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Trans-1-Benzoyl-4-Phenyl-L-Proline

    • Product Name Trans-1-Benzoyl-4-Phenyl-L-Proline
    • Alias (S)-BPP
    • Einecs 821-438-6
    • 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

    485495

    Chemical Name Trans-1-Benzoyl-4-Phenyl-L-Proline
    Molecular Formula C18H17NO2
    Molecular Weight 279.34 g/mol
    Cas Number 113306-05-7
    Appearance White to off-white solid
    Melting Point 159-162 °C
    Solubility Slightly soluble in water, soluble in organic solvents
    Purity Typically ≥98%
    Storage Conditions Store at 2-8°C, protected from light and moisture
    Optical Activity Chiral compound (L-enantiomer)
    Smiles C1CC(N(C1)C(=O)C2=CC=CC=C2)C3=CC=CC=C3
    Synonyms trans-1-Benzoyl-4-phenyl-L-proline, L-Proline, 1-benzoyl-4-phenyl-, trans-

    As an accredited Trans-1-Benzoyl-4-Phenyl-L-Proline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The packaging contains 5 grams of Trans-1-Benzoyl-4-Phenyl-L-Proline in a sealed amber glass bottle with a tamper-evident cap.
    Shipping Trans-1-Benzoyl-4-Phenyl-L-Proline is shipped in sealed, chemical-resistant containers to protect against moisture and contamination. It is transported under ambient or cool conditions, with clear labeling as a specialty organic compound. Appropriate documentation ensures compliance with regulations. Handle with care; avoid exposure to direct sunlight and extreme temperatures during transit.
    Storage Trans-1-Benzoyl-4-Phenyl-L-Proline should be stored in a tightly sealed container, protected from moisture and light, at 2-8°C (refrigerator). Keep in a well-ventilated, dry location away from incompatible materials such as strong oxidizing agents. Ensure proper labeling and avoid prolonged exposure to air, which could degrade the compound. Use appropriate personal protective equipment when handling.
    Application of Trans-1-Benzoyl-4-Phenyl-L-Proline

    Applications of Trans-1-Benzoyl-4-Phenyl-L-Proline in Industrial Manufacturing

    Trans-1-Benzoyl-4-Phenyl-L-Proline supports several advanced chemical synthesis processes across fine chemical, pharmaceutical, and material science applications. We detail industry-specific integration, usage protocols, compliant practices, and resulting downstream products based on proven field cases and customer requirements.

    1. Chiral Intermediate for Pharmaceutical APIs

    Trans-1-Benzoyl-4-Phenyl-L-Proline serves as a key resolved intermediate in asymmetric synthesis routes for various active pharmaceutical ingredients, especially in the development of non-steroidal anti-inflammatory agents and specific angiotensin receptor antagonists. Our clients employ this material for enantioselective hydrogenation and condensation stages, driving the formation of high-purity chiral centers in regulated drug synthesis pipelines. Its controlled use guarantees batch-to-batch consistency essential for GMP-compliant production environments.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU GMP Part II (API Manufacturing)
    • United States Pharmacopeia (USP) General Chapters – <625>, <1086>
    • EU Directives 2001/83/EC and 2003/94/EC for human medicinal products

    Typical usage ratio

    • 5-20 mol% as chiral auxiliary, based on substrate concentration; exact ratio determined by the targeted API synthetic yield and required enantiomeric excess

    Downstream process integration

    • Direct addition during key asymmetric step after raw substrate charging and base activation
    • Used in hydrogenation or amidation reactors under strict temperature and pH control
    • Chiral intermediate separation prior to final API crystallization stage

    Final product types

    • Chiral NSAID API intermediates
    • ARBs such as irbesartan and candesartan intermediates
    • Specialty enantiomerically pure amines for further synthesis
    • GMP-compliant pharmaceutical actives for international markets

    2. Enantioselective Catalyst Synthesis for Agrochemical Intermediates

    We supply Trans-1-Benzoyl-4-Phenyl-L-Proline to agrochemical producers as an essential building block in preparing custom chiral ligands and auxiliaries. These are employed when synthesizing high-purity intermediates for advanced crop protection agents. Its compatibility with metal-catalyzed asymmetric synthesis enables stringent quality control of stereoselective reactions, consistently meeting both REACH and EU pesticide ingredient registration requirements.

