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L-Valine Benzyl Ester Hydrochloride

    • Product Name L-Valine Benzyl Ester Hydrochloride
    • Alias Benzyl 2-amino-3-methylbutanoate hydrochloride
    • Einecs 243-740-7
    • 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
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    Specifications

    HS Code

    159864

    Product Name L-Valine Benzyl Ester Hydrochloride
    Cas Number 22007-83-6
    Molecular Formula C12H18ClNO2
    Molecular Weight 243.73
    Appearance White to off-white powder
    Purity Typically ≥98%
    Solubility Soluble in water and methanol
    Boiling Point Decomposes before boiling
    Melting Point 82-86°C
    Storage Conditions Store at 2-8°C, protected from light and moisture

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

    Packing & Storage
    Packing L-Valine Benzyl Ester Hydrochloride, 25g, packed in a sealed amber glass bottle with tamper-evident cap and clear labeling.
    Shipping L-Valine Benzyl Ester Hydrochloride ships in secure, sealed packaging to protect from moisture and contamination. It is classified as non-hazardous for air and ground transport. Store and transport at room temperature. Accompanied by a certificate of analysis and safety data sheet (SDS) to ensure compliance with regulatory and safety standards.
    Storage L-Valine Benzyl Ester Hydrochloride should be stored in a tightly closed container, protected from light and moisture. Keep it in a cool, dry, and well-ventilated area, ideally at 2–8°C (refrigerator temperature). Ensure it is kept away from incompatible substances such as strong oxidizing agents and bases. Follow all relevant safety and handling guidelines when storing this chemical.
    Application of L-Valine Benzyl Ester Hydrochloride

    Applications of L-Valine Benzyl Ester Hydrochloride in Industrial Manufacturing

    As a direct manufacturer, we support advanced industrial practices by supplying L-Valine Benzyl Ester Hydrochloride for established downstream sectors. Drawing on formulation data and validated market use, we detail core application paths with relevant compliance and use specifications for production professionals.

    1. Protected Amino Acid Intermediate Production for API Synthesis

    L-Valine Benzyl Ester Hydrochloride plays a strategic role as a protected amino acid intermediate in pharmaceutical synthesis, particularly within peptide-based active pharmaceutical ingredient (API) manufacturing. The compound’s protected structure allows it to enter solid-phase or solution-phase peptide synthesis seamlessly, minimizing undesired side reactions while affording selective deprotection at later synthetic stages. Downstream manufacturers rely on its controlled reactivity for building peptide chains under regulated conditions, contributing directly to batch repeatability and regulatory compliance for injectable APIs and other parenteral medicines.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guidance for Active Pharmaceutical Ingredients
    • US Pharmacopeia (USP) General Chapter <1045>
    • European Pharmacopoeia (Ph. Eur.) Peptide Substances Monographs
    • Current Good Manufacturing Practice (cGMP), US FDA 21 CFR Part 210/211

    Typical usage ratio

    • 0.95–1.10 molar equivalents per amino acid coupling, calculated based on peptide sequence and batch size; adjustment depends on length and hydrophobicity of targeted peptide chains.

    Downstream process integration

    • Incorporation during amino acid activation and coupling stages of stepwise peptide chain elongation.
    • Use in solid-phase peptide synthesis (SPPS) resin loading or solution-phase step-wise coupling.
    • Participates in hydrogenolysis-based deprotection after completion of synthesis, releasing free L-valine moiety.

    Final product types

    • Synthetic peptide APIs for oncology, metabolism, and rare disease indications
    • Generic bulk peptide drugs and reference standards
    • Peptide-based injectable formulations, including controlled-release forms
    • Research-use-only peptide standards for pharmaceutical development

    2. Chiral Intermediate in Chemical Synthesis for Agchem & Fine Chemicals

    Manufacturers in the agrochemical and high-value fine chemical industries employ L-Valine Benzyl Ester Hydrochloride as a chiral building block. Its defined stereochemistry supports the selective construction of optically pure intermediates. The raw material is widely utilized during the synthesis of chiral amines, acids, and specialty heterocycles, ensuring high enantiomeric excess in active ingredient production. Incorporation into multi-step syntheses improves control over stereoselectivity and yield, critical for downstream formulation compliance and global registration of crop protection actives and advanced materials.

