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Lobelanine

    • Product Name Lobelanine
    • Alias Lobelidine
    • Einecs 210-103-7
    • 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
    VTB
    Specifications

    HS Code

    189270

    Name Lobelanine
    Chemical Formula C22H27NO2
    Molecular Weight 337.46 g/mol
    Cas Number 477-36-1
    Appearance White to off-white powder
    Solubility Soluble in organic solvents, poorly soluble in water
    Melting Point 239-241°C
    Iupac Name 2,6-bis(1-phenylethyl)piperidin-3-one
    Type Alkaloid
    Source Found in plants of the Lobelia genus
    Storage Conditions Store in a cool, dry place
    Synonyms Lobelanine, Lobelaninum

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

    Packing & Storage
    Packing Lobelanine is supplied in a sealed amber glass bottle, 10 grams, with a tamper-evident cap and clear hazard labeling.
    Shipping Lobelanine should be shipped in accordance with relevant chemical safety regulations. Use sealed, labeled containers resistant to moisture and light. Include proper documentation (SDS, labeling), and package securely to prevent leaks or spills. Transport using a reputable courier experienced with chemicals, and comply with local, national, and international shipping requirements.
    Storage Lobelanine should be stored in a tightly sealed container, away from light, moisture, and incompatible substances. Keep it in a cool, dry, and well-ventilated area, ideally at room temperature. Ensure storage is secure and appropriately labeled. Use personal protective equipment when handling, and avoid exposure to heat, open flames, and sources of ignition to maintain stability and safety.
    Application of Lobelanine

    Applications of Lobelanine in Industrial Manufacturing

    Lobelanine, as produced by our integrated chemical facility, serves as a critical intermediate in specialized pharmaceutical synthesis, biotechnological research, and advanced veterinary medicine production. The following sectors illustrate true-to-market applications, with detailed compliance and process integration for each downstream scenario, verified by customers and industrial partners across regulated geographies.

    1. API Intermediate for Respiratory Pharmaceuticals

    Leading pharmaceutical manufacturers incorporate lobelanine as a precursor in the synthesis of lobeline and related plant alkaloid medications for respiratory therapy. Its structural properties enable direct modification during the conversion to active ingredients for finished drug products used in cessation aids and selected bronchodilators. Downstream customers run in-situ chlorination or methylation processes where precisely dosed lobelanine supports efficient API yield and batch reproducibility under GMP systems.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 210/211 (Pharmaceutical Manufacturing Standards)
    • European Pharmacopoeia monographs (where applicable for API synthesis)
    • Health Canada GMP guidelines

    Typical usage ratio

    • 0.8% – 3% w/w based on the total weight of the reaction mixture; adjusted according to chromatographic determination and yield target for specific synthesis protocols

    Downstream process integration

    • Added during the alkaloid extraction or base-precursor step as an isolated intermediate; exact stage selected based on target API pathway (e.g., N-demethylation, hydrogenation)

    Final product types

    • Active pharmaceutical ingredients (APIs) such as lobeline hydrochloride for prescription and over-the-counter medication formulations
    • Finished solid dosage forms—primarily oral tablets and capsules for nicotine replacement therapy
    • Parenteral solutions used in clinical and hospital respiratory support

    2. Analytical Chemical Standard in Biotech Research

    Biotechnological R&D centers and analytical labs source high-purity lobelanine for use as an internal standard in mass spectrometry and chromatographic assays, particularly in natural product identification and plant metabolic profiling. Rigorous quality metrics drive selection based on traceability, impurity profile, and batch-specific spectral data. Labs require a controlled baseline for calibration and quantification within advanced LC-MS workflows.

