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(S)-Glyceraldehyde Acetonide

    • Product Name (S)-Glyceraldehyde Acetonide
    • Alias (S)-GA Acetonide
    • Einecs 642-729-3
    • 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

    900760

    Product Name (S)-Glyceraldehyde Acetonide
    Cas Number 7252-84-6
    Molecular Formula C6H10O4
    Molecular Weight 146.14 g/mol
    Appearance White to off-white solid
    Optical Rotation [α]D20 +27° to +33° (c=1, H2O)
    Melting Point 79-83°C
    Purity ≥98%
    Solubility Soluble in water, methanol, and ethanol
    Storage Conditions Store at 2-8°C in a tightly closed container
    Synonyms (S)-(+)-2,3-O-Isopropylidene-glyceraldehyde
    Smiles CC1(O)OC(CO)C1=O
    Inchi InChI=1S/C6H10O4/c1-6(2,10-4-7)9-3-5(8)11-6/h3-4,7H,1-2H3
    用途 Chiral building block in organic synthesis

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

    Packing & Storage
    Packing (S)-Glyceraldehyde Acetonide, 5g; supplied in a sealed amber glass vial within a protective screw-cap container, labeled with hazard warnings.
    Shipping (S)-Glyceraldehyde Acetonide is shipped in tightly sealed containers under cool, dry conditions to prevent degradation. The packaging complies with chemical safety regulations, ensuring protection from light, moisture, and air. Appropriate hazard labels are applied, and transport is managed by certified carriers according to relevant chemical shipping guidelines and safety standards.
    Storage (S)-Glyceraldehyde Acetonide should be stored in a tightly sealed container, protected from light and moisture. Keep it in a cool, dry place, ideally refrigerated at 2–8°C. Avoid exposure to air or heat sources to prevent degradation. Ensure clear labeling, and store away from incompatible substances such as strong oxidizing agents. Handle under an inert atmosphere if prolonged storage is required.
    Application of (S)-Glyceraldehyde Acetonide

    Applications of (S)-Glyceraldehyde Acetonide in Industrial Manufacturing

    As a direct manufacturer of high-purity (S)-Glyceraldehyde Acetonide, we supply this specialty chiral building block to a select group of downstream industries with validated applications. Its well-defined stereochemistry and chemical stability make it an essential intermediate for complex syntheses and advanced material manufacturing. Below, we outline core industrial scenarios, outlining technical requirements, integration processes, and end product types relevant for B2B purchasers and process engineers.

    1. Chiral Pharmaceutical Intermediate Synthesis

    Pharmaceutical companies use (S)-Glyceraldehyde Acetonide as a key precursor in the asymmetric synthesis of bioactive compounds, notably for custom chiral alcohols and advanced intermediates required in active pharmaceutical ingredient (API) pathways. Researchers and process chemists incorporate this material in enantioselective reactions, especially in the preparation of anti-diabetic agents, anti-HIV drugs, and other small-molecule APIs, where precise stereocontrol is mandatory. Its role as a synthetic handle in aldol, nucleophilic addition, and epoxidation reactions supports scalable drug manufacturing with batch-to-batch consistency.

    Industry compliance standards

    • Current Good Manufacturing Practice (CGMP, 21 CFR Parts 210/211, US FDA)
    • International Council for Harmonisation ICH Q7 for API production
    • Ph. Eur. 2.2.46, USP General Chapter <1046> for chiral substances
    • Traceability to ISO 9001:2015 certified quality systems

    Typical usage ratio

    • 0.8–3.5 mol% relative to major pharmaceutical intermediates in asymmetric routes
    • Adjusted based on route-specific enantiopurity and scale of target API

    Downstream process integration

    • Added during the early chiral pool step or as the primary substrate in multi-step syntheses
    • Employed in batch and continuous flow processes with in-situ monitoring

    Final product types

    • Non-steroidal anti-inflammatory drug intermediates (e.g., chiral cyclopropylamines, epoxides)
    • Building blocks for antiretroviral APIs
    • Custom enantiomeric fragments for clinical candidate compounds

    2. Advanced Peptide Synthesis

    Peptide and oligonucleotide manufacturers use this compound to introduce custom stereochemistry into modified amino acids or as a protected glyceraldehyde derivative for peptide backbone extension. Its stability enables precise coupling conditions, critical for building unnatural or modified peptides with therapeutic applications. Process engineers select (S)-Glyceraldehyde Acetonide for its tolerance in solid-phase synthesis and controlled deprotection steps, directly influencing final product purity and biological activity.

