and low contaminant load. Fluctuations in active ingredient levels wreak havoc during scale-ups, especially in sectors like pharma where regulators scrutinize every impurity profile. Our team invests real time in upstream analytics—chromatography, spectroscopy, even particle imaging—to guarantee lot uniformity. We take these steps not because the market always demands it, but because a failed batch at the client’s site quickly leads back to the manufacturer.
Regulators don’t offer grace periods. Over the years, passing audits and customer audits has forced us to treat each metric as a baseline, not a finish line. We don’t gamble with the unknown. For pharma-bound Shikimic Acid, we supply full impurity profiles, shelf-life data, and route-of-synthesis documentation—not because it’s required on every sale, but because customers in regulated sectors trust what they can verify. Environmental compliance also comes into play. Our shift to biotechnological sourcing helped us avoid the residue and sustainability pitfalls facing traditional agricultural producers. By focusing on these realities, we trade short-term profit for long-term stability.
Lab managers rarely call to praise ongoing performance, but complaints come fast if materials deviate from established specs. We learned to track these issues early by sending technical teams to client production lines for troubleshooting. If a new lot triggers reaction slowdowns or unexpected byproducts, we’re the first to review the root cause using both tracked production records and retained reference samples. Clients using Shikimic Acid for sensitive stereoselective syntheses appreciate this hands-on follow-up. Open communication means faster problem-solving and greater trust, something the trading middlemen struggle to match.
Profit in chemical manufacturing always comes down to yield, energy cost, and scrap rates. For Shikimic Acid, extraction purity can mask true cost if yields are unpredictable. Yields drop when raw input fluctuates in quality—a reminder experienced teams internalize fast. By stabilizing every input from fermentation feedstock to filtration media, we lock down batch yield and stick to an efficient throughput. Customers benefit from price stability and reliable timelines because we make those variables visible before anything leaves our site.
Drug development is unforgiving. Synthesizing active pharmaceutical intermediates from Shikimic Acid leaves little tolerance for contamination. Our deep relationships with pharma partners emerged out of years of keeping every parameter visible, from process route documentation to batch-to-batch chromatograms. By delivering a material that meets or exceeds published pharmacopoeia standards, we help our partners put new therapies on shelves, on schedule. That kind of collaboration goes beyond paperwork. We hold regular technical exchanges with users, adjusting particle size distribution, moisture profile, or packaging based on direct customer input. This approach pays dividends, not just in repeat business but in zero surprises at process validation.
After years of running both plant extraction and fermentative routes in parallel, we measured the real environmental impact of both. Water and solvent consumption in the extractive plant route ran about double that in our fermentation setup. Waste streams from plant material required added treatment, raising regulatory complexity. By transitioning the majority of our output to closed-loop fermentation, we reduced not only our carbon footprint but also our reliance on external suppliers vulnerable to supply disruptions. Sourcing sustainability isn’t a slogan—it’s an operational truth. That approach won’t earn headlines, but it does matter to customers with long-term contracts and green chemistry principles to uphold.
Chemical end-users don’t need another vendor pitching theoretical benefits. Feedback from medicinal chemists using our Shikimic Acid in antiviral synthesis has been blunt—reproducibility counts for more than any sales pitch. Consistent isomer ratios and low residual solvents shape real reaction outcomes. Our product wasn’t always this foolproof. It took repeated collaboration, real-world failures, and redesigning filtration protocols to reach a point where we can stand behind every lot number. Over time, tweaks like extending drying times or utilizing higher-grade reverse osmosis water moved the product from acceptable to best-in-class for multi-step synthesis.
Errors at the supplier level cascade down a supply chain quickly. We built our batch release standards around the realities clients face: missed timelines, process bottlenecks, and unexpected impurities can all easily arise from seemingly small deviations. With Shikimic Acid, our goal has always been to provide certainty—no hidden residues, predictable particle flow, no seasonal variations. Our presence as the actual manufacturer puts us in the position to catch, and correct, issues before they become customer headaches. We hold reserve samples of every lot for post-sale investigation, a practice that has saved more than a few vital projects for our most demanding partners.
Trust builds batch by batch. As a manufacturer, we never benefit from hiding weaknesses; our clients always find out, one way or another. Regular audits, full access to production logs, and collaborative investigations into out-of-spec events have strengthened relationships with our longest-standing buyers. We share details about our biotransformation process, water sources, and packaging standards upon request. That transparency isn’t an obligation—it’s a cornerstone of how long-term value is built for both sides.
Chemical markets shift without warning. Currency rates, logistics bottlenecks, even changes in safety regulations all impact our ability to deliver Shikimic Acid. Rather than relying solely on long-distance shipping or volatile commodity exchanges, we invested in domestic redundancy and on-site storage. Bulk orders receive active monitoring from production line to packaging and shipment, so that upsets in one facility don’t result in customer shortages. Experience taught us it’s less costly to keep a cushion than to scramble for supplies at the last minute.
Real manufacturing isn’t about flawless batches every time; it’s about learning and adapting. Early runs of Shikimic Acid faced batch-to-batch inconsistencies. Instead of patching over complaints, we returned to process analytics, rechecking every step from inoculum prep to lyophilization. Improvements followed not from wishful thinking but from concrete operator feedback, client case studies, and failed pilot runs. Now, robust upstream controls and analytical sign-offs ensure the product meets real-world demands, not just theoretical models.
Shikimic Acid means different things at different points in the value chain: to a plant biologist it’s a metabolic intermediate, to a pharmaceutical chemist it’s a vital building block, to a flavorist it’s a precursor to subtle aromas. As chemical manufacturers, our focus stays grounded in daily practice—not just words. Our process isn’t the cheapest path, but it’s one shaped by feedback, long-term planning, and knowing every pitfall from raw plant sources to full GMP bioproduction. Decades of practical work taught us that Shikimic Acid, sourced properly, is not a simple commodity. It’s an intricate product whose real value shows in every kilo delivered and every partnership sustained.
The future for Shikimic Acid will keep shifting—new synthetic biology methods, changing regulatory pressures, new downstream applications. As a manufacturer, adaptation drives every part of our operation. By staying close to the process, listening to client experiences, and refusing to cut corners at any stage from fermentation to finished goods, we ensure Shikimic Acid keeps supporting science, medicine, and industry where reliability and trust remain the ultimate currency.