Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing admin@sinochem-nanjing.com 3389378665@qq.com
Follow us:

2-Amidinopyrimidine Hydrochloride

    • Product Name 2-Amidinopyrimidine Hydrochloride
    • Alias 2-Aminopyrimidine, hydrochloride
    • Einecs 401-490-4
    • 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
    VTB
    Specifications

    HS Code

    830833

    Product Name 2-Amidinopyrimidine Hydrochloride
    Chemical Formula C5H7ClN4
    Molecular Weight 158.59 g/mol
    Cas Number 5571-07-7
    Appearance White to off-white powder
    Melting Point 279-281°C (dec.)
    Solubility Soluble in water
    Storage Conditions Store at room temperature, keep container tightly closed
    Purity Typically ≥98%
    Synonyms 2-Amidinopyrimidine monohydrochloride
    Smiles C1=CN=C(N=C1)C(=N)N.Cl
    Usage Intermediate for organic synthesis

    As an accredited 2-Amidinopyrimidine Hydrochloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 2-Amidinopyrimidine Hydrochloride is packaged in a sealed amber glass bottle, labeled, containing 25g, and clearly marked for laboratory use.
    Shipping **Shipping Description:** 2-Amidinopyrimidine Hydrochloride is shipped in tightly sealed containers to prevent moisture absorption and contamination. It should be handled and transported as a non-hazardous chemical under standard, dry conditions, avoiding extreme temperatures. Relevant labeling and documentation, including product identification and safety data, accompany each shipment in compliance with regulatory standards.
    Storage 2-Amidinopyrimidine Hydrochloride should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area. Keep it away from moisture, heat sources, and direct sunlight. Store at room temperature, unless otherwise specified by the manufacturer. Ensure the storage area is appropriately labeled and suitable for chemicals to prevent contamination and unauthorized access. Avoid contact with incompatible substances.
    Application of 2-Amidinopyrimidine Hydrochloride

    Applications of 2-Amidinopyrimidine Hydrochloride in Industrial Manufacturing

    We specialize in the direct manufacturing of 2-Amidinopyrimidine Hydrochloride, providing high-purity material for demanding sectors that require compliance with international standards and rigorous process integration. Below, we outline major downstream application scenarios grounded in long-term market adoption and proven demand.

    1. API Intermediate for Antithrombotic Agents

    Pharmaceutical companies utilize our material as a key intermediate during the synthesis of direct thrombin inhibitors and related antithrombotic drugs. Its unique chemical structure supports high-yield amidination steps under controlled conditions, and batch records consistently reference its input during GMP inspections. Formulators tailor concentration based on target molecule and scale, with analytical QC protocols addressing trace impurities post-reaction. Our product supports stable API intermediate production through established multi-step synthesis routes.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU GMP EudraLex Volume 4
    • US FDA 21 CFR Parts 210/211
    • Pharmacopeia references applicable to synthesized active ingredients (USP, EP)

    Typical usage ratio

    • Input range of 0.5–2.2 molar equivalents, with final amount calculated based on API target batch size and process yield optimizations

    Downstream process integration

    • Introduced during intermediate synthesis stage, typically via acylation, amidination, or cyclization reactions within controlled reactors; QC sampling occurs after each major step

    Final product types

    • API intermediates for small-molecule antithrombotic pharmaceuticals
    • Bulk finished pharmaceutical ingredients for generic or branded drugs targeting coagulation disorders

    2. Specialty Additive in Diagnostic Reagent Production

    Diagnostic reagent manufacturers employ our 2-Amidinopyrimidine Hydrochloride as a functional additive in chromogenic and enzymatic substrate formulations for in vitro diagnostics. Its specific reactivity with trypsin-like serine proteases supports enhanced substrate performance in test kits for clinical laboratories. Stringent batch-to-batch reproducibility remains critical, as downstream QC protocols require traceability throughout reagent formulation pipelines, ensuring compliance with in vitro diagnostics regulation.

