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N-4-Nitrobenzyl-N-Propylamine Hydrochloride

    • Product Name N-4-Nitrobenzyl-N-Propylamine Hydrochloride
    • Alias NBP-HCl
    • Einecs 'EINECS 611-278-2'
    • 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

    731369

    Product Name N-4-Nitrobenzyl-N-Propylamine Hydrochloride
    Cas Number 49670-95-1
    Molecular Formula C10H15ClN2O2
    Molecular Weight 230.69 g/mol
    Appearance White to off-white solid
    Purity Typically ≥98%
    Melting Point 125-130°C (decomposes)
    Solubility Soluble in water and methanol
    Storage Conditions Store at 2-8°C, protected from light and moisture
    Synonyms N-(4-Nitrobenzyl)-N-propylamine hydrochloride
    Smiles CCCN(Cc1ccc(cc1)[N+](=O)[O-])Cl
    Inchikey MFKLUOHYHBKFAJ-UHFFFAOYSA-N

    As an accredited N-4-Nitrobenzyl-N-Propylamine Hydrochloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Packaged in a sealed amber glass bottle, 10 grams, labeled "N-4-Nitrobenzyl-N-Propylamine Hydrochloride," with safety and handling instructions.
    Shipping N-4-Nitrobenzyl-N-Propylamine Hydrochloride is shipped in tightly sealed containers, protected from light and moisture. Packaging complies with regulations for chemical safety, including appropriate labeling and documentation. It is transported as a non-hazardous material under normal conditions, but care is taken to prevent spillage or contact during shipping and handling.
    Storage **N-4-Nitrobenzyl-N-propylamine hydrochloride** should be stored in a tightly sealed container, protected from light and moisture, in a cool, dry, and well-ventilated area. Keep the storage temperature at 2–8°C (refrigerated). Ensure the chemical is kept away from incompatible substances such as oxidizing agents and bases. Label containers clearly, and follow standard chemical storage protocols.
    Application of N-4-Nitrobenzyl-N-Propylamine Hydrochloride

    Applications of N-4-Nitrobenzyl-N-Propylamine Hydrochloride in Industrial Manufacturing

    As a dedicated manufacturer of N-4-Nitrobenzyl-N-Propylamine Hydrochloride, we supply this specialty amine derivative across several established industrial sectors. Below, we detail the specific proven applications, listing relevant compliance requirements, precise formulation ratios, process stages, and representative end products for each segment.

    1. Pharmaceutical Intermediates for Active Pharmaceutical Ingredient (API) Synthesis

    N-4-Nitrobenzyl-N-Propylamine Hydrochloride actively participates as a protected amine building block in multi-step synthesis routes for regulated APIs, especially in central nervous system and oncology segments. Manufacturers rely on this raw material for selective functional group introduction, enabling precise structural modifications required in patented drug substance development and commercial large-volume manufacturing.

    Industry compliance standards

    • Current Good Manufacturing Practice (cGMP) for active ingredients (ICH Q7)
    • U.S. Pharmacopeia (USP) monographs for intermediates and APIs
    • European Pharmacopoeia (Ph. Eur.) active substance guidance
    • FDA DMF submission where applicable

    Typical usage ratio

    • Applied at 0.8–2.5% molar equivalent in target reaction step, determined by required stoichiometry and process validation yield; typical API synthesis platforms finalize optimal dose during scale-up and cleaning validation.

    Downstream process integration

    • Added as a functionalized amine coupling partner or protected group carrier during the reductive amination or nucleophilic substitution step within multi-stage intermediate synthesis; removal and purification follow standard crystallization, flash chromatography, or preparative HPLC, as validated per product specification.

    Final product types

    • Generic and proprietary API molecules (notably containing N-benzyl amine motifs)
    • Central nervous system (CNS) drug substances
    • Oncology small molecule actives

    2. Custom Fine Chemical Synthesis for Agrochemical Intermediates

    Agrochemical producers employ this compound as a synthetic intermediate for the elaboration of complex nitrogen-containing herbicide and insecticide actives. Its nitrobenzyl moiety enables selective downstream modifications, making it valuable in scaled multi-hectare batch and continuous flow production lines for crop protection molecule development.

