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HS Code |
891906 |
| Chemical Name | N-(2'-Cyano[1,1'-biphenyl]-4-ylmethyl)-L-valine methyl ester hydrochloride |
| Cas Number | 1336276-39-3 |
| Molecular Formula | C20H22N2O2·HCl |
| Molecular Weight | 360.87 g/mol |
| Appearance | White to off-white solid |
| Purity | Typically ≥98% (varies by supplier) |
| Solubility | Soluble in DMSO, methanol |
| Storage Temperature | 2-8°C (refrigerated) |
| Synonyms | N-(4'-Methylaminomethyl-biphenyl-2-carbonitrile)-L-valine methyl ester hydrochloride |
| Smiles | CC(C)[C@@H](NCc1ccc(cc1)c2ccccc2C#N)C(=O)OC.Cl |
As an accredited N-(2'-Cyano[1,1'-biphenyl]-4-ylmethyl)-L-valine methyl ester hydrochloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 25 grams of **N-(2'-Cyano[1,1'-biphenyl]-4-ylmethyl)-L-valine methyl ester hydrochloride** provided in a sealed amber glass bottle with labeling. |
| Shipping | N-(2'-Cyano[1,1'-biphenyl]-4-ylmethyl)-L-valine methyl ester hydrochloride is shipped in a tightly sealed container under ambient or cool conditions, protected from moisture, light, and heat. Proper chemical labeling and documentation are included. Shipping complies with relevant regulations for safe transport of laboratory chemicals. |
| Storage | Store **N-(2'-Cyano[1,1'-biphenyl]-4-ylmethyl)-L-valine methyl ester hydrochloride** in a tightly sealed container, protected from moisture and light, in a cool, dry, and well-ventilated area. Keep at 2-8°C (refrigerator) unless otherwise specified. Avoid exposure to incompatible substances such as strong oxidizers, and ensure proper labeling and access control to prevent unauthorized handling. |
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Purity 99%: N-(2'-Cyano[1,1'-biphenyl]-4-ylmethyl)-L-valine methyl ester hydrochloride with 99% purity is used in pharmaceutical synthesis, where it ensures high yield and minimal byproduct formation. Melting Point 178-182°C: N-(2'-Cyano[1,1'-biphenyl]-4-ylmethyl)-L-valine methyl ester hydrochloride with a melting point of 178-182°C is used in solid-state formulation studies, where it provides thermal stability during processing. Molecular Weight 344.82 g/mol: N-(2'-Cyano[1,1'-biphenyl]-4-ylmethyl)-L-valine methyl ester hydrochloride with a molecular weight of 344.82 g/mol is used in analytical method calibration, where it allows for precise quantification in LC-MS analysis. Hydrochloride Salt Form: N-(2'-Cyano[1,1'-biphenyl]-4-ylmethyl)-L-valine methyl ester hydrochloride in hydrochloride salt form is used in formulation development, where it enhances solubility in aqueous drug delivery systems. Stability Temperature up to 80°C: N-(2'-Cyano[1,1'-biphenyl]-4-ylmethyl)-L-valine methyl ester hydrochloride stable up to 80°C is used in accelerated stability testing, where it maintains chemical integrity under stress conditions. Particle Size <50 µm: N-(2'-Cyano[1,1'-biphenyl]-4-ylmethyl)-L-valine methyl ester hydrochloride with particle size below 50 µm is used in tablet manufacturing, where it enables uniform blending and dosing accuracy. Enantiomeric Excess >98%: N-(2'-Cyano[1,1'-biphenyl]-4-ylmethyl)-L-valine methyl ester hydrochloride with enantiomeric excess above 98% is used in chiral drug development, where it guarantees stereochemical consistency for bioactivity studies. |
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We have spent years in the fine chemical sector, seeing trends shift and requirements tighten with every new round of research breakthroughs. Each batch we produce tells us something new about process intricacies and the value of starting materials that perform predictably. The molecule N-(2'-Cyano[1,1'-biphenyl]-4-ylmethyl)-L-valine methyl ester hydrochloride arrived in our production pipeline not because it’s just one more raw material on a catalog, but from consistent demand in targeted pharmaceutical and synthetic research directions. Our teams developed expertise in this compound, refining methods and optimizing output to ensure actual researchers and process engineers can rely on the substance from the first gram to full-scale batches.
We supply this compound in a fine crystalline powder, with stringent specifications for purity, particle size, and moisture content. We have found pure grades—verified by HPLC and detailed impurity profiling—hold up much better in both screening studies and scale-up reactions. Consistency shows up as less rework and reduced surprises during QC, avoiding headaches that come with material from less disciplined syntheses. Specifications for N-(2'-Cyano[1,1'-biphenyl]-4-ylmethyl)-L-valine methyl ester hydrochloride have been shaped by biopharma partners who need reliable performance in transition-metal-catalyzed transformations, asymmetric synthesis, and API intermediate development.
