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HS Code |
617274 |
| Chemical Name | 1-Chloro-4-Phenylbutane |
| Molecular Formula | C10H13Cl |
| Molecular Weight | 168.67 g/mol |
| Cas Number | 6281-36-9 |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 254-256°C |
| Melting Point | -12°C |
| Density | 1.032 g/cm³ |
| Refractive Index | 1.523 |
| Flash Point | 110°C |
| Solubility In Water | Insoluble |
| Smiles | ClCCCC1=CC=CC=C1 |
| Pubchem Cid | 12353 |
As an accredited 1-Chloro-4-Phenylbutane factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, 100 mL, tightly sealed with a screw cap; labeled with chemical name, structure, hazard symbols, and handling instructions. |
| Shipping | **Shipping Description:** 1-Chloro-4-Phenylbutane should be shipped in tightly sealed containers, protected from moisture and strong oxidizers. Transport at ambient temperature, away from heat sources. Comply with applicable regulations for hazardous chemicals (UN 1993, Class 3, PG III – flammable liquid, n.o.s.). Ensure proper labeling and include relevant safety data sheets with the shipment. |
| Storage | **1-Chloro-4-Phenylbutane** should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from sources of ignition, heat, and direct sunlight. Keep it away from incompatible substances such as strong oxidizers. Proper labeling and secondary containment are recommended to prevent leaks or accidental contact. Use appropriate safety measures to avoid inhalation or skin exposure. |
Applications of 1-Chloro-4-Phenylbutane in Industrial ManufacturingAs a direct manufacturer, we provide 1-Chloro-4-Phenylbutane for several advanced chemical synthesis industries. Our production addresses the critical needs of pharmaceutical, agrochemical, and specialty chemical companies, integrating precise quality control and detailed compliance protocols throughout all application sectors below. 1. Pharmaceutical Intermediate SynthesisPharmaceutical companies source 1-Chloro-4-Phenylbutane for use as a key intermediate in the multi-step synthesis of active pharmaceutical ingredients, particularly for central nervous system agents and select anti-psychotic APIs. In commercial-scale operations, the compound enters the synthesis process post-coupling, serving as a controlled alkylating agent for core ring construction or side chain elongation. Stringent process controls monitor residual chloride levels and final purity, with complete documentation traceable to cGMP lot production and validated by rigorous analytical release testing. Our material supports chain extension steps where precise control over reaction yield and impurity profile determines product quality for finished APIs distributed in global regulated markets. Industry compliance standards
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2. Agrochemical Fine Chemical Building BlockManufacturers in the agrochemical sector use this material to synthesize phenylalkane-based insecticide and fungicide actives. It is introduced during the core chain assembly, acting as an efficient alkylating agent for cyclization or ring-extension reactions in technical-grade crop protection chemical production. Downstream processors maintain precise charge calculations, monitor purity via GC or HPLC, and integrate QA checkpoints to comply with international pesticide regulatory requirements for raw material sourcing, stability assessments, and environmental controls. Industry compliance standards
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3. Fragrance and Aroma Chemicals ManufacturingSpecialty chemical firms in the flavors and fragrances industry use this compound as a controlled alkyl chain donor during the synthesis of long-chain benzenoid perfume intermediates. Custom syntheses utilize the material to introduce defined side chains onto aromatic rings, allowing for the generation of finished aroma compounds with targeted volatility and unique scent profiles. In quality-focused production, every batch undergoes organoleptic assessment, GC-MS verification, and stability testing in accordance with fragrance industry standards prior to blending into consumer or fine fragrance applications. Industry compliance standards
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4. Custom Synthesis for Specialty PolymersPolymer manufacturers employ our chemical for the synthesis of specialty copolymers and engineering plastics, relying on its halide functionality to initiate controlled chain-extension or crosslinking reactions. Batch productions in pilot or commercial reactors use it with strict monomer-to-initiator ratios, monitored through in-line NMR and viscosity analysis. Integration occurs in the initial monomer blending stage, allowing for the generation of target molecular weights and uniform polymer architectures as defined by engineering specifications. Industry compliance standards
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5. Organic Laboratory Reagent for R&D and Process Scale-upLeading R&D institutes and pilot plants utilize this compound as an alkylating reagent during the development of proprietary fine chemicals and when scaling laboratory discoveries to pilot or demonstration scale. R&D workflows document each use with batch records referencing applicable safety handling and chemical hygiene plans. The compound enters the process during the exploration of new reaction routes, selectivity studies, and synthetic methodology optimization, demanding consistent purity and reliable reactivity for actionable scientific and industrial process development outcomes. Industry compliance standards
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Our years in manufacturing specialty chemicals taught us one thing: precision makes or breaks a process. 1-Chloro-4-Phenylbutane, with the CAS number 1678-19-5, serves as a dependable building block for complex syntheses. The backbone of its utility is in the trifecta of purity, reliable reactivity, and straightforward handling on the plant floor. Over time, we’ve tuned our process to meet the exacting standards set by research institutions and industrial labs without losing sight of day-to-day practicality. That mix of scalable quality and hands-on production experience sets us apart from firms that just repackage what others make. Results count, so any discussion about 1-Chloro-4-Phenylbutane needs to account for how it performs batch after batch, not just its chemical formula on paper.
