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HS Code |
867234 |
| Chemical Name | 5-Hydroxytryptophan |
| Common Abbreviation | 5-HTP |
| Molecular Formula | C11H12N2O3 |
| Molar Mass | 220.23 g/mol |
| Source | Derived from the seeds of Griffonia simplicifolia |
| Uses | Dietary supplement for mood and sleep support |
| Mechanism Of Action | Precursor to serotonin (5-HT) in the brain |
| Physical Appearance | White crystalline powder |
| Solubility | Soluble in water |
| Cas Number | 56-69-9 |
As an accredited 5-Hydroxytryptophan factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A white, sealed plastic bottle labeled “5-Hydroxytryptophan, 100g,” featuring hazard symbols and a lot number, with a tamper-evident cap. |
| Shipping | 5-Hydroxytryptophan (5-HTP) is shipped in tightly sealed containers under cool, dry conditions to preserve stability and quality. Packaging complies with relevant chemical transport regulations. Standard shipping involves prompt dispatch with tracking, and temperature-controlled options are available upon request to ensure product integrity during transit. Safety documentation is included. |
| Storage | 5-Hydroxytryptophan (5-HTP) should be stored in a tightly sealed container, protected from light and moisture. Keep it at room temperature, ideally between 15–25°C (59–77°F), in a dry, well-ventilated area away from incompatible substances. Proper storage preserves its stability and prevents degradation. Avoid exposure to excessive heat and direct sunlight for optimal shelf life and safety. |
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Purity 99%: 5-Hydroxytryptophan with purity 99% is used in pharmaceutical formulations, where high purity ensures consistent therapeutic efficacy and safety. Particle size D90 <50 µm: 5-Hydroxytryptophan with particle size D90 <50 µm is used in tablet manufacturing, where uniform particle size improves compressibility and dissolution rate. Molecular weight 220.23 g/mol: 5-Hydroxytryptophan with molecular weight 220.23 g/mol is used in clinical research, where precise molecular weight supports accurate dosing calculations. Melting point 293°C: 5-Hydroxytryptophan with melting point 293°C is used in solid dosage development, where thermal stability during processing is ensured. Stability temperature up to 40°C: 5-Hydroxytryptophan with stability temperature up to 40°C is used in nutraceutical blends, where controlled storage conditions maintain product integrity. Assay ≥98.5%: 5-Hydroxytryptophan with assay ≥98.5% is used in dietary supplements, where high assay guarantees maximum active ingredient potency per unit dose. Solubility 10 mg/mL in water: 5-Hydroxytryptophan with solubility 10 mg/mL in water is used in liquid formulations, where enhanced solubility enables rapid bioavailability. Residual solvent <0.1%: 5-Hydroxytryptophan with residual solvent <0.1% is used in injectable preparations, where low solvent content complies with strict regulatory standards. Microbial limit <100 cfu/g: 5-Hydroxytryptophan with microbial limit <100 cfu/g is used in clinical nutrition products, where low microbial load reduces contamination risk. LOD (Loss on drying) ≤1.0%: 5-Hydroxytryptophan with LOD ≤1.0% is used in encapsulation processes, where moisture control enhances long-term product stability. |
Competitive 5-Hydroxytryptophan prices that fit your budget—flexible terms and customized quotes for every order.
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Producing 5-Hydroxytryptophan in-house means the responsibilities—and rewards—begin with us. Unlike the hustle of trading desks or the patchwork of intermediaries, every batch emerges under our direction and meets the same expectations we set for our own team, our families, and the research partners trusting our name. Our focus does not stop at lab-scale purity. In our experience, manufacturing 5-HTP to meet large-scale demand for supplement makers, pharmaceutical formulators, and functional food companies calls for vigilance across every phase: sourcing, extraction, purification, and packaging. Over years of refining equipment lines and fortune garnered from candid feedback in the field, we have learned not to treat 5-HTP as a commodity. It requires intention at every stage if it is to match the diverse purposes it supports.