    Industry compliance standards

    • OECD Principles of Good Laboratory Practice (GLP)
    • European Union Regulation (EC) No 1107/2009 on Plant Protection Products
    • ISO 9001:2015 Quality Management Systems Certifications for Fine Chemicals
    • REACH (Registration, Evaluation, Authorisation and Restriction of Chemicals, European Chemicals Agency)

    Typical usage ratio

    • Ranges from 0.8 to 1.25 molar equivalents, determined by the number of chiral transfer steps; excess controlled by endpoint HPLC analysis to maximize enantiopurity.

    Downstream process integration

    • Entry during initial chiral auxiliary coupling and esterification stages
    • Engaged in hydrogenolytic cleavage or acid hydrolysis for deprotection at predetermined stages
    • Used to generate enantiopure precursors prior to agrochemical or specialty intermediate assembly

    Final product types

    • Chiral amine intermediates for selective herbicides and insecticides
    • Optically pure α-amino acid derivatives for fine chemicals
    • Building blocks for high-performance materials and advanced macrocycles
    • Intermediates for manufacturing plant growth regulators

    3. Research-Grade Reagent for Proteomics and Life Science Laboratories

    Proteomic and biotechnology laboratories depend on high-purity L-Valine Benzyl Ester Hydrochloride as a standard reagent in the synthesis and modification of peptide and protein fragments. Lab-scale users select this compound for controlled side chain protection during custom synthesis, site-directed mutagenesis experiments, and peptide mapping procedures. Accurate use ensures reproducible cleavage, labeling, and sequencing, contributing to the development of novel diagnostics, biomarker validation, and structure–activity relationship (SAR) studies for life science applications.

    Industry compliance standards

    • ISO 13485:2016 Quality Management for In Vitro Diagnostic Reagents
    • GLP Standards for Laboratory Chemicals (OECD/US EPA)
    • US National Institutes of Health (NIH) Guidelines for Recombinant DNA Molecules
    • Local chemical registration and safety requirements (e.g., GHS labeling)

    Typical usage ratio

    • 0.1–1.0 mmol per 1 mmol target peptide, scaled according to peptide length and complexity; excess minimized to facilitate downstream deprotection and purification.

    Downstream process integration

    • Applied in small batch synthesis during N- or C-terminal peptide blocking steps
    • Used in SPPS libraries, site-specific labeling, and adduct formation for mass spectrometry calibration
    • Hydrogenolytic or acidic removal of protecting group performed as part of final purification protocols

    Final product types

    • Peptide libraries for drug discovery research
    • Protein–peptide conjugates for immunoassays and ELISA kits
    • Modified substrates for enzyme activity profiling
    • Internal standards for proteomics and metabolomics

    4. Intermediate for Specialty Polymer and Biomaterial Modification

    Producers of advanced biomaterials integrate L-Valine Benzyl Ester Hydrochloride during the controlled modification of specialty polymers and degradable matrices. The benzyl-protected valine derivative introduces custom side chains and reactive moieties, allowing users precise control over material hydrophobicity, degradation kinetics, and targeted bioactivity. In downstream processing, polymer scientists adjust protective group removal conditions stepwise to enable sequential grafting or block copolymer templating. These adaptations directly support strict physical and biocompatibility profiles required for tissue engineering and drug delivery platforms.

    Industry compliance standards

    • ISO 10993-1, Biological Evaluation of Medical Devices—Part 1: Evaluation and Testing within a Risk Management Process
    • ISO 13485 Quality Management Systems for Medical Devices
    • USP Class VI Plastics Biological Reactivity Tests
    • US FDA Guidance for Industry: Use of International Standard ISO 10993-1

    Typical usage ratio

    • Typically 0.5–2.0 parts per hundred resin (phr); exact ratio varies with polymer architecture and desired modification level.

