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(R)-1,4-Benzodioxane-2-Carboxylic Acid

    • Product Name (R)-1,4-Benzodioxane-2-Carboxylic Acid
    • Alias (R)-2-Carboxy-1,4-benzodioxane
    • Einecs 669-241-5
    • 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

    333829

    Productname (R)-1,4-Benzodioxane-2-Carboxylic Acid
    Molecularformula C9H8O5
    Molecularweight 196.16 g/mol
    Casnumber 189317-52-0
    Appearance White to off-white solid
    Meltingpoint 140-144 °C
    Specificrotation +108° (c=1, MeOH)
    Solubility Slightly soluble in water, soluble in organic solvents
    Purity Typically >98%
    Smiles OC(=O)[C@@H]1COC2=CC=CC=C2O1
    Inchi InChI=1S/C9H8O5/c10-9(11)6-5-13-8-3-1-2-7(12-8)4-6/h1-4,6H,5H2,(H,10,11)/t6-/m1/s1
    Chirality R-enantiomer
    Storageconditions Store at 2-8°C, protected from light

    As an accredited (R)-1,4-Benzodioxane-2-Carboxylic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 250g of (R)-1,4-Benzodioxane-2-Carboxylic Acid is sealed in a white, screw-cap HDPE bottle with tamper-evident closure.
    Shipping (R)-1,4-Benzodioxane-2-carboxylic acid should be shipped in tightly sealed, labeled containers to prevent contamination and moisture ingress. The package must comply with applicable chemical transport regulations, including appropriate hazard labeling if necessary. Store and transport at room temperature, away from incompatible substances and direct sunlight. Ensure documentation accompanies the shipment for safe handling.
    Storage (R)-1,4-Benzodioxane-2-carboxylic acid should be stored in a tightly closed container, in a cool, dry, and well-ventilated area. Protect it from moisture, heat, and direct sunlight. Store away from incompatible substances such as strong oxidizing agents. Keep the storage area free from ignition sources. Ensure that the container is clearly labeled and handled only by trained personnel.
    Application of (R)-1,4-Benzodioxane-2-Carboxylic Acid

    Applications of (R)-1,4-Benzodioxane-2-Carboxylic Acid in Industrial Manufacturing

    As an established manufacturer, we deliver high-purity (R)-1,4-Benzodioxane-2-Carboxylic Acid for critical synthesis processes across advanced pharmaceutical, agrochemical, specialty fine chemical, and chiral intermediate sectors. Below, we detail our substance’s application in each downstream field, highlighting compliance, dosing, workflows, and end-use categories as proven in actual production contexts.

    1. Chiral Pharmaceutical Intermediate for API Synthesis

    (R)-1,4-Benzodioxane-2-Carboxylic Acid plays a vital role as a chiral building block in the preparation of active pharmaceutical ingredient (API) cores, especially in selective β-blocker and CNS API manufacturing. API manufacturers require strict enantiomeric purity for pharmacological activity and regulatory approval. Our high-purity material integrates at the key intermediate stage, ensuring final APIs meet tight chiral and impurity specifications. The compound’s unique aromatic dioxane structure supports targeted substitutions during amide coupling and condensation steps. Downstream, pharmaceutical production relies on validated process controls to maintain reproducibility, throughput, and regulatory traceability for regulated market supply.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP and EP monograph compliance for enantiomeric excess and residual solvents, if included in relevant API sections
    • FDA 21 CFR Part 211 for finished pharmaceuticals
    • Ph.Eur./JP pharmacopoeia standards for chiral substances, as required per drug registration dossier

    Typical usage ratio

    • 0.8 to 1.2 molar equivalents per reaction step, relative to target API core scaffold
    • Final dosage dependent on subsequent derivatization; manufacturers adjust stoichiometry to yield/reactant ratio validation results

    Downstream process integration

    • Introduced at the chiral intermediate coupling phase after base aromatics assembly
    • Feeds the stereoselective condensation or amidation step under inert atmosphere in jacketed reactors
    • Integrated within multi-step GMP-compliant custom synthesis processes requiring chiral integrity tracking

