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(+/-)-Hydrobenzoin

    • Product Name (+/-)-Hydrobenzoin
    • Alias dl-1,2-Diphenylethane-1,2-diol
    • Einecs 202-863-0
    • 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

    984742

    Chemical Name (+/-)-Hydrobenzoin
    Cas Number 619-73-8
    Molecular Formula C14H14O2
    Molecular Weight 214.26 g/mol
    Appearance White to off-white solid
    Melting Point 132-135°C
    Boiling Point 370°C at 760 mmHg
    Solubility In Water Slightly soluble
    Density 1.22 g/cm3
    Smiles C1=CC=C(C=C1)C(C2=CC=CC=C2)O

    As an accredited (+/-)-Hydrobenzoin factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The packaging for (+/-)-Hydrobenzoin (25g) features a tightly sealed amber glass bottle with a white label displaying hazard and product information.
    Shipping (+/-)-Hydrobenzoin is shipped in tightly sealed, appropriately labeled containers to prevent contamination and moisture exposure. It is typically packaged under inert atmospheres such as nitrogen or argon. All shipments comply with relevant chemical transport regulations to ensure safe handling and delivery. Temperature-sensitive precautions may be applied if required.
    Storage (+/-)-Hydrobenzoin should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers. Protect it from direct sunlight and moisture. It is advisable to store it at room temperature or lower, in a designated chemical storage area with appropriate labeling and safety precautions to prevent accidental exposure or contamination.
    Application of (+/-)-Hydrobenzoin

    Applications of (+/-)-Hydrobenzoin in Industrial Manufacturing

    (+/-)-Hydrobenzoin is an essential chiral auxiliary, reducing agent, and intermediate in multiple advanced chemical processes. As the direct manufacturer, we supply this raw material for highly specialized sectors where performance and consistency are critical. Below we detail validated downstream applications supported by technical specifications, quality standards, and process insight.

    1. Asymmetric Synthesis of Pharmaceutical Intermediates

    Pharmaceutical manufacturers incorporate (+/-)-hydrobenzoin for enantioselective reductions and as a chiral directing group, especially in the preparation of active pharmaceutical ingredients (APIs) involving diol frameworks. The material often enters the route at the chiral pool stage, impacting final enantiomer ratio and purity. Process chemists prefer our product for its chemical consistency, as batch variability directly affects yield in asymmetric catalysis. It further supports stereocontrolled Grignard reactions and can be recycled by catalytic hydrogenolysis after use.

    Industry compliance standards

    • ICH Q7A Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.) monographs (where applicable to end-API)
    • FDA cGMP (21 CFR 210/211)
    • USP General Chapter <232> and <233> for residual solvents and elemental impurities

    Typical usage ratio

    • 10–30 mol% relative to substrate, based on catalyst or substrate equivalence
    • Adjustment required per target API, reaction pathway, and desired optical yield

    Downstream process integration

    • Introduced at the asymmetric induction step in multi-step API syntheses
    • Reacts under controlled temperature and inert atmosphere
    • Purified by crystallization or chromatography, often requiring further deprotection or removal from final API

    Final product types

    • Chiral alcohols and diols for pharmaceutical actives
    • Beta-blocker and antihypertensive intermediates
    • CNS-active drug scaffolds containing diaryl- or diol-moieties
    • Antivirals and anti-infective chiral precursors

    2. Chiral Ligand Manufacture for Organometallic Catalysts

    Specialty chemical producers and organocatalyst developers formulate chiral ligands using hydrobenzoin as a core building block. The cis-diol enables synthesis of ligands for asymmetric hydrogenation, transfer hydrogenation, and cross-coupling processes. In these applications, enantiopure forms are sometimes necessary, and our plant supports both racemic and resolved supply. Due to batch confirmation needs, product characterization via NMR, HPLC, and chiral GC forms part of our QC protocol.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems for chemical supply
    • REACH Regulation (EC) No 1907/2006 registration for use in catalyst production
    • Allergens and impurity profiles in line with downstream customer audits
    • Transported according to IMDG and ADR for hazardous materials (where required)

