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1-[2-(Dimethylamino)Ethyl]-1H-Tetrazole-5-Thiol

    • Product Name 1-[2-(Dimethylamino)Ethyl]-1H-Tetrazole-5-Thiol
    • Alias Dazomet
    • Einecs 674-670-8
    • 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
    VTB
    Specifications

    HS Code

    914031

    Chemical Name 1-[2-(Dimethylamino)Ethyl]-1H-Tetrazole-5-Thiol
    Molecular Formula C5H12N4S
    Molecular Weight 160.24 g/mol
    Cas Number 79869-69-3
    Appearance White to off-white solid
    Solubility Soluble in water and polar organic solvents
    Boiling Point Decomposes before boiling
    Functional Groups Tetrazole, thiol, tertiary amine
    Storage Conditions Store in a cool, dry place, tightly closed container
    Synonyms DMTE, 1-(2-Dimethylaminoethyl)-1H-tetrazole-5-thiol
    Pka 7.5 ± 0.5 (for tetrazole ring)
    Hazard Statements May cause skin and eye irritation
    Applications Used as a coupling additive in peptide synthesis

    As an accredited 1-[2-(Dimethylamino)Ethyl]-1H-Tetrazole-5-Thiol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The chemical is supplied in a 25g amber glass bottle with a tamper-evident seal, labeled with product name, structure, and safety information.
    Shipping This chemical, **1-[2-(Dimethylamino)Ethyl]-1H-Tetrazole-5-Thiol**, should be shipped in tightly sealed containers under ambient or refrigerated conditions, depending on storage guidelines. It must be protected from moisture and direct sunlight, labeled as a hazardous material if applicable, and handled according to relevant transport regulations for chemicals.
    Storage **1-[2-(Dimethylamino)ethyl]-1H-tetrazole-5-thiol** should be stored in a tightly sealed container, protected from light, moisture, and sources of ignition. Store in a cool, dry, well-ventilated area, away from incompatible materials such as strong oxidizers and acids. Always label containers clearly and keep them out of reach of unauthorized personnel. Use secondary containment to minimize the risk of spills.
    Application of 1-[2-(Dimethylamino)Ethyl]-1H-Tetrazole-5-Thiol

    Applications of 1-[2-(Dimethylamino)Ethyl]-1H-Tetrazole-5-Thiol in Industrial Manufacturing

    As an original manufacturer, we supply 1-[2-(Dimethylamino)Ethyl]-1H-Tetrazole-5-Thiol for specialized roles in high-value industrial processes. The following sections outline real downstream application scenarios, compliance references, formulation practices, integration process, and typical product outputs.

    1. Energetic Materials – Primary Explosives Synthesis

    Our material functions as a performance modifier in the synthesis of tetrazole-based primary explosives used in detonators and initiator cords. The thiolated tetrazole structure enables the formation of energetic salts with enhanced thermal stability, controlled ignition sensitivity, and tailored decomposition profiles. This material supports the stringent demands for consistent batch control during melt-cast or wet-process routes employed by commercial explosives plants.

    Industry compliance standards

    • UN Recommendations on the Transport of Dangerous Goods, Model Regulations
    • U.S. Bureau of Alcohol, Tobacco, Firearms and Explosives (ATF) Explosives Regulations
    • OSHA 29 CFR 1910.109 for Explosives and Blasting Agents
    • REACH Annex XVII restricts/criteria for energetic materials

    Typical usage ratio

    • Used at 1.5% to 7% by weight in combined primary explosive formulations; dosage varies based on desired detonation pressure, brisance, and thermal stability.

    Downstream process integration

    • Incorporated into wet granulation or solution-phase synthesis immediately prior to crystallization of the explosive salt. Reacted with lead, silver, or copper salts under controlled pH, then filtered, dried, and granulated.

    Final product types

    • Lead tetrazolate initiators
    • Electric detonator charge pellets
    • Pyrotechnic initiator charges
    • Non-electric blasting caps

    2. Specialty Corrosion Inhibitors for Oilfield Formulations

    Used as a key intermediate in oilfield corrosion inhibitor concentrates, this thiolated tetrazole grants robust protection to steel pipelines and equipment exposed to CO2/H2S-rich production fluids. Its strong sulfur coordination forms persistent adsorption films, minimizing both uniform and pitting corrosion rates in critical upstream and midstream installations. Formulators specify exact input levels based on water cut, brine load, hydrogen sulfide presence, and temperature dynamics of each well or gathering system.

