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HS Code |
474050 |
| Iupac Name | (2S,4S)-pentane-2,4-diol |
| Cas Number | 16689-53-7 |
| Molecular Formula | C5H12O2 |
| Molar Mass | 104.15 g/mol |
| Appearance | Colorless liquid |
| Boiling Point | 206-210 °C |
| Melting Point | −1 °C |
| Specific Rotation | +13° to +15° (c=1, H2O) |
| Density | 0.965 g/cm3 at 25 °C |
| Solubility In Water | Miscible |
| Chirality | Chiral, (2S,4S)-enantiomer |
| Synonyms | (S,S)-(+)-2,4-Pentanediol |
As an accredited (2S,4S)-(+)-Pentanediol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 25g amber glass bottle labeled "(2S,4S)-(+)-Pentanediol," sealed with a screw cap, includes hazard warnings and handling instructions. |
| Shipping | (2S,4S)-(+)-Pentanediol should be shipped in tightly sealed containers under ambient conditions. It must be protected from moisture and strong oxidizing agents. Standard shipping regulations for non-hazardous chemicals typically apply, and appropriate labeling should be included. Ensure compliance with local, national, and international chemical transportation guidelines. |
| Storage | (2S,4S)-(+)-Pentanediol 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 from moisture and direct sunlight. Store at room temperature and avoid sources of ignition. Ensure proper labeling and keep it away from food and drink. Use appropriate personal protective equipment when handling. |
Applications of (2S,4S)-(+)-Pentanediol in Industrial ManufacturingAs a direct manufacturer of (2S,4S)-(+)-Pentanediol, we deliver this specialty diol to advanced industrial operations globally. Downstream processors depend on its precise chiral configuration for demanding applications, where purity and consistent molecular performance influence product quality and regulatory acceptance. The following scenarios outline its targeted deployment across key industry segments, with required compliance standards, formulation guidance, process integration points, and the exact types of finished products produced from our material. 1. Chiral Building Block for Active Pharmaceutical Ingredient (API) SynthesisInnovators in the pharmaceutical sector incorporate our stereospecific pentanediol during multi-step synthetic routes for the production of certain APIs, especially chiral intermediates essential in cardiovascular, anti-infective, and CNS drug classes. Strict industry oversight classifies this input as a critical precursor; its molecular integrity and traceability must match the demands of regulatory submissions and GMP audits. Production technicians carefully monitor addition rates during key coupling and reduction reactions to control stereochemistry in target molecules. Industry compliance standards
Typical usage ratio
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2. Monomer for Biodegradable Polyester ProductionPolymer chemists select (2S,4S)-(+)-Pentanediol as a specialty diol monomer in the manufacturing of biodegradable aliphatic polyesters, where controlled stereoregularity and chain length modification optimize biodegradation profiles and tensile properties. Its low odor and high purity support strict food-contact regulatory adherence in downstream consumer packaging or agricultural films. Process engineers meter this raw material with precision during melt polycondensation, controlling molecular weight and branching according to film or resin grade demands. Industry compliance standards
Typical usage ratio
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3. Co-monomer in High-Performance Polyurethane SystemsIndustrial formulators integrate (2S,4S)-(+)-Pentanediol into polyol blends for high-performance polyurethane (PU) systems where structure-sensitive diols enhance network flexibility, solvent resistance, and abrasion characteristics. Applications target specialty foam and elastomer products with stringent chemical exposure or flexural cycle specifications. The unique stereochemistry influences polymer microphase separation, resulting in tailor-made mechanical profiles that differ from those using linear or branched diols. Industry compliance standards
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4. Stereoselective Intermediate in Agrochemical SynthesisSynthesis teams in crop protection manufacturing employ our chiral pentanediol as an intermediate in the multi-stage assembly of stereochemically defined agrochemicals, especially where biological activity depends on enantiomeric purity. The material’s batch traceability and analytical verification facilitate compliance with global agrochemical legislation. Typical operations introduce the diol at the stage of chiral resolution or specific ring-closure reactions during development of active pesticides or growth regulators. Industry compliance standards
Typical usage ratio
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5. Specialty Additive in Cosmetic Ingredient FormulationCosmetic ingredient manufacturers utilize (2S,4S)-(+)-Pentanediol as a multifunctional diol with preservative-boosting properties and a favorable sensory profile in leave-on and rinse-off formulations. Approval for safe topical use hinges on maintaining low impurity profiles and formal adherence to INCI and IFRA standards. The ingredient enters blending stages post-heated phase to ensure compatibility, contributing to humectancy or stability in final formulations for sensitive skin markets. Industry compliance standards
Typical usage ratio
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Manufacturing (2S,4S)-(+)-Pentanediol in-house has taught us the subtleties behind every successful batch. This chiral diol appears as a clear, slightly viscous liquid, with a mild characteristic odor. The configuration produces consistent results batch after batch, supporting stringent research goals and commercial processes alike. We are mindful of every stage—from raw material selection to purification—so the diol's handedness doesn't vary and chemists trust what they receive. Small changes in chirality turn into big changes downstream. We see this firsthand on the production line, and also through feedback from researchers who tie enantiopurity to final yield and product quality.
