Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing admin@sinochem-nanjing.com 3389378665@qq.com
Follow us:

Glutarimide

    • Product Name Glutarimide
    • Alias 2,6-Piperidinedione
    • Einecs 203-483-2
    • 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

    725397

    Cas Number 1120-71-4
    Molecular Formula C5H7NO2
    Molecular Weight 113.115 g/mol
    Iupac Name Piperidine-2,6-dione
    Melting Point 155-156 °C
    Boiling Point 274 °C (at 760 mmHg)
    Appearance White to off-white crystalline solid
    Solubility In Water Moderately soluble
    Density 1.27 g/cm³
    Pubchem Cid 9802

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

    Packing & Storage
    Packing Glutarimide, 100g, supplied in a sealed amber glass bottle with tamper-evident cap, labeled with hazard symbols and product details.
    Shipping Glutarimide should be shipped in tightly sealed containers, protected from light and moisture. It should be handled as a hazardous chemical and transported according to relevant regulations (such as DOT or IATA). Ensure appropriate labeling, cushioning against breakage, and include safety information with the shipment to safeguard handlers during transit.
    Storage Glutarimide should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from direct sunlight and sources of heat or ignition. Avoid moisture and incompatible substances such as strong oxidizers. Proper chemical storage protocols and labeling are essential to ensure safety and maintain chemical stability. Use in accordance with laboratory safety regulations.
    Application of Glutarimide

    Applications of Glutarimide in Industrial Manufacturing

    As a direct manufacturer specializing in Glutarimide, we supply raw material solutions for advanced industrial applications. Our focus aligns with the stringent requirements of downstream users who incorporate Glutarimide into highly regulated and performance-specific environments. Below, we detail established downstream scenarios with their respective standards, process insights, dosage guidance, and final product types.

    1. Pharmaceutical Intermediate for Anticonvulsant Drug Synthesis

    Leading pharmaceutical producers incorporate Glutarimide as a key intermediate in the synthesis of anticonvulsants such as thalidomide and its analogues. The tight control of purity, trace elements, and reaction parameters is mandatory throughout the multi-stage synthesis, with Glutarimide introduced during the pivotal condensation and cyclization step. The manufacturing process adheres rigorously to international pharmacopeial and GMP requirements to ensure consistency and compliance.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients
    • USP/NF (United States Pharmacopeia/National Formulary)
    • EMA Guideline on Manufacture of the Finished Dosage Form
    • 21 CFR Parts 210 & 211 (US FDA Current GMPs for Finished Pharmaceuticals)

    Typical usage ratio

    • Dosage typically between 0.8 to 1.1 molar equivalents depending on the coupling agent and desired yield optimization; precise adjustment based on real-time titration and purity titrimetric analysis

    Downstream process integration

    • Introduced during high-temperature condensation reactions under nitrogen atmosphere, followed by cyclization; inline monitoring ensures batch consistency and impurity control at the intermediate synthesis stage

    Final product types

    • API intermediates for thalidomide and structurally related anticonvulsants
    • Final active pharmaceutical ingredients for oral solid dosage forms

    2. Building Block for Agrochemical Synthesis (Herbicides and Growth Regulators)

    Manufacturers of specialty agrochemicals utilize Glutarimide as a molecular building block in producing highly regulated herbicides and plant growth regulators. The process employs Glutarimide in nucleophilic substitution and functional group transformation stages, necessitating traceability and compliance with international pesticide regulations and hazardous substance management systems.

    Industry compliance standards

    • FAO/WHO Specifications and Evaluations for Agricultural Pesticides
    • REACH Regulation (EC) No 1907/2006
    • China GB 2763: National Standard for Maximum Residue Limits for Pesticides in Food
    • ISO 9001:2015 Quality Management System in agrochemicals

    Typical usage ratio

    • Ranges from 0.5 to 1.5 weight percent of the active matrix, adjusted based on substitution pattern required and targeted biological activity

    Downstream process integration

    • Incorporated during early stage condensation and amidation steps in batch or continuous process units; monitored by HPLC for conversion yield and structural integrity

    Final product types

    • Herbicidal active ingredient intermediates
    • Commercial plant growth regulators and derivative agrochemical actives

    3. Intermediate for Polyimide Monomer Preparation in High-Performance Plastics

    Producers of high-performance engineering plastics rely on Glutarimide as a reactive intermediate to synthesize specific polyimide monomers. The addition of Glutarimide during functionalization steps enables precise control over polymer backbone rigidity and thermal stability, essential for fabricating advanced films and molded parts subject to demanding operational environments.

