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Benzyloxyamine

    • Product Name Benzyloxyamine
    • Alias Benzylhydroxylamine
    • Einecs 221-713-6
    • 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
    VTB
    Specifications

    HS Code

    236808

    chemical_name Benzyloxyamine
    molecular_formula C7H9NO
    molecular_weight 123.15 g/mol
    CAS_number 2687-43-6
    appearance Colorless to pale yellow liquid
    boiling_point 234-236 °C
    melting_point -7 °C
    density 1.07 g/cm3
    solubility_in_water Slightly soluble
    refractive_index 1.535
    flash_point 96 °C
    pubchem_cid 17311

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

    Packing & Storage
    Packing Benzyloxyamine, 25 grams, is supplied in a sealed amber glass bottle with a screw cap, labeled with hazard and safety information.
    Shipping Benzyloxyamine is shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. It should be handled in accordance with local, national, and international regulations, ensuring proper labeling and documentation. Transport is typically via ground or air, with applicable hazard precautions. Store in a cool, dry, well-ventilated area during transit.
    Storage **Benzyloxyamine** should be stored in a tightly sealed container, protected from light and moisture. Keep it in a cool, dry, and well-ventilated area, away from sources of ignition, heat, and incompatible substances such as strong oxidizers and acids. Ensure proper labelling and limit access to trained personnel. Refrigeration is recommended for long-term storage to maintain stability.
    Application of Benzyloxyamine

    Applications of Benzyloxyamine in Industrial Manufacturing

    Benzyloxyamine finds dedicated function across several high-value chemical downstreams. As the direct producer, we ensure consistent supply to support demanding industrial protocols, maintaining traceability from raw input through every step of partner operations. Below, we detail the principal segments where this specialty intermediate integrates into commercial-scale production, referencing actual compliance, dosing, processing, and finished goods parameters encountered by professional users.

    1. Active Pharmaceutical Ingredient (API) Synthesis: Anticancer Intermediates

    Many pharmaceutical manufacturers rely on benzyloxyamine as a building block for selective O-benzyl protection in multistep syntheses of cytostatic drug molecules. The compound participates in nucleophilic substitution and condensation reactions enabling protection and then deprotection of hydroxylamine functionalities during the assembly of key heterocyclic scaffolds. Large-scale chemists integrate its use into GMP-validated process lines, where precise addition and complete downstream removal are monitored by batch record and analytical verification.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice for Active Pharmaceutical Ingredients)
    • European Pharmacopoeia (Ph. Eur.) monographs
    • U.S. Food and Drug Administration (FDA) 21 CFR Part 210/211
    • Chinese Pharmacopoeia production guidelines

    Typical usage ratio

    • 0.9–1.3 molar equivalents per target functional group, adjusted based on substrate reactivity and process validation data

    Downstream process integration

    • Introduced in the first or second step as a hydroxylamine protection reagent; later removed post-condensation via catalytic or acidic deprotection before final purification

    Final product types

    • API intermediates for kinase inhibitors (e.g., protected benzohydroxamic acids)
    • Nitrogen heterocycle scaffolds for oncological actives
    • Small-molecule cytostatics incorporating O-benzyl-protected motifs

    2. Agrochemical Synthesis: Herbicide Precursor Manufacturing

    Leading crop protection firms use benzyloxyamine as a reactive moiety in the synthesis of oxime- and hydrazone-substituted herbicide active ingredients. Its selectivity for O-benzyl functional group introduction allows for controlled modification of precursor molecules during key intermediate stages. Technologies target effective control of reaction kinetics and purity, managed under quality-regulated agrochemical production systems.

    Industry compliance standards

    • FAO/WHO Specifications for Agricultural Pesticides
    • ISO 9001:2015 certified production requirements
    • REACH regulation (EC No 1907/2006 for European markets)
    • GB/T 1604-2006 (China pesticide manufacturing standards)

    Typical usage ratio

    • Generally 1.0–1.5 molar equivalents in oxime condensation stages, refined according to precursor purity and desired conversion efficiency

    Downstream process integration

    • Applied during synthesis of protected intermediates prior to final hydrolysis or trans-oximation for finished herbicide actives

    Final product types

    • S-triazine herbicide intermediates
    • Oxime ether precursors for post-emergence weed controls
    • Selective rice and corn herbicide active compounds

    3. Specialty Polymer Modification: Surface-Functionalized Polymers

    Benzyloxyamine enables chemical manufacturers to introduce and later unmask functional amine or hydroxylamine groups on polymer chains. Specialty film and resin producers employ it as a selective protection-deprotection reagent during post-polymerization modification, supporting customization of compatibility, hydrophilicity, or surface reactivity for high-end coatings and biomedical polymer supplies.

