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HS Code |
353420 |
| Iupac Name | 2-hydroxy-4-aminobutanoic acid |
| Molecular Formula | C4H9NO3 |
| Molecular Weight | 119.12 g/mol |
| Cas Number | 924-49-2 |
| Appearance | White to off-white solid |
| Melting Point | 189-191°C (decomposition) |
| Solubility In Water | Soluble |
| Pka | Carboxyl: ~2.3; Amino: ~9.6 |
| Smiles | C(CN)C(O)C(=O)O |
| Inchi | InChI=1S/C4H9NO3/c5-2-1-3(6)4(7)8/h3,6H,1-2,5H2,(H,7,8) |
| Synonyms | 4-Amino-2-hydroxybutanoic acid; Homo-threonine |
| Storage Temperature | Store at 2-8°C |
| Hazard Statements | Generally regarded as low hazard |
As an accredited 2-Hydroxy-4-Amino Butanoic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | White HDPE bottle labeled "2-Hydroxy-4-Amino Butanoic Acid, 100g," tightly sealed, hazard symbols, lot number, and supplier details. |
| Shipping | 2-Hydroxy-4-Amino Butanoic Acid is shipped in tightly sealed, chemical-resistant containers to prevent moisture and contamination. Packages are clearly labeled according to regulatory guidelines. It is transported under ambient conditions unless otherwise specified. Ensure compliance with local, national, and international shipping regulations for chemical substances. Handle with appropriate personal protective equipment. |
| Storage | 2-Hydroxy-4-Amino Butanoic Acid should be stored in a tightly sealed container, protected from light and moisture. Store at a cool temperature (2–8°C recommended) in a well-ventilated, dry area away from incompatible substances such as strong oxidizers and acids. Handle using appropriate personal protective equipment to prevent inhalation and skin contact. Keep container tightly closed when not in use. |
Applications of 2-Hydroxy-4-Amino Butanoic Acid in Industrial ManufacturingAs a direct manufacturer of 2-Hydroxy-4-Amino Butanoic Acid, we support leading industries worldwide with material solutions precisely aligned to downstream requirements. Below, we detail specialized applications and operational protocols for key industrial sectors now adopting this acid in advanced processing. 1. Chiral Intermediate Production for Pharmaceutical SynthesisThis compound acts as a high-value chiral building block in the synthesis of non-proteinogenic amino acids, peptide mimetics, and select APIs. GMP pharmaceutical plants integrate it during asymmetric synthesis stages, leveraging its functional groups to introduce stereochemistry and tailor molecular frameworks. Appropriate documentation and process controls support traceability from incoming raw material to finished API batch, ensuring regulatory alignment and batch reproducibility. Typical formulation relies on controlled enantiomeric purity and carefully managed impurity profiles to conform to global submission requirements. Industry compliance standards
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2. Functional Component in Nutritional Supplement ManufacturingThis acid appears as a specialty ingredient in the targeted formulation of performance nutrition supplements, especially those designed for amino acid enrichment or metabolic modulation. Food-grade production lines blend it with other micronutrients under monitored environmental and contamination controls, ensuring strict adherence to regulations governing human consumption. Formulation specialists carefully calibrate inclusion based on daily intake limits and specific bioavailability goals, underpinning compliant product launches in global markets. Industry compliance standards
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3. Advanced Monomer in Biodegradable Polymer SynthesisIndustry-scale polymerization units employ this acid as a functional monomer for custom polyamide and polyester chains, fostering the production of bio-based, degradable plastics. Process engineers dose the acid at defined intervals into controlled, catalyst-assisted reactors, adjusting stoichiometry to shape mechanical and hydrolysis properties of the resultant polymer. Batch lot traceability and impurity controls assure compliance with eco-labeling and polymer food-contact statutes, while production documentation supports downstream certifications and product passports for sustainable supply chains. Industry compliance standards
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4. Building Block for Agrochemical Active Ingredient SynthesisChemical process units in agrochemical plants utilize this raw material as a nitrogenous precursor during active ingredient synthesis for select herbicides and plant growth modulators. Its amino and hydroxy structure facilitates ring-forming transformations and modifications tailored to crop protection chemistry. Feed conversion efficiency and intermediate purity receive close attention, with concurrent oversight of environmental release and waste byproduct protocols consistent with agricultural chemical authority requirements. Batch traceability documentation supports downstream stewardship and local product off-shore registrations where applicable. Industry compliance standards
Typical usage ratio
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Every chemist standing on the manufacturing floor knows how finicky some amino acid derivatives can be. With hundreds of compounds cycling through the reactors day in and day out, it’s rare to find one with as wide a practical reach as 2-Hydroxy-4-Amino Butanoic Acid. The chemical, sometimes known as an atypical hydroxy amino acid, developed a niche long before the word “custom synthesis” became a favorite phrase in the fine chemical sector.
