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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 | (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. |
Applications of (S)-Glyceraldehyde Acetonide in Industrial ManufacturingAs 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 SynthesisPharmaceutical 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
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2. Advanced Peptide SynthesisPeptide 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
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3. Chiral Auxiliary for Fine Chemical ProductionProducers 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
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4. Glycosylation Reactions in Carbohydrate ChemistryCarbohydrate 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
Typical usage ratio
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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.
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.
(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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.