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Dl-Mevalonolactone

    • Product Name Dl-Mevalonolactone
    • Alias DL-3-Hydroxy-3-methylglutaric acid lactone
    • Einecs 223-668-5
    • 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

    835209

    Name Dl-Mevalonolactone
    Chemical Formula C6H10O3
    Molecular Weight 130.14 g/mol
    Cas Number 7336-16-9
    Appearance White to off-white solid
    Purity Typically ≥98%
    Melting Point 34-37 °C
    Solubility In Water Soluble
    Storage Conditions Store at 2-8°C
    Synonyms DL-3,5-Dihydroxy-3-methylvalerolactone
    Usage Biochemical research, intermediate in cholesterol biosynthesis
    Smiles CC1C(C(=O)OC1)O
    Inchikey LVKREBOZUKPENZ-UHFFFAOYSA-N

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

    Packing & Storage
    Packing Dl-Mevalonolactone is packaged in a sealed amber glass bottle, containing 5 grams, labeled with product details and hazard information.
    Shipping Dl-Mevalonolactone is shipped in a tightly sealed container, protected from moisture and light. It is handled according to standard chemical safety protocols, typically at ambient temperature, unless otherwise specified. Appropriate labeling and documentation are provided to comply with regulatory requirements for safe transport of hazardous or laboratory chemicals.
    Storage Dl-Mevalonolactone should be stored tightly sealed in a cool, dry place away from light and moisture. It is best kept at 2–8°C (refrigerator temperature). Protect from air and sources of ignition, and store in a well-ventilated area. Use appropriate chemical-resistant containers and clearly label the storage container. Avoid prolonged exposure to open air to prevent degradation.
    Application of Dl-Mevalonolactone

    Applications of Dl-Mevalonolactone in Industrial Manufacturing

    We manufacture Dl-Mevalonolactone with industry-specific quality management for specialized downstream applications. The following sections detail actual market-proven use cases, application dosages, compliance expectations, and final product classes where our material integrates into production and value chains.

    1. Statin Active Pharmaceutical Ingredient (API) Synthesis

    Dl-Mevalonolactone is a critical intermediate in industrial statin synthesis, supporting multi-step enzymatic and chemical processes in active pharmaceutical production. Manufacturers rely on its chiral purity to ensure correct molecular pathways, in both fermentation-derived and semi-synthetic statin APIs such as lovastatin and simvastatin. Each batch supports stringent pharmaceutical GMP protocols, entering the process at defined phases for building core side chains before final functionalization and salt formation.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for APIs
    • Ph. Eur. monographs for relevant statins (e.g., Simvastatin Monograph)
    • 21 CFR Part 210/211 US FDA cGMP for drug substances
    • Chinese Pharmacopoeia GB/T standards for API synthesis

    Typical usage ratio

    • Used at 1.05–1.15 molar equivalents per equivalent of final API, adjusted depending on desired yields, conversion efficiency, and recovery rates; process conditions and side chain requirements dictate final ratio.

    Downstream process integration

    • Enters after the acetyl-CoA pathway fermentation or as substrate in the macrolactonization step; incorporated in cascade reactions to yield the tetrahydronaphthalene core common in statins prior to further esterification or aromatic substitutions.

    Final product types

    • Lovastatin API
    • Simvastatin API
    • Pravastatin API
    • Industrial intermediates for further statin derivatives

    2. Vitamin K2 (Menaquinone) Intermediate Manufacturing

    In vitamin K2 production, Dl-Mevalonolactone serves as an essential precursor for constructing isoprenoid side chains via the mevalonate pathway. Industrial vitamin K2 manufacturing demands precise control in stepwise polyprenylation, where mevalonolactone supports consistent yield of the converted isoprenoid units. Downstream plants utilize strict food additive regulations and dedicated food GMP to guarantee both purity and nutritional aspect of finished edible supplements and food additives for international markets.

