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HS Code |
666592 |
| Cas Number | 4479-86-9 |
| Molecular Formula | C9H11NO2S |
| Molecular Weight | 197.25 g/mol |
| Iupac Name | 2-amino-3-(2-thienyl)propanoic acid |
| Synonyms | L-2-Thienylalanine, (S)-2-Amino-3-(2-thienyl)propanoic acid |
| Appearance | White to off-white crystalline powder |
| Melting Point | 261-264 °C (dec.) |
| Solubility | Soluble in water |
| Optical Activity | [α]20/D +20° (c=1, H2O) |
| Storage Temperature | 2-8°C |
As an accredited L-2-Thienylalanine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | L-2-Thienylalanine, 25g, supplied in a clear, sealed glass bottle with a screw cap, labeled with hazard and product information. |
| Shipping | L-2-Thienylalanine is shipped in tightly sealed containers under ambient conditions, protected from moisture and light. The package is clearly labeled with relevant hazard information and handled in accordance with standard regulations for non-hazardous chemicals. Transportation complies with applicable local and international shipping guidelines for laboratory reagents. |
| Storage | L-2-Thienylalanine should be stored in a tightly sealed container, protected from light and moisture. Keep it in a cool, dry, and well-ventilated area, ideally at 2–8°C (refrigerated conditions). Ensure the storage area is free from incompatible substances, such as strong oxidizing agents. Proper labeling and safety data sheet (SDS) accessibility are recommended for safe handling and storage. |
Applications of L-2-Thienylalanine in Industrial ManufacturingL-2-Thienylalanine serves as a specialized non-proteinogenic amino acid with distinct thienyl functionality, supporting multiple technical sectors through its tailored reactivity and chiral structure. As an experienced chemical raw material manufacturer, we supply this compound to demanding downstream industries that require rigorous compliance, tightly controlled formulation integration, and reliable traceability. 1. Pharmaceutical Intermediates for API SynthesisPharmaceutical manufacturers utilize L-2-Thienylalanine as a critical chiral building block during the synthesis of speciality active pharmaceutical ingredients, especially in peptidomimetic frameworks, small molecule drugs, and certain anti-infective candidates. The material enters multi-step organic synthesis routes where the thienyl ring and chiral amino acid backbone enable selective coupling and intermediate formation. Strict traceability and pharmaceutical-grade handling apply throughout all stages to ensure final API integrity. Industry compliance standards
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2. Advanced Peptide Synthesis for Research and DiagnosticsSpecialty peptide manufacturers and CROs apply L-2-Thienylalanine in the assembly of custom sequence peptides for research antibodies, bioassay substrates, and reference standards. Its aromatic thienyl group introduces unique functional handles into diagnostic probes or screening libraries, supporting structure–activity work and protein interaction studies. Material handling demands precise batch-to-batch reproducibility and full analytical traceability. Industry compliance standards
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3. Building Block in Agrochemical R&DL-2-Thienylalanine supports downstream innovation in crop protection through usage as a precursor for developing thienyl-modified lead compounds in agrochemical research. Synthetic chemists incorporate this compound to modulate bioactivity, improve selectivity, or introduce new binding sites during lead optimization workflows. Agrochemical discovery utilizes multi-step synthesis routes and systematic analytical verification of intermediates. Industry compliance standards
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4. Chiral Intermediate for Fine Chemical SynthesisProducers of specialty fine chemicals rely on L-2-Thienylalanine to introduce both stereochemical complexity and aromaticity within advanced intermediates, especially for industries targeting custom flavors, specialty coatings, or electronic materials precursors. The material’s unique chiral and aromatic combination enables building precise functional groups that define subsequent performance attributes in final goods. Industry compliance standards
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L-2-Thienylalanine has become a familiar name in our facility. This beta-amino acid, recognizable by its sulfur-containing thiophene ring, comes off the line with its own personality—stability, a slightly earthy aroma, and a structure that opens doors to unique applications. Over the years, our experience producing L-2-Thienylalanine has shown us why the subtleties of amino acid construction matter so much to researchers and chemists. Delivering reliable purity, batch after batch, means more than chemical analysis; it reflects how we manage every reaction step, how we handle materials, and how closely we track feedback from partners deep in medicinal chemistry, peptide design, and advanced materials.
