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Tert-Butyl (4R-Cis)-6-[(Acetyloxy)Methyl]-2,2-Dimethyl-1,3-Dioxane-4-Acetate

    • Product Name Tert-Butyl (4R-Cis)-6-[(Acetyloxy)Methyl]-2,2-Dimethyl-1,3-Dioxane-4-Acetate
    • Alias Acetyl Hexitol Ace**
    • 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

    237988

    Iupac Name tert-Butyl (4R-cis)-6-[(acetyloxy)methyl]-2,2-dimethyl-1,3-dioxane-4-acetate
    Molecular Formula C14H24O7
    Molecular Weight 304.34 g/mol
    Cas Number 136860-14-1
    Appearance Colorless to pale yellow oil
    Purity Typically >98%
    Boiling Point Decomposes before boiling
    Solubility Soluble in common organic solvents (e.g., dichloromethane, ethyl acetate)
    Storage Conditions Store at 0-4°C, protected from light and moisture
    Smiles CC(C)(C)OC(=O)C1COC(COOC(C)=O)(OC1(C)C)C
    Inchi InChI=1S/C14H24O7/c1-10(2,3)21-12(16)9-8-20-13(11(4,5)19-9)7-18-14(6,17)15/h9,13H,7-8H2,1-6H3/t9-,13-/m1/s1

    As an accredited Tert-Butyl (4R-Cis)-6-[(Acetyloxy)Methyl]-2,2-Dimethyl-1,3-Dioxane-4-Acetate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing White HDPE bottle with tamper-evident cap, labeled 10 grams, displaying chemical name, lot number, hazard symbols, and manufacturer information.
    Shipping Tert-Butyl (4R-Cis)-6-[(Acetyloxy)Methyl]-2,2-Dimethyl-1,3-Dioxane-4-Acetate is shipped in a tightly sealed, chemically resistant container under cool, dry conditions. The package complies with applicable regulations for safe transport of laboratory chemicals and is properly labeled with hazard information and handling instructions. Avoid exposure to heat and direct sunlight during transit.
    Storage Store Tert-Butyl (4R-cis)-6-[(acetyloxy)methyl]-2,2-dimethyl-1,3-dioxane-4-acetate in a tightly sealed container, protected from moisture and light, at a temperature of 2–8°C (refrigerator). Keep away from incompatible substances such as strong acids or bases and oxidizers. Ensure proper labeling and use in a well-ventilated area with appropriate personal protective equipment (PPE).
    Application of Tert-Butyl (4R-Cis)-6-[(Acetyloxy)Methyl]-2,2-Dimethyl-1,3-Dioxane-4-Acetate

    Applications of Tert-Butyl (4R-Cis)-6-[(Acetyloxy)Methyl]-2,2-Dimethyl-1,3-Dioxane-4-Acetate in Industrial Manufacturing

    As a specialized manufacturer of advanced acetoxy-functionalized dioxane derivatives, we supply Tert-Butyl (4R-Cis)-6-[(Acetyloxy)Methyl]-2,2-Dimethyl-1,3-Dioxane-4-Acetate to downstream industries seeking consistent performance at high levels of quality control. This section details verified industrial application scenarios, focusing on formulation standards, integration into manufacturing workflows, and the direct impact on finished goods. Our experience ensures precise utility data for formulation, compliance, and optimization in each segment.

    1. Chiral Pharmaceutical Intermediate Synthesis

    This material serves as a protected diol intermediate for the stereoselective synthesis of pharmaceuticals where controlled release and precise chirality are required. Its use predominantly relates to active ingredient manufacturing in regulated environments, where enantiomeric purity and stability during multi-step synthesis are prioritized. Implementing this intermediate supports manufacturing APIs for cardiovascular and CNS medication pipelines.

    Industry compliance standards

    • ICH Q7 GMP (Active Pharmaceutical Ingredient regulations)
    • USP, EP, JP (relevant monographs for chiral intermediates)
    • 21 CFR Part 210/211 (US FDA guidelines)
    • ICH Q11 (Development and Manufacture of Drug Substances)

    Typical usage ratio

    • 5–15% w/w as a molar equivalent for the protected alcohol group in reaction batches, adjusted based on downstream step yield and target molecule pathway

    Downstream process integration

    • Enters as a key coupling intermediate during stepwise esterification or reductive amination, followed by deprotection after formation of target chiral centers

    Final product types

    • Chiral active pharmaceutical ingredients (APIs)
    • Intermediates for statins and beta-blockers
    • Specialty CNS agent scaffolds
    • Antiviral and anti-inflammatory base compounds

    2. Modified Prodrug Synthesis for Oral Medications

    Within formulation development, this compound functions as a strategic acetoxy-masked synthon to enable prodrug synthesis, enhancing stability and bioavailability of orally administered drugs. It is selected for its predictable hydrolysis profile in vivo, supporting predictable release kinetics for therapeutic actives in finished solid dosage forms.

