2,2'-Dithiodipyridine

    • Product Name: 2,2'-Dithiodipyridine
    • Chemical Name (IUPAC): 2,2'-Dithiobis(pyridine)
    • CAS No.: 2122-19-2
    • Chemical Formula: C10H8N2S2
    • Form/Physical State: Crystalline Powder
    • Factroy Site: No.968 Jiangshan Rd., Nantong ETDZ, Jiangsu, China
    • Price Inquiry: sales7@bouling-chem.com
    • Manufacturer: Nantong Acetic Acid Chemical Co., Ltd.
    • CONTACT NOW
    Specifications

    HS Code

    821878

    Chemicalname 2,2'-Dithiodipyridine
    Othernames 2,2'-Dipyridyldisulfide
    Casnumber 583-39-1
    Molecularformula C10H8N2S2
    Molecularweight 220.31
    Appearance Yellow crystalline powder
    Meltingpoint 69-72 °C
    Boilingpoint 324.1 °C at 760 mmHg
    Solubility Slightly soluble in water, soluble in organic solvents
    Density 1.31 g/cm³
    Purity Typically ≥98%
    Storagetemperature Store at 2-8 °C
    Flashpoint 145.7 °C
    Ecnumber 209-510-3
    Refractiveindex 1.684

    As an accredited 2,2'-Dithiodipyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 2,2'-Dithiodipyridine is packaged in a 25g amber glass bottle with a red screw cap and detailed hazard labeling.
    Container Loading (20′ FCL) 20′ FCL: 10 MT in 500 kg fiber drums or 8 MT in 25 kg fiber drums, securely packed for export.
    Shipping 2,2'-Dithiodipyridine is shipped as a stable, solid chemical in tightly sealed containers to prevent moisture ingress and contamination. It should be handled according to standard hazardous material protocols, typically packaged with appropriate labeling and cushioning. Shipping may require documentation for hazardous goods, and temperature control is not generally necessary for this compound.
    Storage 2,2'-Dithiodipyridine should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from sources of ignition and incompatible substances such as strong oxidizers. Protect it from moisture and direct sunlight. Store at room temperature and ensure proper labeling. Use in a chemical fume hood to minimize exposure to vapors and dust.
    Shelf Life 2,2'-Dithiodipyridine has a shelf life of several years when stored in a cool, dry place, protected from light.
    Application of 2,2'-Dithiodipyridine

    Purity 99%: 2,2'-Dithiodipyridine with a purity of 99% is used in peptide synthesis, where it ensures high coupling efficiency and minimal side reactions.

    Melting Point 86°C: 2,2'-Dithiodipyridine with a melting point of 86°C is used in redox titrations, where it provides stable assay conditions for accurate endpoint detection.

    Molecular Weight 218.3 g/mol: 2,2'-Dithiodipyridine with a molecular weight of 218.3 g/mol is used in protein thiol quantification assays, where it enables precise molar reactivity calculations.

    Particle Size ≤50 μm: 2,2'-Dithiodipyridine with particle size ≤50 μm is used in homogeneous catalytic processes, where it ensures rapid dissolution and consistent reactivity.

    Storage Stability ≤25°C: 2,2'-Dithiodipyridine with storage stability at temperatures ≤25°C is used in laboratory reagent kits, where it maintains long-term chemical integrity and reactivity.

    UV Absorption 343 nm: 2,2'-Dithiodipyridine characterized by UV absorption at 343 nm is used in spectrophotometric analysis, where it allows sensitive detection of thiol-containing compounds.

    Solubility in Methanol ≥10 mg/mL: 2,2'-Dithiodipyridine with solubility in methanol ≥10 mg/mL is used in organic synthesis protocols, where it enables easy preparation of concentrated stock solutions.

    Free Quote

    Competitive 2,2'-Dithiodipyridine prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please contact us at +8615371019725 or mail to sales7@bouling-chem.com.

    We will respond to you as soon as possible.

    Tel: +8615371019725

    Email: sales7@bouling-chem.com

    Get Free Quote of Nantong Acetic Acid Chemical Co., Ltd.

    Flexible payment, competitive price, premium service - Inquire now!

    Certification & Compliance
    More Introduction

    2,2'-Dithiodipyridine: A Reliable Choice for Thiol Detection and Beyond

    Real progress in chemical research often comes from tools that do their job without causing a fuss. 2,2'-Dithiodipyridine (sometimes called DTDP or dipyridyldisulfide) falls into this category. In laboratories across academia and industry, scientists reach for this compound because it gives crisp, interpretable results. The value of a reagent like 2,2'-Dithiodipyridine isn’t about hype or buzz—it’s about trust built one experiment at a time.

    What Stands Out With 2,2'-Dithiodipyridine?

    The core of 2,2'-Dithiodipyridine’s appeal comes down to its structure: two pyridine rings bridged by a disulfide bond. This setup gives researchers a simple, specific way to interact with free thiol groups in proteins, peptides, and small molecules. If you’ve ever needed to track or quantify mercapto groups, you know how important clear reactivity can be. One of the first things that comes to mind is its ability to participate in disulfide exchange reactions. You add DTDP to a solution with free thiols, and a measurable, yellow chromophore forms. That visual cue isn’t just satisfying, it’s quantifiable—making this compound a mainstay in enzyme characterization, redox biology, and protein chemistry.

