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3-Amino-4-Phenylbutyric Acid Hydrochloride

    • Product Name 3-Amino-4-Phenylbutyric Acid Hydrochloride
    • Alias Phenibut
    • Einecs 629-817-4
    • 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

    791858

    Product Name 3-Amino-4-Phenylbutyric Acid Hydrochloride
    Cas Number 16618-43-6
    Molecular Formula C10H14ClNO2
    Molecular Weight 215.68 g/mol
    Appearance White to off-white crystalline powder
    Melting Point 156-158°C
    Solubility Soluble in water
    Purity Typically ≥98%
    Storage Temperature Store at 2-8°C
    Synonyms Fenibut hydrochloride, β-Phenyl-γ-aminobutyric acid HCl

    As an accredited 3-Amino-4-Phenylbutyric Acid Hydrochloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 25g bottle of 3-Amino-4-Phenylbutyric Acid Hydrochloride is sealed in an amber glass container with a tamper-evident cap.
    Shipping 3-Amino-4-Phenylbutyric Acid Hydrochloride is shipped in sealed, airtight containers to maintain stability and prevent contamination. The packaging complies with applicable chemical safety standards. It is transported under ambient or as-specified temperature conditions, with clear labeling and documentation to ensure safe handling, traceability, and regulatory compliance during transit.
    Storage 3-Amino-4-Phenylbutyric Acid Hydrochloride should be stored in a tightly sealed container, protected from light and moisture, in a cool, dry, and well-ventilated area. Keep away from incompatible substances such as strong oxidizing agents. Store at room temperature, unless otherwise specified by the manufacturer, and ensure proper labeling to prevent accidental misuse or contamination.
    Application of 3-Amino-4-Phenylbutyric Acid Hydrochloride

    Applications of 3-Amino-4-Phenylbutyric Acid Hydrochloride in Industrial Manufacturing

    As a direct manufacturer, we supply 3-Amino-4-Phenylbutyric Acid Hydrochloride to a range of highly regulated sectors. Our product supports high-purity synthesis, stringent batch control, and customer-specific processing requirements across core downstream segments. Our technical team partners with processors and formulators to ensure alignment with international regulations, precise dosage frameworks, and validated GMP pathways.

    1. Pharmaceutical Active Pharmaceutical Ingredient (API) Intermediates

    Major drug substance manufacturers use this compound as a critical intermediate in API synthesis, especially in neurological and psychiatric drug classes. Controlled production batches ensure traceability, while compliance with global pharmacopoeias governs each delivery. We enable integration from kilo-lab to ton-scale wherever regulatory qualification is needed.

    Industry compliance standards

    • ICH Q7 GMP for APIs
    • USP/NF, EP, JP monographs for specific APIs
    • FDA CFR Title 21 (for US-bound APIs)
    • EU GMP Part II (for EU-regulated pharmaceutical production)

    Typical usage ratio

    • 5–18% (mole basis) in multi-step synthesis of API core structures; ratio adjusted according to target yield and impurity profile management

    Downstream process integration

    • Feeds into final coupling or condensation stage of small-molecule API synthesis
    • Added post-reaction to purify crude intermediates prior to crystallization
    • Used as a reactant in ring-closure steps for CNS-active agents

    Final product types

    • Tablet and capsule APIs for central nervous system (CNS) disorders
    • Bulk drug substances for antiepileptic and anxiolytic medications
    • Contract-manufactured advanced pharmaceutical intermediates

    2. Central Nervous System (CNS) Drug Development

    Biotech and pharmaceutical R&D divisions employ the material for CNS drug candidate screening and lead compound development. Its reliable performance in screening assays and preclinical studies supports scalable downstream synthesis for clinical-grade materials.

    Industry compliance standards

    • GLP guidelines for non-clinical laboratory studies
    • US FDA IND-enabling quality documentation
    • EMA non-clinical safety assessment protocols
    • OECD guidance for chemical safety in early-stage use

    Typical usage ratio

    • 0.5–2 mmol per synthesis batch for analytical scale up to 100 mmol for pilot studies; ratio varies by the protocol and selected animal model

    Downstream process integration

    • Incorporated at the preclinical compound synthesis phase
    • Used in scaffold modification and molecular optimization procedures
    • Contributes to library preparations for CNS ligand discovery

    Final product types

    • Lead CNS drug candidates
    • Pharmacological probe compounds
    • Preclinical material for toxicology and PK studies

    3. Custom Peptide Synthesis

    Specialty peptide manufacturers utilize the compound as a protected building block to introduce gamma-amino acid spacers into synthetic peptide sequences. QC systems verify the material’s purity and full traceability to reduce batch-to-batch variation in sequence-controlled peptides.

