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L-Beta-Homoproline Hydrochloride

    • Product Name L-Beta-Homoproline Hydrochloride
    • Alias (3R)-3-Piperidinecarboxylic acid hydrochloride
    • Einecs 695-723-9
    • 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

    723176

    Product Name L-Beta-Homoproline Hydrochloride
    Cas Number 139481-59-7
    Molecular Formula C6H12ClNO2
    Molecular Weight 165.62
    Appearance White to off-white solid
    Purity Typically ≥98%
    Melting Point 206-210°C (dec.)
    Solubility Soluble in water
    Chemical Structure Pyrrolidine ring with carboxyl and amine groups; hydrochloride salt
    Chirality L-enantiomer
    Storage Conditions Store at 2-8°C, protected from light and moisture
    Synonyms L-2-Aminocyclopentane-1-carboxylic acid hydrochloride
    Canonical Smiles C1CC(CNC1)C(=O)O.Cl
    Application Used in peptide synthesis and medicinal chemistry

    As an accredited L-Beta-Homoproline Hydrochloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing L-Beta-Homoproline Hydrochloride, 25g, is supplied in a sealed amber glass bottle with a tamper-evident cap and clear labeling.
    Shipping L-Beta-Homoproline Hydrochloride is shipped in compliance with relevant chemical safety regulations. The compound is securely packaged in sealed, airtight containers to prevent contamination or moisture absorption. It is typically dispatched via ground or air transport, with appropriate labeling and documentation, ensuring safe handling and delivery to laboratories or research facilities.
    Storage L-Beta-Homoproline Hydrochloride should be stored in a tightly sealed container, protected from light and moisture. Keep it at room temperature (15–25°C) in a dry, well-ventilated area, away from incompatible substances such as strong oxidizers. Ensure proper labeling, and avoid exposure to excessive heat. Store in accordance with applicable chemical safety regulations and handle using appropriate personal protective equipment.
    Application of L-Beta-Homoproline Hydrochloride

    Applications of L-Beta-Homoproline Hydrochloride in Industrial Manufacturing

    L-Beta-Homoproline Hydrochloride serves as a specialized intermediate in chemical manufacturing, supporting several advanced sectors through its use in synthesis, process engineering, and product formulation. Our material is produced to meet stringent industry requirements and is consistently inspected for purity, trace metals, and suitability for critical B2B industrial utilities.

    1. Active Pharmaceutical Ingredient (API) Synthesis

    Pharmaceutical manufacturers use L-Beta-Homoproline Hydrochloride as a chiral building block during the synthesis of β-amino acid derivatives, anticancer agents, and enzyme inhibitors. Process chemists incorporate it in multi-step reaction pathways, focusing on stereospecific transformations under GMP controls. Integration occurs mainly after initial assembly of core structures, contributing to molecular chirality and bioactivity demanded by drug substances. Quality teams perform trace-level impurity profiling to ensure batch-to-batch consistency and regulatory compliance for New Drug Applications and generic API filings globally.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • United States Pharmacopeia (USP) General Chapter <1078>
    • European Pharmacopoeia Chiral Substances Regulation
    • FDA cGMP 21 CFR Part 210/211

    Typical usage ratio

    • 5-40 mol% loading in target stage, tuned per synthetic yield and by-product formation profile; adjusted based on final molecule structure demands

    Downstream process integration

    • Incorporation immediately after coupling reaction or reductive amination during multi-step synthesis
    • Employed in enantioselective step—entry point defined by target stereochemistry
    • Solution-phase or solid-phase peptide synthesis adaptation
    • Integrated with continuous flow or batch production platforms

    Final product types

    • Oral and injectable APIs containing β-amino acid motifs
    • Enzyme inhibitors with pyrrolidine rings
    • Small-molecule oncology candidates
    • Peptide-based therapeutic drugs

    2. Peptide Synthesis for Research and Diagnostic Reagents

    Biotech companies and reference laboratories apply L-Beta-Homoproline Hydrochloride in synthetic peptide libraries, oligopeptide standards, and custom sequence reagents for immunoassays and biomarkers. Its use improves peptide backbone conformation and imparts desired structural rigidity, key for high-affinity binding in diagnostic development. Special handling involves controlled addition during Fmoc/t-Boc solid-phase synthesis, enabling restricted side reactions and retention of integrity for high-purity reagent batches.

