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Tetramethylguanidine Chloride

    • Product Name Tetramethylguanidine Chloride
    • Alias TMG-Cl
    • Einecs EINECS 214-275-1
    • 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

    532732

    Chemical Name Tetramethylguanidine Chloride
    Synonyms 1,1,3,3-Tetramethylguanidine hydrochloride
    Cas Number 536-37-0
    Molecular Formula C5H13N3·Cl
    Molecular Weight 151.63 g/mol
    Appearance White to off-white crystalline powder
    Melting Point 138-142°C
    Solubility Soluble in water
    Boiling Point Decomposes before boiling
    Density 1.10 g/cm³ (approximate)
    Storage Conditions Store in a cool, dry place
    Odor Odorless
    Ph 8-10 (10% aqueous solution)
    Ec Number 208-628-9

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

    Packing & Storage
    Packing Tetramethylguanidine Chloride is supplied in a 25g amber glass bottle, sealed with a plastic cap, and labeled with hazard information.
    Shipping Tetramethylguanidine Chloride is shipped in tightly sealed, chemical-resistant containers to prevent moisture absorption and contamination. It should be transported as a hazardous material, adhering to local regulations, with appropriate labeling and documentation. Temperature and handling precautions must be observed to ensure safety during transit. Keep away from incompatible substances.
    Storage Tetramethylguanidine chloride should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from moisture, heat sources, and incompatible chemicals such as oxidizing agents and strong acids. It is important to keep the chemical away from direct sunlight and store it at ambient temperature. Proper labeling and secondary containment are recommended to prevent accidental exposure or spillage.
    Application of Tetramethylguanidine Chloride

    Applications of Tetramethylguanidine Chloride in Industrial Manufacturing

    Tetramethylguanidine Chloride (TMG-Cl) is an advanced organic base used as a key process additive and catalyst in specialized chemical synthesis fields. As a direct manufacturer with established production routes, we supply material meeting stringent global standards for industrial customers seeking consistent quality, controlled purity, and technical documentation. Below are the principal downstream industries where this compound delivers definitive performance value in real manufacturing environments.

    1. Pharmaceutical Intermediate Synthesis

    Pharmaceutical manufacturers employ Tetramethylguanidine Chloride as a nucleophilic catalyst and phase transfer agent in the synthesis of critical heterocyclic intermediates, especially in the formation of imidazoles, pyrimidines, and quinazolines. The material facilitates deprotonation and ring closure reactions in medicinal chemistry pipelines, where precision in purity and residual salt content directly impact API (Active Pharmaceutical Ingredient) qualification. Customers typically utilize in integrated GMP-compliant facilities to address regulatory and customer audit requirements for traceability and impurity profiles.

    Industry compliance standards

    • ICH Q7A Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP–NF and European Pharmacopoeia general monographs for residual solvents
    • EudraLex Vol. 4 GMP Guidelines

    Typical usage ratio

    • 0.5%–3% relative to total reaction mass; tuning based on target intermediate’s reactivity and impurity profile requirements

    Downstream process integration

    • Added during nucleophilic substitution or cyclization steps in multi-step active pharmaceutical intermediate synthesis

    Final product types

    • Imidazole-based APIs
    • Pyrimidine pharmaceutical intermediates
    • Quinazoline derivatives for oncology and antiviral applications

    2. Agrochemical Active Ingredient Production

    In the agrochemical industry, formulators depend on Tetramethylguanidine Chloride to drive alkylation and condensation steps in the production of crop protection agents, enabling efficient catalyst cycles and improved batch yields. Specific herbicide and fungicide molecules incorporate intermediates synthesized using TMG-Cl because of its strong basicity and controlled nucleophilicity, which suppress unwanted side reactions during large-volume continuous synthesis runs, particularly under cGMP and Responsible Care protocols.

