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N-Carbobenzoxy-1,3-Diaminopropane Hydrochloride

    • Product Name N-Carbobenzoxy-1,3-Diaminopropane Hydrochloride
    • Alias Z-Lys(Z)-OH
    • 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

    517204

    Product Name N-Carbobenzoxy-1,3-Diaminopropane Hydrochloride
    Cas Number 54552-11-1
    Molecular Formula C11H17ClN2O2
    Molecular Weight 244.72 g/mol
    Appearance White to off-white solid
    Solubility Soluble in water
    Melting Point 128-133°C
    Boiling Point Decomposes before boiling
    Storage Temperature 2-8°C
    Purity Typically ≥98%
    Synonyms Z-1,3-Diaminopropane hydrochloride
    Smiles C1=CC=C(C=C1)COC(=O)NCCCN.Cl
    Iupac Name N-(Benzyloxycarbonyl)propane-1,3-diamine hydrochloride

    As an accredited N-Carbobenzoxy-1,3-Diaminopropane Hydrochloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 250g of **N-Carbobenzoxy-1,3-Diaminopropane Hydrochloride** packaged in a sealed, amber glass bottle with tamper-evident cap and labeled.
    Shipping N-Carbobenzoxy-1,3-Diaminopropane Hydrochloride is shipped in tightly sealed containers, protected from moisture and light. Packaging complies with standard chemical safety regulations. It is transported at ambient temperature unless otherwise specified, with all appropriate documentation and labeling to ensure safe and secure delivery according to regulatory guidelines for laboratory chemicals.
    Storage Store **N-Carbobenzoxy-1,3-Diaminopropane Hydrochloride** in a cool, dry, well-ventilated area away from direct sunlight and incompatible substances such as oxidizers and acids. Keep container tightly sealed when not in use. Protect from moisture and physical damage. Store at 2–8 °C (refrigerator), unless otherwise specified by the manufacturer, to maintain chemical stability and prevent decomposition.
    Application of N-Carbobenzoxy-1,3-Diaminopropane Hydrochloride

    Applications of N-Carbobenzoxy-1,3-Diaminopropane Hydrochloride in Industrial Manufacturing

    As a specialized manufacturer, we supply N-Carbobenzoxy-1,3-Diaminopropane Hydrochloride to global customers operating in strictly regulated, high-value markets. The following sections highlight its essential downstream roles, specifying industrial use cases where its chemical attributes bring direct manufacturing value.

    1. Peptide Synthesis Intermediates for Pharmaceutical Manufacturing

    Peptide active pharmaceutical ingredients (APIs) require specialized protected diamine intermediates for stepwise synthesis. Our material functions as a critical building block in solid-phase and solution-phase peptide assembly, notably for introducing protected diaminopropane residues into oligopeptides where orthogonal deprotection is required. Controlled use ensures reproducibility and high final product purity demanded by regulatory agencies.

    Industry compliance standards

    • ICH Q7 GMP Guidelines for Active Pharmaceutical Ingredients
    • United States Pharmacopeia (USP) standards for peptide APIs
    • European Pharmacopoeia (Ph. Eur.) requirements
    • FDA’s cGMP regulations 21 CFR Parts 210/211

    Typical usage ratio

    • 0.90–1.05 molar equivalents per protected diaminopropane residue introduced, with minor adjustment based on peptide chain length and protection scheme

    Downstream process integration

    • Added during the protected amino acid coupling step on automated or manual peptide synthesizers following resin preconditioning
    • Deprotection and cleavage occur subsequently as per process controls

    Final product types

    • Pharmaceutical-grade oligopeptides and therapeutic peptides
    • Custom peptide intermediates for downstream modification

    2. Protected Diamine Reagents for Custom API Intermediate Synthesis

    Active pharmaceutical ingredient manufacturers depend on protected diamine reagents in the synthesis of specialty small molecule drugs, especially for nitrogen-bridge structures. Our product's carbobenzoxy group offers temporary protection during multistep reactions, preserving key reactivity for subsequent functionalization. This controlled protection advances selectivity and minimizes byproduct formation in process scale-ups.