    Industry compliance standards

    • ISO 13485: Medical Devices Quality Management Systems
    • FDA 21 CFR Part 820 for diagnostics manufacturing
    • Sigma-Aldrich Custom Peptide Synthesis Protocols
    • Applicable REACH Documentation for import and safe handling

    Typical usage ratio

    • 1-5 residue incorporation per 10–100 amino acid chain; exact loading based on targeted binding specificity and peptide fold stability requirements

    Downstream process integration

    • Introduced during automatic peptide synthesizer cycles
    • Resin coupling and washing controlled within inert reaction chambers
    • Purification via HPLC or preparative LC post-synthesis
    • Spot-checked by mass spectrometry and NMR for fidelity confirmation

    Final product types

    • High-purity synthetic peptides for antibody production
    • Reference controls used in LC-MS diagnostic kits
    • Tagged peptide standards for laboratory traceability
    • Epitope mapping reagents for pre-clinical R&D

    3. Chiral Auxiliary in Fine Chemical Synthesis

    Manufacturers of agrochemical active ingredients and advanced polymers use L-Beta-Homoproline Hydrochloride as a chiral auxiliary to introduce non-racemic centers, supporting reaction pathways that produce high-value fine chemicals. Chemical engineers specify its use for precise control in asymmetric Diels-Alder reactions, Mannich condensations, and hydrogenation protocols, especially under batch and pilot-scale platform conditions. Downstream handlers require traceability for all auxiliary reagents under ISO process audits.

    Industry compliance standards

    • ISO 9001 Quality Management Systems
    • Regulation (EC) No 1907/2006 (REACH)—Annex VI, Section 1–3
    • Chemical Facility Anti-Terrorism Standards (CFATS, USA), Sec. 550
    • Agrochemical FAO Guidelines for Technical Material

    Typical usage ratio

    • 10-20 mol% relative to chiral carbon introduced in single or multiple stages; adapted to desired ee (enantiomeric excess) threshold per product class

    Downstream process integration

    • Added at intermediate stage—directly before enantioselective transformation
    • Recycled or reclaimed after target formation via extraction/wash protocol
    • Work-up includes acid/base partitioning for purity assurance
    • Compatibility with aqueous or solvent-rich process environments validated

    Final product types

    • Chiral agrochemical intermediates
    • Fine chemical blocks for flavor/odorants
    • Non-racemic monomers for specialty polymers
    • Stereochemically controlled fragrance bases

    4. Intermediate for Veterinary Active Compounds

    Producers of veterinary pharmaceuticals rely on L-Beta-Homoproline Hydrochloride to construct β-amino acid analogues for antiparasitic and anti-infective applications. Formulation scientists incorporate the material during critical intermediate coupling reactions, enabling animal health products with improved pharmacokinetics and spectrum. Regulatory submissions require full material trace verification, with synthesis often performed in GMP-like environments tailored to VICH guideline expectations.

    Industry compliance standards

    • VICH GL3 Good Manufacturing Practices for APIs (veterinary)
    • Chinese Pharmacopoeia Veterinary Drug Monographs
    • WHO Technical Report Series for veterinary substances
    • OIE Guide on Minimum Requirements for Veterinary Drug Quality

    Typical usage ratio

    • 5-18 mol% inclusion at key intermediate step; rate varies with desired analog activity spectrum and compound solubility

    Downstream process integration

    • Adopted at semi-synthetic intermediate construction prior to API finishing
    • Batch reaction monitored for possible by-product minimization
    • Subsequent transformations or derivatizations operate under controlled conditions
    • Purge and clear step confirms no auxiliary carry-over into API

    Final product types

    • Oral veterinary antihelmintics
    • Injectable antiparasitic raw materials for animals
    • Intermediate bases for animal feed medicated additives
    • Compounded multi-active dosage forms

    5. Building Block for Functionalized Polymers

    Polymer chemists integrate L-Beta-Homoproline Hydrochloride as a monomer substitute when engineering responsive hydrogels and functionalized resins. Its inclusion modulates the backbone rigidity and improves the selectivity of polymer-based drug delivery devices and analytical separation columns. Process technicians stage its dosing after initial chain polymerization, ensuring β-amino acid residues become covalently anchored within the polymer matrix structure.