    Industry compliance standards

    • FAO/WHO Technical Guidelines for Pesticide Specifications
    • ISO 9001:2015 Quality Management Systems
    • REACH Regulation (EC) No 1907/2006 (Europe)

    Typical usage ratio

    • 0.7%–2.5% by weight relative to substrate; adjusted based on target molecule complexity and batch scale

    Downstream process integration

    • Dosed into condensation reactors at the base-catalyzed alkylation stage during technical grade active ingredient synthesis

    Final product types

    • Triazine-based herbicides (e.g., atrazine intermediates)
    • Pyridine fungicide precursors
    • Sulfonylurea herbicide intermediates

    3. Specialty Polymer and Resin Manufacturing

    Producers of high-performance resins and polymers, especially those used in electronics and advanced coatings, utilize Tetramethylguanidine Chloride for controlled polymerization of heterocyclic monomers and curing of epoxy resins. The compound functions as an advanced guanidine catalyst, sharply accelerating ring-opening reactions while providing a well-monitored thermal profile throughout process reactors. Its controlled basicity preserves integrity of sensitive monomers and contributes to consistent molecular weight distributions, which are essential for specialty coatings and encapsulants in regulated sectors.

    Industry compliance standards

    • RoHS Directive 2011/65/EU
    • UL 94 Flammability Standard (for electronic encapsulants)
    • ISO 14001 Environmental Management Standard

    Typical usage ratio

    • 0.3%–1.0% depending on monomer type and targeted polymer chain length; application trials determine final dosage

    Downstream process integration

    • Introduced as a catalyst at the pre-polymerization or chain extension stage in bulk or solution polymerization set-ups

    Final product types

    • Epoxy potting resins for electronic device encapsulation
    • Polyimide films for flexible circuit boards
    • UV-curable coatings for optical fiber sheets

    4. Silane Coupling Agent Modification

    Manufacturers of functionalized silane coupling agents and specialty surface modifiers apply Tetramethylguanidine Chloride in the transesterification or nucleophilic substitution stages to obtain more reactive silanol derivatives. This step is critical for the electronics, aerospace, and automotive sectors, where precisely modified surface active agents must meet high adhesion and thermal stability requirements. The material’s reliable catalytic performance results in reproducible surface treatment agents with tightly controlled functional group density, supporting high-throughput silanization at downstream customer sites.

    Industry compliance standards

    • ASTM D2578 Surface Energy Test Method
    • ISO 12944 Corrosion Protection Coating Standards
    • UL 746B Standard for Polymeric Materials

    Typical usage ratio

    • 0.2%–0.8% on active silane content; determined by silane substrate reactivity and desired conversion rate

    Downstream process integration

    • Added at the substitution or hydrolysis stage in silane functionalization reactors prior to purification and packaging

    Final product types

    • Silane adhesion promoters for automotive glass bonding
    • Fiber surface treatment agents for composite manufacturing
    • Chemically modified siloxanes for microelectronic wafer processing

    5. Fine Chemical Synthesis of Dyes and Pigments

    Producers in the fine chemical sector, especially those focused on specialty dyes and pigments for electronic, textile, and printing applications, incorporate Tetramethylguanidine Chloride during key steps to facilitate nucleophilic aromatic substitution and cyclization. The compound proves especially valuable for driving high selectivity in diazo and anthraquinone dye syntheses, minimizing side-product formation and achieving reproducible shade and purity essential for global market acceptability. Traceability and analytical support are provided throughout process validation in accordance with both customer and national quality directives.

    Industry compliance standards

    • OEKO-TEX Standard 100 (textile dyes)
    • REACH Regulation (EC) No 1907/2006
    • ISO 9001:2015 Quality Management Systems

    Typical usage ratio

    • 0.4%–2.0% depending on dye class and substrate reactivity; ratio tailored through QC-monitored batch trials

    Downstream process integration

    • Charged prior to or during key amination/condensation reactions in pigment and dye synthesis reactors

    Final product types

    • Anthraquinone and azo dyes for LEDs and LCD displays
    • Colorant concentrates for high-end printing inks
    • Reactive dyes for technical textile coatings
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    Certification & Compliance
    More Introduction

    Tetramethylguanidine Chloride: Experience from the Manufacturer’s Bench

    Introducing Tetramethylguanidine Chloride: Real-World Focus on Utility and Purity

    As a chemical manufacturer, we have watched Tetramethylguanidine Chloride earn respect for its performance in chemical synthesis. This compound, often abbreviated as TMG·HCl or referred to by its IUPAC title, delivers consistent results in demanding environments. Chemists especially rely on it in organic synthesis, where reactivity, solubility, and reproducibility matter day in and out. Unlike resellers, we see its character form in each batch, shaped by raw material handling, process control, and attention to purification. TMG·HCl isn’t just a commodity; success depends on the fine details often easily overlooked outside the plant floor.

