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Methylguanidine Hydrochloride

    • Product Name Methylguanidine Hydrochloride
    • Alias N-methylguanidinium chloride
    • Einecs 208-771-2
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    165278

    Chemical Name Methylguanidine Hydrochloride
    Cas Number 139-02-6
    Molecular Formula CH6N3Cl
    Molecular Weight 111.54 g/mol
    Appearance White crystalline powder
    Solubility Soluble in water
    Melting Point 186-190°C
    Boiling Point Decomposes
    Storage Conditions Store at 2-8°C, tightly closed
    Purity Typically ≥98%
    Synonyms N-Methylguanidine hydrochloride
    Pubchem Cid 12238

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

    Packing & Storage
    Packing Methylguanidine Hydrochloride, 25g, supplied in a sealed, amber glass bottle with tamper-evident cap, labeled with hazard and handling instructions.
    Shipping Methylguanidine Hydrochloride is shipped in tightly sealed containers to protect from moisture and contamination. Packaging complies with chemical safety regulations. It is transported at ambient temperature, with clear hazard labeling, and accompanied by a Safety Data Sheet (SDS). Handle with care during transit to prevent damage or accidental exposure.
    Storage Methylguanidine Hydrochloride should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from moisture and incompatible substances such as strong oxidizers. Keep it at room temperature and protect from direct sunlight. Always label the container clearly and handle under appropriate chemical safety protocols to prevent accidental exposure or contamination.
    Application of Methylguanidine Hydrochloride

    Applications of Methylguanidine Hydrochloride in Industrial Manufacturing

    Methylguanidine Hydrochloride serves as a critical intermediate and functional additive in selected industrial sectors, supporting specific process chemistry and stringent downstream quality requirements. Below, as a direct manufacturer, we outline verified application sectors where this compound has proven practical utility, structured by main industrial scenarios. Each segment covers compliance, application formulation ranges, process fit, and the nature of end-use goods within the respective field.

    1. Pharmaceutical Synthesis: Antihypertensive Drug Intermediate

    In the pharmaceutical industry, Methylguanidine Hydrochloride acts as a building block for manufacturing certain antihypertensive agents, particularly guanidine-based derivatives. Production lines incorporate this material at the initial or intermediate condensation reaction steps. We support drug manufacturers by providing technical documentation for direct process use, ensuring that material traceability and impurity profiles meet the regulatory thresholds required in final product APIs.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • European Pharmacopoeia monographs (where applicable to APIs)
    • US FDA 21 CFR Parts 210/211 (for finished pharmaceuticals)
    • Chinese Pharmacopoeia standards for chemical drug intermediates

    Typical usage ratio

    • 0.8%–3.2% molar ratio based on total guanidine precursor input; adjusted according to the impurity burden and target API yield per batch process control.

    Downstream process integration

    • Introduced at early-stage condensation or cyclization steps, preceding subsequent alkylation and purification phases in pharmaceutical API production lines.

    Final product types

    • Active Pharmaceutical Ingredients for antihypertensive tablets and injectables
    • Bulk intermediates for generic antihypertensive formulations

    2. Agrochemical Manufacturing: Herbicide Intermediate

    Methylguanidine Hydrochloride is employed as a reagent in the synthesis of specialized herbicide molecules, notably those structured around substituted guanidines. Herbicide producers dose it directly into the intermediate coupling reaction via controlled addition to ensure high conversion and minimal byproduct formation. Batch records and COA traceability are maintained for downstream compliance.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • OECD Guidelines for the Testing of Chemicals (relevant to impurities and environmental fate)
    • ISO 9001:2015 certified QC systems for input materials
    • China GB/T 1604 Pesticide Technical Standards

    Typical usage ratio

    • 1.2%–4.5% w/w per reaction mass, fine-tuned according to targeted herbicidal activity and active ingredient synthesis batch size.

    Downstream process integration

    • Fed into guanidation or amidation synthesis units, typically upstream of formulation and granulation stages for technical concentrate production.

    Final product types

    • Pre-emergent and post-emergent herbicide technical grade material
    • Formulated herbicidal actives for crop-specific application

    3. Laboratory Diagnostics: Nitrogenous Reference Reagent

    Diagnostic reagent manufacturers incorporate Methylguanidine Hydrochloride within analytical kits as a reference standard for nitrogenous compound quantification tests. Quality control strictness and high lot-to-lot purity are mandatory, especially for laboratories adhering to ISO-accredited methodologies. The compound functions as a calibrator in automated biochemical analyzer lines for clinical or food-testing applications.

