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Tetramethylguanidine Dihydrogen Phosphate

    • Product Name Tetramethylguanidine Dihydrogen Phosphate
    • Alias TMG dihydrogen phosphate
    • Einecs 629-019-4
    • 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
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    Specifications

    HS Code

    730419

    Chemical Name Tetramethylguanidine Dihydrogen Phosphate
    Cas Number 82941-13-1
    Molecular Formula C5H15N3·H3PO4
    Molecular Weight 197.18 g/mol
    Appearance White to off-white solid
    Solubility Soluble in water
    Melting Point Decomposes above 200°C
    Density 1.34 g/cm3 (approximate)
    Storage Conditions Store in a cool, dry place, tightly closed
    Synonyms 1,1,3,3-Tetramethylguanidine phosphate
    Hazard Classification Irritant

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

    Packing & Storage
    Packing Tetramethylguanidine Dihydrogen Phosphate, 100g, is packaged in a sealed, amber glass bottle with a secure screw cap for safe handling.
    Shipping Tetramethylguanidine Dihydrogen Phosphate is typically shipped in tightly sealed, chemical-resistant containers, often under cool and dry conditions. Packaging complies with hazardous material regulations due to its corrosive nature. Proper labeling, documentation, and transportation by certified carriers are required to ensure safety and regulatory compliance during domestic and international shipments.
    Storage Store Tetramethylguanidine Dihydrogen Phosphate in a tightly sealed container, in a cool, dry, and well-ventilated area away from moisture and incompatible substances such as strong acids and oxidizers. Protect from physical damage and sources of ignition. Clearly label the container and avoid exposure to humidity to prevent decomposition. Always follow standard laboratory chemical storage protocols and use proper personal protective equipment.
    Application of Tetramethylguanidine Dihydrogen Phosphate

    Applications of Tetramethylguanidine Dihydrogen Phosphate in Industrial Manufacturing

    Tetramethylguanidine Dihydrogen Phosphate, produced in our integrated facility, is recognized for its stability and catalytic performance in industrial synthesis. Our manufacturing partners utilize this material in select high-value sectors where strong basicity and phosphate properties advance formulation and process reliability. Below, we summarize key downstream deployment scenarios within chemical and pharmaceutical production, aligned with recognized compliance, technical formulation, and process workflows.

    1. Pharmaceutical Intermediate Synthesis

    Pharmaceutical manufacturers deploy our material as an organocatalyst for phosphorylation reactions, specifically in the synthesis of nucleotide and nucleotide analog intermediates. Detailed monitoring at the stage of nucleoside modification maximizes reaction control, so this phosphate salt’s solubility and low water content suit GMP synthesis lines. The chemical enters the process post-activation of nucleosides, catalyzing phosphate group introduction prior to subsequent purification steps. Careful selection and quantification at the process development stage minimize batch variability and guarantee lot traceability through the regulated pipeline.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU GMP, Annex 1 (Manufacture of Sterile Medicinal Products)
    • 21 CFR Part 211 (US FDA cGMP for Finished Pharmaceuticals)
    • Ph. Eur. (European Pharmacopoeia) reference for raw material control

    Typical usage ratio

    • Used at 0.5–2.2 molar equivalents relative to the nucleoside substrate—dosage depends on reaction kinetics and purity of starting materials, as determined during R&D scale-up.

    Downstream process integration

    • Added directly into phosphorylation reaction batch after nucleoside activation; followed by controlled temperature reaction and solvent-based workup; remnant is removed in downstream chromatographic purification prior to API crystallization.

    Final product types

    • Purified nucleotide intermediates
    • Nucleotide-based pharmaceutical precursors (for antiviral and anticancer drugs)
    • Oligonucleotide API building blocks
    • Specialty fine chemical intermediates for drug pipelines

    2. High-Performance Polymer Catalyst

    Producers of specialty polyurethanes and polyether resins incorporate Tetramethylguanidine Dihydrogen Phosphate as a strong basic catalyst during prepolymer manufacturing steps. This phosphate-guanidine salt advances the chain extension and crosslinking efficiency, especially in elastomer, foam, and adhesive resin lines. Accurate metering ensures narrow molecular weight distribution and reproducible mechanical properties in the final formulation. Implementation requires close engineering process control, including in-line FTIR monitoring for endpoint confirmation and robust post-cure for product safety.