Anyone who’s worked at the bench or the plant knows that specifications on paper don’t tell the full story. Material with the same name can behave wildly differently depending on its source. Several labs complained to us about unreliable product from the open market: brown tints, off-odors, and sticky residue slowing their reactions and costing them research time. From years of operation, we understand the subtle impurities—unreacted starting materials, polar byproducts, or heavier organics—that drag down synthesis outcomes. Through repeated fractional distillations and tight contaminant monitoring, we provide a product clear in color, neutral in odor, with residue and titer confirmed by both NMR and GC retention times. Real-world scientists see the difference during purification and downstream chemistry. Yields increase and reproducibility improves.
The current model supplied features a minimum assay of 99.0%, exceeding the grade typically distributed by trading houses. We never swap in lower purity lots to fill orders during tight market conditions. Each drum batch is tested—no bulk blending, no batch dilution tricks. The boiling range and refractive index fall within published ranges, which means process engineers can monitor for leaks or spills without recalibrating every time a new lot arrives. Our hands-on team tracks the process from reaction kettle to drum, so if a customer flags a batch, we have real traceability right back to an operator on a given shift.
The focus isn’t just regulatory compliance; it’s giving process chemists a level of transparency and control that’s usually missing from commoditized supply chains. The need for consistency runs even deeper during multi-step syntheses or when investigators must reproduce results for publication or drug validation. Making things easy for auditing teams, we openly share supporting documentation like chromatograms and residual solvent scans on request, not buried behind paperwork delays. Chemists and engineers see the difference in downstream reliability the first time they run a scaled-up batch with our product instead of a generic import.
From our own shop floor experience, handling and storage play just as pivotal a role as purity. 1-Chloro-4-Phenylbutane has a manageable boiling point that simplifies collection and transfer but still demands basic industrial hygiene. Operators handle the product in well-ventilated, dry spaces using standard PPE. Over the years, leaks and contamination from packaging have proven costly—so we use moisture-resistant, food-grade liners inside our steel drums to reduce peroxide formation and water pickup. This extra effort reduces downstream issues like color pickup or unexpected decomposition, particularly in humid environments or where drums get stored for more than a few months. Storage advice isn’t just generic—it’s learned from real-world spills and unscheduled plant shutdowns, with tweaks made after every incident review.
The liquid’s physical stability avoids surprises on the line. We make sure each container arrives as a transparent, water-like liquid, with no sediment or phase separation. By holding back inventory after packing, we spot-check drums after transit to verify there’s no layering or polymerization. Old tales from field users often mention partially solidified drums—usually due to poor purification or improper stabilization upstream. We address that not by adding random stabilizers, but by sticking to a clean process and tight temperature control throughout the chain. These aren’t bullet-point claims—they come from on-the-ground efforts in actual chemical plants, responding to problems the next shift will face if left alone.
The real value of 1-Chloro-4-Phenylbutane appears in the broad diversity of applications it supports. Most demand high consistency because this molecule doesn’t sit in inventory long—it’s a feedstock for agrochemical intermediates, fine flavor and fragrance precursors, and active pharmaceutical ingredients. Customers synthesizing phenyl-substituted amines, specialized alcohols, or complicated heterocycles depend upon repeatable product behavior. A failed batch in these lines means more than lost profit; it sets back timelines for crop protection trials or delays drug registration.
Some downstream users require further chemical modification, such as Grignard reactions or nucleophilic substitution. Our team is in regular contact with process engineers and R&D chemists to gather feedback after every campaign. This real dialogue—usually missed by mere distributors—guides continuous process tuning. One customer flagged inconsistent Grignard results several years ago that we tracked back to trace UV-reactive contaminants. Process tweaks and extra purification steps removed the issue across all shipments. These quality improvements don’t arise from laboratory theorists, but from listening to clients who measure pilot plant performance batch by batch. This cycle of communication, adaptation, and documentation provides reliability for research outcomes, scale-up efforts, and patent inking.
1-Chloro-4-Phenylbutane also shows up in organic synthesis as a chain extender, halide intermediate, and semi-bulk precursor. Rather than chase every fleeting opportunity, we focus on building robust relationships with clients needing consistency week after week. Instead of offering the lowest price or promising exclusive “new” grades, we zero in on measurable performance metrics. Order histories show that customers stay because their own downstream yields rise and headaches drop, not because of discounts or excessive marketing.
Living through winter warehouse work and hot summer drum loads shapes our approach to packaging and transit. 1-Chloro-4-Phenylbutane, stable under most conditions, still reacts poorly to moisture pickup or prolonged exposure to air—especially across global supply chains running through damp ports or tropical depots. So our drums leave the plant nitrogen-purged and sealed with tamper-evident closures. We’ve seen firsthand the corrosion and contamination that surface from shortcutting this step. The cost of cleaning up a contaminated batch, especially in an FDA-audited line, far outweighs the modest expense of heavier packaging and inerting. With repeated feedback loops from shipping teams and end-users, our packaging shifted from lighter jugs to high-integrity drums and intermediate bulk containers with heavy liners. This protects both the product and the worker during unloading or transfer, reducing extra sample and QC work for customers.