The most common question we field at technical audits and industry trade shows centers on our 5-HTP’s specification: Why do our lots display such narrow assay variation, and what does this consistency mean for customers? Our standard model—the crystallized pure 5-Hydroxytryptophan with over 99% verified content—is the result of repeated cycles of solvent extraction and filtration, completed by state-of-the-art column purification. The raw Griffonia simplicifolia seeds, which serve as our starting material, pass through quarantine and pesticide screening before extraction ever begins. We never buy from speculative harvests or accept shipments missing their trace documentation. Technical managers in search of reliable batch-to-batch analytical results often cite this traceability as a source of confidence when building new formulations or reporting to regulatory authorities.
Not every producer walks this path. Years ago, we encountered product samples with inconsistent bioactive content, off-odors, and erratic particle sizes, revealing inadequate separation or careless blending. These kinds of inconsistencies can cause headaches for encapsulation, tableting, and finished product testing, often at the worst times. Our process aims to prevent these setbacks. Our careful fractionation helps us consistently exclude peak impurities—especially those derivatives which can emerge from incomplete conversion or residual plant alkaloids—ensuring high color and odor standards even before shipment.
Our work feels most meaningful once the product leaves our floor and enters practical use. Dietary supplement formulators frequently highlight the advantages of defining input quality with high-precision ingredients, and our 5-HTP became a preferred option for encapsulation because its flowability and fine, white crystalline form align with automated capsule fillers and high-speed tableting machines. In beverage and functional food research, we see nutrition groups selecting our 5-HTP for prototypes, knowing that uniform dispersion and shelf stability will translate directly to the final consumer’s experience. Pharmaceutical companies, operating under regional GMP rules, often ask us for supporting documentation on heavy metal residuals and solvent residues because they know the smallest off-spec result can shut down months of development. Our certificate of analysis always reflects exacting in-house and third-party tests. Often, procurement officers charter their purchasing strategy not just on measured purity, but also on the absence of chemical solvent traces—a tightrope we walk constantly by policing our own rinse protocols and verifying post-processing dryness.
5-HTP, unlike synthetic precursors more commonly found in bulk amino acid markets, requires a tight grip on raw material selection. Synthetic alternatives may show similar maximum purity, but they risk carrying forward trace contaminants from their starting chemicals. In our own internal side-by-side QA runs, the naturally derived material consistently yields lower aggregate impurity counts and less regional batch-to-batch variation. Natural-origin 5-HTP also aligns more squarely with consumer preferences in many markets, fitting current demand for plant-based and minimally processed actives.
We don’t craft 5-HTP in a vacuum. Markets shift as consumer needs and regulatory maps change. In some countries, 5-HTP enters the market as a dietary ingredient, while in others it steps under stricter medical oversight, subject to exhaustive quality and purity testing. Meeting diverse compliance codes requires honesty about both process capability and batch accountability. As a manufacturer, we house archived retention samples and reference chromatograms for all outgoings, empowering compliance officers and importers to verify that shipments stay mapped back to unique, traceable runs.
Unexpected changes in regulation or import policy pose less of a threat when you know precisely what sits in each drum, right down to the microgram. Several years ago we adapted our analytical panel to screen for a broader panel of naturally co-extracted alkaloids after new requirements arose from European food safety authorities. Since then, we have kept our documentation dynamic, ensuring it reflects the evolving demands of global partners—whether a health authority in Brazil requests a declaration of drought-resistance farming practices, or a North American auditor wants genotoxic impurity clearance on each lot.
Our research group constantly explores small improvements, often based on lessons learned in problem-solving. Adaptive extraction protocols allow us to address seasonal differences in seed harvests—a factor we once ignored, to our own loss—in the content of 5-HTP precursor compounds. We maintain direct dialogue with growers and in-country agronomists, supporting best practices that lead to richer, more reliable inputs. At the same time, we hunt for opportunities to reduce solvent usage during extraction and switch wherever possible to green, food-safe alternatives. These shifts have contributed to our ability to offer a product with reduced chemical load, pleasing both regulatory reviewers and progressive consumer brands.
One of the challenges we took on involves addressing the presence of unwanted trace substances such as “peak X,” a mysterious compound first reported by Japanese researchers decades ago that caused widespread scrutiny of 5-HTP supplementation. Rather than treat this merely as an issue for paperwork, we integrated methodical UV and HPLC screening into our process. Production runs that display any hint of this or other non-target substances halt for deeper review or reprocessing. By sharing our comprehensive screening data, we enable transparency and confidence across the entire downstream supply chain.