    Industry compliance standards

    • ISO 9001:2015 (QMS for Polymer Manufacturing)
    • REACH Regulation (EC 1907/2006, for use and safety documentation)
    • ASTM D3574 (Standard Test Methods for Flexible Cellular Materials—Slab, Bonded, and Molded Urethane Foams)
    • GHS/CLP chemical hazard classification for automotive and industrial polymers

    Typical usage ratio

    • Usually dosed at 0.02–0.15% by total resin weight (200–1500 ppm), adjusted for resin type, isocyanate index, and catalyst loading trials for reactivity control.

    Downstream process integration

    • Introduced during prepolymer blending phase before chain extension; ensures homogenous mixing; excess removed in devolatilization or downstream devol batch units; final content verified via residual catalyst testing.

    Final product types

    • Polyurethane foams (automotive, bedding, and industrial grades)
    • Polyether and polyester resins
    • Flexible and semi-rigid polymer blocks
    • Two-part adhesive systems

    3. Electronic Grade Chemical Processing

    Manufacturers in the electronics sector rely on Tetramethylguanidine Dihydrogen Phosphate for high purity etching baths and as an ultra-trace-grade buffer in fabrication of semiconductors. Stringent impurity requirements necessitate rigorous filtration and particle size monitoring upstream. Our material is applied in photoresist stripping and residue removal stages, with special attention to ionic contamination and metal impurities. Each production lot is documented for trace metals and organic residue limits per electronics-grade standards.

    Industry compliance standards

    • SEMI C93 (Specifications for Phosphoric Acid Used in Semiconductor Processing—analogous requirements used for all phosphate chemistry)
    • IEC 61340-5-1 (Electrostatic Control—Cleanroom Protocols)
    • RoHS Directive (EU, for restricted substance management in electronic assemblies)
    • ISO 14644 (Cleanrooms and Associated Controlled Environments)

    Typical usage ratio

    • For photoresist stripper baths: 0.1–0.45 M concentration; batch volume tailored to substrate surface area and impurity loading; recirculation and replenishment governed by in-line titration.

    Downstream process integration

    • Charged directly to formulating tanks for wet processing; utilized during post-lithography cleaning sequences; works in combination with solvent blends; recycled and filtered to maintain prescribed ionic levels between process runs.

    Final product types

    • Integrated logic and memory chips (finished wafers)
    • Flat-panel display circuit substrates
    • High-density printed wiring boards
    • Wafer surface preparation consumables

    4. Laboratory and Diagnostic Reagent Production

    Diagnostic product manufacturers use our phosphate-guanidine compound in the preparation of enzyme reaction buffers and as a pH stabilizer in in vitro diagnostic kits. The reliable buffering capacity ensures consistency for molecular detection protocols, including PCR reagent formulations and nucleic acid extraction columns. Cleanroom manufacturing controls cross-contamination and batch labeling supports full regulatory traceability. Downstream, the product is introduced during component mixing under controlled humidity and temperature with lot-based verification by functional assay.

    Industry compliance standards

    • ISO 13485:2016 (Medical device—QMS for Diagnostic and Laboratory Reagents)
    • US FDA 21 CFR Part 820 (Quality System Regulation for Medical Devices and IVDs)
    • CLSI QMS01-A4 (Clinical Laboratory Standards Institute—Quality Management System)
    • CE Marking (EU IVD Directive 98/79/EC compliance for finished kits)

    Typical usage ratio

    • Formulated at 10–100 mM in reaction buffers; specific concentrations determined by enzyme activity and downstream compatibility analysis; verified by pH titration and functional performance testing.

    Downstream process integration

    • Weighing and dissolution in sterile vessels; buffer solution is filtered and then portioned into kit batch lots; enters filling lines prior to lyophilization or liquid packaging; stability verified under accelerated storage.