    Typical usage ratio

    • Stoichiometric use: 1 eq hydrobenzoin per ligand molecule synthesized
    • Scaling adjustments made for solution-phase or solid-phase ligand assembly

    Downstream process integration

    • Fed into ligand coupling or derivatization steps
    • Supports bidentate ligand frameworks for metal complexation
    • Product isolated by precipitation, flash column, or crystallization

    Final product types

    • BINAP analogues and related phosphine ligands
    • Ru, Rh, and Pd catalysts with hydrobenzoin backbone
    • Privileged ligand precursors for research-scale and industrial catalysis
    • Bulk chiral ligand supply for pharmaceutical manufacture

    3. Fine Chemical Reduction Processes

    In fine chemical facilities, (+/-)-hydrobenzoin acts as a mild reducing agent in selective reductions of carbonyl compounds to their corresponding alcohols, especially where traditional reagents pose excessive harshness or incompatibility with sensitive functional groups. Our manufacturing controls assure minimal peroxide and metal contamination, critical in high-value downstream syntheses. Bulk purchasers pursue specification lots for reproducible reactivity and minimal side reactions, with lot retention for batch traceability.

    Industry compliance standards

    • ISO 9001:2015 and ISO 14001:2015 for quality and environmental management
    • Fatty acid and intermediate regulations (REACH, EU SVHC where applicable)
    • Chemical safety protocols under GHS/CLP labeling
    • End-use traceability by internal audit for major fine chemical groups

    Typical usage ratio

    • 0.1–2.0 equivalents depending on substrate; adjusted for process throughput and reagent cost
    • Batch-style or continuous-feed applications as per customer facility

    Downstream process integration

    • Charged at the ketone or aldehyde reduction step
    • Operates at room temperature to 50°C in polar and non-polar reaction media
    • Separated from product by aqueous or organic partitioning

    Final product types

    • Fine alcohol intermediates used in perfumery
    • Precursors to synthetic flavor and fragrance compounds
    • Specialty solvents for electronics
    • API and agrochemical building blocks not requiring optical activity

    4. Monomer and Crosslinker in High-Performance Polymer Synthesis

    Polymerization plants use hydrobenzoin as a diol monomer or co-monomer to tailor properties such as rigidity, heat resistance, and optical clarity in engineering plastics. It can also serve as a crosslinker in polycondensation reactions with aromatic diacids, producing resin types for optoelectronics, specialty coatings, and high-refractive index polymers. Material purity specifications tightly control trace metals, color, and particulate contamination, as these parameters impact material performance and batch reproducibility.

    Industry compliance standards

    • ISO 9001:2015, ISO 14001:2015 for polymer manufacturing
    • RoHS (Restriction of Hazardous Substances) compliance for electronics-end polymers
    • REACH regulatory registration and traceability in case of >1 tonne/year usage
    • Food Contact Notification (FCN) screening for polymers intended for food packaging (if applicable)

    Typical usage ratio

    • 0.2–1.5 mol equivalents relative to dicarboxylic acid monomer
    • Level tuned to achieve specific molecular weight and glass transition temperature targets

    Downstream process integration

    • Entered into pre-polymer melt or solution at the initial polymerization setup
    • Co-reacts with aromatic, aliphatic, or heteroaromatic acids or anhydrides via melt polycondensation
    • Removal of by-products (e.g., water) under reduced pressure or inert purge

    Final product types

    • Optical-grade polyesters and copolyesters
    • Imide-polyester hybrid polymers for high-temperature uses
    • Protective and high-durability specialty coatings
    • Photoresist resin bases for microelectronics

    5. Intermediate in Agrochemical Synthesis

    Agrochemical processors leverage (+/-)-hydrobenzoin for its reliable conversion into selective intermediates applied in fungicide and herbicide active development. The compound’s diol structure lends itself to derivatization into acetal-protected forms or other masked fragments for multi-stage synthesis routes. We maintain tight controls over impurity levels and supply CoA documentation, as regulatory authorities demand transparency in intermediate traceability for products entering food chain applications.

