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D-Luciferin Potassium Salt

    • Product Name D-Luciferin Potassium Salt
    • Alias D-Luciferin K+ Salt
    • Einecs 259-651-8
    • 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
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    Specifications

    HS Code

    868577

    Product Name D-Luciferin Potassium Salt
    Cas Number 115144-35-9
    Molecular Formula C11H7KN2O3S2
    Molecular Weight 318.41 g/mol
    Appearance Off-white to yellow powder
    Solubility Soluble in water
    Purity ≥98%
    Storage Temperature -20°C
    Synonyms Firefly Luciferin, Beetle Luciferin, D-Luciferin
    Assay Method HPLC
    Light Sensitivity Light sensitive
    Usage Bioluminescent substrate
    Ph Of Solution 6.0-7.5 (20 mg/mL in water)

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

    Packing & Storage
    Packing The D-Luciferin Potassium Salt (1g) is supplied in a sealed, amber glass vial with a tamper-evident cap and clear labeling.
    Shipping D-Luciferin Potassium Salt is shipped in tightly sealed, light-protective containers under ambient or cool conditions to ensure stability and prevent degradation. Packages are clearly labeled and comply with chemical shipping regulations. Expedited shipping may be available to minimize exposure to moisture, heat, and prolonged transit.
    Storage D-Luciferin Potassium Salt should be stored at –20°C in a tightly sealed container, protected from light and moisture. The storage area should be dry and well-ventilated to prevent degradation. Avoid repeated freeze-thaw cycles by aliquoting the compound. Proper storage preserves its stability and ensures reliable bioluminescent assay results. Keep out of reach of unauthorized personnel and label appropriately.
    Application of D-Luciferin Potassium Salt

    Applications of D-Luciferin Potassium Salt in Industrial Manufacturing

    D-Luciferin Potassium Salt serves as a specialized substrate in industries focused on biochemical detection, cell-based assay development, diagnostic device production, preclinical imaging, and environmental monitoring. Our manufacturing processes ensure consistent batch quality tailored for rigorous commercial and industrial operations.

    1. In Vitro Bioluminescent Assay Systems for High-Throughput Screening

    Pharmaceutical and biotech companies incorporate D-Luciferin Potassium Salt as a key substrate in engineered firefly luciferase-based screening platforms. It allows sensitive ATP quantification and gene reporter analyses for drug discovery pipelines. QC protocols emphasize minimal batch variance to support reproducible plate-to-plate readouts, with material validated for use in automated liquid handling workflows. Customers integrate the substrate during the reagent addition stage of assay plate setup, often just prior to data acquisition.

    Industry compliance standards

    • USP Reagent Grade where applicable
    • OECD GLP (Good Laboratory Practice) guidelines
    • ISO 13485 for manufacturers of diagnostic testing kits
    • FDA 21 CFR Part 820 for medical device applications

    Typical usage ratio

    • 10–100 μM in assay buffer, dependent on luciferase enzyme concentration and throughput volume requirements
    • Customers adjust based on signal intensity targets and instrument dynamic range

    Downstream process integration

    • Added as a last-step component in multiwell plate reagent loading
    • Prepared in sterile buffer; dispensed by automated liquid handlers or robotic systems
    • Directly involved in substrate-enzyme luminescent reaction under controlled conditions
    • Batch QC includes substrate purity and bioluminescence yield certification

    Final product types

    • Pre-formulated assay kits for ATP/luciferase testing
    • High-throughput reagent packs for pharmaceutical screening workflows
    • Ready-to-use gene reporter systems for genetics laboratories
    • Bioanalytical contract research testing kits

    2. Cell Viability and Cytotoxicity Assays in Biotech Production

    Contract research and cellular therapy manufacturers depend on D-Luciferin Potassium Salt in luciferase-expressing cell line assays to measure viability, proliferation, and cytotoxicity. The substrate ensures single-cell sensitivity for kinetic and endpoint measurements. Integration into cell-based platforms requires careful formulation for serum compatibility, with stringent raw material traceability maintained from lot to lot.

