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Boc-D-Cyclopropylglycine

    • Product Name Boc-D-Cyclopropylglycine
    • Alias Boc-D-cpg
    • Einecs 682-270-6
    • 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
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    Specifications

    HS Code

    395450

    Product Name Boc-D-Cyclopropylglycine
    Cas Number 152766-80-6
    Molecular Formula C10H17NO4
    Molecular Weight 215.25
    Appearance White to off-white solid
    Melting Point 98-102°C
    Solubility Slightly soluble in water, soluble in organic solvents
    Storage Conditions Store at 2-8°C, dry place
    Purity Typically ≥98%
    Synonyms N-Boc-D-cyclopropylglycine
    Smiles CC(C)(C)OC(=O)N[C@@H](C1CC1)C(=O)O
    Inchi InChI=1S/C10H17NO4/c1-10(2,3)15-8(14)11-7(9(12)13)6-4-5-6/h6-7H,4-5H2,1-3H3,(H,11,14)(H,12,13)/t7-/m1/s1
    Optical Rotation [α]20D = +33° (c=1, MeOH)
    Application Amino acid derivative for peptide synthesis

    As an accredited Boc-D-Cyclopropylglycine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The packaging for Boc-D-Cyclopropylglycine (1g) is a sealed amber glass vial clearly labeled with product name, quantity, and safety information.
    Shipping Boc-D-Cyclopropylglycine is shipped in secure, tightly sealed containers to prevent moisture and air exposure. It is packaged according to chemical safety regulations, labeled with hazard information, and protected from extreme temperatures. Shipping complies with local and international chemical transport guidelines, ensuring safe and prompt delivery to the destination.
    Storage Boc-D-Cyclopropylglycine should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from direct sunlight and moisture. Store at 2-8°C (refrigerator temperature) and protect from incompatible substances such as strong acids or bases. Ensure proper labeling and keep away from sources of ignition or excessive heat.
    Application of Boc-D-Cyclopropylglycine

    Applications of Boc-D-Cyclopropylglycine in Industrial Manufacturing

    Boc-D-Cyclopropylglycine is a protected non-natural amino acid intermediate with well-established roles in highly regulated industrial manufacturing settings. Our production is aligned with the pharmaceutical supply chain, supporting advanced peptide synthesis, small molecule API building blocks, and related fine chemical developments. Below, we highlight major application scenarios, covering compliance, precise industrial usage, downstream processing, and end product categories.

    1. Peptide Therapeutics Synthesis

    This chiral cyclopropylglycine derivative serves as a key monomer in the solid-phase or solution-phase synthesis of peptide-based drug candidates, especially where cyclopropyl modifications confer increased metabolic stability or target selectivity. Peptide active pharmaceutical ingredients (APIs) containing cyclopropylglycine residues are advancing in fields such as oncology and metabolic disorders. Production lines supporting GMP batch manufacturing require reproducible sourcing and validated integration of non-natural amino acids at defined sequence positions.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for APIs
    • Current Good Manufacturing Practice (cGMP), 21 CFR Parts 210/211
    • United States Pharmacopeia (USP) General Chapter <1045> Peptide Therapeutics
    • European Pharmacopoeia peptide monographs (Ph. Eur.)

    Typical usage ratio

    • Used at the specific residue positions—typically 1–20% molar incorporation in the main sequence, depending on peptide length and design; chemists adjust Boc-D-cyclopropylglycine loading per synthetic batch scale and peptide substitution pattern.

    Downstream process integration

    • Boc-protected amino acid introduced during automated stepwise chain elongation on solid-phase peptide synthesizers (SPPS); also applicable to segment condensation in solution-phase protocols, with full deprotection and purification steps incorporated post-assembly.

    Final product types

    • Investigational peptide APIs, early-phase clinical batch peptides, and process validation materials for pharmaceutical use
    • Preclinical research peptides for structure-activity relationship (SAR) studies

    2. Small Molecule API Building Blocks

    Pharmaceutical companies employ this protected cyclopropylglycine as a synthon in the construction of complex molecular scaffolds where constrained ring amino acids enhance pharmacological profiles. The Boc group ensures compatibility with standard condensation and coupling reactions, minimizing racemization and facilitating selective deprotection at the appropriate synthetic stage.

    Industry compliance standards

    • International Conference on Harmonisation (ICH) Q11: Development and Manufacture of Drug Substances
    • FDA Q3A/B guidelines for impurities in drug substances and drug products
    • ISO 9001:2015 Quality Management

    Typical usage ratio

    • Varies from 2–10 mol% of final molecule structure, depending on whether the cyclopropylglycine is incorporated as an intermediate or terminal motif; precise equivalents adjusted based on coupling yields and protecting group removal schedules.

