Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing admin@sinochem-nanjing.com 3389378665@qq.com
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(+/-)-Nicotine

    • Product Name (+/-)-Nicotine
    • Alias β-pyridyl-α-N-methylpyrrolidine
    • Einecs 200-193-3
    • 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

    290481

    Name (+/-)-Nicotine
    Chemical Formula C10H14N2
    Molar Mass 162.23 g/mol
    Cas Number 54-11-5
    Appearance Colorless to yellowish oily liquid
    Density 1.01 g/cm³
    Melting Point -79 °C
    Boiling Point 247 °C
    Solubility In Water Miscible
    Pka 8.02
    Iupac Name 3-[(2S)-1-Methylpyrrolidin-2-yl]pyridine
    Flash Point 95 °C
    Specific Rotation ±164° (c=10, ethanol)
    Un Number 1654
    Toxicity Highly toxic

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

    Packing & Storage
    Packing Amber glass bottle containing 25 grams of (+/-)-Nicotine, tightly sealed with a safety cap, labeled with hazard symbols and handling instructions.
    Shipping (+/-)-Nicotine is shipped in accordance with hazardous materials regulations due to its toxicity and flammability. It is packaged in tightly sealed containers, labeled with appropriate hazard warnings. Shipping requires compliance with local, national, and international guidelines, ensuring secure containment to prevent leaks or exposure during transit. Specialized carriers are typically used.
    Storage (+/-)-Nicotine should be stored in a tightly sealed container under an inert atmosphere, such as nitrogen or argon, to prevent oxidation. Store at 2–8°C (refrigerated), away from heat, light, and incompatible substances like strong oxidizers or acids. Ensure storage area is well-ventilated, secure, and designated for toxic, volatile chemicals. Proper labeling and access control are recommended for safety.
    Application of (+/-)-Nicotine

    Applications of (+/-)-Nicotine in Industrial Manufacturing

    As a primary producer of (+/-)-Nicotine, we serve partners in regulated industrial and specialty sectors. Our nicotine supports downstream processes governed by strict compliance standards and is essential in a range of transformation steps for finished goods that require precision and reliable supply. Below we detail verified, real-world applications across select industries.

    1. Electronic Nicotine Delivery Systems (ENDS) Liquids

    Manufacturers in the ENDS sector rely on high-purity nicotine for the formulation of e-liquid bases, which require consistent material input to ensure repeatable pharmacokinetic profiles and adherence to regulatory compositional limits. Our product is dosed directly into pre-mixed propylene glycol and glycerin systems under controlled environments to maintain accurate final concentrations, followed by inline blending and bottling for market-ready cartridges and refill bottles. Downstream producers perform analytical verification prior to packaging, maintaining strict traceability at every step.

    Industry compliance standards

    • European Union Tobacco Products Directive (EU TPD 2014/40/EU)
    • US FDA Premarket Tobacco Product Application (PMTA) regulations
    • ISO 9001 quality management certification
    • ISO/IEC 17025 analytical testing requirements

    Typical usage ratio

    • 0.3%–5% nicotine, adjusted based on finished product strength (3–50 mg/mL range within legal limits)

    Downstream process integration

    • Direct addition post-base blending; metered dosing to bulk tanks before flavor and additive incorporation; inline QC for concentration adjustment; final solution filtration prior to bottling

    Final product types

    • Closed-system and open-system e-liquids
    • Disposable vape cartridges
    • Pod refill liquids

    2. Nicotine Replacement Therapies (NRT) Manufacturing

    Pharmaceutical companies use our material as the primary active agent in various smoking cessation products, observing strict Good Manufacturing Practice protocols. Accurate nicotine addition into controlled-release matrices or aqueous gels is essential to meet pharmacopoeial specifications and dosage accuracy, and validated analytical methods confirm content uniformity before release. The process requires fully closed environments to prevent cross-contamination, especially during conversion to salt forms for specific NRT formats.

    Industry compliance standards

    • European Pharmacopeia (Ph. Eur.) Monograph 1531
    • United States Pharmacopeia (USP-NF) Nicotine Monograph
    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • WHO GMP for pharmaceutical production

    Typical usage ratio

    • Calculated to achieve final product dosages ranging 1–4 mg per unit (lozenge, gum) or 7–21 mg/24h (patches); typically, a 0.1%–2% input in gels or adhesive mass, dependent on format and required release profile

    Downstream process integration

    • Active ingredient addition during admixture step for direct compression or gel blending; conversion to nicotine salt (e.g., bitartrate dihydrate) as needed; inline HPLC and moisture content checks prior to final product shaping; contained packaging under validated cleanroom conditions

    Final product types

    • Transdermal patches
    • Gum and lozenges
    • Oral films
    • Nicotine nasal and oral sprays

    3. Agrichemical Nematicide and Insecticide Synthesis

    Select crop protection producers use synthetic nicotine as a precursor for manufacturing specific systemic nematicides and insecticides for controlled agricultural applications. The active ingredient is processed through esterification or other derivatization steps, producing potent biocidal agents that comply with regional pesticide registration protocols. Input concentration is tightly managed to avoid environmental overexposure, and all batches are analyzed for residuals before formulation into commercial products.