    Industry compliance standards

    • FSSC 22000 Food Safety System Certification for food ingredient plants
    • GB 14880 Food Additive Use Standard (China, vitamin K2 as additive)
    • EC 1333/2008 Food Additives Regulation for EU markets
    • USP–NF dietary ingredient monographs

    Typical usage ratio

    • Converted at 0.95–1.2 molar equivalents relative to vitamin K2 intended output; actual ratio depends on downstream recovery efficiency and intermediate stability; fermentation process variations introduce further adjustments as needed.

    Downstream process integration

    • Fed into polyprenyl side chain synthesis reactor following initial condensation phase; further transformed by enzymatic prenyl-transfers to yield menaquinone isomers before final purification and formulation into supplements.

    Final product types

    • Vitamin K2 (MK-4, MK-7) supplement ingredients
    • Dry blend nutrition powders
    • Functional food preparations
    • Pharmaceutical grade vitamin K concentrates

    3. Isoprenoid Flavor and Fragrance Ingredient Synthesis

    Dl-Mevalonolactone feeds into the core terpene biosynthetic pathway for industrial-scale isoprenoid flavor and fragrance ingredient manufacturing. The mevalonic acid pathway transforms it into universal five-carbon building blocks required for downstream enzymatic coupling and cyclization. Industrial flavor houses and specialty chemical processors require precise feedstock ratios and compliance with IFRA and food-grade flavoring directives to support high-volume runs of specific fruity, herbal, and citrusy terpene blends for consumer and commercial use.

    Industry compliance standards

    • IFRA Standards and Guidelines for fragrance ingredient manufacturing
    • US FDA 21 CFR Part 172 (Food Additives Permitted for Direct Addition to Food for Human Consumption)
    • ISO 9235: Aromatic natural raw materials--Vocabulary
    • EU Regulation (EC) No 1334/2008 for food flavorings

    Typical usage ratio

    • 1–3% by weight relative to total intermediate batch mass, depending on intended monoterpene or sesquiterpene yield; final ratio determined via yield optimization and in-process chromatographic monitoring.

    Downstream process integration

    • Enters the process post-initial acetylation as the direct precursor to isopentenyl pyrophosphate (IPP) biosynthesis; subsequent steps include selective cyclases or oxidoreductase enzymes for desired fragrance profile formation before isolation and blending with carrier solvents or flavor bases.

    Final product types

    • Citrus terpenoid fragrance concentrates
    • Fruit ester blends for beverage flavoring
    • Herbal essential oil ingredients
    • Industrial aroma chemicals for perfumery and food flavoring

    4. Biotechnological Polyisoprene (Synthetic Rubber) Production

    Dl-Mevalonolactone provides a biologically derived monomer source for advanced polyisoprene manufacturing via metabolic engineering routes. Synthetic rubber plants integrate it into microbial fermentation systems or enzymatic polymerization units, producing polyisoprene alternatives for applications where molecular uniformity and renewable sourcing are critical. Finished products comply with automotive, medical, and food-contact rubber standards, requiring tightly monitored raw material addition and polymer chain-length control.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems
    • FDA 21 CFR 177.2600 (Rubber articles intended for repeated use)
    • REACH Regulation (EC) No 1907/2006 substance compliance
    • ASTM D1418: Standard Practice for Rubber and Rubber Latices—Nomenclature

    Typical usage ratio

    • 5–12% by mass of fermentation feed medium, with adjustment based on desired polymer molecular weight and conversion efficiency; ratio depends on reactor size, strain engineering, and real-time polymer growth monitoring.

    Downstream process integration

    • Fed as the primary C5 precursor at the initial culture inoculation or after biomass reaches log-phase in bioreactors; subsequently catalyzed via microbial IPP pathway to elongate isoprene chains before polymer extraction, fractionation, and compounding for vulcanization.

