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Acs-Pnz-Pyrrolidyl-(Boc)-Nso2Nh2

    • Product Name Acs-Pnz-Pyrrolidyl-(Boc)-Nso2Nh2
    • Alias Acs-Pnz-Pyr-Boc-Nso2Nh2
    • 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

    820408

    Product Name Acs-Pnz-Pyrrolidyl-(Boc)-Nso2Nh2
    Molecular Formula C18H25N5O7S
    Molar Mass 455.49 g/mol
    Appearance White to off-white solid
    Purity ≥95%
    Storage Temperature -20°C
    Solubility DMSO, DMF, slightly soluble in methanol
    Protecting Groups Acetyl (Acs), Benzyloxycarbonyl (Pnz), tert-Butyloxycarbonyl (Boc)
    Functional Groups Sulfonamide, Carbamate, Amide
    Cas Number N/A
    Application Peptide synthesis intermediate
    Stability Stable under recommended storage conditions

    As an accredited Acs-Pnz-Pyrrolidyl-(Boc)-Nso2Nh2 factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The chemical Acs-Pnz-Pyrrolidyl-(Boc)-Nso2Nh2 is supplied in a 100 mg amber glass vial, tightly sealed for protection.
    Shipping The chemical **Acs-Pnz-Pyrrolidyl-(Boc)-Nso2Nh2** is shipped in a sealed, chemically compatible container, protected from moisture and light. The package includes appropriate Hazard Communication labels and documentation, with temperature-controlled shipping if specified. Handling complies with all applicable safety and regulatory guidelines to ensure chemical integrity and safe delivery.
    Storage **Acs-Pnz-Pyrrolidyl-(Boc)-Nso2Nh2** should be stored in a tightly sealed container, protected from light and moisture. Keep at -20°C in a dry, well-ventilated area, away from incompatible substances such as strong oxidizers and acids. For best stability, avoid repeated freeze-thaw cycles and ensure the environment is free from humidity to prevent hydrolysis or degradation.
    Application of Acs-Pnz-Pyrrolidyl-(Boc)-Nso2Nh2

    Applications of Acs-Pnz-Pyrrolidyl-(Boc)-Nso2Nh2 in Industrial Manufacturing

    As a specialized manufacturer of Acs-Pnz-Pyrrolidyl-(Boc)-Nso2Nh2, we support advanced industrial sectors that require reliable intermediates for high-value synthesis. Below are detailed application scenarios in core downstream tracks with relevant compliance, technical, and product highlights.

    1. Pharmaceutical API Intermediate for Peptide Synthesis

    This compound serves as a protected pyrrolidyl sulfonamide intermediate during solid-phase peptide synthesis (SPPS) for the manufacture of regulatory-compliant active pharmaceutical ingredients (APIs). Its N-Boc and sulfonamide functionalities ensure site-specific coupling and minimize side reactions in oligopeptide assembly. Our clients integrate it in custom and generic API projects where exact protection and deprotection steps are critical for maintaining molecular integrity under GMP controls. Placement of this intermediate in payload linkage synthesis supports scalable manufacturing for next-generation peptide therapeutics.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice (GMP) for Active Pharmaceutical Ingredients
    • USP, EP, JP requirements for starting materials
    • Chemical registration under REACH for European manufacture
    • FDA 21 CFR Part 211 for documentation and traceability

    Typical usage ratio

    • 0.8–1.2 molar equivalents per amino acid coupling step depending on peptide sequence length and resin loading
    • Adjusted to batch scale and process optimization by in-line MS monitoring

    Downstream process integration

    • Direct addition after resin swelling and initial deprotection steps
    • Engages in selective coupling via Fmoc/Boc protection strategies on automated SPPS platforms
    • Purification through preparative HPLC before final global deprotection and lyophilization

    Final product types

    • Synthetic therapeutic peptides (injectable and oral forms)
    • Peptide-drug conjugates
    • Research-grade oligopeptides
    • API starting units for small-molecule/peptide hybrids

    2. Chemical Probe Development for Target Validation

    Drug discovery labs use Acs-Pnz-Pyrrolidyl-(Boc)-Nso2Nh2 as a protected heterocycle scaffold when building functionalized chemical probes. Its stability and orthogonal protecting groups permit selective modifications and conjugation with fluorophores or affinity tags crucial in biophysical and cell-based target validation. Research organizations refine probe physicochemical properties through controlled deprotection and coupling, enabling high-precision profiling of protein targets in lead identification workflows governed by GLP standards.

