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Nicotine Hydrochloride

    • Product Name Nicotine Hydrochloride
    • Alias Nicotine hydrochloride
    • Einecs 214-131-9
    • 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

    781064

    Productname Nicotine Hydrochloride
    Chemicalformula C10H15N2·HCl
    Molecularweight 198.70 g/mol
    Casnumber 219-737-0
    Appearance White to pale yellow crystalline powder
    Solubility Highly soluble in water
    Meltingpoint 234-247°C
    Boilingpoint Decomposes
    Ph 4.5–7.0 (1% solution in water)
    Odor Characteristic, tobacco-like
    Storageconditions Store in a tightly closed container, protected from light and moisture
    Purity Typically >98%
    Synonyms Nicotine monohydrochloride
    Stability Stable under recommended storage conditions
    Usage Pharmaceuticals, research, and manufacturing

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

    Packing & Storage
    Packing Nicotine Hydrochloride, 100g, securely packaged in an amber glass bottle with tamper-evident seal and clear hazard labeling.
    Shipping Nicotine Hydrochloride should be shipped in tightly sealed, appropriately labeled containers, following all applicable hazardous material transport regulations. Use secondary containment, keep away from heat and incompatible substances, and ensure secure, upright placement. Only trained personnel should handle shipping, and relevant safety documentation (SDS) must accompany each shipment.
    Storage Nicotine hydrochloride should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible substances such as oxidizing agents. Keep the storage area secure and clearly labeled. Store at room temperature, avoiding excessive heat and moisture. Ensure access is restricted to trained personnel, and follow all relevant safety and regulatory guidelines for hazardous chemicals.
    Application of Nicotine Hydrochloride

    Applications of Nicotine Hydrochloride in Industrial Manufacturing

    Nicotine Hydrochloride serves as a high-purity active ingredient in specialized industrial sectors. As a direct manufacturer, we provide consistent specification control and batch documentation to support demanding downstream applications. The following sections outline primary industry scenarios in which Nicotine Hydrochloride is integrated at a formulation and process level by manufacturers operating under strict compliance requirements.

    1. Pharmaceutical Nicotine Replacement Therapies (NRT)

    Pharmaceutical companies use Nicotine Hydrochloride as the reference standard in oral and transdermal nicotine replacement therapies, including prescription lozenges, gums, and patches. Product quality, validated sourcing, and regulatory traceability remain key, with process integration beginning at the initial dose formulation and maintained throughout blending and finished dosage form manufacturing. The addition rate directly affects therapeutic release and regulatory approval, requiring rigorous adjustment during pilot and commercial production stages.

    Industry compliance standards

    • United States Pharmacopeia (USP)
    • European Pharmacopoeia (Ph. Eur.)
    • Good Manufacturing Practices (GMP – ICH Q7)
    • FDA 21 CFR 210/211 for Finished Pharmaceuticals

    Typical usage ratio

    • Active loading: 1–4% w/w in finished oral formulations, adjusted for product form and dose (e.g., 2 mg or 4 mg per lozenge/gum unit, 7–21 mg per patch)

    Downstream process integration

    • Batch-blended during the initial mix of actives and excipients
    • Metered addition in granulation for lozenges and gum base compounding
    • Solution-phase addition for transdermal matrix or reservoir systems before casting and curing

    Final product types

    • Nicotine lozenges (2 mg, 4 mg)
    • Nicotine chewing gum (standardized dose)
    • Transdermal nicotine patches
    • Oral dissolving films containing controlled nicotine content

    2. Inhalation and Aerosol Device Cartridges for Smoking Cessation

    Manufacturers producing closed system refill cartridges and inhalation sticks for medically supervised smoking cessation depend on pharmaceutical grade Nicotine Hydrochloride. Stringent impurity controls and batch traceability guarantee compliance at every step from solution compounding to cartridge filling. Accurate dosage is achieved through tight process control in blending and device loading, addressing the challenges associated with uniform delivery via pulmonary or buccal absorption devices.