    Industry compliance standards

    • ISO 9001 Quality Management System for chemical synthesis
    • EU Regulation (EC) No 1107/2009 for plant protection product intermediates
    • REACH compliance (Registration, Evaluation, Authorisation and Restriction of Chemicals)
    • EPA 40 CFR, Part 158: Data requirements for agricultural chemicals

    Typical usage ratio

    • Used at 1.2–3.0% w/w per target reaction mass in phase-specific condensation or protection steps; adjusted based on the intended transformation efficiency and downstream purification constraints.

    Downstream process integration

    • Charged into jacketed reactor vessels after initial condensation or alkylation stage; commonly subjected to heating and subsequent extraction or distillation for desired intermediate isolation, monitored by in-process GC-MS or HPLC.

    Final product types

    • Sulfonylurea and anilide herbicide intermediates
    • Pyridyl and phenylpyrazole insecticide building blocks
    • Nitro-substituted nitrogen functionalized precursors for finished crop protection actives

    3. Analytical Reagent Production for Chromatographic Derivatization

    Specialty laboratories and diagnostic kit manufacturers utilize this compound for derivatization protocols, enhancing amine, peptide, or amino acid detection in HPLC/UPLC and mass spectrometry applications. Its precise reactivity allows high-yield labeling with minimal byproduct formation, supporting stringent purity and detection requirements in regulated environments.

    Industry compliance standards

    • ISO/IEC 17025: Testing and calibration laboratories
    • Good Laboratory Practice (GLP) for reagent quality assurance
    • USP <467> Residual Solvents (for trace analysis)
    • RoHS 2 (Directive 2011/65/EU) for laboratory instrument compatibility

    Typical usage ratio

    • Dosed into labeling or derivatization reactions at 0.05–0.20% w/v relative to target analyte solution; precise ratio adjusted for molar equivalence to sample protein or small molecule content, confirmed by method suitability studies and QC assay acceptance criteria.

    Downstream process integration

    • Mixed at controlled temperature with sample matrix during pre-column or in-line mixing; derivatized samples are then directly injected into chromatographic instruments. End-point verification achieved by standard chromatogram comparison, followed by washing and column reconditioning per laboratory protocol.

    Final product types

    • HPLC/UPLC test kits for pharmaceutical quality control
    • Mass spectrometry derivatizing reagents for clinical diagnostics
    • Certified reference materials used in analytical contract laboratories

    4. Advanced Material Synthesis for Specialty Polymer Functionalization

    In specialty polymer manufacturing, this compound serves as a chain-end modifier and functional monomer precursor, granting tailored reactivity or light-sensitive features to advanced polymer structures. This method supports dedicated production of responsive films, encapsulant layers, and research-stage electronic substrate coatings where precise side group anchoring is required.

    Industry compliance standards

    • ISO 9001:2015 for advanced polymer manufacture
    • ASTM D883 for terminology relating to plastics standards
    • EN 13432 for biodegradable polymer matrix components (when applicable)
    • RoHS (Directive 2011/65/EU) for electronics-related polymers

    Typical usage ratio

    • Incorporated at 0.3–1.0 mol% relative to overall monomer feed in batch or continuous bulk polymerization processes; level established by R&D compounding trials to achieve target functionalization and optical/light-activation thresholds.

    Downstream process integration

    • Fed into pre-polymerization or post-polymer modification reactors as a functional end-capper or reversible side group. Integration monitored via FTIR or NMR to verify binding efficiency and avoided byproduct formation, with subsequent melt processing or film casting steps standardized per sector practice.

