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HS Code |
355404 |
| Product Name | (S)-(-)-3-Benzyloxy-1,2-Propanediol |
| Cas Number | 21163-41-9 |
| Molecular Formula | C10H12O3 |
| Molecular Weight | 180.20 |
| Appearance | Colorless to pale yellow liquid |
| Purity | Typically ≥98% |
| Optical Rotation | [α]D20 -36° (c=1, MeOH) |
| Boiling Point | 170-172°C at 1 mmHg |
| Density | 1.18 g/cm3 |
| Refractive Index | n20/D 1.541 |
| Smiles | OC[C@@H](COCc1ccccc1)O |
| Storage Temperature | 2-8°C |
| Solubility | Miscible with most organic solvents |
As an accredited (S)-(-)-3-Benzyloxy-1,2-Propanediol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 25 grams of (S)-(-)-3-Benzyloxy-1,2-Propanediol, tightly sealed with a tamper-evident cap and labeled for laboratory use. |
| Shipping | (S)-(-)-3-Benzyloxy-1,2-Propanediol is shipped in tightly sealed containers, protected from moisture and light. The product is typically packed with cushioning materials, labeled according to regulatory guidelines, and shipped via express or ground courier services. Appropriate documentation and safety data accompany the consignment to ensure compliance with chemical transportation standards. |
| Storage | (S)-(-)-3-Benzyloxy-1,2-Propanediol should be stored in a tightly sealed container in a cool, dry, and well-ventilated area. Keep away from light, moisture, and sources of ignition. Recommended storage temperature is 2-8°C (refrigerated). Avoid contact with strong oxidizing agents. Ensure that the chemical is handled using proper personal protective equipment and in accordance with safety protocols. |
Applications of (S)-(-)-3-Benzyloxy-1,2-Propanediol in Industrial ManufacturingAs a specialized manufacturer of (S)-(-)-3-Benzyloxy-1,2-Propanediol, we focus on its application in downstream industries where its stereochemical purity and functional groups are essential for producing advanced organic compounds. Below, we detail several key industrial scenarios where this intermediate plays a critical role, outlining relevant standards, typical formulation ranges, integration in customer processes, and principal end-use products. 1. Chiral Pharmaceutical Intermediate SynthesisMany pharmaceutical manufacturers use this intermediate during the synthesis of chiral active pharmaceutical ingredients—particularly beta-blockers and select anti-HIV medications—where enantiopurity determines drug safety and effectiveness. We supply material that meets the precise purity and traceability requirements for regulated API manufacturing, and our technical teams support process integration in multi-step syntheses where stringent control is paramount. Industry compliance standards
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2. Advanced Fine Chemical and Specialty Ester ManufacturingProducers of specialty esters and ethers for fragrance and flavor applications employ this material as a precursor due to its asymmetric diol structure and benzyloxy leaving group, enabling efficient esterification or etherification. Our high-purity grades cater to fine chemical plants focusing on high-value ester derivatives used in premium consumer products. Industry compliance standards
Typical usage ratio
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3. Synthesis of Chiral Ligands and CatalystsResearch and industrial catalyst producers rely on this compound as a chiral building block for synthesizing ligands used in enantioselective transition metal catalysis. Its precise configuration and hydroxyl profile allow for controlled derivatization, supporting the manufacture of proprietary catalysts for asymmetric hydrogenations and additions in synthetic chemistry scale-up. Industry compliance standards
Typical usage ratio
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4. Biologically Active Glycidyl Ether Intermediate ProductionChemical manufacturers use (S)-(-)-3-Benzyloxy-1,2-Propanediol as a key starting material for making chiral glycidyl ethers via direct epoxidation. These intermediates serve biotechnology and healthcare formulators who synthesize advanced oligomers, bioactive agents, and medical device coatings where enantioselectivity and reactivity underpin product function and regulatory approval. Industry compliance standards
Typical usage ratio
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5. Production of Enantioselective Polymer ModifiersProducers of polymers with tailored stereochemistry deploy this chiral diol as a monomer modifier, especially for specialty polyurethane or epoxy systems where subtle control over optical activity, flexibility, and cross-linking is required. Our consistent shipment quality and traceable batch records ensure reliable performance for industrial polymerization batches. Industry compliance standards
Typical usage ratio
Downstream process integration
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Every batch of (S)-(-)-3-Benzyloxy-1,2-Propanediol we produce leaves our facility with purpose built in from the ground up. This compound draws the attention of chemists looking to build up chiral molecules, and it’s not hard to see why. We’ve watched researchers and industrial users lean on this chiral building block for the same reason: its reliable stereochemistry shapes the backbone of more advanced chemical syntheses. In our years manufacturing this molecule, we have learned that precision at every stage yields confidence downstream.
