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4-Hydroxybutyric Acid Hydrazide

    • Product Name 4-Hydroxybutyric Acid Hydrazide
    • Alias gamma-Hydroxybutyric acid hydrazide
    • Einecs 695-723-1
    • 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

    513060

    Product Name 4-Hydroxybutyric Acid Hydrazide
    Cas Number 7332-22-1
    Molecular Formula C4H10N2O2
    Molecular Weight 118.13 g/mol
    Appearance White to off-white solid
    Melting Point 103-105°C
    Solubility Soluble in water
    Storage Temperature 2-8°C
    Purity Typically ≥98%
    Synonyms Gamma-hydroxybutyric acid hydrazide, GHB hydrazide

    As an accredited 4-Hydroxybutyric Acid Hydrazide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 4-Hydroxybutyric Acid Hydrazide comes in a sealed, amber glass bottle containing 25 grams, labeled with hazard and handling information.
    Shipping 4-Hydroxybutyric Acid Hydrazide should be shipped in tightly sealed containers, protected from light, moisture, and physical damage. It is transported as a laboratory chemical and should comply with local, national, and international regulations. Shipping is typically done via ground or air with appropriate hazard labeling, keeping the material at a stable temperature.
    Storage 4-Hydroxybutyric Acid Hydrazide should be stored in a tightly sealed container, protected from moisture and light. Keep it in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizers and acids. Storage at room temperature is acceptable unless otherwise specified on the safety data sheet. Ensure proper labeling and access only to trained personnel.
    Application of 4-Hydroxybutyric Acid Hydrazide

    Applications of 4-Hydroxybutyric Acid Hydrazide in Industrial Manufacturing

    As a specialized manufacturer of 4-Hydroxybutyric Acid Hydrazide, we supply this compound for select industrial downstream sectors where its unique properties support high-value production processes. Below, we provide detailed, sector-specific application insights, focused on established and regulated industrial scenarios that demonstrate the concrete integration and compliance of our material within real-world manufacturing frameworks.

    1. Pharmaceutical Intermediate Synthesis

    4-Hydroxybutyric Acid Hydrazide is widely implemented as a key intermediate in synthesizing a range of active pharmaceutical ingredients (APIs), particularly for central nervous system agents and anticonvulsant medications. Downstream manufacturers integrate it during the condensation stage of multi-step syntheses, taking advantage of its functional hydrazide group to form heterocyclic cores critical to final drug molecules. Quality control hinges on rigorous adherence to documented impurity limits and residual solvent standards, due to its role in regulated drug substance precursors, with validated analytical methods guiding its monitored inclusion.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice Guidance for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.) monographs where applicable
    • USP General Chapter <1058> Analytical Instrument Qualification
    • Chinese Pharmacopoeia synthesis requirements for intermediates

    Typical usage ratio

    • Integral amount typically ranges from 0.20 to 0.50 molar equivalents relative to target substrate, adjusted based on route efficiency and impurity profile management

    Downstream process integration

    • Batchwise addition at stepwise condensation stage in multi-step API synthesis; subjected to in-process controls and reaction yield assessment

    Final product types

    • Anticonvulsant APIs
    • Psychotropic pharmaceutical actives
    • Other specialty drug intermediates

    2. Agrochemical Active Ingredient Preparation

    Producers in agrochemical manufacturing employ 4-Hydroxybutyric Acid Hydrazide for the targeted assembly of new fungicide and herbicide molecules, particularly those requiring nitrogen-containing heterocyclic scaffolds. It enters the process at the heterocyclization transformation step, giving rise to bioactive moieties with defined selectivity profiles needed for crop protection agents. The batch records and QC data require documented compliance with environmental emissions and worker safety guidelines due to downstream regulatory controls for agricultural chemicals.

    Industry compliance standards

    • FAO/WHO Specifications and Evaluations for Agricultural Pesticides
    • OECD Principles of Good Laboratory Practice (GLP)
    • US EPA 40 CFR Part 158: Data Requirements for Pesticide Registration
    • REACH Regulation (EC) No 1907/2006 for manufacturing and import

    Typical usage ratio

    • Usage typically between 0.10 and 0.30 molar equivalents, tailored according to specific synthetic yield and target compound structure

    Downstream process integration

    • Added during nitrogen introduction or ring closure stages when producing hydrazide-functionalized agrochemical actives; isolated as part of technical-grade intermediates