Our batches consistently meet a purity threshold above 99%, measured by validated analytical methods. Typical single-lot moisture remains under 0.2% w/w, since we have learned low moisture directly assists both reaction rates and material handling during scale-up. Particle size distribution comes dialed in for straightforward dissolution and metering, eliminating the delays that happen with coarser grinds or sticky, hygroscopic residue. The hydrochloride salt version, which our teams optimized, stands up well to ambient conditions during storage and shipping—performance we value as much as our customers do, because it means less re-qualification and fewer hold-ups on delivery.
Through repeated campaigns, we’ve developed stepwise protocols that keep hazardous intermediates under tight control. Skilled technicians oversee each workup, and our in-house chemists solve for bottlenecks with practical tweaks. We source building blocks only from audited suppliers since the quality at this stage turns out to be make-or-break for downstream excellence. Our reactors are set up to manage exotherms and minimize batch-to-batch deviation. Solvent recovery gets factored in to keep environmental impact and cost within reason. Every release passes full spectroscopic and chromatographic analysis: NMR, IR, LC-MS, and HPLC profiles land in a digital archive for traceability.
Over time, we observed that the stereochemistry of the L-valine methyl ester fragment requires close attention, especially in the presence of bases or at elevated temperatures. Early deviations in side chain integrity led us to modify conditions, selecting milder bases and lower reaction temperatures, extending cycle time but greatly increasing ratio of desired product. Achieving and preserving the chiral purity has repeatedly proven to be key for downstream application in chiral ligand synthesis or lead compound modification. In this matter, we never cut corners—we have seen enough false economies in earlier years from traders and resellers to understand that shortcuts here cost much more than they might appear.
Demand for N-(2'-Cyano[1,1'-biphenyl]-4-ylmethyl)-L-valine methyl ester hydrochloride tracks with medicinal chemistry programs exploring novel kinase inhibitors, peptide mimetics, and advanced lead optimization strategies. Over the last few years, several teams working on small molecule scaffolds have landed on the biphenyl cyano motif combined with stereochemically defined amino acid esters as offering improved binding and selectivity profiles in preclinical screens. Our clients bring us real-time feedback about solubility issues or limitations in prior intermediates. We respond with batches adjusted for optimal physical properties and quality standardization, so their screens move forward without interruption.
This compound regularly serves as a core intermediate for Suzuki and Negishi coupling reactions—a role that depends on unambiguous structural integrity. The cyano handle, in particular, offers a launchpad for amide coupling, reduction, or further functionalization. Process development chemists have told us directly that reliable supply avoids the need for repeated prep runs in their own labs, saving weeks during new target development cycles. In this way, what we do on the manufacturing side shows up as greater project velocity in medicinal chemistry companies and university research labs.
Manufacturers often try to compare this material to structurally related biphenyl or amino acid derivatives. The difference comes down to the unique pairing of the 2'-cyano biphenyl motif with L-valine methyl ester in a hydrochloride salt. Some will try valine tert-butyl ester analogs or use other amino acid fragments altogether, but our experience shows L-valine methyl ester brings a balance between lipophilicity and functional group tolerance that supports both modern SNAr transformations and late-stage diversification.
Salts other than hydrochloride can often complicate isolation and handling. For instance, using sodium or potassium salts has led to caking, slower dissolution, and frequent downstream precipitation or filter clogging. We initially ran trials with different salt forms before settling on the hydrochloride—its performance outstripped the others for shelf life, shipment, and process compatibility. The hydrochloride version also makes it easier to bring material into aqueous workups without unintended hydrolysis or side reactions.
Other suppliers might sell partially characterized lots or alternate batches with different counterions, which creates headaches on transfer and scale-up. At our facility, each batch gets the same analytical sign-off, and we match every outgoing shipment with a reference chromatogram and full IR/NMR spectra. This policy cuts troubleshooting for you down the line since the material you ordered six months ago will match what you need to substitute or reorder today.
Every package leaves our site double-sealed, with desiccant packs included for longer transits. As we’ve seen, ignoring moisture control leads to rapid acid uptake from air, dulling material quality before it even reaches the end user. For ambient and cold storage, we advise keeping sealed bags in a low-humidity cabinet—simple precautions learned from real-life slips, not theory. Reactivity with nucleophiles or strong bases where the biphenyl cyano group can play a role in side reactions means we suggest careful monitoring during mix stages. It sounds basic, but the cost of one failed reaction from overlooked impurities or incorrect storage habits always outweighs the extra effort up front.