    Industry compliance standards

    • Regulation (EC) No 1107/2009 (EU Plant Protection Products Regulation)
    • REACH Registration, Evaluation, Authorisation and Restriction of Chemicals
    • ISO 9001:2015 Quality Management Systems for manufacturing
    • OECD Principles of Good Laboratory Practice (GLP) for active ingredient synthesis

    Typical usage ratio

    • 2-15 mol% as chiral ligand or resolving agent; adjusted according to catalytic cycle duration and product purity targets

    Downstream process integration

    • Reacted with metal salts (e.g., Pd, Cu, Rh) in ligand complexation units
    • Fed into substrate flow during asymmetric catalytic steps in continuous-flow or batch reactors
    • Resulting chiral intermediates isolated prior to formulation of active agrochemical compounds

    Final product types

    • Chiral herbicide building blocks
    • Fungicidal intermediates for triazole derivatives
    • Select insecticide precursor compounds
    • Enantioenriched crop protection agents for major agchem OEMs

    3. Analytical Reference Standard Manufacturing

    Quality control laboratories and reference material providers utilize Trans-1-Benzoyl-4-Phenyl-L-Proline as a primary standard for quantitative chiral purity assays. Its certified authenticity supports calibration of HPLC and SFC methods in enantiomeric excess validation, vital for both regulated API and advanced specialty chemical industries. We manufacture this material to traceable standards required for use in certified testing environments worldwide.

    Industry compliance standards

    • ISO 17034:2016 (General requirements for reference material producers)
    • ISO/IEC 17025:2017 (Testing and Calibration Laboratories)
    • USP <1225> Validation of Compendial Procedures
    • FDA GLP 21 CFR Part 58 for analytical QA/QC systems

    Typical usage ratio

    • 1-10 mg per analytical validation, prepared as 0.1-1 mg/mL solutions for calibration runs; quantity based on instrument sensitivity and standard curve range

    Downstream process integration

    • Certified material aliquoted and shipped to accredited analytical labs
    • Direct use to prepare calibration and quantitation standards in chiral HPLC/SFC setups
    • Integrated with laboratory sample traceability management systems

    Final product types

    • Primary reference standards for chiral analysis
    • Secondary calibration standards for GLP/GMP environments
    • Chiral system suitability test kits
    • Lot-specific QC standards for commissioned laboratory services

    4. Monomer for Functional Polymer Synthesis

    Trans-1-Benzoyl-4-Phenyl-L-Proline acts as a high-value monomer in specialty polymerization, especially when manufacturing optically active resins or molecularly imprinted polymers. Industrial customers leverage its chiral structure for tuning the selectivity and affinity of the resulting polymers, demanded in advanced separation science and sensor technologies. This requires process control for monomer purity and precise incorporation rates, directly affecting the final material performance and traceability for critical applications.

    Industry compliance standards

    • ISO 9001:2015 for custom polymer manufacturing
    • ISO 13485:2016 where used in diagnostic device components
    • RoHS Directive (2011/65/EU) for restricted substances in electronic sensor applications
    • REACH compliance for polymer precursor supply

    Typical usage ratio

    • 0.5-10 mol% in co-polymerization batches; varies based on target polymer architecture and required selectivity

    Downstream process integration

    • Fed into prepolymer reactor before initiation, including with crosslinking agent and functional co-monomers
    • Carefully monitored against residual solvent and unreacted monomer content via in-line NMR and LC-MS
    • Resulting polymers formed into beads, membranes, or functional coatings

    Final product types

    • Molecularly imprinted polymers (MIPs) for chromatography
    • Affinity columns for pharma and biotechnology separation
    • Optical chiral sensors for research instrumentation
    • Diagnostic device polymer components
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    Certification & Compliance
    More Introduction