    Industry compliance standards

    • ISO 13485:2016 Quality Management for Medical Devices
    • IVDR (EU Regulation 2017/746) for in vitro diagnostic medical devices
    • US FDA 21 CFR 820 (Quality System Regulation for Medical Devices)

    Typical usage ratio

    • Added at 0.05–0.25% w/v relative to finished buffer volume, adjusted according to specific assay sensitivity and substrate turnover rates determined during pre-formulation trials

    Downstream process integration

    • Dispersed during aqueous buffer preparation phase prior to substrate addition; follows validated mixing sequence documented within standardized work instructions

    Final product types

    • Chromogenic diagnostic test kits (e.g., substrate panels for enzyme activity assays)
    • Clinical laboratory reagent solutions for coagulation and protease screening

    3. Component for Peptide Synthesis Reagents

    Producers of custom peptides and oligonucleotides source our compound for use in solid-phase peptide synthesis (SPPS) and selective peptide side-chain modification. Its amidine functionality enables targeted activation and protection procedures crucial for synthesizing sequence-defined peptides under anhydrous conditions. Scale-up projects rely on tight lot release specifications, as even minor variations in purity impact final peptide yield and chain fidelity, prompting QC teams to integrate additional verification points at each chemical synthesis stage.

    Industry compliance standards

    • ISO 9001:2015 for quality management in chemical manufacturing
    • US FDA guidelines for GMP peptide therapeutics (21 CFR 210/211)
    • International Council for Harmonisation (ICH Q11: Development and Manufacture of Drug Substances)

    Typical usage ratio

    • Employed at 0.8–1.5 molar equivalents per amino acid residue in the coupling step, adjusted based on resin loading and sequence complexity

    Downstream process integration

    • Added during side-chain activation or amidination steps post-coupling in automated peptide synthesizer cycles; inclusion documented per batch process sheet

    Final product types

    • Synthetic therapeutic peptides for pharmaceutical or research applications
    • Biological reference standards

    4. Processing Aid in Paper Wet-Strength Resin Production

    Our material finds application as a catalytic processing aid in the production of polyamide–epichlorohydrin (PAE) wet-strength resins used in high-durability paper goods. Chemical paper producers value the enhanced polymerization efficiency it confers—especially in batch systems calibrated for high throughput—while process engineers scrutinize dosage to prevent resin over-stabilization. Environmental and product safety regulations govern its usage, with downstream operators documenting addition times and completed batch records as required by continuous improvement programs.

    Industry compliance standards

    • REACH (EC) No 1907/2006 registration for chemical safety
    • FDA 21 CFR 176.170 and 176.180 for paper and board in contact with aqueous and fatty foods (if applicable for final use)
    • OEKO-TEX® Standard 100 for chemical content in textiles and paper goods

    Typical usage ratio

    • Used at 0.01–0.05% by mass of total resin batch, with adjustment based on ultimate paper grammage and required wet strength per end-use application

    Downstream process integration

    • Introduced at the pre-polymerization mixing stage within reaction vessels; dosing controlled via automated feedback systems based on on-line viscosity monitoring

    Final product types

    • Wet-strength resins for tissue paper, toweling, specialty labels, and food-grade packaging papers

    5. Intermediate in Fine Chemical Synthesis for Agrochemical Actives

    Manufacturers of crop protection actives and growth regulators incorporate our compound as an intermediate structure during the synthesis of select pyrimidine-based agrochemicals. Tight process control enables consistent conversion during multi-stage synthesis, while formulators consider purity adjustments to mitigate risk of by-product formation. Regulatory submission files reference its usage and trace its removal through validated impurity clearance steps, ensuring that no detectable residue remains in the finished agrochemical active.