    Final product types

    • Photo-reactive polymer films
    • Semiconductor encapsulation resins
    • Surface-modified specialty plastics for lab-on-a-chip and sensor applications

    5. Chemical Research and Custom Synthesis (Order-Based Projects)

    Chemical research organizations and custom synthesis service providers frequently order N-4-Nitrobenzyl-N-Propylamine Hydrochloride for multi-functional group installations and scaffolding during exploratory bench-scale projects. This enables rapid prototyping and piloting of molecular candidates for academic, industrial, and government-funded initiatives focused on new molecule discovery and advanced functional materials.

    Industry compliance standards

    • ISO 9001 for R&D material traceability and batch records
    • Good Laboratory Practice (GLP) for exploratory projects
    • OECD Principles of Good Laboratory Practice
    • Material transfer agreement (MTA) and safe handling protocols compliant with local chemical safety regulations

    Typical usage ratio

    • Usage varies from 0.05 up to 5% (w/w or molar), set by specific project requirements and synthetic target scope; amounts are defined by preliminary combinatorial chemistry and confirmed through analytical verification of reaction progress.

    Downstream process integration

    • Incorporated at bench or pilot scale into manual or automated reactor systems. Often utilized during initial nitrobenzyl installation, amination, or protecting group strategy deployment. Post-reaction, chemists purify intermediates via silica gel flash chromatography, preparative LC, or solid-phase extraction.

    Final product types

    • Lead structure candidates for further development
    • Novel functional materials for electronics or catalysis research
    • Small-batch chemical building blocks for pharmaceutical or academic use
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    Certification & Compliance
    More Introduction

    N-4-Nitrobenzyl-N-Propylamine Hydrochloride: An Experienced Manufacturer’s Insight

    What N-4-Nitrobenzyl-N-Propylamine Hydrochloride Offers

    Manufacturing N-4-Nitrobenzyl-N-Propylamine Hydrochloride comes with unique challenges and opportunities. This compound, carrying the molecular formula C10H15ClN2O2, delivers reliability in advanced synthesis work, especially in fields ranging from pharmaceuticals to materials science. Our team has worked through every batch with the attention demanded by regulated and innovation-driven customers.

    Over years, our attention to process consistency and purity level has shaped the product we offer today. Few intermediates express versatility like this one. It brings a steady nitro-substituted aromatic core tethered to a propylamine chain, set as its hydrochloride salt. With a white to light-yellow crystalline appearance, consistent melting point, and excellent solubility profile, repeatability becomes possible in scale-up and research settings alike.

    Getting the Fundamentals Right: Synthesis and Handling

    Sourcing reliable raw materials sets the ground rules. No shortcut replaces high-purity starting reagents with traceability back to original lots. Our chemists begin with certified compounds and tightly control each step, especially the nitro-group attachment, which defines the compound’s reactivity pattern downstream. Lab validation and process upscaling both reveal the pitfalls of overlooked side reactions—each impurity contributes its own ghost to analytical results and downstream synthesis.

    Temperature swings and solvent quality during the formation of the hydrochloride salt change how crystals form. Many manufacturers overlook humidity and airflow when working at scale, yet these factors shape the particle size distribution and the efficiency of filtration. Multiple filtration runs and re-crystallization sometimes prove necessary, especially with sensitive reactions and downstream biological work in mind. Our team routinely reports yields above industry averages and near-quantitative conversion rates during hydrochloride formation, due to decades refining these seemingly small details.

    Purity, Consistency, and Product Validation

    We routinely see buyers struggling with batch-to-batch inconsistencies from smaller suppliers. N-4-Nitrobenzyl-N-Propylamine Hydrochloride’s applications in active compound synthesis and intermediate production mean that purity isn’t just an analytical number but something reflected in real-world reaction performance. Our minimum spec demands ≥99% by HPLC, with controlled limits for water content, residual solvents, and related substances, using techniques like Karl Fischer, GC-MS, and NMR for each lot.