    Industry compliance standards

    • ISO 10993-5 (Biological Evaluation of Medical Devices – Cytotoxicity for biomedical plastics)
    • ASTM D638 (Polymer tensile testing protocols)
    • EU Regulation (EU) No 10/2011 on plastic materials in contact with food (if for food-contact surface polymers)
    • REACH Annex XVII restriction compliance for polymer additives

    Typical usage ratio

    • Typically 0.5–2.5 wt% in protection steps, with dosage tailored to the desired degree of functional site protection and polymer matrix characteristics

    Downstream process integration

    • Incorporated after primary polymerization as part of a multi-step protection/activation protocol for functional monomer side chains, followed by further derivatization or surface grafting

    Final product types

    • Activated polymer beads for affinity chromatography
    • Surface-modified films for diagnostic biosensors
    • Functionalized medical device coatings

    4. Analytical Reagent Preparation: Derivatization in Chromatographic Analysis

    Contract research organizations and analytical standards producers use benzyloxyamine as a derivatization agent to quantify carbonyl-containing analytes in environmental, pharmaceutical, and food matrices. Chemical transformation to O-benzyl oximes or hydrazones allows improved detection limits, chromophore sensitivity, and peak resolution during HPLC, GC-MS, or capillary electrophoresis runs, all implemented under traceability and validation routines specified for analytical reference chemical workflows.

    Industry compliance standards

    • ISO/IEC 17025 (General requirements for testing and calibration laboratories)
    • FDA Guidance for Industry: Bioanalytical Method Validation
    • USP General Chapter <621> Chromatography
    • Good Laboratory Practice (GLP) directives, OECD Principles

    Typical usage ratio

    • 10–20 times molar excess relative to target carbonyl analyte concentration, with actual amount set per matrix type and detection threshold requirements

    Downstream process integration

    • Dispensed during sample pre-treatment, executing carbonyl group derivatization in solution prior to chromatographic injection

    Final product types

    • Certified analytical kits for food and environmental monitoring
    • Reference standards for pharmaceutical residue detection
    • Stabilized reagent sets for laboratory validation
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    Certification & Compliance
    More Introduction

    Benzyloxyamine: A Closer Look at a Trusted Intermediate

    A Reliable Building Block in Chemical Synthesis

    Producing benzyloxyamine has been a central part of our chemical manufacturing floor for several years. Among the intermediates we work with, this compound stands out for its relevance to both laboratory researchers and industrial process engineers. We know both groups look for dependability, clean reactions, and crisp yields. From daily batch trials to large-scale production, we see benzyloxyamine deliver these reliably.

    Model and Physical Description

    Our standard benzyloxyamine carries a molecular formula of C7H9NO. This specification comes to life as a fine, white crystalline powder, free from impurity streaks or off-odors. Practically, this matters—a dependable physical appearance signals a properly controlled process, something our own operators check throughout every run. Our typical batch reports a purity of no less than 99%, confirmed by HPLC assay. Moisture levels land well below 0.5%, checked by Karl Fischer titration, so both storage and downstream reactions proceed without surprise.

    How We Produce It

    On the production floor, our benzyloxyamine routinely starts from benzyl chloride and hydroxylamine hydrochloride in a controlled-base environment. This route avoids excessive byproduct formation and minimizes waste, which matters as much to our balances at the end of each shift as to the environment. We have invested in controlled-feed pumps and real-time temperature monitoring, both key to steering reaction dynamics and keeping side-reactions away from the main product. Our operators keep regular logs of every batch, watching for color, smell, and consistency changes that don’t always show up in digital readings.

    The Role in Synthesis: Real-world Applications

    Most chemists pick benzyloxyamine as a reagent for derivatization and protection in organic synthesis. In practice, its most common use is as a precursor for oxime formation. Our experience with pharmaceutical clients shows that benzyloxyamine often takes the stage in the synthesis of sophisticated active pharmaceutical ingredients, in particular for blocking or unveiling carbonyl functionalities. Our production team also connects with researchers doing carbohydrate conjugation, who report that benzyloxyamine forms stable O-benzyloximes under mild conditions, reducing product loss and clean-up steps.

