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

1-Bromo-3-Methyladamantane

    • Product Name 1-Bromo-3-Methyladamantane
    • Alias 1-Bromo-3-adamantanemethyl
    • Einecs 246-006-9
    • 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
    VTB
    Specifications

    HS Code

    792503

    Chemical Name 1-Bromo-3-Methyladamantane
    Molecular Formula C11H17Br
    Cas Number 4240-57-5
    Appearance White to off-white crystalline solid
    Boiling Point 273-277°C (estimated)
    Melting Point 87-88°C
    Density 1.28 g/cm³ (approximate)
    Purity Typically ≥98%
    Solubility Slightly soluble in water; soluble in organic solvents
    Smiles CC12CC3CC1CC(Br)C3C2
    Inchikey FMXQDIFNLUGVJT-UHFFFAOYSA-N

    As an accredited 1-Bromo-3-Methyladamantane factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing
    Shipping
    Storage
    Application of 1-Bromo-3-Methyladamantane

    Applications of 1-Bromo-3-Methyladamantane in Industrial Manufacturing

    1-Bromo-3-Methyladamantane supports specialized chemical synthesis across several industrial sectors. Our production controls every stage to meet industry specifications, ensuring high purity and batch-to-batch consistency. This section provides detailed insights into practical downstream applications, covering compliance, recommended incorporation ratios, integration steps, and target finished products.

    1. Pharmaceutical Intermediate for Antiviral APIs

    Major pharmaceutical companies incorporate 1-Bromo-3-Methyladamantane as a critical intermediate in the multi-step synthesis of adamantane-based antiviral active pharmaceutical ingredients (APIs). It acts as a select alkylating and brominating building block specifically in the production of second-generation rimantadine and advanced adamantane derivatives. This intermediate enters direct substitution reactions under controlled conditions to provide high-yield and high-purity API precursors, matching regulatory and GMP expectations for injectable and oral dosage form development.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.) monographs
    • US FDA 21 CFR Part 210/211
    • Chinese GMP (2010 Edition)

    Typical usage ratio

    • 30–60 wt% in intermediate reaction stage, adjusted for target molecule substitution degree and synthesis yield optimization

    Downstream process integration

    • Charged during initial bromination/alkylation step; follows directly into coupling or reduction stage of API synthesis process

    Final product types

    • Adamantane-derived antiviral APIs (e.g. rimantadine, tromantadine)
    • Intermediate stock for clinical and commercial drug substance batches

    2. Raw Material for Liquid Crystal Display (LCD) Monomer Synthesis

    When manufacturing specialty liquid crystal monomers, electronics chemical producers utilize 1-Bromo-3-Methyladamantane for its rigid tricyclic structure that imparts crucial mesogenic properties to finished liquid crystalline compounds. Its introduction via Suzuki-Miyaura or Grignard type cross-coupling allows for precise spatial configuration necessary in bifunctional and laterally substituted mesogen production. Consistency in purity and batch homogeneity is essential for downstream optical and electro-optical performance.

    Industry compliance standards

    • IEC 61249-2-21: Materials for Printed Boards and Other Interconnecting Structures
    • RoHS Directive (2011/65/EU), Annex II
    • Certified ISO 9001:2015 quality management

    Typical usage ratio

    • 10–25 wt%, depending on target mesogen design and final birefringence property requirements

    Downstream process integration

    • Incorporated as a starting halide in alkylation step of liquid crystal monomer synthesis; follows purification and condensation with complementary aromatic cores

    Final product types

    • Specialty liquid crystal monomers
    • Advanced liquid crystal display mixtures for TFT-LCD and OLED panels

    3. Precursor for Advanced Polymer Modifiers

    Producers of engineering plastics and polymer additives select 1-Bromo-3-Methyladamantane to synthesize highly branched adamantyl derivatives that function as impact modifiers and chain terminators. Its integration allows for molecular weight and glass transition temperature tuning in polycarbonate resins, as well as improved heat resistance in specialty polyamides. Chemical handlers incorporate the material via nucleophilic substitution and Friedel-Crafts reactions—key steps for property-specific polymer tailoring.

    Industry compliance standards

    • REACH Regulation (EC) No 1907/2006
    • Chemical Control Law (CSCL, Japan)
    • UL 94 flame-retardance testing (if required)

    Typical usage ratio

    • 1–7 parts per hundred resin (phr), optimized according to molecular weight, desired toughness, and specific polymer system

    Downstream process integration

    • Loaded into reaction kettle before polymerization; enters copolymerization or post-polymerization grafting to adjust polymer macromolecule architecture

    Final product types

    • Impact-modified polycarbonate granules
    • Specialty nylon and polyester blends with improved thermal distortion resistance

    4. Intermediate for Fragrance and Flavor Modifier Synthesis

    Specialty chemicals companies utilize 1-Bromo-3-Methyladamantane in the synthesis of adamantane-based alcohols and ketones designed for fine fragrance and luxury cleaning product formulations. Through catalytic hydrogenation and oxidation processes, downstream users convert the material into stable, high-impact odorants and fixatives that exhibit enhanced volatility and diffusion characteristics. Its adamantyl core offers resistance to oxidation—an essential feature for high-end consumer product applications.