    Industry compliance standards

    • OECD Principles of Good Laboratory Practice (GLP) for registration studies
    • EU Regulation (EC) No 1107/2009 for plant protection products
    • US EPA 40 CFR Part 158 for pesticide registration data requirements

    Typical usage ratio

    • Incorporated at 0.4–1.3 molar equivalents, tailored to stepwise conversion efficiency according to targeted agrochemical structure

    Downstream process integration

    • Reacted during pyrimidine ring-formation or amidination steps, with inline spectrophotometric tracking and staged separation prior to downstream derivatization or formulation

    Final product types

    • Technical-grade agrochemical intermediates
    • Formulated crop protection actives for herbicides, fungicides, and growth regulators
    Free Quote

    Competitive 2-Amidinopyrimidine Hydrochloride prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.

    We will respond to you as soon as possible.

    Tel: +8615371019725

    Email: admin@sinochem-nanjing.com

    Get Free Quote of Sinochem Nanjing Corporation

    Flexible payment, competitive price, premium service - Inquire now!

    Certification & Compliance
    More Introduction

    2-Amidinopyrimidine Hydrochloride: Practical Applications and Insights from the Plant Floor

    Understanding the Role of 2-Amidinopyrimidine Hydrochloride in Modern Chemistry

    Over the years in the lab and on the shop floor, we’ve seen time and again how the right intermediate can change the course of a manufacturing project. 2-Amidinopyrimidine Hydrochloride stands out in this respect. Chemists often seek compounds that solve challenges in both synthesis and final application without introducing unnecessary complexity into the workflow. This material offers a unique blend of reactivity and stability that makes it a trusted component, especially where high purity is a strict requirement.

    Specifications and Handling from Those Who Work with It

    From the very first packaging session, our team recognized the importance of consistency. Moisture and exposure to air rapidly change the appearance and utility of many fine chemicals, and 2-Amidinopyrimidine Hydrochloride shows marked sensitivity to water vapor. Multiple shifts spent optimizing the drying and filling process paid off, resulting in a white crystalline powder with reliable flow and minimal caking. Average purity hovers above 98%, confirmed batch after batch with in-house HPLC. The compound’s melting point, typically around 260°C with some variance, gives further assurance that no extraneous components linger in the final product.

    Many of these features follow from our approach to starting material selection and control of reaction conditions. Recrystallization serves both to improve appearance and wash away residual byproducts—sometimes invisible in solution but always present to cause headaches during downstream processing.

    Real-World Use Cases: What 2-Amidinopyrimidine Hydrochloride Achieves

    Customers, especially those in pharmaceutical and biotech laboratories, come to us with processes that call for selective and controllable aminopyrimidine derivatives. In several stages of active pharmaceutical ingredient synthesis, this hydrochloride salt handles nucleophilic substitution reactions where an amidine group must retain integrity under tough conditions. It persists in high-pH steps and does not degrade quickly upon heating, opening the door to multi-step sequences without complicated protection tactics.

    One medicinal project in particular required a scaffold robust enough for late-stage functionalization. Over dozens of cycles, technicians reported minimal decomposition of the 2-amidinopyrimidine unit itself, even as other moieties fell apart. A handful of grams or a full reactor load, users got the same reliable response.

    How 2-Amidinopyrimidine Hydrochloride Differs from Other Aminopyrimidines

    Sourcing many amidinopyrimidines reveals subtle distinctions in their handling and end-use. Unsubstituted amidines, or compounds with free bases instead of hydrochloride salts, often come with unwanted side reactivity, solubility quirks, or stability issues in ambient conditions. Our product, as the hydrochloride variant, resolves those issues in day-to-day plant operations.

    The hydrochloride salt form brings water solubility improvements for formulation and easier downstream isolation. Compared to the free base, this salt resists atmospheric degradation, storing cleanly over the long term. Years ago, we noted crystallization challenges with the free base version—powders that turned sticky in less than a month. Once the switch was made to the hydrochloride salt, shelf life extended and dosing accuracies improved.

    In actual synthesis, chemists observed the hydrochloride form simplifies pH control, especially in buffered or aqueous systems. It dissolves quickly and doesn’t cause pH swings, giving more predictable results. This difference means less time spent correcting solutions and more productive hours doing real chemistry.