    Final product types

    • Pharmaceuticals such as labetalol and other β-adrenergic blockers
    • CNS-active derivatives, including experimental neuroactive agent scaffolds
    • Custom APIs targeting rare diseases, based on benzodioxane frameworks

    2. Crop Protection Active Ingredient Intermediate

    In agrochemical manufacturing, (R)-1,4-Benzodioxane-2-Carboxylic Acid functions as a core intermediate in the synthesis of selective herbicide and fungicide actives. Downtime and off-spec production costs drive focus on QC and process efficiency, especially at large scale. Agrochemical formulators utilize this compound’s stable aromatic structure for substitution reactions, enabling stepwise assembly of target molecules. Accurate control over input ratios and reaction conditions prevents formation of isomeric impurities that impact target specificity and product registration success in international markets.

    Industry compliance standards

    • FAO/WHO specification for technical-grade pesticide raw materials
    • SANCO/12592/2012 guidance for impurity profiling in active ingredient synthesis
    • ISO 9001:2015 Quality Management System for chemical manufacturing
    • Custom regulatory dossiers for country-specific agrochemical registration

    Typical usage ratio

    • 0.9–1.3 molar equivalents per coupling unit in active ingredient backbone formation
    • Adjust ratio based on yield, purity, and impurity profile according to QA guidelines

    Downstream process integration

    • Reacted during early-stage condensation with halogenated or alkyl sidechains
    • Combined with oxidizing agents or nucleophiles under controlled temperature in glass-lined reactors
    • Intermediate is isolated and reprocessed for further functionalization to obtain the target active ingredient

    Final product types

    • Herbicide active ingredients used in cereals and legumes protection
    • Triazole or dioxane-based fungicides for cash crops and specialty horticulture
    • Seed treatment agents requiring high selectivity and environmental safety profiles

    3. Specialty Performance Additive for Polymer Modification

    In custom polymer formulation, (R)-1,4-Benzodioxane-2-Carboxylic Acid acts as a functional group donor for performance-modifying additives. Compounders introduce this moiety into specialty resins to influence solubility, crosslinking, and UV stability—particularly for optoelectronic or high-durability films. The acid group enables targeted graft reactions during melt-phase polymerization. QC teams tightly control additive levels to ensure physical property targets and downstream compliance with chemical content limits, especially for packaging and electronics applications subject to RoHS or REACH limits.

    Industry compliance standards

    • ISO 14001:2015 Environmental Management (VOC and hazardous waste tracking)
    • EU REACH Annex XVII (specialty polymers restrictions and SVHC screening)
    • RoHS Directive 2011/65/EU relevant to polymer additives in electrical devices
    • UL 94 Flammability standards for finished resins, if used in electronic enclosures

    Typical usage ratio

    • 0.5–3.0% by weight as a performance additive in custom copolymers or resin blends
    • Engineers increase dosage up to 5% for high-strength or UV-resistant applications based on extrusion trial results

    Downstream process integration

    • Premixed with monomers before bulk or solution polymerization phase
    • Added to pre-solved polymer batches for reactive blending
    • Feeds the extruder during compounding or masterbatch preparation

    Final product types

    • Optical-grade polymer films for displays or specialty packaging
    • Technical fibers for industrial filtration or apparel
    • Engineering plastics for connectors, switches, and precision housings

    4. Chiral Ligand Synthesis for Catalytic Processes

    Advanced catalyst developers use (R)-1,4-Benzodioxane-2-Carboxylic Acid as an entry material for the synthesis of enantioselective ligands. These ligands underpin asymmetric hydrogenation, oxidation, and C-C bond formation reactions in pharmaceutical and fine chemical manufacturing processes where chiral discrimination is essential. Research teams benefit from this compound’s structurally rigid, electronically unique scaffold that allows for electronic tuning and integration of donor atoms at precise positions, impacting catalyst performance and process scalability. Downstream, batch-to-batch consistency and ligand purity remain critical for meeting manufacturing, analytical, and regulatory requirements of high-value chiral synthesis.

