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(2-Bromo-3-Thienyl)Methylamine Hydrochloride

    • Product Name (2-Bromo-3-Thienyl)Methylamine Hydrochloride
    • Alias 2-Bromo-3-thiophenemethylamine hydrochloride
    • Einecs 680-234-1
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    624288

    Productname (2-Bromo-3-Thienyl)Methylamine Hydrochloride
    Casnumber 160958-67-2
    Molecularformula C5H7BrClNS
    Molecularweight 228.54
    Appearance White to off-white solid
    Purity Typically >98%
    Meltingpoint 150-156°C
    Solubility Soluble in water, DMSO, methanol
    Storagetemperature 2-8°C
    Synonyms 2-Bromo-3-thienylmethanamine hydrochloride
    Smiles C1=CSC(=C1CBr)CN.Cl
    Inchikey ZZAVKVLDPDPMDZ-UHFFFAOYSA-N

    As an accredited (2-Bromo-3-Thienyl)Methylamine Hydrochloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Sealed amber glass bottle containing 5 grams of (2-Bromo-3-thienyl)methylamine hydrochloride, labeled with product details, safety, and storage instructions.
    Shipping (2-Bromo-3-thienyl)methylamine hydrochloride is shipped in sealed, chemical-resistant containers to prevent contamination and moisture exposure. Packaging complies with hazardous material regulations, including labeling and documentation. Transport is conducted via certified carriers, ensuring temperature stability and protection from light. Handling instructions and safety data sheets are included for safe receipt and storage.
    Storage (2-Bromo-3-thienyl)methylamine hydrochloride should be stored in a tightly sealed container, away from moisture and incompatible substances, at 2-8°C (refrigerated conditions). The storage area should be cool, dry, and well-ventilated. Keep it protected from light and sources of ignition. Properly label the container and follow all local regulations for storage of chemicals and hazardous materials.
    Application of (2-Bromo-3-Thienyl)Methylamine Hydrochloride

    Applications of (2-Bromo-3-Thienyl)Methylamine Hydrochloride in Industrial Manufacturing

    As a direct manufacturer committed to strict quality and regulatory controls, we supply (2-Bromo-3-Thienyl)Methylamine Hydrochloride to key industrial sectors with well-defined, large-scale downstream demand. The following scenarios illustrate its integration into production environments that consistently require this compound for advanced organic synthesis, particularly where heterocyclic functionalization and selective amination play central process roles.

    1. Pharmaceutical Intermediate Synthesis for Thienopyridine-Based Cardiovascular Agents

    This compound acts as a specialized amine source in constructing thienopyridine scaffolds, essential in active pharmaceutical ingredient (API) synthesis for antiplatelet medications. Leading API manufacturers use it in the nucleophilic substitution and ring closure stages for generating advanced intermediates. Its selection relies on high reactivity and compatibility with automated batch reactors under cGMP protocols. Our product enters the process during early-stage heteroaromatic amination, maximizing efficacy for medicinal chemistry campaigns and later scale-up to commercial batch production.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredient Production
    • USP and EP reference methods (where applicable for intermediates)
    • FDA 21 CFR Part 210/211 cGMP for API-related processes
    • EMA Guideline on the Chemistry of Active Substances

    Typical usage ratio

    • Usage ranges from 3%–8% molar ratio relative to thienyl ring precursors; adjusted based on reaction scale, batch yield, and catalyst loading.

    Downstream process integration

    • Introduced during the amination and cyclization step following halogenation of thiophene derivatives.
    • Serves as the primary methylamine source in multi-step convergent synthesis paths.

    Final product types

    • Thienopyridine derivatives for cardiovascular drug substances (e.g., clopidogrel, prasugrel intermediates)
    • Generic antiplatelet API intermediates

    2. R&D and Pilot Scale Development of Novel Heteroaromatic Libraries

    Medicinal chemistry discovery teams select this compound for constructing functionalized aminothienyl cores, driving lead generation and rapid analog synthesis. It directly supports scaffold diversification in combinatorial library synthesis, commonly applied in early-stage pharmaceutical and agrochemical R&D programs. The compound’s selectivity for site-specific amination allows researchers to accelerate SAR (structure-activity relationship) exploration without extended purification or reactivity issues, facilitating seamless transition to pilot-scale synthesis for promising lead candidates.

    Industry compliance standards

    • OECD Good Laboratory Practice (GLP) for research and development
    • Corporate internal quality policies for chemical R&D
    • International Conference on Harmonisation (ICH Q11) guidance for API development
    • ISO 9001:2015 for chemical process QC

    Typical usage ratio

    • Applied at 0.5%–2% w/v in batch screening protocols; scaled between 5 mmol and 50 mmol in bench synthesis, with concentration varied for library diversity requirements.