    Industry compliance standards

    • ISO 10993-1 Biocompatibility for medical polymer materials
    • FDA 21 CFR 177.2600 for indirect food contact substances
    • SQAS (Safety & Quality Assessment for Sustainability) certification
    • ASTM D7209 for hydrogel swelling evaluations

    Typical usage ratio

    • 1-7 mol% substitution within copolymer chain; final ratio set for desired branching or cross-link density, validated by polymer performance testing

    Downstream process integration

    • Introduced at copolymerization phase after primary matrix setup
    • Stirred into monomer solution before catalyst or initiator addition
    • Reactive extrusion or injection molded for solid-state integration
    • Lot-specific characterization via FTIR and GPC

    Final product types

    • Hydrogel beads for protein separation columns
    • Bio-functional membranes for controlled release
    • Chromatographic stationary phases in analytical columns
    • Medical device coatings
    Free Quote

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    Certification & Compliance
    More Introduction

    L-Beta-Homoproline Hydrochloride: Real-World Value from a Manufacturer’s Viewpoint

    Shaping Genuine Quality Through Direct Production

    As one of the specialized producers of L-Beta-Homoproline Hydrochloride, we have found that the process demands a disciplined approach that simply cannot be matched by traders or distributors. Turning this specific amino acid analog into a reliable product asks for real insight into each reaction stage, vigilant purity control, and a dedication to chemical consistency. Every batch reflects our commitment to the small details that matter most in research and industry.

    How Model and Purity Factor into Real-Use Scenarios

    We supply L-Beta-Homoproline Hydrochloride in its hydrochloride salt form, a choice shaped by hands-on lab experience. Chemists appreciate the solid, crystalline powder because it handles easily and dissolves with predictability in water. We developed our HCl salt model specifically for synthesis labs and biopharmaceutical research teams who value low-moisture content and reproducible outcomes. Moisture levels typically run below 0.5%, and we target chemical purity over 99%. While absolute numbers always fluctuate with each batch, regular checks through HPLC, NMR, and optical rotation keep us honest and accountable.

    From the ground up, the specs are tuned for teams working on API intermediates, peptidomimetics, and probing the role of conformationally restricted proline analogs. The compact ring structure, and position of the beta-amino group, introduce unique conformational biases, unlocking uses that ordinary proline derivatives just can’t deliver. Teams building custom peptide libraries or testing new enzyme inhibitors often tell us they see improved selectivity and stability when swapping standard L-proline for our L-Beta-Homoproline Hydrochloride.

    Application-Focused Manufacturing: Meeting Demands in Research and Industry

    Practical feedback from end users has shaped how we scale and purify this compound. Unlike a trader, we recognize that small adjustments downstream—like extra steps for decolorization or targeted recrystallization—matter much to teams downstream. Our facility runs with dedicated reactors for cyclization and protection, separate from our general amino acid lines. This keeps contamination and batch confusion to a minimum. We run full traceability on starting materials, and our operators undergo yearly training in both GMP and research-grade protocols.

    Our clients often use L-Beta-Homoproline Hydrochloride as a chiral building block. The unique beta-substituted ring holds value for custom peptide synthesis, backbone modification, and as a probe in enzyme mechanism studies. Academic groups, CROs, and pharma R&D units look for predictable purity and the confirmation that each shipment will mirror their last purchase. Our in-house controls support what matters most: reliable biophysical behavior during scale-up or combinatorial synthesis, not just numbers on a Certificate of Analysis.

    Why Form Matters: Handling and Access

    Our crystalline powder comes in standard 1kg, 5kg, and 25kg sealed drums, which makes it easy to portion and store—no wasted material, no sudden caking. Labs rarely see degradation under standard storage, which comes down to our focus on minimizing ambient moisture exposure at every stage. Some alternatives in the open market use the free base instead, but we have found the HCl salt avoids stability complaints and helps avoid pH drift in solution preparation.

