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C-(1H-Imidazol-2-yl)-Methylamine

    • Product Name C-(1H-Imidazol-2-yl)-Methylamine
    • Alias histamine
    • Einecs 629-927-6
    • 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

    644826

    Chemical Name C-(1H-Imidazol-2-yl)-Methylamine
    Molecular Formula C4H7N3
    Molecular Weight 97.12 g/mol
    Cas Number 1018-03-9
    Appearance White to off-white crystalline powder
    Melting Point 102-106 °C
    Solubility Soluble in water
    Pka Approximately 9.0 (amine group)
    Smiles NCc1nccn1
    Inchi InChI=1S/C4H7N3/c5-1-4-6-2-3-7-4/h2-3H,1,5H2,(H,6,7)
    Storage Temperature 2-8 °C
    Synonyms 2-(Aminomethyl)imidazole
    Purity Typically ≥ 98%
    Hazard Statements May cause irritation to skin, eyes, and respiratory tract

    As an accredited C-(1H-Imidazol-2-yl)-Methylamine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 25g of **C-(1H-Imidazol-2-yl)-Methylamine** supplied in a sealed amber glass bottle with tamper-evident cap, labeled with safety information.
    Shipping C-(1H-Imidazol-2-yl)-Methylamine is shipped in tightly sealed containers under dry, cool conditions to prevent moisture absorption and degradation. It is packed in accordance with chemical safety regulations, labelled with hazard information, and transported with appropriate documentation to ensure safe and compliant handling during transit.
    Storage **C-(1H-Imidazol-2-yl)-Methylamine** should be stored in a tightly sealed container, under an inert atmosphere such as nitrogen, and kept in a cool, dry, well-ventilated area away from moisture and incompatible substances (such as strong oxidizers and acids). Protect from light and store at room temperature or as recommended by the manufacturer to prevent degradation.
    Application of C-(1H-Imidazol-2-yl)-Methylamine

    Applications of C-(1H-Imidazol-2-yl)-Methylamine in Industrial Manufacturing

    As a direct manufacturer, we maintain robust supply of C-(1H-Imidazol-2-yl)-Methylamine in bulk to support high-volume operations in specialty chemical pipelines. Our technical team collaborates closely with business partners and production engineers, drawing from proven downstream applications in advanced material synthesis and performance chemical intermediates. Below, we outline primary industrial end-uses backed by regulatory compliance, established manufacturing recipes, and integration into large-scale processes.

    1. Synthesis of Pharmaceutical Intermediates

    Producers of small-molecule active pharmaceutical ingredients commonly incorporate C-(1H-Imidazol-2-yl)-Methylamine in the construction of nitrogen-containing heterocyclic intermediates. The compound enters as a critical building block during multi-step processes in the generation of anti-infective, anti-inflammatory, and antifungal agents, especially where high heteroatom functionality is required for bioactivity. Stringent control over trace impurities and amine content is mandatory at this stage to meet regulatory submission requirements.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • USP–NF Monographs for applicable intermediates
    • EDQM CEP submission support
    • FDA 21 CFR Part 210/211 for quality management

    Typical usage ratio

    • 0.25–1.5 molar equivalents, depending on position in synthesis; process chemists adjust based on yield optimization and residual impurity profile

    Downstream process integration

    • Charged to reaction vessels during amide/imidazole ring functionalization and protection steps
    • Amine coupling stages in flow or batch synthesis

    Final product types

    • Pharmaceutical intermediates for final API synthesis
    • Intermediates for anti-infective and anti-inflammatory drugs
    • Biologically active research compounds for medicinal chemistry

    2. Manufacture of Imidazole-Based Corrosion Inhibitors

    The imidazole moiety in this raw material finds targeted application in formulating corrosion inhibitors added to water treatment products and metalworking fluids. Manufacturers employ it to enhance the polar adsorption layer on steel and non-ferrous metals, improving protection under challenging conditions such as high-chloride environments and closed-loop water systems. The amine structure confers specific reactivity in precise inhibitor blends where stability and film formation efficiency remain critical KPIs for industrial customers.