    Final product types

    • PCR and qPCR reagent kits
    • Nucleic acid extraction spin columns
    • Molecular diagnostic buffer concentrates
    • Clinical chemistry analyzer reagents

    5. Specialty Agrochemical Synthesis

    Producers of advanced crop protection agents integrate Tetramethylguanidine Dihydrogen Phosphate as a phase transfer catalyst during the synthesis of organophosphorus intermediates. Accurate catalyst addition enhances selectivity and conversion rate for key step phosphorylation, supporting downstream formulation of water-dispersible granules and active ingredient concentrates. Batch production uses close in-line monitoring for catalyst depletion and byproduct management, supporting full lot traceability for agrochemical regulatory review.

    Industry compliance standards

    • FAO/WHO Specifications for Pesticides (FAO/WHO Joint Meeting on Pesticide Specifications)
    • ISO 9001:2015 (for Agrochemical Manufacturing and Quality Management)
    • Regulations (EC) No 1107/2009 (EU Authorization of Plant Protection Products)
    • US EPA 40 CFR Part 158 (Data Requirements for Pesticides)

    Typical usage ratio

    • Added at 0.1–1.0 mol% relative to limiting reagent; precise ratio determined by target conversion over time and batch size; monitored in pilot scale and established via kinetic assays.

    Downstream process integration

    • Catalyst charged at phosphorylation reaction initiation; mixed under controlled temperature; removed during aqueous workup and neutralization before product isolation and granulation stages.

    Final product types

    • Organophosphorus pesticide intermediates
    • Water-dispersible granule concentrates
    • Emulsifiable crop protection formulations
    • Agricultural active ingredient stock solutions
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    Certification & Compliance
    More Introduction

    Tetramethylguanidine Dihydrogen Phosphate: In-House Experience, Application, and Added Value

    Tetramethylguanidine dihydrogen phosphate, often referred to as TMG·2H3PO4, holds a distinct place in the toolbox of synthetic organic chemists. Here at our production site, we focus on bringing a precise understanding of this compound's properties and performance to our users. Our years in the chemical industry have reinforced just how important attention to detail is when developing reagents that must not only perform in the lab but also scale up to meet the daily demands of manufacturing or research environments.

    Direct Experience with TMG·2H3PO4

    We manufacture Tetramethylguanidine dihydrogen phosphate in controlled batches, using consistent starting materials. Our formulations focus on supporting chemists and process engineers working on complex catalytic or synthetic needs. The compound emerges as an off-white crystalline solid, stable under normal storage conditions if kept dry and away from strong oxidizers. Each batch runs through checks for purity, free amine content, solubility in common solvents, and water content. Our routine work with this compound has helped us streamline production so that customers can rely on a clean product.

    In the chemical synthesis world, TMG·2H3PO4 brings distinct advantages. Its role as a strong, non-nucleophilic base comes from the guanidine backbone and phosphate counterion. For us, hands-on lab experience highlighted how its relatively high basicity and unique ionic structure change reaction pathways. For example, in base-promoted esterifications or certain amidation protocols, TMG·2H3PO4 gives higher yields or cleaner products compared to options like simple tertiary amines or inorganic bases. Our chemists rely on its fast dissolution in polar solvents such as methanol, DMF, or DMSO, allowing for ease of use in scale-up conditions.

    Key Technical Properties: Delivered from the Source

    Our product typically measures above 98% purity by HPLC and melting point consistency. Moisture checks, important for bench-level reproducibility, show levels below 0.5% for standard batches. The compound maintains its physical integrity under nitrogen storage. Measuring its solubility profile, we observe complete dissolution in methanol and ethanol, as well as DMSO. From experience, users benefit most when storing it under a dry atmosphere because atmospheric moisture may influence both solubility and reactivity.

    We dissolve TMG·2H3PO4 for site trials to test its compatibility with substrates carrying delicate functional groups. Because the phosphate counterion introduces new acidic conditions within the medium, adjustment of pH-sensitive steps might become necessary. This has proven useful for us and our clients in projects where other base-promoted protocols yield side reactions, especially with acid-labile intermediates.

    Application Insights: Supporting Industry Needs

    Having supported a wide variety of syntheses in-house, our process team has gathered real-world case data. In some coupling or acylation reactions, chemists move away from hazardous alkali metal hydrides or strong mineral bases and turn to TMG·2H3PO4 instead. Our staff found significant safety improvements in switching from caustic hydroxides to this organic base–phosphate combination, without sacrificing product selectivity. For applications involving epoxy curing, TMG·2H3PO4 achieves the required cure speeds yet limits unwanted background reactivity. Several coatings manufacturers have shared with us how this results in a better balance between shelf-life stability and rapid hardening during use.