    Industry compliance standards

    • European Medicines Agency (EMA) guidelines on inhaled pharmaceutical products
    • USP General Chapter <601> Aerosols, Sprays, and Inhalants
    • ISO 13485:2016 for Medical Device Quality Management
    • Toxicological impurity screening as regulated in ICH M7

    Typical usage ratio

    • Formulated at 0.5–3.0% w/v in cartridge solutions; specific dosing is set to deliver 0.5–2 mg per inhalation event and is optimized for device capacity and vapor generation method

    Downstream process integration

    • Dissolved into vehicle matrix in controlled mixing systems
    • Filtered and sterile-filled into inhaler cartridges or pods under GMP cleanroom conditions
    • Device calibration and QC release aligned with finished fill content testing

    Final product types

    • Prescription and OTC medical inhalers for nicotine replacement
    • Nicotine aerosol cartridges for closed system vapor inhalation
    • Metered dose oral inhaler sticks

    3. Veterinary Insecticide and Ectoparasiticide Formulations

    In animal health, Nicotine Hydrochloride is a reference standard and active agent in certain regulated veterinary insecticides targeting lice and mite infestations in livestock. Strict adherence to animal safety and residue controls define the formulation process, with the material incorporated during pre-mix or concentrate blending stages. Processing adapts to species-specific regulations on maximum residue and withdrawal times, with product forms ranging from liquid pour-on to dusting powders.

    Industry compliance standards

    • Veterinary International Cooperation on Harmonisation (VICH) guidelines
    • OECD Guidelines for Testing of Chemicals – Ectoparasiticide Residue Studies
    • EC 37/2010 on Maximum Residue Limits for Pharmacologically Active Substances
    • Council Directive 2001/82/EC relating to veterinary medicinal products

    Typical usage ratio

    • Incorporation rate: 0.05–0.15% w/w in pour-on or spray formulations; adjusted based on animal species, efficacy studies, and national veterinary guidelines

    Downstream process integration

    • Premixed with solvent or carrier in temperature-controlled tanks
    • Homogenization and controlled cooling to optimize actives distribution
    • Micro-quantification and stability assessment prior to packaging

    Final product types

    • Livestock pour-on solutions
    • Veterinary dusting powders for external parasite control
    • Animal dip concentrate for poultry and ruminants

    4. Analytical Reference Standards for Laboratory Calibrations

    Accredited testing laboratories and quality control departments use high-purity Nicotine Hydrochloride as a calibration and control standard in validated analytical methods, such as HPLC or GC-MS, to quantify nicotine content or residue in pharmaceuticals and consumer products. Sourcing requires tight certification, full characterization (NMR, MS), and certificate of analysis traceability to primary reference standards. Exact solution preparation and analytical workflow integration remain critical to minimize cross-contamination and establish assay reliability in batch release and forensic contexts.

    Industry compliance standards

    • ISO/IEC 17025:2017 General Requirements for Testing and Calibration Laboratories
    • USP Reference Standard Certification
    • FDA Guidance for Industry – Analytical Procedures and Methods Validation
    • ICH Q2(R1): Validation of Analytical Procedures

    Typical usage ratio

    • Used to prepare calibration standards: 1–10 μg/mL in aqueous or organic solvents, exact range set by the validated method and instrument type

    Downstream process integration

    • Dissolution and serial dilution to target concentration
    • Spiking of assay samples or preparation of chemical control lots
    • Instrument performance verification prior to analytical runs

    Final product types

    • Certified reference solutions for HPLC/GC-MS calibration
    • Internal laboratory controls for nicotine content release testing
    • Proficiency testing standards for pharmaceutical and environmental laboratories
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    Certification & Compliance
    More Introduction

    Nicotine Hydrochloride: From Precision Manufacturing to Responsible Application

    Standing at the center of chemical innovation means living with responsibility. Nicotine hydrochloride, often pinpointed for its highly specialized applications, remains one of the more nuanced products in our portfolio. The focus for us as a manufacturer is less about its headline role in high-volume agriculture or nicotine product manufacture and more about the value of purity, consistency, and traceability for scientists and developers. Each lot that leaves our facility enters research environments, precision synthesis projects, or analytical settings where margin for error narrows to almost zero.

