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L-Isoserine

    • Product Name L-Isoserine
    • Alias isoserine
    • Einecs 246-901-8
    • 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

    401843

    Product Name L-Isoserine
    Iupac Name (S)-2-amino-3-hydroxypropanoic acid
    Molecular Formula C3H7NO3
    Molecular Weight 105.09 g/mol
    Cas Number 632-13-9
    Appearance White to off-white powder
    Solubility Soluble in water
    Melting Point Circa 200°C (decomposes)
    Optical Activity Levorotatory (L-form)
    Pka Values pKa1 (COOH): ~2.2, pKa2 (NH2): ~9.7

    As an accredited L-Isoserine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing White, sealed HDPE bottle labeled "L-Isoserine, 99% purity, 100g" with hazard symbols, lot number, and manufacturer details.
    Shipping L-Isoserine is shipped in tightly sealed containers, protected from moisture, heat, and direct sunlight. It is typically packed according to hazardous material guidelines, with clear labeling. Transportation follows standard chemical shipping regulations to ensure safety and product integrity during transit. Ensure compliance with local, national, and international shipping regulations.
    Storage L-Isoserine should be stored in a tightly sealed container, protected from light, moisture, and air. Keep it in a cool, dry place, ideally at 2–8°C (refrigerated). Ensure the storage area is well-ventilated, away from incompatible substances such as strong oxidizing agents. Clearly label the container and handle using standard laboratory safety procedures.
    Application of L-Isoserine

    Applications of L-Isoserine in Industrial Manufacturing

    L-Isoserine, as a synthetic non-proteinogenic amino acid, plays a targeted role in advanced industrial processes. Our direct production supports specialized formulations in pharmaceutical synthesis, peptide research, bioengineering, diagnostics, and fine chemical manufacturing. Below, we detail verified downstream sectors, outlining compliance, inclusion ratios, process points, and representative end products.

    1. Custom Peptide Synthesis for Pharmaceutical R&D

    Leading pharmaceutical innovators incorporate L-Isoserine as a functional building block in structurally modified peptides and peptidomimetics. Its unique stereochemistry introduces backbone constraints and modification points crucial for activity modulation in therapeutic peptide drug candidates. Chemists use our material for sequence diversification, mechanism studies, and enhancing peptide stability throughout non-clinical and early clinical research programs.

    Industry compliance standards

    • Good Manufacturing Practice (GMP) guidelines (ICH Q7)
    • US FDA requirements for active pharmaceutical ingredient (API) manufacture
    • European Pharmacopoeia – General monographs for amino acids and peptides
    • ISO 9001:2015-certified QC management

    Typical usage ratio

    • 0.2–3 molar equivalents relative to target peptide batch size
    • Ratio varies by sequence design, side-chain protection scheme, and amidation endpoint

    Downstream process integration

    • Incorporation during solid-phase peptide synthesis (SPPS) as a protected N-Fmoc, N-Boc, or unprotected residue
    • Use during solution-phase segment coupling
    • Triggered during cyclization or backbone modification for peptide drug prototypes
    • Purification via preparative HPLC prior to further analytical and biological evaluation

    Final product types

    • Investigational peptide pharmaceuticals
    • Preclinical peptide libraries
    • Bioactive peptidomimetics
    • Peptide-based lead compounds for further drug development

    2. Synthesis of Chiral Pharmaceutical Intermediates

    Specialty chemical manufacturers use L-Isoserine as a stereochemically defined precursor for asymmetric synthesis routes. Its non-standard backbone enables selective derivatization, supporting the construction of chiral building blocks and advanced intermediates used in small molecule and peptide API production. Process chemists favor its use for introducing functional groups inaccessible through standard natural amino acids, improving downstream active compound yields.

    Industry compliance standards

    • Current Good Manufacturing Practices (cGMP)
    • REACH compliance for registered substances in the EU
    • Japanese Pharmaceutical Excipients Certificate (when for local synthesis)
    • Internal QMS certified to ISO 9001 or equivalent

    Typical usage ratio

    • 5%–30% (w/w) relative to target intermediate batch composition
    • Dosage driven by conversion efficiency and downstream transformation protocol

    Downstream process integration

    • Direct introduction in racemic or enantiomerically pure form to stepwise synthetic pathways
    • Serves as starting scaffold for derivatization, cyclization, or amide bond formation
    • Often enters at one of the early or mid-steps to set chiral centers
    • Integration into multi-step cascade reactions for product optimization

