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Spermine Dihydrate

    • Product Name Spermine Dihydrate
    • Alias SPM
    • Einecs 218-739-9
    • 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

    523075

    Chemical Name Spermine Dihydrate
    Molecular Formula C10H26N4·2H2O
    Molecular Weight 246.38 g/mol
    Cas Number 306-67-2
    Appearance White to off-white crystalline powder
    Solubility Soluble in water
    Melting Point 124-130°C (decomposes)
    Storage Conditions Store at 2-8°C
    Purity Typically ≥98%
    Synonyms N,N'-Bis(3-aminopropyl)tetramethylenediamine dihydrate
    Ph Of 1 Solution 10.0-11.5
    Ec Number 206-194-5

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

    Packing & Storage
    Packing Spermine Dihydrate, 25g, packaged in a sealed amber glass bottle with tamper-evident cap and chemical hazard labeling.
    Shipping Spermine Dihydrate is shipped in sealed, chemical-resistant containers to prevent moisture absorption and contamination. It is classified as non-hazardous but should be handled using standard laboratory safety precautions. The package includes proper labeling and documentation, and is shipped promptly via trusted carriers to ensure product integrity upon arrival.
    Storage Spermine Dihydrate should be stored in a tightly sealed container, protected from light and moisture. Keep it at 2-8°C (refrigerated) in a well-ventilated, dry area away from incompatible substances such as strong oxidizing agents. Proper labeling and storage conditions help maintain its stability and prevent degradation. Always follow institutional safety protocols when handling and storing this chemical.
    Application of Spermine Dihydrate

    Applications of Spermine Dihydrate in Industrial Manufacturing

    Spermine dihydrate plays a critical role in multiple advanced manufacturing sectors where its cationic properties, chelating ability, and cell stability functions support high-value transformations. Our production focuses exclusively on sectors with established, validated downstream demand for this polyamine compound. The following sections provide a detailed overview of four major application segments, outlining compliance guidelines, usage ratios, integration points, and resulting finished goods.

    1. Biopharmaceutical Cell Culture Media Formulation

    Spermine dihydrate is utilized by biopharmaceutical firms as a growth factor component in upstream mammalian and microbial cell culture media formulations, supporting cell viability, DNA stability, and protein synthesis during recombinant protein production. Manufacturers must precisely control spermine concentrations to avoid cytotoxicity while optimizing cell yield, relying on real-time QC assays throughout the process. Spermine integration occurs at the hydrated powder blending stage before media sterilization and downstream fermentation. Final products include monoclonal antibody drugs, recombinant hormones, and viral vector therapies used in clinical and commercial settings.

    Industry compliance standards

    • USP General Chapter <1043> Ancillary Materials for Cell, Gene, and Tissue-Engineered Products
    • European Pharmacopoeia (Ph. Eur.) compliance for raw materials in biotech manufacturing
    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • 21 CFR Parts 210/211: US FDA cGMP for finished pharmaceuticals

    Typical usage ratio

    • Final concentration in media: 0.01 – 0.1 mM (2–20 mg/L), adjusted based on cell line sensitivity and protein expression requirements

    Downstream process integration

    • Hydrated spermine powder is added during dry-mix blending for media preparation, dissolved and sterile filtered before transfer to fermenters or bioreactors

    Final product types

    • Recombinant monoclonal antibody solutions
    • Therapeutic protein APIs (insulins, cytokines, enzymes)
    • Viral vectors for gene therapy pipelines
    • Cell-based vaccine intermediates

    2. Oligonucleotide Synthesis and Purification

    Synthesis houses in the nucleic acid therapeutics and diagnostics field leverage spermine dihydrate as a stabilizing reagent during oligonucleotide chain assembly and post-synthesis purification steps. The compound’s polycationic nature improves DNA/RNA duplex formation, enhances HPLC separation profiles, and protects against strand depurination, contributing to higher purity yields. Addition occurs either in synthesis solution or mobile phase buffers during reversed-phase chromatography. End-use products manufactured with spermine supplementation include PCR primers, siRNA, aptamers, and antisense oligonucleotide drugs.