    We have watched orders increase from agrochemical manufacturers as well; these buyers incorporate benzyloxyamine during the development of custom pesticides, where fine-tuning molecular structures can make the difference between patent novelty and infringement. Many of these clients want not just purity but also batch reproducibility for regulatory dossiers. Our internal QA records show round after round of tight data, with impurity profiles kept below International Conference on Harmonization (ICH) thresholds, simplifying paperwork for our customers.

    Comparisons with Other Intermediates

    Some manufacturers in our industry might opt for methoxyamine hydrochloride or ethoxyamine when designing routes involving oxime formation. We’ve run comparative pilot batches here, weighing practical parameters like yield, reaction rate, workup, and downstream compatibility. Benzyloxyamine emerges as the preferred choice for those targeting protected or “masked” carbonyls that will later require specific deprotection steps. Its benzyl group brings extra stability—critical in complex multi-step syntheses, especially when temperature swings or strong reagents threaten less robust linkages.

    Also, removing the benzyl group after reaction often calls for mild hydrogenolysis, a procedure our pharmaceutical partners consider gentle enough for sensitive fragments, which would break down if exposed to rougher deprotection. This selectivity is not just a theoretical advantage; we’ve seen less product decomposition and cleaner chromatograms in our pilot lab every time we compare.

    Methoxyamine, by contrast, can hydrolyze too quickly under acidic or basic workups, leading to a higher number of failed purifications. Ethoxyamine often struggles to give the necessary stability during longer steps. Our own R&D group, after years of running test syntheses, settled on benzyloxyamine for longer, multi-stage sequences, especially when downstream hydrogenolysis fits the final steps.

    Packing, Shelf Life, and Handling in the Warehouse

    We fill and seal benzyloxyamine in HDPE-lined fiber drums or aluminum-lined bags, avoiding direct contact with metal to prevent trace contamination. Every batch leaves the plant with a tamper-evident seal and a lot-numbered label, something our warehouse team tracks digitally and by hand. Our experience shows this approach meets the needs of both small-scale labs looking for 100-gram packs and industrial operators who order multi-kilo quantities.

    Inside our storage facility, we keep benzyloxyamine in a dry, cool section to avoid caking or degradation. Product stored this way maintains its integrity for up to two years, based on our own stability trials. Batches stored at higher temperatures or in less regulated climates develop a faint yellow tint and lose their chemical snap over time; our QC team flags and rejects these before any shipment leaves.

    Down-to-Earth Handling Advice

    Our own operators always use a dust mask and nitrile gloves when transferring benzyloxyamine because the fine powder can become airborne and irritate the nose and throat after long exposure. Most of our larger-scale customers ventilate their handling areas with local exhaust. We recommend the same to smaller labs that might underestimate how easily fine benzyloxyamine dust disperses. Clean-up is best managed with a simple HEPA vacuum—water should be avoided, as benzyloxyamine dissolves quickly, complicating disposal.

    From a manufacturing standpoint, the compound handles easily with standard powder-transfer processes, so most customers end up integrating it smoothly into their workflow. Our own crews clean any spilled material with absorbent pads and store contaminated waste for contracted disposal, limiting risk and exposure.

    Quality Assurance Practices Shaped by Experience

    We run benzyloxyamine through several analytics before packing. Our process chemists prefer HPLC to GC for the main assay, mostly because the compound's volatility under high heat can mislead GC readings. We conduct FTIR scans to cross-check the absence of benzaldehyde or unreacted hydroxylamine. This mirrors what we see in our customers’ in-house checks; a clean disappearance of carbonyl peaks signals a successful reaction and no troublesome carry-over.

    Batch-to-batch reproducibility gets attention during plant runs. Each reaction is monitored for pH, reaction time, and yield. Based on years of experience, small variances in aqueous layer pH can alter not just yield, but downstream workup clarity, so our technical crew supervises closely at this stage. After isolation, samples from each drum head for impurity profiling. Our internal reports show fewer than 10 ppm of benzyl alcohol or unreacted amine, a level we maintain through column purification if necessary.

    Our customers share our appreciation for transparency, so we keep and share detailed certificates of analysis. Any deviations prompt immediate investigation—keeping trust strong and making sure no surprises appear down the line.