Manufacturing 5-HTP may look straightforward in a catalog listing, but direct experience shows clear differences that matter for end-users. Many widely marketed products outsource extraction or blend material from multiple origins, occasionally sacrificing purity or transparency for price. We run all steps at our own site: procurement, extraction, isolation, drying, milling, and packing. This control means we can commit to tight purity intervals and robust documentation, supporting audit checks and batch recalls with direct, on-site evidence, not slow international emails.
Production scale matters as well. Small-batch runs sometimes show strong analytical data on a micro level. Scaling those up can lead to bottlenecks, contamination, or inconsistent particle profile unless each increase receives its own validation. We have invested heavily in pilot-scale testing and continuous process checks, closing the feedback loop between our lab chemists and the floor manufacturing crew. Longstanding partners often comment on the low lot-to-lot deviation and clear labeling they receive, compared to the headaches they met with third-party blenders.
Another key differentiator involves moisture and stability. By employing vacuum drying and nitrogen packaging, we shield each batch from hydrolytic breakdown and oxidative loss, extending shelf life and protecting the active content as it makes its journey from warehouse to encapsulation line. Our experience confirms that batches shipped in less controlled packaging often reach final production lines disappointing their recipients, who then manage costly claims and delays. Our protocols keep the product reliable across widely different climate zones.
The ultimate proof lies in the real-life applications and feedback from those working with our product. Pharmaceutical developers scrutinize impurity profiles and demand substantiated documentation of cleaning and cross-contamination risk, which we supply as a matter of routine. Food technologists appreciate the close particle sizing and flow properties, simplifying formulation with protein isolates, hydrocolloids, or micronutrient blends. Supplement brands want solid evidence of both purity and traceability, as claims drive consumer confidence and support regulatory defense if challenged. We support formula changes, pilot study requests, and new label claims with accessible in-house team members, rather than sending our clients to generic web support portals.
Safety is embedded in every decision. Employees on the production floor train in hazard recognition and response, and our production managers double-check every lot before release, not just with automated readouts but also with hands-on inspections—checking for discoloration, scent, or particulate contamination by eye. This dedication runs through our hiring, training, and ongoing process review cycles. In real terms, users gain a 5-HTP product that represents the summed vigilance of a team who care about safety and outcome, from seed to sealed drum.
Testing forms the backbone of our process. Every batch, whether intended for export or domestic partners, undergoes comprehensive HPLC analysis confirming ≥99% 5-HTP by weight, alongside standard microbiological and heavy metal screens. We maintain records for each technical parameter, supporting our claims and enabling end-users’ own QA staff to cross-validate outcomes. In our years of manufacturing, we have encountered and troubleshot nearly every conceivable deviation: unseasonal seed variation, micro-batch contamination, shipment delays, moisture migration, and analytical drift. Each challenge reinforced the importance of documentation, verification, and continuous review.
While some suppliers chase rising demand by stretching lead times or bundling products of varying ages, we keep our scheduling transparent and avoid over-promising. Making clear timelines and dependable release dates matter for every link in the supply chain. In our experience, certainty equals value far beyond price benchmarks alone.
Looking forward, the landscape for 5-HTP continues to evolve. Research teams seek higher potency materials for novel applications, while regulatory authorities heighten their scrutiny. The plant sources themselves shift as climate pressures alter harvest cycles. Our commitment remains rooted in hands-on, responsible production that values transparency, process improvement, and a real backstop for every claim. We draw on our history—both of hard-won successes and lessons from the rare setbacks—to negotiate the future with clear-eyed purpose.
At its heart, creating 5-Hydroxytryptophan that end-users can trust means much more than ticking boxes or posting certificates. It means standing accountable for every kilogram shipped and supporting outcomes, whether it’s in a research paper, a nutritional label, or a finished bag of supplement. Each batch is a chance to demonstrate not just technical capability, but a care that reflects the standards we set for ourselves.
The sense of pride we take in every lot does not just stem from producing an ingredient—it comes from the knowledge that operators in labs, food plants, and research centers worldwide rely on the diligence, transparency, and technical strength built into our process. The story of our 5-HTP is still unfolding, but at every step, we anchor our approach in accuracy, integrity, and the drive for solutions that reach beyond the expected.