Our facility operates with a focus on minimizing impurities and maximizing batch reproducibility. Each run is closely monitored, since scale-up only runs smoothly when process controls line up exactly as designed. The typical lot of (2S,4S)-(+)-Pentanediol ships after thorough gas chromatography and chiral HPLC testing. Purity levels and actual optical rotation are recorded for each shipment—nothing beats a hard number when you want repeatable chemistry, and the tolerance we maintain is strict. Years spent refining this process means chemists do not lose time or confidence when formulating asymmetric syntheses or developing pharmaceutical intermediates.
We set our standards based on granular feedback from people in the lab and on the shop floor. A colorless appearance and moisture content below 0.1% don't happen by accident. It takes careful wash and drying procedures, tight temperature control, and knowledge gained over many production cycles. We found early on that traces of iron or other metals, even at low ppm levels, can interfere with downstream hydrogenation or oxidation reactions. To address this, we revised both cleaning routines and process monitoring, eliminating those trace contaminants and tightening specification sheets accordingly.
The typical batch weighs in at over 99% chemical purity by GC, with optical purity confirmed by validated, modern analytical equipment. Small batches and custom lots are available for those who require it, but our main production lines are capable of multi-kilo scale without sacrificing the specifications that matter to discerning end users. The density, refractive index, and optical rotation values are tightly aligned with the literature, precisely because each detail feeds back into successful project outcomes.
We have handled several pentanediol isomers, and this one stands apart based on what it allows users to accomplish in enantioselective synthesis. The (2S,4S) configuration brings a defined spatial arrangement to molecules, which proves essential during construction of complex targets like statins, beta-blockers, and certain alkaloids. The stereochemistry does not come for free; it takes real work to maintain. Years of customer project troubleshooting have shown us where enantiomeric contamination causes headaches—one off-kilter run can throw off whole pipelines. Our commitment to this precise diol grew out of requests from partners who needed better control in their research, pushing us to innovate cleaner synthesis and sharper analytical methods.
Other pentanediol products lack the defined handedness that matters in pharmaceutical, flavor, and material science applications. Racemates or the (2R,4R) isomer, for example, cannot replace the (2S,4S) version in most asymmetric construction. Only this configuration, in high purity, ensures consistent chiral recognition or desired bioactivity.
The impact of well-made, highly pure (2S,4S)-(+)-Pentanediol turns up in reactions that never stall at intermediate stages, in purifications that yield cleaner fractions, and in patent applications that hinge on exact enantiomer distribution. Many of our long-term collaborators say they have come to trust our batches for use in scale-up routes, be it for APIs or advanced intermediates. Plenty of times we hear frustration about materials purchased from intermediaries: specs may look fine on paper but fail when scrutinized in real reaction conditions. We draw pride from being able to back up numbers not just with a certificate, but also with real stories from routine use in process labs.