    Common End Uses We See in the Field

    Benzyloxyamine routinely appears in orders from contract research organizations, both in synthesis and screening labs. These groups value the intermediate as a building block for creating N- or O-benzyl protected oximes. Many of them synthesize pharmaceutical intermediates, starting with our benzyloxyamine to build structural diversity into their compounds. From past collaborations, we know metabolic stability can often hinge on the right protection strategies, and the benzyl group introduced by benzyloxyamine often carries more weight than originally assumed.

    In the agrochemical sector, we see formulators request large lots as they scale bench trials to kilo-lab runs. The compound’s high melting point helps during storage and transportation, especially in hot summers, when softer amine-based reagents may clump or degrade. Some research centers have approached us with custom functionalization requests, looking for azide-modified benzyloxyamines—those projects keep us busy with continuous process improvements.

    Market Changes and Customer Trends

    Over time, requests for higher-purity benzyloxyamine grew as regulatory requirements in pharma and specialty chemicals increased. We adapted line cleaning procedures between batches, reducing risk of cross-contaminants. Upgrades in our analytical equipment have helped us catch even low-level impurities, aligning with customer demands for product fit-for-purpose in regulated markets.

    Requests for custom packaging, including amber glass jars and vacuum-sealed multilayer bags, surfaced as customers began storing material for extended periods or under challenging climatic conditions. Having flexible packing lines allowed us to respond to these needs without delay. We routinely field queries about stability data at sub-freezing temperatures, as Northern jurisdiction customers winterize their warehouses.

    Global transport disruptions over recent years reaffirmed the value of keeping substantial inventory in house. Delays in raw material arrival led us to increase our own buffer stocks. From experience, being able to guarantee supply through such periods strengthened customer relationships and provided our team with new logistical skills.

    Environmental and Regulatory Considerations

    Operational safety and environmental stewardship rise to the foreground in chemical manufacturing. Our handling and disposal protocol meets national hazardous waste rules; spills and leaks of benzyloxyamine do not enter regular drainage or landfill. Instead, we collect and pack spent material for authorized incineration—minimizing environmental risk.

    Our product does not count as a scheduled controlled substance in our region; regulatory status may differ abroad, leading some buyers to request documentation for their own compliance checks. We prepare full shipping documentation, aligned to international regulations, to avoid customs delays that can halt a tight project timeline.

    Waste minimization gets special attention in our facility. We designed our reactors and purification lines with closed-loop wash and recovery systems, allowing solvent recycling and reducing total discharge volume. As part of continuous improvement, the team regularly reviews and upgrades processes to lower both our environmental impact and plant costs.

    Adapting to Changing Industry Needs

    New drug development, crop protection, and materials science industries often adjust their requirements. Our team responds by refining our benzyloxyamine process for custom needs, sometimes tuning purity, sometimes scaling up or down batch sizes. From practical experience, flexible operations beat rigid systems when customer demands shift overnight.

    We develop custom specification routes for clients needing lower moisture content, special particle size, or documented absence of certain trace contaminants. Our R&D chemists cooperate directly with process engineers from customer companies, often signing NDAs before sharing research. Experience taught us not just to rely on analytical reports, but to invite client feedback on solubility, color, and reactivity—these practical attributes sometimes reveal more than numbers on a page.

    Looking to the Future

    R&D teams in several sectors continue requesting benzyloxyamine in increasingly demanding applications—peptide chemistry, carbohydrate mapping, and custom surface modification, to name a few. We stand ready to adjust our processes and packaging accordingly. As regulatory landscapes tighten and new green chemistry initiatives develop, our team remains alert to potential new reaction routes—perhaps with less solvent, or milder reagents, or shorter cycle times.

    While we have yet to see a direct substitution product match benzyloxyamine's unique blend of stability and reaction selectivity, we regularly experiment with alternative aryl or alkyl derivatives, aiming to offer expanded options. Only clear benefits get released to customers; our own team spends time comparing downstream performance so that no one finds unwelcome surprises mid-project.

    The journey with benzyloxyamine stretches from bulk chemical drums on our loading dock to careful scoops in research labs around the world. In every step, knowledge gleaned from previous batches guides our current processes—from smarter raw material sourcing, to improved QA sampling, to better storage and handling. Every year brings new challenges, but manufacturing benzyloxyamine to ever-higher standards has stayed a rewarding cornerstone for our team.