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HS Code |
936014 |
| Productname | (Boc-Aminooxy)Acetic Acid |
| Casnumber | 74232-72-3 |
| Molecularformula | C7H13NO5 |
| Molecularweight | 191.18 |
| Appearance | White to off-white solid |
| Meltingpoint | 85-88°C |
| Solubility | Soluble in DMSO, methanol, and slightly soluble in water |
| Purity | Typically ≥98% |
| Storagetemperature | 2-8°C (refrigerated) |
| Synonyms | tert-Butoxycarbonylaminooxyacetic acid |
| Smiles | CC(C)(C)OC(=O)ONCC(=O)O |
| Inchikey | UGZCZMMLWGBPKO-UHFFFAOYSA-N |
As an accredited (Boc-Aminooxy)Acetic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 5-gram sample of (Boc-Aminooxy)acetic acid is supplied in a sealed amber glass vial with a tamper-evident cap. |
| Shipping | (Boc-Aminooxy)Acetic Acid is shipped in tightly sealed containers at ambient temperature, protected from moisture and direct sunlight. Packaging complies with chemical safety regulations to prevent contamination or degradation. For bulk or international shipments, appropriate labeling and documentation are provided in accordance with transportation guidelines for laboratory reagents and chemicals. |
| Storage | Store (Boc-Aminooxy)acetic acid in a cool, dry, well-ventilated area away from moisture and incompatible substances such as strong oxidizers and acids. Keep the container tightly closed and protected from light. Recommended storage temperature is 2–8°C (refrigeration). Handle under inert atmosphere if possible to prevent degradation. Always follow relevant safety protocols and consult the product’s safety data sheet for more information. |
Applications of (Boc-Aminooxy)Acetic Acid in Industrial ManufacturingWe manufacture (Boc-Aminooxy)Acetic Acid to supply leading life science, pharmaceutical, and specialty chemical producers with high-purity raw materials for advanced synthesis processes. This section provides detailed, real-world application information based on implementation experience in primary downstream sectors where this chemical plays a critical role. Each scenario focuses on the compliance, formulation, process integration, and end-use specifics that govern its professional use. 1. Peptide Drug Intermediate SynthesisIn GMP peptide manufacturing, (Boc-Aminooxy)Acetic Acid serves as a specialized protected building block for introducing aminooxy groups, crucial for oxime-ligation strategies and post-synthetic modifications. Custom peptide facilities add this compound during the solid-phase chain assembly, directly impacting purity and functionalization of APIs designed for oncology, metabolic, and antiviral treatments. Adjustments in usage ratios depend on the targeted peptide sequence and side-chain compatibility, while adherence to internationally harmonized pharmaceutical regulations is mandatory at all stages. Industry compliance standards
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2. Antibody-Drug Conjugate (ADC) Linker ProductionProducers of ADC payload linkers utilize (Boc-Aminooxy)Acetic Acid as a precursor for the aminooxy-functional domain. This allows selective attachment to aldehyde handles on antibodies or payloads through oxime bond formation. The chemical’s quality and protection profile directly influence final conjugation efficiency and drug payload stability. Formulation is tailored under regulated conditions to minimize cross-linking and control batch-to-batch consistency for clinical and commercial ADC manufacture. Industry compliance standards
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3. Glycoconjugate Vaccine SynthesisSpecialty vaccine manufacturers rely on (Boc-Aminooxy)Acetic Acid as a key reagent for functionalizing polysaccharide antigens with aminooxy groups, facilitating oxime coupling to carrier proteins. This enables precise, site-selective conjugation strategies required for next-generation bacterial and viral conjugate vaccines. The addition rate and process parameters are strictly regulated to maximize functional loading and minimize non-specific binding, ensuring robust immunogenicity and regulatory acceptance. Industry compliance standards
Typical usage ratio
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4. Biopolymer Surface Modification for Diagnostic PlatformsDiagnostic device assemblers incorporate (Boc-Aminooxy)Acetic Acid to functionalize biopolymer surfaces—such as dextran, PEG, or cellulose—with customizable aminooxy handles. This modification is essential for immobilizing biomolecules onto sensor arrays and microplates via oxime linkage, driving assay sensitivity and specificity in high-throughput screening. Integration protocols require reliable, scalable introduction during bulk surface derivatization under protocols validated to traceable standards, supporting QC and regulatory documentation for IVD device release. Industry compliance standards
