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Harmaline Hydrochloride Dihydrate

    • Product Name Harmaline Hydrochloride Dihydrate
    • Alias harmaline-hydrochloride-dihydrate
    • Einecs 252-385-9
    • 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

    942896

    Chemical Name Harmaline Hydrochloride Dihydrate
    Molecular Formula C13H15ClN2O3
    Molecular Weight 282.73 g/mol
    Cas Number 304-21-2
    Appearance White to off-white crystalline powder
    Solubility Soluble in water
    Melting Point Around 281-285°C (decomposition)
    Storage Conditions Store at 2-8°C, protect from light and moisture
    Purity Typically ≥98%
    Synonyms Harmaline hydrochloride, Harmalol hydrochloride dihydrate
    Iupac Name 4,9-dihydro-7-methoxy-1-methyl-3H-pyrido[3,4-b]indole hydrochloride dihydrate
    Ph 1 Solution Approximately 4-6

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

    Packing & Storage
    Packing Amber glass bottle labeled "Harmaline Hydrochloride Dihydrate, 10 grams," with hazard symbols, lot number, and tightly sealed cap for safety.
    Shipping Harmaline Hydrochloride Dihydrate must be shipped in tightly sealed containers, protected from light and moisture. It is typically packaged in certified, leak-proof materials and transported as a non-hazardous substance, following local, national, and international regulations. Appropriate labeling and documentation ensure safe and compliant delivery to laboratories or approved destinations.
    Storage Harmaline Hydrochloride Dihydrate should be stored tightly sealed in a cool, dry, and well-ventilated area away from incompatible substances like strong oxidizers. Protect from light and moisture to maintain stability. Store at room temperature (15-25°C), ensuring the container is clearly labeled. Use appropriate chemical storage cabinets and follow all safety regulations for hazardous substances.
    Application of Harmaline Hydrochloride Dihydrate

    Applications of Harmaline Hydrochloride Dihydrate in Industrial Manufacturing

    As the original manufacturer of Harmaline Hydrochloride Dihydrate, we deliver this specialized raw material for select established industrial and research uses. Our expertise ensures every batch meets demanding compliance and integration requirements across select chemical, pharmaceutical, and analytical applications. The following industrial scenarios demonstrate proven downstream processing, compliance systems, and typical usage practices.

    1. Alkaloid Reference Standards in Analytical Laboratories

    Commercial and governmental laboratories frequently require authentic natural alkaloid reference materials with documented purity and identity. Harmaline Hydrochloride Dihydrate is utilized for calibration and validation in quantitative and qualitative HPLC and mass spectrometry procedures within toxicology, forensic, and phytochemical labs. Stringent characterization makes this material a preferred standard for laboratory quality control workflows, trace impurity analysis, and regulatory determinations of herbal products and beverages containing β-carbolines.

    Industry compliance standards

    • ISO/IEC 17025 laboratory accreditation
    • USP Reference Standards qualification protocols
    • FDA 21 CFR Part 11 (electronic records, electronic signatures)
    • ICH Q2(R1) Validation of Analytical Procedures

    Typical usage ratio

    • Preparation of 10–100 µg/mL stock solutions for analytical calibration; must match instrument detection requirements and reference method guidelines

    Downstream process integration

    • Dissolution and dilution into analytical solvent systems during method validation or routine QA/QC sample runs
    • Direct integration into multi-point calibration curves for quantification of β-carbolines
    • Spiking of control samples for recovery and precision assessment

    Final product types

    • Certified laboratory reference standards
    • Analytical test kits for β-carboline quantitation
    • Documented quality control reports in commercial and regulatory testing

