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1-(3-Dimethylaminopropyl)-3-Ethylcarbodiimide Methiodide

    • Product Name 1-(3-Dimethylaminopropyl)-3-Ethylcarbodiimide Methiodide
    • Alias EDC Methiodide
    • Einecs 285-652-4
    • 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

    617804

    Chemical Name 1-(3-Dimethylaminopropyl)-3-Ethylcarbodiimide Methiodide
    Cas Number 25952-53-8
    Molecular Formula C9H20IN3
    Molecular Weight 297.18 g/mol
    Appearance White to off-white crystalline powder
    Solubility Soluble in water and polar organic solvents
    Melting Point 110-112°C
    Storage Conditions Store at 2-8°C, tightly closed, protected from light
    Synonyms EDCI methiodide, EDC methiodide
    Application Coupling reagent in peptide synthesis
    Purity Typically ≥98%
    Sensitivity Moisture sensitive
    Hazard Class Irritant
    Inchi Key RXSLWZVVQNMLSG-UHFFFAOYSA-M
    Boiling Point Decomposes before boiling

    As an accredited 1-(3-Dimethylaminopropyl)-3-Ethylcarbodiimide Methiodide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The packaging is a sealed amber glass bottle containing 5 grams of 1-(3-Dimethylaminopropyl)-3-Ethylcarbodiimide Methiodide, with labeling.
    Shipping 1-(3-Dimethylaminopropyl)-3-Ethylcarbodiimide Methiodide is shipped in tightly sealed containers, protected from moisture and light, and stored at room temperature. The chemical is classified as non-hazardous for standard shipping, but care should be taken to comply with local regulations and ensure packaging prevents exposure or contamination during transit.
    Storage 1-(3-Dimethylaminopropyl)-3-Ethylcarbodiimide Methiodide should be stored in a tightly sealed container, protected from light and moisture. Keep the substance at 2-8°C in a cool, dry, and well-ventilated area. Store separately from strong oxidizers, acids, and bases to avoid hazardous reactions. Proper labeling and adherence to safety protocols are essential to maintain chemical stability and minimize risks.
    Application of 1-(3-Dimethylaminopropyl)-3-Ethylcarbodiimide Methiodide

    Applications of 1-(3-Dimethylaminopropyl)-3-Ethylcarbodiimide Methiodide in Industrial Manufacturing

    As an established manufacturer, we supply 1-(3-Dimethylaminopropyl)-3-Ethylcarbodiimide Methiodide to specialized sectors that rely on highly selective carbodiimide crosslinking chemistry, particularly where water solubility and efficient activation of carboxyl groups are essential. Our expertise is utilized across regulated life science and fine chemical markets, with each application scenario guided by specific formula requirements, process integration points, and stringent industrial standards.

    1. Peptide and Protein Crosslinking in Biopharmaceutical Manufacturing

    Leading biopharmaceutical producers use this carbodiimide compound extensively for peptide coupling and protein conjugation processes under aqueous conditions, supporting the synthesis of key intermediates and active bioconjugates. Its solubility profile enables controlled activation steps without introducing organic solvents, ensuring compatibility with high-purity production environments and sensitive biological APIs.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • USP General Chapter <791> pH and <1047> Biologics
    • FDA 21 CFR Parts 210/211 cGMPs
    • European Pharmacopoeia guidelines for peptide synthesis reagents

    Typical usage ratio

    • 0.9 – 1.5 molar equivalents relative to carboxyl group substrate; ratio optimized based on amino acid sequence, peptide length, and desired activation efficiency

    Downstream process integration

    • Added at the activation stage in solution-phase or on-resin peptide synthesis processes following deprotection and neutralization cycles
    • Inserted into the protein conjugation workflow post-buffer exchange, enabling carboxyl-to-amine crosslinking in controlled pH media

    Final product types

    • Synthetic therapeutic peptides
    • Antibody-drug conjugates (ADCs)
    • Enzyme-linked proteins for diagnostic kits
    • Drug delivery bioconjugate carriers

    2. Oligonucleotide Functionalization for Molecular Diagnostics

    Producers of nucleic acid-based diagnostic reagents employ our carbodiimide derivative for activating terminal carboxylic acid groups on oligonucleotides, supporting covalent attachment to reporters or surfaces within assay platforms. This process enables downstream immobilization and labeling steps for clinical PCR and sequencing consumables under DNA-grade regulations.

