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L-Dithiothreitol

    • Product Name L-Dithiothreitol
    • Alias DTT
    • Einecs 222-468-7
    • 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

    831971

    Product Name L-Dithiothreitol
    Chemical Formula C4H10O2S2
    Molecular Weight 154.25 g/mol
    Cas Number 3483-12-3
    Appearance White to off-white crystalline powder
    Melting Point 42-44 °C
    Solubility Soluble in water and alcohol
    Storage Temperature 2-8 °C
    Purity Typically ≥99%
    Synonyms Cleland's reagent, DTT
    Pka1 9.2
    Pka2 10.1

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

    Packing & Storage
    Packing The L-Dithiothreitol packaging features a sealed amber glass bottle, labeled with hazard warnings, containing 5 grams of the white crystalline powder.
    Shipping L-Dithiothreitol is shipped in tightly sealed containers, protected from light and moisture. It is typically transported at ambient or cool temperatures, depending on stability requirements. Appropriate hazard labeling and documentation are included to ensure safe handling. Shipping complies with relevant regulations for chemical and laboratory reagent transport.
    Storage L-Dithiothreitol (DTT) should be stored tightly sealed in a cool, dry place, away from light and moisture. Ideally, it is kept at 2–8°C (refrigerated) and protected from air to prevent oxidation. Solutions should be freshly prepared or stored at -20°C in aliquots to avoid repeated freeze-thaw cycles, as DTT is sensitive to air and degrades over time.
    Application of L-Dithiothreitol

    Applications of L-Dithiothreitol in Industrial Manufacturing

    L-Dithiothreitol serves as a highly effective reducing agent in several specialized industrial applications where precise control over redox status is required. The following sections outline genuine downstream scenarios where L-Dithiothreitol is incorporated by manufacturers, focusing on distinct processing environments and regulatory needs.

    1. Biopharmaceutical Protein Refolding

    Biotech producers incorporate L-Dithiothreitol to maintain cysteine residues in a reduced state during recombinant protein refolding and purification, ensuring high structural fidelity and bioactivity. Redox adjustment with this material is critical when upstream fermentation or cell expression conditions risk incorrect disulfide bond formation, which could compromise downstream therapeutic function. Quality-driven manufacturing environments select this material for integration at steps requiring fine-tuned reduction before downstream chromatography or final fill.

    Industry compliance standards

    • USP General Chapter <1066> Biological Reactivity Tests
    • European Pharmacopoeia Monographs for Parenteral Preparations
    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • FDA cGMP (21 CFR Parts 210/211) for Biologics Manufacturing

    Typical usage ratio

    • 0.1 mM – 10 mM; adjusted based on protein concentration and desired folding kinetics; reduction conditions validated by in-process sample testing

    Downstream process integration

    • Added during refolding buffer preparation, immediately after protein harvest; also applied in buffer exchange prior to affinity or SEC purification steps

    Final product types

    • Therapeutic monoclonal antibodies
    • Recombinant enzymes
    • Structural protein pharmaceuticals

    2. In Vitro Diagnostic Reagent Manufacturing

    Diagnostic companies use L-Dithiothreitol in formulations for sample preparation devices and enzymatic reagent kits. The reducing agent is crucial when producing hemoglobin-processing assays or nucleic acid prep reagents, as it preserves target molecule integrity and prevents unwanted oxidation during reagent storage and clinical sample analysis. Manufacturers formulate it at precise concentrations compatible with assay window requirements, consistently validated via both process and stability studies before commercial release.