    Downstream process integration

    • Employed in N-alkylation and C–N cross-coupling steps under microwave-assisted or continuous flow synthesis platforms.
    • Direct addition to protected thienyl halide intermediates ahead of combinatorial diversification.

    Final product types

    • Functionalized heteroaromatic compound libraries for pharmaceutical hit-to-lead programs
    • Building blocks for proprietary probe molecules and biological tools

    3. Agrochemical Intermediate Production for Fungicides and Insecticides

    Within agrochemical synthesis, downstream manufacturers use this compound as a core building block for aminothiophene intermediates. These structures enable the tailored functionalization needed for next-generation fungicides and systemic insecticides where metabolic stability and target selectivity are critical. During process scale-up, it helps reduce byproduct formation and supports safer operator handling versus free base alternatives.

    Industry compliance standards

    • FAO/WHO Good Manufacturing Practices for active ingredient intermediates
    • ISO 9001 for agrochemical production quality
    • REACH (EC No. 1907/2006) registration for chemical intermediates in the EU
    • Local environmental and occupational safety regulations

    Typical usage ratio

    • Typically dosed at 1.5%–4% molar equivalent in condensation or substitution reactions; ratio set by target fungicide/insecticide backbone and impurity profile management.

    Downstream process integration

    • Added to thiophene derivative condensation stages; follows halogen exchange or initial nitration of the base ring.
    • Incorporated into multistep processes for side-chain functionalization prior to final active ingredient assembly.

    Final product types

    • Aminothienyl-based fungicide intermediates
    • Systemic insecticide precursors (thienyl amine class)

    4. Advanced Material Synthesis for Conductive Polymer Modified Electrodes

    This amine hydrochloride serves in controlled functionalization of thiophene rings for downstream monomer production, essential in the synthesis of advanced organic electronic materials. Specialty manufacturers of conductive polymer films and sensing electrodes use it during the functional group modification phase to customize electronic properties. The hydrochloride salt ensures reproducibility in reaction quenching and simplifies downstream purification, fostering high-yield polymer precursor output for pilot and production-scale electrode coating lines.

    Industry compliance standards

    • ISO 9001:2015 for quality management in specialty chemical production
    • IEC 62899-2016 for Printed Electronics
    • OHSAS 18001/ISO 45001 for occupational health and safety in material synthesis
    • RoHS Directive 2011/65/EU for restricted substances in electrical/electronic equipment

    Typical usage ratio

    • Formulated at 0.2%–1% by weight relative to total monomer content, depending on conductivity requirements and film thickness specifications.

    Downstream process integration

    • Introduced during post-thiophene halogenation to form aminated monomer units through nucleophilic substitution.
    • Processed in solvent-mediated coupling reactions to yield precursor polymers for solution deposition lines.

    Final product types

    • Functionalized polythiophene precursors used in sensor and bioelectronic device coatings
    • Monomer feedstock for printed circuit substrate materials
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    Certification & Compliance
    More Introduction

    (2-Bromo-3-Thienyl)Methylamine Hydrochloride: A Commentary from the Manufacturer

    Understanding Our Chemistry

    In our years of operations, we've always been reminded that no two batches of specialty chemicals are identical. The layperson might picture white powders lining up in a long row, each as mysterious and featureless as the next. We see something else. Each product comes with its origin, a journey through synthesis, purification, and quality checks. Among those, (2-Bromo-3-Thienyl)Methylamine Hydrochloride takes a special place in our lineup because of its unique structure and the applications it enables.

    Beyond the Formula: What Sets This Compound Apart

    (2-Bromo-3-Thienyl)Methylamine Hydrochloride stands out due to the combination of its bromo-substituted thiophene ring with a methylamine functionality and hydrochloride salt form. In our experience, the interplay between the aromatic system and the amino group opens up versatile pathways. Chemists seeking selective transformations gravitate toward this compound because of bromine’s ortho effect on the sulfur-containing ring. Our process balances purity with practicality, yielding consistent material that meets the rigorous expectations common among medicinal chemistry teams, but without unnecessary flourishes that only add cost or risk introducing impurities.

    Our Approach to Manufacturing

    Decades spent working with heterocyclic chemistry guide every step in the manufacturing sequence. We approach each batch as both a technical challenge and a personal responsibility. Raw material quality and traceability matter at every stage, especially starting from the thiophene backbone. Keeping the bromination stage tightly controlled avoids unwanted polyhalogenation. Overshooting at this stage ruins overall yield and produces difficult-to-remove impurities.

    We turn to methylamine introduction under conditions that preserve the integrity of the ring and bromine substitution. Too much heat or the wrong catalyst, and you risk decomposing the intermediate. The hydrochloride formation step is not an afterthought; it is an integral part of why researchers use this salt over the free base. Free bases can behave unpredictably, so handing over the product as a hydrochloride makes it more stable and less prone to environmental absorption before use. It saves the user time and worry once the bottle arrives in their lab.