    Industry compliance standards

    • ISO/IEC 17025 (General requirements for laboratory competence)
    • Good Laboratory Practice (GLP) principles per OECD guidelines
    • USP Reference Standards criteria where applicable

    Typical usage ratio

    • 10–100 μg/mL as standard solution concentration; final quantity adjusted according to analytical method sensitivity and instrument limit of detection

    Downstream process integration

    • Diluted and spiked into sample matrices prior to LC-MS, GC-MS, or HPLC analysis; acts as a reference to calibrate retention time, mass accuracy, and quantitation curves

    Final product types

    • Commercial reference standards distributed to third-party analytical labs
    • Validated testing kits for plant alkaloid profiling
    • Research data packages supporting regulatory submission

    3. Veterinary Drug Precursor

    Animal health manufacturers process lobelanine as a building block for non-human pharmaceutical compounds, primarily in the development of respiratory and central nervous system stimulants for livestock and companion animals. Manufacturing integrates this raw material into multi-step synthesis, culminating in API-grade substances evaluated for safety under veterinary drug regulations. Performance consistency depends on impurity controls and lot-to-lot reproducibility maintained under veterinary-specific quality management systems.

    Industry compliance standards

    • VICH GL9 (Good Manufacturing Practice for Active Pharmaceutical Ingredients Used in Veterinary Medicinal Products)
    • US FDA CVM guidelines for animal drugs
    • European Union Regulation (EU) 2019/6 for veterinary medicines
    • ISO 9001:2015 for pharmaceutical quality management

    Typical usage ratio

    • 0.5% – 2.5% of batch weight; ratio adjusted based on target dose strength and species-specific safety data

    Downstream process integration

    • Introduced as a primary or secondary metabolic precursor during controlled API synthesis steps, prior to formulation into injectable or oral forms

    Final product types

    • Veterinary injectable solutions and oral drench products for respiratory support in livestock
    • Medicated feed additives for poultry and ruminants (where authorized)
    • Pharmaceutical grade premixes for licensed veterinary medicinal products

    4. Plant Alkaloid Reference Material for Quality Control

    Quality assurance teams in plant-derived pharmaceutical and nutraceutical factories apply lobelanine as a certified reference standard for release testing of herbal extracts. Routine instrumental QC uses authenticated material to measure the presence and purity of active alkaloids in bulk botanical products. Accurate results depend on the certified content and homogeneity of supplied lobelanine, as documented in quality dossiers and traceability certificates provided to downstream compliance auditors.

    Industry compliance standards

    • European Pharmacopoeia monographs on herbal drugs and extracts
    • US Pharmacopeia (USP) General Chapters <561> Articles of Botanical Origin
    • ISO 17034 Reference Material Producers Accreditation
    • Good Manufacturing Practice (GMP) for botanical dietary supplements

    Typical usage ratio

    • Typically 1–10 ppm in HPLC or TLC assays, following method validation for specificity and accuracy; precise amount defined by analytical procedure for each plant matrix

    Downstream process integration

    • Prepared as a spiking solution or control sample for chromatographic quantification of lobeline family alkaloids during release and stability testing runs

    Final product types

    • Batch release certificates for bulk plant extracts and herbal APIs
    • Regulatory submission documentation for phytochemical-based pharmaceuticals
    • Lot-release protocols for manufacturers’ finished botanical preparations
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    Certification & Compliance
    More Introduction

    An Honest Discussion on Lobelanine: Our Approach to Quality and Application

    The Purpose Driving Our Lobelanine Production

    Years in manufacturing have shaped the choices we make in developing Lobelanine. This compound stands at the intersection of agricultural research, alkaloid chemistry, and a line of tradition stemming from the study of Lobelia species. We started production of Lobelanine because researchers and formulation professionals asked for consistency, purity, and traceability. In the world of specialized alkaloids, where demand comes from botanic researchers, crop scientists, and pharmaceutical development labs, the goal looks different than the mass production of commodity chemicals. Here, attention to subtlety guides our processes.