    Industry compliance standards

    • ISO 13485:2016 Medical Devices – Quality Management (for in vitro diagnostic components)
    • EN 13612 Analytical performance evaluation (medical devices)
    • US CLIA requirements for laboratory diagnostics
    • Chinese SFDA registration for clinical chemistry reagents

    Typical usage ratio

    • 0.01%–0.2% w/v, titrated to match the calibration curve requirements and lot-specific standard concentrations.

    Downstream process integration

    • Used in blending of calibration solutions and control reagents prior to analytical kit assembly and sterilization.

    Final product types

    • Clinical chemistry analyzer calibration standards
    • In vitro diagnostic kits for urea, creatinine, or nitrogenous compound testing

    4. Specialty Chemical Synthesis: Ligand and Catalyst Manufacturing

    Producers specializing in fine chemicals rely on Methylguanidine Hydrochloride for developing specific ligand precursors and catalytic systems. Here, the compound directly enters controlled synthesis routes to prepare guanidine-based ligands or organometallic catalyst supports. QC procedures track residual salt and synthetic byproducts to meet catalyst grade consistency for industrial partners.

    Industry compliance standards

    • ISO 9001:2015 Quality Management for chemical synthesis
    • REACH Regulation (EC) No. 1907/2006 regulatory compliance
    • Internal customer specifications for ligand and catalyst manufacturers
    • Hazardous Materials Regulations for chemical handling and transportation

    Typical usage ratio

    • 1.0%–5.0% stoichiometric ratio, set by catalyst formulation and desired ligand modification protocols.

    Downstream process integration

    • Charged at primary ligand formation stage, before metal complexation and catalyst purification or drying operations.

    Final product types

    • Guanidine-based chelating ligands for homogeneous catalysis
    • Organometallic precursor salts for specialty catalytic applications

    5. Chemical Research Reagents: Nitrogen Donor in Academic Synthesis

    Academic and industrial R&D laboratories utilize Methylguanidine Hydrochloride as a controlled nitrogen donor for mechanistic investigations and pilot-scale novel compound synthesis. Users refer to this material for reliable reactivity profiling and method validation, maintaining close attention to its purity and batch traceability in experimental reports and published protocols.

    Industry compliance standards

    • GLP (Good Laboratory Practice) guidelines for chemical research
    • University or institutional chemical safety protocols aligned with local legislation
    • ISO 17025:2017 requirements for laboratory competence
    • REACH SVHC notification (when scale exceeds research exemption)

    Typical usage ratio

    • Variable, most protocols employ 0.5%–2.5% based on required nitrogen equivalency, reaction mechanism, and scale-up feasibility.

    Downstream process integration

    • Measured into reaction vessels at stepwise additions for proof-of-concept synthesis, then monitored through analytical verification procedures before product isolation.

    Final product types

    • Novel guanidine-substituted compounds for publication
    • Reference samples and small-scale intermediates for further research
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    Certification & Compliance
    More Introduction

    Methylguanidine Hydrochloride: A Closer Look from the Manufacturer’s Perspective

    Understanding Methylguanidine Hydrochloride Production

    Manufacturing methylguanidine hydrochloride gives us a unique vantage point into what chemists and industry specialists search for in a high-purity reagent. Over the years, our team has worked hands-on with every step, from raw material sourcing to the final inspection of each lot, ensuring quality that doesn’t simply pass routine benchmarks but answers the specific expectations that research labs, biotech developers, and pharmaceutical process engineers bring with them.

    The standard model we produce, often specified by purity greater than 99%, comes as a white crystalline powder with a distinct, mild odor that most experienced chemists immediately recognize. We target a particle size distribution that flows well and dissolves consistently for applications where precise molarity makes a difference. Each batch receives quantitative assay validation through titration and high-performance liquid chromatography, offering assurance for anyone calibrating sensitive procedures.

    Why Purity and Consistency Matter in Methylguanidine Hydrochloride

    In downstream uses—ranging from protein modification studies to analytical research—the difference between a consistently manufactured methylguanidine hydrochloride and generic versions shows up in the repeatability of results. Researchers who set up multiple reaction runs in parallel need dependable baseline performance.

    Even a slight contamination by secondary amines or residual moisture can complicate molecular assays, delay parallel synthesis, or trigger batch failures in peptide coupling work. We take every step to minimize side-reactions and carryover, using low-temperature crystallization and dedicated glass-lined reactors designed so previous syntheses do not introduce cross-contaminants.

    From a hands-on perspective, consistency means more than checking purity stats on a certificate. Seasoned technicians in our facility recognize subtle visual hints that indicate a batch may be out of specification. Differences in luster or granule size prompt us to run additional FTIR or NMR checks—a real-world practice that ensures outlier material never leaves our facility.