Our typical finished material offers an enantiomeric excess—testing in our in-house lab usually shows >99% purity on the chiral center, and HPLC confirms it each time. Chemists in pharmaceuticals prefer it over race mates for the simple reason that building drugs with defined chirality means clearer, safer end results. We see our material go into key intermediate stages of anti-infective and cardiovascular compounds. There’s satisfaction in knowing the molecular construction starts here.
We’ve watched the industry shift focus toward single-enantiomer chemistry for much of the last decade. Regulatory agencies now want more clarity on the stereochemistry of active substances. That pushes upstream suppliers like us to do better, not just in the lab, but in how we manage our plant floor. Each kilogram of (S)-(-)-3-Benzyloxy-1,2-Propanediol passes through careful hands. Analysts check for both chemical purity and optical rotation, and any off-standard batch gets flagged for rework. Some customers want certificates showing specific rotations fit a tight range; our policy is to provide these on request because it builds trust in our relationship.
A prodrug synthesis, for example, can lose selectivity if early intermediates don’t hold tight to their handedness. We saw one case where a customer switched from a racemic source bought through a trader to our single-enantiomer supply; their downstream chiral HPLC analysis moved from unclear separation to sharp, dependable peaks.
Long production runs can show subtle drift if equipment isn’t dialed in, so we keep each run of (S)-(-)-3-Benzyloxy-1,2-Propanediol under close watch. Raw epichlorohydrin and benzyl-protected starting materials get tested each time, not only at the start of a new lot. In our experience, quality variations often trace back to solvent or base; we run checks for water content and impurities in advance. Because catalytic hydrogenolysis steps can go off-track with contaminated substrate, our team inspects the set-up before charging any fresh material.
We calibrate glassware and reactors for volume and temperature, but we don’t stop there. Operators record every batch parameter manually alongside the automated system, catching trends that might fall through data reviews. This ‘double coverage’ came up during a customer audit; we could show every time a human stepped in and why. It reassures even the toughest pharmaceutical QA inspector that no short cuts creep in at the critical stages.
Many first-time users handle benzyloxy-protected glycols with a mix of caution and respect. On our end, we maintain strict controls around handling because any glycol ether carries heightened flammability risk, especially in kilo-scale glass reactors with possible static discharge. Our protocols call for grounded lines, continuous ventilation, and routine fire-safety drills tied directly to production operations. Chemical incidents don’t just cost product—they can burn trust forever with a customer.
New operators go through a safety induction where they see not just “what to do” but “why it matters.” We share real stories (no details withheld) about near-miss events and encourage speaking up if procedures don’t seem right. The payoff shows in our insurance record and in customer visits; there have been times where our own attention to minor safety enhancements led a visitor to update their own operations. We believe this kind of real-world knowledge sharing helps raise standards across the whole field, not just on paper.
Quality control isn’t just a completed box on a form. We regard the Certificate of Analysis—a necessity for pharma and fine chemical clients—as the beginning, not the end. Each product certificate references both the lot analysis and the chain-of-custody for raw components. A product like (S)-(-)-3-Benzyloxy-1,2-Propanediol, destined for use in API synthesis, often prompts a request to review trace impurities, even when those levels sit well below typical reporting limits.
Some buyers ask for extended stability data. We maintain retention samples at controlled temperatures, both in-house and with contract QA partners. Staff pull retention samples after three months, twelve months, and two years to look at storage stability, discoloration, or unexpected hydrolysis. If anything flags, we proactively share concerns with customers and, more than once, have helped them troubleshoot their own downstream issues by providing true as-produced and as-stored comparison data.