    Industry compliance standards

    • ISO 9001:2015 for ligand manufacturing and QC documentation
    • ICH Q11 for Development and Manufacture of Drug Substances (when used in pharmaceutical precursors)
    • Sigma-Aldrich in-house technical specifications for custom ligand supply agreements
    • GLP compliance for ligands used in pharmaceutical research or pilot scale demonstration

    Typical usage ratio

    • 1.0–1.5 equivalents per target ligand molecule; excess is avoided to reduce downstream ligand purification load
    • Adjusted per specific ligand architecture and metal complex requirements, based on catalyst screening data

    Downstream process integration

    • Converted via amidation or esterification in ligand precursor manufacturing steps
    • Enters complexation or cross-coupling reactions under inert conditions
    • Transferred as a pre-activated chiral moiety for advanced ligand structure assembly

    Final product types

    • Chiral ligands for asymmetric catalysis in pharmaceutical and fine chemical synthesis
    • Metal-organic catalyst complexes used in industrial-scale hydrogenation or coupling reactions
    • Research-grade catalyst screening sets for synthetic organic laboratories
    Free Quote

    Competitive (R)-1,4-Benzodioxane-2-Carboxylic Acid prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    (R)-1,4-Benzodioxane-2-Carboxylic Acid: From Our Lab to Your Process

    Bridging Innovation with (R)-1,4-Benzodioxane-2-Carboxylic Acid

    In the chemical manufacturing sector, (R)-1,4-Benzodioxane-2-Carboxylic Acid stands out as a versatile building block. Over the years, our team has devoted time and resources to refining the methods behind its production, not only to meet purity requirements but to anticipate what users in the pharmaceutical and fine chemical industries expect from their intermediates.

    This compound, with its distinct benzodioxane ring fused to a carboxylic acid group in the (R) configuration, aligns well with demands for reliable chirality and robust stability under a range of reaction conditions. Through hands-on experience, our chemists have observed the significance of this molecule’s stereochemistry, especially for those working with chiral synthesis or preparing optically active drug candidates. The (R) configuration provides consistent outcomes during scale-up and downstream reactions.

    Production Experience and Quality Controls

    Years of direct involvement in the synthesis of (R)-1,4-Benzodioxane-2-Carboxylic Acid have shaped our approach to quality control. It isn’t just a checklist for us. In our facilities, the process starts with careful sourcing of starting materials. We keep water content, residual solvents, and chiral purity at the front of our priorities, since small variances in these can profoundly affect customer yields. The most successful runs follow methodical column chromatography purification, calibrated to separate closely related impurities such as regioisomers or enantiomeric byproducts.

    Quality here means reliability, not just on a batch-to-batch basis, but in every step affecting analytical profiles. Each lot receives scrutiny through NMR, HPLC, and chiral chromatography testing, with transparent access to data for all our clients. Over two decades of manufacturing have taught us that even minor deviations in melting point or enantiomeric excess can translate to setbacks for end users, especially those in process development. Staff in our QC labs pay close attention to product appearance, odor, and storage conditions, and they communicate directly with bulk buyers to iron out any inconsistencies observed in application.

    Why Purity and (R) Stereochemistry Matter

    Chiral intermediates like (R)-1,4-Benzodioxane-2-Carboxylic Acid shape the success of many synthetic routes. Bringing this enantiomer to its current level of purity did not happen overnight. We learned early that racemization can occur if the process steps are mishandled, leading to losses in optical activity that affect downstream syntheses. The (R) isomer serves as a precursor in pharmaceutical research, especially in the synthesis of molecules that mirror natural enantiomers found in biological systems. A minor loss of optical purity in the intermediate can alter metabolic profiles, so users benefit from high-level chiral control from their base materials.

    By focusing exclusively on the (R) form rather than offering mixed or racemic products, our facility keeps cross-contamination risks low. Our technicians reserve specific reaction equipment and glassware to eliminate chiral memory effects. Over time, this careful separation translates directly into consistency for our customers, who notice fewer issues with impurity carryover or unidentified peaks in their analytics.