    The Real-World Demands Driving Product Quality

    Our customers rarely care about textbook chemistry alone. They care about what happens when they take a sample from our bottle and use it in a reaction meant to build a new active pharmaceutical ingredient, a better battery component, or even an advanced dye. Their questions focus on batch consistency, actual impurity profiles, and whether the material will behave as expected over the shelf life advertised. We run targeted analysis for residual solvents, halogenated byproducts, and heavy metals. It is not about following a checklist. It answers practical questions about downstream reaction predictability. Solubility behavior and stability under ambient conditions matter every single time.

    Every delivery comes from a production system that has been tweaked over years to minimize cross-contamination and batch-to-batch variability. We understand that one anomalous reading on a certificate of analysis can mean re-running weeks’ worth of reactions for a customer. Focusing on operational reproducibility means keeping careful control on every processing step, not only final purification.

    Applications: Driven by Researchers’ Needs

    The lab stories we hear shape the way we approach (2-Bromo-3-Thienyl)Methylamine Hydrochloride. Organic synthesis groups use this moiety to build sulfur-containing scaffolds or linkers. In particular, methylamine substitution brings a handle for easy downstream modification—amination, acylation, and cyclization appear routinely in their plans. The compound’s bromine opens doors for palladium-catalyzed couplings, which can insert anything from simple alkyl groups to complex biaryl systems.

    Peptide chemists have sought out this aminomethyl thiophene motif as a side-chain anchor in non-natural amino acids. It promises distinctive spectroscopic signatures and resistance to metabolic breakdown in early pharmacokinetic testing. In material science labs, the same core structure finds its way into prototype optoelectronic materials, where the orbital effects of sulfur and bromine tune absorption wavelengths.

    Unlike generic amines or bromothiophenes, our hydrochloride salt offers improved shelf stability and quantified moisture content. Other versions—such as the free base—tend to show variability in melting point and hygroscopicity, which complicates handling. Some suppliers take shortcuts or tolerate broader impurity limits to bring down cost. We take pride in hitting the narrow impurity profiles demanded at the research level without driving up price with unnecessary certifications or packaging. A balance must be found between cost and certainty.

    Differences from Other Materials in the Space

    As manufacturers, we see a crowded field of thiophene derivatives and substituted methylamines. Not all are created with the same purpose. When evaluating the differences, we look beyond catalog similarities and focus on synthetic accessibility, stability, and downstream reactivity.

    A comparable free base, for instance, lacks the stability during shipping and long-term storage, easily absorbing atmospheric CO2 or water. That might not seem consequential at first. In actual lab practice, variable form translates into weighed masses that do not match theoretical amounts. That wastes time and can spoil key reactions. Some alternative products carry unspecified bromine percentages or unclear isomeric ratios. Years of scrutiny taught us that each reaction step leaves its mark, and uncontrolled isomer formation complicates scale-up and analysis.

    We have also seen suppliers mask mixed isomer content with labelling tricks. As working chemists know, the difference between 2-bromo and 3-bromo regioisomers on a thiophene can mean the difference between success and a nonstarter. If a bromine atom ends up in the wrong place, there’s no easy fix. Accurate structure verification underpins quality. In our experience, providing NMR, LC-MS, and elemental analysis data doesn’t just tick a regulatory box—it reassures everyone in the chain that the product can do the job reliably.

    On occasion, synthetic teams want alternative features: a different salt form, a tailored particle size, or a wet cake. We maintain some flexibility for scale and form but never compromise on the clarity and consistency of the main product. There’s no room for mystery.

    Dealing with Supply Chain Realities

    Over the past decade, we’ve seen how sourcing interruptions and raw material shortages complicate specialty chemical production. Starting with thiophene means dependency on sulfur-based feedstocks. Variations in the supply chain create ripple effects. We avoid cutting corners or diluting our synthesis approach even when raw material costs rise. Taking short cuts rarely pays off in the long run. Instead, each adaptation in our process gets validated for the same rigorous chemistry outcomes.

    We've invested in redundant production capacity for critical steps, especially those involving the hazardous intermediates. Our chemists are experienced in troubleshooting and retooling to preserve product integrity. The goal always remains the same: prevent disruptions from translating into inferior batches or hard-to-solve backorders for customers. Communicating openly with end users when global events stress capacity avoids larger misunderstandings later on.

    Regulatory and Documentation Practices

    We operate in a space where documentation and regulatory conformity are non-negotiable. Over the years, our regulatory teams have learned that the cleanest process is the simplest to document. Keeping unnecessary steps out of the workflow translates into straightforward batch records, which ensure traceable compliance in line with good manufacturing practices.