    In the pharmaceutical industry, our product enters use in protocols where tight control of base strength and non-nucleophilicity prevents the formation of undesired byproducts. Case studies from our partners demonstrate its advantage in peptide coupling and macrocycle formation, particularly where alternative guanidine bases introduce unwanted nucleophilic effects or suffer from lower thermal stability. The smooth granular form we produce pours easily into process vessels and minimizes operator handling risk compared to dustier analogues.

    Contrast to Other Guanidine-Based Reagents

    We've worked with a range of guanidine derivatives, including tetramethylguanidine (TMG) base itself and other commonly encountered salts such as hydrochloride or carbonate forms. Tetramethylguanidine dihydrogen phosphate offers unique performance traits absent in those alternatives. TMG base remains a strong, versatile organic base, yet the presence of a phosphate counterion alters both its solubility and how it interacts with reaction mixtures. We consistently note that the phosphate salt does not carry the high volatility or pronounced odor associated with pure TMG. From a process safety standpoint, this makes site operations markedly easier, not only for our own blending teams but also for warehouse and shipment logistics.

    Compared to carbonate and hydrochloride versions, TMG·2H3PO4 brings milder handling needs. Carbonate forms, while safe and stable, exhibit less solubility in key polar solvents, sometimes making them less ideal for homogeneous reaction protocols. Hydrochloride salts appear more sensitive to atmospheric moisture and may present challenges with chloride contamination in sensitive product routes. Based on our pilot and production campaigns, TMG·2H3PO4 works as a more stable and cleaner base, especially when customers want to avoid interfering anions.

    Practical Considerations for Handling and Scale-Up

    Our manufacturing shop floor recognizes the day-to-day needs of engineers and technicians–not only the laboratory researcher. At production scale, choosing a base that stores well and allows accurate dosing factors into operational efficiency. Tetramethylguanidine dihydrogen phosphate brings the advantage of minimal caking, free-flowing consistency, and reliable bulk packaging options. We ship it in lined fiber drums and sealed plastic containers, confirmed by both internal batch trials and frontline user reports to maintain transit quality across seasons.

    On-site, our material integrates rapidly in automated feeders, blending tanks, and manual charging steps. Solubility checks conducted in solvents typical to most fine-chemicals or pharma operations show consistent handling without clumping or sediment. These observations become critical for continuous processes or larger reactors where downtime, residue issues, or transfer losses drive up costs.

    We have made our operations more efficient by switching to this product in certain plant lines, eliminating secondary drying steps after drum opening. Customers in polymer synthesis, such as polyurethanes or polycarbonate processes, have seen better batch-to-batch consistency compared to earlier base blends.

    Meeting Environmental and Regulatory Challenges

    The manufacturing world grows more attentive to environmental impact. Tetramethylguanidine dihydrogen phosphate fits well with customers’ efforts to cut hazardous waste and improve workplace safety. Strict regulation around volatile organics and strong mineral bases pushes companies toward less corrosive alternatives. Based on years of health, safety, and environment (HSE) monitoring at our site, this compound requires moderate standard controls–avoiding harsh fumes and limiting the corrosiveness common to stronger inorganic bases like sodium hydroxide or potassium tert-butoxide.

    Our documented disposal routes benefit from the non-chlorinated nature of the compound. Waste phosphate poses less risk to downstream biological treatment units in wastewater, compared to persistent or toxic halide byproducts. To minimize resource use, we have introduced recovery procedures to reclaim phosphate through downstream neutralization where feasible. These improvements translate into waste cost reductions, both for us and for several users with whom we collaborate on closed-loop treatment projects.

    Collaborating to Address Sourcing and Consistency

    Clients, especially in regulated markets, place a premium on repeatability and clear validation data. We provide certificates of analysis backed by our in-house QC analytics, which not only satisfy audits but also support in-process troubleshooting if issues happen downstream. Our priority on traceable raw materials and full documentation helps reduce risks both for production and for end-users seeking FDA or similar approval. Our R&D team handles requests for non-standard particle sizes, or for enhanced purity, working closely with partners to optimize batch yields or reduce downstream purification steps.

