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Thianthrene-1-Boronic Acid

    • Product Name Thianthrene-1-Boronic Acid
    • Alias TT1BA
    • Einecs 606-184-8
    • 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

    973298

    Product Name Thianthrene-1-Boronic Acid
    Cas Number 1980201-53-9
    Molecular Formula C12H9BO2S2
    Molecular Weight 260.15 g/mol
    Appearance Off-white to beige powder
    Purity Typically ≥97%
    Solubility Slightly soluble in organic solvents
    Storage Conditions Store at 2-8°C, protect from moisture
    Smiles B(C1=CC2=C(S1)C=CC3=CC=CC2=S3)(O)O
    Inchi InChI=1S/C12H9BO2S2/c15-13(16)9-5-7-1-3-11-12(17-7)8-6-10-2-4-12/h1-6,15-16H
    Synonyms 1-Borono-thianthrene; Thianthrene-1-boronic acid

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

    Packing & Storage
    Packing 50g of Thianthrene-1-Boronic Acid is supplied in a sealed amber glass bottle with a tamper-evident cap for protection.
    Shipping Thianthrene-1-Boronic Acid is shipped in sealed, labeled containers designed to protect against moisture and light. The packaging complies with standard regulations for chemical transport, ensuring safe handling and delivery. Temperature conditions are maintained as specified in the product's safety data sheet to preserve chemical integrity during shipping.
    Storage **Thianthrene-1-boronic acid** should be stored in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible substances such as strong oxidizers. Keep the container tightly closed and protected from moisture. Ideally, store below 25°C and in an inert atmosphere, such as under nitrogen. Follow all standard laboratory safety and chemical storage protocols to prevent degradation or hazardous reactions.
    Application of Thianthrene-1-Boronic Acid

    Applications of Thianthrene-1-Boronic Acid in Industrial Manufacturing

    As a manufacturer specializing in high-purity boronic acid derivatives, we supply Thianthrene-1-Boronic Acid to global industrial partners for advanced synthesis in demanding downstream sectors. Below, we detail its real-world applications, integration points, compliance protocols, dosage criteria, and the types of end-use products produced across specialized chemical manufacturing pipelines.

    1. Pharmaceutical Intermediates for Small-Molecule Drug Synthesis

    Thianthrene-1-Boronic Acid serves as a key boron-containing coupling component in multi-step organic syntheses that construct biorelevant aromatic frameworks via Suzuki–Miyaura cross-coupling. Its defined purity profile supports consistent reproducibility in pharmaceutical fine chemical production, particularly for molecules with organosulfur functionalities. Our customers integrate this intermediate into the lead optimization and scale-up phases, directly impacting the synthesis of clinical research APIs and patentable molecular entities.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for Active Pharmaceutical Ingredients
    • USP–NF monographs pertaining to residual solvent and element content
    • EU Regulation (EC) No 1907/2006 REACH, Annex XVII (restrictions for organosulfur compounds)
    • FDA DMF submission for non-compendial small-molecule intermediates (where required)

    Typical usage ratio

    • 0.2–1.5 molar equivalents relative to the halide substrate; adjustment based on batch scale and reaction optimization studies

    Downstream process integration

    • Charged into the palladium-catalyzed cross-coupling reactor after base and halide substrate addition; often followed by phase separation and downstream purification

    Final product types

    • Orally available kinase inhibitors
    • Organosulfur-containing preclinical research APIs
    • Advanced pharmaceutical intermediates (APIs requiring sulfur moieties)

    2. High-Performance OLED Material Precursor

    Electronic chemical integrators utilize Thianthrene-1-Boronic Acid as a precursor for synthesizing heteroaromatic compounds incorporated into organic emissive layers and charge-transport materials. Its boronic acid functionality participates in precision cross-coupling, forming thianthrene-based cores that exhibit desirable photostability and charge mobility. This material enters the value chain at the intermediate stage for custom organic electronic device development.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems for Electronic Chemicals
    • RoHS Directive 2011/65/EU for restricted substances in display electronics
    • IEC 62471 Risk Group Classification for OLED device safety
    • Customer-specific impurity and purity thresholds as per OLED manufacturer QC protocols

    Typical usage ratio

    • 0.8–1.2 equivalents in cross-coupling reaction mixtures; precise ratio set during device layer optimization runs

    Downstream process integration

    • Blended into the organic layer precursor solution; following coupling and post-purification, the resulting compounds proceed to vacuum deposition or inkjet printing processes for device fabrication

    Final product types

    • High-luminance OLED emissive blue and green layers
    • Hole-transport materials for display panels
    • Organic semiconductors for flexible touchscreens and lighting films

    3. Specialty Polymer Synthesis—Fluorescent Polymer Precursors

    Manufacturers of advanced specialty polymers integrate Thianthrene-1-Boronic Acid into polymer backbones to impart photoluminescence or redox-active properties. Through Suzuki polymerization, it provides the structural motif for block copolymer architectures in fluorescent sensors and optoelectronics. The feedstock purity critically impacts molecular weight distribution and fluorescence quantum yields.

