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2-(Dimethylamino)Thioacetamide Hydrochloride

    • Product Name 2-(Dimethylamino)Thioacetamide Hydrochloride
    • Alias DMTA hydrochloride
    • Einecs 228-304-7
    • 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

    926221

    Product Name 2-(Dimethylamino)Thioacetamide Hydrochloride
    Cas Number 1758-73-2
    Molecular Formula C4H11ClN2S
    Molecular Weight 154.66 g/mol
    Appearance White to off-white crystalline powder
    Melting Point 164-168°C
    Solubility Soluble in water
    Storage Conditions Store at 2-8°C, tightly closed
    Synonyms N,N-Dimethylthioacetamide hydrochloride
    Purity Typically ≥98%
    Chemical Structure CH3SC(N(CH3)2)H•HCl
    Hazard Class Irritant
    Inchi Key GQJQWYQZGSXRGN-UHFFFAOYSA-N
    Ec Number 217-157-5
    Canonical Smiles CN(C)C(=S)C.Cl

    As an accredited 2-(Dimethylamino)Thioacetamide Hydrochloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The packaging is a sealed 25-gram amber glass bottle, labeled with chemical name, hazard symbols, batch number, and handling instructions.
    Shipping 2-(Dimethylamino)Thioacetamide Hydrochloride is shipped in tightly sealed containers to prevent moisture ingress and degradation. It is typically dispatched as a solid under ambient temperature with appropriate hazard labeling. Packaging complies with local and international regulations for chemical substances, ensuring safety during transit and storage. Handle with care and avoid direct contact.
    Storage Store 2-(Dimethylamino)thioacetamide hydrochloride in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of moisture and incompatible substances such as strong oxidizers or acids. Protect from light and heat. Ensure proper labeling, restrict access to trained personnel, and follow all safety protocols for handling hazardous chemicals.
    Application of 2-(Dimethylamino)Thioacetamide Hydrochloride

    Applications of 2-(Dimethylamino)Thioacetamide Hydrochloride in Industrial Manufacturing

    As a direct manufacturer of 2-(Dimethylamino)Thioacetamide Hydrochloride, we serve process industries in need of precise intermediate functionality, advanced catalysis, and reliable specialty synthesis pathways. Below, we outline verified industrial-scale downstream sectors, with technical details on compliance, dosing, integration points, and applicable end products.

    1. Active Pharmaceutical Ingredient (API) Synthesis

    Our 2-(Dimethylamino)Thioacetamide Hydrochloride plays a key role as a sulfur-donating intermediate in multi-step synthesis for several heterocyclic drug candidates. Pharmaceutical firms use it for constructing thiazole and thiadiazole rings under mild conditions, where reliable salt formation and minimal byproduct formation are essential. Clean supply and strict lot traceability facilitate compliance with regulated market authorizations.

    Industry compliance standards

    • ICH Q7 (GMP for active pharmaceutical ingredients)
    • USP and EP monograph compliance for intermediates (if applicable)
    • FDA 21 CFR Part 211 (Finished pharmaceuticals GMP)
    • REACH Annex VII for intermediate status

    Typical usage ratio

    • Batch charge typically at 0.8–1.2 molar equivalents versus the aldehyde or isocyanate reactant
    • Adjusted to substrate conversion and impurity profile requirements
    • May require further downstream purification steps

    Downstream process integration

    • Introduced during ring-closure or cyclization step within controlled aqueous or mixed solvent
    • Used after initial coupling and prior to final crystallization
    • Residual monitoring implemented via HPLC in crude stages

    Final product types

    • Thiazole-based pharmaceutical actives
    • Thiadiazole-derivative APIs
    • Antimicrobial intermediate compounds
    • Oncology research molecules

    2. Polymerization Catalyst Precursor

    Specialist polymer producers select 2-(Dimethylamino)Thioacetamide Hydrochloride for its function as a precursor to thiol-modified catalysts used in precision radical polymerization. Accurate dosing ensures controlled molecular weight and dispersity, while compliance checks for trace metals and amino group reactivity maintain downstream polymer quality. The material’s easy solubility in mixed alcoholic media supports continuous catalyst preparation.