    Industry compliance standards

    • ISO 9001:2015 in biotech reagent manufacturing
    • ICH Q7 for GMP Active Pharmaceutical Ingredient intermediates
    • FDA 21 CFR 58 (GLP for nonclinical laboratory studies)
    • CLSI (Clinical and Laboratory Standards Institute) C62-A guideline for cell viability/cytotoxicity methods

    Typical usage ratio

    • 15–300 μg/mL in culture media, optimized per cell type and luciferase expression levels
    • Adjustments for different plate formats (6- to 384-well)

    Downstream process integration

    • Supplemented just before luminescence detection phase in cell culture assays
    • Used both in live cell kinetic monitoring and endpoint cell health readouts
    • Documented for compatibility with automated plate readers and imaging systems
    • Supplier validation includes sterility and endotoxin testing

    Final product types

    • Cell viability/cytotoxicity reagent kits
    • Live cell imaging systems and consumables
    • Custom luciferin solutions for gene editing workflows
    • CRO cell analytics service bundles

    3. Bioimaging Substrate for In Vivo Preclinical Small Animal Studies

    Pharmaceutical R&D laboratories and CROs rely on D-Luciferin Potassium Salt as an injectable substrate for live animal bioluminescent imaging. The substrate’s pharmaceutical-grade purity supports biodistribution and pharmacokinetics monitoring using luciferase reporter strains in mice and rats. Manufacturing traceability and contaminant control are critical to meet preclinical study design requirements.

    Industry compliance standards

    • USP Pharmaceutical Grade
    • OECD Principles of GLP
    • Guidelines for the Care and Use of Laboratory Animals (NRC/OLAW)
    • AAALAC International accreditation standards

    Typical usage ratio

    • 15–150 mg/kg body weight for intravenous or intraperitoneal administration
    • Diluted in sterile saline or PBS prior to injection

    Downstream process integration

    • Prepared as a sterile injectable immediately before administration to animals
    • Administered prior to imaging sessions in dedicated BLI (bioluminescence imaging) suites
    • QC validation includes absence of pyrogens and consistent batch luminescence output
    • Potency confirmation with reference luciferase-expressing cell lines

    Final product types

    • Preclinical imaging-grade substrate vials and syringes
    • BLI animal research kits
    • On-demand substrate packs for in vivo contract research services
    • Pharmacological compound tracking test sets

    4. Food and Environmental Pathogen Detection Kits

    Food safety laboratories and water testing companies use D-Luciferin Potassium Salt in real-time bioluminescent assays for detecting microbial ATP contamination in food products, beverages, and potable water. Formulations are developed for compatibility with food processing sample matrices and meet industry protocols for trace analysis. Each lot undergoes release testing for matrix interference and background signal uniformity.

    Industry compliance standards

    • ISO 17025 for testing laboratory accreditation
    • AOAC Official Methods for food pathogen detection
    • FDA BAM (Bacteriological Analytical Manual) methodologies
    • EU Commission Regulation (EC) No 2073/2005 (Microbiological criteria for foodstuffs)

    Typical usage ratio

    • 5–30 μg/mL in swab extraction buffer or test solution
    • Adjusted based on sample type (solid or liquid matrices)

    Downstream process integration

    • Added to sample extracts during ATP bioluminescence step
    • Used in field, laboratory, and factory automation settings
    • QC validation for food contact and environmental trace analytics
    • Material supported by detailed Certificate of Analysis (COA) and traceability records

    Final product types

    • PCR-independent food pathogen testing kits
    • ATP monitoring swabs for hygiene and QC labs
    • On-site water safety bioluminescent kits
    • Ready-to-use ATP luminometers for food processing lines

    5. Clinical Diagnostic Reagents for Molecular Imaging Platforms

    Diagnostic manufacturers formulate D-Luciferin Potassium Salt in reagent systems designed for clinical-grade molecular imaging including detection of luciferase-expressing biomarkers in patient samples and ex vivo tissues. The substrate is processed under stringent cleanroom conditions to minimize contamination risks. Batch-to-batch reproducibility supports precision diagnostic evaluation and compliance with clinical laboratory protocols.