    How Manufacturing Insight Drives Consistency

    Downtime or inconsistency threatens productivity. Delivering TMG·HCl at scale rarely comes with shortcuts. The difference between freshly isolated material and product exposed to moisture or excessive heat shows up first in the lab—sometimes in yields, sometimes in downstream processing headaches. High assay percentages and stable physical forms become vital. For many years, our teams have optimized reaction times and purification routes for TMG·HCl to achieve fine, free-flowing powders that pour cleanly and dissolve without fuss.

    Product Form and Typical Specifications

    TMG Chloride emerges from our reactors as a white to off-white crystalline powder—a reliable appearance when produced under tight environmental controls. Even though the molecular formula (C5H13N3·HCl) is universal, every chemist who receives a lot looks for low water content and a high purity profile on their COA. Analytical content usually exceeds 99% by HPLC or titration, but we also follow up with moisture tests and regularly consult our trained eyes for texture and flow. Our methods avoid residual starting materials—an uncommon problem with less-established processes, but one to watch for with guanidine derivatives since trace levels of dimethylformamide or unreacted guanidine can show up in less controlled environments.

    Batch consistency isn’t accidental. Every kilogram tells a story of diligent drying and careful packaging; this reduces risk of caking or degradation in storage—two problems that haunt distributors and resellers more often than those of us with direct process oversight. Product stability doesn’t just save time; it reduces waste and unexpected failures during scale-up.

    Where Tetramethylguanidine Chloride Earns Its Place

    Organic synthesis rewards durable, predictable reagents. TMG·HCl steps into various roles: as a phase transfer catalyst; an intermediate in pharmaceutical synthesis; and a nucleophilic base in reactions that need both strength and selectivity. Its performance as a non-nucleophilic base outpaces many traditional amine hydrochlorides in reactions sensitive to moisture or other salts. TMG·HCl’s melting and solubility characteristics fit into modern pharmaceutical synthesis, including API development, where measured delivery and traceability matter.

    What stands out in daily manufacturing? Our teams hear regularly from bench chemists who notice faster reactions with cleaner crude yields when switching from traditional guanidines to TMG·HCl. The ability to perform strong deprotonation or act as a buffer, without introducing competing nucleophilicity or myriad byproducts, keeps its application list long.

    In our facility, we listen closely to customer feedback: does the batch dissolve in water or alcohols without haze? Does it arrive clump-free and pourable, even after weeks in storage? These questions reflect real-world problems we address through regular process review and post-packing QC checks.

    Tetramethylguanidine Chloride’s Distinct Properties

    Many seasoned chemists ask for differences between TMG·HCl and similar bases, including 1,1,3,3-Tetramethylguanidine (TMG free base) or guanidine hydrochloride. TMG·HCl brings cationic strength without the safety or volatility concerns tied to free TMG, which is caustic and irritating to handle. Its hydrochloride salt form is less volatile, safer for shipping, and straightforward to store. For reactions sensitive to free amines, TMG·HCl offers a reliable entry point thanks to its stable crystalline form and low hygroscopicity.

    Guanidine hydrochloride acts as a powerful denaturant or protein unfolding agent in biotech applications, but its ionic strength, solvation profile, and basicity differ sharply from that of TMG·HCl. Our direct experience identifies that TMG·HCl serves best in organic transformation and pharmaceutical synthesis, not as a protein chaotrope—the two products, though similar in name, occupy very different spaces.

    As a practical matter, reaction byproducts and product workups vary between these bases. TMG·HCl often avoids emulsions and persistent salt residues seen in guanidine hydrochloride–mediated processes. Chemists committed to process development value those savings in time and effort.

    Technical Nuance Only Seen at Scale

    Small-batch syntheses often mask problems that emerge in commercial process runs. Scale-up labs know TMG·HCl is susceptible to caking if too much time passes between drying and packaging; even minor humidity spikes can lead to clumping that frustrates automatic feeders. We keep careful records and maintain controlled environments to avoid these pitfalls, and constant feedback from both our own internal users and our institutional customers helps us improve. Over years of process refinement, even minute temperature drift during crystallization has been linked to shifts in lattice formation—minute enough to go unnoticed by the end-user, yet significant on the plant floor.