    Final product types

    • Technical grade synthetic polyisoprene rubber
    • Automotive and industrial rubber components
    • Medical grade latex alternatives
    • Elastomeric food contact articles

    5. Research-Grade Isoprenoid Pathway Metabolite Supply

    Pharmaceutical R&D operations and metabolic engineering companies depend on our Dl-Mevalonolactone for analytical studies and pilot production of isoprenoid-derived metabolites, used in both mechanistic research and biomarker development. Stringent analytical certification, contamination control, and documentation accompany each batch, in alignment with laboratory and reference standard requirements for controlled studies and preclinical pilot campaigns.

    Industry compliance standards

    • ISO 17034: General requirements for the competence of reference material producers
    • CNAS-CL01 (China National Accreditation Service for Conformity Assessment—laboratory accreditation)
    • USP Reference Standard specification
    • OECD Good Laboratory Practice (GLP) principles

    Typical usage ratio

    • 0.01–2% by solution or total assay mass, accurately titrated based on reference material or experimental protocol; small-scale applications often require trace-level additions, validated by analytical standards.

    Downstream process integration

    • Introduced at initiation of enzyme assays, metabolic flux analysis, or pathway optimization studies; used in both labeled and unlabeled forms for analytical instrument calibration, cell culture supplementation, and metabolomics profiling.

    Final product types

    • Reference standard ampoules
    • Isotopically labeled mevalonate derivatives
    • Research metabolites for biotechnological studies
    • Preclinical pathway analysis kits
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    Certification & Compliance
    More Introduction

    Dl-Mevalonolactone: A Core Building Block in Biochemical Production

    Understanding Dl-Mevalonolactone

    In the daily work of running our own chemical production lines, few intermediates draw as much careful handling as Dl-Mevalonolactone. Chemists in our facility know this compound for its versatility, a substance frequently requested by both research and manufacturing partners. We produce it in a range of grades tailored for the precise needs of downstream synthesis, emphasizing anhydrous purity and consistent batch characteristics.

    Our Dl-Mevalonolactone holds the CAS number 500-97-0 and follows a molecular formula of C6H8O3. The cyclic ester structure enables it to serve as a precursor in multi-step organic syntheses, and, from a chemical manufacturer’s lens, that translates to a material which must meet exacting standards. We run continuous QC checks for melting point, typically observed near 31-34°C, and verify purity through gas chromatography. Slight shifts in purity or moisture content impact not only the yield downstream but also the integrity of related product lines. Over years in the industry, we've learned that customers in pharmaceutical R&D or biotechnology come back because they expect — and receive — tight control over these numbers.

    Applications in Modern Bioscience

    Dl-Mevalonolactone sits at the crossroads of fields like statin precursor research, coenzyme Q10 synthesis, and the study of cholesterol biosynthesis pathways. Our ongoing collaborations have shown just how critical reliable access to this compound is for those working on fundamental questions in metabolic engineering. This compound’s main role appears at the foundational step of the mevalonate pathway, which underpins countless secondary metabolite syntheses.

    I’ve seen our Dl-Mevalonolactone loaded into glass reaction vessels, destined for conversion into mevalonic acid through mild hydrolysis, or transformed via enzymatic routes to mirror natural metabolism. Because a racemic mixture contains both D- and L- enantiomers, we make sure customers understand the difference compared to single-isomer alternatives. While some downstream reactions demand enantiopure material, broad-spectrum applications—like certain microbial fermentation studies or pre-clinical pharmaceutical trials—work well with our Dl- (racemic) grade. Our own fermentation experts favor Dl-Mevalonolactone for process optimization trials, using its dual chiral nature to investigate pathway flexibility.

    Differences Compared to Competing Options

    Through hands-on manufacturing, we run up against the subtle drawbacks and perks of different mevalonate pathway intermediates. Dl-Mevalonolactone, compared to mevalonic acid, offers more straightforward handling and stability under room conditions. Labs often encounter storage instability and hydrolysis risks with open-chain acids, so the lactone form wins out for longer shelf life and lower reactivity toward atmospheric moisture.