Researchers and commercial producers alike often use this diol as a building block for:
Our technical staff maintains an open channel with users, listening to what does or does not work in the context of each project. Practical issues pop up: solubility variation between batches, unexpected haze, or subtle odor changes. Every time we tweak the process, it comes out of joint discussion with real chemists, not simply a reading of standard tables.
Modifications in handling, packaging, or shipping sometimes arise from on-the-ground conversations: a new solvent mixture can improve material compatibility, or improved container liners prevent micro-contamination. These solutions come together because our team moves between lab and production settings, not via generic desk research. Especially with a compound as nuanced as chiral pentanediols, a sense of what can go wrong—and how to pre-empt it—matters more than memorized protocols.
Full traceability from starting material through to final container labeling has been a major concern among life sciences and materials customers. We document every raw ingredient, each process lot, and every analytical data point—down to variant readings for chiral HPLC, Karl Fischer moisture levels, and heavy metal panels. Once in a while we get requests to investigate batch specifics for quality audits or regulatory submissions; each time, it pays off to have robust systems in place, rather than scramble for records. We keep all batch records accessible for years, sometimes exceeding what regulations strictly require, simply because being able to share exact numbers fosters genuine confidence.
It is not enough these days to offer purity alone. Regulations around chemical sourcing, worker safety, and environmental impact change frequently. The tight oversight over raw materials, especially those sourced internationally, has altered how we vet suppliers and maintain documentation. Our production scheduling accounts for this paperwork load, since unforeseen holdups can disrupt even the best-laid plans. Feedback from our compliance team shapes raw material agreements, disposal routines, and transportation modes long before (2S,4S)-(+)-Pentanediol leaves our loading dock.
The increasing demand for clear, validated routes of manufacture in regulated industries—like APIs, excipients, or flavors—led us to build a unique cradle-to-shipment documentation chain. Customers see this in action not through brochures, but through seamless audits and rapid responses to documentation requests. Our years of in-house recordkeeping mean users spend less time chasing paperwork and more time focusing on their science.
While most specialty chemical suppliers focus on cost or throughput, we have learned the importance of clarity regarding stereoisomer options. Some new users confuse (2S,4S)-(+)-Pentanediol with its racemic or (2R,4R) forms. Each isomer serves a different purpose: racemic mixtures introduce unpredictability into asymmetric syntheses, while alternate enantiomers fit only certain target molecules. What looks like a minor difference on a data sheet often translates into a dead-end reaction or unexpected impurities down the line.
We routinely hear from synthetic chemists that they cannot swap in lower-cost, mixed-isomer diols without undermining their whole project. Loss of optical activity, mismatched melting points, or variant solubilities all trace back to this root cause. For advanced chemistry, that margin is never worth the gamble. We advise researchers and process developers early about these differences, reducing the risk of project delays or regulatory pitfalls.
Manufacturing at scale brings up lessons that you will not find in literature reviews alone. Subtle changes in temperature, even by a degree or two, can lead to increased retention of unwanted byproducts or minor loss of optical rotation. We address these challenges not by simply tweaking parameters, but by identifying the underlying mechanisms—whether through feeding rates, stirring speed, or solvent grade adjustments. In fact, we regularly troubleshoot for external R&D labs who run into trouble mirroring small-scale literature yields at larger volume. We share real-world tips on phase separation, filtration, and drying that have saved both money and time for customers working with sensitive chiral diols.
Handling (2S,4S)-(+)-Pentanediol means more than controlling just moisture or dust; it means anticipating stability issues that can crop up during transport, even with carefully sealed drums. We design all packaging to buffer changes in ambient humidity and temperature, learning through experience that what survives a week on a bench does not necessarily last two weeks in a tropical warehouse. We also monitor for longer-term degradation in storage, advising users on environmental controls to preserve both purity and chirality. These insights don’t come from theoretical advice—they come from hauling, storing, and using real product over years of fielding tough technical questions.