    Industry compliance standards

    • ISO 9001:2015 for polymers and plastics manufacturing
    • RoHS Directive 2011/65/EU compliance for electronic and electrical applications
    • UL 94 Flammability Standard for Plastics Materials

    Typical usage ratio

    • Typically incorporated at 2–6% by mass in the polymerization charge, with adjustments based on desired mechanical and thermal properties of the final resin

    Downstream process integration

    • Added during the precursor salt cyclization and imidization steps; quality control includes FTIR and GPC analysis at the post-synthesis stage

    Final product types

    • High-temperature-resistant polyimide resins
    • Dielectric films and high-performance molded plastic parts

    4. Precursor for Synthetic Modification in API Research and Custom Molecule Development

    Contract research organizations and pharmaceutical R&D units use Glutarimide as a reliable scaffold for rapid development of new chemical entities within medicinal chemistry projects. Scientists employ it for structural diversification through functional group modification at specific loci, with traceability demanded throughout the research pipeline to meet submission and scale-up standards.

    Industry compliance standards

    • OECD Good Laboratory Practice (GLP) for Non-Clinical Safety Studies
    • USP General Chapter <823> Radiopharmaceuticals for research applications
    • Material Transfer Agreement (MTA) compliance for substance traceability

    Typical usage ratio

    • Used from 0.1 to 1.0 mmol scale per reaction during lead discovery and optimization, scaled up as required for pilot batches based on target compound complexity

    Downstream process integration

    • Utilized in early-stage synthesis, with modification steps performed under inert conditions; all intermediates tracked by LC-MS and elemental analysis

    Final product types

    • Research and screening libraries
    • Synthetic intermediates for proprietary active pharmaceutical candidates

    5. Intermediate for Industrial Dye Synthesis

    Manufacturers of specialty dyes employ Glutarimide within the synthetic routes for high-purity organic pigments, especially where imide moieties contribute to specific chromophore properties. The inclusion of Glutarimide provides reactive functionality during ring closure operations, directly impacting hue intensity and fastness characteristics required in technically demanding textile and plastic coloration.

    Industry compliance standards

    • OEKO-TEX Standard 100 (textile dye safety)
    • REACH Registration (EC No 1907/2006) for dye substances
    • ISO 9001:2015 for colorant manufacturers

    Typical usage ratio

    • Formulation may require 3–8% by molecule count within the coupling reaction, with adjustment determined by targeted pigment structure

    Downstream process integration

    • Participates in closed-ring reaction stages after coupling with aromatic substrates; controlled addition during heating ensures optimal imidization

    Final product types

    • High-performance organic pigments for synthetic fibers
    • Technical dye intermediates for polymer coloration systems
    Free Quote

    Competitive Glutarimide prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.

    We will respond to you as soon as possible.

    Tel: +8615371019725

    Email: admin@sinochem-nanjing.com

    Get Free Quote of Sinochem Nanjing Corporation

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

    Certification & Compliance
    More Introduction

    Glutarimide: A Core Building Block in Advanced Synthesis

    Glutarimide stands out in modern chemical manufacturing as a tried-and-true intermediate, recognized for its role in everything from pharmaceuticals to advanced materials. Our team has worked with glutarimide for decades, learning its nuances and its place in the broader world of specialty chemicals. This compound, with its clean, cyclic imide structure, offers stability and reactivity in the precise ways our clients rely on for their formulations and scale-up projects.

    A Purpose-Driven Molecular Scaffold

    What gives glutarimide its value is more than just its five-membered ring with two ketone groups. In the lab, it provides a reliable node for introducing additional functional groups, serving as a central hub in multi-step syntheses. Over the years, chemists from research universities and leading manufacturers have leaned on glutarimide to build more complex molecules, including essential active pharmaceutical ingredients. Our process optimization focuses on providing glutarimide with purity that minimizes unwanted byproducts, an effort that cuts waste and cleanup steps downstream.

    We produce glutarimide in batches that consistently exceed purity thresholds set by regulatory authorities. Each lot comes with analytical support showing not just purity, but clarity on minor isomer and contaminant profiles. Consistent supply, with stable lot-to-lot profiles, makes it easier for our industrial users to validate and scale-up their own reactions. This gives product developers a predictable foundation, especially important for projects moving from the lab to the pilot phase, where surprises can cost both money and time.

    Current Market Specifications and Quality Control

    Our glutarimide typically appears as a white crystalline solid, with a melting point close to 154°C. Those seeking high-precision material for synthesis will find our standard offering meets or exceeds 99% purity by HPLC. Through methodical solvent removal and precise temperature controls during crystallization, we produce material with moisture content reliably below 0.5%. Every drum and kilogram we ship carries a full set of COA data — not just regulatory compliance measures, but nuanced details important for process chemists: residual solvent percentages, trace metal analysis, and particle size distribution where relevant.