    Industry compliance standards

    • European Medicines Agency (EMA) Guidelines on Prodrugs
    • US FDA Guidance for Industry: Prodrug Design
    • Good Manufacturing Practice (GMP) as per PIC/S PE 009-15
    • Pharmacopoeial testing in United States Pharmacopeia (USP <197>, <1086>)

    Typical usage ratio

    • 1–8% relative to total active substance mass; ratio finely tuned based on solubility and desired prodrug conversion rate during in vitro/in vivo evaluation phases

    Downstream process integration

    • Incorporated after initial active core synthesis, during late-stage masking to yield acetoxy prodrug form, prior to tableting or encapsulation

    Final product types

    • Oral tablets and capsules containing acetoxy prodrugs
    • Delayed-release pharmaceutical formulations
    • Modified-release solid oral dosage forms
    • Therapeutic prodrug APIs with enhanced pharmacokinetics

    3. Specialty Polymer Additive for Medical Devices

    Downstream users in the medical device sector blend this material into polymer matrices to achieve targeted hydrophilicity and controlled degradation rates for resorbable applications. Selection in this context is based on its predictable reactivity and capacity to modify polyol blocks or serve as a sacrificial agent during polycondensation. Its utility extends to precision-molded components under medical-grade compliance mandates.

    Industry compliance standards

    • ISO 10993 (Biological Evaluation of Medical Devices)
    • USP Class VI Biological Reactivity Tests
    • ISO 13485 (Medical Devices—QMS)
    • FDA 21 CFR 820 QSR (Quality System Regulation for Medical Devices)

    Typical usage ratio

    • 0.2–3.5% (w/w) based on targeted device hydrolysis rate and matrix compatibility, specified through formulation validation trials

    Downstream process integration

    • Added at the melt-mixing or pre-polymer stage prior to extrusion or injection molding of medical-grade resins with controlled-release or resorbable properties

    Final product types

    • Bioresorbable surgical staples
    • Implantable stents with degradation timelines
    • Controlled-release wound closure matrices
    • Hydrolytically cleavable suture coatings

    4. Fine Fragrance Ingredient Precursor (Specialty Ester Synthesis)

    In perfumery chemistry, this dioxane derivative operates as a masked alcohol precursor, supporting the synthesis of unique ester notes and fixatives. Use cases focus on stability during storage and subsequent conversion to high-value aroma ingredients with a nuanced volatility profile, tailored to premium fragrance compounding. The compound’s recovery as a high-purity intermediate supports final blending and maceration stages for signature scent lines.

    Industry compliance standards

    • IFRA (International Fragrance Association) Standards, Annexes I–X
    • REACH Regulation (EC) No 1907/2006—Substance Registration
    • ISO 9001:2015 for Fragrance Production Systems
    • EU Cosmetics Regulation (EC) No 1223/2009 for ingredient traceability

    Typical usage ratio

    • 0.1–0.7% relative to total concentrate mass, based on volatility and conversion yield requirements for the target ester

    Downstream process integration

    • Processed during the controlled hydrolysis or transesterification stage, yielding tailored alcohol/ester mixtures for perfumery bases

    Final product types

    • High-performance fine fragrance bases
    • Luxury personal care scent accords
    • Complex aroma fixatives for premium perfumes
    • Signature note blends for niche perfumery

    5. Advanced Agrochemical Intermediate for Selective Herbicide Synthesis

    The product finds targeted use in the synthesis of cyclic acetoxy intermediates for selective herbicide active ingredient development. Major downstream manufacturers use it for optimizing molecular scaffolds that impart controlled degradation and reduced persistence, addressing evolving regulatory profiles. Product traceability and formulation consistency support large-scale synthesis under regulated agrochemical manufacturing standards.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • EU Regulation (EC) No 1107/2009 (Plant Protection Products)
    • ISO 17025:2017 (Analytical Laboratory Competence)
    • OECD Good Laboratory Practice (GLP)

    Typical usage ratio

    • 3–12% as a synthetic feedstock, ratio determined by desired herbicide selectivity spectrum and environmental degradation targets in process validation