    Industry compliance standards

    • ISO 9001:2015 for quality management in chemical manufacturing
    • DIN EN ISO 14001 for environmental management (applicable to process operators)
    • Product stewardship initiatives for polymer additives
    • REACH registration and safety data documentation

    Typical usage ratio

    • 0.2–1.0% by weight in the catalyst precursor slurry
    • Proportion depends on target polymerization initiation rate and catalyst loading
    • Requires on-line adjustment for continuous reactors

    Downstream process integration

    • Dosed into homogeneous catalyst formulation kettles pre-polymerization
    • Quality control for thiol conversion conducted upstream of polymer batch introduction
    • Often combined with ferric or cupric salts for tailored reactivity

    Final product types

    • Specialty polymers for coatings
    • Electrically conductive polymer films
    • Advanced hydrogel matrices
    • Polymeric dispersing agents

    3. Agrochemical Synthesis Intermediate

    Major agrochemical manufacturers incorporate this chemical as a building block in the construction of sulfur-containing pesticide molecules. It undergoes selective alkylation and oxidative coupling steps to yield bioactive heterocycles that support crop protection formulations. The product’s high assay and consistent reactivity limit unwanted side reactions in large-scale continuous processes.

    Industry compliance standards

    • FAO/WHO Specifications for Pesticide Intermediates
    • ISO 9001:2015 for batch traceability in agrochemical input chains
    • REACH Annex VIII for environment and workplace safety
    • CLP Regulation (EC) 1272/2008 for classification, labelling, and packaging

    Typical usage ratio

    • Ratios typically range from 1.1–1.5 molar equivalents to halogenated aromatic precursors
    • Precisely managed according to targeted reaction yield and selectivity profile

    Downstream process integration

    • Applied at early-stage heterocycle assembly line
    • Reacts in sequential alkylation or condensation vessels
    • Integrated in both batch and semi-continuous flows for maximum throughput

    Final product types

    • Herbicide technical concentrates
    • Fungicide active substance precursors
    • Insecticide intermediates containing thioamide bridges
    • Plant growth regulator raw materials

    4. Analytical Reagent Compound

    Certified testing labs and chemical analysis companies select 2-(Dimethylamino)Thioacetamide Hydrochloride as a derivatizing agent for exotic sulfur speciation in environmental and food monitoring. The reagent’s purity level and low background interference allow reliable detection limits in photometric and chromatographic methods, essential for regulated sample testing.

    Industry compliance standards

    • ISO/IEC 17025 accreditation for testing laboratories
    • ASTM D3223 for sulfur compound determination
    • EPA 200.8 method compliance (where applicable)
    • Good Laboratory Practice (GLP) requirements for chemical analysis

    Typical usage ratio

    • Standardized in analytical procedures at 1–5 mg/mL solution concentrations
    • Adjusted to matrix and analyte sensitivity in validation protocols
    • Total sample:reagent ratios documented in SOPs

    Downstream process integration

    • Prepared freshly as an aqueous reagent stock in sampling labs
    • Introduced immediately before spectroscopic measurement or extraction step
    • Used during quality control round-robin proficiency tests

    Final product types

    • Water testing reagent kits
    • Certified reference standards for sulfur detection
    • Environmental monitoring sampling solutions
    • Food safety laboratory consumables

    5. Dye and Pigment Intermediate

    Synthetic dye and pigment manufacturers employ 2-(Dimethylamino)Thioacetamide Hydrochloride as a functional intermediate in the preparation of sulfur-rich chromophores for high-stability pigments. The intermediate delivers specific electron-donating properties that support strong shade intensity and lightfastness, essential for demanding textile, ink, and plastic coloration.

    Industry compliance standards

    • OEKO-TEX Standard 100 for textile chemicals
    • EN 71-3 for migration of certain elements from toy colorants
    • ISO 9001:2015 for colorant batch consistency
    • EU REACH Annex XVII for restricted substances in dyes

    Typical usage ratio

    • Formulation input typically at 0.5–2.0 molar equivalents to aromatic backbone
    • Adjusted to final chromophore hue and target spectral properties
    • Dosing confirmed by in-process LC-MS validation

    Downstream process integration

    • Added during pigment condensation and coupling step
    • Supports thioether bridging for enhanced pigment durability
    • Integrated in both solid-phase and solution-based synthesis routes

    Final product types

    • Sulfur-based organic pigments
    • Textile disperse dyes
    • High-purity inkjet pigment dispersions
    • Heat-resistant plastic masterbatch colorants
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    Certification & Compliance
    More Introduction

    2-(Dimethylamino)Thioacetamide Hydrochloride: Beyond the Data Sheet

    A Closer Look at a Niche Intermediate

    Producing specialty chemicals such as 2-(Dimethylamino)thioacetamide hydrochloride feels a bit like handcrafting a unique tool for researchers. Every batch carries our commitment to both purity and reliability. This compound doesn’t often grab headlines, but in laboratories and process plants, it fills a role that wide-market chemicals simply cannot handle. Our work with 2-(Dimethylamino)thioacetamide hydrochloride (often known by its CAS 16641-27-1) comes directly from regular conversations with organic chemists and custom synthesis designers who need materials for precise tasks. There’s a practical satisfaction in answering that need with thoughtfully produced chemicals.