    Industry compliance standards

    • FAO/WHO International Code of Conduct on Pesticide Management
    • EPA FIFRA standards for active ingredients
    • EU Regulation (EC) No 1107/2009 on pesticide approval
    • ISO 9001 for agrochemical production facilities

    Typical usage ratio

    • 0.5%–2% by weight as precursor input; adjusted by target derivatization yield and final product specification

    Downstream process integration

    • Input at the esterification or salt formation stage; monitored with GC or HPLC for precursor conversion; post-processing includes dilution or encapsulation for formulated concentrate or wettable powder/final spray products

    Final product types

    • Nicotinoid nematicide concentrates
    • Insecticidal sprays and granules
    • Seed treatment coatings for regulated crops

    4. Analytical Laboratory Reference Standards

    Research and analytical laboratories require certified nicotine as a calibration reference in routine and regulatory testing of nicotine-containing consumer and environmental samples. Highly pure material is aliquoted or diluted to precise gravimetric standards, supporting traceable quantification in chromatography and mass spectrometry workflows. These standards are critical for method validation, proficiency testing, and ensuring compliance with legislative residue thresholds.

    Industry compliance standards

    • ISO 17034 reference material production
    • ISO/IEC 17025 laboratory accreditation for chemical testing
    • FDA and EMA guidance on analytical method validation
    • CFR 21 Part 58 (GLP for laboratory practices)

    Typical usage ratio

    • Preparation of stock solutions at 100–1,000 μg/mL; working standards typically diluted as needed for specific assay calibration (no finished product dosage)

    Downstream process integration

    • Gravimetric dilution and ampule filling under documented conditions for secondary standard preparation; aliquoting into sealed vials; distribution to analytical laboratories for calibration use

    Final product types

    • Certified nicotine standard solutions
    • Quality control reference ampules
    • Proficiency testing sample kits
    Free Quote

    Competitive (+/-)-Nicotine prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    Introducing (+/-)-Nicotine: From Chemistry to Application

    Real Manufacture, Real Commitment

    As one of the chemical manufacturers working directly with alkaloids, our journey with (+/-)-Nicotine starts at the source—raw botanical processing. Every gram we produce comes from a continuous line rigorously monitored for both precision and purity at industrial scale. Our nicotine is a racemic mixture, representing both enantiomers, offering the chemical versatility that many research-driven, synthetic, and flavor industry clients demand. Over years of development, we've refined extraction and purification to answer the needs that chemists, formulation scientists, and product engineers face in both routine and challenging applications.

    Model and Specifications

    Our standard offering of (+/-)-Nicotine reaches high purity through multiple-stage distillation and targeted chromatographic fractionation. Typical batch purities exceed 99%, supported by repeated gas chromatography assays and NMR characterization. Customers seeking analytical grade or those dealing with specialized synthesis requiring micro-contaminant control will find our solvent stripping and in-line inert atmosphere packaging especially beneficial. Each production run follows a detailed lot record: parameters such as absorbance, polarity, refractive index, and residual solvent content come with each order, not as an afterthought, but as standard documentation. Consistency matters, and as hands-on manufacturers, we have systems to minimize variability from run to run.

    Storage conditions play a role in both immediate usability and long-term stability. We supply (+/-)-Nicotine stabilized with nitrogen and light-protective containers, since oxygen and UV exposure rapidly alter alkaloid structure and reduce shelf life—a hard lesson from early batches managed without such controls. For clients handling extended formulation times or shipping across diverse climates, our packaging support cuts down on product loss and reprocessing.

    Why Racemic Nicotine?

    Much of the world recognizes nicotine as (S)-nicotine, the naturally dominant enantiomer found in tobacco leaves. Our (+/-) product—equimolar (R)- and (S)-nicotine—steps outside that singular biological profile into broader chemical territory. In industrial labs, scientists often require both optical isomers for reactivity studies or as analytical standards. Some client groups run assays to compare the behavioral or receptor binding differences between enantiomers. Others exploit the racemate as an intermediate for novel salt formation or as a precursor in custom alkaloid synthesis. We've watched pharmaceutical researchers, agricultural chemists, and specialty chemical designers request the racemic format for its role in stereoselective synthesis optimization and for ease of comparative toxicology screening.