    Industry compliance standards

    • US FDA Guidance for Peptide Synthesis and Impurity Control
    • Japanese Pharmacopeia (JP) peptide monographs
    • ISO 13485:2016 for medical-grade peptide component manufacturing
    • European Pharmacopoeia 10.0 (Peptide Active Substances)

    Typical usage ratio

    • 1.0–5.0 mol% per modified residue in non-proteinogenic amino acid segments
    • Quantity adjusted according to peptide chain length and site-specific modifications

    Downstream process integration

    • Incorporated during the synthesis of chiral glycine or unnatural amino acids prior to resin loading
    • Used in solution-phase and solid-phase peptide synthesis (SPPS) where side-chain protection is critical

    Final product types

    • Therapeutic peptides with enhanced stability or receptor selectivity
    • Peptide-based drug candidates for diabetes and oncology
    • Diagnostic imaging peptide probes (radio-labeled or fluorescently modified)

    3. Chiral Auxiliary for Fine Chemical Production

    Producers of fine chemicals and specialty monomers employ (S)-Glyceraldehyde Acetonide as a stereocontrolled auxiliary in the production of optically active compounds, such as α-hydroxy acids and sugar derivatives. Its protected dioxolane structure allows for high-yield syntheses under strongly acidic or basic conditions, after which the auxiliary can be selectively removed. This compound’s inclusion as a chiral template offers predictable enantiomeric excess, underpinning the manufacture of flavors, fragrances, and advanced materials with highly specific chirality.

    Industry compliance standards

    • REACH (EC 1907/2006) for registration and safety of chemical intermediates
    • ISO 9001:2015 for specialty chemical quality management
    • Food Chemical Codex (FCC) standards for certain aroma chemical production
    • JECFA specifications where applicable

    Typical usage ratio

    • 3–10 mol% relative to starting aldehydes or alcohols, depending on targeted fine chemical
    • Content tailored based on d/l ratio and downstream chiral separation requirements

    Downstream process integration

    • Mixed at the initial chiral step, followed by reaction with Grignard reagents, reduction, or alkylation
    • Auxiliary cleavage performed during final purification using mild hydrolysis or acidolysis

    Final product types

    • Optically active α-hydroxy acid flavor ingredients (e.g., lactic acid derivatives)
    • Chiral building blocks for aroma compound manufacturing
    • Custom ligands for metal catalyst synthesis

    4. Glycosylation Reactions in Carbohydrate Chemistry

    Carbohydrate research and specialty sugar manufacturers integrate this material in stereospecific glycosylation processes, facilitating the synthesis of protected hexose sugars and intermediates used in oligosaccharide assembly. The cyclic acetonide group ensures selective reactivity and provides stability during multi-step routes. Analytical and preparative chemists rely on its predictable behavior in protecting group strategies and its utility in preparing rare sugar isomers with applications in vaccine adjuvant development and pharmaceutical excipient production.