    Industry compliance standards

    • ISO 14001 Environmental Management (for environmentally controlled polymer manufacturing)
    • ASTM D638 for polymer resin mechanical property assessment
    • REACH chemical registration and notification for new polymeric materials
    • Local fire code compliance for aromatic polymer processing

    Typical usage ratio

    • 1.0 equivalent per repeating unit in Suzuki polycondensation reactions; final incorporation rate depends on targeted polymer molecular weight

    Downstream process integration

    • Dosed into monomer feed stream for catalyst-driven polycondensation; reaction progresses under inert atmosphere before downstream extrusion or casting

    Final product types

    • Redox-active polymer films for sensory devices
    • Fluorescent polymer coatings and adhesives
    • Conductive resins for printed electronics

    4. Agrochemical Active Ingredient Development

    Agrochemical innovators employ Thianthrene-1-Boronic Acid during active ingredient research, synthesizing sulfur-containing aromatic scaffolds with targeted bioactivity. Its use in boronic acid-mediated cross-coupling allows for diversification of pesticide or fungicide cores. Production processes carefully monitor for residuals and byproduct minimization to meet environmental and regulatory standards.

    Industry compliance standards

    • FAO/WHO Food and Agriculture Organization Technical Guidelines for Active Ingredients
    • OECD Good Laboratory Practice (GLP) for pesticide R&D
    • EU Regulation (EC) No 1107/2009 for plant protection products
    • Regulatory submission requirements for new agrochemical actives (e.g., EPA 40 CFR Part 158)

    Typical usage ratio

    • 0.3–1.1 equivalents relative to halide partners, tuned for each candidate active synthesis and scale-dependent productivity targets

    Downstream process integration

    • Fed into the catalyst bed for coupling with halide intermediates; post-reaction handling includes solvent recovery, purification, and formulation into technical concentrate

    Final product types

    • Sulfur-enriched fungicide actives
    • Custom aromatic herbicide candidates
    • Technical-grade pesticide formulations

    5. Custom Dye Intermediate in Analytical and Imaging Chemistry

    Laboratories and analytical-grade dye producers incorporate Thianthrene-1-Boronic Acid as a tailored intermediate to build conjugated sulfur-rich frameworks with unique photophysical properties. Precision coupling controls the electronic structure for high-sensitivity probes and specialty stains. Purity, trace metal content, and consistent reactivity are strictly observed to avoid analytical interference in end-use applications.

    Industry compliance standards

    • ISO/IEC 17025 Laboratory Quality Management for chemicals in analytical reference standards
    • CLSI (Clinical and Laboratory Standards Institute) protocols for in vitro diagnostic substances
    • EN 71-3 for heavy metal content in laboratory dyes used in educational products
    • Internal corporate specifications for nuclear purity and spectral quality in imaging probes

    Typical usage ratio

    • 0.5–1.3 stoichiometric equivalents relative to the dye scaffold; loading selected for optimal absorbance/emission performance

    Downstream process integration

    • Added during the synthetic route for functional chromophore extension, followed by purification via chromatography and formulation for analytical-grade markets

    Final product types

    • Photostable imaging dyes
    • Fluorescent markers for analytical chemistry
    • Specialty chromophores for spectroscopic standards
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    Certification & Compliance
    More Introduction

    Thianthrene-1-Boronic Acid: A Reliable Choice for Modern Synthesis

    Building With Thianthrene-1-Boronic Acid: Insights from the Manufacturer

    Manufacturing chemicals teaches you a lot about the hidden frameworks of modern science. Thianthrene-1-boronic acid has earned its place as a building block for challenging molecular construction, particularly in pharmaceuticals and advanced materials research. From my daily work in synthesis, I see demand shifting toward more sophisticated reagents, and this is a strong example.

    In our plant, each charge of raw material undergoes a strict vetting process before we start any reaction. We produce thianthrene-1-boronic acid using a multi-step synthesis that draws on clean feedstock, high-purity solvents, and a set of intermediate checks. Consistency is more than a promise—it’s essential for the types of cross-coupling developers and medicinal chemists who depend on our product. A single out-of-spec batch can disrupt the entire flow of a discovery project.

    Specification Brings Results

    We manufacture thianthrene-1-boronic acid to a purity above 98%, as confirmed by H-NMR and HPLC. Even minor impurities can trigger catalyst poisoning or leave residues that confound analytical interpretation. The white to off-white powder has a melting point in the expected 240–250°C window, and moisture content remains well below 0.5% thanks to dedicated vacuum drying. These numbers drive efficiency in the lab, slashing time on pre-purification steps and helping research teams focus on what matters—their synthesis, not troubleshooting.