    One point we see overlooked: L-Beta-Homoproline’s distinct chemical backbone creates clear separation between it and common proline analogs. For example, whereas alpha-homoproline features an extended methylene bridge at the alpha position, altering local folding and receptor targeting, our beta homolog introduces a different bias on conformational space and disrupts cis-trans peptide bond dynamics differently. For synthetic chemists and protein engineers, these fine details translate to changes in biological activity and solubility, opening space for new molecular properties and potential therapeutic applications.

    Supporting Innovation through Specifications, Not Just Promises

    Some customers ask us why we do not chase absolute highest purity or lowest endotoxin numbers, as seen in analytical reagent supply. From a manufacturing stance, every decimal point above 99% pays rapidly diminishing returns for most R&D users and increases costs without added practical benefit. We audit our entire synthesis chain for residual solvents and heavy metals, and set limits according to experience, regulatory guidance, and typical application requirements for pharmaceutical intermediates. When a project approaches preclinical or GMP steps, we step up measures for documentation and extra purification, as needed. As a chemical manufacturer, we can do this in-house rather than relying on volumes or off-the-shelf offerings from others.

    L-Beta-Homoproline Hydrochloride’s lot-to-lot consistency comes from owning the whole process, from protected precursor to final salt isolation. We know every input—who supplied it, the batch, the trace elements present. Unlike a reseller piecing together supply from multiple re-processors, we answer directly for the integrity of what leaves our gates. Our technical team reviews every client’s route-of-use, offering honest suggestions if an application may call for a different grade or a modified specification.

    Practical Differences from Other Beta-Amino Acids and Proline Analogs

    Looking across the field of proline derivatives, specific handling and synthesis quirks define the best choice. Take beta-homoalanine: while it extends the aliphatic chain, it lacks the rigidifying ring necessary for peptidomimetic conformational constraint. Alpha-homoproline shifts the methylene, opening up different rotational pathways and often leading to altered or less predictable secondary structure. L-Beta-Homoproline Hydrochloride, with its substitution pattern, forces peptides into specific geometries that resist random coil formation and deliver sharper biochemical signatures.

    This rigour in backbone design is invaluable for those exploring structure-activity relationships or working with constrained peptide scaffolds. Our experience in packing and storage suggests that, compared to other lysine or proline salts, L-Beta-Homoproline Hydrochloride resists caking and decomposition. This traces back to both its crystalline habit and our focus on eliminating hygroscopic impurities during final isolation.

    We have invested in closed-system drying and packaging tech to handle the challenge. Teams switching from commodity amino acid suppliers frequently come to us with complaints about sticky, imprecise material. Once they try our approach, returns and support requests drop almost to zero. It is these details, built up from years of production, that make the difference in actual use—not just what is written on a spec sheet.

    Addressing Challenges: Cost, Scalability, and Reliability

    Producing L-Beta-Homoproline Hydrochloride at commercial scale brings its own economic and technical challenges. The interesting chemistry that makes the beta homolog valuable also entails longer production cycles and higher raw input sensitivity compared to conventional L-proline. Sourcing precursor chemicals that meet high standards for impurity limits doesn’t always line up with what’s readily available in bulk markets. Over the years, we have developed relationships with reliable starting material suppliers and invested in direct pre-purchase inventory during periods of global price volatility.

    Natural disasters, regulatory changes, or raw material shortages can impact supply stability, so we maintain both local and international alternatives for source chemicals. Large-scale peptide manufacturers and leading research organizations have grown accustomed to our ability to deliver on schedule—even if global trade conditions change. In tough years, having full command of our own process lets us pivot faster and deliver material without delays caused by subcontracting or market fluctuations.

    Quality Control from Start to Finish

    Most complaints in the industry boil down to poor consistency: off-spec color, batch-to-batch variation, or unexpected side-products. Our process incorporates routine monitoring for every step—cyclization, deprotection, salt formation, drying, sieving, and packing. Infrared spectroscopy, mass spectrometry, and advanced moisture analysis run side by side with standard titrations and chromatographic assays. Each step gets double-checked by experienced staff familiar with both the chemistry and the real challenges faced by end users working with sensitive peptide or pharmaceutical systems.