    Industry compliance standards

    • IPEC-PQG GMP Guide for Pharmaceutical Excipients
    • USP-NF for excipients used in oral solid dosage forms
    • ISO 22000 food safety management (for ingredients used in pharmaceutical nutrition)
    • Regulation (EC) 1333/2008 for food additive handling (for non-medicinal carbohydrate use)

    Typical usage ratio

    • 0.5–2.0 equivalents per protected sugar moiety for regioselective glycosylation steps
    • Range modified according to chain length and complexity of carbohydrate assembly

    Downstream process integration

    • Employed in the initial preparation of protected carbohydrate frameworks before elongation or branching
    • Deprotection scheduled as the final stage after full glycosylation and purification

    Final product types

    • Rare sugar-based pharmaceutical excipients
    • Oligosaccharide vaccine adjuvants
    • Protected hexose derivatives for analytical standards
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    Certification & Compliance
    More Introduction

    (S)-Glyceraldehyde Acetonide: Advancing Chiral Chemistry

    The Foundation for Reliable Chiral Synthesis

    Every batch of (S)-Glyceraldehyde Acetonide we produce carries the weight of practical demands in modern chemistry. This material, also known by its chemical name 1,2-O-Isopropylidene-(S)-glyceraldehyde and catalogued as CAS 7252-83-7, helps researchers and process engineers build consistent, repeatable results in both laboratory and manufacturing settings. Years of scaling this compound have taught us where it counts: purity, reproducibility, and supply chain stability are not optional but mandatory, especially where one chiral building block can change the outcome of an entire synthesis.

    Understanding Purity and Quality Control: Lessons from the Plant Floor

    Our teams have learned, often through costly troubleshooting and batch reviews, how minor impurities in (S)-Glyceraldehyde Acetonide impact downstream reactions. Synthetic organic scientists rely on reliable chirality, so we keep a tight grip on enantiomeric excess and chemical purity, measured rigorously through chiral HPLC and NMR. Specifications typically fall in the 98%+ purity range by GC and HPLC, with enantiomeric excess measured above 98%. We refuse partial loads from suppliers for key solvents and acetonide precursors, stemming from one too many headaches with off-grade starting materials. Chromatographic fingerprinting, off-odors, and subtle color changes have flagged avoidable problems. From these experiences, we verify every new lot against archived reference standards to prevent unwanted surprises.

    Physical Form and Handling Realities

    (S)-Glyceraldehyde Acetonide tends to arrive as a colorless to pale yellow oil or low-melting solid, depending on ambient conditions. This apparent variability can catch newer labs off guard. Our experience shows that refrigeration limits color changes and helps avert polymerization, especially if samples sit for a while. We pack under inert gas and ship with absorbent pouches in sturdy glass bottles, avoiding metal contact that can affect stability. Left open in humid conditions, (S)-Glyceraldehyde Acetonide slowly absorbs moisture and degrades. Chemists who scale up can underestimate how fast an aldehyde will react with trace water or air; those who plan reactions carefully with fresh portions rarely run into trouble. For long-term storage, our team settles on −20°C as the best practice, having seen degradation increase dramatically at higher temperatures.

    (S)-Glyceraldehyde Acetonide vs. Unprotected (S)-Glyceraldehyde

    Some labs attempt to shortcut procedures by using neat (S)-Glyceraldehyde, hoping to simplify chemical steps. In reality, the unprotected compound suffers from instability and polymerizes readily at room temperature. Acetonide protection, achieved by reaction with acetone and acid catalyst, shields the sensitive backbone and makes the aldehyde group selectively available for further transformations. Direct use of (S)-Glyceraldehyde without protection leads to frustrating results: yield drops, product purity declines, and trace byproducts form. What seems like a shortcut on paper becomes an operational headache, especially when process traceability matters. Chemical intuition, honed by repeated failures on the bench, demands the use of the acetonide-protected form to remove these headaches and unlock efficiency.

    Key Uses in Chiral Building Block Synthesis

    We have shipped (S)-Glyceraldehyde Acetonide into a broad spectrum of industries, from pharmaceutical R&D to catalyst screening and flavors development. Its primary value lies as a staple chiral synthon for constructing diverse chemical architectures. Our conversations with synthetic chemists revolve around the ability to induce asymmetry early in multicenter molecule synthesis. For example, downstream steps leading to nucleoside analogues, chiral amino acids, sphingolipid mimics, or even non-peptide drugs all often start from one clear chiral anchor. (S)-Glyceraldehyde Acetonide, with its defined stereochemistry, lets scientists set absolute configuration and maximize downstream selectivity. Reliable sources remain critical when regulatory filings depend on reproducible stereochemical outcomes.