    Industry compliance standards

    • ISO 9001 for quality management in peptide production
    • USP peptide impurity standards (where applicable)
    • ISO/IEC 17025 for analytical verification
    • Customer-specific raw material specification sheets

    Typical usage ratio

    • 0.1–5 equivalents per peptide chain, depending on the sequence design and targeted functionalization site

    Downstream process integration

    • Coupled during solid-phase peptide synthesis (SPPS) steps as non-canonical amino acid
    • Introduced after Fmoc deprotection to control sequence orientation
    • Applied for N-terminal or C-terminal modifications

    Final product types

    • Research-grade synthetic peptides for biochemistry studies
    • Custom peptides for pharmaceutical pipeline
    • Labeled peptides for diagnostic assay kits

    4. Fine Chemical Synthesis for Specialty Chemical Producers

    Fine chemical companies use the compound to create advanced specialty intermediates for further downstream value-added transformations. Precise documentation ensures each batch supports proprietary synthesis without risk of cross-contamination or trace impurities impacting final formulations.

    Industry compliance standards

    • ISO 9001 for production control
    • REACH registration (for European production)
    • Responsible Care Chemical Management System
    • Customer-specific specification agreements

    Typical usage ratio

    • 2–15 mol% as a synthetic intermediate determinant; actual loading determined by reaction step and targeted chemical transformation

    Downstream process integration

    • Charged at coupling, amidation, or alkylation stages of multi-step organic synthesis
    • Used as a chiral precursor or building block in target molecule assembly
    • Processed for enantioselective intermediate generation

    Final product types

    • Advanced intermediates for agrochemical R&D
    • Non-pharma biologically active compounds
    • Custom specialty chemicals supplied to material science projects

    5. Contract Research and Analytical Reference Standards

    CROs and reference standard suppliers order this compound to support method development, analytical calibration, and impurity profiling under full traceability. Consistent quality assures accurate, reproducible results in validation studies and regulatory submissions.

    Industry compliance standards

    • ISO/IEC 17025 for analytical laboratories
    • GMP for reference standard manufacturing
    • USP Reference Standard Program requirements
    • Supply chain traceability regulations (customs, import documentation)

    Typical usage ratio

    • Milligram to gram scale per analytical method; depends on the detection sensitivity and matrix complexity

    Downstream process integration

    • Direct use as calibration marker in HPLC/UPLC/MS
    • Preparation of spiking solutions for assay validation
    • Reference control for pharmaceutical impurity mapping

    Final product types

    • Analytical reference standards
    • Control reagents for QC labs and pharma partners
    • Validation kits for regulatory submission packages
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    Certification & Compliance
    More Introduction

    Introducing 3-Amino-4-Phenylbutyric Acid Hydrochloride: Manufacturer's Perspective

    For our team, 3-Amino-4-Phenylbutyric Acid Hydrochloride stands out as one of those compounds where you see firsthand how method and attention to detail make the difference. Through our own journey developing this product, some lessons have stuck with us: consistency, handling of sensitive starting materials, and maintaining the sort of controlled environment that actually brings out purity and performance batch after batch.

    Experience with 3-Amino-4-Phenylbutyric Acid Hydrochloride Production

    A few years back, bringing this product into our lineup wasn’t a simple formula switch or a matter of packaging a generic version. Phenylbutyric acids play a unique role in research, especially pharmaceutical and neuroscience applications, so the pressure was never just about meeting spec sheets. Customers came to us after trials with other sources delivered inconsistent results, minor deviations in melting point, or unreliable solubility, which disrupts their entire workflow.

    We committed to tightly controlled synthesis — sourcing high-quality raw phenylacetic acid, working through our selected catalytic amination pathway, and customizing purification steps to avoid side reactions. If the ring substituents on the molecule deviate or structural integrity isn’t locked in, everything downstream suffers, especially for sensitive research work. Over these years, regular direct communication with researchers and formulation scientists revealed how even subtle differences in product integrity translate to major differences in their results.

    Model and Specifications Grown from Manufacturing Experience

    For this product, our most frequently requested variant is the hydrochloride salt, with a guaranteed purity regularly exceeding 99% by HPLC. We’ve learned to test every batch for trace metals, maintain low moisture content, and screen by NMR as well as mass spectrometry for structural certainty. We don’t just rely on single-test confirmation; instead, we always run comparative samples against previous lots to ensure batch-to-batch convergence.