    Product Identity and Our Direct Knowledge

    Nicotine hydrochloride, molecular formula C10H14N2·HCl, emerges from careful synthesis, not as a byproduct but by deliberate reaction and highly controlled extraction. In our own lines, we prioritize a fine, crystalline powder free of odor and visual impurities. End-users reference our model classifications closely: not only for concentration, which regularly runs to 99% or higher, but also for clarity on hydration state, pH profile, and freedom from secondary alkaloids. This changes the conversation from commodity purchasing to solutions built for exacting standards.

    By keeping active oversight over precursor selection and reaction conditions, we see firsthand the pitfalls of even minor deviations. Minor impurities in the precursor funnel through every downstream step. Our continuous batch analytics make a difference—on-site chromatography and mass spectrometry do not just verify a number on a document; they shape revisions in real time. Purity above 99%, often reaching pharmaceutical quality, is not a marketing concept here. It’s the result of unwavering process discipline and years of incremental improvement.

    Specifications — More Than Purity

    We have manufactured nicotine hydrochloride to a spectrum of specifications over the years. Most commonly, users request material that runs 99.5% pure or higher, forming an almost-white crystalline powder with a defined melting range. Moisture content matters in sensitive synthetic chemistry—too much, and reactions derail. Customers working on complex chiral syntheses use our lowest-moisture lots to reduce unwanted byproducts. Research requests often demand full impurity profiles, including detection of nornicotine, anabasine, anatabine, and trace metals.

    Weight and volume measurements form only the foundation; we add value through our ability to manufacture lots with pre-determined particle distributions. Certain analytical applications require carefully milled particles, achieved by using multistage grinders and exhaustive sieving. Product entering the food or pharmaceutical stream must also withstand additional scrutiny—here, our in-house quality control chemists run targeted pesticide residue and solvent screens unique to these fields. The standards keep evolving, and our facility adapts each time, often well ahead of regulatory shifts.

    Direct Experience: The Process and the Challenges

    Transforming extracted nicotine into a hydrochloride salt takes more than following a formula. Our team starts with plant-sourced, high-purity nicotine—solvent washes, phase separations, and repeated filtrations remove chlorophyll, plant fats, and tars. Even before hydrogen chloride exposure, the precursor faces extended GC-MS analysis on the plant lot itself.

    Converting to nicotine hydrochloride involves targeted acidification. Poor control here produces off-white, sticky masses or aggressive odor—a sign of incomplete conversion or mixed salt forms. We run temperature and pH monitoring at every significant step. This matters: research institutions rely on us because we demonstrate every single lot with full certificate of analysis, including batch chromatography and full MS spectrum. Our familiarity with what goes wrong at scale lets us troubleshoot with customers far beyond the basic “purity and grade” bullet points.

    We recall a year where even minor variation in ambient humidity in our facility changed not just yields, but solubility profiles, crystallization time, and bulk transport behavior. That episode shaped SOP revisions in our drying and final packaging areas. Customers engaged in solid oral dose manufacture rely on these subtleties—what looks like a minor shift during crystallization ends up affecting tableting, homogeneity, and storage stability over months.

    Safety, Handling, and Environmental Stewardship

    Nicotine hydrochloride, like all nicotine salts, commands respect in any setting. Most outside the direct chemistry field hear “nicotine” and bring strong preconceptions. Our team approaches its manufacture with protocols anchored in hazard awareness, ventilation, containment, and operator training. Direct skin contact, inhalation, and accidental ingestion get equal attention. Facilities build out dedicated glovebox workstations, maintain eye washes and shower stations, and run routine drills for spill and exposure management.

    Key customers consult with us not only on product specifics, but on design of their own handling spaces. We advise on compatible plastics and glass quality; we notice, for instance, contamination from plasticizers in low-grade transfer equipment. Training focuses on accuracy, mix-up prevention, and fail-safes in packing and storage. Our environmental controls never fall behind either—effluent and fume treatment follow best-in-class industry benchmarks, not the loose minimum.