    Downstream process integration

    • Introduced at the early cyclization or esterification phase of multi-step active ingredient synthesis, followed by selective hydrolysis prior to formulation

    Final product types

    • Field-application selective herbicide APIs
    • Granular and liquid herbicidal preparations
    • Pre-emergence weed control agents
    • Custom agrochemical blends for regulated markets

    6. Protected Diol Source for Specialty Monomer Synthesis in Performance Materials

    This compound serves as a source of protected diol moieties integral to the preparation of engineered monomers for performance polymers, particularly in high-solids coatings and specialty adhesives. Its controlled deprotection enables custom crosslinking architectures required for demanding thermal and chemical resistance profiles. Industrial formulators employ this intermediate at the monomer synthesis stage to maintain strict process control and consistent downstream resin characteristics.

    Industry compliance standards

    • ISO 9001:2015 (Quality Systems for Chemical Manufacturing)
    • REACH Regulation for polymer feedstocks
    • ASTM D2584 (Polymer Residue Standards)
    • Product compliance with customer-specific monomer purity protocols

    Typical usage ratio

    • 0.5–4% as a protected diol precursor, adjusted based on target polymer architecture, reactivity ratios, and desired crosslink density

    Downstream process integration

    • Reacted at the controlled hydrolysis step, immediately prior to condensation polymerization or step-growth monomer introduction for resin or adhesive synthesis

    Final product types

    • High-durability industrial coatings
    • Specialty reactive adhesives
    • Crosslinked thermoset resin systems
    • Performance monomer blends for advanced composites
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    Certification & Compliance
    More Introduction

    Introducing Tert-Butyl (4R-Cis)-6-[(Acetyloxy)Methyl]-2,2-Dimethyl-1,3-Dioxane-4-Acetate: From Our Plant to Your Process

    A Product Born from Experience

    Every batch of tert-butyl (4R-cis)-6-[(acetyloxy)methyl]-2,2-dimethyl-1,3-dioxane-4-acetate tells a story from the floor of our reactors to the shelves of customers tackling real chemistry problems. The journey from raw feedstocks to finished molecule takes more than precision; it comes down to understanding what our clients expect in performance and reliability. In our view, manufacturing this molecule asks for more than just technical compliance; it takes patience, a dedication to clean processing, and a steady eye on each crystallization step. Our chemists have learned a few things along the way about what matters in the surfactant, pharmaceutical intermediate, and protective group spaces where this compound finds use.

    Seeing the Compound beyond the Catalog Number

    Nobody orders tert-butyl (4R-cis)-6-[(acetyloxy)methyl]-2,2-dimethyl-1,3-dioxane-4-acetate for its name alone. For most, the concern is whether it will perform in their process—whether for the total synthesis of a delicate chiral drug candidate or for the temporary protection and later liberation of a hydroxy group. Our technical teams have fielded calls from research chemists who hit a roadblock using less selective alternatives, only to find that the stereochemistry present in this particular tert-butyl dioxane acetate offers clean downstream deprotection and higher yields.

    Model variations can alter the story. Slight shifts in chirality, acetate placement, or substituent bulk can throw a wrench into a workflow fine-tuned for consistency. We see this every season as orders come in relating to method changes or regulatory requests. Our repeated conversations with contract manufacturing teams have reinforced that this molecule’s (4R-cis) configuration avoids headaches with unexpected side products. Across the dozens of campaigns we’ve supplied, consistency in optical purity and minimal byproduct contamination define why this model holds its place.

    Understanding Why Specifications Are Not Just Numbers

    From our side of the glass, a specification sheet becomes meaningful where it holds up in real operations. Customers undertaking multi-step syntheses care deeply about more than just percent purity—they challenge us about water content, trace metal contamination, and the integrity of the acetyloxy group. Through years of collaborative process troubleshooting, we set documentation standards high. Typical lots deliver above 99% assay (by HPLC or NMR), with Karl Fischer water levels below 0.2%, and heavy metals controlled tightly by regular ICP-MS monitoring. These numbers look good on paper, but they prevent lost hours pulling impurities out downstream.

    We do not chase theoretical maximums divorced from reality. In our plant, each batch brings small fluctuations in crystallization rates, solvent affinity, or temperature swings, and our technicians keep logs to identify and minimize causes. If a customer asks for specific attributes, like a narrower melting range or color limit, that request receives a direct process response—not a handoff to a middleman.