    Final product types

    • Chiral pharmaceutical intermediates
    • Substituted beta-amino acids
    • Protected amino acid derivatives
    • Chemical precursors for active ingredient synthesis (e.g., antihypertensive agents, CNS-active compounds)

    3. Biochemical Reagent Production for Diagnostics

    Producers of diagnostic assay kits and life sciences reagents employ L-Isoserine for calibrators, enzyme substrate controls, and system suitability testing. Its distinct structure provides non-interference with common proteinogenic peptides, supporting accuracy in amino acid profiling and method validation. Our molecule ensures lot-to-lot reproducibility essential to OEM diagnostic manufacturing, particularly for chromatography and electrophoresis methods requiring specialized reference standards.

    Industry compliance standards

    • ISO 13485:2016 – Quality management for medical devices and reagents
    • CLSI (Clinical and Laboratory Standards Institute) guidelines for reference material traceability
    • US FDA 21 CFR Part 820 – QSR for in vitro diagnostic manufacturing
    • Lot traceability documentation

    Typical usage ratio

    • 0.01–0.1% (w/v) in reference solution or calibration mixture
    • Ratio determined by analytical detection range and performance requirements

    Downstream process integration

    • Addition to calibration standards before lyophilization or solution packaging
    • Blending with natural amino acids in quantitative amino acid analysis kits
    • Usage as process positive/negative controls in kit manufacturing workflows
    • Incorporation during development of custom laboratory standards and quality controls

    Final product types

    • In vitro diagnostic assay kits (e.g., amino acid quantitation panels)
    • Reference standards for clinical analysis
    • OEM biochemical reagents
    • Custom analytical controls for research hospitals and biotech firms

    4. Research-Grade Fine Chemical Manufacturing

    Fine chemical producers source L-Isoserine as a highly pure, well-characterized intermediate for academic and industrial research applications. This amino acid analog expands the synthetic options for creating novel molecular probes, enzyme substrates, and molecular scaffolds. Researchers value our stable, high-grade product for exploratory work in chemical biology, catalytic studies, and material science applications, where purity and defined structure impact project outcomes.

    Industry compliance standards

    • ISO 9001:2015 QMS for specialty chemicals
    • Chemical Abstracts Service (CAS) traceability
    • Material Safety Data Sheet (MSDS) availability
    • Product specification transparency for research supply

    Typical usage ratio

    • Precision-weighed amounts based on research protocol – generally 10 mg to 1 g per run
    • Adjustments according to substrate screening or catalyst evaluation scale

    Downstream process integration

    • Utilized as a direct reactant or probe in exploratory screening reactions
    • Integration during advanced organic synthesis for functional group modification
    • Testing in bioconjugation, labeling, and structural studies
    • Preparation of custom derivatives for method development

    Final product types

    • Novel molecular scaffolds for academic publishing
    • Molecular probes for chemical biology
    • Substrates and inhibitors for enzymology studies
    • Research samples for high-throughput screening
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    Competitive L-Isoserine prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    L-Isoserine from the Manufacturer’s Perspective: What Sets It Apart

    Introduction to L-Isoserine: Beyond the Basics

    As a direct manufacturer of synthetic amino acids, we work with practical challenges and see first-hand how each fine adjustment in the production process shows up in the lab, the warehouse, and the end results for our customers. L-Isoserine, known by its catalogue reference Mod-LIS0225 in our range, stands out in the world of non-proteinogenic amino acids. Since it’s not incorporated into proteins by ribosomal translation, L-Isoserine occupies a niche territory, often underestimated or misunderstood by those outside academic or pharmaceutical chemistry circles.

    Unlike L-serine, which exists as a canonical amino acid with a clear path in the biosynthetic world, L-Isoserine brings a rare set of properties to synthesis and research projects. We have spent years adapting our fermentation reactors and purification lines to achieve not only high yield but also batch-to-batch consistency, because the unique stereochemistry of L-Isoserine doesn’t forgive shortcuts.

    The Real Work Behind Purity and Consistency

    L-Isoserine often comes under scrutiny in synthetic chemistry because it can easily get confused with its constitutional isomer, L-serine. This creates real risks if purity or isomerism falls even slightly out of spec. Through hands-on process tweaks—improved enantioselective synthesis, rigorous HPLC testing, and a careful choice of starting reagents—we reach and regularly verify chemical purity at the 99+% level, with optical rotation matching reference standards. Lab results stop being hypothetical figures once you run scale-up; only then do you realize the smallest deviation in reaction conditions can throw off the product.

