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4-Benzyl-2-(Chloromethyl)Morpholine

    • Product Name 4-Benzyl-2-(Chloromethyl)Morpholine
    • Alias 4-Benzyl-2-chloromethylmorpholine
    • Einecs 681-476-3
    • 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

    317207

    Chemical Name 4-Benzyl-2-(Chloromethyl)Morpholine
    Cas Number 1053912-73-4
    Molecular Formula C12H16ClNO
    Molecular Weight 225.72 g/mol
    Appearance Colorless to pale yellow liquid
    Solubility Soluble in organic solvents
    Purity Typically >98%
    Smiles C1COC(N1CCCl)CC2=CC=CC=C2
    Inchi InChI=1S/C12H16ClNO/c13-9-11-14-6-8-15-12(14)10-7-5-3-1-2-4-7/h1-5,7,12H,6,8-11H2
    Storage Temperature Store at 2-8°C

    As an accredited 4-Benzyl-2-(Chloromethyl)Morpholine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 250g of 4-Benzyl-2-(Chloromethyl)Morpholine is supplied in a sealed amber glass bottle with a tamper-evident cap and hazard labeling.
    Shipping 4-Benzyl-2-(Chloromethyl)morpholine is shipped in tightly sealed, chemical-resistant containers, compliant with hazardous material regulations. It is transported under controlled conditions to prevent exposure to moisture, heat, and direct sunlight. Appropriate labeling and documentation, including safety data sheets, accompany the shipment to ensure safe handling and compliance with international chemical shipping standards.
    Storage Store 4-Benzyl-2-(Chloromethyl)morpholine in a tightly closed container, in a cool, dry, well-ventilated place, away from direct sunlight and incompatible substances such as strong oxidizers and acids. Keep away from ignition sources and moisture. Use and store under fume hood if possible. Ensure proper labeling and secondary containment to prevent accidental leaks or spills.
    Application of 4-Benzyl-2-(Chloromethyl)Morpholine

    Applications of 4-Benzyl-2-(Chloromethyl)Morpholine in Industrial Manufacturing

    As an original manufacturer of 4-Benzyl-2-(Chloromethyl)Morpholine, we support advanced industries with a production-grade intermediate tailored for specific chemical synthesis pathways. Its practical function as a building block for active and specialty molecules enables downstream partners to control purification, yield, and production scale in regulated environments. Below, we present differentiated scenarios where this intermediate is strategically integrated into established industrial processes, complying with stringent application requirements.

    1. Pharmaceutical Intermediate for Active Pharmaceutical Ingredients (APIs)

    This material finds dedicated use as a key intermediate in the synthesis of select heterocyclic APIs, particularly within morpholine-based and benzyl-substituted therapeutic compounds. Pharmaceutical manufacturers utilize its reactive sites for nucleophilic substitution and condensation steps, under tightly controlled conditions, ensuring traceability and reproducibility in high-value synthetic routes for drug substance production.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • 21 CFR Part 210/211 U.S. cGMP Regulations
    • EU GMP Part II
    • Relevant USP/Ph. Eur. specifications for API synthesis inputs

    Typical usage ratio

    • 0.85–1.2 mol equivalent relative to the core substrate in stepwise synthesis, adjusted based on process mass intensity targets

    Downstream process integration

    • Charged as a condensation or alkylation intermediate in mid-stage batch reactions, introduced after initial substrate derivatization, then directly isolated or further processed while maintaining control of residuals and byproducts

    Final product types

    • Antihypertensive API intermediates
    • CNS-acting drug substance precursors
    • Morpholine-based pharma intermediates

    2. Agrochemical Synthesis: Fungicide and Herbicide Precursors

    Major agrochemical formulators, focusing on next-generation crop protection products, introduce this compound into the synthesis of select systemic fungicides and herbicide molecules. The structure serves as a modifiable anchor enabling the production of tailored azole and morpholine fungicide scaffolds featuring enhanced bioactivity and controlled release, in compliance with agrochemical registration dossiers and pre-market requirements.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • REACH Regulation (EC) No 1907/2006
    • OECD Guidelines for Testing of Chemicals
    • ISO 9001:2015 for quality management in production facilities