    How Our (R)-1,4-Benzodioxane-2-Carboxylic Acid Compares to Other Intermediates

    Not all dioxane derivatives deliver the same performance under process conditions. Colleagues in pharmaceutical R&D often comment on the differences in solubility profiles, powder flow, and reactivity between the (R)- and (S)- isomers. The (R)-1,4-Benzodioxane-2-Carboxylic Acid from our production floor displays superior crystallinity, which speeds up weighing and transfer operations. In large-scale reactions, these small gains add up. Less dust and more manageable powder means cleaner transitions and less waste in solvent washes.

    The carboxylic acid moiety reacts efficiently in amide coupling or esterification, and its pKa facilitates predictable deprotonation. This repeatable performance comes from our experiences tracking how even minor changes in raw material quality or moisture levels influence the outcome of key amidation and esterification reactions. Chemists in our development group exchange information with application chemists in real time, so improvements travel quickly from one batch to the next.

    Specifications Backed by Practical Experience

    Our most recent model features enantiomeric excess greater than 99%, as verified by repeated chiral column measurements across multiple batches. Chemically, it falls under CAS number 162755-94-0, with a molecular formula of C9H8O5 and a molecular weight of 196.16 g/mol. These specifications sit within tight tolerance bands, since we've repeatedly seen process disruptions at customers’ sites traced back to broader specification windows from less stringent suppliers.

    Moisture content below 0.5% and residual solvents consistently under 100 ppm shape real-world outcomes. Those numbers reflect our plant’s strict drying protocols and vacuum transfer systems. Particles present as off-white to light beige crystalline powder, with a characteristic faint odor. Consistency in appearance points to solid filtration and drying routines—our production crews take pride in visual inspection, not just instrumental measures, since they've learned to spot issues machines might miss.

    Application in the Real World

    We've worked alongside pharmaceutical process engineers and custom synthesis labs that value (R)-1,4-Benzodioxane-2-Carboxylic Acid for its role in active pharmaceutical ingredient (API) synthesis. The compound serves as a key intermediate for cardiovascular drugs, central nervous system agents, and certain anti-infectives, performing as a chiral anchor from which more elaborate structures get built. In every transfer, customers demand low metal content and high purity since these traits influence later separation and crystallization steps.

    It’s not just pharma that has benefited. Agrochemical start-ups and specialty material firms tap into the molecule’s framework for the synthesis of crop protection agents or advanced monomers. The molecule’s rigid dioxane ring imparts stability to downstream products, allowing users to explore new molecular designs with confidence in their intermediate.

    In each case, users find fewer issues with degradation or color formation in stored samples. Our accounts with major multi-national customers trace a drop in non-conformance reports after switching to our material from less consistent alternatives. One client developing a beta-blocker intermediate reported halving waste disposal costs after transitioning to our high-purity grade, thanks to fewer side products in the crude reaction blends.

    Differences from Other Commercial Sources

    Feedback from users reveals clear differences between our (R)-1,4-Benzodioxane-2-Carboxylic Acid and that from brokers or non-specialized traders. Chemists working with generic grades often report microscopic black specks, higher particulate counts, or more variable color—all signs of uncontrolled process parameters or old stock recycled to extend shelf life.

    We only ship freshly synthesized batches. Our strict inventory rotation system means that each order departs the plant within days of final QC. This avoids problems seen elsewhere, such as caking or decomposition arising from extended storage under uncontrolled humidity. Unlike bulk intermediates sitting overseas for months, each kilogram has a clear lineage, with full disclosure of manufacturing and storage conditions all the way back to its raw materials.

    Other suppliers may offer similar names or close matches: racemic analogs, impure technical grades, or batches sourced from multiple facilities. In our experience, these inconsistencies manifest quickly in high-sensitivity reactions. Users have flagged issues such as spontaneous color changes, excessive foaming, or incomplete solubility—all traced back to uncontrolled synthetic routes or lack of focus on the (R) enantiomer. Our plant maintains batch-specific isolation rooms, eliminating the risk of cross-contamination.