    Producing racemic nicotine starts with either partial synthetic routes or resolution from plant-derived sources. Over time, we've optimized the latter for cost and scalability by working directly with our raw material partners, a network built over decades. In contrast, traders and resellers rarely see or touch source material, so quality control at the plant level is usually a blind spot for them. Our quality team frequently visits leaf preparation facilities, ensuring that only clean, traceable biomass enters the extraction stream. As a result, the racemic blend remains free from many plant secondary metabolites and agrochemical impurities. Chemists recognize the difference when running their own purity or side-product screens.

    Applications and End Uses

    Most customers buying (+/-)-Nicotine from a primary manufacturer like us operate in regulated, technical sectors. Pharmaceutical researchers require reference standards against which to validate detection assays, measure isomeric purity, or conduct animal pharmacology studies. Racemic nicotine forms a crucial baseline for comparison to optical isomers or product impurity profiles. We often supply research centers tasked with developing new analytical methods, or exploring the environmental fate of synthetic and natural alkaloids. Inhalation and transdermal delivery researchers utilize racemic nicotine to understand metabolic and pharmacodynamic differences, contributing to safer product design.

    Beyond pharma, the flavors and fragrances sector explores racemic nicotine as a flavor modulator or process raw material. We’ve collaborated with academic groups determining odor thresholds, and food chemists analyzing nicotine derivatives in flavor encapsulation research. Crop science innovators use racemic nicotine for product development in nematicides or pest management, where regulatory frameworks require both isomer profiles for risk assessment. Whether the end use lands in a patch, a spray, or a laboratory dish, technical specialists order from us to guarantee the controlled specifications required for downstream analysis and compliance.

    Because we manage every production step, clients frequently request custom concentrations or salt forms. For instance, if a research protocol needs a 0.05M aqueous solution, our engineers adjust mixing and aliquoting processes to guarantee concentration homogeneity from drum to vial. This level of flexibility rarely exists with bulk traders dependent on a fixed external supply.

    Technical Challenges and Improvements

    Producing nicotine—especially in racemic form—pushes manufacturing into challenging territory. Nicotine oxidizes quickly, forming brown tars and losing reactivity if handled without air and light control. Early in our manufacturing history, we learned through wasted batches that short downtimes or improper seals cost significant material losses and open the door to contaminated product recalls. By investing in high-integrity nitrile-closure systems and automated oxygen scavenging, we've lowered oxidized impurity rates to negligible levels. On the analytical side, implementing in-line headspace analysis flags volatile contaminants before product leaves the process line.

    Scaling up without running into charring or runaway exotherms requires hands-on process engineering. Our team designed continuous-feed evaporators to avoid dead-volume “hot spots”—a far cry from batch systems that once led to unpredictable purity swings. Our technical staff shares manufacturing data with client-side chemists, offering a transparent look into each lot’s thermal and chemical profile, which enables easier troubleshooting at the research and formulation stage. Large-scale users—tobacco product developers, agricultural formulation labs, and analytical reference suppliers—rely on our documentation to clear both internal QA and regulatory audits. We offer full trace element analysis and batch-specific impurity breakdowns by default, saving our customers time and money during downstream qualification.

    Differences from Other Products in the Market

    Not all nicotine products serve the same needs. Synthetic (S)-nicotine, highly attractive for e-cigarette and pharmaceutical use, comes with the benefits of high stereoselectivity and near-absolute optical purity. For applications where only the natural isomer matches regulatory or biological requirements, that product fits best. Yet synthetic routes tend to increase costs and require additional purification steps to strip side-products and residual solvents. A trader or distributor may not understand the difference, but in our plants, these distinctions influence both how we price and how we schedule production runs.

    In contrast, natural nicotine extract (S form) arrives with a profile shaped by the original biomass: variable minor alkaloids, glycosidic residues, and trace pesticides, sometimes below detection limits, sometimes not. Racemic (+/-)-Nicotine, especially when created through controlled extraction and in-house racemization, delivers a tightly specified chemical starting point for comparative research or synthetic derivatization studies. Specialty industrial buyers request it for fine chemical synthesis and advanced material development, not just for its molecular scaffold, but also for the confidence that comes from supply stability. Only vertically integrated manufacturers offer this blend of traceability and adaptability.

    We’ve noticed that customers who tried buying from resellers often found inconsistent supply, variable purity, and a lack of technical support during periods of changing regulatory policy. Over the years, we’ve partnered with both academic and industrial groups transitioning from “off-the-shelf” product to custom manufacturing, reducing analytical failures, and increasing long-term R&D productivity. Unlike bulk commodities, chemicals like (+/-)-Nicotine rely on technical support, reliable documentation, and process feedback—this is where in-plant expertise, not just distribution networks, make the difference.