    Final product types

    • Systemic fungicide concentrates
    • Novel herbicide technicals
    • Pre-formulation intermediates for downstream agrochemical production

    3. Specialty Polymer Crosslinking Agent

    Manufacturers integrating specialty polymers, such as hydrazide-modified polyurethanes or other functionalized elastomers, use 4-Hydroxybutyric Acid Hydrazide as a crosslinking agent to achieve enhanced chemical resistance and mechanical performance. The compound is charged into the reactor during the chain extension or prepolymer modification step to enable covalent bonding and controlled gelation. Careful documentation under process safety and product stewardship systems controls the dosage and process parameters, aligning with both in-house protocols and external safety data communication.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems
    • EU Regulation No 1272/2008 (CLP) for chemical safety labeling
    • National Fire Protection Association (NFPA) chemical process safety codes
    • Customer-specific product stewardship requirements

    Typical usage ratio

    • Dosage ranges from 0.50% to 2.00% by polymer mass, dependent on required crosslink density and final physical properties; determined by pre-scaling and mechanical property validation

    Downstream process integration

    • Introduced during chain extension or curing reactions in step-growth polymerizations; monitored for uniform distribution and thermal curing profile

    Final product types

    • Hydrazide-functionalized polyurethane foams and elastomers
    • Specialty polymer coatings with chemical resistance
    • Crosslinked polymer composite materials for engineering applications

    4. Active Ingredient for Diagnostic Reagent Development

    The IVD (in vitro diagnostic) sector uses 4-Hydroxybutyric Acid Hydrazide to introduce hydrazide functionalities into chromogenic substrates and linker molecules required in enzymatic diagnostic kits. In this application, it serves as a derivatization reagent, facilitating the covalent immobilization of biomolecules onto assay surfaces. Traceability and assay specificity define formulation procedures, while manufacturing is subjected to continual clinical and analytical verification, requiring full traceability and regular process validation for regulated diagnostic use.

    Industry compliance standards

    • ISO 13485:2016 Medical Device Quality Management Systems
    • US FDA 21 CFR Part 820: Quality System Regulation (QSR) for medical devices
    • European In Vitro Diagnostic Regulation (IVDR) 2017/746
    • Analytical method validation guidelines (CLSI, EP05-A3)

    Typical usage ratio

    • Dosage typically ranges from 0.01 mmol to 0.10 mmol per assay substrate batch, adjusted after optimization for reactivity and substrate color intensity

    Downstream process integration

    • Applied during immobilization or substrate derivatization stage of diagnostic reagent synthesis; product batch traced by unique process lot number

    Final product types

    • Chromogenic diagnostic substrates
    • Enzyme-linked immunosorbent assay (ELISA) plates and auxiliaries
    • Chemical sensor surface-modified reagents
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    Certification & Compliance
    More Introduction

    Introducing 4-Hydroxybutyric Acid Hydrazide: A Practical Approach to Synthesis and R&D Applications

    Real-World Use of 4-Hydroxybutyric Acid Hydrazide in the Lab

    Every production run reminds us that chemical synthesis isn’t just about achieving yield. Pure, dependable intermediates set the stage for consistent results and predictable performance down the line. 4-Hydroxybutyric Acid Hydrazide, also known as gamma-hydroxybutyric acid hydrazide, is a specialty intermediate we’ve been offering for years because it repeatedly meets such standards where routine reagents often fall short.

    For bench chemists and development teams, 4-Hydroxybutyric Acid Hydrazide presents a solid blend of utility and reliability. It carries a straightforward molecular backbone, consisting of a four-carbon aliphatic chain with a terminal hydrazide group. Our most common model is the pure free acid hydrazide in crystalline form, offered at assay levels above 98%. We see its primary demand in pharmaceutical research, especially in custom route design for GABA analogs, active pharmaceutical ingredient (API) synthesis, and probe molecule preparation.

    Why Consistency Matters in Intermediate Manufacturing

    Several teams we work with have switched over from generic hydrazide sources. Most report frustration with variable impurity profiles, poor lot traceability, or inconsistent handling properties. From our end, we house every batch under controlled conditions, monitor the pH after preparation, subject each lot to thermal testing, and provide thin-layer chromatography (TLC) snapshots for on-request documentation. Having full control over the process means feedback from customers channels directly to the production line—leading to tweaks in purification, filtration, or drying times. For labs running tight timelines or delicate reactions, confidence in the intermediate supports higher throughput and less rework.