    We have fine-tuned our process over years, not just to meet the market’s general expectations, but to solve the real problems encountered in high-stakes manufacturing. Clients have come to us, for example, after finding that glutarimide from other sources contained persistent organic impurities that altered downstream reactivity. Through focused distillation and crystallization tweaks, we offer material targeted to avoid those headaches. Analytical feedback loops from major end-users guide nearly every production cycle. We routinely field requests for custom particle size or solvent-wetted glutarimide for specialized blending and downstream compatibility, and our facility is equipped for these needs.

    Handling and Application Experience

    The use of glutarimide has evolved alongside changing manufacturing needs. Early in our experience, most glutarimide flowed into the agricultural sector and small-molecule pharmaceuticals, where it formed part of larger transformation ladders. Over the last decade, demand has shifted into high-purity applications, particularly for modern drug discovery and industrial catalysts. Our technical team spends time with both established process engineers and university researchers working on next-generation routes that rely on the predictable behavior of our product.

    Glutarimide holds value not just in what it can do alone, but in how it streamlines surrounding chemistry. In the hands of practiced synthetic chemists, it transforms through N-alkylation, condensation, or hydrolysis reactions, providing access to a spectrum of intermediates otherwise hard to build efficiently. We have seen demand spike for our product in contract manufacturing projects, particularly where reliability matters — clients want to avoid the fatigue of inconsistent intermediates undoing weeks of careful work. For those working with route scouting or process development, knowing the baseline of your starting materials is critical, and glutarimide’s well-defined profile lowers the risk of variable outcomes.

    The Real-World Edge Over Generic Suppliers

    Not all glutarimide on the market meets the benchmarks the modern process industry expects. We have tested material from other sources — material supposedly of similar purity — and found batch-to-batch fluctuation in impurity profiles that threaten reaction yield and scalability. For example, a compound traced at less than 0.1% can still catalyze side reactions in large runs, generating waste and requiring extra purification. Anybody running a pilot plant or managing kilo-lab scale reactions knows the disruption that comes from product recalls, rework, or, worse, process shutdowns due to inconsistent input.

    Our operation focuses on more than just purity for its own sake. We actively monitor for trace contaminants, residual solvents, and even particulates that slip through basic screening at less experienced operations. This discipline emerges from our direct involvement in troubleshooting customer problems — such as one client who encountered catastrophic foaming during crystallization due to nonvolatile residue from inadequately purified glutarimide from a broker. Our team adjusted our solvent wash protocols to address similar risks, and now routinely reports on these findings with every production batch.

    Supporting Scientists and Engineers with Transparency

    Beyond shipping drums or bottles, our primary job supports progress by offering a predictable, transparent supply base. Over the years, we have expanded our data reporting so clients see not just basic spectral characterization, but in-depth impurity profiles, test method descriptions, and detailed batch notes. Rapid feedback on any deviations has proven invaluable for our partners running continuous or large-scale processes, allowing for rapid investigation and mitigation of issues.

    Some customers pursue exploratory chemistry — new transformations using glutarimide as a starting framework for molecules unknown a decade ago. Our technical support works with these groups to optimize solvent ratios, reaction times, and work-up conditions based on the nuances of our material. In many cases, published literature lacks real-world details about processability at larger scale, or about side reactions triggered by invisible contaminants. We regularly facilitate exchanges between early-stage researchers and industrial process leaders to capture hard-won experience in the field. The effect shows: clients return not just for material, but for insight and process solutions we’ve picked up from years at the bench and in the plant.

    Safe Handling: Built on Experience

    No synthetic discussion is complete without considering safety and scale effects. Our history with glutarimide includes safety reviews ranging from lab bench to freight containers. Key to our approach is regular storage audits and comprehensive package tracing — never cutting corners with labeling, weight, or shipment documentation. Our field engineers have worked onsite with customer EHS teams to refine SOPs around transfer and storage, particularly where ambient humidity can impact product stability. While glutarimide itself is relatively robust, careless handling of drums or bags leads to aggregation and clumping, both of which create process bottlenecks and unnecessary handling.

    Direct experience teaches that well-documented material movement, joint safety drills, and timely feedback keep people safe and processes running efficiently. As regulations tighten, sharing hazard management data not only helps our direct clients, but shapes industry norms for everyone using this specialty chemical. Open communication about lessons learned — even from rare incidents — builds the knowledge base for the next generation of chemists and plant operators. Through these collective efforts, we make sure that glutarimide’s benefits reach end products safely and efficiently.

    Continuous Improvement Guided By Real Needs

    Our focus on continuous improvement springs from frequent conversations with those working in process development and bulk manufacturing. Feedback often loops rapidly: if a new impurity pops up, or a formulation challenge arises, we bring those lessons back to the plant for immediate review. In one case, a customer scaling up an API synthesis reported unexpected color formation traced to a heat-sensitive byproduct. Within days, we tightened our crystallization windows, adjusted solvent choices, and brought the next batch in line with the most demanding requirements.