    2. Intermediate for β-Carboline Derivative Pharmaceutical Synthesis

    API manufacturers use Harmaline Hydrochloride Dihydrate as a semi-synthetic precursor for β-carboline derivative compounds, targeting various CNS investigative therapies. Controlled functionalization, methylation, or demethylation routes rely on its established structure and salt form, integrating fully into validated API synthesis flows under regulated manufacturing conditions. Pharmaceutical-grade purification, trace control, and batch consistency support downstream efficacy and regulatory approval efforts in advanced API production scenarios.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU GMP Part II for API manufacturing
    • US FDA DMF (Drug Master File) requirements
    • Relevant pharmacopeial monographs (USP, Ph. Eur.) for starting materials

    Typical usage ratio

    • 0.7–1.2 molar equivalents relative to target β-carboline synthesis output, adjusted based on conversion efficiency and downstream chemical step requirements

    Downstream process integration

    • Enters as the primary alkaloid substrate in controlled semi-synthetic transformations
    • Subjected to catalytic methylation or demethylation in anhydrous or aqueous media, followed by intermediate isolation
    • Integrated into multi-step batch or continuous synthesis for CNS investigative API production

    Final product types

    • Semi-synthetic pharmaceutical-grade β-carboline derivatives (e.g., harmalol, harman)
    • API intermediates for clinical trial synthesis
    • Research-grade and pilot-scale CNS drug substances

    3. Plant Extract Standardization in Herbal Dietary Supplement Manufacturing

    Producers of herbal dietary supplements containing Peganum harmala (Syrian Rue) and related species employ Harmaline Hydrochloride Dihydrate as a quantitative marker to standardize extract profiles. Accurate spiking and reference enable precise adjustment and verification of alkaloid levels, critical for quality control and labeling compliance, particularly within EU and North American regulatory frameworks governing herbal alkaloid content in dietary supplements. QC teams utilize this material in validated HPLC and GC runs throughout the blending and encapsulation process.

    Industry compliance standards

    • EU Regulation (EC) No 1925/2006 on the addition of vitamins, minerals and certain other substances to foods
    • US FDA 21 CFR Part 111 (Current Good Manufacturing Practice in Manufacturing, Packaging, Labeling, or Holding Operations for Dietary Supplements)
    • ISO 22000:2018 Food Safety Management Systems
    • AOAC Official Methods for botanical ingredient analysis

    Typical usage ratio

    • 0.005–0.02% w/w relative to total plant extract mass, based on target alkaloid profile specifications and confirmation batch testing

    Downstream process integration

    • Added as a reference during extract blending, prior to batch homogenization and granulation
    • Utilized as an internal standard for QC validation at multiple manufacturing checkpoints
    • Enables specification adjustment during encapsulation and finished product testing

    Final product types

    • Standardized herbal capsules/tablets with declared β-carboline content
    • Quality-controlled liquid tinctures
    • Batch-certified bulk plant extracts for global supplement supply

    4. Neurochemical Research Tools for Life Science Institutions

    Life science R&D groups at universities and research centers utilize Harmaline Hydrochloride Dihydrate in both in vitro and in vivo neurobehavioral studies. Its well-documented effect as a monoamine oxidase A inhibitor allows investigators to explore serotonin metabolism, neurotransmitter dynamics, and toxicological endpoints in mammalian models. Researchers rely on tightly controlled formulation and documented traceability for dose-response experiments, mechanistic biochemistry, and neurological toxicology assessment.

    Industry compliance standards

    • NIH OLAW PHS Policy (Public Health Service Policy on Humane Care and Use of Laboratory Animals)
    • EU Directive 2010/63/EU (protection of animals used for scientific purposes)
    • Institutional Animal Care and Use Committee (IACUC) protocols
    • GLP (Good Laboratory Practice, OECD)

    Typical usage ratio

    • Ranges from 2–15 mg/kg body weight for in vivo rodent studies; 1–100 µM concentration in cell culture in vitro, dictated by research protocol endpoints and species/model sensitivity

    Downstream process integration

    • Dissolution into sterile saline or appropriate vehicle for animal administration
    • Incorporated into culture media for biochemical assays
    • Applied as a reference compound or challenge agent in in vitro receptor binding, enzyme inhibition, or transporter function studies