Our customers work the product through optically active epoxide opening, glycidol derivatization, and amide bond formation. Over the years, several shared examples of improved ligand preparation for asymmetric synthesis, where the (S) configuration proved crucial. One particular medicinal chemistry group described how switching to our lot led to sharper yields in a key hydrogen boronation step—something they’d struggled to stabilize with off-the-shelf material from a bulk trader.
Even in flavor and fragrance R&D, the fine control this benzyloxy-protected diol gives has drawn positive feedback. The need for precise, predictable reactivity—especially during scale-up from gram to kilogram—can’t be overstated. Repeat orders and direct dialogue with researchers often shape minor process adjustments on our end. For example, we helped a long-running customer modify drying protocols to avoid unwanted benzyl cleavage, shortening their total cycle time and reducing color issues in the finished ingredient.
Chiral intermediates come in many shapes, but our (S)-(-)-3-Benzyloxy-1,2-Propanediol stands out because we built its production around hands-on feedback from field chemists. Over time, the demands of a single enantiopure product pushed us to redevelop purification steps, upping the clarity and consistency of every output. Many competitors sell racemates for economy’s sake; we chose the harder path of optically pure output, dialed in with catalytic steps and in-line chiral monitoring.
In-house, the chemists keep a direct line to production—no paperwork bottlenecks. Requests for alternate packaging or higher-dryness lots get answered by the same team making the product, because we know those requests flow straight from the reaction flask. We supply to custom kilo-scale runs for process validation, then ramp up to drum lots, adapting the handling conditions each time based on customer real-world feedback. This shorter feedback cycle keeps us sharper than automated support desks or chain-of-command structures.
Scale-up from benchtop to plant floor rarely behaves like a copy-paste job, especially with chiral glycols bearing sensitive protecting groups. We learned through hard experience that even slight changes in stirring or pH handling can tilt the stereoselectivity away from spec. There was a time we battled minor racemization during neutralization—our operators isolated the cause as barrel-to-barrel base variability. We moved to homogenous inline blending, reducing off-spec lots dramatically.
That sort of hands-on learning doesn’t show up on standard operating procedures but it keeps big projects from derailing. In one customer case, we lent our plant engineers to advise on their new pilot set-up. Their successful first-time yield on an epoxide nucleophilic opening sequence using our diol as the base speaks to real-world results rather than marketing.
Responsible chemical manufacturing unfolds through choices at every stage. Our (S)-(-)-3-Benzyloxy-1,2-Propanediol process uses high-purity solvents, and we have invested in a closed-loop recovery system to cut emissions. Waste streams pass through on-site neutralization, and we post our effluent data on community boards each quarter.
We source raw materials from suppliers meeting global Responsible Care standards. Workers train on the latest hazard communication, not just to tick legal boxes, but because lives depend on it. Periodic process audits, both voluntary and through our client’s requests, drive steady improvements. Some solvent streams now feature 85% recovery thanks to upgrades sparked by client conversations about long-term supply chain resilience.
Because this molecule often forms a building block for drug or cosmetic ingredients, we treat each shipment with full lot traceability. This traceability runs forward and backward through supply chain ledgers and staff logs, not just ERP entries. In cases of recall or impurity investigation, we have retrieved full lot records years after shipping, which gives peace of mind to the quality teams at the end of our supply line.
Customers working at both gram and multi-kilo scales have different needs. Our team draws on experience to match packaging formats to actual usage, whether for a university spin-off or an established API supplier. Newly produced (S)-(-)-3-Benzyloxy-1,2-Propanediol gets nitrogen-purged at fill, then sealed in containers with tamper-evident closures.
Some specialty pharmaceutical clients request pre-weighed aliquots or pharma-ready glass containers; the packaging crew adapts, building cleanroom operations as needed. In the rare event of a shipping error, direct access to staff gets issues sorted quickly, not via forms but real phone calls and photos. These small fixes kept a critical project on schedule last year when a mislabel left a customer unable to pass an import checkpoint.
Feedback from returning clients prompted us to add QR-coded labels that link directly to lot-specific QA documents—a paper saving and a speed-up for regulatory audits downstream. In a field where every day’s delay echoes through multiple projects, this seemingly simple step has shortened verification steps for several customers.