    Where Nicotine Hydrochloride Stands Apart

    Nicotine hydrochloride often confuses non-specialists because of its proximity to other nicotine products: nicotine sulfate, plain nicotine (freebase), and newer synthetic salts. Clients in analytical chemistry and pharmaceutical development look specifically for the hydrochloride salt form, seeking its unique stability, predictability in aqueous media, and consistent ionization for titration or HPLC studies. Freebase nicotine oxidizes and degrades quickly; it suits applications where volatility is desired, but not for fine research. Sulfate salts dissolve differently, often complicating reproducibility and pH control in complex buffers.

    Over the years, requests for hydrochloride have grown from simple demand for a “more stable salt” to nuanced, application-specific conversations. A lab working on receptor binding assays needs the tightest profile on secondary alkaloids and wants assurance on batch-to-batch consistency. A customer in advanced inhalation device research insists on low-level solvent testing because device performance can shift with even trace acetone or ethanol. As manufacturers, we listen, adapt, and invest in the infrastructure that delivers reliability on these points.

    Research, Regulation, and Market Pressures

    Regulatory environments shift quickly, particularly in the areas of nicotine chemistry, pharmaceutical excipient standards, and food ingredient safety. We navigate this with deliberate transparency. Our documentation runs deep and always includes original lot data, production date, chain-of-custody logs, and repeated in-house verification—this comes from direct experience fielding regulatory requests in multiple countries. Documentation is not an afterthought—too many users assume that “high purity” equals compliance, but inspectors care very much about provenance, testing authority, and reproducibility.

    Policy changes—like tighter rules on nitrosamine content and labeling—never sneak up on us. Our analytical teams stay in constant contact with regional agencies, and we invest early in new detection systems or protocols where signals emerge. Rather than reacting to new limits, we build our targets ahead of implementation, running lots below the maximum allowed content before outside forces require it.

    For the R&D sector, the trend toward alternative nicotine delivery (like aerosolization and implantable matrices) increases demand for highly controlled material, where even rare impurities can shift pharmacokinetic outcomes in early-stage studies. From a manufacturer’s perspective, we engage directly with researchers, not as anonymous suppliers, but as dedicated partners troubleshooting method challenges together.

    Sustainability and Supply Chain Realities

    The ethical conversation around nicotine chloride manufacture cannot be overlooked. We draw from vetted agricultural sources, full supply chain mapping, and transparent certification processes. Our operations aim to minimize solvent waste, recycle non-reactive fractions, and audit partners for both labor and environmental practices. We have seen firsthand that shortcutting in these areas translates to both regulatory exposure and direct risk to long-term viability.

    These measures affect price, lead time, and procurement policy—sometimes making our offering less attractive than mass-market, semi-regulated imports. We stand by this direction because cutting corners in precursors or running uncertain chain-of-custody operations hurts trust. In our field, loss of traceability or contamination event happens rarely, but when it does, the impact cascades outward—to product recalls and to years-long recovery of reputation.

    End-Use Sectors: Our Experience Bridges Gaps

    Our nicotine hydrochloride heads to diverse applications. Pharmaceutical researchers deploy it as reagent or reference standard. In biochemical settings, it allows precise study of nAChR (nicotinic acetylcholine receptor) pathways. Analytical labs needing standard addition or blind reference blends use it for its solubility and ease of quantification. Emerging discussions with engineers prototyping new medical delivery platforms reveal new requirements on solubility, aerosolization properties, and particle stability across a range of pH values.

    We have guided agricultural users, but the hydrochloride salt rarely fits large-scale crop protection where nicotine sulfate remains preferred for water tank mixes. We clarify this routinely: hydrochloride shines in controlled lab work, not in open-field environments. Its highest value continues to lie in controlled-release research, device testing, and pharmaceutical-grade synthesis. Over years of production and direct troubleshooting, these distinctions matter deeply—wrong material selection wastes effort and can derail tightly funded research.