    Final product types

    • Dose-formulated research solutions for neurochemical assays
    • Validated animal model testing protocols
    • Peer-reviewed publications featuring controlled β-carboline exposure models
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    Certification & Compliance
    More Introduction

    Understanding Harmaline Hydrochloride Dihydrate: Manufacturer’s Perspective

    The Foundation of Quality: Materials and Methods Matter

    Producing Harmaline Hydrochloride Dihydrate is not just a technical process—it reflects decades of questions, challenges, and adjustments. This compound, with the chemical structure C13H15ClN2O2•2H2O, often takes center stage during our production week. Unlike plant extracts that come with batch variability, Harmaline Hydrochloride Dihydrate in our hands emerges from a controlled synthetic route. Each time, the same yellowish crystalline powder leaves the final stage, reflecting laboratory conditions monitored at every checkpoint.

    Stability issues always come up in early stage projects. Customers working in pharmacological research want to know why our dihydrate form remains so consistent hydrating over time, and the answer lies in the way we manage molar ratios and crystallization. This isn’t about just throwing chemicals into a flask. Teams work with temperature and humidity control, especially during recrystallization, where water content can make or break usability for those in analytical chemistry or in the synthesis of reference standards.

    Model and Specifications: Beyond the Numbers

    People often ask about “models” or “grades” as if quality snaps cleanly into Standard or Superior. That isn’t how this business works. Our Harmaline Hydrochloride Dihydrate typically falls into research and pharmaceutical grade, most batches landing with an assay of greater than 98.5% by HPLC, residual solvents far below the levels required by current compendia, and moisture verified by automated Karl Fischer titration. Melting point range tells a story too; you cannot ignore it during QC. Impurity profiles get attention since the primarily anticipated impurity—harmalol—crops up if the oxidation step gets rushed. This approach to specifications comes from our own headaches troubleshooting customer issues a decade back.

    No two customers come to us with the same tolerances. We’ve worked with buyers who want detailed polymorph data and others content with a single certificate of analysis. We bake our experience with process analytics directly into our quality assurance process, not just to meet an abstract requirement, but because we have dealt with unhappy calls about unstable batches in summer heat or delayed analysis because of failed purity checks.

    Usage: Why Laboratories and Researchers Turn to Harmaline Hydrochloride Dihydrate

    Chemists continue to demand Harmaline derivatives in neuropharmacology and alkaloid studies. Common uses include MAO inhibitor research, as Harmaline displays both selective and non-selective inhibition. Standardization allows researchers to produce consistent results. Labs appreciate that our Harmaline Hydrochloride Dihydrate dissolves easily in both water and polar organic solvents, helping them prepare analytical standards or primary solutions quickly.

    A lot of our orders come from university groups working on CNS-active compounds, both for in vitro enzyme inhibition assays and small animal testing protocols. The fact that our dihydrate form resists clumping under standard storage helps avoid lot-to-lot variability in dose preparation. There’s an ongoing need for analytical labs to test biological specimens for harmala alkaloids—particularly in forensic settings—making reliable standards crucial.

    Preparation of reference materials for forensic toxicology depends on sourcing a dihydrate with tightly controlled water content. The value of low residual solvent and stable hydrate form cannot be overstated—years ago, we fielded complaints from partners whose samples lost mass or changed color after months in storage, usually when sourcing from less careful suppliers. These are not minor inconveniences in regulated environments.

    The Difference: Why Not Just Buy Any Harmaline?

    A big question for scientists: why bother with the hydrochloride dihydrate? The free base exists, so does a simple hydrochloride. For those not steeped in synthetic chemistry, the dihydrate form appears to add unnecessary complexity.