    Industry compliance standards

    • ISO 13485:2016 Medical Devices – Quality Management
    • FDA 21 CFR 820 Quality System Regulation
    • CLSI MM01 guidelines for nucleic acid reagent preparation
    • Relevant national diagnostic product registration guidance (e.g., NMPA, CE-IVD)

    Typical usage ratio

    • 0.8 – 1.2 equivalents per carboxy-terminated oligonucleotide strand; ratio modulated according to length and desired modification density

    Downstream process integration

    • Dosed into aqueous labeling buffer during terminal activation, followed by rapid purification to remove excess reagent before quality control and final product formulation

    Final product types

    • Fluorescently labeled PCR primers
    • Microarray probes
    • Sequencing adapters
    • cDNA immobilization modules

    3. Water-Soluble Polymer Crosslinking for Medical Hydrogels

    Medical device manufacturers exploit the high water solubility of this carbodiimide for crosslinking carboxyl- and amine-functional water-soluble polymers under mild, physiological conditions, central to producing bio-compatible hydrogels for wound dressings and drug-eluting devices. This approach avoids the need for organic solvents and mitigates extractables risk, supporting compliance in regulated healthcare markets.

    Industry compliance standards

    • USP Class VI Biological Reactivity Tests
    • ISO 10993 Biological Evaluation of Medical Devices
    • FDA 21 CFR Part 820 Device GMP
    • ISO/TR 22971 for Hydrogel Devices

    Typical usage ratio

    • 0.5 – 2.0% w/w based on total polymer mass; dosage determined by polymer type, molecular weight, and degree of crosslinking desired for end-use mechanical properties

    Downstream process integration

    • Introduced as a solution to pre-blended polymer dispersions under controlled pH and temperature, immediately prior to molding or casting operations; final removal by extensive washing steps

    Final product types

    • Hydrogel wound dressings
    • Drug delivery patches
    • Soft tissue scaffolds
    • Bioadhesive sheets and coatings

    4. Activation Agent for Specialty Coating Resins

    Leading formulators in electronics and specialty coatings sectors use this compound to activate carboxyl-reactive intermediates during the synthesis of functionalized resins, especially when water-compatible crosslinking is required for applications in anti-fouling, antistatic, or bio-responsive coatings. The reactivity profile allows fast in-line processing, minimizing batch times and improving throughput control.

    Industry compliance standards

    • ISO 9001 Quality Management
    • RoHS (Restriction of Hazardous Substances Directive) for electronics
    • REACH (Registration, Evaluation, Authorization and Restriction of Chemicals – EU)
    • Specialty resin raw material purity specifications (per end-user contracts)

    Typical usage ratio

    • 0.5 – 1.0 molar equivalents per carboxyl function; adapted for resin-solids content and required level of functional group conversion

    Downstream process integration

    • Metered into polymerization reactors during resin modification stages or directly into pre-mix tanks for inline coating formulation; pH and temperature monitoring used to control reaction profile

    Final product types

    • Anti-fouling film coatings
    • ESD-protective layers for electronic substrates
    • Bioactive polymer coatings for medical equipment
    • Surface-modified packaging films
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    Certification & Compliance
    More Introduction

    Introducing 1-(3-Dimethylaminopropyl)-3-Ethylcarbodiimide Methiodide: Precision Chemistry from the Source

    Understanding the Compound

    Innovation in chemical synthesis takes more than high-purity bottles on shelves—it takes consistency, reliable science, and a transparent connection with the bench. Our team manufactures 1-(3-Dimethylaminopropyl)-3-Ethylcarbodiimide Methiodide, designed to serve as a versatile coupling agent trusted by peptide chemists, bioconjugate researchers, and oligonucleotide synthesis specialists. Each batch comes directly from our reactors, never from intermediaries or repackagers. Our process starts with selectively sourced raw materials, handled with exacting care at every step, because every reaction tells a story about its origins.