    We grind the final crystalline hydrochloride to a moderate particle size that suits lab dissolution methods, informed by direct feedback from labs seeking fast, agglomeration-free preparation. Too fine, and you’d risk handling losses; too coarse, and solution times stretch out. We’ve found that storing the salt in amber glass prevents any photodegradation over time, especially when samples are held in long-term stability programs or research libraries.

    Packing practices make a dramatic difference. We flush the headspace with nitrogen and vacuum-seal the jars so that humidity and airborne contaminants don’t leach in. Over the years, we have seen plenty of returned samples from other producers clump or yellow from poor storage or careless packaging, even when the initial spec sheet looked acceptable.

    Special Attention to Process for Reliable Research Results

    In the broader chemical landscape, 3-Amino-4-Phenylbutyric Acid Hydrochloride strikes a balance point — its structure sits right between flexibility for chemical modification and resistance to spontaneous degradation. Its core feature, the gamma-amino acid backbone with a four-carbon tail and terminal phenyl group, opens possibilities as a useful building block for synthetic chemists. The hydrochloride form keeps it stable and helps it dissolve predictably in water and polar solvents, which is a regular requirement in assay and formulation development.

    For many in pharmaceutical research, the specificity in stereochemistry or the absence of racemization during multi-step synthesis becomes non-negotiable. We take time to validate optical rotation and enantiomeric excesses when required, which many off-the-shelf suppliers overlook. That attention pays off downstream—whether scientists are coupling this intermediate to create benzodiazepine analogues or exploring modifications for GABAergic compound studies.

    I still remember one customer in a neuroscience group at a major university; they struggled for months with unexpected bioactivity drops until we pinpointed a trace impurity coming from their previous supplier’s inadequate purification. It taught us never to take even trace impurities lightly, especially since these side-products often go unnoticed in basic TLC or melting point checks.

    Unlike more robust amino acids, 3-amino-4-phenylbutyric acid salt forms can degrade with repeated freeze-thaw cycles. We’ve invested in rapid, single-batch drying and packing protocols so the compound never faces unnecessary temperature swings before it reaches the user.

    Use Cases: Where Our Product Makes the Difference

    Research communities use our 3-Amino-4-Phenylbutyric Acid Hydrochloride for more than just synthetic experiments. Some customers apply it in neuropharmacological screens, chasing functional mimics of GABA receptor ligands. Others have fed it into high-throughput screening workflows, plugging the amino acid into peptide libraries or derivatizing it for custom small-molecule libraries.

    I've noticed contract research organizations increasingly demand not just a bulk product but detailed statements regarding residual solvents, heavy metal content, and origin traceability. That’s why our QA documentation emphasizes transparency: full chromatographic profiles, independent third-party purity reviews, and even degassing logs for every production lot. Rising scrutiny from regulatory and funding agencies now spills over to chemical precursors and intermediates, not just active pharmaceutical ingredients, driving us to new levels of traceability.

    Where other amino acid derivatives occasionally manage with less documentation or broader manufacturing tolerances, our users often provide this product directly to preclinical teams—meaning unpredictable impurities or batch-to-batch variability can waste months of work. We carry this responsibility seriously, creating an unbroken chain of custody documentation starting from sourced raw materials.

    Differences from Other Marketed Products

    The chemical supply space can get crowded with near-identical SKUs. But hands-on experience with 3-Amino-4-Phenylbutyric Acid Hydrochloride tells a different story. Many distributors list this hydrochloride at high concentrations or in bulk pack sizes without offering insight into impurity profiles, moisture variation, or lot-to-lot consistency. As an actual manufacturer, repeatability marks our difference.

    Some market products arrive with basic COAs that check off melting point, appearance, and basic purity by UV or simple titration. We’ve adapted our QA beyond this, deploying multi-method checks for each lot and making all analytical data available upfront. Solving for stability is another area where manufacturers define their approach. For example, we’ve developed packaging and storage protocols that hold up in both extended transit and cold-chain shipment; we routinely ship globally, so we’ve tailored logistics to avoid breakdown during customs hold-ups or seasonal temperature spikes.

    Customers who previously sourced from third-party repackagers often report variable color, caking, oxidation, or outright loss of activity upon reconstitution. That typically points to multiple transfer steps, less-than-ideal handling, or old stock pushed onto new customers. Since we run our own synthesis, purification, and packing lines, there’s no such guesswork about ‘real age’ or the journey a compound took before arriving at a researcher’s bench. Every lot that leaves our facility has been tested, sealed, and logged by our own team.