    Downstream process integration

    • Used during pre-polymer mixing or controlled post-polymerization functionalization steps
    • Protecting group selectively cleaved mid-process to expose free valine for secondary reactions
    • Supports integration in both solvent-based and melt-processing equipment

    Final product types

    • Bioactive hydrogels for drug-release systems
    • Cell culture scaffolds and engineered extracellular matrices
    • Polymer nanoparticles for targeted medical imaging
    • Functionalized fibers for wound dressing composites
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    Certification & Compliance
    More Introduction

    L-Valine Benzyl Ester Hydrochloride: Manufacturer’s Perspective on Its Value and Role

    Introduction to a Key Intermediate

    After years of working in chemical process manufacturing, you notice trends. Some products persist because they solve very specific problems for our customers, whether in pharma, research, or specialty synthesis. L-Valine Benzyl Ester Hydrochloride falls in that group. Its role looks simple – it’s an intermediate by most accounts – but the consistency, purity, and reliability people expect only come from experience and a close understanding of what’s happening at a molecular level.

    Understanding L-Valine Benzyl Ester Hydrochloride by a Manufacturer

    L-Valine Benzyl Ester Hydrochloride is a derivative of L-Valine, one of the three branched-chain amino acids. We’ve seen this material requested both for its specific reactivity in peptide synthesis and as a protecting group during segment coupling. We produce this compound under the model number LVBE-HCl98, indicating its minimum purity, which our in-house QCs regularly confirm at or above 98%.

    Daily, our team handles raw material selection, reaction monitoring, isolation, and purification with a close eye on chiral integrity, since racemization during esterification is a risk without careful process control. Beyond final HPLC assays, our staff also draw on experience—watching resins swell in solvents or recognizing subtleties in filtration patterns—to spot any run-to-run variation. Manufacturing is personal. You keep learning from the batch before, and you fix whatever didn’t work perfectly.

    Key Features in Our Product

    What separates our L-Valine Benzyl Ester Hydrochloride from generic alternatives is tight handling of side reactions and consistent control over particle size. This small detail shapes how smoothly customers execute solid phase peptide syntheses or build protected derivatives. We also pack the powder in controlled humidity so clumping doesn’t catch users off-guard right out of the drum. Too often, inconsistent particle flow leads to dosing errors on automatic dispensing systems; our process from drying through packing helps avoid that.

    Prioritizing absolute purity is not just a marketing pitch for us—impurities, especially those associated with over-alkylation or incomplete hydrochloride formation, disrupt downstream steps. Our product undergoes two-point verification, including IR and NMR profiles. By doing so, we minimize the batch-to-batch surprises that customers sometimes see from non-manufacturers: for example, odd moisture retention or small peaks in the NMR spectra.

    Explaining Its Usage: Not All Applications Are Equal

    Chemists working with peptide synthesis rely on L-Valine Benzyl Ester Hydrochloride due to its stability under conditions that cleave other groups. Its benzyl ester moiety survives reagents and pH steps that wreck methyl and ethyl esters. In reductive conditions, the benzyl group can be specifically removed, which gives people flexibility to build up polypeptide chains using solid-phase or solution-phase routes.

    Through discussions with users in both small-scale research and commercial process development, we adjust our manufacturing protocol accordingly—batch size, granulation, and inert-atmosphere drying all get tuned depending on feedback about handling issues during coupling, deprotection, or resin attachment. We welcome calls about how it dissolves in different solvents and which lots showed better dissolution in DMF or THF. Small usability questions drive real, plant-floor change. Peptide chemistry seldom forgives shortcuts or missed details.

    Comparisons with Related Intermediates

    For those weighing L-Valine Benzyl Ester Hydrochloride against plain L-Valine or other esters, it helps to recognize what happens in practical synthesis. L-Valine as a free acid or simple methyl ester easily undergoes undesired side reactions, especially when you run couplings in the presence of strong acid chlorides or under hydrogenolysis. The benzyl ester locks in the carboxyl protection yet can be removed under controlled palladium-catalyzed conditions. That selectivity saves rework and purification steps.