    Applications: Real-World Experience in Lab and Industry

    Methylguanidine hydrochloride’s appeal lies in its versatility. For those working in the lab, its role as a strong chaotropic agent is key, denaturing proteins for extraction and purification. Enzyme mechanisms often require it to disrupt non-covalent bonds, especially during purification of nucleic acids or separation protocols supporting next-generation sequencing sample prep.

    In diagnostic research, methylguanidine hydrochloride assists with rapid cell lysis and selectively disrupting hydrogen bonding. Our manufacturing data show that medical diagnostic companies rely on our material for precise lysis buffer formulations, where batch-to-batch variation isn’t an option. Several bioprocess clients have noted more stable yields in immunoassay runs, attributing the improvement to our low trace impurity levels—something mass-market chemicals do not reliably offer.

    Customers in pharmaceutical synthesis report using this product to prepare intermediates for heterocyclic chemistry and guanidine-functionalized drugs. In these synthetic cascades, the amine group configuration and salt form influence overall reactivity. We calibrate our process to avoid over-drying, which would make weighing inaccurate and can foster static buildup, possibly risking airborne transfer in large-scale environments.

    Quality Control Backed by Real-World Experience

    Having worked with university researchers, industrial QC analysts, and scale-up teams, we understand that technical data only tells part of the story. What our partners often ask for is evidence that a manufacturer stands behind their claims. In our case, we routinely cross-reference stability and batch uniformity using long-term storage samples. Material that doesn’t meet year-over-year benchmarks gets decommissioned.

    After speaking with hundreds of end-users each year, we have refined our approach to batch release. Rather than depending solely on analytical certificates, we complement instrumentation with sample feedback. Sent batches undergo random sampling, with project leaders running critical application-specific tests—cell lysis times, spectral clarity, solubility checks—before bulk shipment proceeds. This approach, born from experience rather than textbooks, helps clients avoid surprises once the material is in their workflow.

    What Sets Our Methylguanidine Hydrochloride Apart

    Not every methylguanidine hydrochloride on the global market goes through the same rigorous protocols. Generic importers may repackage drum stock sourced from multiple facilities, resulting in unpredictable results. As the manufacturer, we maintain full control from raw ingredient verification—vetting suppliers using in-person audits and chemical fingerprinting—through each step of production.

    Customers tell us a major pain point with commoditized products is batch variability. Over the past decade, we’ve prioritized process upgrades: sealed-environment milling to avoid airborne moisture, double-filtration purification to lower organic carryover, and inline pH monitoring. These steps don’t only support purity; they make a difference when using methylguanidine hydrochloride for analytical calibration or pharmaceutical benchmarking, where the margin for error shrinks and every variable matters.

    Molecular biologists conducting DNA shearing or chemical denaturation find their results less reproducible with material cut from multiple suppliers. Our single-source, single-lot approach provides tighter performance windows. Our documentation crosses from the production line into the lab, meaning that if an experiment needs to be repeated, labs can trace exactly which lot went into which step—a traceability that import repackagers rarely offer.

    Handling and Storage: Lessons Learned Through the Years

    Having handled methylguanidine hydrochloride across scales, from kilogram samples for research to multi-ton drums for industry, we have learned the importance of reliable moisture protection. The salt form tends to attract water from the atmosphere, making dedicated climate-controlled storage critical. Failing to seal containers immediately after opening leads to altered consistency and decreased shelf life.

    Repeated feedback from customers who have used less well-managed alternatives confirms the value of desiccant-packed containers sealed with inert gas. Oxidative breakdown or caking from humidity quickly reduces effective concentration—something you don’t pick up until it throws off a critical titration or an extraction protocol underperforms. Our team checks each lot for residual water and includes handling guidance based on real in-factory and laboratory experience rather than generic documentation.

    Environmental and Safety Perspectives

    From a manufacturer’s standpoint, safety isn’t just about complying with the paperwork—it comes from year-round training and incident prevention. We’ve seen firsthand the minor mistakes that can happen when operators don’t understand the precise nature of methylguanidine hydrochloride: accidental skin contact, spills, or mixing with incompatible acids. Over decades, our protocol development—implementing closed transfer lines and well-explained operator checklists—has reduced near-miss events.

    Disposal practices show similar variation across customers, and we work directly with chemical waste processors to minimize downstream risks. Some generic versions come tainted with halogenated organics or mixed amines, leading to hazardous waste complications. Through our system of in-house purification and post-production verification, we limit hazardous contaminants, making downstream management more straightforward.