    Routine Quality Control: Lessons Learned by the Manufacturing Crew

    Routine quality checks reveal real world truths. A material may pass a standard laboratory assay, but if it cakes under pressure or toughs up in solution, process operators face delays and losses. Each batch of 2-Amidinopyrimidine Hydrochloride receives hands-on scrutiny, not just automated HPLC or NMR runs. Plant staff scoop, funnel and weigh the powder under working conditions mirroring those of our largest clients. If it clumped or exhibited static issues, a recipe change followed. These adjustments eliminated failures during bulk flask charging at customer sites.

    One client running a 500-liter vessel once pointed out that minor color shifts signaled issues in previous supplier batches. With tighter control of recystallization staging and a tweak to neutralization timing, faint yellowing was eliminated. These process tweaks resulted in improved perceptions from procurement through to the API production floor.

    Safety, Storage, and Trust in Supply

    Materials with amidine character demand attention in handling—corrosivity, dustiness, and inhalation risk don’t disappear at the point of sale. Our team treats every gram with the expectation that a missed step may ultimately find its way into a client’s reactor. Every production run is scrupulously bagged, double checked for seal integrity, and housed in controlled humidity spaces to protect the material from hydrolysis.

    Drums get clearly labeled, but more importantly, staff carry out regular walk-bys and visual inspections instead of relying solely on documentation. Containers marked out-of-spec get quarantined. Over time, these habits build trust with partners who value supplier vigilance as much as price or capacity.

    Supporting Innovation and Problem-Solving in Synthesis

    In the custom synthesis space, adaptability matters. Chemists sometimes request slight modifications—tighter sieving cuts, altered moisture content, or specific blends to match pilot plant requirements. Because we control our own upstream supply chains, rapid turnaround on adjustments is possible. Our engineers know the pressures buyers face, having troubleshot doznes of scale-ups themselves.

    Long-standing customers occasionally reach out mid-project with complications. Does a trace contaminant interfere with their catalyst? Is the salt form compatible with a non-aqueous process? Experience points toward fast, honest responses over generic assurances. Instead of canned answers, we review available data, sometimes shipping out rapid micro-lots for their own bench evaluation.

    On-site feedback sometimes results in direct process upgrades: if one team detects a heat-drying artifact or a pH shift in a batch, we gather plant operators, technical management, and QA specialists to walk through the process steps. A single observed impurity through a customer’s LC-MS kicks off a root cause analysis. Such cycles of review distinguish a conscientious manufacturer from traders who simply repackage bulk.

    Environmental Aspects and Waste Management

    Efficient plants cannot afford to ignore their byproduct streams. The separation of chloride fractions during neutralization and careful mother liquor disposal keep 2-amidinopyrimidine hydrochloride production clean and safe for both plant operators and the broader environment. Rather than dilute streams or let wash waters collect, our setup recycles as much as possible, and waste handling is tightly tracked using real-world checkpoints instead of unchecked downstream treatment.

    In recent years, regulations on chloride emissions and fine particulate release have prompted ongoing investment in scrubbers and closed-system filtration. Continuous operator training equips all staff to spot issues before they escalate, whether during a night shift or post-maintenance restart. As a result, downstream users gain confidence their own environmental reviews will not trigger concerns from unexpected impurities.

    Comparing Plant-Prepared Material to Repackaged Goods

    Feedback from contract labs and scale-up teams has been candid: off-the-shelf amidinopyrimidines from third-parties often present more problems than they solve. Unlabeled blending, variable granule sizes, and unpredictable residual solvent content complicate even simple recipes. Manufacturer control over every step allows for tighter quality and direct fulfillment.

    Early on, dealing with complaints about slow dissolution rates or inconsistent melting points, our technical group responded by opening up internal batch records and inviting customer audits. This openness, rare in much of the contract manufacturing sector, helped separate trustworthy producers from mere marketers. Documented records, not just glossy certificates, back up each drum and every kilogram sent out.