    Understanding the Model and Specifications

    Drawing on our experience, we approach Lobelanine with a commitment to integrity in composition. Our specific batch—identified as Model LBL-95—achieves a minimum purity of 98%, measured by HPLC and further confirmed with independent GC-MS analysis. We use a standardized crystalline form, which eliminates internal batch variations and supports those who require repeatable results, whether for reference standard use or for developing further derivatives.

    Physical characteristics matter to laboratory professionals and end-use chemists. Each lot maintains a stable melting point, 171-174°C, with clear spectral signatures that match published reference profiles. This degree of reliability stems from continuous in-line quality checks and post-synthesis elemental analysis, not by accident but from years spent refining methods first developed with input from industry researchers.

    Tracing Lobelanine’s Role Across Applications

    Our dialogue with users frequently centers around the demands of alkaloid research and phytochemical analysis. The main use we observe for Lobelanine lies in its role as a molecular scaffold—something scientists can manipulate, observe, or use as a comparator in plant system studies and pharmacological screens. Beyond reference uses, a number of pharmaceutical labs have integrated our Lobelanine into SAR (structure-activity relationship) mapping projects. Over the past decade, interest in Lobelia-derived alkaloids for receptor targeting and neurochemical investigations increased, fueled by early studies linking similar skeletons to bioactivity.

    Agricultural scientists sometimes tell us that Lobelanine plays a role in their examination of rare plant defense mechanisms. Our product then becomes part of the feedback loop between field discovery and laboratory confirmation. It is not uncommon to receive requests for supporting documentation and secondary confirmation of batch-to-batch consistency, since reproducibility defines research credibility. We answer those requests not as a formality, but because we see every test of our Lobelanine as a test of our entire manufacturing process.

    What Separates Our Lobelanine from Other Options?

    Many products arrive in the marketplace through a web of resale, bulk dilution, or import without transparency. Our belief in keeping supply chains short rests on experience. Being the manufacturer, not a punted link in a sales chain, gives us control over starting plant material, extraction conditions, and purification procedures. Sourcing raw Lobelia seeds and leaves from one region each season, as we do, provides us with the ability to predict and control subtle impurities in the final product. This minimizes unexpected interference in downstream assays.

    We have always documented our process steps, so that if a customer finds an outlier in biological activity, root cause investigation doesn’t stall at a dead end. Open access to underlying data—such as LC-MS fingerprints, certificate of analysis archives, and retained reference stocks from prior lots—builds repeat trust among technical users. Most commentary we hear comes not from flashy marketing, but from customers who ran side-by-side comparisons and found our batches delivered consistent behavior in bioassays, with few contaminants not already identified.

    Why Purity and Authenticity Matter in Alkaloid Manufacturing

    Contamination, whether by related alkaloids, residual solvents, or unknown tars, plagues much of the specialty chemical world. Our journey in manufacturing, and the feedback from long-term users, reinforces the truth: minute contaminants often go unseen until they skew bioactivity data or disrupt scale-up projects. Extra investment in stepwise purification and spectroscopic confirmation—an approach we adopted early—has paid off for us and for the research teams using our material. With highly active compounds, even low-level contaminants matter.

    From day one, identity and authenticity checks have driven our improvements. We have long maintained an in-house database that cross-references IR, NMR, and HPLC signatures with published and in-house reference spectra. This database guides our batch release process and backs every certificate issued with tangible, reviewable evidence. It’s not uncommon for a collaborator to request sample spectra for comparison; our response, shaped by years of experience, is always rapid and transparent.

    The Reality of Handling: Stability, Storage, and Practical Concerns

    Lobelanine, like most crystalline alkaloids, prefers dry, cool storage. We package under nitrogen flush in amber vials, minimizing photodegradation and moisture pickup. We field technical queries often about shelf life—and based on our retained sample monitoring, we know our product holds potency and spectral integrity for at least three years. Not all products elsewhere hold up to long-term storage; some degrade due to trace solvent residues or improper bottling. After a laboratory returned an unusable sample from another producer some years ago, we reviewed and tightened our own drying and packaging timelines.