    Years of experience in reactor scale-up have taught us to watch for solubility shifts and to track crystallization kinetics carefully. Not all boronic acids handle as predictably during production—some resist filtration and keep more solvent, dragging down purity. Thianthrene-1-boronic acid, prepared on our lines, separates cleanly and takes on package stability that lets it travel without trouble, even if the route is half a world away.

    A Workhorse for Advanced Chemistry

    Boronic acids opened whole new doors in organometallic chemistry. Thianthrene-1-boronic acid stands out to seasoned researchers due to its unique aromatic scaffold. The thianthrene moiety brings sulfur, shape, and electronic character not found in simple phenylboronic acids. This lets users build up molecular libraries for hit-to-lead exploration, particularly in target areas where redox properties or chalcogen atom placement matter. In our experience, it has contributed to key hits in kinase inhibitor programs and beyond.

    Suzuki-Miyaura coupling remains the dominant application. We hear from customers—teams at biotechs, academic labs, and contract research groups—who push the compound into conditions that challenge more temperamental substrates. Because our thianthrene-1-boronic acid is produced under anhydrous, inert conditions and sealed to prevent air exposure, it keeps its original activity beyond standard shelf life. This property reduces project risk for formulators and downstream chemists.

    Why Consistency Matters in Specialty Chemicals

    We don’t take shortcuts with cleaning protocols or batch documentation. Each production run is traceable down to the lot and operator, with real-time monitoring for pH, temperature, and reagent addition rate. Early on, we learned the importance of in-process controls—if a color change runs ahead of schedule or the filtration step slows unexpectedly, we halt and investigate. These process habits grew out of years serving chemists who notice everything. Minor deviation reflects directly on yield, and in drug development, inconsistency means delays, extra analytical runs, and likely regulator scrutiny.

    Unlike distributors or traders, we field questions directly from scientists wrestling with route design. Sometimes we modify drying routines to match a sensitive user’s process, or coordinate shipments with a project lead’s calendar. We actively seek out feedback from downstream users, integrating learnings across campaigns so the next lot lands faster and offers even tighter specs. The level of service builds trust, but so does manufacturing know-how. Researchers working under pressure need to minimize surprises, so reliability in a specialty building block like thianthrene-1-boronic acid makes a tangible difference.

    Comparing Thianthrene-1-Boronic Acid with Alternative Boronic Acids

    Every boronic acid brings distinct physical and chemical traits. Simple aryl and heteroaryl boronic acids suffice for basic couplings, but often fall short when electronic tuning or specific three-dimensional structure is needed. The thianthrene ring introduces a rigid, extended aromatic system with two sulfur atoms positioned diametrically. This structure modulates both electron density and local geometry—two points that influence reaction rate and final compound properties.

    Users frequently mention the heightened reactivity of thianthrene-1-boronic acid in palladium-catalyzed couplings, especially with hindered partners or electron-poor aryl halides. Where some boronic acids might show sluggish conversion, this reagent reliably affords higher yields under comparable conditions. Useful in iterative cross-couplings, thianthrene-1-boronic acid rarely succumbs to boronic acid protodeboronation or competitive reduction, two failures that waste valuable time and material.

    In solid-state form, our product exhibits lower hygroscopicity compared to several heteroaryl boronic acids, which means easier handling on an open bench and less caking over storage time. It tolerates brief atmosphere exposure, an undocumented benefit that often becomes clear only to those who spend their days weighing and dosing small quantities for parallel synthesis.

    Meeting Modern Challenges: Quality and Sustainability

    Every kilo of specialty chemical we release draws on a full spectrum of know-how, much of it learned by confronting setbacks. Early attempts to synthesize thianthrene-1-boronic acid on large scale highlighted issues with waste salt management, off-gassing, and occupational exposure to volatile intermediates. We engineered new containment, updated fume scrubber design, and introduced real-time monitors on vent lines. Many boronic acids, if mishandled, produce strong odors or hazardous atmospheres during hydrolysis or workup; thianthrene-derived intermediates carry unique sulfur compounds that demand something extra in waste control.

    We worked closely with local waste partners to set up closed-loop recycling for solvents and installed on-site treatment of aqueous streams. These practices stem not from regulatory compliance alone but from an ethos of stewardship. The cost of waste treatment climbed over the years, yet the discipline pays back through community health and team morale. Sustainability can mean something concrete—engineers on our team know every ton of solvent we recover keeps both margins and groundwater safer.

    Some of our users operate under green chemistry mandates or must document the lifecycle impacts of their reagents. We invested in pre-weighed sealed packaging for thianthrene-1-boronic acid, so each aliquot dispenses directly into a reaction flask. This step drastically cuts handling waste and limits user exposure. Fewer broken vials, less leftover material, and simpler disposal all add up to tighter operations, both in the manufacturing site and in the R&D lab running multiple projects on a deadline.