    Downstream process integration

    • Incorporated during amidation/carboxylation steps of multi-step organic synthesis, often during convergent assembly or late-stage modifications of API candidates where chiral center retention is critical; deprotection occurs before final salt formation or purification.

    Final product types

    • Route intermediates for anti-infective or central nervous system (CNS) APIs
    • Advanced pharmaceutical intermediates used for final API crystal forms or salts

    3. Specialty Peptide Diagnostic Reagents

    Boc-D-cyclopropylglycine is incorporated into custom peptide chains produced for use as antibody epitope mimics or standard calibration peptides in ELISA, LC-MS, and other analytical platforms. Synthetic peptides containing cyclopropyl-modified residues enhance specificity and stability in diagnostic test manufacturing and immune assay development.

    Industry compliance standards

    • ISO 13485:2016 Medical Devices—Quality Management for In Vitro Diagnostics
    • U.S. FDA 21 CFR Part 820—Quality System Regulation
    • CLSI (Clinical & Laboratory Standards Institute) standards for IVD raw materials

    Typical usage ratio

    • Typically 1–5% of total peptide batch, inserted at one or more defined sites within synthetic diagnostic peptides to mimic critical structures or provide unique mass signatures for reference standards.

    Downstream process integration

    • Introduced during custom peptide synthesis stage by C-terminal or N-terminal elongation in SPPS protocols; final peptides undergo further biotinylation, labeling, or conjugation before use in diagnostic kit assembly.

    Final product types

    • Peptide standard materials for immunoassay kit calibration
    • Reference controls for LC-MS peptide identification

    4. Research-Grade Peptide Library Production

    Academic and biotech research groups use Boc-D-cyclopropylglycine in the synthesis of combinatorial peptide libraries for ligand screening, protein interaction profiling, and structure-based lead optimization. The cyclopropyl group confers steric and conformational diversity to libraries, often yielding hits with improved biological properties for downstream drug discovery.

    Industry compliance standards

    • Institutional research chemical safety guidelines
    • OECD Good Laboratory Practice (GLP) for non-clinical safety studies

    Typical usage ratio

    • Up to 10% of a given peptide library’s variants contain the cyclopropylglycine residue, either at fixed or random positions; actual proportion depends on screening library design and desired scaffold diversity.

    Downstream process integration

    • Applied during parallel automated SPPS or split-pool combinatorial synthesis; compound mixtures are purified via HPLC and characterized before screening assays or structural analyses.

    Final product types

    • Diversified research peptide libraries
    • Screening sets for target engagement studies and initial lead identification

    5. Chiral Auxiliary for Stereoselective Synthesis

    Chemical manufacturers and contract research organizations utilize protected D-cyclopropylglycine derivatives for the induction or control of stereochemistry during asymmetric synthesis steps, especially when constructing stereochemically complex pharmacophores. Use as a chiral auxiliary ensures high stereoselectivity and can be recovered or removed after synthesis, minimizing downstream purification burden.

    Industry compliance standards

    • EU REACH regulations for specialty chemical intermediates
    • ISO 9001:2015 for chemical and pharmaceutical manufacturing
    • Supplier-specific quality agreements and Certificate of Analysis (CoA) requirements

    Typical usage ratio

    • Applied in stoichiometric amounts relative to the substrate (usually 1:1 molar ratio), adjusted for completeness of stereocontrol in asymmetric transformations; excess removed after key reaction step as per process validation results.

    Downstream process integration

    • Added at the stage of enolate alkylation, Michael addition, or aldol reaction in chiral auxiliary-based stereoselective processes; removed via acid/base or reductive cleavage before final structure isolation or further functionalization steps.

    Final product types

    • Intermediates for stereochemically defined active compounds
    • Chiral building blocks for further transformations by process chemists or custom synthesis services
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    Certification & Compliance
    More Introduction

    Introducing Boc-D-Cyclopropylglycine: A Reliable Building Block for Modern Peptide Synthesis

    Pursuing Quality and Consistency in Every Batch

    Several years ago, we decided to enhance our line of protected amino acids to answer the demands coming from both established research institutions and innovative pharmaceutical companies. The outcome of this effort is Boc-D-Cyclopropylglycine, a specialty D-amino acid we prepare specifically for teams working at the frontier of peptide science. This compound has done much to facilitate the design of bioactive molecules where conformational rigidity, chirality, and structural precision play crucial roles in experimental and therapeutic outcomes. Behind this capability stands a focused manufacturing process born of hands-on experience, the careful selection of raw material sources, and a commitment to measurable purity.