    Long-Term Partnerships and Customization

    Regular discussions with research partners open up insights that don’t always make it into public specifications. Some projects call for modified batch sizes—either larger for continuous operations, or small batches for feasibility work. Our team works directly with supply chain planners and chemists to tweak production scheduling or adjust packaging, eliminating weeks of delay and unnecessary repacking.

    With pharmaceuticals especially, clear communication routes allow us to anticipate spikes in demand or specification changes. Once, a partner in oncology research requested a lower chloride content. The process team responded within days by revisiting product washing, collecting pilot samples, and securing third party confirmation. This agility can only exist at a producer with in-house capability, not a distant broker.

    Process Insight from Decades on the Line

    Manufacturing teams learn which formulas “just work” and which bring noise and confusion to a continuous flow system. In years building this operation, it became clear that each amidinopyrimidine variant reacts differently to high-speed mixing, heat shock, and even drum transfer. The hydrochloride version fends off static pickup and yields a pourable powder that remains workable after months on the shelf.

    This level of performance arises from tuning both the synthetic route and the finishing steps. We maintain precise control over neutralization stages and use multiple checks during crystallization. A commitment to these methods grew from watching early failures—shipping sticky or over-dried material that cost clients thousands in clean-up or lost time.

    Collaboration with Analytical Chemists

    Critical applications require more than batch-level purity claims. We coordinate closely with analytical chemists, sharing reference spectra and collaborating on troubleshooting. Our plant routinely supplies IR, NMR, and advanced chromatographic panels, not just standard COAs. Customers in drug discovery or scaling campaigns welcome this transparency, shaving weeks off internal assessments.

    Joint efforts improve futures for both sides. For a major fermentation client, we supplied not only kilograms of 2-Amidinopyrimidine Hydrochloride but tracked low-level impurities that might affect bioassay results far downstream. These deeper data sets provided R&D teams with the confidence to move to next development steps.

    Responding to Industry Evolution

    As regulatory frameworks evolve, manufacturers face increased scrutiny over raw material traceability, documentation, and batch reproducibility. Instead of waiting for regulators to set new bars, our plant continually upgrades records management, adopting digital entry and automated validation checks. Each container carries a clear, unbroken history, holding up under random audit or sudden customer inquiry.

    Sometimes, long-term clients approach us seeking help to reduce costs or streamline a process involving 2-Amidinopyrimidine Hydrochloride. Rather than pushing back, we sit down, review all process data, and suggest tweaks—ranging from bulk-scale handling interventions to optimizing drying cycles. This kind of partnership stems from understanding not only the chemistry but also the business pressures our end users confront.

    Pride in Manufacturing, Not Middlemanning

    From the first time we produced 2-Amidinopyrimidine Hydrochloride, every step, from sourcing raw pyrimidines to final drum tie-offs, was intent on producing repeatable, thorough results. Being a manufacturer means more than converting reagents. It requires understanding logistics, storage, field use, regulatory implications, and real-world batch performance—not just in our warehouse, but at the point of consumption.

    Seeing material loaded in our facility and then cited in published process patents years down the road gives a sense of satisfaction not found in simple reselling. Troubleshooting issues, processing minor modifications, and serving as a chemist’s direct link to the production plant creates mutual growth and advancement.

    Future Prospects and Continuing Improvements

    Production systems keep moving. New users discover 2-Amidinopyrimidine Hydrochloride in process optimizations and target library syntheses. Each feedback cycle—positive or otherwise—gets folded back into process development. Our focus remains on advancing internal controls, exploring greener chemistry, and maintaining open lines of communication with our partners.

    As technology grows and pharmaceutical projects shift toward smaller, more focused endpoints, demands for traceability and adaptability surge. By holding the skills, supply chains, and experience in-house, our team meets these requirements, piece by piece. Steady investment in equipment and people ensures each kilogram, each drum, does its job, and enables clients to focus on their own innovations, rather than solving problems that shouldn’t exist in the first place.