Typical usage ratio
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5. Site-Specific Protein Labeling Reagent ManufacturingChemical biologists and custom labeling manufacturers use (Boc-Aminooxy)Acetic Acid to introduce protected aminooxy motifs into protein labeling reagents, enabling stable and site-selective coupling of fluorescent labels or biotin to carbonyl-functionalized biomolecules. Stringent formulation and purification steps ensure that final products offer minimal nonspecific labeling, with application-specific adjustments driven by targeted labeling efficiency and downstream detection modalities. Quality requirements enforce trace analysis of protection group removal and residual contaminants. Industry compliance standards
Typical usage ratio
Downstream process integration
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At our chemical plant, the team dedicates years to creating and refining specialty amino acid derivatives. (Boc-Aminooxy)acetic acid made its way through our research pipeline not from the need to pad a portfolio, but because researchers kept asking for a robust aminooxy carboxylic acid with reliable Boc protection, easy handling, and consistent results. This compound occupies a clear spot in peptide synthesis and bioconjugation workflows, acting as a crucial linker and reactive building block.
Unlike large catalogue suppliers that split focus between endless intermediates, our lab and production operators know exactly who asks for (Boc-Aminooxy)acetic acid and why—a good share of our clients develop stable oxime linkages, peptide extensions, or chemical probes. These are projects where every impurity and every percent of yield matters.
Our process for (Boc-Aminooxy)acetic acid starts from pharmaceutical-grade raw materials. The main feedstock picks up no mystery side-products because we avoid the routine “one-pot shortcuts” that others might adopt. We work at moderate scale, in reactors that hold up to a few hundred liters—big enough for reliability, small enough to keep control of every batch variable.
Judgement about purification makes or breaks an aminooxy acid: you can’t tolerate residual oxidants or boc-cleavage byproducts at this stage, or the acid will fall short in downstream coupling. Our team purifies each batch using tailored extraction and crystallization, passing every lot through LC and NMR validation. Spectra show no baseline scatter, and water content consistently lands within anhydrous range, with typical color always bright white to off-white.
Customers measure their work by structure and yield, not just by a spec sheet. We track purity for (Boc-Aminooxy)acetic acid above 98 percent by HPLC, with identity confirmed by both NMR and mass spectrometry. The melting point sits within a narrow range; from experience, batches outside the 85–91 degrees Celsius window never meet our shipment criteria. Residual solvents drop far below ICH thresholds, since peptide synthesis is unforgiving about these traces.
Some powders look acceptable yet give inconsistent weighing or spill during transfer. Ours packs densely to avoid static “fluffing.” Each batch arrives in HDPE bottles, sealed for atmospheric stability. Visual checks under full lighting keep away any hint of discoloration. Our people know from handling hundreds of lots that even slightly yellowed product causes uncertainty at customer labs—someone there will write to point it out before you even see it.
Laboratories rely on (Boc-Aminooxy)acetic acid for solid-phase peptide synthesis, especially when building blocks require oxime or hydrazone linkages to aldehyde or ketone partners. In our early client feedback, most users occupied research roles in universities and biotechs looking to attach payloads to proteins, antibodies, or small molecules—always aiming for gentle reaction profiles that avoid damaging side reactions.
Chemists commonly dissolve the acid in DMF or DMSO, activating the carboxyl group with standard carbodiimides or mixed anhydrides. The Boc group shields the aminooxy function during coupling, but surrenders easily to TFA cleavage at the later deprotection step. Our preparation holds up through multiple freeze-thaw cycles and survives refrigeration without visible hydrate formation.