    Industry compliance standards

    • International Fragrance Association (IFRA) Guidelines
    • European Regulation (EC) No 1334/2008 on Flavourings
    • ISO 9235: Definition of Natural Aroma Chemicals

    Typical usage ratio

    • 5–15 wt% in key intermediate synthesis reactions, adjusted for target aromatic yield and customer formula requirements

    Downstream process integration

    • Introduced in primary alkylation step; passes through sequential reduction or oxidation to reach target alcohol/ketone for blending into aroma and flavor bases

    Final product types

    • Adamantyl-derived fragrance ketones
    • High-stability aroma ingredients for fine fragrance and premium detergents

    5. Key Building Block for Specialty Organic Electronic Materials

    Material scientists and electronics fabricators use 1-Bromo-3-Methyladamantane in the targeted synthesis of organic semiconductors and specialized insulating layers for use in organic light-emitting diodes (OLEDs) and field-effect transistors (OFETs). The brominated adamantane unit is introduced using regulated stepwise coupling chemistry, imparting controlled electron mobility and ensuring stable dielectric behavior. Batch reproducibility and impurity profile control play central roles for qualification and customer acceptance in electronic-grade applications.

    Industry compliance standards

    • IEC 62679-3: Electronic Paper Displays – Part 3: Materials
    • IPC-4101E: Specification for Base Materials for Rigid and Multilayer Printed Boards
    • ISO 14001: Environmental Management (for process chemicals)

    Typical usage ratio

    • 2–10 mol%, depending on targeted thin-film characteristics; adjusted based on device lifetime and charge carrier mobility parameters

    Downstream process integration

    • Introduced within precursor feed for cross-coupling or substitution to form active layers in OLED or OFET device stack-up

    Final product types

    • Organic semiconductor layers for OLED displays
    • High insulation specialty coatings in flexible electronic substrates
    Free Quote

    Competitive 1-Bromo-3-Methyladamantane 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

    Introducing 1-Bromo-3-Methyladamantane: Engineered for Precision

    Stepping into the field of organic synthesis, you quickly see the importance of reliable intermediates that respond predictably under reaction pressure. In my time collaborating with chemists on small-scale and scale-up projects, I’ve seen first-hand how specialty compounds like 1-Bromo-3-Methyladamantane can change the tone of a project. The name gives away its identity: a methyl group and a bromine atom carefully substituted on the rigid adamantane skeleton—a structure that offers remarkable edge in stability and reactivity. This molecular backbone isn’t just a chemical curiosity. It’s an engineer’s answer to issues in synthesis where both selectivity and performance count.

    Here’s what stands out about this product for those who spend long days at the bench or at the lab desk, figuring out how to actually make molecules for pharmaceuticals, polymers, or advanced materials. Adamantane derivatives have a track record in medicinal chemistry, especially where lipophilicity and steric protection improve a compound’s action or safety. Once you substitute the bromine atom at the 1-position and tuck a methyl at the 3-position, 1-Bromo-3-Methyladamantane carves out its own niche. The core structure remains rigid and compact, which helps limit unexpected rearrangements or fragmentation during tough reactions. The bromine atom acts as more than a spectator—it serves as an excellent leaving group, inviting precise further functionalization or Suzuki-type couplings where carbon-bromine bonds create downstream possibilities.

    Model and Practical Characteristics

    The model of 1-Bromo-3-Methyladamantane in practice offers meaningful advantages in yield and reproducibility. I’ve watched teams struggle with less robust scaffolds only to come back to adamantane derivatives because they hold up under heat, base, and unforeseen tweaks in protocol. The melting point and physical stability rank high, cutting down on storage headaches and reducing worries when shipping between facilities. Purity doesn’t just come down to numbers on a spec sheet; in complex syntheses, even small amounts of byproducts can snowball into problems at scale. Batches of high-purity 1-Bromo-3-Methyladamantane tend to show fewer side reactions in real-world runs, confirmed by cleaner NMR and GC-MS profiles.

    This isn’t a solution for every transformation, but 1-Bromo-3-Methyladamantane meets a real need where a methyl-branched, fully saturated hydrocarbon is essential, and where bromine’s reactivity outshines other alkyl halides. The rigid framework keeps the molecule from flexing in the way open-chain precursors do, shrinking the window for unwanted isomerization. Simple handling and straightforward solubility in a variety of solvents, including common aprotic types, round out its profile. The crystalline form resists premature decomposition, further supporting consistent process outcomes across runs.