In practice, the acid’s structure—bearing both a hydroxy and an amino group—opens doors for bioconjugations, pharmaceutical building blocks, and chiral auxiliaries. This compound carries the formula C4H9NO3, and, at the molecular level, that single extra hydroxy moiety can make life a lot easier for process chemists. Its presence can increase reactivity in a broad range of condensation and cyclization reactions. We have witnessed firsthand its effect in smoothening some of the toughest couplings that usually stall with straightforward amino acids.
Batch after batch, we produce 2-Hydroxy-4-Amino Butanoic Acid to meet demanding tolerances in purity and moisture content. Typical material, by our GC/MS and HPLC validation, achieves purity above 99% with a moisture profile controlled well below 0.2%. The acid’s crystalline form makes it easy to weigh and transfer, avoiding unpleasant clumping or inconvenient sticking inside bulk containers.
Producing this molecule at scale needs close monitoring of the pH through synthesis and isolation. Unlike simpler α or β amino acids, this compound’s hydroxy group reacts unpredictably under alkaline conditions, so you won’t see us relying on recipes that work for just any amino acid batch. Nuanced pH shifts and temperature holds, developed after countless pilot runs, make sure each lot aligns with the customer’s chromatograms, not just the catalog’s words.
As a manufacturer, we field plenty of calls from researchers interested in novel ligands or pharmaceutical starting points. 2-Hydroxy-4-Amino Butanoic Acid often enters those conversations because it acts as a reliable, highly functional intermediate for several key transformations.
Academic and industrial partners lean on this acid to develop peptide analogues with greater stability or tailored hydrophilicity. Certain research programs in neurochemistry have experimented with it as a mimic of GABA analogues. It’s not just a curiosity for those in advanced synthesis; those leading scale-up projects grab for it when they need a robust backbone that supports both hydrogen bonding and further functionalization.
From a practical view, the molecule slips easily into automated peptide synthesizers. Processes built around solid-phase peptide synthesis benefit from its clean coupling efficiency and low racemization risk, a distinction we have confirmed through dozens of scale-up runs. Researchers in chiral pool chemistry also appreciate its ability to serve as a precursor for more complex, high-value molecules. The hydroxy group on the chain helps direct regioselectivity, so complex rearrangements or substitutions find a firmer foundation.
We also see the acid used in specialized formulations. Some agricultural and veterinary researchers request this compound for use in nutrient blends and as a building block for newer generation plant growth regulators. Its stability and polarity help it dissolve in both water and polar organic solvents, unlike the more hydrophobic α-amino acids. Several food chemists, particularly in sports nutrition development, prefer the compound because of these characteristics, though it is important to note that regulatory acceptance for ingestion remains a complex issue in many jurisdictions.
Chemists familiar with the amino acid field often treat such compounds as a homogenous group, but chemistry on the plant floor isn’t so forgiving. – Use glutamic acid, glycine, or alanine in a reaction—results diverge fast as soon as side chain interactions come into play. In our experience, 2-Hydroxy-4-Amino Butanoic Acid can outperform these standard workhorses in specific transformations.
Compared to γ-aminobutyric acid—one of the more closely related structures—the hydroxy on the 2-carbon atom isn’t just a flowery addition. It acts as a handle for O-acylation, carbonate formation, or for carrying out asymmetric synthesis. This feature promotes more complex modifications and introduces options not accessible with basic amino acids.