    Industry compliance standards

    • API RP 932-B, Corrosion Control in Hydroprocessing Refinery Units
    • NACE Standard TM0177, Laboratory Testing of Metals for Resistance to Sulfide Stress Cracking
    • ASTM D665 for Rust-Preventing Properties
    • OSHA Process Safety Management of Highly Hazardous Chemicals

    Typical usage ratio

    • Injected at levels of 100 - 700 ppm (weight/weight aqueous phase), with monthly adjustment during field trials to match scaling, emulsion tendency, and produced water chemistry.

    Downstream process integration

    • Dosed as a blended concentrate to water injection lines or crude gathering loops; added just upstream of major corrosion-risk zones, or batched for hydrostatic testing.

    Final product types

    • Ready-to-use oilfield corrosion inhibitor blends
    • Pipeline rust prevention fluid
    • Well completion fluid treatment packages
    • Enhanced corrosion protection slugs for pigging operations

    3. Advanced Pharmaceutical Building Block in Heterocyclic Synthesis

    This tetrazole analog acts as a niche intermediate in creating API substructures bearing the tetrazol-5-thiol motif, notably in the development of novel antifungal, antiviral, or anti-inflammatory agents. Pharmaceutical companies opt for this route when seeking lead molecules with improved metabolic stability and unique hydrogen-bonding patterns. Custom synthesis protocols define optimal conditions for protection, condensation, and ring formation steps exploiting the reactivity of the dimethylaminoethyl side chain.

    Industry compliance standards

    • USP–NF Monograph Requirements for starting chemicals
    • ICH Q7A Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients
    • EU GMP Annex 15 Qualification and Validation
    • Local Pharmacopeia recognition if used in registered API synthesis (e.g., ChP, Ph. Eur.)

    Typical usage ratio

    • Included as a reactant at 0.2–0.8 molar equivalents, determined by target substitution pattern and final yield optimization during scale-up.

    Downstream process integration

    • Charged at alkylation, cyclization, or thioether formation steps at the laboratory or pilot-plant scale, typically after initial heteroaromatic core assembly.

    Final product types

    • Tetrazole-based drug intermediates
    • Pharmaceutical research compounds
    • Late-stage API synthons
    • Reference standards for regulatory submissions

    4. Electroplating Additive for Non-Cyanide Silver Deposition Baths

    This raw material serves as a bath brightener and leveling agent in the formulation of non-cyanide silver electroplating electrolytes. It chelates silver ions and moderates metal deposition rates, ensuring uniform grain orientation and minimized porosity in decorative and technical silver layers. Electroplater operations select input concentrations based on bath turnover rate, desired layer thickness, and component geometry, enabling repetitive, defect-minimized operation within regulatory guidelines.

    Industry compliance standards

    • ASTM B700 Standard Specification for Electrodeposited Coatings of Silver
    • RoHS 2011/65/EU Directive compliance (Heavy Metal Restrictions)
    • EN ISO/IEC 17025 for testing laboratories, when verifying finished layer composition
    • National Wastewater Discharge Permits (e.g., EPA Clean Water Act, China GB 21900-2008)

    Typical usage ratio

    • Employed at 0.05 – 0.40 g/L in silver bath concentrates. Precise input must be validated by Hull cell testing and surface analysis for each plating scenario.

    Downstream process integration

    • Added to make-up or makeup-plus-maintenance dose for the working bath; introduced during electrolyte preparation after pH and temperature stabilization.

    Final product types

    • Decorative silver-plated jewelry
    • Electronic contact surfaces for connectors
    • Silver-plated cutlery and tableware
    • Precision optical reflectors
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    Certification & Compliance
    More Introduction

    1-[2-(Dimethylamino)Ethyl]-1H-Tetrazole-5-Thiol: Manufacturing Insight

    About the Molecule

    In the day-to-day work at our chemical plant, 1-[2-(Dimethylamino)Ethyl]-1H-Tetrazole-5-Thiol stands out as a specialty intermediate that finds increasing demand in both research and industry. With a molecular formula of C5H11N5S and a molar mass around 173.24, the compound sits comfortably in the class of tetrazole-based heterocycles. In our facilities, we synthesize this compound with a focus on reproducibility, yield, and minimization of impurities. As the chemists on the ground, we know that stability, purity, and handling ease make a real difference in the lab or workshop—outcomes we address every batch.