Producing L-2-Thienylalanine calls for solid understanding and careful hands-on work. Our team draws on years of hands-on synthesis, scaling, and troubleshooting. The molecule, with its thiophene ring attached to the alpha carbon of alanine, challenges classic peptide synthesis conventions. Sulfur brings reactivity to the game. In the plant, our production routes avoid over-oxidation, manage moisture exposure, and reject cheap shortcuts. The isolation and crystallization phases demand sharp attention, especially as by-products can sneak in and purity swings wildly without close supervision. This way, we bring forward an amino acid that fits in snugly with high-precision research, not just industrial bulk chemistry.
Our model for L-2-Thienylalanine includes careful control over chirality, focusing on the L-isomer. Racemization chips away at yields and undermines functional outcomes in pharmaceuticals. We address this by intentionally controlling temperature profiles and opt for proven, gentle reagents rather than aggressive bases or acids. The end result—a crystalline, free-flowing powder—displays a purity often 99% or greater by HPLC, keeping impurities and D-isomer contamination well below recognized thresholds for fine chemical work.
Specifications are written on paper, but the real world rarely follows that script exactly. We have seen how even tiny shifts in starting material quality influence the finished batch. Our L-2-Thienylalanine walks out in lots that measure up across the board: white to off-white crystalline powder, optical rotation matching reference standards, single sharp peak on the chromatogram, and low moisture content. Ash, heavy metals, and residual solvents fall below tough internal standards. Over the past decade, our on-site analytical team has tuned methods around feedback from customers running NMR, MS, and peptide sequencing—so issues get solved before leaving the site.
Particle size often comes up in conversations with customers. Some peptide scientists noted clogging or dissolution delays in automated synthesizers using other suppliers’ material. With this in mind, we’ve refined grinding and sieving steps to deliver a consistent fine powder without excessive fines. This simple change, born from a direct call with a research group running long peptide chains, reduces wasted runs and slashes downtime.
Water content leads to several headaches in coupling chemistry. We manage risk by maintaining storage below 4°C and use desiccants in sealed drums. These steps matter less to a catalog trader and more to those who use this compound at scale, where each failed coupling run represents real time lost and true cost.
Researchers approach us because L-2-Thienylalanine does something ordinary alanine or phenylalanine cannot. Its thiophene moiety stands in for phenyl rings in structure-activity studies. This subtle switch can improve binding selectivity and tweak metabolic vulnerability in lead compounds. Medicinal chemists regularly ask us to keep the sulfur ring “pristine”—they fear oxidation, so we work with oxygen-free packaging and check for sulfoxide or sulfone formation as a matter of course.
We have supplied lots earmarked for protease inhibitor development. In our experience, the sulfur offers routes to tunable ligands—a mechanism to extend half-lives or sidestep metabolic breakdown. Teams working in agrochemical design and material sciences also reach for our compound to find new architectures in polymer research, thanks to the sulfur heterocycle’s electronic character. On occasion, we’ve seen creative use as a “handle” for subsequent functionalization—something you can’t quickly pull off with plain, unsubstituted amino acids.
Academic and industrial labs use our product to build custom peptides, exploring resistance to enzymatic degradation. Veterinary researchers have sometimes chosen L-2-Thienylalanine over more common analogues to probe species-specific metabolic pathways. In every case, there is a technical reason to choose this molecule, further justified by clear analytical proof that our batches do not introduce unknowns—no undeclared hydrazine, no ambiguous byproducts, no masking agents in the blend.
From time to time, novel bioconjugation approaches land on our desk. A recent project required the introduction of a sulfur ring for downstream click chemistry. Our technical support team held direct conversations on dosing, optimal storage, and purification. Collaborating this closely, we ensure users get the performance and transparency needed for sensitive innovations.
L-2-Thienylalanine departs from standard amino acids because of its heteroaromatic ring. In peptide chains, it alters backbone flexibility and local electronic distribution. Phenylalanine and tryptophan, although aromatic, remain far less reactive and lack sulfur’s unique impact. The thiophene ring introduces new conformational dynamics, which sparks interest for building better enzyme inhibitors and peptide therapeutics.
We have run side-by-side trials in peptide coupling, substituting L-2-Thienylalanine for phenylalanine and tyrosine. The shift in reactivity is clear—coupling times adjust, and yields fluctuate unless protocols address the sulfur. Our insight from monitoring hundreds of syntheses is that the presence of sulfur not only changes final molecule performance, but it can also imprint legacy reactivity into reaction vessels and lines. It pays to rinse glassware thoroughly and to monitor for trace oxidation products. Any chemical producer ignoring these lessons risks unpleasant surprises for the next downstream user.