    Industry compliance standards

    • ISO 13485:2016 for Medical Device and IVD Quality Systems
    • IVDR (EU 2017/746) for In Vitro Diagnostics Regulation
    • CLSI GP44-A4 Sample Handling Guidelines
    • FDA 21 CFR Part 820—Quality System Regulation

    Typical usage ratio

    • 1 mM – 100 mM, concentration tailored to specific reagent activity and shelf-life study results for assay kit components

    Downstream process integration

    • Blended into master batch buffer solutions prior to aliquoting or lyophilization; sometimes applied directly to swab tubes or sample buffer vials during kit assembly

    Final product types

    • Blood cell lysis buffers for hemoglobin analysis
    • RNA/DNA extraction reagents
    • Clinical chemistry analyzer kits
    • Point-of-care diagnostic devices

    3. Molecular Biology Enzyme Manufacturing

    Enzyme suppliers deploy L-Dithiothreitol in production and stabilization protocols for DNA- and RNA-processing polymerases as well as restriction enzymes. The material prevents oxidation-induced loss of enzymatic activity during both purification and formulation. It is incorporated at precise points in downstream filling and lyophilization to guarantee lot-to-lot reproducibility demanded by research and diagnostic customers globally.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems
    • REACH Regulation (EC) No 1907/2006
    • Technical requirements per Clinical Laboratory Improvement Amendments (CLIA)
    • OECD Principles of Good Laboratory Practice (GLP)

    Typical usage ratio

    • ~1 mM – 50 mM, defined by each enzyme’s structure and redox sensitivity, with levels locked after activity and stability profiling

    Downstream process integration

    • Introduced immediately after final purification (SEC/ion exchange), directly into enzyme glycerol buffer prior to filter-sterile dispensing and packaging

    Final product types

    • Taq polymerase master mixes
    • Reverse transcriptase preparations
    • Restriction enzyme bulk and custom aliquots
    • Ligation enzyme reagent sets

    4. Agricultural Biotechnology Tissue Culture Media Preparation

    Plant biotech operations integrate L-Dithiothreitol in tissue culture protocols, specifically for protoplast isolation and regeneration. The material maintains cellular thiols during enzymatic digestion of cell walls, improving cell viability and transformation rates. Reproducible formulation and tight analytical control of reducing conditions are required for batch success and downstream application in trait development pipelines.

    Industry compliance standards

    • OECD Consensus Documents for Transgenic Plant Applications
    • FAO/WHO Codex Alimentarius Guidelines on Safety Assessment of Foods Derived from Biotechnology
    • ISO 9001:2015 for Laboratory Quality Management
    • Local GM crop approval regulations (for downstream use)

    Typical usage ratio

    • 0.25 mM – 2 mM, adjusted per crop species, protoplast yield goals, and viability QC checks

    Downstream process integration

    • Added to enzyme digestion buffers used for the initial release of plant protoplasts; present in subsequent wash and regeneration media

    Final product types

    • Regenerated plant tissue for transformation
    • Transgenic plantlet stocks
    • Elite trait donor cell lines for seed or vegetative propagation

    5. API Synthesis—Peptide Production

    In commercial peptide synthesis, process chemists employ L-Dithiothreitol at cleavage and deprotection stages to ensure correct reduction of disulfide bonds and side-chain functional groups, particularly for peptides containing multiple cysteine residues. Controlled dosing prevents over-reduction and byproduct formation, which is essential for regulatory conformance and reproducible API release specifications in regulated environments.

    Industry compliance standards

    • ICH Q7 GMP Guidance for APIs
    • European Pharmacopoeia General Purity Tests
    • US FDA QSR and DMF (Drug Master File) requirements
    • Ph. Eur. 2.2.28—Peptide Mapping Analytical Criteria

    Typical usage ratio

    • 5 mM – 100 mM, optimized for specific peptide sequence and resin loading, with process control based on reduction progress and purity endpoint analysis

    Downstream process integration

    • Incorporated during post-synthesis cleavage from resin beads, often included in subsequent HPLC mobile phases prior to crude peptide purification

    Final product types

    • Therapeutic peptide APIs
    • Peptide reference standards and analytical controls
    • Custom peptide fragments for immunodiagnostics
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    Competitive L-Dithiothreitol prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    L-Dithiothreitol: Reliable Reductant from a Manufacturer’s Workbench

    Our View on L-Dithiothreitol in the Lab and Factory

    L-Dithiothreitol, familiar to many as DTT, earns a solid reputation on the bench for reducing disulfide bonds without fuss or drama. As a chemical manufacturer who spends plenty of time on both the production line and quality control bench, I have seen L-Dithiothreitol serve as a staple in research and industrial applications for decades. When we produce DTT, we prioritize crystalline purity, tight moisture control, and real consistency—every batch meets the demands of scientists in genomics, proteomics, and pharmaceutical development. We work with the most scrutinizing labs and production partners, so every gram carries the effort of careful monitoring, not to mention regular feedback from partners who actually use it, not just stock it.