    Differentiating True Manufacturer Material: Real-World Challenges

    Many sources claim “manufacturer” status, but direct production tells a different story. Trust only builds after resolving logistical issues, managing solvent residues, and scaling from grams to kilos repeatedly. In the plant, exotherms during acetonide formation need careful monitoring. Overheating delivers side-products, not the target material. We learned to phase in acetone slowly, control water content rigorously, and monitor catalyst loadings carefully. Final purification stages separate genuine material from persistent byproducts like unprotected aldehyde and acetic acid impurities. Each phase teaches lessons that a copy-paste intermediary never experiences. Batches crashing out as sticky films or developing unexpected odors signal problems; an actual manufacturer adapts process steps on the fly to resolve bottlenecks without hiding behind specification sheets.

    Specifications That Respond to User Demands

    Discussions with formulation chemists and pilot plant managers clarify which data matter most: consistent melting range, color index, enantiomeric excess, and solvent content (especially if used in API synthesis). Our standard grade comes with a GC purity above 98%, color below 30 APHA, and residual solvent content below 0.5%. We meet customer requests for custom packaging or bulk lots with validated kilo-scale batches, giving batch-specific reference spectra with shipments. This openness pays off when a pilot run flags some offbeat impurity. We work directly with users to trace roots, adjust purification, or change solvent systems where feasible. This hands-on relationship outperforms faceless catalog product offerings, especially when year-on-year supply consistency counts.

    Supply Chain Security and Why It Matters

    Unplanned interruptions in raw material deliveries can sideline production and stall vital research. We have lived through resin shortages, shipping delays, and even regulatory blockades. Our facility stockpiles enough raw input and intermediates to guarantee resilience during minor supply chain shocks, and maintains additional standing orders to buffer against market price swings. Partners describe lost time and labor when buying from unknown “manufacturers” who actually broker from trading houses. Our team shares COAs tied directly to output from our own reactors, giving partners confidence in traceability. Serial number tracking, periodic retesting, and archiving samples from each lot anchor compliance for both internal QA and external audits. These are not “features” but hard-learned standards for materials that anchor regulated manufacturing.

    Practical Differences from Other Chiral Compounds

    Some researchers ask whether other chiral aldehydes or diol derivatives can fill similar roles. Our observations show that both reactivity and selectivity of (S)-Glyceraldehyde Acetonide, especially as a protected aldehyde, make it uniquely versatile compared with common alternatives. For instance, unprotected glyceraldehyde offers low stability and requires specialty handling. Other mono-protected or benzylidene-derivatized aldehydes often deliver less predictable results in enamine or Wittig-type reactions. The isopropylidene acetonide group blocks both vicinal hydroxyls, focusing selectivity on the aldehyde moiety and drastically improving outcome reliability for C–C bond-forming transformations. Laboratories performing carbohydrate synthesis or stereoselective alkylations typically find that acetonide-protected material gives fewer side reactions and a cleaner product workup.

    On-Site Quality Control: Human Judgment Trumps Catalog Specs

    Our chemists run process checks, not just paperwork reviews. Visual cues, subtle odors, or changes in oil consistency do not always show up on a standard certificate of analysis. One instance involved a color shift that masked an impurity spike, flagging the need for spectral retesting. Every operator enforcing in-plant checks prevents costly issues for downstream users. We pull random drips and run TLC spot-checks, verifying against archived samples to catch trends early. Every kilogram receives unique tracking numbers and findings are logged into our plant database, forming a clear audit trail for regulatory or customer scrutiny. This in-house attention defends against blowback from misidentified shipments, especially for partners relying on precise chiral purity.

