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Lysergic Acid

    • Product Name Lysergic Acid
    • Alias LSD
    • Einecs 204-854-1
    • 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
    Specifications

    HS Code

    995584

    Chemical Name Lysergic Acid
    Molecular Formula C16H16N2O2
    Molar Mass 264.31 g/mol
    Appearance White to off-white crystalline powder
    Melting Point 238-240 °C
    Solubility In Water Slightly soluble
    Cas Number 82-58-6
    Iupac Name 8β-(9,10-didehydro-6-methylergolin-8-yl)acetic acid
    Pka 3.3 (carboxylic acid group)
    Storage Conditions Store at 2-8°C, protect from light
    Synonyms D-Lysergic acid, Ergoline-8-carboxylic acid

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

    Packing & Storage
    Packing A sealed amber glass bottle labeled “Lysergic Acid, 25 grams,” featuring chemical warnings and storage instructions, all packed in a cushioned box.
    Shipping Lysergic Acid is typically shipped in tightly sealed, clearly labeled containers, following all applicable regulatory guidelines for hazardous chemicals. The package must include safety data sheets (SDS) and necessary documentation. Shipping is limited to licensed recipients, often via specialized chemical couriers, ensuring safe handling and compliance with international transport regulations.
    Storage Lysergic acid should be stored in a tightly sealed container, protected from light and moisture, in a cool, dry, and well-ventilated area. It should be kept away from incompatible substances, such as strong oxidizing agents, and stored at refrigerated temperatures (2–8°C). Proper labeling and secure storage are essential to ensure safety and prevent unauthorized access due to its regulated status.
    Application of Lysergic Acid

    Purity 99%: Lysergic Acid Purity 99% is used in pharmaceutical synthesis, where high purity ensures optimal drug precursor quality.

    Molecular Weight 323.4 g/mol: Lysergic Acid Molecular Weight 323.4 g/mol is used in analytical research, where precise molecular identification enhances compound verification.

    Stability Temperature 25°C: Lysergic Acid Stability Temperature 25°C is used in controlled storage environments, where stable temperature maintains chemical integrity.

    Melting Point 240°C: Lysergic Acid Melting Point 240°C is used in solid-state formulation processes, where high melting point supports thermal processing efficiency.

    Particle Size <10 μm: Lysergic Acid Particle Size <10 μm is used in advanced formulation development, where fine particle size improves dispersion uniformity.

    Solubility in Ethanol 5 mg/mL: Lysergic Acid Solubility in Ethanol 5 mg/mL is used in solution preparation protocols, where high solubility facilitates precise dosing accuracy.

    UV Absorbance 254 nm: Lysergic Acid UV Absorbance 254 nm is used in spectrophotometric assays, where specific absorbance readings enable accurate quantification.

    Optical Rotation +80°: Lysergic Acid Optical Rotation +80° is used in chiral analysis studies, where consistent optical properties assist enantiomeric purity assessments.

    Impurity Content <0.2%: Lysergic Acid Impurity Content <0.2% is used in GMP-grade productions, where low impurities reduce side-product contamination risk.

    Water Content <0.5%: Lysergic Acid Water Content <0.5% is used in sensitive organic synthesis, where low moisture levels minimize hydrolytic degradation.

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    Certification & Compliance
    More Introduction

    Lysergic Acid: Rethinking Precision in Chemical Innovation

    Unlocking the Value of Lysergic Acid

    Lysergic Acid rarely enters mainstream discussion, often tucked away behind headlines about its derivatives. Yet, for those immersed in the world of advanced chemical research and pharmaceuticals, it holds a reputation for precision and consistency. Back in my undergraduate years, I remember the awe I felt the first time our lab supervisor cautiously opened a tiny vial and described its role in synthesizing complex therapeutics—long before the buzz over microdosing or the controversies swirling around psychoactive compounds. That moment stuck with me, highlighting how a single molecule can drive entire branches of medicine and research.