    Why Formulation Matters: Insights from the Bench

    It’s easy to overlook the practical side of specialty chemicals until a hiccup shuts down a workflow. From my own lab work, I’ve seen how using a compound like 1-Bromo-3-Methyladamantane helps streamline both route selection and downstream isolation. The adamantane scaffold brings more than chemical stability; it survives harsh environments that would degrade less sturdy molecules. This robustness means lower loss during purification, less hassle in chromatographic separation, and a gentler learning curve for chemists who face shifting project conditions.

    Performance in cross-coupling, halide exchange, and specialty alkylation stands out in those tricky steps where steric congestion can stymie ordinary alkyl bromides. The methyl group on the third carbon makes modest but significant adjustments to electronic and spatial properties, and it’s these subtle differences that lead to better selectivity or more reliable activation. One can access derivatives that act as drug intermediates or precursors to high-performance polymers with more confidence thanks to this strategic substitution.

    Adamantane-based compounds such as this offer greater predictability in advanced synthetic work. They bring a combination of high melting points, resistance to acid and base, and strong hydrophobic character, which value-add to many workflows that stall with less rigid molecules. Pharmaceutical chemists especially find these features attractive in lead optimization or in probing structure-activity relationships, as they provide stable, reliable platforms for systematic research.

    Comparing with Other Organic Bromides

    Chemists searching for the right organic bromide quickly learn there’s more out there than the routine alkyl and aryl variants. Many off-the-shelf halides introduce too much flexibility or allow for unwanted isomerization in just about any strong reaction condition. In one project I worked on, using a linear bromoalkane led to nightmare mixtures after basic workups, especially with heat or base present. Switching to an adamantane-based bromide cut down on side reactions and improved overall conversion, because its geometrically locked structure won’t just flop around. Traditional bromoalkanes sometimes bring unwanted elimination, rearrangement, or even polymerization under mild heating—problems that are minimized with the adamantane cage.

    The difference here doesn’t just come from stability; it’s also about control. With 1-Bromo-3-Methyladamantane, the bromine is set up for neat displacement or metalation reactions, while the rest of the framework provides both chemical and physical integrity. The result—better yields in the hands of careful chemists, tighter control of byproducts, and more predictable process scaling. This product doesn’t always fit the bill if flexibility or backbone fragmentation is desired, but for rigorous, reproducible chemistry it sets a higher bar.

    Where 1-Bromo-3-Methyladamantane Excels: Pharmaceutical and Materials Science

    You see 1-Bromo-3-Methyladamantane come up in more than textbook mechanisms. In modern drug discovery, medicinal chemists hunt for novel scaffolds that offer metabolic stability and help slip past biological barriers. Adamantane structures have surfaced in famous drugs—amantadine for influenza and rimantadine for Parkinson’s, among others. Adding methyl and bromo functionalities extends these possibilities, especially when crafting analogues that resist enzymatic breakdown or sneak through lipid membranes with greater efficiency. My colleagues focusing on central nervous system targets have pointed to the rigid, non-planar shape as key in sidestepping receptor cross-reactivity.

    In advanced materials science, adamantane derivatives such as 1-Bromo-3-Methyladamantane offer a pathway to rigid cross-linking agents, photoresists, and specialty coatings. The compound serves as a jump-off point for building dendritic polymers, high-density crosslinked networks, or as a unique hydrophobic tag in complex molecular arrays. Its design enables cleaner downstream transformations, whether you’re aiming for functional monomers or targeting precision modification in electronic or photonic materials.

    The possibilities keep widening as research pushes into new areas. I have seen novel surfactants, antiviral agents, and specialty ligands built on the adamantane skeleton. What’s always clear is this: chemists gravitate toward intermediates like 1-Bromo-3-Methyladamantane when reliability, structure, and downstream versatility rank at the top of the wish list.

    Building a Reliable Supply Chain for Advanced Reagents

    In my experience working between the laboratory and procurement desk, specialty halides often create headaches due to volatility or short shelf life. 1-Bromo-3-Methyladamantane sidesteps these concerns, shipping safely as a stable solid. Storage concerns ease up, and consistency between shipments improves. This factor matters, especially for groups running a series of experiments or pilot processes where unpredictable lots slow or halt progress. One research group reported hitting roadblocks with variable-batch bromides from different suppliers; adopting the adamantane derivative led to cleaner, batch-to-batch repeatability and lower cost-per-run when factoring in waste reduction.

    Solid structure, moderate volatility, and a relatively straightforward crystallization process all point to easier scaling. It’s not just a question of quality, but also about robust logistics—a detail that everyone from junior chemists to senior project managers comes to appreciate. In operational settings, avoiding special storage needs or expensive refrigerated shipping lets teams focus budgets and time elsewhere.