    Industry compliance standards

    • ISO 13485:2016 Quality Management Systems for medical device and diagnostic raw materials
    • Ph. Eur. monographs for oligonucleotides (where applicable)
    • US FDA Guidance for Industry: CGMP for Combination Products
    • ICH Q9: Quality Risk Management in oligonucleotide manufacturing

    Typical usage ratio

    • Ranging from 10 – 200 µM in synthesis or purification buffers, based on oligo length and desired stabilization

    Downstream process integration

    • Added during solid-phase synthesis deprotection and in HPLC eluent phases for enhanced oligo resolution and strand integrity

    Final product types

    • Research-grade and GMP-grade short RNA/DNA oligonucleotides
    • siRNA therapeutics and chemical gene silencers
    • Diagnostic PCR/RT-PCR primers and probes
    • Antisense drug APIs for rare disease pipelines

    3. Biotechnological Enzyme Stabilization and Storage

    In biotechnological enzyme manufacturing, spermine dihydrate is valued as a conformational stabilizer, maintaining enzyme activity during long-term storage and lyophilization. By binding to nucleic acid and protein residues, spermine mitigates denaturation and aggregation, especially for therapeutic enzymes and molecular biology kits. The compound enters at the formulation tank stage after the main active has been purified, with levels optimized to maximize shelf-life while avoiding precipitation. The major outputs are stabilized enzyme bulk actives and commercial ready-to-use molecular kits.

    Industry compliance standards

    • ISO 9001:2015 certified QC systems for enzyme production
    • Good Manufacturing Practice (GMP) per EudraLex Volume 4 for biotech APIs
    • US Pharmacopeia enzyme product monographs
    • OECD principles of Good Laboratory Practice (GLP) for quality batch release

    Typical usage ratio

    • 0.005 – 0.1% w/v (50–1000 mg/L), tailored according to enzyme type and target storage duration based on real-time stability data

    Downstream process integration

    • Incorporated into formulation blends post-chromatography purification, prior to sterile filtration and aliquoting into final containers or lyophilization vials

    Final product types

    • Bulk stabilized therapeutic enzymes
    • Molecular biology reagents (e.g., DNA/RNA polymerases, restriction enzymes)
    • Diagnostic test kit master mixes
    • Lyophilized enzyme powder products

    4. Specialty Polyamine Additive for Biodegradable Polymer Production

    Manufacturers developing advanced biodegradable polyamide and polyester materials use spermine dihydrate as a chain-extending polyamine, contributing to improved mechanical properties, flexibility, and hydrolytic stability in bio-based plastics. Spermine participates in condensation reactions, functioning as a structural monomer during polymer synthesis via melt processing or solution polymerization. Addition ratios are carefully chosen for target molecular weight and physical property optimization. The finalized polymers serve markets for precision medical devices, drug delivery carriers, and eco-friendly packaging films.

    Industry compliance standards

    • EU Regulation (EC) No 10/2011 for food-contact plastics
    • ISO 10993-1: Biological Evaluation of Medical Devices (for polymer implants)
    • REACH Regulation (EC) No 1907/2006 for chemical safety
    • ASTM D5338 for biodegradability test methods of plastics

    Typical usage ratio

    • 0.5% – 5% by molar ratio relative to diacids/diesters; final dosage based on polymerization pathway and final product mechanical requirements

    Downstream process integration

    • Introduced as a reactant in the main polymerization reactor, either batch or continuous, combined with diacid or ester components under nitrogen atmosphere

    Final product types

    • Medical-grade biodegradable polymer rods and scaffolds
    • Resorbable surgical suture filaments
    • Biodegradable flexible packaging films
    • Bioabsorbable microcapsule carriers for sustained drug release
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    Certification & Compliance
    More Introduction

    Spermine Dihydrate: Quality from the Source

    Our Direct Experience with Spermine Dihydrate in Chemical Manufacturing

    For decades, our facility has dedicated research and production lines to polyamines, including Spermine dihydrate. This compound, with the chemical formula C10H26N4·2H2O, rarely leaves our loading dock without a story. It often means weeks of precise batch control, careful handling of intermediates, and strict oversight from regulatory authorities. Many times, our chemists have debated batch strategies for Spermine because water content, crystalline structure, and even storage can influence whether a lab or production facility achieves the result they want. Spermine dihydrate—specifically as a dihydrate—shows differences in solubility, stability, and compatibility, which distinguishes it from the anhydrous or tetrahydrate grades. Our regular customers depend on consistency, so we don’t treat this as a commodity or just another catalog item.

    Understanding Spermine Dihydrate

    Few polyamines have the same impact across research and biotech circles as Spermine dihydrate. Our reactors typically produce this material for labs investigating DNA stabilization, gene editing, or cellular processes. Spermine binds and compacts DNA; its two extra water molecules shape both its crystal form and its shelf life, which experienced chemists immediately recognize as an edge over the anhydrous material when they need easier dissolution at room temperature. For example, we have seen partners in protein crystallization rely on our dihydrate due to its predictable behavior during formulation and its lower tendency to cluster or precipitate. That predictability has catapulted our product into custom synthesis for both hospitals and research institutes.