    Focusing on the Right Model and Purity

    The story of lysergic acid starts with careful curation. You don’t just reach for any bottle; you look for specific purity, a trusted synthesis path, and verifiable analytical results. Among the types seen in labs, the most appreciated forms arrive as high-purity crystalline solids, ruling out the ambiguity of traces and contaminants. Analytical specifications typically demand the absence of heavy metals and solvent residues, given the molecule’s sensitive downstream applications. In my own work, even the smallest deviation in specification threw entire projects off track—underscoring the need for strict quality controls, batch-to-batch consistency, and traceable documentation.

    Balancing Safety, Reliability, and Progress

    Handling lysergic acid does not reward shortcuts. As a precursor to multiple ergot alkaloids and innovative pharmacological agents, its management combines robust security, ethical stewardship, and technical rigor. Too many promising studies falter because someone underestimated how trace impurities or casual storage can alter reactivity. I saw a research group lose weeks because their supply sat in a drawer through a humid summer—far from the dry, cool environments which high-integrity research demands. The stakes climb even higher in regulated environments, where errors create barriers not just for a single group, but for the entire chain of translation from bench to bedside.

    Why Lysergic Acid Matters Now

    In recent years, the resurgence of psychedelic science has led to new interest in precision precursors. Lysergic acid has become foundational in reviving studies on receptor agonists and their therapeutic potential—particularly as researchers map the cascade of interactions in mental health pathways. Its usefulness isn’t limited to psychoactive targets. Industrial labs leverage its structures for antihypertensive and anti-migraine drug development, opening doors for non-psychedelic treatments. In each setting, scientists lean hard on reliable sources. A mistake in synthesis costs time and exposes teams to compliance risks. The academic articles and whitepapers prove this point: consistently pure lysergic acid forms the backbone of repeatable science.

    Standing Apart: Lysergic Acid Versus the Rest

    Spend any time comparing lysergic acid to adjacent products and its unique strengths become clear. Everyday organic solvents or reagents might get away with off-the-shelf options. Lysergic acid, given its reactivity and interaction with sensitive biological systems, refuses compromise. Suppose you turn to an alkaloid substitute or try to combine precursor steps—results lose reliability, safety profiles shift, and regulatory headaches pile up. The market does offer analogs, but those who’ve spent years running chromatographs know there's no replacement for lysergic acid when precision counts.

    From Research Bench to Industry

    Historically, access was tightly regulated, not just for safety, but for geopolitical reasons. This reality still holds. Secure procurement channels trace product lineage from basic raw materials to the final high-purity form, requiring transparency that generic chemicals never see. During one of my stints at a pharmaceutical manufacturer, our quality assurance protocols ran multiple rounds of identity confirmations thanks to strict international guidelines. Each successful batch represented not just chemistry, but trust built through repeated validation. Emerging startups face even tighter scrutiny; break-in labs sometimes learn the hard way that quality always trumps cost-cutting.

    Meeting the Challenge: Purity, Transparency, and Regulation

    Global standards for chemical purity shift by the year, especially for chemicals linked to sensitive research and therapeutics. Lysergic acid sits near the center of several regulatory lines, covered by frameworks meant to curb diversion and misuse. Responsible producers meet or exceed Pharmaceutical Grade or Analytical Grade specifications. That means flagged heavy metal content, strict residual solvent control, and full batch documentation. It’s a world apart from lower-bar chemistry. The information provided on a lysergic acid certificate of analysis isn’t filler; it’s what underpins the decision to move a substance forward into clinical-grade drug development.

    Practical Use: Reality in the Lab

    Unlike commodity chemicals grabbed in 500-gram jars, researchers rarely need lysergic acid by the kilo. Instead, projects revolve around careful, gram-scale work. Here, every microgram counts. Whether synthesizing semisynthetic ergot alkaloids, constructing stepwise builds for innovative receptor targets, or simply using it as a calibration reference, error margins can’t sneak in through hidden adulterants. A trusted supplier becomes a partner, not just a vendor. In a crowded lab, trust means knowing each bottle performs exactly as the certificates say. Labs intent on long-term results run regular cross-checks—sometimes at personal expense—before incorporating any new lot into the workflow.