Direct dialogue with research chemists and process engineers helps us keep pace with discovery trends. We encourage visiting partners to walk through the site, ask operations staff about their own lab-scale issues, and bring samples back for collaborative troubleshooting. The process chemists running kilo labs see their own challenges reflected in the queries we field from end-users. Because (S)-(-)-3-Benzyloxy-1,2-Propanediol often plays a role in proof-of-concept studies, we sometimes adjust a purification or supply higher-purity material for a time-sensitive academic milestone.
Some customers seek out joint development—shared risk and all. The team here has supported collaborations focused on finding greener protection routes for glycidol analogs, including candidate runs where final product needed new impurity-cutting steps. These joint efforts bear fruit both in yield and in professional trust. We take pride in seeing patents credit not just a molecule, but the steps and knowledge that let it solve a problem.
Supply disruptions—raw material shortages, logistics blockages—hit chiral intermediate users hard. Manufacturers like us now anticipate these bumps by talking with global logistics partners, mapping alternate transport, and setting emergency inventory aside. A few years back, an abrupt border closure meant one API manufacturer faced imminent line stoppage. Quick thinking across both sides enabled air lift of enough (S)-(-)-3-Benzyloxy-1,2-Propanediol to bridge their gap.
Priced commodities will always have resellers promising identical product, but the reality on the receiving end often brings surprises. One customer’s story sticks with us: switching to our direct-made lots eliminated unexpected UV impurities and moved their regulatory audit timeline forward by months. A well-documented, directly managed production chain stands apart; there’s less risk, and less guesswork about unseen intermediates or swapped suppliers.
Exports must fit each region’s specifications, so we customize documentation to support everything from standard European pharmacopoeia references to Asian custom declarations. Staff maintain language and technical correspondence to ensure no hiccups in customs or regulatory pushback—a small detail, but it keeps the supply flowing.
Chiral diols share broad functional resemblance but differ in the details. Our (S)-(-)-3-Benzyloxy-1,2-Propanediol, for instance, remains benzylated at the secondary hydroxyl, a feature that adds both synthetic flexibility and protection against base-catalyzed side reactions. Customers contrast it with plain (S)-1,2-propanediol, where no protective group can mean reduced selectivity in glycidol etherification or epoxidation pathways.
Other market options, like the (R)-enantiomer or racemates, simplify supply costs but risk undermining later performance where chirality-specific reactivity pays off. Several clients described drifting yields, or even regulatory obstacles, when switching away from single-enantiomer routes. The benzyloxy group’s stability through a wider range of pH also lets our intermediate play well in ambitious syntheses where conditions shift during scale-up.
We hear from customers that documentation accompanying bulk materials from traders often falls short—trace impurity lists, stability data, or spectra missing or unreadable. Our approach keeps full transparency, not simply as a regulatory must, but because synthetic teams want their questions answered without a sales filter in between.
End-users invest in assurance above all; nothing derails costly project timelines faster than a failed batch traceable to an unknown supplier. Our model bypasses third parties—every lot comes with full records, direct staff support, and the readiness to dialogue about specific needs or hurdles. Over the years, this open approach forged relationships beyond mere transactions.
Our production team welcomes site visits, external audits, and outside QA reviews. We benefit too: customer input often shapes our next improvement. Whether answering tough regulatory questions, tweaking a custom lot, or lending technical advice, we prioritize technical accuracy and candor, never aiming to overpromise.
Regular industry conferences and technical panels offer opportunities to learn new applications, identify bottlenecks, and compare notes with both peers and clients. We share our findings, whether about minor shifts in epoxide opening best practices or solvent recovery pathways, believing that good chemistry spreads by conversation, not just invoices and samples.
The demand for chiral intermediates like (S)-(-)-3-Benzyloxy-1,2-Propanediol isn’t fading any time soon. As new synthetic routes open up and the drive for safer, more selective pharmaceuticals and specialty materials grows, standards will only rise higher. We believe meeting and exceeding these challenges calls for transparency, technical depth, and daily engagement with both science and industry realities.
Our years making this molecule, listening to its users, and refining the process reflect more than just economic motive. The satisfaction in supporting breakthrough therapies, improved material science, or academic progress brings shared wins. In the world of chiral chemistry, knowledge and open partnership count as much as purity and paperwork. We stand ready to meet the needs of each partner, eager to push what’s possible with each new lot produced.