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DL-2,3-Dimercapto-1-Propanesulfonic Acid Sodium Salt Monohydrate

    • Product Name DL-2,3-Dimercapto-1-Propanesulfonic Acid Sodium Salt Monohydrate
    • Alias DMPS
    • Einecs 611-255-5
    • 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
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    Specifications

    HS Code

    816605

    Product Name DL-2,3-Dimercapto-1-Propanesulfonic Acid Sodium Salt Monohydrate
    Cas Number 17766-26-6
    Molecular Formula C3H7NaO4S3·H2O
    Molecular Weight 246.3 g/mol
    Appearance White to off-white powder
    Solubility Soluble in water
    Melting Point Decomposes
    Storage Temperature 2-8°C
    Purity ≥98%
    Ph Value 6.5 - 7.5 (50 mg/mL in water)
    Synonyms DMPS sodium salt monohydrate
    Chemical Structure HSCH2CH(SH)CH2SO3Na·H2O
    Ec Number 241-989-1

    As an accredited DL-2,3-Dimercapto-1-Propanesulfonic Acid Sodium Salt Monohydrate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing White, opaque plastic bottle containing 25 grams of DL-2,3-Dimercapto-1-Propanesulfonic Acid Sodium Salt Monohydrate, with tamper-evident seal.
    Shipping **Shipping Description:** DL-2,3-Dimercapto-1-Propanesulfonic Acid Sodium Salt Monohydrate should be shipped in tightly sealed containers, protected from moisture and light. Transport as a non-hazardous chemical; avoid extreme temperatures. Follow standard chemical shipping regulations, including clear labeling and documentation. Store and handle under cool, dry conditions upon arrival to maintain product stability and quality.
    Storage DL-2,3-Dimercapto-1-Propanesulfonic Acid Sodium Salt Monohydrate should be stored in a tightly sealed container, protected from light and moisture. Keep it in a cool, dry place, ideally at 2–8°C (refrigerated). Ensure good ventilation in the storage area and keep away from incompatible substances such as strong oxidizers. Always follow standard chemical storage safety protocols.
    Application of DL-2,3-Dimercapto-1-Propanesulfonic Acid Sodium Salt Monohydrate

    Applications of DL-2,3-Dimercapto-1-Propanesulfonic Acid Sodium Salt Monohydrate in Industrial Manufacturing

    As the direct and specialized manufacturer, we supply DL-2,3-Dimercapto-1-Propanesulfonic Acid Sodium Salt Monohydrate (DMPS-Na) for well-established downstream industry segments. Our material supports advanced processing requirements, strict regulatory environments, and ensures process consistency for demanding formulations. Below, we outline its principal downstream applications with technical specifics relevant to formulation chemists, process engineers, and QC managers.

    1. Parenteral Chelation Therapeutics Manufacturing

    Pharmaceutical producers incorporate DMPS-Na in the formulation of injectable antidotes for heavy metal poisoning, especially for the chelation of mercury and arsenic. Critical requirements include maintaining stability, minimal excipients, and stringent endotoxin controls during aseptic processing. Dosage in final drug product necessitates precise titration to patient weight and toxic load, determined through validated pharmacopeial methods and clinical guidelines.

    Industry compliance standards

    • USP-NF and European Pharmacopoeia monographs for parenteral active substances
    • ICH Q7 GMP for active pharmaceutical ingredients
    • FDA 21 CFR Part 211 and EMA guidelines for medicinal product manufacture
    • EDQM TSE/BSE-free compliance documentation

    Typical usage ratio

    • Typically 0.2–2.0% w/v in reconstituted infusion or injection solution; exact concentration adjusted for pediatric/adult dosing and heavy metal burden as per physician direction and therapeutics protocol

    Downstream process integration

    • Added as the primary chelating agent during bulk solution preparation, followed by filtration, sterile fill/finish, and thorough in-process release bacterial endotoxin testing

    Final product types

    • Ready-to-use ampoules and vials for hospital and emergency room use
    • Concentrated powder vials for reconstitution by healthcare professionals

    2. Oral Pharmaceutical Chelation Products

    Manufacturers of solid orals deploy DMPS-Na in tablet, capsule, or powder sachet formulations to support outpatient management of heavy metal exposure. The raw material requires blending with stabilizers and palatability agents, while meeting oral-specific residual solvent specifications and bioavailability targets defined through in-vitro dissolution profiles.