    Users often ask how our hydrochloride salt stacks up against the plain benzyl ester. The salt form gives greater stability and easier handling, especially for those tasked with weighing and dissolving in production suites without inert-atmosphere enclosures. Our staff have learned not to underestimate the value of stable storage—customers running high-throughput peptide assemblies see less variability in coupling efficiency when the starting ester doesn’t degrade from light or humidity.

    Manufacturing Discipline Informs Quality Every Day

    We’ve noticed that shortcuts in esterification or drying create headaches for everyone down the line. Water content, for example, not only complicates weight calculations but can trigger partial hydrolysis and turn an entire run into unusable byproduct. Our facility’s focus on vacuum drying and moisture testing isn’t just for the paperwork. It’s reaction yield and customer trust on the line.

    Our team has developed a habit of checking both small and large batches for subtle differences—sometimes, product lots at the ton scale behave differently from kilogram runs, simply because heat transfer and agitation can shift the crystal habit or mean certain batches pick up impurities from vessel wall adsorption. Over several years, a pattern emerges: simplest methods, like regular Karl Fischer titration and batch-to-batch comparison of TLC or HPLC chromatograms, prevent most quality issues. Nothing is assumed; every shipment gets checked for the details that matter.

    Process Improvements: Not Just a One-Time Fix

    Chemical manufacturing is never static. We work through solvent recovery cycles, optimizing catalyst loads, and investigating alternative protective group strategies. Each batch of L-Valine Benzyl Ester Hydrochloride rides on these daily improvements. Sometimes, we learn from our customers—peptide chemists who find a side reaction or solubility issue in a new automated synthesis protocol. Those conversations flow right back into our process. If we need to tweak a drying temperature or extend a recrystallization hold, we do it based on what real users are actually experiencing, not just on the established protocol.

    Our labs maintain processed sample inventories reaching back several years. Any time a returning customer requests “product as supplied five years ago,” we can cross-verify using retained samples and records—retrospective analysis heads off consistency issues long before they scale up. Real-world manufacturing connects the office, the production floor, and the warehouse. Each group contributes because each faces the consequences of a missed detail or misunderstood use-case.

    Why Model, Specification, and Habitual Quality Matters

    Some buyers fixate on spec sheets, but decades of watchful process control show where those specs come from—and where they sometimes hide important variation. Our LVBE-HCl98 achieves a minimum 98% purity by both HPLC area and NMR without deliberate suppression of minor peaks. Impurities above 0.2% get flagged for deeper analysis. We don’t simply ship product meeting a number; we investigate each outlier and try to prevent a recurrence. It costs more time, but reducing unknown variables saves much more for us and for end-users.

    Customers tend to notice when a regular batch changes color, gains odor, or dissolves slower than before. That feedback cycles right back to us. In our plant, a yellow cast to the material or a faint medicinal odor often warns of trace byproducts from overreduction or solvent carryover. We train crews to spot these signals early, before any shipment leaves our control. These habits keep the product’s value high—not just on paper, but in each real-life use.

    Differences from Non-Manufacturer Sourcing

    Peer chemical producers know the difference between direct-from-plant sourcing and buying from traders or resellers. Material from a third party often comes with minimal documentation, ambiguous origin, or unexplained differences from order to order. As the original manufacturer, we keep method-of-preparation records and can clarify any change in process or supply chain. We don’t relabel or remix.

    Direct buyers appreciate fast answers to technical questions: solvent recommendations, compatibility issues, planned changes to packaging, or whether we can supply custom lot sizes for particular process trains. That level of dialogue only works when you make the product yourself. Questions don’t disappear into bureaucratic queues or unanswered emails.

    Safety Observations and Handling Nuances

    On the plant floor, the staff become sensitive to characteristic features of L-Valine Benzyl Ester Hydrochloride: its fine white or off-white crystalline nature, slight tendency to attract moisture, and the need to protect from strong acids or bases during storage. The compound emits low odor under most temperatures, but open containers in high humidity draw attention by increasing caking. We instruct handlers to keep bulk containers tightly closed and use rapid transfer techniques. Over the years, these procedures become instinctual.