On rare occasions customers added our (Boc-Aminooxy)acetic acid to microwave-assisted couplings or flow chemistry rigs. Performance never faltered. Every time we heard about failed reactions, the root cause traced back to bulk reagents or poor handling, not to our product’s core integrity.
Not every carboxylic acid linker performs at this level. Standard amino acids do not include an aminooxy group, so simple glycine or alanine never replaces the reactivity profile. Compared to N-hydroxysuccinimide esters or other “pre-activated” building blocks, (Boc-Aminooxy)acetic acid gives far more flexibility—users control both the activation and the coupling step, minimizing hydrolysis risks from storage or transfer.
Some labs consider omitting the Boc group, but experience reveals that unprotected aminooxyacetic acid suffers oxidation and polymerization, especially on the bench. A Boc group shields the reactive moiety, keeps the compound shelf-stable, and ensures deprotection occurs cleanly at a stage and time chosen by the researcher, not by accident.
Other manufacturers on the market offer versions with higher residual salt, lower purity, or ambiguous NMR traces. Some provide mixed Boc and Fmoc derivatives. After speaking with process developers during validation stage, most end-users ask for dedicated, single-protecting group materials. The reason ties to purification: mixed protecting groups stretch downstream chromatography runs and make finished peptides harder to characterize.
No researcher develops a new probe or peptide drug with a one-off batch. Large programs lock in supplier relationships for years. We structure our production so that every lot matches the last, using the same downstream isolation and the same quality checks. Scientists tell us their validation work comes down to knowing today’s batch will behave the way last year’s did—no drift in coupling efficiency, no shift in deprotection conditions, no new peaks in the HPLC.
For customers scaling new drug candidates, trace impurities from side reactions can destroy process economics or cause regulatory issues. Our team has sweated out many rounds of cleaning, extraction, and drying to bring (Boc-Aminooxy)acetic acid up to the level demanded by GMP pilot plants, though we also make plenty for non-GMP projects. Every feedback alert—whether a stray impurity, a lumpy bottle, or a packaging gripe—goes back to production right away. We learn faster here than at companies further removed from the plant floor.
A research group developing antibody-drug conjugates once ran into trouble with a rival vendor’s batch: high background, skipped reactions, lower product yields. They asked us to help troubleshoot, so we went over their protocol side-by-side with them. Within a few days, they realized the previous supplier’s batch barely crossed 90 percent purity, and their HPLC trace hid ethanol residue. They switched to our batch, and yields rebounded above 94 percent with no need to rework their process or spend on extra purification.
Tech transfer managers in process chemistry appreciate simple documentation but care more about analytical transparency. We share typical NMR, LC-MS, and elemental analysis whenever asked—not just the numbers on a page, but the raw spectra and all lab notes leading up to batch release. Open, direct communication keeps mistakes rare and lets customers spend time on science, not QA documentation.
Peptide synthesis generally runs on tight deadlines. Our shipping cycle factors this in by holding safety stock for high-frequency buyers and building in flexibility for pilot runs and research spikes. All shipments include clear batch numbers, proper labels, and traceable records. No fancy QR codes or smart packaging; just robust labels that stay readable no matter how much traffic a bottle sees in a research lab.
Some years back, one biotech asked for (Boc-Aminooxy)acetic acid that could hold up to higher temperature reaction steps. After analyzing decomposition byproducts and talking it through with our R&D, we fine-tuned drying conditions and, at batch scale, switched container liners to a new grade that kept thermal stability higher by about 2–3 degrees. That batch ran through their entire pilot run without a single crystallization defect.
A few customers request alternate grades—higher purity, lower endotoxin, or specific particle sizes. While the product generally arrives as a fine powder, we have delivered it semi-granular for certain automated dispensing equipment. Whenever requests stretch our technical limits, we work through the trade-offs on the bench, document all changes, then update our SOPs.