    Industry compliance standards

    • USP <795> and <1078> for non-sterile pharmaceutical compounding
    • ICH Q3C for residual solvents and Q6A for specifications
    • Local pharmacopoeia (e.g., JP, BP, IP) monographs based on distribution market
    • WHO GMP for finished dosage forms

    Typical usage ratio

    • Active ranges from 25 mg up to 300 mg per unit dose, composition adjusted based on age group, severity of intoxication, and regulatory prescription limits

    Downstream process integration

    • Blended into excipient matrices during direct compression or granulation, with additional coatings applied as needed for stability and masking taste

    Final product types

    • Oral tablets and capsules for pharmacies and clinics
    • Pediatric powder sachets for manipulation into liquid suspensions

    3. Veterinary Antidote Formulations

    Veterinary pharmaceutical firms source DMPS-Na for incorporation into antidote solutions and drench preparations, addressing intoxication from environmental or accidental heavy metal ingestion in companion and livestock animals. Production must address withdrawal periods, residue testing, and animal-specific pharmacokinetic considerations.

    Industry compliance standards

    • VICH GL40 (Stability testing for veterinary medicinal products)
    • EU Regulation 2019/6 (veterinary medicinal products)
    • FDA CVM Guidance for Industry #61 (Special considerations for animal drug manufacturing)
    • GVP-V (Good Veterinary Practice Manuals)

    Typical usage ratio

    • Generally incorporated at 0.1–0.5% w/v in oral drench or solution format, subject to veterinary toxicology assessment and species-specific dose requirements

    Downstream process integration

    • Dissolved into vehicle bases post-filtration or mixed with flavor-masking agents, then filled into bulk containers or single-use dose bottles under cGMP protocols

    Final product types

    • Oral solutions for cattle, swine, and equine heavy metal exposures
    • Dose-measured bottles for companion animal use (dogs, cats)

    4. Environmental Detoxification and Water Treatment Chemicals

    Specialist companies producing reagents for contaminated wastewater employ DMPS-Na as a heavy metal sequestrant in tertiary treatment modules. The material’s high chelation specificity permits controlled removal of dissolved mercury, cadmium, and arsenic in industrial effluent, validated through accredited environmental monitoring.

    Industry compliance standards

    • EPA Method 1631/EPA SW-846 for mercury in wastewater
    • ISO 14001:2015 (Environmental management systems)
    • REACH Annex XVII restrictions for hazardous substances
    • EN 14886 (water treatment chemical safety)

    Typical usage ratio

    • Usually dosed at 1–20 ppm, actual rate set by influent heavy metal levels and continuous process feedback from inline sensors or lab titration results

    Downstream process integration

    • Injected into holding tanks or pipeline mixers post-primary filtration, with contact time and agitation parameters optimized for quantitative precipitation or chelation prior to dewatering or filtration units

    Final product types

    • Customized liquid formulations for municipal and industrial wastewater plants
    • Pre-packaged reagent sets for on-site effluent testing and remediation operations

    5. In-vitro Diagnostic Reagent Manufacturing

    Diagnostic reagent manufacturers use DMPS-Na as a standard for calibration of chelation capacity or as a stabilizer in assay kits measuring heavy metal concentrations in clinical and environmental samples. Lot to lot traceability, documentation, and negligible assay interference are central to component release for regulated diagnostics.