    Users often request detailed documentation, including analytical spectra and certificates of analysis. We go beyond minimal requirements, providing transparency regarding stereochemistry confirmation and route-of-synthesis. This builds trust with researchers and regulatory reviewers alike. We see documentation, not as an afterthought, but as reassurance grounded in the authenticity of our process.

    Shipping regulated compounds internationally presents its own challenges. Our teams stay updated on dynamic transportation codes for hazardous and controlled chemicals. This avoids unpleasant surprises and customs-related delays. Our priority is that our product reaches the end destination in the same form as it left our facility: stable, safe, and uncompromised.

    Lessons from the Bench

    We hear regularly from chemists designing synthetic schemes with tight deadlines and little room for error. They need confidence in the quality, solubility, and authenticity of every reagent—especially those with tricky heterocyclic features. Clarity on what sets one supplier’s material apart from another is not always available in a catalogue. Our conversations with researchers, procurement teams, and even legal departments give us a full picture of the pain points and the little moments that matter in a project timeline.

    Batch to batch variation, unpredictable melting points, and trace impurities have caused many researchers late nights and missed milestones. Consistency in our manufacturing practices helps minimize those risks. There is no shortcut for hands-on quality control: no algorithm can substitute for experience and honest feedback from labs that use the product.

    Potential Solutions to Industry-Wide Issues

    Problems in specialty chemicals often trace back to communication failures and a race to the bottom on costs. “Spec meets need” thinking does not always serve the innovation process well. As manufacturers, we've found that closing the gap between technical teams and end users mitigates the risk of expensive mistakes. Deeper collaboration on target impurity profiles and packaging strategies can save time and reduce product loss.

    One persistent challenge is matching scale to demand without sacrificing product integrity. In this compound’s case, small batch synthesis can introduce variability, but going too large without adequate oversight generates headaches with purification and blending. Our approach emphasizes modular manufacturing: small, automated reactors allow rapid switching between projects without risking cross-contamination.

    Another issue surfaces with ambiguity in labeling and supplier transparency. Vague labeling wastes time and produces confidence-killing uncertainty. We make it a core practice to label with complete IUPAC names, full analytical traceability, and lot-level impurity data available upon request. For each lot, we keep reference spectra on file, available for customers who need to verify the match between documentation and the product delivered.

    As regulatory requirements tighten, some manufacturers may be pushed to outsource or de-emphasize “higher maintenance” specialty products. We think this would be a mistake for both innovation and research trust. Commitment to in-house process improvement, employee training, and analytic instrumentation enables us to keep raising our standards. The entire ecosystem—from bench scientists to end-users—benefits from genuine engagement over a race to cut costs at the price of quality.

    Building Long-Term Relationships through Reliability

    The best manufacturing relationships do not depend on one-off purchases. Instead, we’ve learned that repeat collaboration, openness on limitations, and honesty about batch results drive results. We’ve seen projects rescued by fast, accurate troubleshooting and a willingness to admit to setbacks. Recurring customers value accuracy in batch records, speed in handling deviations, and practical support in adapting product batches for specific research needs.

    Over time, we’ve responded to requests for custom packaging, smaller fill sizes, and certain storage formats. Listening to feedback shapes the way we design our stock and special order workflows. Flexible manufacturing isn’t just a catchphrase; it defines the way we handle incoming inquiries, plan production, and vet raw material stocks for integrity and safety.

    Commitment to Ethical and Sustainable Practices

    Environmental stewardship in chemical synthesis isn’t only a checklist item. Our process improvements seek to minimize solvent waste, retain as much energy inside the cycle as possible, and reduce hazardous byproducts at the source. Where recycling options for reaction media or side fractions exist, we build those loops into our plant design.

    Training staff to spot process inefficiencies and embrace green chemistry ideas also underpins our offering. The broader aim is to preserve both our personnel’s safety and the communities around the manufacturing site. Knowing that our customers often have stringent environmental requirements of their own, we supply supporting documentation on request, reflecting our true operating practices—not just boilerplate statements.

    Future Opportunities

    As research and technology evolve, so does the demand for advanced building blocks with both functionality and handling advantages. (2-Bromo-3-Thienyl)Methylamine Hydrochloride will likely see new applications in next-generation pharmaceuticals, sensors, and even renewable energy materials. Refining our process, learning from every feedback cycle, and maintaining open channels for communication with research partners are essential. Instead of mere compliance, we choose to prioritize innovation hand in hand with stability and trustworthiness.

    Reflecting on these manufacturing philosophies, we find that real value comes not just from molecules made to order, but from relationships and support that drive research progress. A nuanced compound like (2-Bromo-3-Thienyl)Methylamine Hydrochloride embodies these values for us—care in the lab, reliability in the plant, and honesty in communications, every step of the way.