    Quality Control and Regulatory Standards

    In our operation, no product leaves the plant without a chain-of-custody record and individually signed quality certificates. This is more than a regulatory checkbox—it comes from decades supplying quality-driven sectors where even a few ppm deviation in nicotine content can skew study results or invalidate a regulatory submission. Our labs conduct full-spectrum HPLC, GC-MS impurity profiling, and water content analysis on every batch. Clients in research and development, as well as those scaling up to pilot lot production, rely on our transparency and technical detail. Each product label and digital file includes production date, lot number, and detailed storage guidance based on recent stability studies.

    Within our compliance system, we audit both internal processes and upstream supply partners. Tobacco extractors must provide residue and traceability reports. Our in-house environmental controls keep solvent emissions below international thresholds, and periodic external audits monitor both staff safety and ecological impact. Customers seeking international registrations under frameworks like REACH or US EPA pesticide guidelines access our product registration dossiers, which include all technical and environmental datasets relevant for regulatory submission.

    As regulations evolve to cover novel applications like vaping or precision agricultural treatments, our chemists participate in external working groups and technical forums. In one recent policy revision, we prepared extended impurity analysis and formulated supporting documents for clients facing a higher regulatory hurdle. Both our R&D and manufacturing teams focus on anticipating stricter analytical expectations: lower nitrosamine thresholds, tighter control over extractables, and improved documentation interfaces with laboratory information management systems.

    Supporting Technical Innovation

    Science does not stand still, and neither does chemical manufacturing. Many of our clients develop next-generation delivery systems, forensic identification methods, or new environmental applications for alkaloids. We provide more than a bottle or a drum; we support each application with scale-appropriate formulations, from milligram research vials to industrial-liter volumes. Our ability to quickly pivot—processing new requests, adjusting purity, or providing bespoke salt forms—depends on in-house expertise. This integrated approach encourages innovation at both the user and supplier end.

    Close collaboration between our R&D and customer technical teams leads to process improvements that benefit all partners. For instance, a vapor-phase purification system, originally requested by a government research lab studying smoke toxicology, is now standard in our main line. Many clients shared their analytical protocols, which led us to increase our reporting levels for non-targeted impurities. These changes reduce both pre-approval mistakes and surprise findings during later regulatory reviews.

    We stay committed to advancing our own technical frontiers by investing in equipment upgrades and staff training. In practice, this means bringing in new detection technologies, expanding synthetic process capability, and refining our data management systems to support more detailed, on-demand reporting. Users who adopt emergent analytical techniques—like high-resolution mass spectrometry or extended isotope tracing—find our batch records and impurity profiles match their advanced detection standards.

    Looking at Challenges in the Sector

    Supplying racemic nicotine brings ongoing challenges. The market sees fluctuations in input biomass quality, driven by agricultural shifts, legal changes, and climate effects. Active monitoring of source characteristics and continuous adaptation of extraction processes keep our finished product consistent. We maintain buffer stocks and multiple backup suppliers for raw materials to weather short-term supply disruptions. On the chemical synthesis side, controlling for process contaminants at scale requires vigilant monitoring and regular recalibration of distillation and chromatographic equipment.

    Staff training and safety represent another challenge. Nicotine acts as a potent toxin—errors in handling, especially at scale, expose staff to risk. Over years and thousands of production hours, our protocols evolved: daily training, personal exposure monitoring, multi-stage containment strategies, and real-time environmental sensors. These real-world control measures provide not only regulatory compliance but genuine workforce protection.

    Major shifts in regulation, consumer preference, or industrial demand force constant adaptation. We track evolving analytical requirements worldwide and invest in forward planning. Maintaining flexibility—through both process improvements and new chemical process investments—keep us resilient no matter the policy environment. Only through this proactive approach can we continue to provide value to scientists and engineers tackling both today’s questions and tomorrow’s unknowns.

    Partnering for Real Progress

    Members of our technical staff work directly with client scientists, troubleshooting difficult formulations, setting up analytical methods, and offering training as requested. Many of our partners are engineers, project leads, or hands-on bench chemists—they value being able to connect with those actually running the reactors and purification lines. Sharing out real-time process data and custom lot details dramatically reduces time wasted tracking down errors or testing poor-quality material. Some long-term customers co-develop new procedures for post-purification stabilization or rapid concentration adjustments, improving both in-plant and lab-side process reliability.

    We avoid the pitfalls that come from being just an intermediary. Our production planners, technical service chemists, and QA analysts all communicate daily to anticipate shifts in demand or resolve batch-to-batch differences. As the legal climate around nicotine changes—driven both by public health regulation and broader chemical policy updates—our in-house regulatory team works on documentation, keeping pace with or anticipating new compliance requirements.

    The result? Application-focused support, not just product delivery, and a relationship with users based on transparency in production and responsiveness during every new technical challenge. Our experience as true manufacturers, not traders, defines the way we interact with every client, every batch, and every innovation in the field of alkaloids.