    Industry compliance standards

    • ISO 13485:2016 for medical device quality management
    • FDA 21 CFR Part 820 for IVD manufacturing controls
    • CLSI EP06 guidelines for linearity and calibration
    • CE-IVD Mark requirements for European market

    Typical usage ratio

    • Employed at 0.05–0.2% w/v or as specified by test protocol, adjusted to kit design and detection sensitivity requirements

    Downstream process integration

    • Formulated into buffer solutions or lyophilized mixtures during bulk batch compounding, then subjected to sterile filtration and vialing or strip-coating

    Final product types

    • Heavy metal test kits for clinical laboratories (urine, blood analysis)
    • Calibration and reference solutions for automated analyzers
    Free Quote

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    Certification & Compliance
    More Introduction

    DL-2,3-Dimercapto-1-Propanesulfonic Acid Sodium Salt Monohydrate: Proven Utility in Chelation Chemistry

    Our Experience with DL-2,3-Dimercapto-1-Propanesulfonic Acid Sodium Salt Monohydrate

    Working hands-on with DL-2,3-Dimercapto-1-Propanesulfonic Acid Sodium Salt Monohydrate for years has made its uncompromising utility clear. As a manufacturer, we see its popularity grow for good reasons. Plants worldwide use it as a well-balanced chelating agent, especially in heavy metal detoxification research, analytical chemistry, and clinical formulations that target metal poisoning. The compound offers strong chelation properties while maintaining robust water solubility, which meets the needs of both established processes and innovative development projects.

    Our process refines the compound to strict standards, keeping water content consistent and ensuring the sodium salt remains stable and free flowing. Withdrawal from the reactor is performed only after spectral purity matches profiles required for therapeutic and analytical use. Over time, we’ve learned where measures count: small fluctuations in moisture content, even within monohydrate ranges, can influence solubility and handling. These details show up clearly during scale-up, especially in climates with fluctuating humidity and temperature. We monitor batches for organoleptic qualities, making sure no sulfuric off-notes affect downstream utility.

    Model and Specifications: Practical Needs Dictate Manufacturing Choices

    For the chelating agent market, our DL-2,3-dimercapto-1-propanesulfonic acid sodium salt monohydrate follows international standards. The chemical model—more commonly known within the lab as DMPS-Na monohydrate—carries the CAS number 177-96-0. Purity regularly hits or exceeds 99%, according to HPLC and titration data from final batch release. Customers appreciate that we focus on forming the monohydrate, not anhydrous or dihydrate versions, since this balance of water content delivers reliable performance in both analysis and formulation. Particle size distribution remains controlled to support benchwork or pilot scale reactions, so clumping and caking don’t delay production or require additional processing.

    In our line operations, the biggest challenge is not chemical purity—it is logistics: keeping powder from drawing extra moisture or oxidizing, which can create an off-color yellow tint. To avoid this, we rely on inert atmosphere packaging and use sealed HDPE containers. This approach prevents the release of free thiol odor and preserves product for long-term storage. From the start, our formula development has addressed customer feedback—such as clumping or drop in activity during hot, humid shipping—to guide packaging updates and storage recommendations.

    Differences from Competing Chelators and Similar Chemicals

    Any seasoned development chemist knows chelators come in many forms: EDTA, DTPA, DMPS, and DMSA all serve similar markets, but with significant differences. Our DMPS sodium salt stands out through its high selectivity for soft heavy metals like mercury and arsenic, compared to legacy chelators which struggle to release these tightly bound toxins. Unlike EDTA, which grabs both essential ions and toxins indiscriminately, DMPS forms very stable complexes only with the most problematic metals—the sulfhydryl groups in its structure play a vital role.

    In direct work, we’ve seen that this selectivity reduces the risk of depleting crucial elements such as calcium, zinc, and magnesium in patients, or interfering with enzyme activity in lab diagnostics. In the clinic, that difference shows up as fewer side effects and less need for mineral supplementation during detox regimens. Other chelators can enhance kidney load, causing renal stress over time. DMPS, due to its higher water solubility (partly from the sulfonic acid sodium salt group), clears from systems efficiently and safely, which is reflected in systematic urine samples drawn during chelation therapy studies.