Most research teams receive our material for direct use in palladium- or nickel-catalyzed cross-couplings. Dissolution in common polar aprotic solvents works without fuss due to the fine powder format and low residual water. In solid phase peptide synthesis, the L-valine methyl ester backbone maintains integrity even in prolonged couplings, as long as base strength stays controlled. When clients aim to hydrolyze the ester and expose the free acid, our product’s purity shows up as sharp, predictable transitions with no extraneous spots in TLC or unexplained peaks on LC-MS.
Over the years, the most meaningful relationships we have built are with process chemists and sourcing managers who push for truth in data and honesty in performance. Hearing back from clients facing crunch timelines—where one subpar lot could throw a month’s work into jeopardy—keeps us focused on thorough vetting and real guarantees. We do not send out batches with uncertain origin or half-done QC, because we know what happens to a project pipeline after encountering contaminated or misidentified material. If unexpected results arise from a batch, our technical team reviews the data log, rechecks samples, and stands ready to troubleshoot, not pass blame.
Few other products carry the same blend of complexity and reliability as N-(2'-Cyano[1,1'-biphenyl]-4-ylmethyl)-L-valine methyl ester hydrochloride. Researchers switching from generic biphenyl intermediates to our offering consistently mention the boost in synthetic versatility and smoother workup protocols, directly traceable to the controlled chiral integrity and the robust salt form. As process chemists ourselves, seeing material go into successful submissions for IND-enabling studies or new IP filings feels like a tangible return on years of factory-level learning and discipline.
No production process ever stays perfect. Over the last five years, we adapted to raw material shortages, energy constraints, and new compliance regimes by tightening documentation and pushing forward on greener chemistry. We took a closer look at waste management when stricter oversight came into force, updating our solvent management and capturing higher fractions of by-products for recycling. Technicians run regular error-tracking sessions, drawing on everything from operator experience to batch log data, hunting out redundancies and streamlining steps where possible.
Batch deviations, whenever they surface, become training opportunities—not blame sessions but moments to learn which variables hold the greatest downstream risk. In synthesizing N-(2'-Cyano[1,1'-biphenyl]-4-ylmethyl)-L-valine methyl ester hydrochloride, we have found the crystallization sequence can tip product stability if temperatures swing too wildly. Early on, we lost several days to failed crystallizations and learned that tighter control—plus improved temperature monitoring with redundant probes—catches trouble before it becomes a shipment issue. These lessons feed directly back into both updated SOPs and the orientation of new staff, ensuring forward momentum.
On the supply chain side, pandemic-era disruption pushed us to dual-source every key precursor, never leaving reliability to chance. This approach costs more on paper, but the payoff in zero missed deliveries outweighs any line-item savings. We partner with logistics providers who understand how to clear customs with specialist chemicals and who track temperature and humidity readings—not just to tick a box but to prevent the rare, catastrophic event that wipes out a shipment’s reliability.
Beyond the factory gates, researchers count on this molecule as a springboard for new molecule discovery campaigns and pilot-scale validation batches. Case studies from medicinal chemistry teams reveal that lead series synthesized using our material show cleaner spectra, higher reproducibility, and smoother regulatory filings—since impurity profiles and origin data line up date-for-date with project timelines. In peptide chemistry, reliable access to this compound means no interruptions for re-qualification cycles, which can save weeks at critical moments.
Our staff regularly track literature and patent filings to see which new scaffolds incorporate the biphenyl cyano core, using that information to tweak process design and anticipate emerging user needs. By maintaining an open channel with academics and industry project leads, we troubleshoot process bottlenecks, such as filtration-time slowdowns or unexplained color formation in isolated product. Many of our partners share data on reaction yields, suggesting process tweaks that improve outcomes both at our facility and downstream in their labs.
We have seen waves of new requirements from both regulatory bodies and end users, and we know that staying ahead of these changes requires continual reinvestment in quality systems, people, and process technology. Ongoing training, up-to-date analytical infrastructure, and a culture of transparency underpin our supply of N-(2'-Cyano[1,1'-biphenyl]-4-ylmethyl)-L-valine methyl ester hydrochloride. We encourage auditable trails, real-time feedback, and open-book problem solving.
Our approach depends not only on excellent raw materials but also on rigorous execution, honest communication, and an active willingness to admit errors and improve. This compound, more than most, has taught our team that attention to detail in structure, salt form, and chiral purity transforms not just reaction outcomes, but also the ease with which research projects hit their milestones. We view each batch not just as a product for sale but as a solution delivered from our lab to yours—with all the know-how, care, and hard-won insight our industry can offer.
We keep our focus on batch integrity, technical transparency, and responsiveness, because the real value of our product shows up in the achievements and confidence of those who use it—bench chemists, process engineers, and research leaders alike.