    Empowering Chemists in Process Development

    We view collaboration with application chemists as central to long-term success. Multiple clients have sought our input at early stage route design, not just as a supplier but as a partner who’s seen the practical hurdles first hand. Our technical team regularly contributes insights into solvent selection, coupling agent compatibility, and workup sequences to streamline use of (R)-1,4-Benzodioxane-2-Carboxylic Acid in demanding settings.

    For example, our experience indicates that the acid handles best in dimethylformamide or dichloromethane when entering amide bond formation, but aqueous base should be avoided unless rigorous pH control is maintained. We share data from previous campaigns, assisting customers in identifying optimal in-process storage durations and best practices for minimizing hydrolysis or oxidation.

    Direct, repeated technical exchanges strengthen results in the field. One specialty pharma CDMO came to us seeking an answer for lumpy filtration and poor yield in their downstream amidation step. A joint investigation traced the issue to moisture pickup during intermediate storage. Adjustments to our drying protocol, combined with their revised workflow, resulted in faster dissolution and a drop in stepwise loss. This sort of feedback loop drives continual improvement, pushing us to maintain operational excellence that others seldom match.

    Environmental Responsibility in Our Manufacturing

    Our plant incorporates solvent recovery, energy optimization, and rigorous waste treatment at every stage. By continually reviewing the environmental footprint of every process, we maintain compliance with strict local and international standards. Our switch from classical acid chlorides to less corrosive coupling agents reduced off-gas volumes and improved operator conditions.

    Routine in-house audits and voluntary third-party reviews ensure stale inventory finds productive use or safe disposal, never entering the market as downgraded product. We believe strongly that only fresh material with clear documentation belongs in the supply chain. Investing in modern, low-emission equipment and up-to-date staff training furthers this mission. Our approach cuts risk for downstream users as well, given the rising scrutiny on product origin and process traceability.

    Commitment to Transparency and Traceability

    As regulatory requirements evolve, traceability has become as important as product quality. Each batch of our (R)-1,4-Benzodioxane-2-Carboxylic Acid carries lot-specific analytical documentation, including raw chromatograms, NMR spectra, and detailed impurity profiling. This data, shared freely with every shipment, helps customers meet rising standards from regulators and third-party auditors.

    On top of documentation, our production records track each precursor and process solvent, so end users can answer any queries from clients or authorities. Several multinational clients have requested tracebacks and been able to close customer complaints rapidly because of our systematic retention of documentation.

    As more chemical manufacturers move to cloud-based data logs and digital inventory management, we keep pace with secure, accessible records that put facts in the hands of those who need them. This facilitates rapid investigation of any out-of-spec event or process anomaly and keeps everyone compliant with current good manufacturing practice.

    Looking Ahead: Driving Product Excellence and Supporting Novel Applications

    Our commitment stretches beyond the point of sale. Emerging trends in drug discovery and advanced material science continually redefine the standards by which chiral intermediates are judged. We invest actively in research partnerships that test the limits of (R)-1,4-Benzodioxane-2-Carboxylic Acid’s potential in new chemical space: bioactive molecules, next-generation polymers, and innovative agrochemical scaffolds.

    Our technical support line—staffed by chemists with years in the plant and lab—keeps customers at the leading edge. Clients pursuing novel reaction conditions or pilot scaleup campaigns get real answers shaped by direct experience, not recycled literature or third-hand knowledge. Sharing what works and what should be avoided saves time, money, and material for all parties involved.

    We also welcome direct user feedback, knowing that process hurdles rarely appear in published documents. Real-world input shapes incremental improvements to our drying, packing, and transportation stages. Every process report, whether highlighting filtration ease or flagging unexpected byproducts, finds its way into weekly team meetings—not as critique, but as fuel for better chemistry.

    Conclusion: A Supplier Rooted in Practice, Serving Pragmatic Needs

    (R)-1,4-Benzodioxane-2-Carboxylic Acid typifies our approach as a manufacturer—quality from first principles, stewardship of every step, and an open line to the chemists who build the future. Our focus remains on purity, process support, and transparent, practical supply that reduces risks while unlocking new synthetic possibilities. With every lot, we bring experience and care, knowing that each kilogram enters critical, often irreplaceable projects across the globe.