    Logistics: From Production to Delivery

    Shipping nicotine hydrochloride means more than just ticking off hazmat declarations. We handle it as a strictly controlled material, both due to international transportation laws and due to real risk of diversion for illicit purposes. Each outbound container faces checks for seal integrity, moisture exclusion, and proper secondary containment. We record batch number, packager, and tracking codes; final review by our trained compliance staff breaks any chain of complacency.

    Seasonal temperature variance can impact deliveries. Our teams have learned which couriers handle high-sensitivity packages with the care and timeliness research clients demand. Years in export logistics teach us that clear labels, up-to-date paperwork, and rigorous pre-dispatch inspection dramatically improve reliability. We have developed stable partnerships with couriers experienced in high-liability chemicals, minimizing customs holds and loss incidents.

    Supporting Research Goals With Our Experience

    For every lot of nicotine hydrochloride, trust in the final product depends on visible verification, technical support, and direct involvement. We don’t just take an order and ship blind. Our team remains available to discuss deviations, offer technical troubleshooting, and guide users through analytical techniques. Manufacturers like us solve problems, not just supply materials.

    Lectures, webinars, and onsite training expand our reach—many researchers have cut time off their project timelines after direct workshops with our process or analytical staff. We have seen how hands-on support closes gaps in method development or troubleshooting, and how full transparency in sourcing and process documentation strengthens long-term partnerships.

    Troubleshooting and Technical Collaboration

    Because nicotine hydrochloride sits at a technical intersection—regulation, product purity, and safety—our relationship with customers often involves more than paperwork. Targeted troubleshooting helps researchers resolve questions about solubility, degradation, or compatibility with novel excipient systems. In our experience, methods that fail often trace back to misunderstanding of the salt’s unique chemistry: its acid/base profile, potential to form hydrates, or tendency toward slow degradation with poor packaging.

    Facing a challenge, our process specialists share insights from actual production line data, not just generic charts. Explanation of how a particular pH corridor during crystallization produces more stable forms or how atmosphere-controlled packaging extends shelf life by months—these operational realities matter to end-users more than sales talk.

    Trust, Consistency, and Future Readiness

    Delivering nicotine hydrochloride at the standard our customers expect isn’t just about chemistry. It’s about trust earned through every batch, every certificate of analysis, and every technical call fielded with urgency and transparency. We invest not only in analytical instrumentation, but also in ongoing staff training and plant safety modernization. Our goal is not to compete at the lowest cost, but to set the standard for transparency, service, and reliability.

    Decades in the business bring perspective: customers value not only the product but also the partnership and the problem-solving that goes beyond the original inquiry. Standing firmly as the actual manufacturer, we provide these assurances without intermediation, empowered to answer any question and face any problem with direct experience and commitment.

    The Real-World Impact of Manufacturing Standards

    We have seen rapid shifts—a decade ago, demand focused heavily on large-lot commodity, sometimes at the expense of safety and traceability. Now we work with partners prioritizing pharmacopoeial compliance, reduction of nitrosamine precursors, and ecologically responsible production cycles. Academic and private-sector groups want to know about labor practices behind the raw tobacco, not just the numbers on a spec sheet. Our doors remain open to audits and third-party verifications; this confidence flows from our unbroken chain of evidence and ongoing investment.

    Supply chain turbulence in recent years tested every part of the specialty chemical sector. We buffered those shocks by holding strategic inventories, diversifying agricultural sources, and building direct relationships with key customers to forecast needs. Our investment in redundancy meant no missed deliveries or compromised quality, even while global disruptions strained raw material and logistics flows.

    Final Thoughts on the Value of Direct Manufacture

    Manufacturing nicotine hydrochloride carries weight—both chemical and ethical. Every stage, from precursor selection and facility controls to batch analytics and secure delivery, shapes not only the success of our customers’ research but also broader debates about transparency, compliance, and sustainability. Direct manufacturers step forward in these conversations with the credibility built on technical rigor, process visibility, and a collaborative approach to challenges.

    We measure our success by the trust we earn and the support we provide to researchers, developers, and production chemists worldwide. By standing behind each batch with granular data and open communication, we serve not just as suppliers but as technically accountable partners who advance the field and uphold the highest standards of science and safety.