    Industry compliance standards

    • ISO 13485:2016 for medical device manufacturing
    • EU IVDR (In Vitro Diagnostic Regulation) 2017/746
    • FDA 21 CFR Part 820 (Quality System Regulation, Diagnostics)
    • CLIA (Clinical Laboratory Improvement Amendments) requirements for clinical testing workflows

    Typical usage ratio

    • 10–75 μM in clinical reagent cocktails
    • Adjusted per diagnostic platform’s sensitivity and sample input

    Downstream process integration

    • Integrated as a substrate in single-use diagnostic cartridges or cuvettes
    • Added to clinical test samples handled in controlled laboratory environments
    • Automated pipetting and reagent reconstitution at point of diagnostic analysis
    • Extensive documentation and traceability included with each batch

    Final product types

    • IVD cartridges for molecular imaging
    • Blood biomarker detection test kits
    • Automated bioluminescence diagnostic platforms
    • Reference standards for clinical laboratory QC
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    Competitive D-Luciferin Potassium Salt prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    D-Luciferin Potassium Salt: From Factory Floor to Research Bench

    Understanding the Basics of D-Luciferin Potassium Salt

    At our facility, we handle D-Luciferin Potassium Salt by the kilogram, pouring it from drums and running it through strict quality checks. As chemical manufacturers, our perspective on this compound is shaped by years of direct production, batch testing, and close work with technical teams at labs and biotech companies. D-Luciferin Potassium Salt is more than a reagent name on a bottle; it serves as a vital substrate for firefly luciferase in one of the most reliable bioluminescent reactions used in science. Researchers rely on its clean performance for luciferase-based bioassays, live animal imaging, and a growing list of molecular biology applications.

    Our factory model, DFP-1, comes as a white to off-white crystalline powder, stable under standard storage, and manufactured in lots averaging greater than 99% purity by HPLC analysis. We’ve honed our process to keep heavy metals and organic impurities to the low single-digit ppm range, meeting stringent requirements common in pharmacological labeling and preclinical imaging pipelines.

    Bioluminescence goes far beyond novelty or visual effect. Its quantitative accuracy and safety in non-invasive in vivo monitoring explain why D-Luciferin Potassium Salt now ranks among the most-requested luciferase substrates globally. Whether targeting luciferase gene reporters in cell populations or mapping tumor boundaries in small animals, labs depend on luciferin’s consistent emission signal. Reliability comes from upstream: as producers, our focus is on batch-to-batch reproducibility, solubility in buffers, and avoidance of microcontaminants that might interfere with photon yield or background signal.

    The Path from Synthesis to Use in the Lab

    Producing D-Luciferin Potassium Salt requires tight control from raw material intake to the final packaging. Some producers cut corners on synthesis pathways, leading to byproduct contamination or unstable salt forms. We use a direct, multi-step route starting with L-cysteine, avoiding unnecessary chiral intermediates, and ensuring the key potassium counterion is incorporated cleanly, without sodium or heavy metal crossovers. This detail makes a clear difference for users working with sensitive in vivo models or high-throughput quantitative assays.

    After synthesis, handling and storage shift the focus to protecting luciferin’s delicate thiazole ring and methoxy groups from hydrolytic breakdown and UV light exposure. Even slight oxidation or hydrolysis, invisible to the naked eye, can undermine signal reliability. That’s why every batch passes not only UV-vis and NMR testing, but also functional luciferase assay validation — a step skipped by some less rigorous operations. By implementing a final round of vacuum desiccation and bottling under nitrogen, we keep each shipment at optimal stability, whether destined for university freezers or industrial high-volume automation systems.

    From Animal Models to Cell-Based Assays: Real-World Experiences

    We’ve worked with biologists monitoring stem cell engraftment in real-time, oncologists tracking tumor metastasis in living mice, and synthetic biologists building intricate gene circuits. Many customers share early feedback on their assay results: inconsistent performance when switching suppliers, unexplained background signals, or solubility problems that block reliable quantitation. Drawing on these conversations, we focused production development on trouble spots. For example, our standard DFP-1 grade can dissolve rapidly and fully in common injection or buffer media at up to 15 mg/mL, even after months in long-term storage at –20°C.

    Solubility alone doesn’t define a usable luciferase substrate. Researchers care about zero background auto-luminescence and freedom from colored contaminants, both of which can swamp signal-to-noise in sensitive chemiluminescent assays. That means every step of our quality control — from visual inspection to LC-MS and bioassay performance — plays a role in minimizing unexpected signal interference.