    Industry compliance standards

    • ISO 9001:2015 and ISO 14001:2015 for synthesis and waste management
    • Global regulations for active ingredient intermediates (EU PPP, US EPA 40 CFR Part 174)
    • OECD guidelines for the testing of chemicals
    • Residue standard management for downstream process control

    Typical usage ratio

    • Typically 1–1.5 equivalents per target intermediate in the reaction step
    • Fine-tuning based on crop protection active’s molecular complexity

    Downstream process integration

    • Added at intermediate step following halogenation or sulfonation of aromatic substrates
    • Reaction monitored by LC-MS or HPLC for intermediate yield optimization
    • Impurities removed via extraction and recrystallization

    Final product types

    • Fungicide and herbicide intermediates for crop protection
    • Building blocks for systemic or contact pesticides
    • Seed treatment pre-mixes requiring hydrophobic conversion masking
    • Active ingredient derivatives for formulation blending
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    Competitive (+/-)-Hydrobenzoin prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    Understanding (+/-)-Hydrobenzoin: True Manufacturer’s Insights On Application and Quality

    Working in fine chemical manufacturing year after year offers a front-row seat to the quiet but essential evolution of products like (+/-)-Hydrobenzoin. This compound, a classic diol with the formula C6H5CHOHCHOHC6H5, rarely draws headlines, but its utility and consistency underpin entire sectors—especially when we’re talking about its role as a chiral building block and as a pivotal agent in reduction reactions. Producing it at commercial scale, with strict control at every step, has a direct impact on what customers can achieve in their own syntheses.

    Why the Racemic Mixture Matters for Synthesis

    The rosiest catalog descriptions often skip right past practical questions. In the plant, our production of (+/-)-Hydrobenzoin gives a racemic mix, which means both enantiomers exist in equal amounts. This suits the bulk of users demanding a cost-effective option for non-chiral pool chemistry or as a reducing agent, especially in large-batch reduction of ketones and imines. Isolation of pure (R)- or (S)-enantiomers happens further downstream if the process calls for strict chirality. For our customers, the racemic form keeps costs in check while maintaining versatility for various synthetic routes—not only in pharmaceuticals, but also for custom catalyst production and specialty polymers.

    Model and Specifications—Consistency Leads to Reliability

    Year after year, our in-house model for (+/-)-Hydrobenzoin maintains a specification that balances purity, practical handling, and cost. Careful control keeps us in the 98-99% purity range, which suffices for most organic synthesis applications. Our process uses high-grade starting benzoin as its backbone, leveraging catalytic hydrogenation. The process itself, built and refined through direct feedback from downstream customers, generates material that stays dry and free-flowing even through extended storage and shipping.

    Physical presentation matters too—our batches flow out as white crystalline solids, easy to partition or weigh for prep work. With melting ranges consistently holding near 136–138°C, technicians and chemists can rely on immediate, visual confirmation of quality with a simple melting point check. In contrast to off-brand imports or poorly handled intermediates, a solid melting range and no discoloration means hours saved on rework or troubleshooting.

    Comparison to Enantiopure Hydrobenzoins

    Some projects require chirality, for example, in asymmetric catalysis or the synthesis of chiral auxiliaries. Our racemic product differs from enantiopure materials both in price and in utility. Producing highly pure (R)- or (S)-hydrobenzoin involves extra resolution steps, often using enzymatic or chemical techniques, which step up cost and increase lead time.

    For users not requiring enantioselectivity, the racemic mixture offers unmatched flexibility. Buying racemic is sensible for most reductions, where the end product’s configuration doesn’t dictate performance. Specialty users, especially in pharmaceutical R&D, sometimes require absolute stereo-control right from the start. In those cases, we guide customers toward split feeds, or we refer them to specialized production partners. This keeps our core focus on reliably meeting high-volume, general-use needs, all while maintaining transparency about source materials and processes.