    Upgrading analytical methods and installing more sensitive detection tools, we now routinely capture and resolve shifts in impurity patterns that might otherwise go unnoticed. Clients tracking regulatory compliance, or preparing for audit, find this transparency invaluable during both documentation and process validation. We also provide material tailored for downstream testing — a need that emerged as more customers conducted their own method development. Lessons learned from our production floor now inform raw material specs for some of the world’s largest pharmaceutical and industrial contractors.

    Comparing Glutarimide With Other Core Imides

    Glutarimide shares its core chemistry with other cyclic imides like phthalimide and succinimide. Differences matter to advanced users. Phthalimide, with an aromatic ring, holds value in amide bond-forming reactions and is less flexible for ring-opening applications. Succinimide, with a four-membered ring, is more polar and often used in peptide chemistry. Glutarimide sits between them in both structure and function: it brings a balance of ring strain and reactivity. This gives it an edge for N-alkylation and various ring-expansion or cleavage strategies.

    We have supported clients transitioning from phthalimide routes to glutarimide, particularly where control over side-product profiles or reactivity windows matters most. Our production team tracks observational data on yield, byproduct creation, and purification challenges from these route changes. The consensus among experienced scientists — based on repeated plant trials — is that glutarimide offers higher process control and fewer recalcitrant impurities in multi-step synthetic routes. For those in contract manufacturing with strict impurity specifications, this flexibility translates to real cost and time savings.

    From Sourcing To Scale-Up: Behind Each Batch

    Starting material quality matters. We source maleic anhydride and ammonia from top-tier suppliers, then closely monitor each conversion step. Our reactors are custom-fitted for precision in temperature and pressure — a necessity learned through long runs where batch variability could spoil days of work. Modern sensors and high-throughput analytics have cut both manual error and production lag to nearly zero. Experience teaches that by driving down the time between reaction and isolation, we preserve both purity and yield for the customer.

    Besides technical upgrades, our staff cross-trains on both legacy and digital batch monitoring systems. Procedures blend direct experience — an operator’s instinct for color and texture shifts — with modern data analysis, so potential problems never slip through unnoticed. Every lot gets tracked from raw material through packaging, with full batch histories available for customer traceability. This degree of accountability supports pharmaceutical clients, industrial producers, and innovators working on new fields that rely on glutarimide as a stable, responsive core intermediate.

    Responding to Shifting Industry Demands

    We have seen industry demand shift not just in volume but in expectation. Early in our manufacturing, glutarimide’s customers needed reliable, affordable supply. Today, clients require tighter specs, transparent processing data, and technical collaboration on custom grades. Shifts like this require our team to upgrade not just production lines, but the way we communicate — frequent tech calls, detailed written protocols, and rapid sampling for new projects. As regulation tightens around pharmaceutical intermediates, we have been working in close step with auditors and customers alike, ensuring that quality systems support compliance from batch release to final delivery.

    Requests for new packaging formats or specific blending needs come in almost monthly. Whether it concerns material for kilogram pilot runs or drum-scale full production, we’re equipped to deliver, drawing on lessons from both successful and difficult projects. This keeps us honest: real-world operating conditions often differ wildly from lab simulations, and we listen closely to client feedback as the most valuable guide to process improvement.

    Glutarimide’s Place in Future Innovation

    Innovation in small-molecule chemistry and materials science keeps glutarimide relevant year after year. Researchers continue to discover applications in areas like polymer modification and crop protection, alongside its well-established use in drug synthesis. One trend we’ve noted comes from startup clients exploring specialty building blocks derived from glutarimide’s backbone — turning what used to be a basic intermediate into a launching point for original product families. Our technical staff frequently engages in joint development work, learning from both academic partners and industrial R&D labs about new requirements for purity, form, and reactivity.

    Whether for classic transformations or new frontiers, glutarimide’s robust, predictable chemistry means it rarely surprises in use. Our job as manufacturer involves more than filling orders — it rests on active involvement in every step, from upstream sourcing to end-use troubleshooting. This culture of engagement, built brick by brick over years, reflects in both the quality of the chemical itself and in the outcomes our customers achieve.

    Conclusion: Industry Trust Built Through Action

    Behind every container of glutarimide we ship lies years of cumulative expertise, ongoing communication, and a commitment to problem-solving at the pace modern chemistry demands. Our knowledge is not abstract or borrowed; it comes from decades on the production floor and ongoing dialogue with those on the front lines of process innovation. Whether supporting a new drug launch or a radical material design, glutarimide from our line arrives as more than a reagent — it is the sum of real-world lessons, careful monitoring, and sustained effort toward the highest standards of chemical manufacturing. In the world of specialty intermediates, this makes all the difference.