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4-Morpholinobenzaldehyde

    • Product Name 4-Morpholinobenzaldehyde
    • Alias 4-(Morpholin-4-yl)benzaldehyde
    • Einecs 631-041-2
    • 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

    594457

    Cas Number 698-80-6
    Molecular Formula C11H13NO2
    Molecular Weight 191.23 g/mol
    Appearance White to light yellow crystalline powder
    Melting Point 91-94°C
    Boiling Point 348.2°C at 760 mmHg
    Density 1.195 g/cm3
    Solubility Soluble in organic solvents such as ethanol and DMSO
    Purity Typically ≥98%
    Synonyms 4-(Morpholin-4-yl)benzaldehyde
    Structure Para-substituted benzaldehyde with morpholine ring
    Smiles O=Cc1ccc(N2CCOCC2)cc1

    As an accredited 4-Morpholinobenzaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 250g of 4-Morpholinobenzaldehyde is packaged in a sealed amber glass bottle with a secure screw cap and clear labeling.
    Shipping 4-Morpholinobenzaldehyde is shipped in secure, airtight containers compliant with hazardous chemical regulations. Packaging ensures protection against moisture, light, and breakage during transit. All shipments include appropriate hazard labeling and documentation, adhering to local and international transport guidelines. Handle and store in a cool, dry place upon receipt.
    Storage 4-Morpholinobenzaldehyde should be stored in a tightly sealed container, away from moisture and incompatible substances such as strong oxidizing agents. Keep it in a cool, dry, and well-ventilated area, ideally in a laboratory chemical storage cabinet. Protect from light and avoid exposing it to extreme temperatures. Ensure that all storage vessels are clearly labeled to prevent accidental misuse.
    Application of 4-Morpholinobenzaldehyde

    Applications of 4-Morpholinobenzaldehyde in Industrial Manufacturing

    As a direct manufacturer of 4-Morpholinobenzaldehyde, we serve specialized industrial sectors that require precise chemical performance and regulatory alignment. The following application scenarios reflect established use-cases in downstream industries, where our product supports formulation, processing, and end-product consistency. Each scenario details compliance standards, usage ratios, process positioning, and resulting finished goods.

    1. Active Pharmaceutical Ingredient (API) Intermediate Synthesis

    4-Morpholinobenzaldehyde functions as a selective building block in high-value synthesis routes for certain APIs, contributing to molecular complexity in CNS-acting compounds and oncology drugs. Pharmaceutical manufacturers rely on its reactivity and purity to support multi-step synthesis under stringent regulatory oversight, where traceability and impurity profiles remain central during process validation and scale-up.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • 21 CFR Part 211 (US FDA cGMP for Finished Pharmaceuticals)
    • European Pharmacopoeia monographs (traceability in impurity control)
    • Chinese Pharmacopoeia (ChP) and DMF submission requirements

    Typical usage ratio

    • 5–20 mol% relative to total API precursor; adjusted by target yield and impurity limits

    Downstream process integration

    • Added during early or mid-stage synthesis via nucleophilic addition or condensation reactions, generally in reactor charging steps under inert atmosphere; inclusion often precedes catalytic transformations or cyclization steps in route design

    Final product types

    • CNS drug intermediates
    • Oncological agent pre-forms
    • Specialty pharmaceutical fine chemicals
    • High purity custom synthesis compounds for R&D

    2. Agrochemical Synthesis – Herbicide and Fungicide Intermediates

    Agrochemical formulators employ 4-Morpholinobenzaldehyde as a core intermediate in multi-step syntheses leading to selective triazole-based fungicides and benzaldehyde-derived herbicide actives. Its application supports production of environmentally stable crop protectants with precise activity spectra, where route selectivity and minimal by-product formation determine overall cost efficiency.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products (FAO/WHO)
    • ISO 17025 (test method validation for agrochemical actives)
    • REACH (EC No 1907/2006) registration and downstream user notifications
    • Chinese Ecology and Environment Standards for pesticide manufacturing

    Typical usage ratio

    • 2–10% by mass in precursor mixture, scalable based on process yield and catalytic cycle efficiency