    A fact I learned early on doing biochemistry research: not every reagent tells the story of your molecules as cleanly as DTDP does. Many alternatives require complex or time-consuming protocols. With DTDP, the reaction runs at room temperature, in aqueous or mixed solutions, and wraps up quickly. These practical advantages mean more time spent interpreting data, less time troubleshooting.

    Key Specifications and Purity Considerations

    Quality matters in any lab setting. Reproducible results often trace back to thoughtful choices about which supplier or grade to use. For 2,2'-Dithiodipyridine, purity above 98% by HPLC is the standard that most professionals rely on. Lower grades might introduce background signals or unexpected byproducts, especially in sensitive assays. The fine, pale-yellow crystalline form signals good handling; clumping or color variations imply moisture uptake or contamination, and that can throw off your measurements.

    Most suppliers package DTDP in amounts ranging from a few grams to hundreds of grams, making it versatile for both small-scale and industrial applications. The solid dissolves well in water, ethanol, or buffer—so you’re not fighting with solubility at the bench. Detailed batch analysis, such as NMR or melting point checks, help confirm identity and rule out residual pyridine or other organic impurities. I’ve learned not to skip these checks, especially with high-value protein samples in play.

    Real-World Uses: More Than Just a Thiol Reporter

    Chemists and biologists alike use 2,2'-Dithiodipyridine for more than just labeling or quantifying thiols. In biochemistry, it shines in Ellman-type assays, where it helps measure active site cysteines in enzymes. Clinical researchers rely on its selectivity when screening blood samples for reduced or oxidized glutathione—a key marker of oxidative stress.

    In industry, manufacturing quality control often runs up against the need for fast turnaround. DTDP’s high sensitivity plays into real-time monitoring of drug, food, or cosmetic production. Processes that risk oxidation or contamination benefit from on-the-spot verification, and nothing beats a ready signal in the visible range for convenience.

    The pharmaceutical sector also gets good mileage out of DTDP in shelf-life testing, where preservatives or stabilizers can modify thiol content over time. The ability to detect subtle shifts creates space for process optimization and safer, longer-lasting products.

    Avoiding False Positives: Handling and Compatibility

    Anyone who’s spent time with DTDP knows reactivity cuts both ways. The compound’s high sensitivity to thiols can turn up false positives if sample prep isn’t careful. Reducing agents like DTT or β-mercaptoethanol interfere directly, so protocols often omit them or use milder alternatives. Even traces of free cysteine or other small thiol-containing compounds change the readout.

    Lab comfort hinges on stability, and here DTDP delivers. The crystalline solid stores well at room temperature, away from moisture and light. I’ve seen unopened bottles keep performance for over a year, but after opening, airtight sealing and desiccation add peace of mind. This stability isn’t just a convenience—it means less waste and tighter cost control.

    What Sets DTDP Apart From The Crowd?

    As reagents go, DTDP lives in the company of several other disulfide-based chromophores. The classic comparator is Ellman’s reagent (5,5'-dithiobis-(2-nitrobenzoic acid), or DTNB), which also signals thiols through a chromophore shift. DTNB has wider recognition and is milder in terms of background reactivity. DTDP’s edge, in my experience, comes from its higher reactivity toward protein thiols and greater tolerance for low-pH buffers. It also offers sharper, less ambiguous color development—meaning operators spot changes with less ambiguity, even on busy plates.

    Compared to maleimide derivatives, which react irreversibly with thiols to introduce fluorescent tags or crosslinks, DTDP remains a gentler option. The disulfide bond can participate in reversibility, crucial when samples need to stay intact for downstream analysis. DTDP also operates without the cost or complexity of enzyme-coupled detection kits.

    It’s not just about biochemistry. In pure organic synthesis, 2,2'-Dithiodipyridine works to activate carboxyl groups for peptide coupling and to protect thiols during multi-step sequences. Classic protocols lean on DTDP’s predictable, well-characterized mechanism to swap protecting groups without scrambling other sensitive bonds. Any tool that helps streamline synthetic planning and troubleshooting becomes a recurring player in the chemist’s toolkit.

    Safety, Handling, and Sustainability Considerations

    Responsibility in the lab starts with knowing the hazards behind every bottle, no matter how familiar. DTDP has a profile that’s reassuringly modest. At standard concentrations, contact with skin or eyes can still cause irritation, but sensible protective measures—gloves, goggles, and local ventilation—keep risks low. Spills clean up with water and a little patience.

    Environmental considerations get more attention every year. DTDP breaks down in typical chemical waste processing, and under neutral pH, it doesn’t persist in water like heavier metals or halogenated residues. Most protocols keep working solutions in glass or polyethylene, since the compound’s slight reactivity might degrade softer plastics over long periods. Anyone working with students or trainees knows the importance of simplicity and low hazard—DTDP rarely raises red flags, and its disposal pathway isn’t tangled in extra paperwork.