    Residue minimization is another point where manufacturers outpace simple repackagers. By running advanced filtration and washing sequences, it’s possible to produce ultra-low residue grades to meet API or advanced synthesis needs. Analytical teams check for heavy metals, volatile organic solvents, and other trace contaminants that threaten sensitive downstream processes.

    The Unseen Impact of Supply Chain Control

    Supply chain integrity directly shapes quality. As a manufacturer, we benefit from upstream chemistry knowledge. Sourcing clean raw guanidine, predrying it, and controlling reagent addition steps enables us to adjust lot-to-lot, watching for slight changes that could otherwise snowball into process headaches. Handling oxidizers, strong acids, and bulk TMG always involves safety infrastructure—respirators, neutralization baths, and continuous monitoring for leaks or spills. Regulatory demands also shape our workflow, so every drum of TMG·HCl comes with full batch traceability and complete documentation.

    Sustainability and Waste Handling Concerns

    Industry-wide, environmental responsibility pushes manufacturers to find better ways to minimize process waste and lower emissions. Chloride-based products commonly generate high-salt water streams; we invest in recovery and remediation systems to cut down on byproduct salt discharge. Our approach to process water treatment now includes closed-loop recovery for rinse streams and secondary containment for accidental releases. This mitigates our environmental footprint and keeps us compliant with regulatory audits.

    Product loss at any stage—spillages, failed drying, improper storage—represents lost effort and environmental burden. Continuous process oversight and practical training for handling, storage, and response reduce these risks. Our warehouse maintains controlled humidity, and all packaging follows a carefully sequenced system that minimizes oxygen and moisture exposure before sealing—no shortcuts here.

    Real Safety Observations from the Plant Floor

    For operators and users alike, TMG·HCl requires standard PPE—gloves, goggles, proper ventilation. Comparing notes with long-time users and internal safety staff, we have found dry powder TMG·HCl less caustic and volatile than free TMG base, which is a riskier inhalation hazard. Still, accidental spills do occur, and our experience with cleanup and neutralization underscores the importance of prompt, thorough response with proper equipment. In rare cases, misuse of incompatible metals or hasty water washdowns has led to corrosion or stubborn residues—painful lessons that sharpen our internal training and recommendations to synthesis teams.

    Any batch destined for export faces an audit of safety documentation and labeling. We print hazard identification prominently and include updated Safety Data Sheets, shaped by manufacturer experience rather than third-party summaries. Keeping downstream users informed reduces accidents and expedites emergency response if needed.

    Feedback Loops from Process Chemists and End Users

    Our work isn’t finished when a drum leaves our dock; customers bring back valuable process observations: solubility in mixed solvents, reactivity with novel substrates, handling quirks at pilot scale. Several partnerships have led to improvements in our drying cycles and adjustments to particle size distribution based on feedback pointing to easier transfer or improved dissolution rates. Process limitations, such as issues with trace iron or other metallic contaminants affecting API purity, have prompted investments in new filtration modules.

    Unlike resellers, who gather reports third-hand, we invite direct communication between manufacturing chemists and customers. Every process hiccup—sticky powder, odd color changes, delayed solubility—triggers a discussion and a chance to improve. That back-and-forth nurtures loyalty and produces a better product with each improving cycle.

    Applications Supported by TMG·HCl’s Profile

    Academic and industrial labs order TMG·HCl for amide couplings, catalyst preps, and rare organic transformations. In the pharma sector, its purity and low moisture contribute to crude yield improvements—yield increases that might seem minor in the lab, but scale to substantial output at batch scale. Our long engagement with client chemists has highlighted its effectiveness in reactions sensitive to basicity and ionic strength. Homogeneity batch-to-batch prevents sudden failures or unplanned reruns, cutting down on lost material and wasted labor.

    Some customers once used TMG free base and have switched to TMG·HCl due to improved safety and storage convenience, especially in humid climates or shipping across borders. Even slight reductions in product volatility or stability translate into cost savings for logistics and quality control.

    Emerging fields—such as advanced polymer synthesis or electronic material R&D—have sparked demand for guanidinium salts, including TMG·HCl, where trace metal control and defined crystallinity help drive innovations. We engage directly with these users, sharing analytical data and process recommendations.