    For research groups tracing metabolic pathways or exploring peptide analogues, contamination or isomeric mix-ups simply aren’t acceptable. We manufacture L-Isoserine as a white crystalline powder, with a molecular weight of 105.09 g/mol and a CAS number of 632-18-0, making sure we maintain an impurity profile that supports reproducible results in rigorous research settings.

    Why and Where L-Isoserine Matters

    Practical applications make a difference. In peptide synthesis, for example, L-Isoserine isn’t a simple swap-in for serine. Its unique side-chain orientation leads to different folding patterns and reactivity in peptide backbones. Our experience shows that medicinal chemists often use L-Isoserine to probe structure-activity relationships in peptide drug leads—to tweak hydrogen bonding or modulate polarity without completely overhauling the backbone architecture.

    We’ve supplied this amino acid to labs developing enzyme inhibitors, colleagues in biochemistry departments testing non-standard amino acid incorporation, and companies modeling how small substitutions alter pharmacokinetics. Each time, feedback zeroes in on one thing: tiny variations in the raw material make huge differences to final biological performance.

    Reliable Supply and Transparent Specifications

    We see confusion in the market, especially when traders mix up similar-sounding amino acids. Many resellers list L-Isoserine with unclear assay values or mixed enantiomeric composition. As a direct producer, our batch documentation includes chromatographic analysis and optical activity measurements, so researchers don’t roll the dice on their inputs. Our long-term clients in academic and pharma settings report fewer reproducibility errors and less wasted effort because the origin and handling of the L-Isoserine they use are clear.

    We manufacture L-Isoserine in 100 g, 500 g, and multi-kilogram lots to match typical scales for discovery and pilot projects. All handling and packaging steps use inert atmospheres since this amino acid can slowly absorb water over time if left exposed. Our experience tells us packaging in tightly sealed, rugged HDPE containers cuts down on unwanted hydration and decomposition during shipping or storage.

    L-Isoserine vs. L-Serine, D-Isoserine, and Related Agents

    Many new users ask how our L-Isoserine differs from standard serine or even its D-isomer. Chemically, L-Isoserine (2-amino-3-hydroxypropanoic acid) differs from L-serine by the location of the amino and hydroxy groups, leading to distinct physical and biochemical properties. L-serine features a 2-amino-3-hydroxypropanoic acid backbone but in a different layout. Our customers who’ve tried substituting one for the other in synthetic routes or as metabolic probes quickly discover enzymes recognize the mismatch—and reactions behave differently.

    We don’t produce D-Isoserine in-house, but every so often, we analyze competitor samples by request, and the differences jump out right away. D- and L-isomers display different optical rotations, and D-isomers typically don’t fit into biocatalytic systems engineered for L-configurations. This catches people off-guard who source from generic lists or brokers lacking stereochemical controls.

    Peptide chemists also use derivatives—N-protected or methylated forms, for example—but we focus on the unmodified L-form. From what we’ve witnessed, modifications to the amino or carboxyl groups can alter solubility or make coupling less efficient. Most researchers return to native L-Isoserine for reliability in solid-phase syntheses after mixed results with more obscure derivatives.

    Formulation, Solubility, and Downstream Use

    Solubility in water, typical of small polar amino acids, remains one of L-Isoserine’s strong suits. Customers working in peptide assembly or bioconjugation often report that it dissolves cleanly without foaming or aggregate formation. We supply the product in a micro-crystalline form with a particle size distribution tailored to dissolve within minutes with stirring. Fine powders dust easily, so our teams have adopted low-dust packaging methods—wearing out lab coats in the process, but reducing wastage.

    L-Isoserine holds up well under standard warehouse conditions, but based on our stability runs, cool, dry storage offers the best shot at a long shelf life. Researchers tell us the product stays pure when desiccated, while open containers pick up moisture in ambient air over weeks or months. For pharma pilot teams or biochemistry labs that need to revisit archived samples months down the line, this storage discipline saves time and frustration.