    Industry compliance standards

    • ICH Q11: Development and Manufacture of Drug Substances
    • Pharmaceutical Inspection Co-operation Scheme (PIC/S) GMP requirements
    • Japanese Pharmacopoeia (JP) synthesis protocols, if relevant

    Typical usage ratio

    • 1.0–1.2 equivalents per diamine moiety targeted for protection, with optimization depending on impurity profile and recovery procedures

    Downstream process integration

    • Introduced during the initial protection reaction prior to main synthetic transformations of complex API intermediates
    • Deprotected at final purification or prior to API crystallization

    Final product types

    • Key intermediates for cephalosporin and carbapenem antibiotics
    • Bridged nitrogen heterocycles incorporated into synthetic APIs

    3. Raw Material for Bioconjugation and Linker Technologies

    Biopharmaceutical companies utilize protected diaminopropane derivatives as coupling units for advanced drug delivery systems, including antibody-drug conjugates (ADCs) and peptide-drug conjugates. The selective deprotection chemistry of the carbobenzoxy group supports linker assembly, maximizing conjugation efficiency and downstream reproducibility in antibody or ligand modifications.

    Industry compliance standards

    • USP General Chapter <665> Plastic Components and Systems Used to Manufacture Pharmaceutical Drug Products
    • GMP for ADC linkers and conjugates
    • EU Directive 2001/83/EC for medicinal product intermediates

    Typical usage ratio

    • Variable: typically 0.7–1.1 equivalents relative to available conjugation sites, modulated by payload-to-antibody ratio targets and desired linker density

    Downstream process integration

    • Utilized in solvent-phase linker synthesis and subsequent conjugation to therapeutic proteins or peptides under controlled hydrophilic/hydrophobic conditions

    Final product types

    • Commercial antibody-drug conjugates (ADCs)
    • Peptide-drug delivery compounds for targeted therapies

    4. Intermediate for Advanced Fine Chemicals and Performance Additives

    Manufacturers of specialty fine chemicals use this protected diamine in multi-step routes to produce high-purity specialty amines and polyamines used in coatings and advanced polymer modifiers. Its stable protection group allows sequential modifications and improved control of amine-reactive steps, supporting consistent performance characteristics in finished additives.

    Industry compliance standards

    • REACH Regulation (EC) No 1907/2006 for chemical intermediates
    • ISO 9001:2015 certification for fine chemical production
    • Compliance with customer-specific raw material assessment programs

    Typical usage ratio

    • 0.8–1.3 molar equivalents; adjusted based on downstream functionalization steps and batch size requirements

    Downstream process integration

    • Charged into reaction vessels during amine protection stages of polymer or additive precursor synthesis, with removal of protecting group post-derivatization

    Final product types

    • Epoxy curing agents for high-performance coatings
    • Functional polyamines for specialty resins and adhesives

    5. Precursor for Custom Synthesis in Research & Development

    Contract development and manufacturing organizations (CDMOs) and research institutions select this raw material for customizable synthetic routes, particularly when developing novel molecular libraries for pharma or material science applications. Its defined protection profile makes it a tool of choice in laboratory-to-kilo scale trials requiring precise incorporation of diamino moieties before deprotection and downstream modification.

    Industry compliance standards

    • ISO 13485:2016 for R&D of medical compounds
    • GLP (Good Laboratory Practice) for non-clinical safety studies
    • Internal SOPs for controlled research chemical handling

    Typical usage ratio

    • Highly variable: typically 0.5–1.5 equivalents depending on experimental protocol and library size, with adjustment for analytical validation or lead compound scale-up

    Downstream process integration

    • Weighing and charging into bench-scale reactions as the initial protected diamine input; adjusted for reaction yield optimization during exploratory work

    Final product types

    • Molecular library members for screening in drug discovery
    • Small batch specialty compounds for patent and lead optimization
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    Certification & Compliance
    More Introduction