    Nuances in Processing and Packaging

    From bulk drums to modest lab bottles, form and function cannot be separated. We have seen poorly packaged TMG·HCl lose flowability and develop persistent clumps that frustrate precisely dosed syntheses. For consistent results, our plant uses nitrogen-blanketed filling lines and heat-sealed moisture-barrier bags, often double-packed for large runs. Every container, large or small, receives a unique identifier that links to batch documentation, analytical results, and trace histories of storage and transfer.

    Technical rigor, not marketing, guides packaging improvements. We track humidity and temperature exposure from pack-out to delivery, so we know which shipping environments best preserve product quality. Working with reliable carriers who understand chemical logistics further reduces breakage, contamination, or temperature-related degradation.

    Comparing TMG·HCl to Other Guanidine and Base Reagents

    Process chemistry often cycles through different bases before settling on the best fit. We field calls weekly asking why not stick with sodium hydroxide, potassium carbonate, or simpler amine salts. Our routine answer looks at stability, reactivity, compatibility, and ease of use. TMG·HCl is easier to dose than free TMG and less hazardous than caustic alkalis. It handles moisture better and stores longer without breaking down.

    Compared to guanidine hydrochloride, TMG·HCl’s lower hygroscopicity and more defined melting range matter for advanced syntheses, avoiding troublesome slurries and hard-to-handle residues. Unlike volatile amines, TMG·HCl doesn’t present storage headaches once packed tightly and shielded from light and air. These differences aren’t academic—they drive time and cost savings at every step from procurement to waste management.

    Scaling TMG·HCl Production: Challenges and Solutions

    As demand for guanidinium derivatives rises, plant-scale challenges mount. Running TMG·HCl synthesis requires tight control of exotherm during salt formation, or else product color or purity suffers. We use jacketed reactors and dedicated temperature monitoring throughout charge and quench stages, always logging deviations for fast troubleshooting. Skilled operators anticipate foaming or gas evolution—issues that cause problems in less closely managed plants.

    Another key: wash cycles and drying times. Too little, and trace mother liquor ruins purity. Too much, and the product cakes or powders out unevenly, complicating downstream handling. By tuning every process parameter, and calibrating drying ovens and nitrogen flow, we cut down on batch failures and unpredictable yields.

    Optimizing production scheduling also ensures freshly synthesized product is dried and packaged without delay, blocking out time-sensitive runs to avoid overlaps or mischarging. This approach comes from years of feedback—seeing where small delays or mix-ups have consequences for customers who need dependable deliveries.

    Advances in Analytical Testing for TMG·HCl

    Routine testing in our labs includes HPLC purity, moisture by Karl Fischer titration, and heavy metal analysis by ICP-MS or AAS. Each of these methods, developed and verified in partnership with R&D teams, evolved in response to actual end-user findings—where even minor drift in water content impacted downstream reaction reproducibility. Our QA teams routinely stress-test retained samples by storing them under adverse conditions and examining changes in physical and analytical properties.

    Transparency builds trust. We release test results alongside every batch, enabling chemists to adjust their own reaction parameters with confidence. Regulatory-driven testing around nitrosamine precursors or trace formaldehyde, even when below statutory limits, further enables use in sensitive pharmaceutical or biotech environments, supporting industry and public health objectives.

    Customer Education and Product Knowledge

    Most success stories with TMG·HCl rest on open communication. Training sessions, user guides, and site visits help bridge the knowledge gap between plant floor and R&D labs. We provide storage and handling tips—keep sealed, minimize air exposure, and store in temperature-controlled spaces—to help customers avoid preventable quality issues. Our technical staff answer queries from researchers and scale-up engineers, sharing lessons drawn from years of operational troubleshooting.

    Rather than relying on generic, third-party data, our support draws from factory experience—what survives shipping, what reacts to glassware or plastic, and what shows up during scale-up that never appeared at the bench. Customers value actionable, honest feedback, especially where risk of product loss or safety is at stake.

    Shaping the Next Generation of TMG·HCl Production

    By staying engaged with scientific communities and regulatory bodies, we continue to refine TMG·HCl—improving throughput, safety, and sustainability. Ongoing investment in automation improves reproducibility, while partnerships with academic and industrial researchers unlock new applications. Every improvement—no matter how small—translates back into longer shelf life, lower waste production, and smoother customer scale-up efforts.

    Every day, hands-on experience and open feedback loops steer product improvement, making Tetramethylguanidine Chloride not only a staple for organic chemists but also a benchmark for responsible, science-driven chemical manufacturing.