    Our Experience with Controlled Synthesis

    We learned early that just producing a compound isn’t enough. 2-(Dimethylamino)thioacetamide hydrochloride needs controlled conditions through synthesis, purification, and finishing. The hydrochloride salt form significantly influences stability under storage, especially compared with the free base. At scale, the product must stay consistent between every kilogram, otherwise a small variance can complicate the reaction yields downstream for our partners. We use high-grade raw materials and optimize every crystallization step, which pays off in reproducible results on the customer’s bench.

    Production begins with quality dimethylamine and a precise handling of thioacetamide under controlled pH and temperature. Over time, we've fine-tuned filtration, solvent removal, and drying, so the finished product stays free from significant levels of residual solvents or moisture. While these details might not seem thrilling, any lapse quickly stands out under analytical testing. Numerous clients bring us stories of failed experiments sourced to poorly controlled impurity levels. Hearing researchers relieved that our products hold up in their own quality checks makes those hours of process monitoring worthwhile.

    Understanding Specifications: Why the Numbers Matter

    Markets often gloss over what’s in a specification sheet, treating it as marketing rather than a true measure of reliability. Through years of scaling this product, we've learned that reported assay and purity are only two pieces of a much bigger puzzle. Depending on the end use—such as pharmaceutical intermediates, peptide coupling, or heterocyclic synthesis—the tolerance for contaminants, color, and even bulk density can have outsized consequences. While some industries accept looser guidelines, research teams and pilot lines expect a tighter range. That’s why most of our batches carry a purity exceeding 98%, with documented limits on residual solvents and heavy metals, even if customers don’t always request those figures in writing.

    Our standard batch comes as a free-flowing, off-white crystalline powder. Humidity, temperature, and even packaging material can impact long-term stability and ease of dispensing, especially during winter shipments through dry climates or storage in less-controlled lab environments. Our in-house protocols maintain strict limits on water content—routinely below 0.5% by Karl Fischer titration. Speaking directly with chemists who ran into caking or clumping with lower-cost imports drove us to develop a range with optimized particle size, protecting flow properties without sacrificing the purity standard.

    The Science Behind Its Use: Applications and Limitations

    What sets 2-(Dimethylamino)thioacetamide hydrochloride apart isn’t just its core structure but the versatility it brings to the synthetic chemist’s bench. Commonly, this molecule steps into reaction sequences as an intermediate when other acylating agents introduce side products. It’s a frequent choice in the synthesis of sulfur-containing heterocycles and in modification of biologically active compounds, particularly where gentle reactivity and defined selectivity are needed. Unlike its analogues, the dimethylamino group imparts increased solubility in water and polar organic solvents, while the hydrochloride salt bolsters its shelf-life under standard storage conditions.

    In direct practice, researchers value the reagent for forming thiazoles and related scaffolds, often under conditions that challenge less robust inputs. It brings unique electron-donating effects to condensation reactions, supporting stable yields and minimizing undesired rearrangement. Pharmaceutical chemists often mention its role in the generation of building blocks for enzyme inhibitors and drug discovery targets. For those of us involved in quality control and logistics, it’s hard not to appreciate that each kilogram sent out supports months of patient, careful discovery inside customers’ labs.

    Drawing comparisons to closely related chemicals offers useful context. Plain thioacetamide, although cheaper and widely available, lacks the functional group adaptation that makes 2-(Dimethylamino)thioacetamide hydrochloride distinct in certain coupling reactions. The additional methyl groups on the nitrogen and the stabilized hydrochloride form change reactivity, making it a favorite for chemists avoiding pathways that generate complicated mixtures or where subtle control over nucleophilicity matters.

    How This Compound Differs from Others in the Bench Chemistry Arsenal

    To the untrained eye, many thioamide compounds seem practically interchangeable. Our time on the manufacturing line and in technical support tells another story. 2-(Dimethylamino)thioacetamide hydrochloride stands out among thioamides by offering both improved handling and greater solubility. It resists oxidation better than the base form and stores well in basic laboratory containers without the need for elaborate desiccators.

    Alternative thioamide salts, or those without the dimethylamino functionality, can break down or form colored byproducts far more quickly. Several research clients mention previous headaches with batch-to-batch inconsistency in products sourced from supply chains lacking deep oversight into process conditions. Such stories underscore the value in producing every lot with a clear chain of documentation, full traceability, and open analytical data.

    Physical properties—such as melting point and hygroscopicity—don’t just show up on the certificate of analysis; they reflect how the compound will behave during real-world storage and use. One pharmaceutical partner once detailed how unmilled grades from a third party caused inconsistent integration in their automated dosing system. Our shift to narrower particle size distribution, guided by this feedback, solved that practical bottleneck. These lessons remind us that understanding the product’s real chemical fingerprint is as much about listening to user experience as it is about reading through technical literature.