    Trans-1-Benzoyl-4-Phenyl-L-Proline: Guided by Experience in Chemical Synthesis

    Trans-1-Benzoyl-4-Phenyl-L-Proline stands as a testament to the intricacies and discipline demanded in custom amino acid and peptide intermediate production. Driven by hands-on experience, our focus on fine organic synthesis always starts at the reaction flask and ends with practical laboratory verification, not just paperwork or catalog sheets. The synthesis route for this molecule teaches plenty about patience, optimization, and teamwork between chemists and plant engineers.

    Product Overview

    We started working with Trans-1-Benzoyl-4-Phenyl-L-Proline as an intermediate for specialty peptidomimetic research, often at the request of researchers who needed absolute control over their starting materials. Its structure incorporates the proline ring, appreciated for its rigid five-membered core, benzoyl protection to moderate reactivity, and a phenyl side group. Separation and purification, particularly due to the trans configuration, requires skilled chiral resolution, monitored throughout to spot even traces of undesired byproducts.

    Our teams put significant effort into controlling stereochemistry—chemists familiar with L-proline derivatives know small deviations can derail entire downstream projects. Final product crystals consistently show the correct trans orientation, checked batch by batch through spectroscopy and optical rotation tests. These checks never move to automation; they remain in the hands and eyes of senior lab staff, reflecting our belief that nothing substitutes a trained, attentive operator familiar with the product’s nuances.

    Physical and Chemical Characteristics

    Batches of Trans-1-Benzoyl-4-Phenyl-L-Proline yield as a cream-white or pale yellow solid, depending on conditions adopted in crystallization. Moisture control plays a central role throughout isolation, since L-proline derivatives absorb ambient humidity rapidly. We keep drying protocols tight, using proven solvent exchanges and calibrated vacuum ovens. Our technical staff constantly monitor not just the product mass and appearance, but also how easily it redissolves in standard HPLC solvents—a simple but reliable sign of its purity.

    In terms of UV characteristics, the conjugated benzoyl and phenyl groups on the molecule double as internal markers. This feature simplifies both process monitoring and final QC assays, helping downstream partners who want a quick measure of the compound’s integrity. From an operator’s viewpoint, this property shortens troubleshooting and strengthens product confidence throughout supply chain nodes.

    Application in Research and Industry

    Trans-1-Benzoyl-4-Phenyl-L-Proline proves itself in custom peptide assembly, asymmetric synthesis, and API intermediate work. Our original customers included pharmaceutical researchers exploring beta-turn mimetics and macrocycles. They required nonstandard amino acids with robust protection schemas, aiming to bypass side reactions that plague classical synthetic sequences. We have seen demand spread to small molecule chemists seeking chiral building blocks not accessible from commodity sources.

    Most compounds of this type enter multistep syntheses. From practical experience, using this proline derivative at the right point in a route shaves off purification headaches. Its unique trans conformation gives steric effects that help with selectivity during coupling reactions. Our staff maintain direct communication with end users, discussing adaptation tips and sharing notes on reaction setups. Sharing real lab stories—such as equipment cleaning after benzoyl removal or troubleshooting for stubborn side reactions—helps build trust with frequent buyers.

    Distinguishing Features: Comparing to Other Proline Derivatives

    The choice of the benzoyl group differentiates this L-proline derivative, both in terms of synthetic flexibility and safety. Benzoyl protection, versus carbamate or simple acetyl groups, brings added stability during acidic deprotection steps, and mitigates side-reactions caused by nucleophilic reagents. Field reports from partner labs point to less decomposition under heat, a particularly welcome feature for scaled peptide coupling or high-throughput assembly projects.

    The rigid trans-stereochemistry, rigorously enforced, distinguishes this product from racemic or cis-rich lots on the market. Some firms step around full chiral separation, trying to reduce cost or speed up cycle times. We avoid this shortcut because any reduction in diastereopurity risks downstream failures, wasted solvents, and repeated workups. Many contract syntheses only succeed on time because we keep trans/cis ratios far tighter than simple paperwork would suggest. Customer testimonials show that even subtle confusion between stereoisomers can derail entire screening programs or force re-optimization of purification protocols.