    What Sets Us Apart as the Manufacturer

    Experience shows up in small details. The consistency of our thianthrene-1-boronic acid comes from everything we learned—not just tuning reaction temperature, but knowing which supplier batch of thianthrene works best and double-checking the optimum base for boronation. A manufacturing team with years in the lab understands the pain points for users: blocked filters, slow dissolution, or those moments during a late-night reaction where only one batch of starting material sits on the shelf, and it has to work.

    We run periodic stability trials on retained lots, checking for changes in melting point and active content over months at both ambient and accelerated conditions. This practice isn’t just for certificate documentation—it directly impacts downstream studies, where researchers sometimes need archived material to repeat a finding or support regulatory filings years later. Confidence in a well-documented lot history can make or break a submission.

    Listening to customers means understanding where the pain points lie. We track every instance where a client raises an issue, no matter how small—maybe a batch felt dustier or presented with slightly altered flow. These observations fuel continuous improvement efforts on packing, milling, and drying. Sometimes we even tweak particle size to help automated dispensing systems in high-throughput screening labs. With every adjustment, the product gets closer to what users need, rather than ticking off generic spec tables.

    Addressing Bottlenecks in Modern Research Environments

    Chemists today work in environments that value speed and data integrity. Projects meant to deliver a clinical candidate or a new material for electronics depend on reliable access to high-purity building blocks. Thianthrene-1-boronic acid, produced to strict controls, removes a critical point of failure in product pipelines. Each batch comes with a full analytical suite: NMR, HPLC, moisture, and for specialty clients, trace metal analysis—all produced in-house under a robust QA/QC framework.

    Because we manage the whole synthesis process, we can guarantee traceability through every upstream supplier and handle batch recall or replacement directly, not through a faceless distribution chain. This responsiveness reduces downtime and simplifies project management for the research chemist. Speed also matters. Our on-demand production capability handles both standing orders and urgent requests, and we ship within hours for in-stock inventory. This level of control delivers peace of mind that only comes from real, direct manufacturer-client relationships.

    Supporting Scientific Progress with Real Solutions

    Our role goes beyond shipping a material. We know our customers ask for thianthrene-1-boronic acid because it isn’t just another off-the-shelf supply. Often their application demands innovative chemistry—targeted modification of a complex API, assembly of a new diagnostic agent, or installation of chalcogen motifs in a molecular array. We’ve seen the range of reactions stretch from straightforward Suzuki couplings to photoredox catalysis and oxidative protocols, each requiring subtly different handling. We worked side by side with development teams to adapt our drying and milling sequence, sometimes incorporating user notes into process revisions that benefit every future lot.

    Technical support involves much more than a troubleshooting phone call. We routinely provide additional documentation—chromatograms, spectra, and customized protocols—especially for regulated work or for investigators developing new coupling methodologies. Building these partnerships with bench scientists gives us an inside view of emerging needs. We feed discoveries from these partnerships back into our production teams and use customer experience to shape product improvements.

    Innovation Through Steady Craftsmanship

    Cutting-edge science never stands still. We invest heavily in ongoing training for production staff, constantly trialing better catalysts or greener workups. This focus on craftsmanship ensures that thianthrene-1-boronic acid combines purity with tangible benefits: less downtime, simpler weighing, and consistent results from one project to the next. Our reactors operate using programmable controls with built-in redundancy, and we regularly recalibrate analytical instruments to maintain accuracy at every quality checkpoint.

    One challenge unique to specialty chemicals lies in scaling from milligram research batches all the way to multi-kilogram production. Our flexibility in reactor sizing means we can support both early-stage SAR projects and late-stage scale-ups with the same level of documentation and reliability. Not every manufacturer commits resources to custom lot production or maintains smaller dedicated lines for sensitive intermediates—these investments make a difference for those who depend on each batch’s traceability.

    Looking to the Future

    The field of boronic acid chemistry keeps moving forward. New advances in functional group interconversion and automation expand the role of specialized compounds like thianthrene-1-boronic acid. We continuously keep pace by reviewing latest literature and maintaining open channels with research collaborators worldwide. Our labs serve not just as suppliers but as real-world partners for those trying to solve difficult synthetic puzzles. Each batch stands behind the experience and commitment of scientists and engineers who respect the trust placed in a reagent supplier.

    For researchers pushing the boundaries of what’s possible in medicinal chemistry, functional materials, or academic discovery, reliable reagents mean fewer dead ends. We see firsthand that attention to detail—from synthesis through packaging—translates to real-world project success. By offering thianthrene-1-boronic acid at the highest grade possible, we support every step in the creative process, helping turn ambitious ideas into new realities.