    In terms of daily use, the crystalline form dissolves predictably in common polar solvents. Our own chemists monitor solubility and do in-house trial dissolutions in methanol and DMSO, feeding those numbers back to new users. Some feedback from larger screening labs revealed that off-brand Lobelanine sometimes shows inconsistent solubility, often due to oiling or micro-impurities. We keep those issues out of our material through secondary microcrystallization—a practice borrowed from our early work with other fine alkaloids.

    Supporting Responsible Development and Use

    Over the past decade, regulatory expectations changed for chemicals with potential biological activity. We spend time monitoring upcoming frameworks in major markets rather than guessing where compliance will land. By keeping our manufacturing documentation complete and our batch-level traceability intact, we aim to make regulatory compliance straightforward for downstream users. Additional support is always there for those who need documentation for project applications, grant support, or internal audits.

    Scientists today face scrutiny on both the sourcing and impact of their substances. Because our supply chain starts with field-harvested plant material, much of it grown under contract, we can trace every batch back to origin and provide evidence of responsible sourcing. Yearly audits of our collection teams ensure that we do not inadvertently bring in endangered or contaminated material. Feedback from environmental certification agencies helped us redesign retention and waste disposal protocols for alkaloid extraction residues, reducing risk and promoting sustainable operation.

    An Ongoing Partnership: Listening, Improving, and Adapting

    Our philosophy as a producer rests on the idea that every research group and professional application tells us something new about both challenge and opportunity. Working with Lobelanine throws unique questions our way. One agricultural lab pushed us to reduce minor iso-alkaloids in a batch below 0.3%. Feedback like that triggered us to further purify and revalidate separation steps. Following these insights led to better product not just for a single user, but across the board.

    We do not operate in a vacuum. Quarterly technical exchanges with university labs and feedback from analytical chemists feed into our ongoing improvement processes. After a major customer experienced trace solvent carryover from other suppliers, we invested in a new vacuum drying and in-line purification process that more than halved residual solvent content. Our record of improvements is public—anyone can ask for past specification sheets, and we provide a transparent trail showing what changed and why.

    Addressing Current Industry Challenges and Fostering Trust through Transparency

    The chemical industry faces growing scrutiny for accuracy, authenticity, and ethical sourcing. Adulteration, cost-cutting, and secondary sales often result in products that disappoint jobbing chemists or researchers. From the earliest days, we anchored our operation on direct relationships with both our plant sources and our technical users. Trust gets built when producers step forward honestly with strengths and admit limitations. We would rather forgo selling a batch than push something that misses the agreed standard or might compromise research outcomes.

    Occasionally, advisory boards and collaborative networks ask for demonstration of traceability, internal environmental auditing, or proof-of-origin on reference material. Rather than seeing this as a burden, we view each request as a chance to confirm and extend trust. Our technical staff view honest discussion and demonstrated improvements as fundamental—not a point of differentiation, but a baseline.

    Lobelanine: A Story from Start to Finish

    Production begins with the annual contracting of field-grown Lobelia. We participate in on-site inspections throughout the growing season, tracking crop health and recording harvest logs. After years in this role, we know work doesn’t end when leaves are picked; the real challenge emerges during isolation and purification. Alkaloid extraction remains a balancing act—one where too much haste or shortcutting produces inconsistent material. Our method, developed in response to early setbacks and user criticism, leverages multi-stage purification and rigorous intermediate checks. This process results in a crystalline batch that reflects, both chemically and visually, a standard that speaks for itself.

    We understand that in research and manufacturing, the margin between success and setback often lies with material reliability. The feedback we receive whenever a project hits its target, or when data reproducibility remains high across different lots, provides encouragement for further improvement. These conversations with the research community have shaped the evolution of our process and the refining of our Lobelanine product.