We’ve watched scale-up projects falter because the material on hand pooled moisture or failed to dissolve beyond 10 g/L. Our crystalline 2-Hydroxy-4-Amino Butanoic Acid, with its consistently high purity, dissolves easily in water and methanol, avoiding those frustrating setbacks that can waste weeks of work. The acid’s relatively neutral odor and high melting point deliver extra convenience for operators who often have to deal with foul-smelling side chain amino acids and sticky syrups.
Another field where comparison matters is chiral purity. Many amino acid derivatives present racemization risks under standard peptide coupling conditions. Thanks to our controlled manufacturing approach—careful temperature regulation, use of optically pure starting materials, real-time monitoring for optical rotation—the risk of unwanted isomer formation drops to negligible levels. This quality assurance gives our customers a smoother path from gram to multi-ton synthesis.
Sourcing reliable raw materials sets the tone for each batch. Early on in our history, inconsistencies in aldehyde purity or ammonia solver grade caused unexplained color changes and yield drops. Today’s raw material intake program tracks every lot with spectral fingerprinting before entering the reactor. This traceability has prevented recurring headaches—your synthesis won’t stall from upstream surprises.
During synthesis, we steer the process through a tightly controlled, multi-stage reaction path. Strong attention goes into the hydroxy group protection during some transformations to prevent scrambling side-products that can haunt downstream purification. For most batches, a controlled-temperature acidic hydrolysis step liberates the amino group at just the right phase, allowing us to hit the target purity.
Solvent choice influences yield and crystallization. While greener solvents have received justified attention, our internal data still support traditional water-methanol systems for higher yield and cleaner filtration. We recapture solvent vapor and maintain containment through recovery systems—no corners are cut on waste management. Filtration and crystallization parameters run to tight tolerances based on historical batch analysis. Any process outlier triggers detailed QA review, not just a pass/fail slip.
Pelletizing and packaging hold equal weight. Granule size affects everything from dust formation in the warehouse to ease of use at the customer’s lot. Through upgraded centrifuge and drying equipment, we ensure even particle sizing and residue-free drying. Final containers—HDPE lined fiber drums—get sealed under nitrogen atmosphere, locking out moisture and preserving shelf life during long-haul shipping.
Each drum and small bag receives a batch-specific certificate that lists full spectral, chromatographic, and elemental analysis. In our manufacturing setting, random in-process checks set a high bar for reproducibility. We back each lot with full documentation—chromatograms, moisture content, and melting point data—so clients pursuing regulatory filings won’t have to chase paper trails.
In long-term storage, free-flowing product maintains integrity for over a year in stable, dry conditions. Some clients who store compounds for years appreciate our long track record of shipping product with the same purity and particle quality batch after batch. If storage conditions deviate or containers remain open for too long, we advise rechecking spectral and chromatographic consistency before resuming sensitive work.
We invite client facilities to visit and observe testing, since transparency forms the backbone of repeat business in this sector. Customer feedback loops supplement internal review cycles. If a new client’s chromatogram shows a minor impurity at a non-reported retention time, we feed that back into sourcing and process steps to ensure future batches match all performance expectations.
Manufacturers face growing scrutiny over the environmental cost and safety record of specialty chemicals. Over two decades in the industry, we have watched regulations tighten and stakeholder expectations rise. From effluent control to occupational exposure, our plant design incorporates rigorous safeguards: closed transfer systems, on-site effluent treatment, and continuous air filtration.
No waste leaves the facility untreated; all reaction mother liquors pass through advanced neutralization and biological digestion. Solid waste streams undergo hazardous materials assessment before off-site dispatch. Our high efficiency recovery units slash solvent use per kilogram of product. Not every manufacturer feels this pressure, but product stewardship is written into core planning and audited every year.
On the regulatory front, we’ve supported many clients through REACH registrations and US FDA preclinical filings. Each certificate of analysis aligns with international norms, and we regularly provide underlying data for technical files. If regulatory frameworks shift, internal compliance teams adapt labeling and reporting protocols, making the path from lab to market less fraught for downstream innovators.
Scaling specialty compounds from 100g drums to multi-ton reactors isn’t a matter of linear adjustment. Thermal gradients, mixing efficiencies, and solid–liquid separation behave differently at high volume. We’ve lost product to unexpected exotherms in jacketed vessels or filter blockages from batch-to-batch variance in crystal habit.