    The bioimaging world keeps setting the bar higher. As animal imaging systems demand precise quantitative data and lower detection limits, even trace chemical impurities become unacceptable. Issues like high sodium contamination lead to electrolyte imbalances in vivo, altering animal responses and throwing off experimental replicability. To stay ahead, we refined our potassium exchange and purification steps. Routine screening for sodium content and transition metal residues catches flaws early, cutting down on failed experiments after product leaves our facility.

    Differentiating D-Luciferin Potassium Salt: What Matters Most in Production

    Manufacturing D-Luciferin Potassium Salt might look simple to outsiders, but the process lives or dies by attention to detail. Unlike so-called “luciferin” blends, which may cut costs by mixing multiple salt forms to mask impurities, a pure potassium salt puts sensitivity and safety first. Users gain predictable luciferase activation, reduced risk of cell viability artifacts, and a gentle handling profile for animal injections.

    Our production line relies on automated crystallization and purification. These steps help us avoid typical pitfalls: sulfate, chloride, or acetate carryover, which lead to mixed signals in kinetic and endpoint assays. DFP-1 matches both the classic firefly luciferase biochemistry and the needs of imaging hardware calibrated for maximal light collection in the 560 nm (green-yellow) range.

    Some competitors market D-Luciferin Sodium or mixed salt forms. Sodium salts can increase the chance of background ionic interference, especially in in vivo experiments, and create solubility headaches. Other alternatives like coelenterazine often demand expensive luciferase enzyme systems, or lack equivalent stability and signal duration. We stick to high-purity potassium salt because academic users and major pharmaceutical companies have repeatedly chosen it for robust performance, clean pharmacokinetics in animal work, and integration into FDA-reviewed imaging protocols.

    Compliance, Traceability, and Trust from a Manufacturer’s Viewpoint

    As production chemists who interact directly with end users and regulatory auditors, we understand that chemical quality depends on complete traceability, not just purity figures on a spec sheet. Every drum of raw material comes with full documentation, allowing us to trace any lot by date, route, personnel, and validated analytical records. We’ve sat across the table from compliance teams for contract research labs, animal facilities, and government contributors. They want a vendor who manages a transparent, repeatable process and takes ownership if an issue arises — which means giving real answers if a customer encounters a performance glitch or a testing anomaly on their end.

    Over the years, we have seen how incomplete transparency or vague product histories have disrupted ambitious animal imaging projects. Many life science companies burn through time and budget when third-party suppliers source D-Luciferin from traders or resellers, and then struggle to repeat published results. That chain of custody breaks trust. Our approach is direct and open: all synthesis, testing, packaging, and data collation occurs in house at our manufacturing facility. Buyers dealing with regulatory filings or non-clinical studies get access to full batch documentation, certificate of analysis, and quality assurance data.

    Feedback from auditors and reviewers has led us to expand stability studies, develop redundant contamination controls, and integrate extra ID verification at every bottling stage. Not every project needs this level of rigor, but animal imaging and pharmaceutical R&D often do. Building a solid, trust-based relationship with repeat customers means adapting to new regulatory requirements, not just offering a static product.

    Challenges in Manufacturing High-Purity Luciferin and Solutions We Apply

    Every raw batch starts with scrutiny. Sourcing pure L-cysteine and thiazole intermediates proves harder each year as global supply chains fluctuate and new contaminant risks emerge. Fluctuating input quality carries downstream risk: heavy metals, residual solvents, or optical isomer contamination can lead to bad substrate, unexpected toxicity in animals, or failed imaging sessions. Cost pressures sometimes tempt less experienced producers to buy the cheapest inputs. In our experience, this a dangerous shortcut — especially for academic labs staking research careers on image-based data.

    Our solution: develop relationships with vetted raw material suppliers, keep incoming acceptance requirements high, and perform in-house identity and purity verification before production begins. Scale helps: running D-Luciferin at production rather than pilot scale lets us keep quality up and cost reasonable, compared to labs who buy through hobbyist or research-scale operations that skip deep cleaning, filtration, or validation steps.

    The next hurdle is process control. Small manufacturing slips — a misplaced temperature setpoint, a skipped filtration pass, or a rushed drying period — end up costing users hours spent tracking down mystery background signals or lost pharmacokinetic windows in live mouse imaging. Solutions are routine: production SOPs with multiple checkpoints, double confirmation before critical synthesis and crystallization steps, and regular skills refresher training for process chemists.