    Optimization Tips From Long-Term Users

    Over the years, a few best practices have surfaced from researchers who spend days, not just hours, with 2,2'-Dithiodipyridine. One, always prep fresh stock solutions. The chromophore can oxidize slowly in air or under strong light, so the practical approach uses just-in-time mixing and shields vials with foil. Two, buffer pH matters. Color development sharpens at neutral to slightly basic pH, though the signal remains usable even as pH drops. Stable, reproducible absorbance means less fuss during method validation and reporting.

    Thorough mixing is another low-tech way to improve results. The DTDP reaction depends on even exposure across the sample, and undissolved particles slow things down. Sonication or gentle vortexing clears things up quickly, which beats troubleshooting sluggish reactions downstream. Once, running a protein quantification series, I cut background variability in half simply by pre-filtering the stock. Small tweaks like this, learned from repeat experience, shape confidence under pressure.

    Quality Data: Relevance in the “Reproducibility Crisis” Era

    Research lives and dies by reproducibility. The pressure to cut corners rarely pays off; anything that adds noise or ambiguity stands out during peer review or regulatory inspection. DTDP earns its place by creating crisp signals with modest sample prep, as long as you respect the limits of interference and stability noted above. This transparency matters more today, not less, as the pressure to publish or deliver new formulations intensifies.

    One factor I’ve seen crop up lately is supply chain reliability. Getting the right product, on time, and with full documentation matters for both grant deadlines and regulatory filings. Reputable suppliers back batches with certificates of analysis, confirm purity using more than just standard melting points, and offer up support for unusual sample types. These safeguards give research teams more confidence to design robust protocols—especially when troubleshooting tough samples or testing new detection hardware.

    Beyond Detection: R&D Innovations Using DTDP

    Recent years have broadened the horizons for 2,2'-Dithiodipyridine. Redox biology—an area exploding with new insights—counts on specific, sensitive thiol detection to map how cells and tissues respond to stress. DTDP’s rapid, measurable response lets teams spot subtle changes that might signal early disease or tissue damage. Personalized medicine and biopharma development both draw on such tools to speed up the path from exploratory research to clinical validation.

    The chemical stability and well-understood interaction with thiols opens the door for DTDP in sensor development. A few years ago, I worked on a project exploring thin-film biosensors. Our group found that immobilizing DTDP on sensor surfaces let us pick out sub-micromolar amounts of cysteine and other amino acids in complex samples. This selectivity set our prototypes apart from more generalized, less specific platforms. The proof of concept owed as much to DTDP’s tradition as to the flashier engineering.

    The Regulatory Angle: Documentation and Compliance

    Quality and traceability work together these days, given increasing regulatory scrutiny in pharmaceuticals, food, and environmental science. With DTDP, most reputable suppliers provide transparency on origin, purity, and contaminants. That information stays useful whether setting up a new validated method or answering questions from a regulatory body. Consistency in documentation turns what seems like paperwork into leverage during unexpected audits or external method reviews.

    In some of my projects, the move to automated, high-throughput instrumentation forced us to examine not just the chemistry, but the paper trail behind every reagent. Lot-to-lot variation—even minor—shows up fast with tight detection windows. With high-quality DTDP, I rarely worry about that noise creeping into my final data. Instead, routine cross-comparisons with other batches or competitors confirm tight performance—building confidence, not just compliance.

    Industry’s Push for Greener and Safer Solutions

    While DTDP already avoids many hazards facing older reagents, industry always asks for more. Green chemistry measures—like low energy use, benign waste, and drop-in compatibility with established workflows—continue to drive adoption. Many companies prefer reagents that align with new ISO or environmental standards. Since DTDP is not a heavy-metal compound and avoids halogenated waste, it earns a nod from many sustainability review panels.

    In the best cases, greener chemistry partners with cost control and reliability. Products that hit both targets stay popular year after year because they respect budgets as much as safety or audit readiness. DTDP’s combined low toxicity, ease of handling, and ready compatibility with water-based systems make it a standout choice for labs keen to keep up with both scientific and corporate responsibility demands.

    Wrapping Up On Making Better Choices

    Every lab veteran collects a mental catalog of tools and reagents, shaped by real successes and failures. 2,2'-Dithiodipyridine sticks in my mind among the “quietly essential” players. It rarely shows up in glossy brochures or splashy news headlines, yet its impact echoes across disciplines—from biochemistry and pharmacology to industrial chemistry and analytical quality control. In those fields, speed, accuracy, and safety matter more than marketing, and here DTDP continues to earn trust.

    Talking to colleagues at conferences or on advisory panels, I hear more stories than sales pitches. Success tracks back to details most people take for granted: unambiguous reactivity, manageable hazard profile, stable shelf life in real-world labs, and results that hold up over years, not just months. If a chemistry tool delivers that, it wins respect, stays stocked, and helps new researchers find their footing.

    Countless experiments, big and small, rely on tools like DTDP. From quantifying thiol groups in complex samples to enabling rigorous process controls, it proves its worth daily. Labs that prize clear data and reproducible outcomes keep it close at hand—building on tradition, but always looking forward.