Overcoming these issues required investment in statistical process control and high-frequency data logging during every run. By compiling process data year over year, we adjusted not only the synthesis order but also the addition rates, agitation speeds, and hold times. Improvements in process analytical technology caught outliers before they became costly batch failures. Rarely do we rely on intuition alone—hard numbers and historical records drive decision-making.
Sometimes, seemingly minor changes—such as valve settings on the filter press or the angle of discharge spouts—have produced unexpected gains in throughput and powder uniformity. Open communication between process engineers and plant operators delivers more improvement than any piece of automation software. Everyone, from head of synthesis to pack-out laborers, feeds back their observations, so the system evolves organically over hundreds of campaigns.
Research organizations often ask us to modify specifications to fit short-lived application needs. For example, clients in bioconjugate development may request lower salt levels, while those focusing on solid formulations prefer a particular range of particle sizes. Working directly with brand owners, we offer custom crystallization and drying options, documented in mutually reviewed batch records. Nothing ships without customer sign-off.
We also routinely participate in joint process improvement projects. Recently, a major pharmaceutical partner outlined issues with side-product formation during coupling with hydrophobic peptide substrates. By adjusting the sequence and cooling phases of the 2-Hydroxy-4-Amino Butanoic Acid purification, we reduced trace impurity levels to non-detect. The outcome shaved weeks off their development timeline and established a specification pathway now standard for all peptide-grade product.
For larger custom runs, we dedicate specific reactor lines and follow isolation protocols that reduce cross-contamination risk. Our customers demand this level of specificity, and our plant flexibility makes us a ready partner on both routine and specialized contracts.
Having worked through hundreds of campaigns over decades, our team recognizes the direction users of 2-Hydroxy-4-Amino Butanoic Acid are heading. Projects in fields like advanced peptide therapeutics, enzyme modification, and asymmetric synthesis need higher cleanliness and traceability. The emphasis now falls less on commodity volume and more on reliability, transparency, and long-term technical partnership.
In recent years, we have expanded our validation capabilities. Mass spectrometry and NMR analysis now supplement traditional titration and TLC. By sharing full spectral libraries with partner organizations, we enable quicker troubleshooting and accelerate early-stage research. Feedback from pharmaceutical customers confirmed that rapid, open data sharing trimmed months off regulatory document preparation.
Adopting renewable feedstocks presents a longer-term transition. Pilot projects show that certain bio-based starting materials can produce comparable yields, though process economics and purity demand careful assessment. We engage with research institutes exploring sustainable synthesis, and internal R&D budgets support process adaptation in response to both legislative and market signals.
From operational standpoint, training the next generation of plant operators matters as much as developing the product itself. We hold skill-building workshops, promote knowledge transfer between teams, and encourage cross-functional collaboration. Operators who understand both the batch protocol and the underlying chemistry prove more likely to catch anomalies and suggest improvements. This human capital investment creates value beyond simple asset upgrades.
We recognize clients’ growing demand for vertical integration and single-source supply. End-to-end manufacturing control boosts confidence in material origin and process integrity. As a manufacturer, we facilitate traceability from incoming material intake to shipment tracking and retain samples for every lot.
Large-scale consumers appreciate visiting the plant floor, seeing the process equipment, and talking with operators who manage the reactors. This transparency builds genuinely collaborative relationships. By listening to client needs—whether on release criteria, tailored packaging, or on-demand documentation—we stay aligned with those at the forefront of fine chemical innovation.
From our perspective, handling 2-Hydroxy-4-Amino Butanoic Acid is not only about filling orders; it’s about refining each link in the supply chain so that researchers, formulators, and process engineers receive consistent, reliable material every time. Deep experience, rigorous tracking, and open communication form the backbone of our operation. The acid may be a specialty item in many catalogs, but for those of us who handle its production, it represents years of technical problem solving and a commitment to continuous improvement.
2-Hydroxy-4-Amino Butanoic Acid, handled at its source, stands apart in the myriad world of amino acid derivatives. Years of direct manufacturing experience shape every kilogram leaving our plant. The collaboration between production crew, clients, and technical teams ensures each batch supports work that advances pharmaceutical research, chemical synthesis, and specialized formulation development. The real difference lies not only in the chemical’s structure, but in the expertise and dedication invested into every production cycle.