Comparing to unnatural isomers or functionalized analogues, L-2-Thienylalanine keeps an edge in ease of peptide bond formation and predictable crystallization. Its model form under standard conditions remains stable for months under inert gas, without pancaking, discoloration, or clumping. We log weights and perform spot checks for loss on drying every quarter, and retain samples for five years to support any analytical queries post-delivery.
Some labs chase after racemic or D-form thienylalanines for chiral probes. We do not blend, dilute, or mask our product—what ships out is the L-isomer at full declared strength. Peptide pharmacologists that have trialed both forms in parallel often find activity profiles diverge sharply; D-isomers can completely blunt activity in biological assays. We keep impurity levels in D-form below 0.5% by chiral HPLC, preventing unexpected off-target results for our customers.
Several years ago, a biotech partner flagged elevated micro-impurity in an early lot. That audit reshaped how we approach solvent recovery and requalification of starting thiophene. Such moments prove that constant refinement, not blind adherence to protocols, builds better product. Our technical and QA teams developed a new filtration system and documented protocols for intermediate sampling, tightening our impurity profile. We didn’t need an outside auditor to tell us where things fell short—operators, analysts, and end-users provided real stories that guide each technical decision.
On the operations side, we process feedback into action. If a late batch developed a missed oxidation spot, we not only replaced that order but tracked the source—oxygen ingress during a facility-wide power cut. A backup generator, air purge system, and improved drum sealing procedures now keep these problems away. Users in synthesizer runs benefit directly—consistent coupling reactions, cleaner peptides, and no surprise “ghost” peaks in LC-MS.
Direct conversations with end-users improve more than our chemistry. A peptide design shop mentioned their glassware held sulfur odor for weeks after a particularly large run. This observation let us explore cleaning solvents and adjust internal recommendations. We note that not all manufacturers possess this experience—traders may copy specifications, but rarely carry insight from a week’s worth of troubleshooting residue stuck to borosilicate.
Technical documentation grows in strength because of these partnerships. Real photos of batches, spectroscopic traces, and recommendations for handling flow through our digital channels. Our sales team draws answers from the chemists and operators who pull levers and read dials, not just marketing collateral.
Consistent batches drive reputation in the fine chemical world. We run pilot lots for every change in raw material supplier, no matter the price savings. This stubbornness, learned from an old failed batch long ago, now sets our work apart from less careful producers. Every drum of L-2-Thienylalanine gets checked for color, UV absorbance, and smell—in addition to the routine chromatographic and spectroscopic screens. If one shift operator thinks a batch looks off, we halt packaging until QA clears it. This hands-on streak across our whole staff keeps surprises scarce for our customers.
As scale varies, challenges surface. Small, research-grade batches often carry a slightly different impurity signature than bulk chemical runs—sometimes a trace of parent thiophene, minor over-reduction, or very rarely, a low-mass by-product. We share these findings openly with advanced users who need full transparency for regulatory filings or patent applications. Our openness stems from a simple truth—the long-term relationships that define our business grow from honesty, not from making traces disappear in paperwork.
Several pharmaceutical partners have tested our lots under their own rigorous screens. Reports often flag sub-ppm impurities uncatchable by classic TLC or routine HPLC. Instead of dodging responsibility, our R&D team investigates, running spiked controls, LC-MS checks, and expansion of reference libraries. We keep every set of analysis on file, and update our controls so that even unusual contaminants, detected once in a thousand kilos, fall under routine surveillance going forward.
Procurement managers sometimes overlook the trailing paperwork behind each drum of a research amino acid. Regulatory changes in Europe, North America, and parts of Asia impact how L-2-Thienylalanine gets labeled, logged, and tracked. We update labeling and shipping manifests regularly rather than get caught by surprise inspections or customs reviews. Material safety data sheets undergo annual review by the same scientists who operate the reactors, meaning theoretical hazards never disconnect from the real process environment.