    Research and Development: Evolving with End Users

    Chemistry never stands still, and we adapt our production strategy as downstream research shifts. When API developers or specialty polymer researchers request modifications — higher purity, solvent-free, or pre-dissolved formulations — we retool and validate new approaches. Sometimes a research group pushes chiral purity demands up a notch; instead of hedging, our team spins up additional purification batches and documents the outcome. Over time, this feedback loop from user to plant floors to synthesis planning creates a more robust supply chain. Our approach differs from brokers selling one-size-fits-all catalog entries, who rarely hear about user experiences beyond a returned shipment or complaint. Instead, user trust relies on a manufacturer’s willingness to listen, adjust, and share insights on best practices for new applications.

    Strategic Partnerships, Not Just Material Deliveries

    Years of collaboration teach us trust builds slowly but disappears quickly. Process teams remember partners who help debug issues, adapt specifications, or redirect batches on tight deadlines. Whether an academic group scaling a new synthetic route or a process chemist in a GMP facility, we approach every conversation as a technical exchange. Customizing final solvent content or packaging not only adds value but translates to fewer headaches and field reports. One customer required extra-tight moisture control, so we adjusted packaging and warehousing to extend shelf life and reduce spoilage during cross-continental shipping. Such experiences drive home the point: chemical manufacturers earn customer loyalty by sharing practical expertise and solving real-world bottlenecks, not by hiding behind generic web listings.

    The Real Value of Technical Documentation

    Our technical team dives beneath surface-level certificates and specification sheets to deliver batch-specific spectra and process notes. Customers in regulated spaces rely on this detail when facing audits or troubleshooting reactions. Close records ensure researchers know the history of every batch — date, process conditions, impurities flagged, and lot cross-references. Sometimes a process chemist needs to prove the origin of a trace impurity. Demonstrating full traceability back to a named reactor run reassures both regulators and users that each kilogram meets their stringent requirements. This extra investment saves time, builds long-term confidence, and underpins relationships that last beyond a single project or compound.

    Environmental and Safety Considerations

    Direct manufacturing experience brings a deep understanding of handling hazards and waste minimization. (S)-Glyceraldehyde Acetonide, though relatively manageable compared to more reactive aldehydes, still needs careful treatment regarding exposure, evaporation, and residual waste. Plant protocols stress the importance of PPE, proper ventilation, and neutralizing any spilled aldehyde immediately before it reacts. We treat every container as a potential exposure source. All plant personnel undergo training in handling air- and moisture-sensitive chemicals, and we maintain up-to-date MSDS documentation accessible to every team member. Cleanup protocols include solvent segregation and aldehyde-specific waste collection, minimizing environmental impact and assuring safe disposal. Ongoing audits and feedback lead to updated process flows as regulations shift, ensuring continued compliance and operator safety.

    Adapting for the Future: Continuous Improvement in Synthesis

    Chemistry evolves, and so does our approach to (S)-Glyceraldehyde Acetonide. As cost pressures, purity demands, and sustainability standards increase, we continually optimize our synthesis route. For example, we have reduced solvent use through improved extraction techniques, trimmed cycle times by refining catalyst selection, and cut waste output with greener workups. These insights accumulate over years, not months, and reflect not only chemical expertise but a real stake in the smooth operation of our partners’ labs. Innovations often spring from cross-industry collaborations, as clients share where standard material falls short and ask for targeted improvements. Sustaining performance across global supply networks requires just this kind of adaptability and practical wisdom.

    A Manufacturer’s Perspective on Reliability

    We know stability, predictability, and consistent supply mean much more than an online product listing. Every bottle of (S)-Glyceraldehyde Acetonide we ship draws on hands-on experience in diagnosis, troubleshooting, and adaptation. Customers trust in facts — traceable raw inputs, transparent purity metrics, and on-demand technical support — not claims or catalog superlatives. Our approach comes from years in chemical plant operation, not marketing copy. What matters most: reliable material, honest communication, and the collaborative problem-solving that helps end users reach their research and production milestones swiftly and confidently.