    Differences from Common Hydrazides and Alkanoyl Hydrazides

    Once you move out of standard acetyl or propionyl hydrazides and into functionalized systems like 4-Hydroxybutyric Acid Hydrazide, new synthetic windows open up. The gamma-hydroxyl function alters both solubility and reactivity, giving controlled access to cyclization reactions, acyl substitutions, or stable linkage with bioactive scaffolds. The four-carbon backbone of 4-Hydroxybutyric Acid Hydrazide makes it flexible for extension or shortening, while the terminal hydrazide serves as a strong nucleophile for condensation steps.

    During optimization, researchers face difficult choices with common acyl hydrazides. Solubility often skews reactions, or drying introduces artifacts. With 4-Hydroxybutyric Acid Hydrazide, its slightly higher polarity and defined melting point (which we routinely check within tight spec) make it a more manageable participant in multi-step synthesis. No batch comes with residual solvents left over from crude workup—a detail we prioritize in final quality control.

    Specifications That Advance Process Control

    Chemists request analytical data, but live testing reveals how a lot actually performs. In our workflow, we prioritize practical usability on top of purity. Every production run passes through repeat runs of NMR and HPLC, confirming both identity and the absence of secondary hydrazide isomers that could complicate downstream steps. We grind crystalline product to a specific size range, so users handling subgram to multi-kilogram scales get consistent flow in reactors, vials, or scoops.

    Moisture content often throws off yields with hydrazides. Our dehydration step, handled at low temperature under vacuum, gives a finished content below 0.2%. We back this up with Karl Fischer titration spot checks for every lot. Because some customers map impurities at sub-ppm levels, we certify metal content (where possible) at each packing cycle. Subtle changes in color—moving from fully white to faintly off-white—show up quickly under our final inspection lights, and off-spec lots get held aside until we clarify the underlying reason.

    Why Synthetic Details Make or Break Discovery Projects

    We often hear from labs optimizing lead series or scaling new analogs. Standard supply chain summed the story up: patchy deliveries, unexplained activity loss, or inconvenient documentation. With direct manufacturing, chemists send unique feedback about how 4-Hydroxybutyric Acid Hydrazide hits their targets or brings up new issues—maybe a minor impurity clouds spectral reads, or a texture shift affects powder flow. Direct control means adjustments happen quickly.

    On the synthesis side, a classic route for hydrazides runs through the acid chloride. For 4-Hydroxybutyric Acid Hydrazide, we use a direct acid-activation method with hydrazine, side-stepping unnecessary functional group migration and keeping unwanted byproduct formation in check. This approach reduces hints of over-condensation or ladder structures in the solid phase. Batch tracking closes feedback loops so chemists receive what worked last month, not a subtly changed formulation that throws off controls.

    Comparison with Similar Functionalized Intermediates

    Some buyers weigh the merits of 4-Hydroxybutyric Acid Hydrazide against offerings like 3-hydroxybutyric acid hydrazide or plain butyric hydrazide. The position of the hydroxyl group matters. In 4-Hydroxybutyric Acid Hydrazide, the terminal gamma position supports formation of stable five- or six-membered rings in cyclizations. This builds structure–activity relationships (SAR) in drug analog libraries, especially for central nervous system (CNS) targets and prodrugs. By contrast, the three position in the beta-hydroxy compound introduces strain, which many teams avoid due to unpredictable cyclization and low reproducibility.

    In direct bench use, 4-Hydroxybutyric Acid Hydrazide stays manageable as both a reactant and a storage compound. Our experience finds few stability issues under sealed, dry conditions for over a year—outperforming many aliphatic hydrazides that degrade or pick up peroxides. Labs often comment on the clean break from precursor and its traceability through multi-step routes.

    Field Data from Customer Syntheses

    With every major lot sold, we follow up with principal investigators or scale-up chemists on their results. Pharmaceutical clients use this intermediate in coupling reactions where the gamma-hydroxyl helps solubilize large aromatic fragments. Others employ it as a protected handle in CNS-active molecule libraries. As new analytical routines emerge, some turn to mass-directed prep or LC-MS, so we tweak the process to support higher levels of cleanliness and data clarity.

    Custom requests come from polymer developers or dye companies, needing stable hydrazide building blocks that won’t break down in functionalization steps. Our 4-Hydroxybutyric Acid Hydrazide handles heat cycles in melt reactions, and the absence of strong aromaticity keeps background reactivity to a minimum—useful in screen preparations and pilot plant runs.