    Those who have worked with analogues know a minor contaminant can change crystallization habits or introduce unpredictable reactivity under reducing or alkylating conditions. Even a small level of by-products, like unreacted amines or nitrotoluene isomers, cause headaches later on. Tighter analytical control and experience tracing the origin of anomalies have helped us solve issues for both generic and proprietary synthesis applications, where regulators and scientists demand paper trails and supporting data.

    Applications Backed by Experience

    Our technical customers value the role this intermediate plays in medicinal chemistry and complex molecule construction. Its combination of an electron-deficient aromatic ring and secondary propylamine side chain offers unique positioning for substitution reactions, reductive aminations, and stepwise derivatization. Years of supply to peptide, ligand, and intermediate manufacturers proved its value both as a nucleophile precursor and as a protected amine in multi-step syntheses.

    Manufacturers in the fine chemicals and pharmaceutical sectors leverage this compound for active ingredient synthesis, with the nitrobenzylic group serving as a modifiable handle. Custom API building blocks often require reductive removal or transformation of the nitro group, where a reproducible starting material shaves weeks off project timelines. Our process knowledge aids developers who need to optimize yield and product isolation, especially where downstream hydrogenation or coupling steps take place. Researchers who build tailored molecular scaffolds report cleaner results and easier isolation thanks to the controlled purity and consistent performance.

    Beyond pharma, new applications have surfaced in materials science and specialty polymer research, with the nitro group participating in controlled-release formulations and novel functionalization pathways. We tracked increasing interest from teams attempting site-specific labeling or constructing photo-reactive surfaces. As new fields push chemistry to more demanding extremes, the demands on starting materials rise in parallel.

    Critical Differences from Related Products

    Decades in the industry taught us that structural cousins of N-4-Nitrobenzyl-N-Propylamine Hydrochloride often fail to deliver identical results. The unique combination of nitrobenzylic functionalization and a secondary, not primary, amine determines reactivity. This compound resists alkylation at nitrogen under conditions where primary amines cannot, allowing greater selectivity in downstream modifications. Substituted analogues—either lacking the nitro or using benzyl chloride cores—produce different reactivity profiles, reduction pathways, and isolation challenges.

    Hydrochloride formation brings its own advantages. Other manufacturers ship free bases and leave downstream salt formation to end users. We found that delivering material as a pre-formed hydrochloride not only boosts solubility in water and common alcohols but also improves storage stability and batch uniformity. Free base material often picks up ambient moisture and atmospheric CO2, while hydrochloride samples remain consistent and flowable well past standard shelf lives without caking, especially under high humidity. This sharply reduces product loss and simplifies handling in GMP and non-GMP environments alike.

    Regulatory, Traceability, and Quality Matters

    Complex syntheses depend on full traceability and regulatory assurance, something most traders and third-party packagers overlook. Direct sourcing from our facility guarantees paperwork completeness, process control, and batch integrity. Auditable documentation, validated methods, retained samples, and full analytical archives support both routine use and unexpected troubleshooting.

    Our production incorporates in-process controls, with every sensitive stage monitored for reaction conversion and trace impurity. During hydrochloride formation, we tested multiple acid titration regimes and settling conditions until repeatable batch homogeneity resulted. This makes compliance with international standards more than a paperwork exercise—it’s a reflection of day-to-day lab work and transparent, ongoing improvement. Our team’s experience navigating regulatory filings with both domestic and global authorities has streamlined supply chains for customers facing rigorous quality audits.

    Challenges in Production and Continuous Improvement

    Scaling up from bench to plant presents technical hurdles. We’ve invested decades overcoming solvent management, waste minimization, and local environmental requirements. Nitro-chemistry poses explosion and toxicity risks that less experienced operators often underestimate. Safe plant design, real-time monitoring of reaction exotherms, and full hazard analysis for nitration and reduction steps mean fewer surprises and less downtime.