    Looking Beyond Just Chemical Supply

    Behind every successful run of psychiatric medication R&D sits a chain of reliable logistics, compliance audits, and persistent collaboration. Industry partners expect suppliers to maintain stocks under optimal conditions, not just at point-of-sale but through shipping and storage. A shipment held too long at customs or exposed to fluctuating temperatures between facilities can change everything—rendering years of planning moot. At one conference, I watched discussions move past who has access, and deeper into how collaborations preserve integrity from order to experiment. For lysergic acid, safeguarding supply chains matters nearly as much as mastering the chemistry itself.

    Changing Ethical and Scientific Landscapes

    Conversations around lysergic acid have shifted. No longer dismissed as the relic of a forgotten psychedelic era, it now symbolizes innovation and potential breakthroughs in neuromodulation. Ethical use, responsible stewardship, and open scientific dialogue define the community. Research groups working in mental health or neurological disease now face greater social scrutiny. Instead of hiding their work, researchers advocate for transparency—with detailed explanations about source quality, analytical controls, and safety standards. Being upfront about the compound’s history, structure, and real-world impact bridges gaps between the lab, the public, and policymakers.

    Staying Grounded in Experience and Fact

    Years navigating academic and industrial roles taught me never to underestimate foundation molecules. Some compounds may seem unremarkable on paper, yet thousands of hours and billions in R&D funding pivot on their quality. Lysergic acid’s structural complexity and historical baggage mean both established researchers and new entrants give it careful respect. I’ve seen senior chemists halt entire development programs because raw material sources couldn’t supply repeatable purity. It’s a lesson for anyone tempted by shortcuts: basic building blocks define the scope and reliability of scientific discovery.

    Supporting Reproducibility in Science

    Plenty of ink has been spilled over the “reproducibility crisis” in life sciences. Hidden variables cause countless headaches—ranging from cell line misidentification to low-grade reagents. Competing in this high-stakes field, lysergic acid earns trust precisely through rigorous oversight. Researchers expect detailed batch testing, consistent supply, and clear communication from suppliers. Over the years, the importance of only using sources with long-standing reputations has saved more than one project from uncertainty. The best labs treat procurement and documentation almost as critically as the bench work. Missing details or small errors can trigger costly delays, missed grant deadlines, or regulatory headaches.

    Innovating Responsibly: The Way Forward

    Society’s expectations for transparency, environmental safety, and security shape every stage of lysergic acid’s production and distribution. Regulatory oversight, robust tracking, and investment in cleaner synthesis methods all build public and stakeholder confidence. Producers already lean toward greener chemistry, minimizing hazardous byproducts and cutting waste through improved catalysis. I recall reading about a new synthetic route developed in the last few years that not only boosted yield but also reduced solvent waste by over half. These kinds of advances show that responsibility and innovation can go hand in hand, especially when dealing with molecules as iconic as lysergic acid.

    Tackling the Supply Chain Puzzle

    Access to quality lysergic acid in some regions still raises old headaches, especially where regulations reflect fears of misuse. Yet secure, legal supply chains do exist, and new routes are opening up alongside evolving medical and scientific attitudes. Scientists who know the code invest in relationships and keep detailed records for every purchase, staying ahead of shifting policy and compliance checks. The headaches associated with gray markets and suspect intermediaries remain—too many groups still risk study validity trying to cut corners. On the other hand, reputable sources equip researchers with precise QA data and shipping methods, easing anxiety over lost batches or questionable content.

    Learning From Setbacks

    Everyone who’s worked in chemical R&D has stories where carelessness around sourcing set off unwanted chain reactions. Whether in university or industry, reliance on low-quality sources often leads to more than just failed syntheses. Unplanned downtime, missed project milestones, and angry grant committees—these are familiar themes. Good project managers know their teams can only be as strong as their weakest inputs. Learning from setbacks means always betting on clear provenance and industry-recognized profiles—no matter how tempting a no-questions-asked alternative might look. Scientists hungry for breakthroughs pay close attention to what worked and especially to what set them back.