    Consistent engagement with customers allows us to adapt our manufacturing protocols. We've taken feedback from many regional and international buyers, implementing barcoded batch tracking and refining our QA sampling plans. For partners developing novel chemical routes, we have provided custom packs of TMG·2H3PO4 for rapid lab evaluation—shortening their design and scale-up cycles. These collaborative efforts have given us better insight into where our material helps process optimization, or where changes in formulation deliver further benefits.

    Technical Support Based on Real-World Use

    Technical queries about reactivity, side-product risks, or solubility come directly to our application chemists. We address these based on practical lab experience and production records, not only published literature. Over the years, we’ve found that TMG·2H3PO4 displays robust performance during multi-step syntheses, even with extended reaction times or higher temperatures. Usage in resin manufacturing and industrial cleaning formulations stands out, as it brings a unique balance: enough strength to drive reactions, without the harshness that can damage sensitive molecules or equipment.

    We support clients with real QA data, including impurity profiles and stability observations across storage periods. For special projects, we document how the material handles in continuous versus batch modes and provide detailed handling recommendations. In one instance, a process team working on scale-up for a flavor compound found improved control of reaction endpoints using our TMG·2H3PO4 as the base, reducing side reactions that earlier protocols with stronger bases produced. By sharing first-hand observations as well as analytical data, we empower users to optimize their own workflows.

    Building Trust Through Manufacturing Rigor

    As principal manufacturers, we control every aspect from incoming raw material approval to the finished lot sign-off. By maintaining direct communication between operators, R&D, and sales, we adjust our process to suit the demands of each application. This investment in cross-team transparency helps us anticipate potential quality issues and solve them before they reach the customer. When new contaminants or degradation pathways become apparent, our teams regroup to redesign purification, rather than simply reworking specifications on paper.

    Through years of shipping to export customers and local partners alike, we have built processes around clear labeling, secure logistics, and transparent documentation. Tank farm operators and warehouse managers have highlighted reduced spill incidents and simpler incident response after switching to Tetramethylguanidine dihydrogen phosphate compared to earlier high-volatility bases. As new regulatory frameworks emerge–especially for pharmaceutical and agricultural use–we stay ahead by engaging with certification audits, adjusting batch records, and updating safety training for all production staff.

    Supporting Industry Evolution Through Product Improvement

    We see the future of Tetramethylguanidine dihydrogen phosphate evolving with the industries it supports. For example, as demand grows for greener chemical processes, our team targets innovation in synthesis and crystallization steps to cut out hazardous reagents and solvents. Progress in solid-state formulation has reduced dust, making site hygiene and inhalation risk easier to manage in large-volume operations.

    Our process innovations—guided by staff suggestions from batch operators—have yielded shorter residence times within reactors, saving energy and improving output consistency. As a direct result, batch processing throughput increased and operational costs declined. Clients in electronics and specialty resins report improved electronic grades, free from ionic impurities, after switching to our higher-purity TMG·2H3PO4.

    Research pipelines in pharmaceuticals frequently seek bases with better selectivity for key C–N or C–O formations. Feedback links these new drug synthesis routes to the efficiency and handling profile of our Tetramethylguanidine dihydrogen phosphate. These projects drive us to further purify and characterize our product, meeting stricter standards and providing clear, accessible certificates for submission to oversight bodies.

    The Value of Direct Manufacturing Input

    By producing and supplying our own Tetramethylguanidine dihydrogen phosphate, we can shape its specifications to reflect practical needs. Our investment in purity and handling pays off when process interruptions decrease, storage times lengthen, and operator safety improves. The lessons learned by our teams–from bench to bulk drum–go into every order. For clients, this means less time troubleshooting base performance and more time focusing on chemistry or downstream operations.

    Chemists, engineers, and operators benefit from materials made with both quality control and an understanding of end-use realities. Tetramethylguanidine dihydrogen phosphate has changed how our customers approach base-driven synthesis, either by cutting operational hazards, boosting reactivity in challenging transformations, or minimizing downstream purification burdens. Through every batch, we keep learning from feedback and new applications, driving us to ensure our product meets the challenges of evolving industry standards.