    Our Manufacturing Approach and Why Hydration States Matter

    Inside our plant, hydrating Spermine demands precision. Water content shifts everything—from how a batch dissolves in water, down to the yield from chromatography. Each specification on our data sheets reflects years experimenting with temperatures, mixing times, and solvent systems. We watch for visual cues, measure residual moisture, and verify purity through HPLC and NMR before filling the drums. Controlling the hydration state has practical consequences. Some competitors cut steps or rush crystallization, ending with ambiguous hydrates that don’t meet the standards set by pharmaceutical, biotech, or cell therapy clients. We don’t aim for the cheapest material on the market. Instead, our drives are purity, identity, and traceability, all measured from our own facility floor.

    Common Uses and Applications We See in the Field

    Most of our Spermine dihydrate leaves the factory for gene therapy and molecular biology. Customers, usually with extensive technical backgrounds, call us to discuss specifics of buffer formulations, pH effects, or potential routes to minimize enzymatic degradation in storage—the sorts of questions that only hands-on, routine experience can answer. We maintain a direct feedback loop with some of the world’s leading nucleic acid and cell biology researchers. Beyond biotech, Spermine dihydrate shows up in industrial enzyme stabilization, some liquid crystals, and polymer technologies, but our most consistent use cases anchor around lab-scale and manufacturing-scale applications in DNA and RNA processing. Spermine’s role in stabilizing nucleic acids has been established by peer-reviewed research, and conversations with our long-term partners often cite these publications during early-stage planning for a project.

    Differences from Other Spermine Products

    The form in which Spermine arrives—anhydrous, dihydrate, or tetrahydrate—has a measurable impact far beyond "just" appearance or label. In practice, our clients confirm that the dihydrate form dissolves more easily under typical preparation conditions. We draw on our own in-lab comparisons: anhydrous Spermine often cakes if exposed to humidity, rendering part of the order unusable unless it’s ground back into solution—an unwelcome hassle for fast-paced research teams. The dihydrate, by contrast, resists clumping, even in humid climates, and stays free-flowing. This difference reduces waste at the benchtop, which matters especially when budgets are tight or lead times for resupply stretch on for weeks. Tetrahydrate, less common and less stable in ambient conditions, attracts fewer orders. We stick to producing dihydrate because our partners report fewer headaches, smoother workflows, and—perhaps most tellingly—reorders year after year.

    Purity, Contaminants, and In-House Controls

    Every drum of Spermine dihydrate starts under our roof with raw materials sourced only after multiple lots pass our incoming QC testing. Over the years we have learned that lot-to-lot variability introduces unanticipated chromatographic peaks or shifts in solution pH, even with small-scale adjustments at upstream suppliers. Some off-the-shelf lots of Spermine on the market show impurity levels that can disrupt enzyme reactions or DNA binding. We work without shortcuts, investing in locked-in raw material pipelines and batch-by-batch transparency. Each production run is characterized using mass spectrometry, NMR, and Karl Fischer titration, so customers can consult a real certificate rather than a recycled generic analysis. We run stability trials at both room temperature and refrigeration, tracking any decomposition products and measuring their impact on downstream applications. We have no tolerance for unexplained impurities; our partners in regulated industries ask for—and receive—full impurity profiles and stability data with every order.

    Specifications We Commit To

    We define Spermine dihydrate with a minimum assay, typically 98% or above by HPLC, limiting heavy metals and residual solvents below recognized thresholds for chemical and biotechnological research. Loss on drying is measured to confirm the 2:1 hydration, which our technicians monitor in real time. Visual checks, FTIR spectra, and melting point data backstop analytical testing. Our direct involvement in all these steps means no matter how demanding the request—larger batch size, tighter impurity limits, special packaging—we can put experienced eyes on it and provide authentic documentation for each drum. Our refusal to offload QC onto external laboratories or distributors is rooted in a belief that only hands-on attention at the source, with continuous operator training and analytical review, delivers reproducible quality every time.

    Customer Experience Informed by Feedback

    We support long-term partnerships with transparent communication. Many repeat clients contact us after disappointing encounters with third-party traders, where inconsistent hydration levels or unlabeled contaminants torpedoed research or wasted manufacturing cycles. The trust we build comes not just from consistent delivery, but from sharing technical advice based on data, not on speculation. For example, we have walked new users through modifications to their buffer prep protocols to compensate for environmental conditions, helped scale up from milligram to kilogram quantities without loss of quality, and coordinated rush orders for urgent clinical needs. We often see the best research come from open lines and real-time troubleshooting instead of just shipping a bottle and closing a sale. Our chemists and production managers routinely field technical queries themselves, rather than pushing the conversation to non-technical staff. This close attention translates into fewer delays, smoother onboarding, and results that speak for themselves.