Chiral purity is no longer a box-ticking exercise; more partner labs now target sub-0.1% enantiomeric excess for method validation or regulatory compliance. These demands prompted us to upgrade our analytical tools ahead of the industry curve. Custom LC-MS and NMR methods, developed in collaboration with academic and industrial clients, allow us to pinpoint trace contaminants and resolve enantiomers far beyond basic chiral GC. Each major facility run includes a cycle of reference standard checking. Cross-validation on different platforms lowers the odds of escaped outliers, turning “just good enough” into real, evidence-backed confidence for people who depend on our batches.
Partnerships with clients lead to method innovations. For example, sample preparation protocols now account for potential interference from new process solvents or stabilizers. Several process chemists working on new synthetic routes brought us their methods for side-by-side validation, resulting in better accuracy for both sides. We continue testing new approaches based on user feedback; historically, many improvements to our analytical suite came about not through top-down decree, but actual problem-solving in response to a partner’s needs.
Environmental demands grow year by year. We learned how small changes in solvent recovery, water use, or packaging design add up through repeated operations. Our latest cycles of environmental auditing encourage us to invest in closed-loop water systems and solvent reclamation. No shortcut replaces real resource conservation—waste disposal bills and stakeholder demands both drive this home. Many users selecting a chiral diol also want the assurance that supply chains run cleanly, so we openly discuss both successes and remaining challenges.
A lot of chemical manufacturers claim green credentials, but tangible progress shows up in lower emissions numbers and less hazardous waste generation across multiple quarters. We publish batch-by-batch environmental statistics to all downstream users who request them, supporting auditing not with slogans but with data showing improved footprint. Customers working in pharmaceuticals or food-chain products say these numbers are now expected, not optional. The real benefit comes as systems are pushed to reduce solvent volumes and energy use without shifting risks onto product purity.
Real feedback drives our evolution. One common issue users face: unanticipated instability of (2S,4S)-(+)-Pentanediol in certain aggressive reactions. Our technical staff now provide up-front guidelines on compatible reagents and recommended pH ranges—lessons derived from in-house stress testing. Some customers also found that standard drying routines fail to remove all water, especially when using older glassware or non-ideal solvents. We suggest alternative solvent systems, plus a detailed vacuum drying protocol tailored to both small and large scale batch operations. Sharing these approaches has saved projects that would have otherwise stalled with off-spec material.
In the early days, we noticed certain customers winding up with unexpected discoloration after long storage. Digging into logistics, we traced this to interaction with container walls at certain humidity levels. The solution: introduce inert liners and monitor shipment environments across different logistical partners. As fields like peptide synthesis and chiral catalysis demand even more from starting materials, continuous learning—by sharing both failures and fixes—proves invaluable. We are not immune to setbacks, but opening our process to feedback and acting on it has built up the quality users now expect.
Experience tells us that global supply of chiral starting materials gets volatile, swinging with new regulatory rulings, transportation hiccups, or upstream factory incidents. Only those who control every production step maintain supply continuity for critical building blocks. External shocks—a winter storm, a new shipping regulation—have forced us to dual-source select raw materials and build up buffer inventory, learning that security of supply matters as much as batch quality.
Chemical innovation often rides on timely access to specialty products. We have invested in both process scale-up and extra storage to shield customers from sudden disruptions that can knock whole research or production campaigns off schedule. Honest discussions with users about real lead-times and contingencies matter more than any marketing boilerplate. Those who’ve scrambled to secure rare building blocks during boom cycles understand the value of supply guarantees coming from direct, local manufacturing.
Chemistry advances not by keeping secrets, but by expanding shared knowledge. We see our work with (2S,4S)-(+)-Pentanediol as part of a broader project—ensuring reliable, reproducible building blocks for future scientific breakthroughs. Our team shares as much as we can about best practices, quirks, and lessons learned, aiming to raise the baseline for fine chemical manufacturing across the board.
Every disgruntled phone call or new challenge pushes us to improve process, not gloss over hurdles. Our staff spends time walking through experimental plans with young researchers, sharing tips on scaling and purification, and advising on long-term storage—all born of hard-earned experience. That sharing mentality, more than technical advantage, sets the stage for lasting relationships and steady progress for years to come.