    What Sets Our L-Dithiothreitol Apart

    As a team dedicated to hands-on manufacturing, we appreciate the subtleties that matter—moisture can ruin a batch, trace metal impurities can skew experimental data, and crystalline form affects shelf life as well as ease of measurement. We send out crystalline L-Dithiothreitol with a purity of not less than 99%, moisture less than 0.5%, and residual metals well below 10 ppm. This commitment follows from hard-won lessons: a batch of DTT that oxidizes too fast sabotages protein chemistry, while contaminated lots just lead to wasted effort. Our plant stays vigilant, using inert atmosphere packaging and sealed, moisture-proof containers. Staff test every lot on freshly prepared solutions to make sure there’s no lag or unexpected behavior—no scientist likes to see a weak or slow reagent on the morning of an important protein extraction.

    Lab techs work best when they can trust reagents. As manufacturers, we pay attention to details far beyond the final test certificate—we know that product ascorbic acid, mercaptoethanol, or TCEP have their place, but nothing swaps in quite the same way as DTT. Customers tell us so when a project requires reliable thiol presence with little background interference. That means DTT must stay white, not yellow out, not clump under humidity, and most importantly, dissolve cleanly in buffers, even at low temperatures.

    Why Is DTT Still a Core Reducing Agent?

    Ask any protein chemist or molecular biologist to describe an ideal reductant, and you’ll hear three answers: strong, reliable, leaves no mess. DTT meets those standards nearly every time. The pair of sulfhydryl groups in the molecule forms a stable six-membered ring upon oxidation, making this compound stubbornly good at resisting air re-oxidation and maintaining reduced protein environments. As a manufacturer, we see demand for DTT stay steady among users handling protein folding, RNA stabilization, and reduction of antibody disulfides. In industrial settings, our DTT enables cleaner processing of enzymes and active pharmaceutical intermediates where unwanted oxidized byproducts ruin process yields.

    During the past five years, DTT never really slipped in terms of demand, even as TCEP or β-mercaptoethanol gain ground in certain workflows. End-users in biotechnology and pharma say "don’t fix what isn’t broken"—as long as the DTT performs as expected, there’s little urge to change. We listen closely to those who use large-scale fermenters, protein isolations, or diagnostic kit preparation lines. Feedback shows that stability on the shelf, quick dissolution, and low odor give our DTT the edge against substitutions that may bring other side-effects or loss of activity.

    Specifications and Batch Consistency

    Throughout our facility, purity control really happens long before packaging. Fresh thiol content, minimal optical impurities, and controlled crystal growth all start with careful sourcing of starting materials—nothing undermines quality quicker than inconsistent raw threo chemistry. Batches must always show the correct melting point and low moisture before we move forward with QA checks. We run batch chromatograms, titrimetric thiol tests, spectroscopic verification, and controlled forced-oxidation studies to simulate real working conditions.

    A chemical supplier who simply "relies on trusted partners" for raw DTT stock often ends up with mixed lots and unpredictable reduction power. We never allow that risk into our supply stream, because we know that contamination with iron, copper, or sulfate affects how DTT works with sensitive enzyme preps and antibody purification. Researchers have reported how some "high-purity" DTT from unrelated sources sometimes leaves colored residues, untimely precipitates, or even accelerated protein degradation—the last thing anyone wants after months spent on expression constructs. Our DTT stays true to specification even after months in storage, thanks to disciplined handling, dry-room filling, and resealable inner liners built to keep oxygen and water at bay.