    Supporting Knowledge, Traceability, and Compliance

    Researchers and commercial users expect more than high-purity material; traceability and documentation are non-negotiable. Each shipment of Spermine dihydrate from our facility carries full batch tracing, dating back through raw materials, production records, and analytical data on file. We maintain audit-ready archives and submit willingly to third-party inspections because many of our partners undergo regular regulatory audits themselves. We document compliance with region-specific and global chemical regulations, always aiming to stay ahead of emerging restrictions or disclosure requirements. Years of communication with procurement and regulatory teams taught us that clear, accessible records save headaches at customs checks and during qualification runs. We proactively notify customers of any regulatory or specification changes, and we provide ongoing updates if global standards shift that might affect usage in sensitive applications. This up-front approach respects our partners’ time and safeguards supply chains from surprise interruptions.

    Batch Production Challenges and Solutions

    Spermine dihydrate’s scale-up from gram quantities to multi-kilogram lots is rarely straightforward. Challenges span from temperature-sensitive hydration to minimizing contact with airborne moisture. In practice, controlling crystallization temperature within a tight window can separate high-purity, crystalline dihydrate from a sticky mass unusable at scale. Our solution involves both automated monitoring and careful human oversight. Old-fashioned laboratory know-how proves invaluable: our operators monitor batch color, texture, and particle size by eye as well as by instrument. Humidity-controlled rooms, filtered water, and nitrogen blankets ensure that no additional water gets into the product during packaging. On several occasions, we have had to adjust batch processes in real time to compensate for fluctuations in ambient humidity—an issue magnified during seasonal shifts. We keep extra processing time and backup staff available to intervene if unexpected issues arise, believing that flexibility at the production stage beats rigid, one-size-fits-all automation, especially for specialty chemicals like Spermine dihydrate.

    Storage, Packaging, and Shipping Considerations

    Proper storage preserves product quality and ensures user safety. Spermine dihydrate benefits from being sealed quickly after crystallization, ideally in double-lined polyethylene containers with minimal headspace. Over the years, we have tested various storage formats; barrels that were not tightly sealed often absorbed atmospheric moisture or picked up contaminants, particularly if transferred to glassware in a humid lab. We recommend storing the product in a cool, dry place, away from incompatible substances, although the dihydrate’s stability affords easier handling compared to the anhydrous form. For shipping, we coordinate documentation so that customs officials and receiving labs encounter no ambiguity with labeling, batch records, or regulatory paperwork. Couriers are briefed on handling and storage requirements, and we supply rapid technical support if any issue surfaces during transit. These steps, though they add some overhead, have reduced complaints, product returns, and delays from customs holds—payoffs that matter for high-value, time-sensitive research materials.

    Supporting Research and Innovative Applications

    We regularly consult with universities, pharmaceutical start-ups, and government labs investigating novel biomaterials, drug delivery systems, or gene editing platforms. In several published collaborations, our Spermine dihydrate served as a polycationic scaffold, facilitating DNA transfection, nanoparticle stabilization, or targeted delivery of genetic cargo. Customers value access to technical staff who understand not just purity, but how the compound performs under the challenging demands of real-world research protocols. We routinely share unpublished data about batch stability, hydration/dehydration rates under controlled conditions, and interference with commonly used buffers or enzymes, so sophisticated users can integrate the material seamlessly into their systems. Practical know-how—gleaned from years on the production floor and in the research lab—helps downstream users optimize their own formulations and maximize the performance of our Spermine dihydrate.

    Continuous Improvement and Future Developments

    Feedback from partners fuels our pursuit of improved manufacturing and testing protocols. Our current focus: reducing trace byproducts through optimized reaction engineering, investigating new anti-caking agents that increase shelf life without interfering with bioreactivity, and tightening impurity profiles through secondary purification. Some improvements come directly from customer feedback: one university partner flagged sporadic clumping under refrigeration, which led us to redesign packaging and update drying cycles. We see value in ongoing collaboration, so we invite partners from across the chemical and life sciences spectrum to propose pilot projects, joint trials, and product modifications. Staying ahead in this field requires vigilance, investment in training, and openness to change. We meet regularly with global experts and regulatory officials to anticipate future standards for traceability, biocompatibility, and environmental compliance. Our commitment remains rooted in producing Spermine dihydrate that meets today’s needs while anticipating tomorrow’s discoveries.