    The goal is never about selling the most units, but to anchor confidence from bench to bedside. Straightforward manufacturing, tight tolerances, and a willingness to take responsibility when users run into real-world issues sets high-quality luciferin apart from generic or blended products.

    Handling, Storage, Shipment, and User Guidance

    Over time, we’ve seen customers face unanticipated challenges not covered in standard product datasheets. D-Luciferin Potassium Salt, even at high purity, degrades quickly if exposed to oxygen or light for too long, impacting its bioluminescence response. Some researchers expect it to behave like stable salts, then call us after observing signal drop-off or unexplained background in their plate readers or imaging systems.

    To minimize risks, we package in light-resistant, vacuum-sealed containers, with easy-to-read, lot-linked labeling and full temperature logging during shipment. All large-volume orders go out with a tamper-evident seal and enclosed instructions outlining recommended storage at -20°C for long-term stability. Smaller research lots ship with quality documentation and fresh test data, not just generic “for research use only” stickers.

    Shipments destined abroad go out with full paperwork, MSDS notarization, and storage guidance for customs clearance. We see product arrive across continents up to two weeks after dispatch, and quality holds when users follow our handling guidance. Several times a year, universities call after running low on stock held in ambient conditions — and ask if we can rush replacement following an unexpected signal failure. Over-communicating proper storage and handling keeps everyone from losing precious samples or wasting research dollars.

    Fielding Technical Questions: Practical Tips from a Producer’s Bench

    We find ourselves fielding technical calls from users testing unknown buffer combinations, stress conditions, or system integrations. Our perspective isn’t based on theoretical chemical knowledge, but on the gritty realities of upscaling and working with trial-and-error feedback from end users. Instead of deferring these situations, we work through common sticking points:

    Direct technical support — not just generic answers — matters most when working with delicate biological systems. By embedding troubleshooting into our outreach, we help troubleshoot site-specific or organism-specific issues, whether high-throughput screening or longitudinal live model studies.

    Comparing Potassium Salt Against Other Salt Forms and Substrates

    End-users occasionally ask why we recommend the potassium salt form over sodium or mixed salts. It’s a question that circles back to stability, solubility, and in vivo handling. In our production runs and customer reports, potassium salt demonstrably outperforms mixed or sodium versions, reducing serum interference and biological side effects, especially in systemic animal injection. Some animal models show acute ionic changes in sodium-sensitive pathways, impacting animal health or readout reliability. By offering only the high-purity potassium version, we help customers bypass these issues — and they return for more consistent scientific output.

    D-Luciferin also stands apart from other luciferase substrates like coelenterazine or synthetic furimazine. While those substrates power different reporter enzymes, D-Luciferin offers greater light output, lower background, and well-understood pharmacokinetics. For gene expression assays and cell or animal imaging using firefly luciferase, D-Luciferin Potassium Salt stays the standard for signal strength and scientific reliability.

    We steer clear of product lines that blend multiple luciferin analogs under vague labeling. That approach muddies batch documentation, reduces the chance of troubleshooting successful results, and leaves researchers chasing ghosts in their data. By sticking to single-molecule, high-purity production, our manufacturing team ensures scientists can meet publication and regulatory standards, audit chemical history, and replicate results across years or sites.

    A Manufacturer’s View: Trust Earned Through Consistency and Collaboration

    Our experience manufacturing D-Luciferin Potassium Salt runs wide, from scaled-up industrial synthesis to supporting single-bench academic studies. What doesn’t change is our commitment to transparency, reproducibility, and real-world scientific progress. We’ve seen how lapses in quality or inconsistent product histories cost scientists time, resources, and data credibility. Our chemical process, workflow, and commitment to sharing detailed product batch records directly address these risks.

    Keeping up with evolving imaging technology, animal labeling approaches, and quantitative assay formats requires not only adaptation at the process level, but also willingness to engage with technical users daily. Manufacturing D-Luciferin Potassium Salt as a core, documented, and consistent product helps keep the glow of biological discovery bright — from our factory floor through the glass of every research vial.

    In a market full of brokers, re-packagers, and partial producers, a genuine chemical manufacturer offers more than product; we offer partnership, knowledge, and tangible reliability throughout every stage. Our D-Luciferin Potassium Salt is not only a molecule, but a commitment to scientific accuracy, safety, and the advancement of life science research everywhere.