    Downstream process integration

    • Introduced during core condensation, cyclization, or coupling reactions in batch reactors; typically positioned just before heterocyclic ring closure or amidation steps to anchor morpholine moieties to target scaffolds

    Final product types

    • Triazole fungicide intermediates
    • Benzaldehyde-derived herbicide building blocks
    • Crop protection technical concentrates
    • Formulated agricultural actives

    3. Fluorescent Dye and Imaging Chemical Synthesis

    Chemical manufacturers producing advanced imaging agents and fluorescent dyes utilize 4-Morpholinobenzaldehyde as a key ring-opening or electron-donating intermediate. It supports the development of pH indicators, fluorescent stains, and biomedical tracers by enabling specific electronic transitions within the chromophore structure, crucial for detection sensitivity and imaging contrast.

    Industry compliance standards

    • ISO 9001:2015 (Quality management for specialty chemical synthesis)
    • USP <51> Biological indicator controls in medical dye manufacture
    • RoHS Directive 2011/65/EU (heavy metal content in laboratory dyes)
    • OECD Principles for Good Laboratory Practice (GLP) in imaging reagent development

    Typical usage ratio

    • 0.5–5% of target dye batch weight; tailored to desired chromophore excitation wavelength and quantum yield requirements

    Downstream process integration

    • Incorporated during key condensation or ring-extension steps; typically added to reaction vessels during chromophore assembly to introduce morpholine-substituted benzaldehyde units, pivotal for tuning fluorescence

    Final product types

    • Biomedical fluorescent tracers
    • Analytical imaging dyes
    • Industrial pH sensors
    • Diagnostic staining kits

    4. Specialty Polymer Modifier Synthesis

    In specialty polymer and advanced resin manufacturing, formulators use 4-Morpholinobenzaldehyde as a chain-modifying co-monomer, lending selectivity in crosslink density and hydrophilicity to finished thermosets. The morpholine functionality imparts targeted changes to polymer glass transition temperature and enhances compatibility in high-performance coatings and adhesives, where precise modification is critical for downstream application conditions.

    Industry compliance standards

    • ISO 14001:2015 (Environmental management in polymer synthesis)
    • EN 13900-1 (Pigments and extenders – Quality requirements for plastics and paints)
    • UL 94 (Flammability for polymer materials)
    • REACH Annex XVII restrictions for polymer additives

    Typical usage ratio

    • 0.3–2% by total monomer weight; adjusted according to target physical modification and final product application (e.g., flexibility, crosslinking)

    Downstream process integration

    • Blended directly into monomer/prepolymer mixture during initial reactor charging; participates in in-situ polycondensation or step-growth polymerization to introduce morpholinyl functionalities into polymer backbone

    Final product types

    • Modified epoxy and phenolic resins
    • Performance adhesives for electronics and aerospace
    • Antistatic and hydrophilic coatings
    • Specialty polymer additives

    5. Analytical Reagent and Chromatography Derivatization

    Producers of analytical reagents and high-sensitivity derivatization kits select 4-Morpholinobenzaldehyde for its unique aldehydic activity in forming stable derivatives with primary and secondary amines, facilitating detection of specific analytes by HPLC or spectrophotometry. Its purity and reactivity permit consistent peak identification and quantification in regulated laboratory workflows.

    Industry compliance standards

    • ISO/IEC 17025 (Analytical laboratory quality management)
    • USP General Chapter <621> Chromatography
    • GLP (Good Laboratory Practice) in analytical reagent preparation
    • FDA 21 CFR Part 58 (Requirements for non-clinical laboratory studies)

    Typical usage ratio

    • 0.05–1 mmol per analyte sample; amount depends on detection sensitivity and reagent molarity for derivatization

    Downstream process integration

    • Supplied as a component in reconstitution vials for chemical derivatization; utilized during sample preparation or inline mixing prior to chromatographic or UV-Vis detection of amino compounds

    Final product types

    • Pre-packed reagent kits for amine detection
    • Chromatography derivatization agents
    • Standardized spectrophotometric test solutions
    • Laboratory reference reagents

    6. Fine Chemical Synthesis for Electronic and Optical Materials

    Precision manufacturers in electronic and optical device materials leverage 4-Morpholinobenzaldehyde within synthesis steps for charge transport compounds and specialty aromatic modifiers. Its specific benzaldehyde structure optimizes carrier mobility or electromagnetic responsiveness in devices such as OLEDs, sensors, and photoconductors, where molecular tuning can significantly impact component performance.