    Shipping teams maintain logs on packaging performance, and we rarely find broken seals or wetting on arrival at a customer’s site. Extra desiccant and double-bagged polyethylene liners have made a measurable difference; one lost drum is too many, so feedback from experienced users led us to adjust our approach. Our shipping department even logs humidity trends before release, which has led to packaging changes that reduce transit risk, especially in monsoon seasons or for export by sea.

    Scaling Up: Practical Lessons in Large-Scale Production

    As a manufacturer, batch scale brings its own surprises. At small scales, certain crystalline forms redissolve quickly and filter well. On hundreds-of-kilos runs, the same compound might cake at the vessel outlet, requiring agitation redesign or slower cooling. Our operations group runs pilot batches before shifting to full-scale production, and we maintain data on all critical process variables—agitation rate, solvent blend, temperature ramp—to smooth the learning curve each time.

    An unexpected benefit of large-volume manufacturing is the early spot-checking of minor impurities that would otherwise go unnoticed at small scales. Customers processing multi-kilo runs spot even tiny shifts in downstream conversion and report back. That communication keeps suppliers honest—without direct feedback from people doing real chemistry at scale, minor problems can balloon.

    Adaptation Based on Customer Feedback

    Real-world users shape how we make and sell L-Valine Benzyl Ester Hydrochloride. Sometimes we get a call from a university lab working in discovery peptides; other times it’s an established pharmaceutical group working on a kilogram synthesis. The concerns of small- and large-scale users aren’t always the same. Customers synthesizing oligopeptides in solution care deeply about residual moisture and byproduct load, since their downstream deprotection steps can fail otherwise. Large-scale operations demand granular lot traceability—if one barrel causes downstream yield to drop by even two percent, the cost runs into real money.

    Our technical support team works directly with research chemists and plant engineers to implement feedback. If a barrel generates static that causes powder to hang up, we switch liners. If a foreign material gets flagged, we pull split samples from our retained batch for reanalysis. We update batch records with every complaint and trend feedback to inform our next process tweak.

    Technological and Environmental Advancements

    Environmental pressure has compelled us to review solvents, waste management, and air quality controls. L-Valine Benzyl Ester Hydrochloride synthesis traditionally utilizes organic solvents; our plant cycles waste through a closed-loop recovery. Each year, we reduce our solvent consumption by incremental process improvement—understanding that our customers and partners prefer “greener” chemical options. The compounds handled here almost never reach the waste stream untreated, as every step is measured, managed, and improved for both compliance and sustainability.

    Technical improvement doesn't always involve large capital investment. Over the years, our production line switched from single-stage reactors to multi-step continuous systems where feasible. The result is tighter process control, better yields, and a dramatic reduction in energy needed per kilogram of product produced. As a result, customers benefit from more stable pricing and more reliable supplied product. We source raw materials locally when possible to reduce supply chain risk.

    Common Questions Manufacturers Hear—And How We Answer

    From time to time, technical directors and procurement specialists reach out about issues ranging from solubility in niche solvents to compatibility with certain catalysts. Our in-house chemists work with actual material on site, so we investigate using material pulled straight from the same batch shipped to the customer. Data and observations never arise from theoretical tables; we base recommendations on tested reality.

    Common customer questions include handling instructions for inert-atmosphere transfers, dissolution speed in polar versus apolar solvents, storage strategies for extended shelf life, and impact of humidity during multi-day synthesis. We answer directly—having seen how the product behaves in bulk, not just as an analytical curiosity. This real world knowledge sets manufacturers apart from third-party sources who can’t replicate on-floor chemistry.

    Looking Beyond Specifications—A Manufacturer’s Mindset

    Every successful synthesis, especially in peptide chemistry, rests on reliable intermediates. L-Valine Benzyl Ester Hydrochloride, from a manufacturer’s viewpoint, is more than a raw material: it represents hundreds of process improvements, small and large, layered over years of production. Each positive outcome for the end user confirms that constant attention, skilled QC, and direct customer engagement matter as much as any piece of process equipment or fancy analytics.

    We stand ready to discuss technical details, usage experiences, and adaptation requests that can take the product’s role further. It’s the collective wisdom of dozens of chemists, operators, maintenance crew, and customers feeding back into the process that creates not just a product but a proven solution, batch after batch.