    Industry compliance standards

    • ASTM D6107-13 guidelines for corrosion and deposit control
    • ISO 8044 terminology and ISO 8044:2023/E for corrosion inhibitors
    • REACH registration and CLP regulations for classification
    • RoHS Directive 2011/65/EU for end-use limitations

    Typical usage ratio

    • 0.1–1.5% w/w in finished inhibitor concentrate; precise dosing varies with system volume and corrosion rate testing

    Downstream process integration

    • Blended into additive packages via emulsion or direct dissolution after liquid/liquid formulation steps
    • Post-reaction stabilization with other azole-based anti-corrosive agents

    Final product types

    • Industrial water treatment corrosion inhibitor blends
    • Metalworking fluid additives
    • Cooling system protection formulations
    • Boiler and closed-loop treatment chemicals

    3. Custom Monomer Synthesis in Polymer Research

    An established downstream use for this chemical involves research-driven production of specialty monomers for high-performance polymers and advanced resins. Polymer manufacturers integrate the imidazolyl methylamine fragment into monomer units through condensation or amidation, supporting the development of materials with improved charge transport, flame resistance, and thermal stability. Research partnerships often specify purity and color index criteria due to influence on the resulting polymer morphology and electronic behavior.

    Industry compliance standards

    • ISO 9001:2015 Quality Management System
    • OECD Test Guidelines for chemical intermediates
    • REACH-compliant raw materials registration for EU supply
    • Technical data alignment with individual customer R&D specifications

    Typical usage ratio

    • 3–10 mol% relative to total monomer load; chemist adjusts based on desired copolymer chain composition

    Downstream process integration

    • Employed during pre-polymer functionalization step for inclusion in step-growth or radical polymerization
    • Directly introduced into monomer precursor blend prior to catalyst addition

    Final product types

    • High-performance engineering plastics
    • Specialty resins for electrical insulation
    • Membrane materials for chemical separation
    • Research-grade polymer samples for material science institutes

    4. CO2 Capture and Separation Facilitation Agent

    Large-scale gas treatment facilities adopt imidazole derivatives in advanced CO2 capture chemistries, where the methylamine group serves as an affinity-enhancing site for acid gas binding. Integration into formulated scrubbing agents or solid-supported adsorbents delivers tailored selectivity, boosting gas purification efficiency in natural gas processing and post-combustion carbon capture projects. Each system requires conformance to environmental and process safety regulations, including control of secondary amine emissions.

    Industry compliance standards

    • ISO 14001: Environmental Management Systems
    • EU Industrial Emissions Directive (IED)
    • US EPA Clean Air Act Section 112 standards
    • Relevant process safety management (PSM) and exposure limit guidance

    Typical usage ratio

    • 0.5–5% by weight in gas treatment solution or immobilized adsorbent; scaled based on CO2 partial pressure and regeneration cycle requirements

    Downstream process integration

    • Impregnated into solid support via wet-impregnation during adsorbent preparation
    • Mixed into amine blend solutions during plant compound make-up stages

    Final product types

    • CO2 capture adsorbent pellets
    • Solvent-based scrubbing fluids for flue gas & biogas
    • Integrated gas-processing units for industrial separation systems
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    Certification & Compliance
    More Introduction

    C-(1H-Imidazol-2-yl)-Methylamine: Practical Insights from the Manufacturer’s Floor

    Rooted in Real Manufacturing Experience

    C-(1H-Imidazol-2-yl)-Methylamine has earned a spot among our steady performers not only due to its unique molecular structure but also because of its resilience across applications. Handling this compound day in, day out on our production lines, we’ve seen its adaptability and reliability firsthand. There are stories behind every batch, from precise temperature controls during synthesis to the satisfaction of hitting purity benchmarks consistently. Among the amine-modified imidazoles, this molecule strikes a balance between reactivity and stability that few others sustain under manufacturing scrutiny.

    Molecular Model and Practical Production

    With the chemical formula C4H7N3, C-(1H-Imidazol-2-yl)-Methylamine features an imidazole ring bonded through its 2-position to a methylamine group. This seemingly simple arrangement goes deeper than academic recognition; during synthesis, our teams pay attention to controlling ring integrity and side chain reactivity. Our model emphasizes optimizing temperature ramps to maintain selectivity, which matters when unforeseen shifts could feed through to product performance.

    We don't look at this compound as just another item in a catalogue. Each batch passes through several purity checks using HPLC and NMR, targeting specification levels that match the demands of research and industrial synthesis communities. The white to off-white crystalline powder signals not only quality but also careful drying and material handling on our side—no shortcuts or outsized variability from lot to lot.

    Purpose & Use: Not Just a Theoretical Candidate

    End-users know C-(1H-Imidazol-2-yl)-Methylamine’s real-world value through its robust performance as an intermediate. Our experience shows that major demand arises from pharmaceutical building blocks and specialized fine chemical synthesis. In multi-step medicinal chemistry workflows, this molecule regularly plays a key functionalization agent, helping assemble more complex heterocycles and facilitating linkages where both imidazole-derived and amine functionalities are needed in the same parent molecule.