    Industry compliance standards

    • IEC 61249 (Materials for printed circuit boards)
    • RoHS Directive 2011/65/EU (electronic material content limits)
    • ISO 9001:2015 (Quality management for advanced material synthesis)
    • IEC 60068 (Environmental testing of electronic materials)

    Typical usage ratio

    • 0.2–1.5% relative to specialty material batch mass; adjusted by targeted device specifications and substrate compatibility

    Downstream process integration

    • Integrated into fine chemical synthesis sequence prior to device precursor formulation, typically during late-stage aromatic substitution or charge carrier modification steps; feedstock purity and batch consistency directly influence device parameter uniformity

    Final product types

    • OLED charge transport layers
    • Optical sensor coatings
    • Specialty polymers for photoconductors
    • Functionalized electronic chemical intermediates
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    Certification & Compliance
    More Introduction

    4-Morpholinobenzaldehyde: Practical Experience in Production and Application

    What Makes 4-Morpholinobenzaldehyde Unique in the Lab and the Factory

    Supplying 4-morpholinobenzaldehyde straight from our own reactor means seeing closely how the compound behaves and what customers demand from it. Our product, known by its chemical name 4-(Morpholin-4-yl)benzaldehyde, usually appears as a pale yellow crystalline powder. Chemists in our team work directly with the raw intermediates and finished batches. The main draw for this molecule is the morpholine group, attached directly to the para-position of a benzaldehyde ring, which gives it several benefits over related benzaldehyde derivatives.

    In practical synthesis, 4-morpholinobenzaldehyde stands out due to its dual reactive sites. The aldehyde function is useful as a building block in condensation reactions—such as reductive amination or the construction of more complex organic frameworks—while the morpholine group adds solubility in polar solvents and an ability to tune the reactivity in pharmaceutical intermediates. In our hands, the product routinely passes purity levels of 99% GC, with water content and heavy metals well below the widely accepted industry limits. From quality control to logistics, producing this compound ourselves means we track every step, from handling morpholine to washing and isolating the crystal.

    Meeting the Demands of API and Fine Chemical Makers

    Much of the global demand for 4-morpholinobenzaldehyde comes from the pharmaceutical and specialty chemical sectors. API manufacturers want reliability and traceability, because this molecule often features at early or midway points in complex organic syntheses. Our main customers are looking to form new C–N or C–C bonds, where a morpholine ring brings desired pharmacological effects or solubility enhancements in drug candidates.

    Producing this aldehyde involves using specific routes—typically Vilsmeier-Haack or Duff formylation, followed by purification and crystallization. Handling the process in-house, we prevent contamination from trace byproducts that can trouble downstream applications. Every batch comes off the line after passing analytical methods such as NMR, HPLC, GC-MS, and melting point screening. By producing and analyzing the product ourselves, we pick up subtle differences in crystal habit, particle size, and batch-to-batch color, all of which may matter for a customer’s outcome in scale-up runs.

    Specifications and Consistency—Why It Matters for R&D and Production

    Trying to assemble active compounds in bulk or at bench-scale depends on getting the main aldehyde in reliable condition. Out of factory, our 4-morpholinobenzaldehyde fits a melting point of 81–84°C and a molecular weight of 191.22. Most requests settle on custom pack sizes in sealed drums or bottles, filled and tested under nitrogen protection, as the aldehyde function does not like excess air or moisture during long storage. High-purity material ensures that super-stoichiometric reactants do not build up dangerous aldehyde impurities in a finished API or advanced intermediate.

    Handling it daily, our staff routinely observe how even minor contaminants (like N-oxide or trace metallics) disrupt downstream hydrogenations or oxidations. Many resellers and traders do not track the origin, and in that case, unexpected side-products sometimes appear, especially in amine condensation steps. By making the aldehyde ourselves and controlling the whole route, we cut out this uncertainty. Finished material always includes a certificate analyzed against a library of reference spectra, not just a typical COA with a pass/fail line for purity.