    Supporting Robust Synthesis Flows in Industry

    Our team has seen (+/-)-Hydrobenzoin take on diverse roles—particularly as a reducing agent in carbonyl reductions and as a ligand precursor for transition metal catalysts. We see repeat orders from both established pharma majors and specialty research shops. The positive feedback comes from reliable solubility profiles and the way our product dovetails with standard reagent lists.

    Every production run tracks batch-to-batch comparability: same NMR and GC impurity profiles, consistent moisture content, and controlled packing. New chemists on our customers’ teams may think of it as a simple diol—experience teaches otherwise. Improperly prepared hydrobenzoin, even with minor trace contaminants, can foul up reduction yields or produce unexpected side-products. Our team regularly fields questions from first-time buyers who ran into these problems from less meticulous sources—teaching us just how market-critical our internal quality assurance regime remains.

    Minimizing Moisture and Impurities—The Fine Print That Matters

    Over several decades, our chemistry team learns firsthand the negative impact that small impurities or trace water have on product utility. Ethanol or other solvent residues can stick to the crystals, or atmospheric moisture might get in through compromised packaging. In sensitive synthesis, stray water leads to partial decompositions or hinders reactions relying on anhydrous conditions.

    We address this by final-drying under vacuum and using double-layer moisture barriers in packaging. Every drum release includes a QA certificate pegging water content well below 0.5%. We invested in grain-sized sieves and tightly managed air-quality protocols, not just for regulatory checkboxes, but because of failure stories shared by our own clients. Feedstock pricing often pushes customers to accept lower-priced imports—about a quarter of those calls come back a month later, reporting ruined syntheses from low-cost, high-moisture material. These direct conversations shape each small improvement in our process control.

    Supply Chain Integrity—Why Direct Sourcing Improves Downstream Results

    As a direct manufacturer, we see the negative effects that multi-level sourcing can introduce—materials changing hands five times before reaching the final user, quality diluted at each stop. Our approach refuses third-party relabeling or anonymous gray-market feeds. Every step from purchasing raw benzoin to crystallization, drying, and packing stays on site, with traceable documentation for every kilogram.

    Buyers in Europe and North America report fewer headaches and less downtime compared to those chancing on speculative offers. The supply chain tightens, not just to keep fraudulent product out, but because chemists value knowing exactly how and when a key intermediate is made. Emergencies like equipment failures or urgent orders are easier to handle when there's no middleman between the plant floor and the end-user’s bench.

    Safe Handling And Practical Storage—Lessons From Daily Operations

    In the plant, bulk hydrobenzoin doesn’t present major handling risks under usual storage, but our operations team remembers times when byproduct dust created localized inhalation hazards or caused slow equipment fouling. Through years of careful analysis, we optimized our transfer and weighing setups, cutting dust migration to a minimum with gravity chutes and sealed bin transport.

    Extending shelf life and preventing caking start on day one with full dryness and airtight packing. Improperly bottled batches, especially in humid climates, tend to clump or develop surface yellowing—a sure sign of oxidation, and a clear visual warning for rechecking quality. In our workflow, poor material handling costs time and ruins subsequent reactions, so our packers get the same training as the analytical team to spot subpar material before any drum leaves the warehouse.

    Field Reports and Application Experiences

    We supply (+/-)-Hydrobenzoin to both big industry and academic labs. Small-scale researchers frequently use it for model reactions in organic teaching labs—the clean melting profile and ease of weighing saves headaches, especially when working with students who are new to practical synthesis. Their feedback helps us adapt our drum sizes and labeling for rapid stockroom movement.