    On the environmental side, we have spent years developing a closed-loop solvent recovery process, keeping waste low and ensuring better outcomes for the communities near our plants. Beyond meeting regulatory benchmarks, we believe these practices create a better product that reflects our commitment to safety and long-term stewardship.

    Comparing Methylguanidine Hydrochloride to Similar Reagents

    Competent chemists evaluating reagents often compare methylguanidine hydrochloride to other guanidine derivatives, such as guanidine hydrochloride or methylguanidine sulfate. We have spent countless hours running head-to-head application trials. Our findings reinforce a few key distinctions.

    The presence of the methyl group in methylguanidine hydrochloride creates slightly different solubility characteristics and a modified reactivity profile compared to guanidine hydrochloride. In protein denaturant roles, this variant exhibits altered strength during chaotropic applications. Each subtlety can matter in finely tuned protocols for molecular biology, peptide chemistry, or pharmaceutical intermediate production.

    Methylguanidine sulfate, for example, introduces additional sulfate anions that may interfere with downstream reactions or create solubility issues in certain organic media. We often receive requests from customers who tried to substitute sulfate or carbonate-based salts in their system—only to deal with inconsistent assay results or filtration blockages. Our production team fields questions about these differences and offers hands-on advice tailored to actual lab feedback, not just what a data sheet suggests.

    While some competitors attempt to market off-spec methylguanidine hydrochloride as interchangeable with lower-purity forms, our work with repeat customers shows this shortcut often results in longer troubleshooting cycles. Research teams who tried switching between products frequently turn back to us after losing days of work to failed reactions. The robust documentation, traceability, and real-world experience embedded in our product lines mark the difference between smooth runs and costly downtime.

    Solving Sourcing and Reliability Challenges

    Any research team or production manager sourcing methylguanidine hydrochloride faces potential pitfalls—delayed shipments, variable specification, or incomplete documentation. Having built up a manufacturing network that stretches from raw ingredients to global logistics, we are positioned to handle these real-world challenges head-on.

    One of the most common issues we see comes from rush buying through third-party traders. Middlemen may not verify storage conditions or expiry status before reselling to new markets. We work without intermediaries, reducing the risk of damaged, outdated, or tampered material reaching critical projects. On the rare occasion that supply logistics encounter unexpected disruptions, our in-house team updates clients with factual timelines and proposed alternatives based on actual production schedules.

    Real supply reliability comes from eliminating guesswork. Over the years, we have refined inventory forecasting using data models built on previous ordering patterns and seasonal demand cycles. For projects with stringent timeline requirements, we can hold safety stock under controlled conditions—providing assurance for high-stakes clinical, diagnostic, or commercial manufacturing campaigns.

    What Experience Has Taught Us: Building Trust with Every Batch

    Our journey in the fine chemicals industry has shown that trust relies on transparency, communication, and continuous feedback. Clients reach out with diverse application needs, and our technical staff engage directly with queries—sharing not just the metrics from quality tests, but stories from our routine. Whether it’s helping a new startup scale their synthesis or troubleshooting an established biotech’s workflow, our collective memory forms the backbone of reliable methylguanidine hydrochloride production.

    Strict regulatory compliance follows, but our experience on the shop floor and in the analytical suite creates a deeper guarantee. From annual validation of our calibration routines to regular review sessions for batch records, every step bends toward real-world accountability. The years have proven that any lapse in communication or quality lands hardest on the client’s project; for us, a tight feedback loop and open dialogue eliminate repeating errors and refine our future output.

    Forward-Looking Approaches and Industry Collaboration

    We continue to evolve our process, encouraged by feedback from pharmaceutical developers, academic researchers, and industrial polymer chemists. Whenever a new regulation or lab technique demands a shift in specifications, we’re quick to trial expanded testing regimes and trace new impurity pathways. Our collaboration with end-users allows our methylguanidine hydrochloride to remain relevant as protocols shift and technology advances.

    Some clients share their custom protocols or ask us to evaluate the reagent’s performance in pilot-scale runs before launch. These partnerships underpin advancements in production—sometimes identifying previously unseen impurities, or opportunities to fine-tune drying and packaging steps that further stabilize our product. We recognize that a dynamic manufacturing process cannot remain static; instead, it follows the demands and innovations of those at the project’s front line.

    Conclusion: Experience Shapes Quality and Trust

    Producing methylguanidine hydrochloride means more than synthesizing a molecule to specification. Our job requires vigilance, hard-earned knowledge, and honest dialogue with each customer. The differences between our product and mass-market alternatives result from decades spent refining every step, learning from every mistake, and adapting to a changing field where every lab, process line, and research objective adds to a shared body of expertise. Our commitment means that every batch offers not just high purity and consistent performance, but also the backing of a team invested in your project’s success.