    How 4-Morpholinobenzaldehyde Differs from Other Benzaldehydes

    Organic chemists often compare this product with related benzaldehyde derivatives—such as the unsubstituted benzaldehyde, 4-methoxybenzaldehyde, or the similarly structured 4-piperidinylbenzaldehyde. Each brings its own set of solubility, reactivity, and toxicity profiles. The morpholine ring at the para-position brings both a less harsh nitrogen, due to the ether oxygen in the heterocycle, and higher solubility with polar solvents like ethanol, methanol, or DMF.

    From a synthetic perspective, this added ring softens conditions in reactions involving nucleophilic attack or Lewis acid catalysis. In our reactions, the morpholine group tends to be more stable to basic hydrolysis and less prone to unwanted rearrangement than piperidine or dimethylamino groups at the same position. Large-scale users report fewer side products and lower levels of unwanted tars when running Mannich, reductive amination, or Chichibabin reactions from our product. Less time lost to purification means higher throughput and more predictable trial synthesis on the R&D side.

    Scaling Up: What We Learned Making Multi-Ton Supply Chains Work

    Scaling this synthesis from kilograms to tons meant developing practical solutions for solvent use, waste streams, and in-process analysis. To keep aldehyde content high and formation of unwanted by-products low, we optimized temperatures, nitrogen blanketing, and in-line filtration. Troubles in early runs—such as color impurities or resin formation—taught us to use buffered workups and food-grade filtration media, rather than cruder methods common with low-cost suppliers.

    By isolating the solid in a way that avoids contact with iron or copper, we keep heavy metal readings below 5 ppm. Many global companies rely on this to pass the stricter regulatory regimes in pharma, such as EU GMP and US FDA standards for drug precursors. Shipping the product cross-border requires strict adherence to local customs and environmental protocols, so we document trace solvents, residuals, and compliance with the latest RoHS and REACH guidance.

    Packing and handling protocols also matter for end users. Aldehydes generally absorb oxygen, turning yellow or brown if exposed. Real-world experience suggests that resealable, light-blocking packaging works better than simple clear containers, especially in humid or warm regions. We field dozens of customer inquiries a year tied to storage or shelf-life. Our staff regularly check retention samples under varying temperatures so we can offer real support to anyone running into discoloration or melting issues.

    Supporting Custom Synthesis and Downstream Innovation

    Many of our customers do not just use 4-morpholinobenzaldehyde as a simple reactant—they incorporate it as a core motif in new drug candidates, imaging agents, or performance polymers. This compound’s structure makes it a favorite for building up piperazine, morpholine, or other nitrogen-containing scaffolds with pendant aldehyde groups.

    Our technical team has worked with process chemists to adjust the particle size and purity depending on application—whether for solution-phase synthesis, batch reactions, or flow chemistry setups. In one case, producing custom-milled batches allowed a multinational research group to speed up reaction rates and avoid filter clogging, a time-saving major enough to justify a change in procurement policy. Collaborations like this, grounded in day-to-day factory work, deliver stronger outcomes for R&D and plant scale-up.

    Beyond pharma, sectors like agrochemicals and specialty polymers increasingly adopt this molecule. In crop protection, it can serve as a precursor to selective herbicide candidates, while polymer researchers explore its use in polyfunctional crosslinkers or in molecular electronics. Demand for larger, impurity-free batches has risen in the last five years, especially from contract manufacturing organizations (CMOs) that supply to multiple global brands.

    Transparency and Traceability from Direct Manufacturing

    Our plant-level documentation reflects this shift. For each batch, we retain synthesis notes, analytic data, and storage logs, so any customer can trace the origin back to the exact reactor run and analytical signature. Unlike distributors or third parties, we carry the risk and responsibility for errors, and we fix issues directly. If an end-user in Europe requests a specific impurity profile to comply with EMA guidelines, or a US biotech wants radiopurity for labeled precursors, we provide samples from retained stock or fresh production.