    Industry compliance standards

    • OECD Principles of Good Laboratory Practice (GLP)
    • NIH reagent quality and documentation guidance
    • Control of hazardous substance (COSHH) regulations for laboratory use
    • Material registration under TSCA (US) or REACH (EU) for R&D supply

    Typical usage ratio

    • 0.9–1.5 equivalents per probe design iteration
    • Adjusted for probe target density and desired substitution patterns

    Downstream process integration

    • Enter initial probe synthesis via amide coupling or click chemistry
    • Selective deprotection for subsequent fluorophore or chelator conjugation
    • Final purification by silica gel chromatography or preparative reverse-phase chromatography

    Final product types

    • Fluorescent and biotinylated chemical probes
    • Target identification tools for HTS assays
    • Proprietary SAR reagents for lead optimization
    • Functionalized affinity capture agents

    3. High-Value Agrochemical Intermediates

    Manufacturers of advanced agrochemicals rely on this intermediate during the preparation of next-generation active ingredients featuring cyclic sulfonamide groups. The N-Boc protection allows multi-step reactions without unwanted hydrolysis, ensuring yield stability when synthesizing specific herbicide or fungicide scaffolds. Agrochemical formulators incorporate this key building block in process routes that meet strict residue and performance criteria, optimizing stepwise conversion under controlled, traceable plant conditions.

    Industry compliance standards

    • ISO 9001:2015 Quality Management System for plant operation
    • Regulation (EC) No 1107/2009 for plant protection product approval in the EU
    • US EPA pesticide registration and inert ingredient review
    • GLP (Good Laboratory Practice) for safety assessment studies

    Typical usage ratio

    • 0.5–1.0 molar equivalents per target molecule depending on route complexity
    • Adjusted to optimize purity and minimize by-product generation in specific active ingredient syntheses

    Downstream process integration

    • Implemented at the heterocycle construction stage following core aromatic substitution
    • Retains protection until final formulation or droplet encapsulation steps
    • Monitored via HPLC/GC during process scale-up for impurity control

    Final product types

    • Selective herbicides (amide-linked sulfonylureas)
    • Fungicidal agents with cyclic sulfonamide cores
    • Advanced safeners for seed treatment formulations
    • Custom synthesis intermediates for agrochemical innovators

    4. Specialty Polymer Additives for Engineering Plastics

    Producers of high-performance engineering plastics use Acs-Pnz-Pyrrolidyl-(Boc)-Nso2Nh2 as a functional monomer precursor, particularly for synthesizing sulfonamide-containing copolymers with enhanced toughness and solvent resistance. Its incorporation ensures controlled functional group introduction, facilitating block or random copolymer structures required by automotive and electronics segments. The intermediate’s protection chemistry supports stepwise functionalization without undesired crosslinking, streamlining QC for technical-grade polymer production under regulated plant conditions.

    Industry compliance standards

    • ISO 14001:2015 Environmental Management for chemical processing
    • RoHS (Restriction of Hazardous Substances) compliance for electronics applications
    • UL 94 flammability approvals for engineering plastics
    • REACH registration for European imports

    Typical usage ratio

    • 1–5 wt% based on total monomer content for specific copolymer formulations
    • Adjusted by melt flow index or mechanical property targets during process trials

    Downstream process integration

    • Precursor charged during monomer blending before polymerization (solution or suspension)
    • Deprotection occurs in post-polymerization to activate sulfonamide groups
    • Integrated with online spectroscopic QC for batch consistency

    Final product types

    • Specialty polyamides for automotive housings
    • Solvent-resistant electrical insulation materials
    • Wear-resistant plastic gears and components
    • Custom compounded technical plastics

    5. Fine Chemical Building Block for Advanced Organic Synthesis

    Chemical manufacturers and contract research organizations source this compound for use as a selective nitrogen and sulfonamide donor in complex molecule assembly, including pharmaceutical impurities, reference standards, and specialty ligands. The dual protection elements allow stepwise transformation via acylation or alkylation, providing flexibility in multistep synthesis where intermediate isolation and high purity are required. This building block supports projects with rigorous traceability and analytical documentation under cGMP and ISO systems.

    Industry compliance standards

    • ISO 17025 for chemical analytical methods
    • USP/Ph. Eur. substance purity requirements (for reference standard synthesis)
    • GMP documentation for pharmaceutical fine chemicals
    • REACH and TSCA records for specialty chemical handling

    Typical usage ratio

    • 1.0 molar equivalent as limiting reagent in custom transformations
    • May increase to 1.5 equivalents in multistep reactions requiring excess for completeness

    Downstream process integration

    • Used in the early to mid-stages of organic synthesis for fragment coupling
    • Incorporated into telescoped routes with protection/deprotection scheduling
    • Final processing involves high-resolution purification and documentation for customer QA

    Final product types

    • Pharmaceutical impurity markers
    • Specialty ligands for catalysis research
    • Reference standards for analytical labs
    • Complex molecule intermediates for downstream validation
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