No chemical process runs out of sight of environmental and safety concerns. Our plant heels to local and national controls over solvent emissions, waste water, and solid byproduct handling. The process for (Boc-Aminooxy)acetic acid minimizes aggressive oxidizers; waste streams at our facility include neutralization and activated carbon treatment. Technicians wear full-scale PPE and receive training to handle all aminooxy intermediates, since exposure risks increase above gram scale.
For anyone working with the acid in the lab, standard good practices suffice: avoid breathing dust, don’t ingest or expose to bare skin, and never store next to volatile acids or oxidants, which can trigger off-odors or degradation. Product labeling includes all GHS hazard and precautionary statements to help guide new users. Experience shows that well-sealed, room-temperature storage often suffices, though for extended shelf life, a refrigerator extends product life beyond two years with no change in HPLC profile.
We collect and log each incident report internally, using the analytics to spot trends. If a customer finds a safety data sheet unclear or a bottle arrives leaking, every issue gets same-day escalation straight to plant management. We’ve trimmed errors to low single digits each quarter and keep working the rate down.
Much of the scientific impact stems from what our product allows in the lab. High-yield peptide ligation opens doors to new diagnostics, targeted therapeutics, molecular tags, or imaging agents. Projects that stretch commercial boundaries—antibody-drug conjugates, synthetic vaccine candidates, metabolite probes—often succeed or fail depending on the quality and consistency of each synthetic step.
We hear scientists tell stories of failed scale-ups, missed milestones, and wasted contracts, all from ill-fitting intermediates. People who switch to our (Boc-Aminooxy)acetic acid rarely turn back. What drives repeat business isn’t just price or paperwork speed. Time and again, the difference comes down to knowing their raw material won’t throw a curveball into a complex synthesis.
Within our own plant, we share pride in every program where our efforts speed a discovery, guarantee a pilot run, or keep a promising peptide drug on track. We stay close to our clients, answer technical questions without delay, and share both product know-how and real troubleshooting strategies. Other shops may ship more SKUs, but few invest in the hands-on, batch-by-batch oversight that drives breakthroughs at the bench.
Continuous improvement in (Boc-Aminooxy)acetic acid manufacturing doesn’t stop at batch yield or lab validation. We regularly revisit every workflow: sourcing, reaction time, solvent recovery, and even picking the right spatulas for charge-in to prevent cross-contamination. Every technician’s suggestion gets field-tested at small scale and shared across shifts.
Sometimes we cycle raw materials from different suppliers. Before any reaches the big reactors, we characterize everything with our own in-house methods. We do not wait for outside complaints to spring into corrective action—every operator knows that a single off-spec lot can disrupt weeks of downstream synthesis for a client.
Our team maintains close contact with chemical safety and compliance advisors. Product updates trickle back to customers as technical service announcements; new packaging, improved stability, and expanded quality testing all come from dialogue with the people who use our acid at the bench.
We have seen the long view of chemical manufacturing—new products roll out each year, but only a handful land as essential tools in drug discovery, proteomics, or advanced materials. (Boc-Aminooxy)acetic acid claims a spot on that short list for anyone designing oxime-linked peptides, labeling proteins, or building custom probes. Most big commercial milestones, from diagnostic reagents to next-generation antibody conjugates, start with small, high-purity intermediates that arrive on time, batch after batch.
Many scientists overlook the value of strong supplier relationships until something goes wrong—a late shipment, a contaminated lot, or an unforeseen stability failure. We have lost sleep ourselves over raw material surprises and know just how much pain a single rotten drum can cause. Every time a customer sends feedback, we treat it as both an audit and a chance to improve, never just as a transaction.
Our own plant’s future depends on upholding trust—by owning up to issues, investing in repeatable quality, and keeping lines open for technical exchanges. (Boc-Aminooxy)acetic acid isn’t just one more line in a catalogue; for us and our clients, it’s a platform for scientific creation, process performance, and long-term reliability. We continue turning out each batch with this in mind, pursuing new solutions and supporting the real-world work behind every reaction.