    Producing Boc-D-Cyclopropylglycine calls for an environment where skill drives decision-making, not stenographic compliance. Technicians oversee each stage, using in-house chiral analysis to verify that no racemization clouds the finished product. What reaches our clients earns its D-stereochemistry through scrutiny rather than assumption. We have spent years writing, revising, and refining batch protocols to weed out minor impurities that can derail peptide coupling, especially when stringent stereocontrol over sequence integrity is expected.

    Specifications That Grow Out of Lab Needs

    We listened closely to what peptide chemists and process developers wanted from their protected cyclopropylglycine: clear and reliable characterization, low moisture content since traces of water can drive premature deprotection or side reactions, and packaging in containers that limit light and moisture ingress long-term. Boc-D-Cyclopropylglycine leaves our facility as a finely crystalline powder, reflecting typical material properties aligned with its molecular structure—white color, low bulk density, swift solubility in most organic solvents commonly used in solid-phase synthesis, and well-defined melting behavior. Our chromatographic data demonstrate that main peaks account for over 99% of the observed sample, while residual solvents never exceed controlled levels. We have seen what even a minor percentage of residual unprotected acid can do to reaction outcomes, and so we pursue a margin that cuts no corners.

    As a native D-isomer bearing the tert-butyloxycarbonyl (Boc) protection on its alpha-amino group, this building block answers the need for both chirality and compatibility with Boc-based synthetic strategies. We keep records of every lot’s specific rotation, moisture content, and purity profile. There are no surprises for the peptide chain growing in the reaction vessel—just the confident expectation that the final sequence will match design, not some invisible variance introduced upstream during production.

    Applications That Demand Precision

    Most of our customers work on sequence-defined specialty peptides and research-targeted oligopeptides, either for proof-of-concept pharmacology or for advancing a clinical candidate. Boc-D-Cyclopropylglycine enters their process as more than a placeholder. Its cyclopropyl side chain provides rigid geometry that resists unwanted backbone flexibility, often creating points of metabolic stability and distinctive bioactivity. Experienced peptide chemists have shared stories with us about the pronounced effect a cyclopropylglycine residue has on turning rate metrics, protease resistance, and receptor affinity patterns in target molecules. These results reflect not hope but the accumulated evidence drawn from the bench—for example, how backbone protection schemes can prevent isomerization and safeguard function, when the starting material lives up to specification.

    Teams using Boc-D-Cyclopropylglycine frequently work in peptide coupling protocols where exposure to acid-labile components occurs. Boc protection gives them the latitude to orchestrate clean deprotection steps, with minimal risk of premature removal under mild conditions. This contrasts with Fmoc-protected analogues which require distinct deprotection cycles, sometimes complicating purification logistics or exposing side chains to conditions that prompt side reactions. We have tuned our process so that Boc-D-Cyclopropylglycine achieves a specific rotation in line with reference standards, so customers can verify stereochemistry at a glance.

    Our experience in collaborative support has shown that medicinal chemists and peptide engineers choose Boc-protected cyclopropylglycine when they want direct incorporation into growing peptide chains without waiting for in-lab purification of starting materials. This is not an idle convenience—time saved in cleanup translates to lower risk for batch failure, less downtime for equipment, and ease in keeping project timelines on track. In certain peptide-mimetic and structure-activity relationship experiments, teams have specifically highlighted the need for D-isomer selectivity. False readings or compromised yield from use of low-grade or incorrectly-protected sources become a thing of the past.

    Key Differences: Real-World Impact, Not Just Catalog Entries

    Comparisons between Boc-D-Cyclopropylglycine and other protected cyclopropylglycines, or even its Fmoc-protected cousins, often hinge on practical factors that shape project outcomes. Choosing the D-isomer over L responds to the trend toward using stereochemical diversity for modulating in vivo metabolism and peptide architecture. Our own data alongside customer feedback support that using meticulously prepared Boc-D-Cyclopropylglycine not only improves coupling efficiency but also decreases peptide chain aggregation on solid supports.

    Clients who have relied on off-brand or bulk commodity materials report challenges ranging from inconsistent yield to the unpredictability of crude peptide purity. During the purification process, minor impurities in raw protected amino acids can add hours or even days to project timelines—not to mention costs. The difference, in our view, traces directly to how much oversight and expertise go into maintaining purity, limiting byproduct profile, and packaging for transport and storage without introducing hidden liabilities for the end user.