    Molecular Features That Matter

    The structure combines a tetrazole ring—highly valued for its nitrogen-rich, stable framework—with a thiol at the 5-position and a 2-(dimethylamino)ethyl side chain at the 1-position. The thiol group imparts significant nucleophilic reactivity for further modification, while the dimethylaminoethyl fragment provides solubility and increases versatility in downstream reactions. Over time, we have seen direct benefits from these features. For example, the thiol enables robust conjugation in bioconjugation and material functionalization steps, and the basic dimethylamino group gives the molecule a handle for salt formation and enhanced water solubility, critical for ease of processing in modern laboratories.

    Batch Consistency and Real-World Handling

    From a manufacturing lens, shelf stability and consistent purity influence how well a chemical fits into scaled operations. We have invested in batch control, tracking, and in-line monitoring so each run of 1-[2-(Dimethylamino)Ethyl]-1H-Tetrazole-5-Thiol minimizes side products. Challenges show up often: moisture sensitivity from the thiol moiety and color changes if the material picks up trace oxidants. We focus on glass-lined reactors and nitrogen atmosphere handling, and standardize vacuum drying to keep levels of oxidized sulfur species low. This isn’t abstract quality management—it’s born of real missteps, where a few ppm of oxidized impurity gave customers headaches in downstream synthesis. Such hands-on learning keeps our production refined and our approach practical.

    Purity and Specifications

    Typical production outputs hover above 98% HPLC purity, as assessed on-site within hours of isolation. Thin-layer and NMR checks catch process drift fast. Our plant separates colorless to pale yellow solid, a telltale sign of minimal sulfur-containing impurities and consistent crystallization. We know from recurring analytical work that trace amines, oxidized thiols, or ring-opened species can impact final product performance. Through repeated runs—tweaking base equivalents, refining solvent swaps, making changes to quench conditions—we settle on an optimized method: start with slightly excess aminating agent and control pH immediately post-reaction. It’s the details that protect yield and quality.

    User Applications: From the Synthetic Lab to Scale-Up

    We see the demand for this compound stretch across custom synthesis teams, bioconjugate chemists, and emerging materials researchers. Tetrazoles like this one have seen uptake for building block use in pharmaceutical synthesis, click chemistry, linker chemistry, and sulfur-rich intermediates for agrochemical work. In our practical experience, the presence of both the basic amine and the thiol in one molecule cuts out extra protection group steps—a small but tangible reduction in waste and time. Research partners mention this repeatedly: a single compound able to react as both nucleophile and weak base in a series of steps means fewer multitask reagents cluttering up the bench.

    Material scientists also value specialized molecules like this for post-polymerization functionalization. We have watched this product join the catalog of bioconjugators, as the tetrazole ring can achieve robust ‘click’ reactions with alkynes or azides, while the thiol provides classic S-alkylations. Every time a researcher writes back about a complex multi-label conjugate achieved through our product, it underscores why raw purity and regularity of output matter in our line of work.

    Comparison to Related Tetrazole and Thiol Analogs

    Working on the manufacturing side, real differences set this compound apart from similar intermediates. The most basic tetrazole-5-thiol lacks the attached 2-(dimethylamino)ethyl group. That difference isn’t just academic; without this side chain, you don't get the same solubility in polar solvents or the same ease of subsequent amine-coupling reactions. Multiple labs requesting closely related analogs often run into solubility or reactivity headaches precisely at this point. The dimethylamino aromatic analogs, meanwhile, show higher melting points and reduced thiol activity—making them clunky for some conjugation steps or polymer modifications.

    By making and using both, we see firsthand: 1-[2-(Dimethylamino)Ethyl]-1H-Tetrazole-5-Thiol often allows for salt formation with inorganic acids, leading to better-defined handling and storage. Free base versions of parent compounds tend to be more odorous and oxidize more readily—issues we’ve corrected primarily by choosing this dialkylamino ethyl substitution pattern.

    Operational Benefits and Practical Shortcomings

    No product is free from quirks. The thiol group picks up oxygen unless stored tightly; we rotate batches and test for peroxide formation regularly. The amine, for all its benefits, can absorb water and CO2 out of air, leading to small but measurable product drift over storage time. In practice, these aren’t purely theoretical vulnerabilities. They guide our packing: vacuum-sealed, moisture-barrier liners, smaller packaging sizes for research use, and stabilization additives for customer requests.