    Packaging Choices Matter for Longevity

    From our experience, different users look for different packaging. Bulk buyers need drum lots, but research labs want small, sealed vials. Over the years, we learned that DTT holds up better in narrow mouth glass, with a tough desiccant pouch. Some labs tried switching to plastic or polyethylene bags for convenience but quickly reverted after seeing product degradation or caking. Those calls from annoyed postdocs taught us to stick with moisture barrier systems. Our packaging lines now always deliver DTT in amber glass with nitrogen purges and clear tamper-evidence bands, based on years of hands-on end-user requests, not just regulatory suggestions.

    Costs always draw attention, especially from industrial accounts, but we never cut corners on container sealing or inner lining. Shelf life extends beyond two years under proper conditions, something we back up with stability studies run side-by-side with storage under normal and stressed environments. Though some dealers try to push alternative pack sizes or non-standard closures, our partners appreciate the reliability and predictability that comes from proven packaging protocols. Every year, we review all feedback and failure cases, iterating the packaging based on direct, real-world use cases.

    Comparison with Other Reducing Agents

    Several options compete with DTT in reducing disulfide bonds. β-Mercaptoethanol works for large-scale solutions, but its overpowering smell and lower stability push many away, especially in shared academic spaces or GMP-regulated pilot plants. TCEP offers odorless reduction and has the advantage of working at low pH. Our in-house tests, and those reported in mainstream journals, show that TCEP sometimes brings unwanted side reactions, particularly when reducing specific proteins or interacting with reactive buffers.

    DTT presses its advantage in terms of selectivity, low toxicity (at practical handling levels), and efficient ring-closure upon oxidation. Unlike dithioerythritol, which often crystallizes with significant moisture and handles less predictably in the milligram scale, DTT offers reliable dosing and stays stable when handled with reasonable care. A handful of newer proprietary reducing chemistries exist, but most carry high costs or require special waste handling protocols, eroding any supposed improvement in pure effectiveness.

    Lab techs often tell us they returned to our L-Dithiothreitol after trying alternatives which seemed promising in promotional flyers but didn’t cut it in day-to-day work. Unpredictable rates of reduction, poor handling properties, and complications in enzymatic assays crop up with these newcomers. We often help troubleshoot protein recovery and provide direct recommendations, and DTT continues to deliver under the widest range of applications. For those running long, complex purification chains, predictable reduction time and stable product mean fewer surprises and less troubleshooting.

    Who Actually Uses L-Dithiothreitol—and How?

    Out in the field, our L-Dithiothreitol shows up in hundreds of labs and production lines. Molecular biologists use it to maintain RNA and DNA integrity during isolation and purification—keeping nucleases at bay, for example. Protein biochemists rely on it to hold disulfide bonds in the reduced state, crucial for enzyme assays or the preparation of functional antibodies. Industrial users often employ DTT during fermentation optimization, helping maintain enzyme activity where oxidative stress can lead to degradation.

    We routinely hear stories from pharma customers manufacturing therapeutic antibodies or biosimilars. They depend on premium-grade DTT when reducing disulfide linkages prior to downstream processing steps or when running analytical checks for product consistency. Diagnostics kit manufacturers blend DTT into lysis buffers to disrupt sample proteins, enabling more efficient extraction of target analytes.

    Academic groups often buy smaller lots, sometimes rotating out several containers in a matter of weeks for coursework or focused research. Scale-up facilities and GMP suites lean heavily on larger batches or custom pack sizes—these users value lot tracking, certificate-backed purity, and guaranteed traceability from source to shelf. We maintain ongoing records and split-sample reserves, a practice born out of many years handling regulatory audits and troubleshooting unique customer requests.

    Risks and How We Address Them

    No reductant stays useful in the face of careless handling. DTT, exposed to air and moisture, oxidizes until it can no longer perform. In our facility and during shipping, we minimize these risks by requiring sealed packaging lines, dedicated cold-room storage, and annual retraining of all logistics teams. Any split or cracked container triggers a hold notice and is replaced, not re-used—wasted product is less costly than lost scientific or industrial output.

    We have faced cases where unexpected environmental swings—heat spells, humidity spikes during transit—threatened product consistency. To counter this, we strengthened shipping protection, built-in multiple humidity sensors in batch storage, and created checklists for distributors, with reminders about refrigeration and resealing. These might seem like details only a manufacturer obsesses over, but end-users have thanked us privately for reduced spoilage rates and fewer troubleshooting headaches.