    Removing color bodies, unwanted isomers, and trace metal contaminants requires iterative tweaking, not simply copying literature methods. High-throughput analytical tools, paired with hands-on process chemists, drove method refinements. We put our operators through continual skills training—not just once, but as part of a company-wide mindset that values craft, oversight, and responsibility. As regulatory expectations and customer demands rise, these lessons form the backbone of our practical knowledge.

    Supporting Customers Through Shared Experience

    Customers benefit from direct lines to experienced staff. Chemists, not just salespeople, answer real-world questions. When fermentation scientists, medicinal chemists, or analytical development labs call us needing advice on solubility in unusual solvents, process modifications, or troubleshooting side product formation, we pull data from in-house runs and historic lot records to provide actionable support.

    End users often describe frustrating experiences with one-off traders or brokers—material arrives without supporting documentation, batch properties drift unpredictably, and technical questions go unanswered. We learned over the years that investing in dialogue, data sharing, and technical writing pays back through repeat business and fewer supply chain snags. Our technical bulletins, usage guides, and analytical data sets stem from actual production batches, not overseas spec sheets.

    Comparison with Other Sourcing Routes

    Direct manufacturer supply means tighter control on shipment timelines, lot recertification, and immediate support during transit. Distributors sometimes swap out manufacturers or blend lots to meet inventory obligations, complicating regulatory traceability and consistency. Working with a single manufacturer eliminates these risks, especially for clients with validation and regulatory approval timelines to manage.

    Competitors using lower spec requirements or looser batch controls often encounter reactivity outliers, especially in pilot trials or scale-up demonstrations. We’ve been invited onto customer sites around the world to diagnose inconsistent reaction results or batch failures, only to find source material out-of-spec. Backward traceability and transparent investigation have allowed us to help fix processes, not just ship more product.

    Commitment to Process Safety, Worker Training, and Environmental Responsibility

    Manufacturers bear the direct responsibility for safe chemical handling and environmental stewardship. Running a plant built around nitration and amination means every vent, drain, and temperature alarm stays under constant scrutiny. Staff training in safety procedures, regular maintenance cycles, and triple checks before every high-risk batch keep us on track.

    We upgraded ventilation, installed advanced filtration systems, and implemented waste reduction programs long before compliance became an industry catchword. Our experience handling nitroaromatics and secondary amines informed these improvements, matching process efficiency with the safety needs of skilled operators and the integrity of the environment. Our policies stem from on-site risk, not just regulatory paperwork.

    Future Perspectives: Listening to Customers and Evolving Alongside Innovation

    Every new research direction, from bioconjugate chemistry to next-generation imaging probes, stretches upstream requirements on intermediates. Dialogue with leading-edge scientists and formulation specialists points us toward new purification thresholds or alternative salt forms. This feedback loop helps us keep pace with brisk shifts in technology, anticipating process changes and customer needs before they become mission-critical.

    Our production improvements—optimized drying cycles, advanced analytical profiling, lab-to-plant integration—emerged in direct response to detailed customer feedback and our own push for higher reliability. These small, steady investments underpin the trust customers place in us when deadlines approach and errors aren’t an option. We see the details in intermediate manufacturing as not just technical achievements but as a foundation for scientific progress across industries.

    Guiding Principles that Define Our N-4-Nitrobenzyl-N-Propylamine Hydrochloride

    Building better chemicals means sweating hundreds of decisions, from procurement through shipping. Real expertise comes from lived experience: years of batch reports, process tweaks, regulatory audits, and direct customer dialogue. The credibility of a manufacturer grows not from marketing claims but from reliable, reproducible supply and the ability to support users at every stage—whether your need is for gram samples to de-risk a pathway or for metric tons under validated process conditions.

    This approach defines our N-4-Nitrobenzyl-N-Propylamine Hydrochloride. By holding ourselves to standards that anticipate where science will push next, and pairing technical facts with experience in the plant, we offer both product and partnership built for the real world of modern chemical manufacturing and research. If your next program depends on reliability and open feedback with real chemists behind the compound, decades of experience stand ready to support your goals.