    We see one other notable feature: odor, typical of low molecular weight thiols, stays faint if purity is managed stringently. This matters—overlooked odors show up in poorly purified analogs, quickly souring user experience even before real analysis begins. Our people pay attention to this, knowing the end-user (and sometimes their safety review board) will too.

    Production Volume and Environmental Factors

    1-[2-(Dimethylamino)Ethyl]-1H-Tetrazole-5-Thiol mainly moves in kilogram quantities, with clear peaks for project-driven research lots. Bulk production brings its own pressures: heat control during ring closure, sufficient inerting to avoid darkening or off-spec runs, and waste minimization. We treat our aqueous waste for sulfur and nitrogen load—and use preferred, low-toxicity solvents. This comes from years of cleaning up after past standard reagents, where small mistakes created much bigger headaches with persistent halogenated waste or acrid byproducts.

    We pay particular attention to energy efficiency in drying and solvent recovery. On-the-ground, reducing batch times and solvent volume equals less cost for us, and less environmental impact—all while keeping analytical results within specification. This is not corporate platitude; it's lived experience. Operators see the value directly, from reduced fume exhaust to less noncompliant waste.

    Traceability and Analytical Confidence

    Each batch receives a unique lot code and is tracked from synthesis through to packaging. Quality control laboratories scrutinize final product against historic analytical data, stored in a robust digital database. Regular reference runs calibrate our systems. Every time we spot-day a sample with NMR, HPLC, and mass spec, we are verifying our own track record, not just following a checklist.

    Suppliers often talk about traceability; we live it. We keep archived retention samples for every batch two years past delivery. We’re constantly updating analytical methods to account for new insights in degradation pathways or side product formation, driven by actual customer sample feedback—not just regulatory requirements.

    Supporting Research and Collaborative Adaptation

    Research partners have brought challenging requests, like chromatography-free isolation or low-odor requirements. These push us to adapt process parameters and think about scalable solutions using less hazardous reagents or milder conditions. Hours spent troubleshooting a single step with a collaborating group have helped us revise our amination approach, reducing exotherms and improving selectivity.

    Practical issues matter: the size of packaging, the material in seals, and the method for tracking shelf life all feed back into our manufacturing routine. Customers often need documentation about origin, control, and purity that is not just a paperwork exercise. We anticipate regulatory changes on new uses for tetrazoles in fields from energetic materials to diagnostics, remaining prepared to update safety, shipping, and technical data as those shifts occur.

    Reliability Through Real-World Experience

    On the production floor, trust builds by delivering the same output time after time and solving problems as they appear, not just quoting data sheets. Colleagues have handled last-minute orders, retested off-hours samples, and reorganized packaging lines because the real-world consequences of shipment delays or out-of-spec batches go beyond cost—they affect partnership and trust.

    Feedback loops from research customers and synthesis teams shape our ongoing development. Whether a batch review uncovers a stability problem or a downstream application points to a side reaction, we keep notes, modify practice, and share updates with our clients. This ensures our 1-[2-(Dimethylamino)Ethyl]-1H-Tetrazole-5-Thiol is not just chemically within specification, but reliable in the hands of actual users.

    Solutions and Forward Steps

    As product use cases grow, we see fresh challenges. Analytical techniques improve, and minor impurities visible only to the most sensitive detectors now drive refinement projects in our labs. We update our internal reference standards and tweak small details—sample grinding, solvent drying, extra filtration steps—to stay ahead.

    Shipping stability remains an area of focus, as international delivery times extend. We work regularly with logistics teams to adjust label content and temperature-control measures to best protect the product until it reaches each researcher’s bench. Shelf-life testing in accelerated conditions helps us give customers up-to-date guidance, grounded in real observation rather than wishful thinking.

    What Sets Our Material Apart

    Years of developing and manufacturing 1-[2-(Dimethylamino)Ethyl]-1H-Tetrazole-5-Thiol have taught us that the details matter most. A clear synthesis path, careful functional group balancing, attention to solvent choices, and strict process controls all produce a reliable specialty intermediate. The value lies in predictable, high-quality material—always ready, always known. Feedback from actual users still shapes improvements, and even small advances—more convenient packaging, improved documentation, faster turnaround—arise directly from recognizing what our peers in research and industry deal with every day.

    All these details form the backbone of our approach: bridge the gap between robust, scalable manufacturing and highly sensitive end use. With real experience behind every batch, we remain committed to providing a product that chemists, engineers, and collaborative partners can rely on, not just to meet their present needs, but to expand what’s possible for tomorrow’s science.