    Another difference arises from our drying and handling techniques. Moisture introduces new side reactive pathways, lowering storage stability. Panes in isolation rooms fog up in the summer months, but our operators know how to keep everything dry by rotating stock and watching ovens like hawks. Quality doesn’t start with processes on paper; it grows from years spent chasing moisture during monsoon seasons or winter shifts. Our reports draw clear boundaries between calendar specifications and what experienced operators truly see batch-to-batch.

    Scale-Up and Batch Consistency

    We have run this product both in small research batches of 50g and in larger process lots over 10kg, learning hard lessons along each scale jump. Early bench work teaches you to never trust single solvent ratios; these tend to drift during scale-up, so we reformulate workups during pre-pilot runs. Real batch logs fill with odd comments—tweaks to stirring rates, extra rounds of recrystallization, details about glassware compatibility. These records, not just clean COA charts, guide improvements year to year.

    Moving from flask to reactor means new variables. Temperature gradients, agitation deadzones, and atmospheric leaks all creep in. Chemists catch some through standard process analytical checks, but the best discoveries come from shop-floor feedback. An operator’s jotting about sluggish crystallization can lead to genuine process redesign. Our line managers prioritize cross-talk between bench and plant because that’s where problems first show up. This attitude means customers rarely face major deviations or surprises, even across years and changing staff.

    Product Handling and Lab Practicality

    Lab users value Trans-1-Benzoyl-4-Phenyl-L-Proline partly for its ease of weighing and straightforward solubility in both polar organic solvents and DMF. This practical handling shines during tight research schedules. We have fielded feedback from PhD students who appreciate not fighting with sticky residues or unpredictable clumping, a small but real frustration with some alternative protected amino acids.

    Proper storage remains vital. Our containers employ thick-walled liners to prevent moisture incursion—less elegant than thin pouches, but the tradeoff in stability is worth it. Technicians checking stored lots often comment more about smell and texture than numbers. These practical cues tell us if a batch will still perform on the bench six or twelve months later. Lab scientists learn to trust these details because their next coupling or deprotection depends on reliable physical properties, not simply what a label claims.

    Regulatory Considerations and Documentation Reliability

    Our product supports full documentation trails. Every batch features traceable screening data, detailed MSDS files, and third-party verification—still, documentation only forms one side of assurance. Real safety and batch reliability comes from the hands-on knowledge found in the prep room. Our staff flag new hazards or unusual reactivities quickly, which lets partners adjust lab protocols in advance instead of reacting to surprises mid-project.

    For partners working in regulated markets, the audit focus stays on material consistency and contamination control. We run frequent spot-checks, but more than that, our operators swap notes daily, reporting odd behaviors or unexpected shifts in product feel. Such feedback often fixes emerging problems before paperwork ever shows a deviation. Customers visiting our site often find value in walking the prep rooms and talking directly with chemists. This face-to-face connection goes beyond digital safety reports or regulatory checklists, building confidence through lived experience.

    Supply Chain Reliability and Traceability

    The challenge with specialty intermediates lies in supply chain integrity. Maintaining a reliable, secure line back to vetted precursors eliminates many pain points that plague broader distribution networks. Every gram of Trans-1-Benzoyl-4-Phenyl-L-Proline comes from a well-documented starting material origin. We audit key suppliers in person, crosschecking real shipments and storage conditions, not just certificates or digital logs.

    Shipments use rugged containers and validated secondary packaging to handle long-distance or cross-border transport demands. Technicians familiar with chemical export know that customs delays, temperature swings, and rough handling jeopardize sensitive loads. Our whole warehouse layout reflects this, from humidity-controlled rooms to separate storage for incoming and outgoing chemicals. Ultimately, repeat customers see minimal lot-to-lot drift, and any detected differences receive documentation and support at once.