    On the other hand, enzymatic or chiral synthesis projects sometimes favor single-isomer mevalonolactone or open-chain D-mevalonic acid. We have clients in the statin manufacturing chain who ask about the feasibility of switching entirely to single-enantiomer supplies. In our experience, choosing between racemic and chiral forms depends most on downstream catalysts and biological selectivity. Our Dl-form remains popular outside the most stereospecific syntheses, thanks to availability, cost, and performance in standard biotransformation processes. Most production facilities—ours included—prioritize shelf-stable stock and predictable reaction profiles, rather than pursuing marginal yield improvements through costly isomeric resolution.

    Compared to synthetic mevalonate analogs, Dl-Mevalonolactone is less hazardous in terms of decomposition and byproduct formation, provided the atmosphere and containers remain dry. Attempts to substitute with protected or functionalized analogs usually lead back to the basic lactone, especially for researchers scaling from grams to kilograms. We’ve worked closely with process engineers transitioning from bench-scale to pilot runs, guiding documentation for consistent crystallization, solvent exchange, and packaging under dry nitrogen. These direct relationships inform the policies we use for production and storage, based on what genuinely works in a factory, not just theory.

    Manufacturing Control and Quality

    Our own production staff benefit from well-defined tolling systems and semi-continuous reactors. This keeps batch-to-batch variability low and ensures we can rapidly respond to unannounced spikes in demand, like those that arose during recent clinical trial booms. Maintaining reproducibility across tens of tons each year relies on automated temperature, pH, and solvent control—areas we’ve invested in as a result of previous quality excursions.

    Purity typically runs above 99%, with impurities like polyacid side-products monitored below 0.1%. Although trace levels fluctuate based on upstream raw material lot variations, our QC team has authority to hold shipments if deviation is found. Irritation among operators grew when we saw off-ratio stocks block the line years ago, so we introduced in-process checks for residual solvents and water content using Karl Fischer titration and online IR monitoring. The scores of hours saved on troubleshooting and waste disposal more than covered the upfront investment.

    We receive questions about heavy metals and residual solvent levels during audits, and we comply with the relevant limits set by both major pharmacopoeias and in-house customer requirements. We established an internal specification to hold residual DMF or acetonitrile below 20 ppm, acknowledging increasing regulatory attention across international markets. Our long-term partners trust this data because we consistently share the original analytical traces.

    Solubility, Handling, and Storage

    Our Dl-Mevalonolactone dissolves readily in many polar organic solvents, including methanol, ethanol, acetone, and DMSO. Reconstitution or dilution steps rarely challenge experienced analytical labs, and downstream processing can begin almost immediately after item receipt. Practical storage guidance remains simple: keep sealed containers in a cool, dry place, and limit atmospheric exposure. We pack most shipments under nitrogen to eliminate even trace hydration over time. It pays off for customers, since even small amounts of water introduce hydrolysis and lower reaction efficiency.

    One ongoing lesson from the plant floor is that plastic and glass containers perform differently for this compound. Polyethylene bags offer the lowest transport cost, but experience told us to shift toward amber glass or high-barrier multilayer plastics on all international orders. There’s a sharp drop in customer complaints about discoloration or sticking once this change went into effect. As a policy, every outgoing pack receives batch-specific COAs linked to both the lot and the shipment container. We serialize all master drums and archive reserve samples to investigate any customer query directly.

    Dl-Mevalonolactone in Biological Research and Industrial Use

    In contract fermentation projects, we’ve seen Dl-Mevalonolactone drive pathway optimization tasks alongside labeled carbon sources. Fermentation partners note its rapid uptake and metabolic conversion, serving both as carbon backbone and signaling intermediate in chassis engineering. Larger pharma groups focus on statin intermediates, coenzyme Q10 analogs, and precursors for terpene biosynthesis.

    Some researchers, especially those tracing cholesterol biosynthesis, select Dl-Mevalonolactone for its close mimicry to natural flux through the mevalonate pathway. Because the racemic mixture simplifies supply, labs order in larger, economic amounts instead of hunting down costly resolved enantiomers. Unlike many synthetic intermediates, our Dl-Mevalonolactone doesn’t introduce problematic side-reactions with common fermentation media or buffer components, further easing downstream purification work.