    Over time, we learned that some customers try to cut costs with cheaper, unverified sources. These usually lead to higher reject rates and more time troubleshooting failed syntheses. Manufacturing L-Beta-Homoproline Hydrochloride in-house means standing behind what we sell, not hiding behind a stack of paperwork. Our technical documentation is prepared by the same chemists who run the actual reactions, which gives labs added confidence. They know any anomalies will be traced, explained, and, if necessary, fixed by the experts who know the process end-to-end.

    Collaborative Development: Adjusting Models Per Industry Feedback

    Sometimes end users need adaptations: custom crystalline grades, degassed packaging, or formal documented origin for regulatory submissions. We can run bespoke campaigns, large or small, to address these demands. Working from direct feedback, we tested and implemented improvements over several cycles, such as enhanced sieving and additional chemistries for protecting groups to minimize cross-reactivity for combinatorial synthesis.

    Over the last decade, working directly with R&D partners has deepened our understanding of how unexpected issues can crop up downstream. Common issues—like undissolved residues or chromatographic tails—often relate to trace by-products from shortcut synthesis elsewhere. We have reworked batches to suit high-throughput needs, such as removing extra ionic content or adopting tailored counter-ion exchange for advanced screening assays. Where others simply source from a supplier and offer the standard grade, being a true manufacturer means honestly advising if our process cannot meet a project's custom specification, and, when possible, proposing a route adaptation that can.

    Environmental and Regulatory Considerations in Modern Manufacturing

    Waste management and green chemistry principles now play a growing role in how we run our L-Beta-Homoproline Hydrochloride lines. Process optimization comes not only from economic pressure but from the ethical responsibility to minimize environmental impact. Solvent recovery units, closed emissions scrubbers, and effective effluent treatment reduce both regulatory risk and operating costs. Strict audit trails and documentation ready for inspection aren’t an afterthought, but a routine part of how material moves from raw source through synthesis and purification to final product.

    Turning a complex beta-amino acid into a practical, usable chemical takes more than buying cheap raw materials and batch-blending. Provenance matters, both to regulatory reviewers and to research chemists who build their next project on top of reliable chemical data. We have passed numerous third-party audits, hosted regulatory pre-approval inspections, and implemented robust training for process personnel. The result: material that meets not only internal standards but can stand up to investigation or import review in restrictive markets and regulatory climates.

    The Road Ahead: Adapting to New Science and Changing Requirements

    As peptide therapeutics and non-standard amino acid chemistry advance, new requests and requirements continue to arrive. Each new innovation—a novel peptide backbone, a folded protein analog, a constrained small molecule—brings its own quirks. L-Beta-Homoproline Hydrochloride, in many projects, shows unexpected promise as peptide chemists seek ways to introduce novel hydrogen bonding patterns or stabilize traditionally unstable regions of folded proteins. Working as a direct producer lets us adapt recipes, test new crystallization strategies, and verify unconventional uses that would challenge a generic third-party supplier.

    Customers working on scaffold design or medicinal chemistry appreciate the clear, detailed answers our team offers, built up from years on the production floor, not just sales literature. No supply chain, no layer of intermediaries, just direct lines from our process chemists and plant technicians. If manufacturing challenges arise, we tackle them upfront and inform buyers early—not after the fact.

    Choosing Direct Production: Real Gains in Reliability and Trust

    The market for L-Beta-Homoproline Hydrochloride is filled with choice. Many routes tote claimed grades and specs, but only producers with full control offer the tight process discipline, open feedback, and custom adaptation that drive both research and industry innovation forward. Every kilogram shipped represents more than a commodity—it is the product of years refining chemistry under practical conditions, not just bench-scale theory. We continue to invest in our people, process, and partnerships to ensure the material we make works as intended, batch after batch, year after year.

    Customers depend on more than price and paper claims: they need tested, consistent, and easily handled material produced by those who know each step in exhaustive detail. By refining each part of our production process, maintaining open contact with users, and learning from each application, we keep raising the standard for what L-Beta-Homoproline Hydrochloride can deliver—for scientists, manufacturers, and innovators pushing boundaries in chemistry and life sciences.