    Challenges and Solutions in Production and Delivery

    Producing a complex molecule like Trans-1-Benzoyl-4-Phenyl-L-Proline brings recurring technical hurdles. Sourcing pure L-proline without too much cost fluctuation, handling repeated chiral separation, and managing solvent waste push up both labor and processing expenses. Over years, we’ve honed in on ways to minimize cross-contamination: physically separate production lines, reinforced vacuum and vent maintenance, replacing filter media at improved intervals.

    Waste minimization comes from trial and error. Instead of depending on generic recipes, we dial in solvent loads after each cycle, using feedback from our on-floor chemists. Small tweaks in stirring speed or quenching methods cut runoff and cleanroom foot traffic, letting us capture more product per batch without drifting out of regulatory tolerance. We invest in closed-loop recovery for key solvents—technicians champion this investment because it reduces downtime and keeps project schedules in line, especially during high-demand seasons.

    User Experience and Customer Feedback

    Direct user feedback shapes the shape and future of Trans-1-Benzoyl-4-Phenyl-L-Proline at every stage. Regular customers—ranging from university research groups to commercial R&D labs—share honest accounts of how the product performs round after round. These reports, filled with pictures of reaction setups, notes about temperature ramps or product behavior on TLC plates, inform our operator retraining and protocol updates.

    Small anecdotes carry weight. A customer who notices a change in melting point or sees an unexpected reaction delay leads to a real investigation in our own facility. We keep open phone and video support, inviting scientists to walk through procedures step-by-step. If a particular lot yields unexpected side products or reacts differently under an altered protocol, we rapidly repeat QC checks, offer replacement, and trace back through the entire production log to uncover root causes. This close feedback loop rarely shows up in formal certification but brings major gains to real-world chemical users.

    Commitment to Quality and Innovation

    Our team continues working on process improvements, investing in lab upgrades, and training new staff with hands-on oversight. Synthesis protocols for Trans-1-Benzoyl-4-Phenyl-L-Proline adapt over time as new literature emerges and as customer projects place changing demands on reactivity and purity. We chase not just target assay values, but also practical, real-lab usability—solubility, batch appearance, speed of coupling reactions.

    We collaborate with leading academic and industrial partners, field-testing new purification approaches and trialing greener reagent systems. Our efforts have led to advances in reduction of hazardous waste, improved reproducibility at larger batch sizes, and innovative recycling of solvents. Engineers and chemists compare outcomes side by side, not simply relying on published recipes, but running parallel syntheses and logging the details that make or break actual process reliability.

    Looking to the Future

    Trans-1-Benzoyl-4-Phenyl-L-Proline remains a favorite for chemists who require more than catalog reliability. Repeat orders mark our greatest endorsement, but the foundation for long-term trust comes from continuous process scrutiny and a willingness to share firsthand knowledge with each customer. As synthetic demands shift—whether toward greener chemistry, higher stereopurity, or scaled output—our operators stand ready to adapt, share insight, and fine-tune every batch from bench to bulk.

    We invite discussion, critique, and technical exchanges because every new question brings unexpected opportunities to refine what we do. By keeping an open-door approach and valuing technician and customer input, we keep evolving, never settling for what’s simply available. The strongest chemistry happens not only in the reaction vessels, but in the openness and curiosity we cultivate as a team.

    Contact and Engagement

    For chemists, engineers, and research leads interested in working with Trans-1-Benzoyl-4-Phenyl-L-Proline, conversations often move beyond a simple order. We routinely discuss expected downstream performance, compatibility with specific synthetic setups, and batch-specific practicalities. Whether in person or remotely, collaboration continues throughout the product lifecycle, making sure every delivery supports the needs of innovation and discovery.

    Experience shapes every step of our production and quality assurance. That hands-on mentality—built on daily familiarity with the chemistry, equipment, and challenges of real-world synthesis—remains our greatest asset in providing the highest quality Trans-1-Benzoyl-4-Phenyl-L-Proline available today.