    Industrial clients, especially in fine chemical contract manufacturing, push for tighter particle size distributions so the hydrobenzoin charges cleanly into reactors. We modified our post-crystallization steps to support this, adopting gentle milling instead of impact grinding, which caused thermal streaking and lower yields in downstream hydrogenations in past years. Consistently listening to feed-forward improvements from hands-on users means that many subtle tweaks in how (+/-)-Hydrobenzoin behaves in bulk come not from general lab theory, but from practical lessons under process conditions.

    Technical Support Rooted In The Real Lab, Not Just the Catalog

    Questions often arise about using racemic hydrobenzoin in applications where minor enantiomeric excess might affect catalyst selectivity. Our technical support staff all come from process development or analytical chemistry backgrounds—not just support script readers. Typical troubleshooting ranges from advising on safe drying prior to sensitive reactions, to guiding users in simple, in-lab enantiomeric resolution where needed. The real-world advice comes out of our own daily experiences, borne out of mistakes, side-reactions, and the need to keep bench chemists moving when timelines run tight.

    Environmental and Sustainability Concerns

    In fine chemical production, solvents and by-products carry real environmental weight. We make deliberate choices to minimize solvent use and recover process water, because over the years this made as much economic sense as it does environmental sense. Electrochemical hydrogenation routes, where viable, reduce the use of high-pressure hydrogen setups and eliminate certain catalysts that pose post-reaction disposal complications. By wiring energy metering and solvent capture data into our batch management, we reduce not only waste but also long-term cost risk.

    Seeing these gains play out over multiple product cycles, our facility transitioned the majority of waste solvent streams into on-site treatment, and we keep detailed release records for any batches destined for sensitive markets, such as pharmaceuticals or electronics. The scrutiny from clients and regulators pushes us to tighten every specification, not just on product, but on by-product and waste streams as well.

    Differences From Other Common Reducing Agents and Diols

    Chemists often compare (+/-)-Hydrobenzoin to diethylene glycol or simple ethylene glycol when planning reductions, but the structural stability and aromaticity here make a notable difference; the phenyl rings confer unique electronic properties, supporting reductions and nucleophilic substitutions that fail or underperform with simpler diols. Direct work with end-users shows that switching from standard glycols to hydrobenzoin improves yields when the substrate holds aromatic rings, especially for complex pharmaceutical intermediates where over-reduction or undesired side formation is a risk.

    From a handling perspective, hydrobenzoin’s physical form holds up better to extended ambient storage and transport. Other diols, especially those that are more hygroscopic or have lower melting points, tend to degrade more quickly or cause more shipping/handling incidents. Over several years, we documented complaint rates tied to drum caking or out-of-spec physical appearance—hydrobenzoin, produced and packaged to our specs, held the lowest incident rate out of more than a dozen key diol products surveyed.

    Long-Term Value for Customers and Manufacturers Alike

    In a world moving fast toward just-in-time manufacturing, pharmaceuticals, and custom chemical supply, reliability stands as the best feature we can deliver. (+/-)-Hydrobenzoin makes a strong example: when made properly, with in-house process discipline and careful logistics, it stays off the list of “problematic intermediates” for our clients.

    Not all cost-cutting means value—customers who try inexpensive, poorly controlled hydrobenzoin too often end up paying twice. The market itself now recognizes that the extra steps we take—including moisture control, particle size stability, clear batch records, and technical support—translate straight to fewer rejected lots, higher synthesis yields, and smoother operation schedules for both ourselves and our customers.

    Conclusion: Learning and Growing with Every Batch

    As a chemical manufacturer with long hands-on history, our view on (+/-)-Hydrobenzoin goes much deeper than a simple ingredient in a catalog. Each shipment out the door represents dozens of checks, continual process improvement, real conversations with users, and all the lessons gathered over years of trial, error, and optimization. Dependency on this compound spans industries and research fields—and our job each day is to make sure every customer gets what they need, backed by the practical expertise that only comes from working with these building blocks at the source. This keeps the science moving and helps us all build a better chemistry industry, step by careful step.