    N-Carbobenzoxy-1,3-Diaminopropane Hydrochloride: Shaping the Future of Peptide Synthesis

    Commitment to Quality from the Laboratory Floor

    As a producer deeply involved in the synthesis of advanced fine chemicals, the journey with N-Carbobenzoxy-1,3-Diaminopropane Hydrochloride (CBZ-DAP-HCl) reflects ongoing dedication to high-purity manufacturing, reliable batch reproducibility, and continual process improvement. Daily exposure to evolving market questions pushes focus onto the features of each molecule, strengthening the ability to support customers, especially those undertaking peptide builds, innovative medicinal chemistry projects, and demanding academic research.

    In the world of protected diamines, CBZ-DAP-HCl has earned a distinct reputation for reliability and performance. Our teams specialize in small to medium batch production for laboratories where each gram matters. We pay close attention to product attributes beyond the commonly cited purity or assay—narrow melting point ranges, controlled moisture content, and shelf stability receive as much scrutiny as analytical data.

    The Practical, Hands-On Approach to Synthesis

    From years on the production line, it becomes clear that the best chemical isn’t simply the one that meets a specification, but also the one that handles predictably at every stage. Careful selection of raw materials sets the foundation for every hydrohalide salt—there is simply no substitute for steady hands and careful process control. For CBZ-DAP-HCl, limited exposure to atmospheric moisture during final stages prevents unwanted hydrolysis. This attention ensures the product stays free-flowing and easy to weigh, even after weeks on a shelf.

    Each batch receives its CBZ group through precise carbamylation, followed by hydrochloride salt formation. The result? A crystalline, off-white solid that flows consistently from vial to reaction vessel. Product identity and purity receive verification through NMR, HPLC, and titration, as customers expect and deserve. By inspecting every stage in-house, we keep control over quality and avoid the pitfalls that come from outsourcing critical steps. Mistakes in this process show up downstream, so the team treats every gram as a reflection of the whole operation.

    Specification-Driven Production: CBZ-DAP-HCl at Its Core

    We usually set our product standard above 98% HPLC purity, with chloride content and water levels falling well within tight limits. Typical batch lots offer a melting point between 196°C and 200°C. Consistent quality allows medicinal chemists to plan their syntheses without worrying about variable impurity profiles from lot to lot. N-Carbobenzoxy-1,3-Diaminopropane Hydrochloride’s formula, C10H17ClN2O2, along with a molecular weight of roughly 248.7 g/mol, simplifies stoichiometric calculations.

    It’s easy to overlook how vital trace impurity control becomes in scale-up or regulatory submissions. Any degradation in the protecting CBZ moiety, or incomplete hydrochloride exchange, shows up during acetylation or deprotection steps later in a synthesis route. Years of direct troubleshooting with customers highlight that impurity sources usually track back to inconsistent upstream chemistry, not laboratory technique. We learned early that prevention beats cure, so each lot faces full analytical assessment before shipment leaves the plant.

    Beyond the Bench: Reactivity, Handling, and Workflow Integration

    Laboratory staff need reagents that integrate smoothly with peptide synthesis strategies. The CBZ-PG (carbobenzoxy-protecting group) balances protection during multi-step condensation or chain extension, while yielding to deprotection when exposed to standard hydrogenolysis. The hydrochloride salt form confers added stability and ease of handling compared to free-base analogs. Unlike many unprotected diamines, which absorb atmospheric carbon dioxide and rapidly form sticky viscous oils, CBZ-DAP-HCl maintains a solid form and resists hydrolytic breakdown across typical benchtop exposures.

    Reactions involving 1,3-diaminopropane tend to require careful timing and measured conditions, because the bare molecule’s reactivity causes side reactions and product loss. Carbobenzoxy-protection, introduced decades ago, now remains the method of choice for managing diamine reactivity during chain assembly. Chemists familiar with the difference in stability between free diamines and CBZ-protected forms reach for this product by name, as it not only shields both amine functionalities but also suppresses unwanted cyclization.