    What Sets the Compound Apart

    In the world of carbodiimides, subtle molecular details translate into major practical differences. Lab teams often ask what makes an ethyl-substituted derivative like ours distinctive, especially when compared to common counterparts such as EDC hydrochloride or DCC. The methiodide salt brings enhanced water stability. Our formulation resists hydrolysis better than non-methylated analogs, allowing longer processing times under aqueous conditions. The cationic methyl group makes purification easier—precipitates settle, minimizing resin clogging and sidestepping lingering traces in final products.

    Many connect carbodiimides exclusively with peptide bond formation, but 1-(3-Dimethylaminopropyl)-3-Ethylcarbodiimide Methiodide opens doors for a range of bioconjugation chemistries. Biologists searching for high-activity amidation in the presence of labile functional groups select this product for its mildness. It supports urea and amide linkages without unleashing side reactions that can plague less selective reagents. Our clients—whether research universities focused on cell labeling or manufacturers scaling up diagnostic conjugates—notice the performance, batch after batch.

    From Production to Practice: Quality Control in Action

    Workflows in chemistry thrive on predictability, not promises. We continually monitor and calibrate synthesis—chromatography and NMR analysis guide each stage, but it’s the practical insight garnered from decades on the floor that shapes adjustments. Inconsistent batches waste time, solvent, and morale. We battle contamination by investing in closed systems and glass reactors dedicated to quaternized intermediates. Regular impurity checks with LC-MS and titration confirm you receive material matching the stated assay every time. Yield metrics matter to us because we run the same processes at pilot and plant scales, closing the feedback loop between R&D, production, and application.

    Hands-On Reliability in the Lab

    Chemists count on reagents that don’t surprise during workups. Ethylcarbodiimide methiodide dissolves quickly, leaving only a faint signature that won’t mask subtle color changes or interfere with UV-based assays. It pairs exceptionally well with both organic and aqueous solvents, so switching protocols or troubleshooting new recipes won’t require juggling incompatible salts. If a reaction fails, it’s usually not because of the coupling agent, at least when used fresh and dry.

    Some customers report clogging issues using traditional carbodiimides because byproducts can crystallize during lengthy reactions or during cold storage. Our experience shows that the methylated iodide byproduct from this compound remains highly soluble in common solvents and rarely impedes subsequent purification. The difference becomes clear in preparative chromatography, where sample losses trace more often to overloaded columns than to residue from reagent decomposition.

    Common Applications: Solutions Guided by Experience

    Peptide synthesis remains core business for many chemical companies, but we see increased demand from bioconjugate developers aiming for site-specific modification on proteins, antibodies, or nanoparticles. Our compound performs in carbodiimide crosslinking for DNA and RNA probes, allowing attachment of dyes or affinity tags with minimal non-specific interactions. Immunologists and molecular biologists turn to this chemistry for making toxin–protein conjugates or antibody–enzyme constructs—products that require not only consistent yields but a reagent that won’t introduce immunogenic impurities.

    Protein immobilization on chromatography supports has turned into a routine process in our customers’ workflows. Each immobilization step gets evaluated for coupling efficiency, stability, and leak of bound protein under repeated wash cycles. We have compared our ethylcarbodiimide methiodide to standard water-soluble carbodiimides, documenting superior bond strength and fewer cases of random alkylation. Our chromatographers value this as it supports regeneration and repeated use of high-value resins, stretching procurement budgets without sacrificing analytical integrity.

    Comparing Alternatives: Picking the Right Tool

    New users sometimes ask if they can substitute our compound for EDC hydrochloride or DCC. Both EDC.HCl and DCC continue to hold ground for certain protocols, especially where extreme water solubility or cost minimization drives decisions. DCC, for example, creates urea byproducts stubborn to separate, posing routine headaches for high-throughput peptide synthesis labs. Its crystalline byproduct can blind filter membranes or contaminate downstream analysis. EDC hydrochloride, while more water-friendly, breaks down rapidly in the presence of carboxylate reactants, cutting process windows and forcing repeated runs if timing goes astray. Our ethylcarbodiimide methiodide bridges these gaps—a stable, crystalline solid, easy to weigh, and manageable in both gram and multi-kilogram orders.