Documentation extends beyond compliance. Certificates of analysis, spectrum printouts, and batch records live on our intranet and can be provided to clients without delay. New requests around chain-of-custody and raw material sourcing are common—especially from global pharma and food developers. Traceability starts with vetting suppliers for feedstocks, down to the lot numbers and temperature logs on incoming barrels. Every bottle of L-2-Thienylalanine shipped includes QR-coded batch histories, so technical recipients in any country can pull raw data during their own QC checks.
We support partners handling strict regulatory audits by providing historical impurity tracking, lot-specific stability data, and detailed handling recommendations honed from years of internal use. This level of access and attention arms our customers with what they need to clear their own technical and regulatory hurdles—without delays or guesswork. It often surprises newcomers to see how much paperwork and behind-the-scenes discipline keeps a modest kilogram of amino acid compliant across borders. But years of practice have taught us that well-organized records mean fewer headaches, faster clearances, and happier collaborators.
Every year brings fresh curveballs. Changes in raw material prices sometimes make supply tight, but we keep strategic reserves and long-term contracts to buffer customers from sudden outages. Staff training keeps skills fresh, ready for new equipment, and adapted for changing safety standards. We invest in regular fire and environmental drills, building habits so lapses don’t creep in when operators get busy.
Disposal and waste management raise special challenges. The sulfur content of L-2-Thienylalanine means spent mother liquors and wash-downs need special handling to avoid downstream pollution. We maintain records of wastewater analyses, conduct third-party audits on our discharge, and look for tweaks to lower environmental impact year after year. Green chemistry remains more than a slogan. R&D searches for optimized stoichiometries, recycling solvents where possible, and reducing energy needs for purification.
Price pressures come and go, but quality never drops. Shortcuts in filtration, energy savings by switching to questionable solvents, or skimping on purification lead to trouble every time. Years watching product recalls from imported materials teach us the cost of cutting corners doesn’t only show up in dollars and cents—it echoes in brand reputation, customer retention, and the trust built after delivering that first reliable drum.
Our technical team meets regularly to review recent literature, patent filings, and feedback from leading peptide houses. L-2-Thienylalanine does more than fill a slot in a catalog; it prompts questions: how can the sulfur be leveraged for click-style chemistry, radiolabel infusion, or pathway-specific probes in advanced medical diagnostics? Every idea worked out in the plant either scales to support innovation or dies in the pilot plant before it can disrupt a customer’s timeline.
We share samples and collaborate on method development. New fields in radiopharmaceuticals, custom biomaterials, and next-gen agrochemicals prompted quality upgrades not just for reputation, but out of practical necessity. We invest in small-batch pilot lines geared for rapid iteration, so emerging startups get responsive support, not just “off-the-shelf” answers from a distant supplier.
A chemist once asked why L-2-Thienylalanine comes at a premium compared with phenylalanine or other simple aromatic acids. Twenty years in the field tells us why: sulfur chemistry walks hand-in-hand with reactivity, purity risk, and the delicacies of managing oxygen and trace metals. Every controlled environment we maintain comes from lessons given by failed reactions, lost product, and hustling to salvage batches flagged after hours by a line operator’s nose.
Distributors may carry bulk amino acids labeled for technical use, but the difference shows in side-by-side application: lower-level impurities translate to clean MS spectra, clear NMR assignments, and confident regulatory filings. We respect other manufacturers for their craft but stake our reputation on deep experience and responsiveness—the sort that answers “why did this batch smell different?” with someone ready to walk the floor at 6 AM, rather than an auto-response from a contact center.
Longevity, in our view, comes from sweat equity and always aiming for technical and regulatory betterment, batch after batch. Our history proves that success lies not only in hitting targets, but in investigating every deviation, sharing data, and working alongside innovators from global pharma, startups, and university labs alike.
The future of L-2-Thienylalanine calls for both innovation and steadfast commitment to proven practice. More industries are discovering what this sulfur-rich amino acid can bring to their platforms. Our plant hosts regular visits from R&D teams around the world, looking for technical insight, real-time troubleshooting, and guidance on process improvement. Each collaboration brings new questions about L-2-Thienylalanine's deeper chemical possibilities—from new solid-phase syntheses to the latest in controlled-release mechanics.
We look forward to where this journey goes. Decades of hands-on chemistry, voice-of-customer improvements, and openness in operation drive us to reach for cleaner product, safer processes, and more versatile applications. In a field where details count and each batch carries the fingerprint of those who made it, we take pride in supplying L-2-Thienylalanine not just as a product, but as a partner in the progress of science.