    Spotlight on Usability: Storage and Longevity

    As manufacturers, we know that procurement and storage habits impact project reliability. CBZ-DAP-HCl’s resistance to deliquescence separates it from many alternative salts—this translates into extended shelf life, reduced risk of caking, and hassle-free handling in periods of high humidity. Uncoated containers inside moisture-barrier packaging prove sufficient for multi-year storage. No nitrogen backfilling or inert atmospheres are needed under normal laboratory conditions, making this product straightforward in stock management and re-use.

    Tracking complaints and customer queries over the years revealed something less obvious: researchers face recurring headaches from product packed carelessly or inadequately sealed. So, we package under dry air, avoiding exposed surfaces and sealing each vessel promptly after filling. It cuts waste, prevents cross-contamination, and reduces need for expensive re-purification steps on customer premises. By controlling every last step of packaging, retrieval rates on CBZ-protected diamines remain extremely high, and the residue loss stays minimal during weighing or transfer.

    Distinctive Features and Real-World Performance

    In our view, the real value of CBZ-DAP-HCl stems from more than an attractive analytical report; it lies in the way this molecule functions in everyday chemistry. Free diamines, while cheaper to produce, bring with them handling challenges, unpleasant odors, and sensitivity to oxidation—traits that disrupt workflows and threaten reproducibility. We have seen users suffer batch failures or column overloading when switching from protected to unprotected forms, thinking the savings in cost could offset trouble in purification. Consistently, the results speak otherwise.

    CBZ-protected diamines, particularly the hydrochloride salt, enable stepwise assembly of peptide chains and branched amino acid derivatives because the molecule keeps its identity throughout the process. Heating, coupling, and deprotection operations run more reliably, giving synthetic chemists predictable endpoints and cleaner reaction workups. Each year, customers planning custom peptide preps or route scouting for scale-up projects specifically request our CBZ-DAP-HCl because past efforts using unprotected or mono-protected alternatives caused delays, reduced overall yields, or failed to scale.

    Comparisons: CBZ-DAP-HCl vs. Alternatives in the Lab

    Other protection options exist—Boc, Fmoc, or Tosyl derivatives offer different stability and deprotection kinetics. Boc-protected diamines, for example, demand acidolysis, introducing side products and complicating purification if not tightly controlled. Fmoc-protected analogs often show higher costs, can be light sensitive, and sometimes introduce steric hindrance unsuitable for all peptide strategies. For everyday work, CBZ protection stands out by delivering strong oxidative stability and convenient deprotection under hydrogenation without strong acids or bases.

    In-house testing with comparative peptide assemblies shows that switching from free-base to CBZ-HCl salts yields higher isolated product mass, with NMR spectra free from unassigned singlets or obscure sidebands. Process operators regularly report that CBZ-DAP-HCl cuts purification workload, since the main product crystallizes well and any side reactions remain manageable. A few stories stick out—researchers in Europe struggled with persistent orange discoloration when using unprotected diamines from a discount supply house; shifting to a reliable CBZ-protected batch quickly returned product purity above 97% with unambiguous mass spectrometry data. This pattern repeats year after year, regardless of the project or researcher background.

    Applying Knowledge to Everyday Benchwork

    Nothing replaces the confidence that comes from knowing a raw material’s provenance and processing history. Our team learned early that the smallest variations in pH, temperature, or solvent system during protection steps create lasting effects, sometimes invisible to HPLC but painfully clear to the practicing chemist. Carefully controlled crystallization, supported by slow solvent exchanges, controls particle size in the final product for better weighing and dosing accuracy in micro-scale and gram-scale syntheses alike.

    Direct feedback from academic and pharma labs led to incremental improvements; dried product free of visible clumps, batch-to-batch tracking, and colour coding for better inventory management all followed direct input from users, not abstract regulatory mandates. We listen not only to the procurement teams, but also to bench chemists shipping samples between sites, so every package places readiness in the hands of the end user, not in the system.