    Technical Support and Process Honesty

    Feedback loops with research chemists keep us alert to potential hang-ups or misfeatures. One cycle, an unexpected color change in late-dried product pointed to a previously insignificant trace impurity (residual solvent peak in the ^1H NMR). Adjusting the wash sequence and ramping up vacuum application solved what could have undermined a kilogram-scale run elsewhere. Unlike batch-brokering setups, direct access to the process lets us mount the right controls and respond without passing the concern around.

    While spec sheets tell the official story, informal dialogues and calibration samples share the real details customers rely on. If someone needs a nonstandard mesh size, alternate packaging, or extra analytical validation, production pivots toward the actual need—skipping unnecessary bureaucracy and giving hands-on chemists what fits their benches or flows into their reactors.

    Environmental and Regulatory Priorities

    Demand for process transparency continues to climb. Chemical buyers now look beyond synthetic performance, asking about compliance and environmental impact. In our operation, routine waste hydrazine and acid residues undergo closed-system neutralization and off-gas capture before neutral material enters waste streams. Regulatory guidance frequently changes; we keep all safety datasheets, local registrations, and compliance logs up to date so users can slot our material into documentation-heavy programs without delay.

    With 4-Hydroxybutyric Acid Hydrazide, supply chain length stays short and traceable. Every supply run draws from raw materials screened for heavy metals, residual pesticides, or phthalates, keeping the finished material inline with pharmaceutical and technical grade needs. Colleagues familiar with the shifting regulatory landscape understand the headaches of incomplete documentation—we hand over analytical or manufacturing records as needed so no part of the process remains unclear.

    Scale-Up and Customization—Supporting Pilot and Production Lines

    Requests often begin with grams or tens of grams, but technology transfer projects scale to kilograms or higher. Building up these quantities for 4-Hydroxybutyric Acid Hydrazide takes more than a larger vessel—batch mixing, drying profiles, and temperature ramps respond differently as size increases. Based on feedback and actual trial runs, we adapt filtration and post-processing steps. This prevents bottlenecks that might appear in high-throughput or continuous synthesis setups and allows labs to avoid repeated scale-up surprises.

    Repacking and shipping protocols include direct fill at final mesh size and vacuum sealing in double-layer barrier bags. Standard operating procedures target moisture pickup, so each drum or bottle opens with no sticky agglomerates and no static buildup that would hinder automatic dosing or precision weighing on the line.

    Supporting Next-Stage Development with Reliable Supply

    Research lab managers and project chemists reserve inputs for “mission-critical” steps in their campaigns. Poor-quality intermediates, off-standard batches, or lot-to-lot inconsistency threaten both time and funding. With 4-Hydroxybutyric Acid Hydrazide, the process closes the loop from order, manufacture, dispatch, and post-delivery performance. Analysts confirm every certificate matches real test data, and order histories stay available for repeat buyers matching prior success.

    Long-term collaborations started small. Over time, mutual experience built shared protocols—reducing overhead, anticipating recurring issues, and cutting down on avoidable communication. Project chemists who stay in touch with direct production keep methods current and minimize supplier risk, especially during patent drafts and regulatory filings.

    A Broader View: Evolving Needs in Research and Process Chemistry

    The growth of medicinal chemistry and advanced material research calls for more specialized intermediates. For too long, “commodity” hydrazides filled many gaps—with little consideration for performance nuances, subtle product-defining properties, or how specs played out in live runs. With 4-Hydroxybutyric Acid Hydrazide, analytical transparency and batch control shift the conversation from “Can we retrofit?” to “How do we extend our results?”—a crucial difference for modern discovery work.

    Face-to-face with production teams, in direct communication about what a specific process or synthetic pathway asks of an intermediate, creates pathways for practical, not theoretical, solutions. Chemists handling demanding programs want input into how raw material cuts down impurity carryover, how adjustments in particle size or dryness shave hours off repeated rework, or how a difference in shipment temperature affects stability on the shelf. By keeping the link tight between manufacturing floor and customer bench, misconceptions and process hiccups fade and reliable results become the rule, not the exception.

    Conclusion: The Value of Manufacturer-Chemist Collaboration

    4-Hydroxybutyric Acid Hydrazide stands out as a highly functional yet approachable intermediate. With roots in day-to-day laboratory use, its design and delivery speak more to practical chemistry than marketing gloss. Reliable supply, responsive feedback, and targeted customization mark the difference for chemists and project teams. With every batch, the focus stays on what works: consistent, traceable material responding to research needs with no shortcuts.