    Quality and Consistency: Not Just Buzzwords

    Years ago, a customer reached out after spending months troubleshooting spotty reaction outcomes. Investigations pointed to micro-impurities in a reagent supplied elsewhere. After receiving our product—and repeating the same experiments—those inconsistencies faded. That story stuck with the team and reshaped how we evaluate controls throughout the process. Batch assessment doesn’t end with purity certification. It includes checks for trace metals, unreacted starting materials, and even color tests under full-spectrum lighting to flag oxidation or thermal degradation. This comprehensive approach doesn’t happen by accident; it reflects both what regulations require and what our own lab experience proves necessary.

    We source analytical-grade water and solvents for every synthesis run. Our process analytics team regularly audits through gas chromatography, titration, and spectroscopic methods, not just spot-checking but running full validation runs several times a year. There’s no silver bullet for maintaining consistency. Vigilance, continuous feedback from users, and sustained investment in process upgrades make the difference between a product that simply passes a shelf-life claim and one that holds up through months of real use.

    As global logistics have become more complex, especially through interruptions in supply chains, more buyers reach out for verified country-of-origin documentation or assurance that no banned or high-residue process chemicals enter upstream. We address these requirements not because of external pressure but as a natural evolution in responsible chemical manufacturing. Such transparency, driven by market and regulatory demands, builds greater confidence between lab staff and producers like us.

    Addressing Risk: Safe Handling and Environmental Choices

    Safe handling isn’t just a theoretical concern; in daily production, it guides layout, containment, and even staff training. 2-(Dimethylamino)thioacetamide hydrochloride, like most thioamides, poses moderate hazards through dust inhalation and skin contact. Through first-hand experience, we learned that packaging integrity plays a significant role not only in worker safety but also in minimizing losses and off-gassing. Our lines shifted from simple PE bags to multi-layer barrier bags for the bulk product, limiting odorous emissions and exposure risk. We conduct regular drills and refreshers on spill control and first-aid for chemical exposure, not just because standards call for it but because it builds trust within our team that everyone’s well-being remains a priority.

    Dealing with residual process materials or byproducts calls for clear protocols. We operate onsite scrubbers and solvent recovery systems, targeting reduced waste and a closed-loop process wherever feasible. Chemical stewardship isn’t an option; it’s a necessity that endures through real scrutiny. As regulatory limits shift on emissions or waste streams, especially in response to local and international updates, staying ahead in environmental performance ensures uninterrupted production and keeps product acceptance high, particularly for those customers supplying into regulated pharmaceutical supply chains.

    Supporting Research and Innovation: Our Ongoing Commitment

    2-(Dimethylamino)thioacetamide hydrochloride rarely appears in public headlines or major trade shows, yet it underpins important progress in fields ranging from drug discovery to specialty polymer research. Our technical staff follow emerging publications and patent filings closely, recognizing that improvements in synthetic methods often trace back to changes in reagent selection. Through routine engagement with our clients, we regularly tune batch parameters and storage recommendations to align with new findings and shifting user requirements.

    A few years ago, a university group approached us for a batch custom-modified with a defined isotope label, for advanced mechanistic work in enzyme simulations. Supporting such specialized requests brings unique challenges, but helps us stay at the edge of development rather than locked into legacy techniques. These collaborations often prompt refinements in small-batch process intensification or nuanced adjustments to purity profiles, which in turn feed directly into our standard production routines.

    Not every project we support brings instant commercial success for the client, but each new synthesis or screen helps us better understand the practical realities of synthetic chemistry today. We believe in steady, incremental improvement—listening more than talking, asking for feedback, making errors transparent, and placing pride in every delivered drum or jar. These attitudes, grown directly from time on the plant floor and at the customer’s bench, shape what we see as genuine manufacturing expertise.

    Partnering for the Future

    Chemistry continues to evolve through the tireless labor of behind-the-scenes scientists, researchers, and supply chain specialists. As one of the few hands-on producers of 2-(Dimethylamino)thioacetamide hydrochloride, we see our role as a bridge between the rigor of the lab and the realities of production—balancing capacity with flexibility, efficiency with traceability, and cost management with unyielding standards for quality and safety.

    Years of feedback and first-hand observation taught us that excellence comes from doing countless small things right—batch after batch, year after year. Every client conversation, technical troubleshooting session, and internal audit feeds back into how we operate. Our goal remains straightforward: provide reliable, high-standard inputs to enable discovery, scale-up, and innovation for everyone who depends on our work. As needs and technologies shift in the coming years, we’ll stay focused on continuous improvement, honest dialogue, and a commitment to both the people and science that drive specialty chemistry forward.