    Lab directors tell us about its known compatibility with a variety of solvents—aqueous, alcoholic, and polar aprotic—all managed with ease. Reaction rates benefit from its clean nucleophilic profile, meaning chemists worry less about off-pathway reactions that can plague other amines. Its imidazole core helps buffer conditions, which we have directly measured to prolong intermediate shelf lives—a point valued in custom peptide and nucleotide syntheses. We’ve supplied bulk and research quantities alike, and feedback often focuses on less waste, fewer purification steps, and consistent yields.

    Specifications That Matter In Everyday Work

    C-(1H-Imidazol-2-yl)-Methylamine typically ships with a minimum assay of 98%. The product shows a melting point range above 80°C, reflecting both solidity and ease of processing—a trait appreciated by technicians managing solid transfer and weighing. Moisture control receives particular attention; water content remains consistently below 0.5% right up to final packaging, backed by real time Karl Fischer titrations conducted on-site. This prevents degradation in moisture-sensitive synthesis steps.

    Particle size rarely gets discussed until it’s a problem—for those scaling reactions or filling reactors, we standardize sieve cuts to minimize dust and clumping. This speeds up not just formulation but also downstream filtration. Our operators monitor batch consistency through physical properties as much as through chemical analytics, observing color and free-flowing status in real time, not just relying on tabulated numbers.

    Addressing Real Differences in Similar Reagents

    Many in the field lump together imidazole derivatives with amine side chains, assuming broad interchangeability. In practice, structure-activity relationships and practical handling set C-(1H-Imidazol-2-yl)-Methylamine apart. Other compounds, such as 1-methylimidazole or imidazole-4-acetaldehyde, each bring their own limitations—ranging from volatility issues in the case of some methylimidazole isomers, to unwanted reactivity or odor in mixed amine derivatives.

    Direct hands-on comparison with isomers and structural relatives, like 4-methylimidazole or imidazole-2-carboxaldehyde, confirms the point: only the 2-yl methylamine keeps side chain basicity and ring π-stacking properties tuned at just the right level for cross-coupling and catalytic studies. Customers working with metal coordination chemistry often note the high affinity and clean complexation C-(1H-Imidazol-2-yl)-Methylamine achieves – outperforming standard imidazole and ethylenediamine derivatives. Our in-house R&D team regularly stress tests this molecule’s reactivity against others, documenting side reactions and byproduct thresholds that guide users away from avoidable troubleshooting.

    Meeting Regulatory and Quality Demands

    We have learned the importance of traceability and transparency. Customers, especially those in pharmaceutical synthesis and regulated industries, expect up-to-date certificates and reliable supply. Sourcing and handling of all precursor raw materials undergo thorough vetting—often exceeding statutory requirements. Each C-(1H-Imidazol-2-yl)-Methylamine batch receives a full documentation trail, starting with raw material identity through to in-process controls and final packaging under controlled atmosphere.

    Typical contaminants such as residual solvents, heavy metals, or traces from catalyst use receive special attention. Our process development team sits with QA/QC staff weekly, sharing actual analytical data trends, not just passing quality control at the end of a process. This reveals and solves long-term process drift early, whether around trace byproducts from side-chain formation or seasonal raw material fluctuations impacting final purity. Third-party audits remain welcomed, given our record of process improvements born from everyday factory realities.

    Supporting Sustainable Operations

    Chemical manufacturing today faces environmental scrutiny, and we see supply partners and buyers alike holding us accountable for waste minimization. C-(1H-Imidazol-2-yl)-Methylamine synthesis has been optimized internally over the years to reduce solvent use and decrease the number of organic extractions. Solvent recycling now forms a default part of batch work-ups. Waste byproducts—like minor methylamine impurities—are captured and processed for energy recovery, not just sent off as liquid effluent. Often, operators suggest tweaks on the flow lines to further cut down on waste; these changes show up directly in lower annual disposal costs and cleaner audit results.

    We favor energy-efficient reaction conditions, reducing heating and chilling demands by fine-tuning both catalyst loadings and reaction dwell times. On a yearly basis, metrics get reviewed against environmental targets openly in front of the production team, showing how each step with C-(1H-Imidazol-2-yl)-Methylamine plays into broader sustainability commitments.