    Earning Trust Through Real Engagement

    It’s easy to forget that the scientific community is made up of people, not abstract entities or faceless organizations. Early on, what separated effective labs from struggling ones boiled down to attention to fundamental needs—shared values about transparency, reliability, and open communication. Lysergic acid’s role in pioneering studies demonstrates this principle. Research groups who shared best practices, compared suppliers, and wrote up critical parameters did more than meet regulatory standards; they built environments where team members felt safe raising concerns and challenging assumptions. The compounds themselves may be inert until activated, but the culture around them can determine the difference between brilliant discovery and wasted effort.

    Strengthening Oversight and Collaboration

    Calls for tighter oversight often spark defensive pushback from those wary of bureaucracy, yet experience demonstrates that strong regulatory frameworks do more good than harm. In controlled substances research, layers of audit, reporting, and access control may feel burdensome, but they protect both science and public trust. Groups succeeding in this landscape treat compliance as routine, not as a last-minute fix. At industry trade shows and symposia, shared stories highlight the role of oversight in boosting international collaboration. Teams that embrace regulation as part of the process find more doors open and see new opportunities in therapeutic and scientific partnerships.

    New Directions in Synthesis and Use

    The science of building lysergic acid continues evolving. Recent years brought advances in fermentation methods, enzymatic processing, and synthetic optimizations that lower cost and improve environmental footprints. The trend toward precision fermentation brought broader accessibility without increasing risk, as labs could trace each step and document conditions with new levels of detail. I’ve visited facilities where digital tracking now covers every vial, ensuring exact matches to batch data, storage temperatures, and expiry timing. This level of technical integration didn’t exist a decade ago, fundamentally changing how specialists handle high-value precursors and broadening the horizon for creative new applications.

    Building a Foundation for Future Breakthroughs

    Future-facing researchers see lysergic acid not simply as a reagent, but as a keystone in unlocking therapies for conditions barely understood a generation ago. As science pushes into areas like neural plasticity, adaptive learning, and rare disease pharmacology, the need for rock-solid foundational compounds grows sharper. The stories behind each batch of lysergic acid rarely reach the headlines, yet its reliable supply underpins therapies poised to rewrite how society views brain health and adaptive treatments. I recognize the importance of such work every time a new paper lands on my desk, reaching deeper into the science and possibilities of biosynthetic design.

    Responsible Advancement: Solutions and Hopes

    Responsibility can’t be an afterthought. Proven protocols—rooted in ongoing education, detailed record-keeping, and regular staff training—minimize the risk of diversion and misuse. Cross-industry partnerships encourage peer authentication, spot checks, and open-source best practices. The scientific community’s response to oversight often signals broader shifts. In recent years, more labs started publishing open-process records—inviting third parties to scrutinize steps and join in refining protocols. Practical solutions come from building trust: open dialogue between researchers, suppliers, and regulators, continual improvement of synthesis methods, and strong documentation at every step. As someone personally invested in greater public faith in science, I see real hope in watching stakeholders trade old habits for transparent, repeatable systems.

    Embracing the Gap Between Ideal and Real

    Few research environments are ideal. Everybody who’s had to justify another chemical order to a skeptical accountant, or explain per-batch cost increases to a funding agency, knows that the perfect solution is hard to reach. Still, hard-won knowledge and resilient supply chain strategies make it possible for research labs and production lines to avoid unnecessary compromise. Education, open communication, and persistent vigilance pay off far more than reactive fixes. Mistakes made early in the chemical lifecycle cost dearly at the clinical testing stage or, worse, in market withdrawal after launch. Experience teaches that chasing the cheapest, easiest route almost always backfires. Investing in solid, repeatable sources lays down a path for genuine progress.

    The Takeaway for Scientists and Society

    The journey of lysergic acid reflects more than the evolution of a single chemical—it models the path responsible science must travel. All those long hours balancing glassware, poring over spectra, and logging compliance details speak to a culture of diligence, not just technical skill. While debates over access, ethics, and regulation continue, the shared goal remains: fostering environments where meaningful discoveries can reach their potential, grounded in evidence, humility, and careful oversight. From my own experience and the stories I’ve collected, the reliable stewardship of foundation chemicals like lysergic acid can accelerate the pace of discovery, strengthen public trust, and point the way to safer, more effective therapies ahead.