    Direct experience tells us why this difference matters. The free base form oxidizes and darkens more quickly, especially when left out in humid air. By choosing the hydrochloride dihydrate, users sidestep many storage headaches and can expect much longer shelf lives under similar conditions. Batch after batch, the dihydrate form maintains a crystalline structure that safeguards against sudden clumping or caking—unlike the free base, which can take on atmospheric moisture and degrade before you notice.

    The difference between the hydrochloride anhydrate and dihydrate isn’t just water weight. The dihydrate form yields more consistent solubility and filtration properties. In our plant, we have adopted crystallization protocols that encourage robust formation of dihydrate. Years ago, we compared long-term samples side-by-side. Anhydrous samples tended to clump and darken, developing what our chemists called “stickiness” that made sample prep much harder for customers. The dihydrate simply performs in a way that suits labs requiring reliability and repeatability.

    Those differences trace back to real-world lab challenges. Analytical teams don’t want to recalibrate balances or dry samples overnight just because material flows differently. By keeping water content steady, we remove variables before our product even leaves the factory. Our process evolved after repeated rounds of customer feedback, with requests for more reliable storage and less time spent prepping samples. Each feedback loop changed the way we run quality checks and packaging.

    Manufacturing Insights: Crafting Stability and Purity

    Synthesizing Harmaline Hydrochloride Dihydrate at scale comes with its own set of demands. We source starting alkaloids in bulk, and since purity varies from different origins, all incoming material undergoes full screening for trace contaminants—lead, arsenic, and cadmium get special attention due to their prominence in botanically derived materials. We built our batch process around solvent systems that strip away unwanted plant byproducts and residual biomass, steps that smaller shops might skip.

    Critical quality attributes—from particle size to light absorption—are tracked throughout production. The dihydrate crystallization step turns up pain points, especially if environmental controls fluctuate. Overshooting humidity or letting the temperature dip too low sometimes leads to incomplete crystallization, trapping solvent or encouraging off-forms. Workers know what happens if a batch dries out too quickly: the material takes on a dusty quality and doesn’t pass muster during lab verification.

    Every container gets a tamper-evident seal, and we use moisture-barrier packaging for all shipments. That decision came after we fielded multiple requests from customers working in warm climates who noticed that other suppliers’ material lost mass during transit. We determined that robust barrier packaging makes a measurable difference when storing the dihydrate at room temperature for months at a time.

    Practical Concerns in Distribution and Storage

    We ship Harmaline Hydrochloride Dihydrate worldwide. From our viewpoint as producers, maintaining quality during long shipments is as important as the synthesis itself. Review of returned goods taught us that not all transportation systems give priority to environment controls. Placing silica gel packets inside every jar and using foil bags prevents shifts in the water content that can impact research accuracy. This isn’t about over-engineering; it’s an answer to genuine problems encountered over decades in the field.

    Customers in dry or hot climates need to know their product won’t degrade ahead of use. We routinely advise storage below 25°C in tightly sealed containers. Past experience with air-exposed jars taught us small details go a long way, such as minimizing headspace and checking closures before shipping.

    Challenges From Research to Application

    Early requests for Harmaline Hydrochloride Dihydrate often came from academic collaborators working on pharmacological profiling. Over the years, new applications entered our radar—bioassays involving MAO-A, use as a pharmacological tool in neurotransmitter modulation, and preparation of reference standards for forensics. Each new project added another layer of requirements: one month, it’s high-volume chromatography calibration; next time, it’s batch-to-batch purity reports for an oncology trial.

    Handling forums and direct calls, we’ve heard the same question countless times: how can we guarantee the product will work in their unique setup? Modern labs require traceable, reliable materials. Five years ago, a surge of counterfeit and subpar alkaloids entered the market, and we received panicked inquiries regarding product identity and heavy metals. Those conversations shaped our certification and documentation process. We invested in third-party analyses not because of outside pressure, but because researchers rely on objective, reproducible information.