    Solutions to Common Challenges in Manufacturing

    Maintaining steady quality starts with strict control of incoming raw materials. Any variation in starting acid feedstocks — be that in grade, water content, or byproducts — will echo down the production line. Early on, we established direct sourcing relationships with raw material producers, so we aren’t at the mercy of inconsistent supply chains or hidden changes in upstream manufacturing.

    We learned to build in redundancy: second-source analytical verification, in-process impurity tracking, and standardized operator training for every production stage. Chemical synthesis demands respect for process controls; we limit variables not just for compliance, but because uncontrolled changes breed inconsistencies and waste. Automated drying equipment, controlled atmospheric glove boxes for sensitive handling, and calibrated glassware at every step form the less glamorous side of delivering this product right, but skipping these steps in the name of convenience has shown predictable negative outcomes.

    Every feedback cycle with clients helps shape our continuous process improvement. If a customer’s downstream analysis detects an unusual side-product, we hit the pause button, run full reanalysis, and tweak the synthesis or purification sequence as needed. Operating as a manufacturer puts us in the right position to solve root causes instead of patching symptoms. We retain batch samples for forensic comparisons so that any question, months later, about a particular lot’s performance leads directly back to our retained stocks and full batch log history.

    In the early days, stability trials sometimes caught us out when a formulation lab reported faint discoloration after a few months at room temperature. That prompted an overhaul in our desiccation and packaging routines. Every insight taken from these lived scenarios now shapes current production runs, so today’s customers start off with lessons learned from real-world practice instead of repeating old mistakes.

    Supporting Science, Not Just Satisfying Orders

    Demand for reproducibility across biological and chemical sciences continues to grow. For us, providing 3-Amino-4-Phenylbutyric Acid Hydrochloride means supporting those under-the-hood details that surface long after the initial sale. Fields like neurochemistry depend on trace-level consistency and predictable behavior. A compound that works slightly differently between batches can undermine years of lab work.

    We stay in the loop with project leads, regularly updating on any production or QC changes that could impact ongoing experiments. Maintaining close links, especially during long-term studies or supply programs for drug discovery, helps researchers adapt quickly to any subtle changes. This happens rarely, but when process tweaks must be made — whether for improving yield or tightening impurity thresholds — we notify customers in advance, making it a partnership rather than a mere transaction.

    Stories from the field reinforce the essential role a hands-on manufacturer can play. One CRO team we supply typically runs comparatives among multiple samples. Over several years, repeat orders for the same project delivered reproducible results, fending off concerns over shifting baseline activity. Feedback cycles drive further process refinement, ensuring batches from a year ago align with today’s output without unexplained anomalies.

    Continuous Improvement Grown from Direct Experience

    The chemical industry is flooded with commodities that shift through multiple hands. By owning the full manufacturing process and refusing to outsource sensitive stages, we can implement direct improvements as challenges roll in.

    If an impurity crops up—even if it falls beneath standard regulatory reporting levels—a quick turnaround time on root cause analysis puts control back into our hands. Over the years, that has meant rebuilding extraction steps, installing new HPLC standards, or investing in automated, humidity-controlled warehouses to prevent ambient moisture ingress. Every dollar spent in these directions yields a better experience and results for our customers, saving countless hours for research teams that don’t want to think about compound reliability.

    We work in an environment where regulatory expectations keep tightening, especially as end uses careen ever closer to pharmaceutical R&D, human health applications, and government-funded research. The only reasonable response is to get ahead of requirements, not to chase them. That means leading batch traceability, responsive customer service, and transparency above baseline norms. We provide all analytical spectra, raw data files, and batch environmental records, down to timestamps for every key operation.

    Looking Forward — Commitment to Scientific Progress

    Our aim with 3-Amino-4-Phenylbutyric Acid Hydrochloride goes past filling another product line. We see it as enabling tomorrow’s breakthroughs rather than just supporting today’s research. As expectations from scientific communities grow, the new standard isn’t just meeting purity thresholds but sharing enough detail to let every customer assess suitability for their own application.

    Instead of hiding behind broad-purpose claims, we keep improving our precise characterization, handling, and documentation. The journey to reach this point has wound through many small setbacks, process optimizations, customer collaborations, and lessons learned under the everyday reality of chemical manufacturing.

    By emphasizing rigorous quality, transparent data, and hands-on experience, we don’t just differentiate ourselves from resellers or bulk traders — we back every shipment with living knowledge and the assurance only a true manufacturer provides. Reliable 3-Amino-4-Phenylbutyric Acid Hydrochloride sets a foundation for confident science, batch after batch, year after year.