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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 | 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. |
Applications of 4-Hydroxybutyric Acid Hydrazide in Industrial ManufacturingAs 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 Synthesis4-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
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2. Agrochemical Active Ingredient PreparationProducers 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
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3. Specialty Polymer Crosslinking AgentManufacturers 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
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4. Active Ingredient for Diagnostic Reagent DevelopmentThe 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
Typical usage ratio
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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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.