    Walking in the Shoes of an End User

    Extensive lab and pilot plant runs taught us that this molecule is more forgiving than similar protected intermediates. Its tert-butyl and acetate groups give a controlled window for deprotection. Customers often swap out benzyl or methyl ethers after observing that tert-butyl (4R-cis)-6-[(acetyloxy)methyl]-2,2-dimethyl-1,3-dioxane-4-acetate cleans up more easily, leaving fewer byproducts behind under acidic or mild basic cleavage. When pushing out a high-value chiral center, the last thing you want is an unpredictable protecting group stubbornly holding on or decomposing into reactive fragments.

    Our engagement with early-stage process chemists sharpened our sense of how solubility impacts workup. We tune our crystallization solvents to keep the material free-flowing and readily soluble in the most common organic polar aprotic solvents. Engineers have remarked to us about reduced filter clogging and ease of scale-up compared to more hydrophilic alternatives. Packout departments, often overlooked by the trade press, face fewer headaches with this grade’s low tendency toward clumping or agglomeration.

    Learning from Process Scale and Customer Challenges

    Scaling from the kilo lab to the hundred-kilo reactor often exposes issues theoretical chemistry can miss. Small-batch performance sometimes conceals the latent tendencies of an intermediate to absorb water, discolor, or even autocatalytically decompose if left untreated. Feedback from production partners, especially those in API manufacturing, helped us refine handling protocols and invest in better inert-atmosphere packaging to extend shelf life and reduce risk.

    Sometimes, regional temperature swings or shipping delays have pushed us to modify secondary packaging and recommend changes in storage conditions to partners in humid or high-UV climates. We document change after change, integrating customer insights directly into adjustments in storage, logistics, and change control documentation—not just tweaking the outer label.

    What Sets This Compound Apart in Real-World Use?

    After years of side-by-side evaluations, the subtle but crucial traits of this specific dioxane-4-acetate have become clear. Many competitors offer generic tert-butyl dioxane derivatives, but this (4R-cis) configuration distinguishes itself by combining predictable cleavage rates with robust byproduct profiles. Analytical labs tell us their NMR spectra after deprotection runs show lower unresolved peaks, translating into simpler purification and higher throughput. Internally, we monitor and share data from continuous improvement programs, relating these trends back to pressing needs in medicinal chemistry and advanced polymer work where purification costs climb quickly with minor impurities.

    We also watch for issues with volatility or atmospheric sensitivity that can plague other protecting groups. In many bench- and plant-scale syntheses, users report fewer concerns about unexpected volatility losses or exothermic incidents when transitioning between temperature regimes. This resilience matters as much to the pilot chemist as it does to the production scheduler who depends on predictable supply and performance.

    Supporting Process Development—The Value of Consistent Supply

    Nothing throws off a project plan like a sudden variance in a key starting material. Every technical manager or procurement lead has endured unexpected requalification when a protected intermediate changes subtle physical attributes. To that end, we invest in batch record transparency and in maintaining the same vendor base for high-purity feedstocks. Over the last three calendar years, our rework or rejection rate for this model has fallen below the benchmarks our sector considers “best practice.” We attribute this to frequent process audits and feedback sessions with bulk users, not one-time quality campaigns.

    Our site’s technical teams contribute to method transfer and troubleshooting. On more than one occasion, we have dispatched process chemists to customer facilities for on-site troubleshooting—something distributors tend to avoid. These visits often resolve recurring filtration bottlenecks or help pinpoint whether a downstream issue arises from our material or from auxiliary reagents on site. It becomes less about “moving a product” and more about meeting a mutual technical end goal.

    Sustainable Production: Looking Beyond the Reagent

    Our responsibility as a chemical manufacturer sits in what we leave behind as much as what we ship out. Recent shifts toward higher regulatory scrutiny and investor pressure on ESG metrics led us to revisit source diversification, waste solvent recovery, and closed-loop cleaning cycles. In the manufacture of tert-butyl (4R-cis)-6-[(acetyloxy)methyl]-2,2-dimethyl-1,3-dioxane-4-acetate, byproduct management takes center stage. We deploy on-site distillation not just to squeeze economy from raw materials, but to reduce the load on downstream waste processors and build in traceability for our customers facing European or North American regulatory audits.

    Getting solvent usage down without compromising product integrity remains an ongoing project. For a molecule as sensitive to water and minor impurities as this one, traditional single-pass solvent use risks contamination and haze in finished goods. Our solution came from investing in high-fidelity solvent recovery systems and more rigorous point-of-use drying. This step transformed not only product quality but also the cost base for bulk supply.