    Typical usage ratio

    • 5–10% w/w relative to the main active compound precursor in multi-stage synthesis; adjusted according to desired substitution degree and ultimate activity profile

    Downstream process integration

    • Added as a nucleophile or alkylating agent in the intermediate stages of batch synthesis, prior to final formulation and purification, to ensure strong molecular integrity in target actives

    Final product types

    • Morpholine-based systemic fungicides (e.g., wheat or barley disease control)
    • Pre-emergence and post-emergence herbicide bases

    3. Specialty Chemical Manufacturing: Advanced Epoxy Curing Agents

    Chemical producers in the advanced materials sector utilize this intermediate to synthesize bespoke morpholine-based curing agents for two-component epoxy systems, addressing requirements for controlled crosslink density, pot life, and chemical resistance. Integration supports both small batch R&D and large-scale continuous production for sectors such as industrial flooring, coatings, and electronics encapsulation.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems
    • REACH Regulation (EC) No 1907/2006
    • Environmental Protection Agency (EPA) guidelines on chemical intermediates in coatings and adhesives
    • UL 746C polymeric materials safety standards

    Typical usage ratio

    • 1.5–4.5% w/w as a targeted crosslinking monomer in curing agent synthesis, depending on the reactivity ratio with epoxy resin and the desired mechanical property profile

    Downstream process integration

    • Introduced during pre-polymerization, typically in solvent-free or minimal solvent systems, followed by post-addition purification to achieve precise molecular weight and epoxide equivalent values

    Final product types

    • High-performance epoxy curing agents
    • Specialty industrial adhesives
    • Chemically resistant floor coatings

    4. Custom Synthesis for Fine Chemical Intermediates

    Fine chemical manufacturers, serving niche sectors such as advanced dye precursors, performance additives, and chiral building blocks, employ this intermediate for its reactive benzyl and chloromethyl functionalities. Its involvement in tailored nucleophilic substitution or alkylation steps permits adaptation to a broad range of synthetically demanding molecules, each governed by distinct quality, purity, and traceability demands.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems
    • REACH compliance for precursor restrictions
    • Applicable ICCA global chemical intermediates best practices

    Typical usage ratio

    • 2–12% w/w, determined by desired product batch size and specificity of downstream reaction pathways; precise formulation based on stoichiometric calculations validated in pilot trials

    Downstream process integration

    • Charged as a controlled reactant in primary batch reactors, often followed by automated monitoring for conversion level and intermediate isolation for final transformation or purification

    Final product types

    • Specialty dye precursors for electronics
    • Chiral fine chemical intermediates
    • Functionalized additives for performance polymers

    5. Active Monomer Integration for Polymer Modification

    Polymer compounders leverage this material as a functional co-monomer or chain modifier in the development of advanced engineering plastics, where nitrogen and benzyl moieties enhance polymer compatibility, processability, and performance in demanding applications such as automotive and electronic housings. Role focuses on fine-tuning polymer matrix properties guided by customer and regulatory specifications.

    Industry compliance standards

    • ISO 9001:2015 Quality Management
    • UL 94 flammability standards for plastics
    • RoHS compliance for electronics-related polymers
    • Relevant ASTM standards for polymer performance testing (e.g., ASTM D638, D790)

    Typical usage ratio

    • 0.3–2.0% w/w, precisely measured according to the targeted polymer chain architecture and mechanical property specification sheets

    Downstream process integration

    • Compounded during melt blending or reactive extrusion as a functional monomer, followed by in-line or batch QC testing to verify property enhancements and compliance

    Final product types

    • Impact-modified polyamides and polyesters
    • High-performance copolymers for automotive and electronics
    • Electrically insulative plastics for device housings
    Free Quote