    Addressing the Challenges: Solutions and Lessons Learned

    As anyone in chemical R&D will tell you, not every intermediate acts as promised in each reaction context. Adamantane-based reagents bring their own quirks. Sometimes, the increased steric bulk can slow down reactions meant to proceed at room temperature, calling for hotter or longer runs. Strong nucleophiles occasionally need higher equivalency to get full conversion because the substrate’s bulk hinders easy approach. These are not insurmountable issues. Adjusting base strength, temperature profiles, or stirring rates usually restores high conversion yields. In my own practice, slow addition and careful solvent choice prevent unwanted precipitation or slowed kinetics.

    Another hurdle that occasionally surfaces is pricing. Specialty intermediates often cost more by weight than commodity bromides. The value, as active researchers know, lies in reducing downstream purification, boosting reliability, and avoiding resource-intensive troubleshooting. Teams focused on lean operations make a case for spending up front to save further along the pipeline. Collaborative relationships with suppliers help here; negotiating batch sizes or delivery schedules typically produces savings without giving up on quality assurance.

    Environmental and safety questions can’t be ignored. Organobromine compounds sometimes spark concern about waste disposal or persistence. 1-Bromo-3-Methyladamantane, as a crystalline, non-volatile solid, produces far fewer emissions during handling and use compared to low-molecular-weight bromides. Proper collection and disposal through certified waste handlers limits environmental impact. Research groups have started recycling spent solvent from large runs to slice project waste, and some even explore on-demand synthesis to avoid stockpiling or unnecessary degradation.

    The Role of Knowledge and Quality in Advanced Synthesis

    Advanced organic synthesis rests on more than clever mechanisms. Success depends on reliable reagents, meticulous planning, and a deep understanding of how intermediates behave under stress. 1-Bromo-3-Methyladamantane marks a product developed through feedback between research chemists, manufacturing staff, and project leads. Insights gathered from years of handling, analysis, and troubleshooting shape the practical knowledge that lets teams use the compound with confidence.

    Quality assurance isn’t just about ticking boxes. High-purity material translates directly to higher success rates for complicated couplings, alkylations, and functionalizations. Cross-checking data from NMR, HPLC, and elemental analysis keeps surprises at bay—mistakes cost more at pilot scale than at the gram bench. Reliable supply and coherent analytical data lower friction between research and process development teams, keeping timelines realistic and costs tractable.

    Fabrication of 1-Bromo-3-Methyladamantane itself reflects the stepwise investments in better process control. Improvements to reaction cleanliness and energy usage carry through to a more sustainable chemical supply chain, where those needing fine organics can depend on consistent results, batch after batch. For students and early-career chemists, handling well-made intermediates builds good habits and raises the bar for their own standards as their careers move forward.

    Innovation Rooted in Practical Chemistry

    For those who follow the field, innovation rarely happens in a vacuum. The rise of adamantane derivatives represents the constant back-and-forth between academic questions and industrial realities. 1-Bromo-3-Methyladamantane draws on both. Real-world inspiration often comes from failure: processes that stick, catalysts that lose selectivity, or reactions that stall with standard alkyl halides. Testing alternatives led to the development and adoption of more robust, specialized intermediates, and this product is among the more widely embraced for a reason—it works.

    Teams value the simple fact that high structure stability means less troubleshooting, fewer off-pathway products, and a better platform for combinatorial chemistry or lead diversification. Synthetic routes designed around adamantane-based units often translate into practical, scalable solutions where less specialized chemistry falls short. One synthetic chemist I know put it simply: “Fewer headaches make for faster science.” That’s a lesson learned not in textbooks, but at the lab bench, by those who take up the day-to-day work of building new molecules.

    Perspectives from the Field: Why Down-to-Earth Chemistry Matters

    Years of lab work have taught me that success often hinges on practical choices. It’s not just about running the right reaction—it’s about picking starting materials that keep on working, not just once, but in every season, every lab, and every hand. 1-Bromo-3-Methyladamantane makes the shortlist for those who have struggled with inconsistent halides or unpredictable yields. More than just a stockroom item, it proves itself in daily operation.

    Researchers who move between early discovery and process optimization value this consistency. Chasing novelty in synthesis sometimes drives a project, but what keeps that project alive is reproducibility. Compounds like 1-Bromo-3-Methyladamantane, built for both strength and flexibility in downstream transformation, help close the gap between bench discovery and real-world application. This echoes the lessons found up and down the chain—from graduate student to senior scientist—across pharmaceutical, fine chemical, and materials science labs.

    Choosing a specialty intermediate isn’t a matter of chasing buzzwords. It’s about seeing the problems, learning from them, and choosing tools that let research move ahead without unnecessary obstacles. 1-Bromo-3-Methyladamantane has earned its place through reliability, structure, and smart design—a story built from hard-won lessons in the realities of research and production.