    Supporting Innovation in Peptide and Medicinal Chemistry

    Nearly every breakthrough in complex peptide synthesis and structure-based drug design has relied on an arsenal of reliable building blocks. CBZ-DAP-HCl belongs to that family of protected scaffolds opening up new synthetic routes, especially those needing carefully masked diamines for aza-peptide, lactam ring, or cross-linking studies. In the last decade, an increasing share of requests originate from teams exploring unusual amino acid derivatives or complex chemical space, not just typical peptide coupling. CBZ protection remains a go-to solution for new ligation strategies requiring compatibility with diverse solvents, mild bases, and tailored functional group conditions.

    Pharmaceutical innovators mention that CBZ-DAP-HCl helps them bypass bottlenecks that arise from fragile or highly hydrophilic free diamines. Less attention often goes to purification teams, who appreciate how protected diamines shorten column chromatography procedures, deliver better recovery rates, and prevent cross-linking or decomposition in downstream steps. Cost remains an important factor, but over years of running pilot and commercial batches, it’s clear that reducing failed synthesis outweighs small price differences at the raw material stage.

    Upholding Safety and Process Responsibility

    Feedback from staff and partners helps us continuously improve occupational health standards, material handling, and exposure prevention. CBZ-DAP-HCl remains relatively benign compared to many other laboratory chemicals; it’s not volatile, nor does it emit hazardous vapors under normal temperatures. Still, fine dust handling and repeated exposure prompt us to favor enclosed charging systems, clear labeling, and routine refresher training for plant staff. Over time, smaller container sizes and reduction of open transfer steps cut loss rates and improved lab hygiene.

    Direct communication channels with key customers lead to ongoing discussions about packaging waste, solvent recycling, and improved documentation. A recent partnership with a contract manufacturer resulted in a fully recyclable enclosure for the CBZ-DAP-HCl vial inserts, minimizing micro-plastic generation in busy facilities. As process chemists, we prefer practical solutions to regulatory headaches—so our focus falls on cleaner, safer work spaces, not only code compliance.

    Anticipating Needs: The Future Outlook

    Ten years ago, barely a dozen researchers worldwide requested custom specs or high-reproducibility CBZ-protected diamines. Today’s launch cycles in pharmaceutical and biologics companies demand a sharper response: smaller lot sizes, tighter ship windows, and batch records traceable by barcode rather than paperwork alone. The lesson from the field stays clear—successful projects start with well-chosen building blocks, applied consistently, and delivered on schedule with clear documentation.

    Supplies of CBZ-DAP-HCl no longer flow only to academic peptide synthesis labs. Diagnostics manufacturers, chemical biology start-ups, and contract research organizations all recognize that the smallest differences in raw material handling metrics can make or break milestones. In the past year, we ramped up parallel synthetic routes to guarantee steady output, even when supply chain disruptions hit raw material sources. This change came at the urging of customers who value continuity, predictability, and close manufacturer relationships over price alone.

    Final Thoughts on Shared Success

    Our commitment to making N-Carbobenzoxy-1,3-Diaminopropane Hydrochloride arises not from blind routine, but from listening to every challenge and query coming from the field. Each technical request, shipment review, or call for batch traceability becomes a point for process improvement, and collective learning strengthens our operations as well as our customers’ bottom lines. The years spent on the production floor, handling each physical bag and batch sheet, reinforce the value of direct experience—no marketing claim stands up to the reality of successful project delivery run after run.

    CBZ-DAP-HCl’s role in protected diamine chemistry cannot be understated. The molecule brings real gains in handling, stability, and synthesis reliability. These advantages rest not just on decades-old procedures, but on a modern approach to traceability, user feedback, and relentless quality control. As a manufacturer embedded in the pulse of fine chemical production, our mission stays focused on supporting creativity, spearheading innovation, and fostering long-term partnerships—one smart building block at a time.