    From a process chemistry view, the sodium monohydrate version of DMPS dissolves quickly in aqueous media without sticking to glassware or leaving residues, making cleanup routines faster. Analytical labs benefit from predictable extraction efficiency, which lets them avoid inconsistencies and reruns. The absence of residual solvents and stability against hydrolysis yield longer shelf life even under routine storage, something not all analogues like DMSA can claim without additional stabilizers.

    True-to-Application Use Cases: Detoxification to Analytical Chemistry

    Across our own client requests, the largest demand comes from clinical research groups and drug formulation teams easing the burden of heavy metal exposure. DMPS’s proven profile in treating inorganic mercury or arsenic toxicity lines up with historical data from published trials. Its inclusion in oral or parenteral chelation mixes depends on simplicity: the sodium salt monohydrate dissolves readily in saline or buffered systems, minimizing lag in preparation.

    Industrial labs working with metal plating, mining, and battery recycling rely on DMPS to capture free ions in process water, lowering discharge values to meet tightening regulatory targets. In these applications, speed of chelator uptake matters—DMPS’s reactivity ensures minimal residual load, reducing both risk and cost at the effluent discharge point. We’ve provided technical support to many customers in these sectors, sometimes even adapting drying protocols to local water chemistry, to maintain definitive endpoint titration results in process control labs.

    In analytical chemistry, DMPS acts as a very strong masking agent for several transition metals that can interfere in trace analysis. Heavy metal assays that once suffered high blanks or poor selectivity now show improved accuracy with its use. Our product’s narrow particle size and consistent monohydrate ratio make it easy to blend into assay preparations, so the only surprises come from the sample, not the reagent.

    Manufacturing Insights: Keeping Quality Consistent for End Users

    Producing DL-2,3-Dimercapto-1-Propanesulfonic Acid Sodium Salt Monohydrate at commercial scale tests every part of a manufacturer’s process discipline. Handling raw thiol intermediates, for example, presents safety and stability challenges. We use jacketed vessels and nitrogen purges to avoid oxidation—this practice delivers whiter, odor-free product compared with open reactor runs. Monitoring monohydrate water content requires more than simple drying; Karl Fischer titration delivers reassurance that the product’s hydration stays in spec, especially when summer humidity climbs.

    Matching physical characteristics batch after batch builds trust for clients running validations in regulated industries. Process tweaks may look small on paper—minor adjustments to agitation, for instance—but play a massive role in avoiding intermediates that can lead to colored off-spec product later. We actively track complaints and maintain a rolling review of field feedback: tweaking mill settings to prevent dust, adjusting storage recommendations for new climates, and offering direct advice on solvent compatibility. This feedback loop with customers leads to better performance in the final application.

    Our raw material sourcing uses long-standing supplier relationships, checked by regular in-house QC. Skipping middlemen lets us adjust incoming feedstock specifications as upstream conditions change; if supply interruptions strike, we catch them before downstream problems set in. The close connection between lab and plant keeps issues small—the scale-up team sits next to quality assurance, so meaningful changes don’t vanish under bureaucracy. This proximity delivers practical fixes, keeping our DMPS sodium monohydrate consistent for every drum and kilo pack made.

    Product Handling and Storage Based on Real Experience

    Any bulk chemical shows weaknesses if stored poorly; DL-2,3-dimercapto-1-propanesulfonic acid sodium salt monohydrate is sensitive to both moisture and air even within the monohydrate form. Our team found early on that stats about “shelf stability” rarely match reality on busy production floors, where containers face repeated open-closings. Repeated exposure can shift the moisture content, affecting handling and dosage. We advise storing the product in tightly sealed original containers at room temperature, away from direct sunlight, and recommend minimal transfer between storage containers to maintain predictable batch performance.