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    Certification & Compliance
    More Introduction

    Introducing 4-Benzyl-2-(Chloromethyl)Morpholine: Direct from the Manufacturer

    Genuine Quality Through Factory Insight

    Here on the production floor, we handle 4-Benzyl-2-(Chloromethyl)Morpholine every day, moving it straight from the reactors to the drums with our own hands. Each batch leaves our facility after strict in-house monitoring because the end use often demands both purity and reliable consistency, especially for development labs and specialty synthesis where margin for error can’t creep in. We see the orders, we track the product, and we keep records on every reaction parameter and analytical outcome. This chemical doesn’t travel through a chain of traders before it reaches you.

    Structure, Model, and Specification: The Manufacturer’s Perspective

    We synthesize every production run of 4-Benzyl-2-(Chloromethyl)Morpholine based on a single, well-defined structure—the morpholine ring fused with a benzyl group, accompanied by a unique chloromethyl side chain. Chemists in our lab monitor its identity by NMR and its purity through HPLC, assuring a solid specification for the needs of pharmaceutical research and intermediates manufacturing. Typical purity finds itself above 98%, and we have seen that small variations in synthetic process create differences in color or clarity, so we've worked out every step to keep those variables in check. The compound comes to life in our reactors, not through remote sourcing; we stand behind its chemical fingerprint.

    What Sets 4-Benzyl-2-(Chloromethyl)Morpholine Apart

    The reason folks come to us for this molecule usually comes down to two things: its versatile reactivity and its ability to serve as an intermediate in organic transformations where morpholine functionality and benzylic activation make a difference. Plenty of clients have tried more common halomethyl morpholine derivatives, but the benzyl group makes ours unique. The presence of the benzyl substituent not only tunes the nucleophilicity and solubility but often allows downstream chemistry that the plain chloromethyl analog just does not open up. We get asked why someone can't simply use a more standard 2-(chloromethyl)morpholine, and having seen dozens of reaction schemes across years, we know experimentally that the aromatic influence from the benzyl provides pathways in alkylation or cross-coupling that simply stall with simpler morpholine rings.

    There isn’t much on the market that matches the selectivity offered by this structure once it gets to work as a building block. In process chemistry or medicinal series, some teams run thousands of variants before landing on a structure, but our customers have described finding new activity when moving from methyl or ethyl to benzyl substitutions on the morpholine nitrogen. That simple step means that intermediates made with 4-Benzyl-2-(Chloromethyl)Morpholine often map out lead candidates more efficiently.

    Usage and Applications: Beyond Neutral Descriptions

    We have seen its story many times: a pharma startup working late hours, a material science group running iteration after iteration of synthesis, a crop-protection team pushing timelines. Their recipes often hinge on chemical steps enabled by 4-Benzyl-2-(Chloromethyl)Morpholine. In pharma, it steps up as an intermediate for APIs with nitrogen ring systems. Custom synthesis shops tell us they use it for introducing both the morpholine moiety and a benzyl group in a single step—which cuts down on separate protections and deprotections. In agrochemical research, it provides the platform for designing more selective and persistent actives, capitalizing on the morpholine’s ring stability and the benzyl’s contribution to hydrophobicity in target ligands.

    One team reported higher yields and cleaner NMR spectra after swapping out their old precursor for this chemical, thanks to our careful control over chloride content and trace impurities. It’s these results—documented on their end, checked again on ours—that keep them coming back. We also see research into CNS-active molecules, where small tweaks to morpholine-related scaffolds shift selectivity for neurotransmitter sites.

    Comparing to Other Products: Lessons from Real Experience

    A few times a year we field calls from frustrated teams who bought morpholine-based reagents from generic sources and ran into sticky products, failed purifications, and signals in NMR that just shouldn’t be there. They ask about the differences. We walk them through our controls: No residual benzyl chloride, no overchlorinated morpholine, and a tight sulfated ash window. The difference comes down to more than a certificate of analysis—our QC manager inspects process logs for every run. If we see signs of side-chain substitution or over-alkylation, the batch won’t leave.