    In-Field Applications and End-User Feedback

    The biggest wins often come from stories shared by users. Researchers working on kinase inhibitors have documented how inclusion of the C-(1H-Imidazol-2-yl)-Methylamine segment increased lead compound solubility and metabolic stability. Those in the dye and pigment sector reported easier coupling with chromogenic aldehyde partners, reducing color bleeding and improving lightfastness. Diagnostic kit developers noted batch-to-batch predictability, helping them truncate validation runs and lower development costs.

    We’ve learned from scale-up partners that switching from related amine-imidazole hybrids over to this molecule cuts downstream purification by half, delivering cleaner products directly from column or crystallization steps. Smaller contract synthesis labs appreciate the transparent supply chain and stability in pricing, giving them freedom to plan without unwelcome substitutions.

    Shelf-Life and Storage Lessons

    Nobody in the supply chain thanks a producer for short shelf-life. We prioritize storage stability. Climate-controlled warehouses store C-(1H-Imidazol-2-yl)-Methylamine under low humidity, and all drums and small packs arrive to customers with tightly sealed liners. Having sampled archive material up to eighteen months after manufacture, we documented unchanged physical appearance and assay. We log all stability tests openly and collect real feedback from customers, especially when they report storing opened containers for extended periods with no visible change in performance.

    We view shelf-life not only as retaining chemical structure but also as maintaining ease of handling. If caking develops—usually an early warning of moisture ingress—our production team investigates root causes, which often leads to prompt corrections in either packaging or drying steps. These practical measures prove more meaningful to end-users than any blanket warranty period.

    Shipping and Handling with Integrity

    Shipping can feel routine, but the logistics behind sending C-(1H-Imidazol-2-yl)-Methylamine safely impact both performance and trust. We have designed custom packing systems to limit transfer losses, using both moisture-barrier liner bags and heavy gauge fiber drums. Palletization matches the requirements of cold chain or ambient routes, based on transport distances and local climate. For research-scale buyers, smaller units and repack options keep exposure minimal, reducing problems during storage. Our logistics and technical support staff field direct calls about special labeling or transportation instructions for each order, passing on practical advice that they themselves have found works best.

    Continuous Improvement Built Around User Experience

    Listening to feedback from bench chemists and production engineers, we maintain an open door approach to improvement. We hold quarterly user panels, not just relying on brochures or datasheets. Adjustments have ranged from shifting sieve fractions for less dust, to rolling out tamper-evident closures in response to supply chain security requests. One notable case involved a specialty API manufacturer, who flagged trace residuals detected by their LC-MS screening. Our process team re-examined purification and raw material tracking, ultimately leading to the implementation of an extra polishing filter and upgraded analytical methodology.

    We do not chase every temporary market trend but focus on reproducibility and fairness across every drum or ampoule of material we send out. A sustained relationship with groups in biotech, petrochemicals, and higher education verifies that word-of-mouth referrals matter more than any catalog blurb. We put our name on every container, knowing that each kilo could wind up in a life-saving pharmaceutical or a next-generation piece of technology.

    Why Real-World Manufacturing Input Matters

    Textbook summaries rarely capture the daily challenges faced on the line. Scalability, purity, and dependable logistics only come together when manufacturers maintain dialogue with their own staff and their customers—chemists, engineers, and operators alike. All the bench-scale convenience and yield in the world does not count if products fluctuate from order to order, or if small formulation changes create headaches for downstream process engineers.

    What differentiates our C-(1H-Imidazol-2-yl)-Methylamine is not only its chemistry but the real-world process behind it. Process optimization is continuous—borne out not only of raw performance metrics but actual production observations: energy savings, recovery of minor reactants, and error tracking for trace contaminant detection. Documentation is more than an afterthought; it forms the backbone of user confidence and repeatability.

    Stability studies and field trials show that careful process control at every stage—from synthesis to drying and final packaging—translates directly to better value for both research and bulk applications. We never lose sight of the fact that end-users depend on our diligence not just for product, but also for the certainty that comes with every shipment. That's knowledge gained from hands-on production—a culture built on experience, accountability, and trust.

    Your Needs, Our Craft

    The value of C-(1H-Imidazol-2-yl)-Methylamine reaches beyond structures and numbers. Each refinement to our protocols reflects lessons learned from both successes and setbacks on the factory floor and at the customer’s site. We work every day to earn confidence by delivering not just quality, but practical benefits—predictable performance, straightforward handling, and honest support. Our whole approach, shaped by years of actual manufacturing practice, stands behind every supply of C-(1H-Imidazol-2-yl)-Methylamine we send your way.