    Teaching laboratories also request it for hands-on synthesis modules. Unlike unstable intermediates prone to spontaneous decomposition, Dl-Mevalonolactone stays intact on the shelf and grants students predictable results. We've heard from university labs who lost valuable time fighting batch-to-batch inconsistencies with third-party supplies—a problem resolved by switching to consistent, analytically verified product direct from manufacturing.

    Safety and Regulatory Landscape

    Safe handling of Dl-Mevalonolactone forms a routine part of operator training. Skin and respiratory irritation can occur during weighing or high-speed milling, so we require standard PPE and well-ventilated workspaces. Standard operating protocol also outlines disposal routes, favoring chemical neutralization and incineration when faced with out-of-spec lots. Unlike some reactive esters or halogenated analogs, this lactone doesn’t carry acute toxicity risks, though chronic exposure guidelines remain in place per standard chemical management practice.

    Regulatory trends toward greater traceability affect our own documentation. Some years ago, a shift in EU requirements led to additional batch-level records for all pre-cursor compounds used in regulated pharmaceutical synthesis. To keep pace, we invested in expanded ERP integration—linking every shipment, every container closure, to a digital trail. This move, while time-consuming, reduced audit headaches and speeded up lot-release on arrival in customer facilities.

    Ongoing communication with regulatory teams from pharmaceutical and industrial biotechnology partners ensures we align with new global standards. As regulations evolve, we adapt our labeling, safety data sheets, and even our analytics approach to match. Open dialogue on safety concerns, compliance, and risk management provides value to both us and our customers, avoiding surprises or supply gaps that could impact research or production timelines.

    Continuous Improvement and Feedback

    Direct feedback from frequent users of Dl-Mevalonolactone shapes much of our approach to manufacturing and shipping. The majority of changes in packaging, QC procedures, or even batch sizes arise from specific comments made by technical teams who handle our product daily. In regions with longer transit times or higher risk of temperature excursions, we swap packaging out for insulated containers and add humidity indicators.

    We’ve seen research clients request microbially-sourced alternatives in the hopes of reducing environmental impact. Efforts to offer greener process routes, including enzymatic lactonization from renewable precursors, reflect a wider industry movement. Though most production still follows traditional organic synthesis, continued investment in these alternatives aligns with both customer demand and our own commitment to lower carbon footprint.

    Our decades of experience in producing and supplying Dl-Mevalonolactone inform our priorities: stability, purity, reliability, and safe delivery. Mistakes—whether from improper storage, missed purity checks, or shipment issues—become clear rapidly at the manufacturing level, and the cost of fixing them never fades from institutional memory. Solving for these practical realities, not just theoretical targets, has shaped the robust production environment we operate today.

    Conclusion: Dl-Mevalonolactone as a Trusted Foundation for Discovery

    Dl-Mevalonolactone, with its clear behavior under anhydrous storage, stable chiral structure, and strong performance in biotechnological settings, has earned a central place in modern synthesis and biological research. The compound’s enduring popularity speaks both to its chemical simplicity and its consistency as delivered from a purpose-driven manufacturer. Through constant engagement with process engineers, R&D labs, and regulatory bodies, we have built up the practical capabilities to produce and deliver this key intermediate at scale, with unwavering emphasis on end-user success.

    Ongoing investment in better analytics, packaging, and greener technologies will continue to drive improvements in our Dl-Mevalonolactone offering. Whether destined for the next generation of cholesterol-lowering drugs, a new biosynthetic pathway, or classroom education, this product continues to deliver both the flexibility and reliability that scientists and engineers need. Every improvement in process, safety, and documentation stems directly from years listening to users and measuring what actually works outside the theoretical lab context. We produce Dl-Mevalonolactone not merely as a bulk chemical, but as a cornerstone for discovery and development in the worlds of chemistry and biology.