    Another major concern in the research field involves regulatory expectations. Laboratories working in regulated environments—particularly in the European Union and North America—must keep documentation of sourcing, purity, and batch traceability. Our long-term production scheduling now includes built-in documentation routines, saving clients significant trouble during annual audits.

    Comparing Harmaline Hydrochloride Dihydrate With Other Analogs

    Researchers sometimes wonder why not opt for Harmalol, Harmine, or simple Harmaline hydrochloride without extra hydration. From our perspective, the difference depends upon the intended application. Harmaline Hydrochloride Dihydrate displays specific stability and solubility profiles, allowing for clean dissolution—a key requirement in preparing research solutions for cell culture media or buffer systems. Users working with free base Harmaline, for example, regularly report rapid color changes and crystallization problems as soon as the compound hits solution. The dihydrate overcomes most of those concerns.

    Harmine, another common option in the harmala alkaloid family, features a methyl group that changes both the biological and physical profile. The hydrochloride salt of harmine offers differences in activity and a narrower viability in certain analytical systems. We have shipped various harmala alkaloids side-by-side, and customer feedback consistently tells us the dihydrate form of harmaline wins out during storage, reconstitution for HPLC, and ease of handling—no excessive static or messy spills.

    From the perspective of a manufacturer, the reasons behind choosing Harmaline Hydrochloride Dihydrate arise from the sum of experience, demand, and direct trial. Lower-grade harmala alkaloids too often contain secondary plant alkaloids, leading to cross-reactivity in sensitive analytical assays. We built routines around stripping away those contaminants.

    Each analog presents its own advantages, but as we see in repeat orders and customer reports, the balance struck by Harmaline Hydrochloride Dihydrate between long-term stability and processing ease continues to make it a favorite.

    Experiences and Solutions in Working With Clients

    Through decades of running a chemical manufacturing operation, we have found that product reliability is the single most cited demand from our long-term clients. Several years ago, we took a close look at support tickets and saw a clear pattern: the biggest issues stemmed from improper storage and handling. We revised our packaging protocols, invested in better training for our warehouse team, and supplied customers with straightforward guidance on keeping their Harmaline Hydrochloride Dihydrate samples active and stable.

    Maintaining low moisture ingress became essential. We introduced dual-seal systems and tamp-resistant containers, moving away from generic packaging. Every time a client reported inconsistent results, our investigation traced back to environmental lapses, not production chemistry. By collaborating directly with analytical labs and research teams, we adjusted our logistics setups to avoid weekend layovers, exposure to high humidity, or excessive transit times. These seem like minor changes, but the overall impact is measurable.

    We continually revise our analytical certificates and batch reports based on conversations with the people using our materials. Assays reflect real-world needs, and the supporting data allows seamless integration into laboratory workflows. Our phone lines remain open for direct support, and our technical staff regularly interfaces with partner labs to troubleshoot issues as they arise. Real-time problem-solving has become embedded in our operational structure.

    Continuous Development Through Experience

    Our ongoing R&D projects feed directly into better Harmaline Hydrochloride Dihydrate. Each synthesis run provides another dataset for our process analytics team, and ongoing relationship with university collaborators exposes new needs for purity, solubility, and stability. We watch regulatory guidelines for emerging safety and documentation standards. Every audit yields tweaks to our internal SOPs, ensuring materials continue to meet the expectations of next-generation researchers, not just legacy users.

    We never treat Harmaline Hydrochloride Dihydrate as a static product line. Racing for the cheapest price rarely benefits anyone involved—especially in a market where low-cost versions mean higher impurity loads and little care for consistency. Our goals have always revolved around upholding strong client relationships built on reliability and technical transparency. Every technical support request becomes an opportunity to adapt our products for real-world research, not just artificial metrics.

    Harmaline Hydrochloride Dihydrate remains at the crossroads of advanced synthetic chemistry and practical laboratory demands—a position refined not by marketing, but by conversations, feedback, and technical lessons learned through years of chemical manufacturing.