    Peer review in chemistry means sharing not just the assay but the details: what solvents were used, which filtration aids, which lot of morpholine, and even the purity data for those. Over years of supplying this product, we have seen that advanced users perform NMR fingerprinting rather than rely only on HPLC. We share our spectra, analyze for residual solvents beyond standard specs, and routinely update our methods to match changing industry guidelines. In this field, details count.

    Sustainability and Safety: More than Compliance

    Producing chemical intermediates in volume brings inevitable questions about process safety and environmental impact. For 4-morpholinobenzaldehyde, the main process risks involve handling formaldehyde sources, chlorinated formylating agents, and the resulting organic residues. In scaling up, we engineered closed-loop solvent recycling and VOC abatement, using in-plant scrubbers and continuous emission monitoring. Protecting our operators means using PPE and scrubbers even in open transfer steps, with regular monitoring of volatile organic concentrations.

    The plant follows international and local safety standards, but hands-on learning has taught us the importance of short transfer lines, inert gas blankets, and real-time temperature probes. Our leadership reviews each safety incident and upgrades the process, piping layout, or alarm systems as real cases dictate. Waste streams from morpholine-containing syntheses are neutralized in on-site plants, and solid wastes end up only in licensed incineration sites.

    We view sustainability as an evolving target. For example, in recent years, we switched from chlorinated to less hazardous formylation reagents for in-house runs destined for eco-sensitive European customers. Annual audits include not just paper compliance but real on-the-spot walkthroughs and air/water monitoring. The environmental performance has boosted our status with multinational API partners who carry out their own on-site verifications.

    Comparing 4-Morpholinobenzaldehyde with Other Supplies in the Market

    Purchasers occasionally ask what sets our factory-made 4-morpholinobenzaldehyde apart from products circulating from resellers or other makers. The big differences appear in side-by-side analytics. It is easy to measure melting point depression or note a yellow tint in a crude sample, but problems usually reveal themselves in subsequent chemistry: incomplete conversion, foul odors, or reaction mixtures that require extra purification.

    Several years ago, customers receiving material from generic supply houses reported more batch-to-batch inconsistency in yield and side-product content. Synthesis teams found themselves discarding entire test runs due to a lack of reproducibility. By comparing mass spectra, NMR, and impurity profiles from direct and indirect sources, our clients started tracking improvements in their production metrics. Fewer failures translated to less wasted time in formulation, QA release, and scale-up batches.

    These real-world outcomes reinforce our choice to keep manufacturing in-house, tightly control supply chain inputs, and reinvest in process improvements rather than low-cost outsourcing. This decided difference matters even more for customers making high-purity intermediates or pilot batches for regulated industries.

    Problem-Solving and Continuous Improvement

    Producing specialty aldehydes invites ongoing challenges. Once, a major pharmaceutical client flagged a subtle impurity in their GC trace. Instead of deflecting blame or passing the complaint along, we re-examined both processes and intermediates. We traced the contaminant to a morpholine feedstock supplier, and our technical team reformulated procedures to purchase only from approved vendors with up-to-date audit trails. By staying close to raw material producers, we’ve reduced similar surprises.

    Not every batch runs perfectly, and equipment fouling sometimes threatens timelines. Our engineers responded by installing in-line cameras and new filtration systems. This vigilance results in a lower rejection rate and tighter feedback for both production teams and customers. Over a decade supplying 4-morpholinobenzaldehyde, continued dialogue with scientists, purchasing managers, and end-users shapes our data-driven improvements to process and analytics.

    Partnering for the Long Term

    Chemicals like 4-morpholinobenzaldehyde do not just represent a single transaction. Our team views every order as a starting point for longer partnership. End-users trust us to provide more than just a product—they expect sound data, flexible logistics, and ongoing technical support, especially when regulatory hurdles get stricter every year.

    Manufacturing chemical intermediates comes with direct responsibility for quality, safety, and downstream impact. Staff in our plant see the effects of decisions made every day in purchasing, maintenance, storage, and shipping. These practical lessons translate into greater reliability for those who use our 4-morpholinobenzaldehyde, in research labs or full-scale production alike.