    In use, the compound’s free-flowing nature supports direct addition to mixers or reactors with minimal dusting. Even so, managers should review handling practices to reduce exposure to the air. Protective equipment, such as gloves and masks, not only follows standard safety policies but also maintains product quality and minimizes health risks. Waste from cleaning or accidental spills requires prompt neutralization and removal; for larger facilities, investing in well-ventilated storage rooms with humidity control lowers the need for reclamation or rework.

    To reduce product degradation through oxidation, we developed protocols that prioritize quick use once the original seal breaks. Whether the setting is a compounding pharmacy or a manufacturing plant, re-sealing procedures cut down on oxidized losses. Some larger clients have introduced argon-purged bins for bulk storage—something that initially seemed overkill, but delivered considerable waste cuts after several months in operation.

    Facing Challenges in the Modern Chemical Market

    Market requirements never stand still. Across the industry, chemical manufacturers face increasing scrutiny about trace contaminants, especially potential impurities from legacy processes or old intermediate suppliers. DMPS’s route includes several sulfur-bearing intermediates, and any contamination or incomplete reaction can introduce unwanted byproducts. Our testing covers residual starting materials, solvent traces, and heavy metals left from the reactor itself. We invested early on in ICP-MS analysis and validated all cleaning cycles. This gives peace of mind to pharmaceutical and analytical clients, who face ever-higher standards from health authorities and environmental bodies.

    Sourcing reliable raw materials represents a frequent challenge for any specialty chemical. Over the years, geopolitical shifts in raw material production zones and freight disruptions have made it vital to maintain healthy supplier relationships and ample inventory. Maintaining flexibility in reagent choices and updating supply chain plans help us ride out short-term disruptions with minimal effect on finished goods. For downstream users, this translates to uninterrupted production schedules and consistent quality. We work with our end users to anticipate swings in demand and to support scale-up or formulation changes well ahead of regulatory deadlines.

    Safety regulations also grow tighter each year. The compound’s handling risk profile pushes manufacturers to keep on top of evolving standards. We regularly retrain line operators and update protocols for material handling and waste—these steps seem minor individually, but over time they keep batch records impeccable and boost operator safety for both us and our partners.

    Continuous Improvement from Field and Lab Perspectives

    Chemical manufacturing sits at the intersection between repetition and constant change. Every manufactured kilogram brings new details, each shaping future protocols or user advice. The field constantly returns lessons on process optimization and troubleshooting—sometimes from seasoned techs in large plants, other times from independent researchers sharing real-world feedback. Tightly controlled monohydrate content turned out to matter more than any flowability spec; specialty filtration supplies solved an unexpected filtration issue in a formulation study. We’ve built a running record of what delivers the best outcomes for everyone along the production, distribution, and research pathway.

    Feedback mechanisms have become central to maintaining DMPS sodium salt monohydrate’s role as a reliable tool for detoxification and analytical needs. A robust technical support system, both in email and direct calls, has minimized downtime for customers hit by unexpected issues—incorrect solution prep, pump fouling, or simple packaging mixups. Frequent short trainings and user guides based on real-world workflows, not just the package insert, close the loop further. The result is a product that works well not just in the controlled setting of a QC lab but also in busy facilities tackling industrial effluents, drug production, and environmental testing.

    Why DL-2,3-Dimercapto-1-Propanesulfonic Acid Sodium Salt Monohydrate Earns Long-Term Trust

    Any specialty chemical must prove itself through reliable field performance, and DMPS sodium salt monohydrate has earned its place through consistent results. Its balance of chemical reactivity, safety, and ease of use spring from careful process design and non-stop attention to shifting customer priorities. Each year, analytical standards grow stricter and application fields more diverse, but the backbone—the quality of the manufactured product—remains fundamental.

    Direct engagement with customers, ongoing investment in state-of-the-art analytical tools, and adaptability in packaging, storage, and documentation ensure delivery of DMPS sodium salt monohydrate that users can trust. The value it brings is built into every drum delivered.