    Lab teams find themselves balancing performance against cost of waste disposal. Handling iodide salts calls for routine attention, but the reduced toxicity and easier filtration of byproducts mean less expense in hazardous waste management. Since our process leaves minimal free amine or unreacted starting material, end users report less need for laborious secondary purifications, enabling faster scale-up without hidden delays.

    Ensuring Consistency: Manufacturing and Logistics

    From the moment we receive a new order to the day shipment leaves the dock, a chain of events unfolds in our facility. Bulk synthesis batches usually range from a kilogram up to several hundred, with smaller custom lots available on request for intricate research projects. Every vessel receives only the appropriate reactants—cross-contamination control comes from dedicated piping, segregated storage for methyl iodide, and regularly validated cleaning protocols.

    Our experience with ambient shipping suggests that this compound does not degrade under typical warehouse and ground transport conditions. Re-sealable, inert-packed containers keep moisture out, so by the time it arrives in customer hands, it remains pure, clump-free, and ready for immediate use. When regulatory paperwork or customs procedures add complexity, we guide customers through the process grounded in practical logistics—real-time coordination across our production, QA, and export teams.

    Supporting Chemists at the Bench

    Manufacturing a chemical like 1-(3-Dimethylaminopropyl)-3-Ethylcarbodiimide Methiodide invites ongoing dialogue with those who use it. Our phone never goes unanswered when a researcher reaches out, whether about solubility quirks or scale-up advice. We routinely help troubleshoot protocols—sometimes reviewing HPLC traces, sometimes walking through reaction timing, sometimes working through tricky solvent systems for custom conjugations. The insights chemists share drive iterative improvements; if two labs on opposite continents struggle with precipitates under specific pH ranges, our R&D team tests new tweaks and reports back.

    Proprietary methods and optimal ratios often vary, but sharing experiences grounds our commitment to transparency. We do not hide behind reluctant disclaimers or force users into rigid protocols. Whether working with automation in high-throughput peptide synthesis or fine-tuning reaction times for precious milligram-scale conjugates in academic settings, our compound supports flexibility without sacrificing performance.

    Safety Practices: A Matter of Habit and Principle

    Risk management starts long before a bottle enters a research lab. Manufacturing with methyl iodide as a precursor triggers stringent ventilation and real-time exposure monitoring, ensuring all team members go home healthy. Our safety standards exceed local regulations because years of working with quaternized salts have shown the value of proactive control. Reagent spills, rare in our lines, receive immediate response—spill kits, secondary containment, and routine drills build muscle memory that pays off in uncertain moments.

    Customers routinely ask about compatibility with standard lab waste streams. Experience shows that the byproducts do not accumulate in commonly used extraction solvents or linger beyond routine water washing. Used containers, triple-rinsed and decontaminated, can join standard waste, reducing both cost and regulatory headache for busy research facilities.

    Building for Tomorrow’s Needs

    The chemical landscape shifts as new applications emerge. We watch trends in fluorescent antibody labeling, nanoparticle surface modification, and solution-phase oligonucleotide synthesis. Every advance in biomedicine or diagnostics challenges existing chemistry, demanding purer, more predictable intermediates. Our work with 1-(3-Dimethylaminopropyl)-3-Ethylcarbodiimide Methiodide continues to evolve: ongoing partnerships with research institutions drive changes in scale, packaging, and analytical testing.

    We see increasingly stringent assay requirements for raw material suppliers serving regulated environments. Pharmaceutical customers, in particular, demand documentation confirming impurity profiles, process validation, and stability data. We manage these expectations by providing up-to-date certificates of analysis and maintaining robust archive data for reference during audits or product registration. Our investment in digital recordkeeping ensures every transaction links back to real-time manufacturing data, not just a generic specification sheet.