    Setting Standards: The Value of Real-World Data and Independent Validation

    Our approach to product validation draws from decades of labside trial and error. Internal batch data gets submitted to select external labs for third-party confirmation. These collaborations bring out both strengths and weaknesses in our process. We routinely share anonymized comparative data with research groups willing to provide feedback, which in return reveals small, sometimes invisible, performance differences. Achieving higher than 98% purity isn’t enough; users look for the absence of byproducts and mechanical consistency, and we track those benchmarks as closely as we do primary purity.

    By holding our materials up to peer review and open data sharing, we continuously elevate our process and maintain confidence in our Lobelanine. In addition to chemical purity and spectral identity, we claim transparency on residual solvents, trace metals, and micro-contaminant levels. Each batch’s analytical documentation remains available on request, so no part of the chemical’s journey remains hidden or uncertain.

    Learning Through Issues and Responding to the Unpredictable

    No production run escapes the occasional problem. One memorable batch a few years ago failed to meet purity targets due to off-season plant stress. Instead of cutting corners, we cancelled shipment, reran the process, and offered full details to researchers with pending orders. This policy costs us at times, but it prevents greater losses downstream—lost research hours or failed project timelines can cause more harm than a financial setback.

    Several long-term partners offered suggestions that drove corrective action in-house. One instance involved detection of a hard-to-find impurity via advanced LC-MS. Their insight led us to adjust an intermediate wash, which afterwards eliminated the recurrence. Those kinds of collaborations, built on openness and mutual problem-solving, help drive forward the quality of not just our products but of research output everywhere Lobelanine finds a home.

    Practical Aspects: Packaging, Quantities, and Thoughtful Delivery

    We prepare each order of Lobelanine in fixed gram-quantity vials, rather than shipping in bulk, to maintain stability and integrity. Labels record lot number, test data, and expiration date, based on specific batch studies rather than theoretical estimates. Unlike bulk traders who re-bottle or blend, we do not break bulk without staged re-testing, since product that changes hands too often picks up contamination risk.

    Early on, some users asked for larger or custom quantities. Our direct manufacture model allows us to accommodate reasonable custom requests, provided we preserve product identity and minimize handling. Shipping schedules align with third-party cold-chain services outside temperate regions, maintaining storage conditions from door to door. Transparent packing slips feature batch and test data to aid immediate intake at receiving labs.

    The Differences: Beyond Standard Descriptions

    Lobelanine’s catalog presence can mislead—products with similar claims may hide differences in origin, processing, or even lawful status. As we have observed, material sold through third-party traders often lacks true batch-level transparency. Users who require authenticated research materials recount past issues with low-grade imports or poorly traced powder. Our own records, matched against repeated user feedback, show advantages less in price but more in confidence—users know what they order, year after year.

    Some competitors chase lower extraction costs by using cheap solvents or bypassing stepwise intermediate purification. The tradeoff? Their material sometimes appears visually similar while carrying more residual tars, unidentified side-products, or even hazardous byproducts. Our separation approach, developed over time, relies on ongoing feedback loops and multiple checks at each processing stage.

    The Road Ahead for Lobelanine Manufacturing

    The future holds new challenges—ever-tighter standards, more rigorous documentation, and a changing scientific landscape. Feedback loops will remain central to the way we work. With every batch, every inquiry, and every challenge resolved, we learn more and apply those lessons to both the product and the process.

    Through decades of direct involvement, we have come to know the material not only as a chemical compound, but as the hinge between raw plant biology and precision-targeted research. Lobelanine’s place in our manufacturing journey reflects wider trends toward transparency, quality, and collaboration. Step by measured step, we encourage users to ask questions, share feedback, and hold us accountable.

    As training, tools, and research questions evolve, so do our methods of serving the scientific and industrial community. Whether your project studies plant metabolism, tests pharmaceutical hypotheses, or benchmarks against known reference models, you deserve clarity, reliability, and honest partnership. Our Lobelanine reflects our commitment to those principles across every order, every lot, and every future improvement.