    Batch Traceability, Data Transparency, and Problem-Solving

    Process reliability and traceability have become more important over the past decade. With more scrutiny on reproducibility in published studies, documentation matters. Every L-Isoserine batch comes with serial numbers, production dates, and full certificates containing HPLC and chiral purity results. When our customers run into unexpected assay failures or synthesis hurdles, our technical team cross-references archived run data and, if necessary, pulls retention samples from the original batch for reanalysis. Having that depth of information means clients can pinpoint process bottlenecks instead of guessing at raw material issues.

    In instances where a researcher’s downstream enzyme or coupling reagent seems incompatible, we sit down with them, study what’s happening at the bench level, and review both our analytical data and theirs. We’ve re-optimized a purification process or even modified the grind size for specific users needing particular solubility or filtration profiles. These practical tweaks come from a culture of direct manufacturing, not a generic sense of customer service.

    Regulatory and Compliance Considerations

    Now and then, regulation changes nudge the landscape. While L-Isoserine’s regulatory footprint remains limited owing to its niche and rare applications, it still falls under wider frameworks on the transport and use of fine chemicals. Our internal QA systems run in line with ICH Q7 guidelines, and audits from our pharma and biotech customers push us to keep documentation, handling, and labeling strong—even where no explicit regulation forces our hand. We’ve experienced spot inspections by major pharmaceutical partners, and their feedback leads us to harden both our production logs and chain of custody.

    Researchers in regulated industries, especially those generating study data for new drug applications or medical devices, need traceable, standards-compliant inputs. Our investment in these systems comes from years of fielding tough questions and troubleshooting across the synthesis chain, shaping both how we make L-Isoserine and how we support its use.

    Supporting Research, Learning from Experience

    L-Isoserine doesn’t get the same limelight as mainstream amino acids, but it attracts groups pushing forward in medicinal chemistry or enzyme design. We’ve seen new requests for this product from companies exploring unnatural peptide analogs, start-ups probing new catalysts, and bioengineering labs rigging up novel biosynthetic pathways. In each case, project success often comes down to confidence in raw materials and close support from their suppliers.

    Experience teaches that the more esoteric a building block, the more care its supply and documentation require. We don’t see L-Isoserine as just another catalog item. Our process engineers regularly analyze waste streams and side-products to improve yield and purity. Lab-to-warehouse feedback cycles have pushed us to streamline neutralization stages during synthesis, replace legacy filtration gear that left product losses, and reduce cycle times for large-batch crystallizations.

    Sometimes, customers bring us unexpected puzzles: off-spec melting points or inconsistent TLC spots. We respond by running the same batch under our own protocols, comparing instrument setups, and sometimes uncovering a temperature gradient or a calibration issue behind an apparent chemical problem. From a manufacturer perspective, these everyday investigations turn directly into product and documentation improvements.

    Moving Forward: Sustaining Reliable, Research-Grade Supply

    As demand diversifies, we keep investing in analytical equipment—HPLC, chiral detectors, moisture analyzers—and staff training. Our team rotates across production lines and QC labs, gaining cross-functional experience and a sense of accountability that doesn’t exist in more hands-off supply chains. We make adjustments to our process flow when recurring customer feedback points to a systemic problem.

    L-Isoserine isn’t volume-driven like the commodity amino acids, so our process never gets fully automated or distant. We work from raw material stocks that undergo stringent incoming QC, with synthesis, work-up, and purification steps that have built-in points for sampling and in-process control. This close management translates directly to the reliability of the product over time—something our long-term collaborators value.

    We promote open dialogue with research partners. Sharing our knowledge of reaction quirks, storage behavior, and analytical methods not only reduces end-user headaches but raises overall standards across research teams. On several occasions, research partners have returned to us with published findings attributed to the dependable performance of our L-Isoserine. Our manufacturing teams take pride knowing the impact of their work reaches across scientific fields and innovation pipelines.

    Conclusion: Trust Through Experience and Detail

    Producing L-Isoserine means living through the sticking points, from crystallization bottlenecks to analytical puzzles to regulatory paperwork. The non-standard nature of this amino acid puts us in close contact with the scientists who use it, challenging us to constantly improve both process and support. Each technical advance or process tweak stems from real-world experience, not abstract metrics.

    In our view, the success of L-Isoserine in research settings depends less on flashy product features and more on sustained, attentive manufacturing. By focusing on robust chemistry, accurate record-keeping, and honest communication, we deliver a product that helps chemists and biologists take confident steps forward in their work—knowing that the building block at the foundation of their experiments arrived with the attention to detail only a dedicated manufacturer can provide.