    Stewarding the Supply Chain

    Trusted suppliers mean little without traceability. Each container we ship receives a unique production identifier, and we can trace every shipment—from mimimum research-use-only volumes to large industrial orders—back to the batch and even raw material lots. This investment in traceability means if an industry standard shifts or an unforeseen impurity emerges, our team acts quickly. Immediate root-cause analysis and rapid response stem not from rigid bureaucracy but from direct experience troubleshooting complex reactions.

    As global attention on chemical provenance grows, end users look for more than just a low price point. They request transparent documentation and want material that stands up to inspection in GMP audits or university grant reviews. We regularly undergo third-party audits and welcome customer visits; walking the floor with researchers or QA specialists sharpens both our process and theirs.

    Continuous Improvement: Listening and Responding

    Feedback from research customers has shaped subtle—but crucial—adjustments in our production process. Early customers experienced occasional static buildup during weighing. By switching filling lines and upgrading humidity control in our packaging areas, we eliminated powder loss and container sticking. Regular client surveys led to a resize in our default container selection, supporting both bulk buyers and those just running a handful of reactions.

    Our technical support channels stay open for ongoing conversations, not just purchase orders. We need your honest assessment if a reaction stalls, if a packaging flaw appears, or if a new regulation calls for tighter documentation. Each point of friction in the user experience becomes a project for improvement in our process chain. Growth, for us, doesn’t come from outpacing competitors—it comes from building partnerships anchored by real-world results.

    Ethics, Environment, and Responsibility

    Chemical manufacturing creates environmental challenges. Our ethos grounds itself in practical, achievable stewardship; solvent recovery and energy minimization stay top of mind in planning both facility design and day-to-day operations. Whenever possible, we recover and repurpose process streams, minimizing both water and energy footprints. Regulatory compliance never marks the end of accountability: we study emerging data on iodide salt waste, keep abreast of evolving discharge regulations, and look for ways to further close the loop on raw material sourcing.

    Every kilogram shipped represents a pledge not just to clients and collaborators, but also to the communities and ecosystems around our facilities. We support third-party environmental audits and adjust procedures as new data and community priorities surface. Pressures toward green chemistry shape our development calendar: we constantly seek to improve atom economies, reduce hazardous byproduct formation, and increase yield efficiency, learning from both regulatory science and practical field experience.

    Strength in Experience—The Manufacturer’s Perspective

    To make a compound that stands up to scrutiny from discerning researchers, logistic managers, and regulators demands both dedication and humility. Supplying 1-(3-Dimethylaminopropyl)-3-Ethylcarbodiimide Methiodide means carrying a responsibility for outcomes in peptide synthesis, conjugate development, and analytical workflows. Our reputation grows not from abstract quality claims, but from consistent supply, complete transparency, and technical dialogue.

    Few things matter more than sending material that works—every time, at scale, with no surprises. This commitment colors every decision, from raw material purchasing to equipment investment and documentation. We benefit from decades spent troubleshooting real-world issues alongside chemists: whether supporting startups entering biotherapeutics or seasoned teams scaling up new diagnostic platforms, our process gets refined by demand for reliability and scale-up expertise.

    Looking to the Future: Evolving with Discovery

    Discovery doesn’t pause, and neither do we. Every week brings new requests for data or slightly altered product variants matched to the evolving needs of advanced chemical biology. Some scientists want tighter control of trace iodide contamination; others experiment with reactions under inert atmospheres or adjust ratios for unexpected substrates. Each request teaches us something new, sharpening production forecasts and aligning analytical methods to today’s best practices.

    We owe our progress to a diverse set of users—newcomers and old hands alike—who notice differences batch by batch, report anomalies, and share papers showing the compound at work under fresh conditions. Their results, paired with our manufacturing improvements, drive the cycle forward. Each bottle shipped connects a chemical reaction with manufacturing history, built on experience, not speculation or marketing gloss. This remains the heart of making not just a product, but a partnership in discovery.