    Several points set our product apart. The careful selection of Boc-D-Cyclopropylglycine is rooted in real-world outcomes observed across a wide range of synthesis and screening environments:

    Where some procurement teams focus only on catalog numbers and price sheets, our end users see the downstream costs of a poorly characterized ingredient each time a peptide column blinks red mid-cycle. The value of a premium, accurately characterized starting material comes in shorter project cycles and fewer disruptions—a lesson driven home not just by theory but by the hard-won experience of chemists with skin in the game.

    Production Journey: A Chemist’s Perspective

    Many challenges come up during the production of Boc-D-Cyclopropylglycine, ones that don’t always get airtime in glossy brochures. The cyclopropyl ring calls for particular attention during both glycine derivatization and Boc protection steps to preserve the three-membered structure against ring expansion or unintended opening. Some of these technical hurdles seized up early research-grade runs for other producers, prompting complaints about trace level byproducts or unexpected melting points that threw off process scale-up.

    We encountered the same pitfalls. Rather than slap a “premium” label on an inconsistent product, we overhauled the initial synthesis and workup, doing away with unnecessary impurities and introducing staged drying and crystallization conditions to lock in the right physical characteristics. Multiple runs refined our approach to prompt, gentle isolation and accurate storage parameters, with each lesson documented and shared within the production team to drive process learning.

    Feedback from clients at peptide facilities led us to address a packaging issue: product sticking to container walls, making full retrieval tricky. After in-depth consultation, we swapped out generic plastics for customized, moisture-barrier vials. Fewer grams lost per bottle, higher consistency in transfer weights, and less hassle for end users. These improvements stem not from following lab manuals but from listening to the lived frustrations and practical requirements relayed by those handling the product on the floor.

    Direct Support and Shared Problem Solving

    Industry moves quickly, and requirements change without much warning. Teams developing new analogues or transitioning from research to small-scale GMP often hit new pain points. In those situations, it pays to have an open channel to the manufacturer, not a faceless third-party reseller who forwards queries without context. Our own staff are chemists and process engineers, so we enter every inquiry with the benefit of understanding how process bottlenecks, analytical hiccups, or sourcing concerns unfold during real synthesis.

    Questions about solubility, coupling behavior under specific conditions, or how to handle tricky couplings often come up. We provide not only standard technical data but also help interpret how observed variations might trace back to local scale-up conditions, agitation rates, or even warehouse humidity levels. Years spent in the production and R&D spaces mean we see the context, not just a data point.

    For teams worried about cross-contamination with other amino acid derivatives, especially in facilities with broad product portfolios, we have implemented dedicated equipment and regular cross-verification cleanouts. That approach drives the quality of our Boc-D-Cyclopropylglycine far beyond the “meets specification” requirements—these protocols respond to the reality of peptide purity expectations at the point of application.

    We don’t view questions about shelf life, packaging compatibility, or specific coupling scenarios as afterthoughts. By maintaining lines of communication with teams at pharma, biotech, and academic labs, we help troubleshoot issues before they cascade into project delays. In return, we get a ground-level view of emerging needs as the field advances.

    Why We Believe in Boc-D-Cyclopropylglycine

    A product’s profile gets shaped over time, through its real-world impact rather than just claims made at the sales counter. Boc-D-Cyclopropylglycine earns its place by consistently standing up to the rigors of modern peptide synthesis, from small-molecule drug discovery to more exploratory chemical biology studies investigating new modes of action. Peptide chemists have pointed out to us that the cyclopropyl motif—rare, stable, and resistant to metabolic breakdown—still remains a source of innovation and differentiation among side chain variations. This isn’t a commoditized ingredient, but a specialty building block with tangible benefits for stability, conformational control, and downstream bioactivity.

    Our production team takes real satisfaction in seeing papers, patents, and investigational compounds that name our material as a critical input. These aren’t generic outcomes—they are the cumulative result of shared expertise, deliberate process management, and a respect for the science our customers practice. By bringing both historical knowledge and continuous improvement into play, we contribute not just a product, but a forward-moving partnership that grows through mutual learning.

    As regulations evolve, new synthetic strategies emerge, and expectations for traceability grow more demanding, we will continue to adapt every aspect of our Boc-D-Cyclopropylglycine supply chain. We draw insight from every conversation, delivery, and troubleshooting session, pushing us to re-invest in analytical infrastructure, to listen even closer, and to continue validating every batch produced. Our commitment traces its roots to a simple idea: what leaves our door should raise confidence, speed up discovery, and ease the critical path to innovation, one bottle at a time.