    Real-World Feedback Drives Refinement

    Nothing influences our process development and batch improvements more than direct feedback from users. Some years ago, a large-scale protein purification plant saw inconsistent reduction rates that we traced back to minor excipient changes from an upstream partner—fixing that problem forced a rethink on qualifying suppliers and led to stricter in-process monitoring. One biotech group struggled with batch-to-batch color differences, so we overhauled our storage protocols, investing in upgraded cold rooms with active moisture extraction.

    Every serious manufacturing group understands that even the best certified chemical means little if not accompanied by traceable provenance and rapid customer support. We invite regular audits, share detailed batch records, and open our doors for site visits. Users frequently ask about batch-specific lot numbers or wish to replicate our in-house testing methods; we provide those resources willingly because real transparency builds trust. The move to more robust digital batch tracking came directly from partners in the pharmaceutical industry, who needed seamless data trails for regulatory filings and internal reviews.

    L-Dithiothreitol in New Biotech Workflows

    As high-throughput genomics, synthetic biology, and precision fermentation spread, DTT increasingly finds use beyond traditional protein or nucleic acid work. Researchers employ our DTT during CRISPR/cas preparation steps, for preserving single-cell extracts, and preparing viral vectors. Kit manufacturers designing rapid diagnostic cassettes demand sub-gram DTT lots with absolute photostability and no impure odor—a trend we saw coming by monitoring shifts in end-user protocols, not just market reports.

    In the world of bioinformatics-linked biochemistry, where throughput sometimes eclipses finesse, DTT can mean the difference between a week’s worth of data or a wasted run. Our technical support and R&D partners often request special lots for new platform launches or pilot batches for device qualification. Each new use case pushes us to develop even tighter controls, faster feedback, and more transparent documentation.

    Sustainability and Responsible Chemistry

    Chemical manufacturing does not escape scrutiny on environmental impact, and L-Dithiothreitol handling presents its own challenges. We implemented solvent recovery at every synthesis stage, reduced purge gas volumes, and improved wastewater treatment to cut total organosulfur emissions well below regulatory thresholds. Our solid waste from DTT production undergoes onsite neutralization before removal, with annual independent audits of each environmental safeguard.

    As new regulations emerge on organic chemical handling worldwide, we collaborate with regulatory experts and client compliance teams to keep our DTT aboveboard from lab to large-scale suite. We design our continuous process improvements to lower resource usage per kilo produced, documenting every reduction and change so that clients—especially those supplying medical and diagnostic markets—can verify the chain of custody and compliance history.

    Direct Experience Shapes Real-World Chemistry

    Years spent making DTT led to a philosophy of accountability over convenience. From the earliest pilot runs, we watched how even a degree’s difference in storage, or a barely visible color shift, could shape lab outcomes. This culture of vigilance carries over into everything from material receipt checks, filtration upgrades, and on-the-floor troubleshooting. Junior technicians train alongside experienced supervisors, learning how minor process variations or packaging flaws multiply downstream.

    We do this work not from obligation, but because it pays off in relationships with users who rely on DTT to move science, medicine, and industry forward. Our loyalty is to the people who actually measure, mix, and apply the chemical—not traders, not catalog compilers, but the hands and minds conducting essential experiments.

    Summary: An Ongoing Partnership with the Real World

    L-Dithiothreitol remains a central tool for reduction chemistry in molecular biology, biochemistry, and pharmaceutical science. The past two decades bore witness to evolving techniques, but reliable, clean DTT is still in demand because of the way it works, how it keeps proteins and nucleic acids stable, and the confidence it provides when results truly matter. As manufacturers, our attention centers on real-world outcomes—not just the certified analysis. Each container reflects the accumulated feedback, adjustments, and support from many sectors. Direct contact with diverse user groups—academic labs, commercial biotech, scale-up manufacturing—continually drives the refinement of our product. The tradition of hands-on quality shapes every batch, and by staying accountable, we ensure our DTT meets the benchmarks today’s scientists expect.