    Compared to commercial 2-(Chloromethyl)Morpholine or other benzyl derivatives, our product’s defining feature is the assurance in side-chain placement. Some sources don’t preserve regioselectivity, leading to side-products that pop up later. That means headaches in scale-up, delayed timelines, and costly re-analysis. Our spectrum of batch-to-batch consistency comes straight from sticking with one validated process and in-house testing—full transparency, no outsourcing. That’s how we keep our product lineup sharp and dependable, so that research groups and process engineers don’t get unpredictable variables in their workup.

    Reliability, Consistency, and Traceable Supply

    Plenty of chemical suppliers treat morpholine intermediates as a commodity, selling drums at an arm’s length. We approach every order as the result of synthesis in our own reactors and the result of work by our own team. Several big projects have trusted us not just for the specification, but for our commitment to traceability—from precursor selection to shipment documentation. Our customers get the whole story for every drum, including synthetic lot, in-lab QC sheets, and, for long-term buyers, archived NMR comparisons across years of production. Keeping direct control is the way we make sure each order supports ongoing research and meets increasing regulatory requirements for traceability.

    Any unexpected shift in purity or a hint of byproduct can set an entire R&D project back weeks. We have learned that through direct dialogue with customers. Every time we field a complaint or troubleshoot an unexpected analytical result, we take it directly back to process improvement. We’ve done root-cause analysis on process hiccups, fine-tuned crystallization steps, and tightened analytical windows for exactly these reasons. That’s the difference when the producer takes responsibility—from initial batch to delivered material.

    Regulatory and Safety Considerations Straight from Production

    In our experience, regulatory demands only grow tighter year by year. 4-Benzyl-2-(Chloromethyl)Morpholine fits into evolving frameworks, especially once clients in pharma or fine chemicals need proof of absence of regulated impurities or compliance with local transport conventions. We keep MSDS documentation and support inquiries about handling, but we also train our own plant operators in best practices for personal safety and environmental responsibility. Every handling step has evolved as regulations have stiffened, including improvements in ventilation, residue capture and waste water treatment. Years ago, this was viewed as an unnecessary hurdle—now, the safety margin means long-term trust from every lab or pilot plant we supply.

    It’s not only about paperwork compliance. Our team deals with the realities of handling chloromethylated aromatics every day. We invest in closed transfer systems, keep scrubbing systems for off-gases maintained, and drive regular reviews of staff training. We’ve developed protocols for spill response and emergency action because the trust built over years springs from actually living with these chemicals, not simply pushing them down the line.

    Sourcing and Authenticity: The Value of Going Direct

    Working with us, buyers avoid the confusion that comes from multiple middlemen. Often, material traded repeatedly between intermediaries collects storage residues, unclear batch histories, or even dilution. We keep direct chain of custody. Buyers have told us they spent weeks unraveling sources until landing on us and tracing back origins to a single facility with clear records. That has stopped their procurement issues cold. For organizations building documentation trails for regulatory filings, having full records from source to shipment simplifies their path, especially with increasing scrutiny from health and safety authorities worldwide.

    The reputation our product carries in the market doesn’t stem from big marketing campaigns. It grows through return customers and references among research leaders who experienced smoother reaction performance, fewer surprises in scale-up, and successful regulatory checks. Our team hears directly from scientists and engineers after their projects cross the finish line.

    The Troubles of Impure or Unreliable Morpholine Reagents

    Over our years manufacturing 4-Benzyl-2-(Chloromethyl)Morpholine, we have fielded more than a handful of quality-related calls stemming from earlier bad experiences in the supply chain. Our QC log includes reports of off-specification lots from unknown sources—results such as high water content, detectable benzyl chloride traces, and NMR profiles with ghost peaks. Some labs even ended up halting programs to rework or isolate the desired compound anew. The costs in lost time and extra labor always outweigh any supposed savings from generic or re-packed supply. For us, the smartest pathway means sticking to validated in-house protocols for synthesis and purification and refusing to compromise on quality. Making this commitment visible to the customers has fostered deep working relationships across the industry.