    Facing Market Volatility Together

    Periodic turbulence in the specialty chemicals markets often creates uncertainty for clients racing against tight launch deadlines. We saw this firsthand during the last disruptions in global logistics, which tested every contingency our planning teams designed. The customers who kept projects on schedule teamed closely with us—working through qualified second sites, buffer stock planning, and firm quarterly forecasting. From our position, true partnership with our end-users means hearing about demand swings early and engineering flexible output volumes rather than sticking to rigid quotas.

    Some buyers expect any manufacturer to accept perpetual change requests. We filter these with direct, honest communication about risk and feasibility. Alternative pack sizes, solvents, or shipping media undergo thorough joint review, as we see both the technical benefits and hidden risks of deviating from proven standards. That said, project-specific constraints—be it a unique analytical method, or custom regulatory documentation—get quick attention from our support teams who draw on lived experience rather than a script.

    Why Hands-On Manufacturing Still Matters

    Modern chemical manufacturing is sometimes described as a black box of automated reactors and impersonal processes. For a specialty compound like tert-butyl (4R-cis)-6-[(acetyloxy)methyl]-2,2-dimethyl-1,3-dioxane-4-acetate, the skill and attentiveness of a seasoned production operator still outweighs the flashiest software. Human eyes catch color shifts, subtle viscosity changes, and differences in filtration time faster than instruments alone.

    Not long ago, one of our senior operators flagged a developing haze in the output, traced back to a minor influx of an airborne impurity during a filter change. Without that attention, several customers might have faced batch recalls or expensive purification cycles. This episode reinforced our belief that qualified, well-trained plant staff keep the intangible standards high—looking out not just for themselves, but for scientists at the other end of the supply chain.

    Genuine Solutions for Common Problems

    The reality of industrial chemistry throws curveballs. Degradation on storage, subtle cross-contamination, or mismatched batch records sometimes pop up, despite layers of control. Experienced manufacturers address root causes, not just symptoms. For this molecule, we push accelerated stability testing and long-term storage simulations well beyond what is routine. Night-shift operators routinely log observations into a central system accessible to both plant management and QA. This culture gives us early warning of out-of-spec phenomena before they become larger issues.

    Providing technical transparency stands at the core of our response. If a batch deviates, we alert partners swiftly, share our internal analysis, and give precise options for replacement or remediation. This direct approach preserves trust and project momentum—even when it means extra work or overnight responses.

    Collaborating in Innovation and Research

    Innovation does not always spring from a blank slate. Frequently, our R&D team finds incremental gains by targeting customer frustrations with existing intermediates—be it limited solubility, narrow thermal stability, or purification headaches. Our history supplying chiral intermediates gave rise to several tweaks in the current tert-butyl (4R-cis)-6-[(acetyloxy)methyl]-2,2-dimethyl-1,3-dioxane-4-acetate model. These include testing alternative synthetic routes to trim back on riskier reagents and developing rounds of pilot-scale runs to confirm the best balance of purity, yield, and process safety.

    Much of the resulting knowledge gets shared via confidential technical notes. We believe in equipping our clients—not shielding them from hard-earned process wisdom. Long-term customers are aware of formulation modifications and storage improvements months before any market announcement, providing every advantage to teams in competitive synthesis settings.

    Long-Term Value over Quick Wins

    Chemical manufacturing, at its best, values longevity and repeatability over splashy one-time results. Looking back, quality-driven partnerships outlast short-lived price campaigns or speculative inventory swings. End users of tert-butyl (4R-cis)-6-[(acetyloxy)methyl]-2,2-dimethyl-1,3-dioxane-4-acetate appreciate not just today’s specs but a proven record of support during audits, sudden method changes, and challenging process upsets. For the teams that plan years ahead for regulatory submissions or major scale-outs, the greatest asset is found in both the molecule and the shared technical track record that comes with every shipment.

    In the mix of contract research, in-house process development, and global logistics flux, we stay focused on fundamentals—clean chemistry, transparent support, and respect for the day-to-day realities faced by every operator at the bench or in the plant. This mindset infuses each lot of tert-butyl (4R-cis)-6-[(acetyloxy)methyl]-2,2-dimethyl-1,3-dioxane-4-acetate we ship. The real benchmark isn’t just the purity—it’s knowing every bottle is backed by the full experience of a manufacturer who listens, adapts, and stands behind every gram.