    Every time we put a product out the door, it goes with the hands-on backing of production chemists who know what should and shouldn’t appear in a spectrum. If any ambiguity ever turns up in customer labs, we go back to our archived comparative runs and offer technical help with investigation—it’s as much about constant learning as risk management. That’s how direct feedback from the researchers and formulation scientists using our morpholine derivatives drives ongoing changes in batch process and logistics.

    Supply Chain, Lead Times, and Program Support

    Unlike distributors who buy on speculation, as the direct source we schedule production to match ongoing demand, with surge capability for larger specialty projects. We work hand-in-hand with clients to project materials need based on their scale-up plans, test reactions, and pilot programs. Regular customers often reserve future runs, so we’ve built logistics and storage options to accommodate those needs. Our planning team balances current manufacturing schedules with updated consumption rates—so material is rarely out of stock and clients can count on fulfillment for tight project deadlines.

    For labs racing to reach the next discovery, nothing derails progress faster than waiting for resupplies or finding inconsistencies between batches. More than once, we’ve expedited synthesis and arranged direct-shipment logistics to keep a drug discovery campaign or a pilot line on track. Direct communication lines with the plant mean customers get accurate information and timely updates, not generic tracking numbers or ambiguous promises.

    Looking Ahead: A Manufacturer’s Take on Evolving Demands

    Our facility tracks ongoing trends in research chemistry, and the demand for specialty intermediates like 4-Benzyl-2-(Chloromethyl)Morpholine continues to climb. The growth in combinatorial synthesis, expanding libraries for medicinal and agrochemical screening, and the continual pursuit of patentable series have all contributed to a steady rise in interest. To meet this, we have responded by fine-tuning reactor scale, safeguarding raw material inventory, and investing in analytical upgrades for faster turnaround.

    Some buyers used to view specialty morpholine derivatives as niche requests—now these compounds anchor regular schedules. Our team spends more time than ever discussing structure-activity relationships with scientific customers, as each new SAR program or API candidate brings fresh synthetic challenges. Direct dialogue shortens the gap between chemical supplier and innovator, leading to solutions that a warehouse-based seller can’t often match. It’s a two-way street; production methods and handling protocols adapt as feedback from the researchers circulates back to our QA and process improvement cycle.

    Potential Solutions to Industry-Wide Issues

    We’re keenly aware of the persistent issues dogging the specialty intermediates market—unclear origins, scattered specifications, and chasing certificates after-the-fact. For project managers hoping to avoid these headaches, starting with the original manufacturer removes layers of complexity. In response, we have adopted direct digital document transfers, in-depth lot records, and routine customer support calls where technical questions can be answered by the actual synthetic chemists, not just sales representatives.

    We encourage customers to request full analytical documentation, chain-of-custody logs, and, where possible, reference spectra for comparison with incoming materials. Bringing open, two-way communication into the supply relationship solves many headaches before they start. Trust, transparency, and hands-on technical engagement set us apart from faceless suppliers marketing the molecule on paper without direct production experience. We welcome site audits and video calls from technically oriented customers, so the people responsible for each batch stand behind every claim and answer every question. That is the level of engagement we believe the specialty chemical market deserves.

    Conclusion: The Manufacturer’s Promise

    Speaking as the people behind the reactors, not remote offices, we know 4-Benzyl-2-(Chloromethyl)Morpholine inside and out. We handle its risks, watch its spectra, answer for its batch history, and work in partnership with every customer laboratory who puts it to the test. There is no substitute for chemical products crafted and delivered by the team who made them—no shortcuts, no disguises. Our commitment runs from first reaction to delivered drum, and the proof sits in every successful synthesis achieved by those who trust our expertise.