We’ve learned over countless shipments that materials like this don’t sit on shelves—they get moved, opened, sampled, and divided. Each process introduces the risk of contamination or accident. Labels, lot numbers, and manifests are handwritten in parallel to digital tracking so that if a shipping mixup occurs, a real person can resolve it promptly. Even minor process interruptions, like a stuck drum bung or a leaking seam, have led to practical changes. Feedback-driven improvements enhance the reliability of deliveries. Our team believes manufacturing doesn’t stop at the reactor wall—it continues until the customer’s last drum opens, gets sampled, and dispensed into a live production process without surprises.
Problems in scaleup or formulation rarely match clean textbook scenarios. Chemists who encounter haze, color, low conversion, or gassing in their syntheses often trace problems back to the raw material, not always equipment or technique. We field technical calls from process teams across North America, Europe, and Asia, troubleshooting issues side by side. Sometimes the culprit is a minor contaminant, solvent residue, or the presence of light-sensitive byproducts. We’ve modified our finishing steps—longer vacuum stripping, UV exclusion, and deeper in-process analysis—to prevent these headaches before shipping. These tweaks go unnoted by third-party repackers, but our operators record each process deviation and improvement for future training and continuous QA cycles. That institutional memory saves money for all parties.
One recurring customer concern involves compatibility with nucleophiles in scale-up synthesis. Anecdotes from several fine chemical makers pointed to unexpected byproducts arising from secondary chlorination or ring closure reactions. Our QC team traced this to the presence of structurally similar impurities arising from side reactions. We responded by implementing tighter in-process controls during the chlorination step and investing in reactor cleaning protocols, not just relying on end-of-line analysis. The outcome: cleaner API pathways, simpler purification, and robust product for challenging chemistry. These are concrete, daily choices rooted in real factory-floor dynamics, not theoretical idealizations or unattainable purity that vanishes from lot to lot.
Experience tells us plenty about what sets a manufacturer apart from a trader. Countless stories come in from research chemists and production managers frustrated by inconsistent supply. They list problems like off-odor shipments, gels or crystals forming during storage, or fluctuating reactivity in experimental runs. The root cause? Decoupled supply lines from commodity resellers who blend, relabel, or dilute product to pad margins. These repackaged chemicals often sit too long in generic warehouses, where stability is lost and contamination sets in. Direct manufacturing avoids that drift because every lot comes from our continuous process, under the same trained team of plant engineers and chemists who see each shipment as a direct reflection of their work. Our focus always returns to performance on the customer’s bench and feedback from production sites, not upstream brokerage deals.
One major pharma company faced batch failures due to unexpected side products showing up as late eluting peaks in their QC checks. A quick audit traced the issue to a reseller-purchased batch of 1-Chloro-4-Phenylbutane. Our customer sent both samples for side-by-side NMR and GC-MS, and the difference was clear—our product matched the reference spectrum, the reseller’s did not. That lab switched their supply chain entirely, saving both project time and regulatory headaches. Their QC reports highlight the practical value of manufacturer-direct sourcing: fewer unknowns, documentation on demand, fast answers to batch-specific questions.
Volume buyers in the chemical industry share similar priorities: speed, predictability, and batch uniformity. Distribution firms may promise any lot size or specification, but they rarely track accountability over years of audit cycles. In cases of product recall or deviation, we produce a full chain of custody from raw material gates to reactor logs and finished packing records. There’s a handshake culture inside our factory; each operator owns their product, understands the client’s application, and feeds improvement ideas straight to management without getting lost in red tape. That’s what builds relationships lasting through downturns as well as growth.
The feedback loop from actual users drives everything we adjust, from raw material switches to the details written on lot slips. In one instance, a specialty polymer maker using our 1-Chloro-4-Phenylbutane flagged slow dissolution during a formulation trial. A review of storage conditions and drum handling identified a change in liner thickness as a contributing factor; this led us to source a different drum liner and review cleanness standards at the packaging stage. Such direct user input goes back into SOP changes, weld inspections, and in-process cleaning cycles. Adjustments come not from abstract continuous improvement mantras but from the lived reality of getting interrupted at 3 a.m. by a customer reporting off-specification material. Every unscheduled audit, lab fail, or supply hiccup moves right back into the process for course correction.
We take a hands-on approach to training each plant operator in the specifics around 1-Chloro-4-Phenylbutane. Learning doesn’t stop at textbook chemistry. Crews walk the lines and review batch slips for irregularities, weekly. All production runs for this product are logged, analyzed, and checked against reference specs stored in-house. This isn’t bureaucratic paper-pushing—tracking deviations and trend lines protects both our operators and every downstream process step in a tight chemistry chain. Many issues get caught because of this continuous real-world vigilance, not just the latest analytical method someone read about at a conference. Technology helps, but engagement on the shop floor makes the difference.
Certifications matter, especially with pharmaceutical or food chain customers. Each batch follows standard documentation, including Certificates of Analysis (CoA) and detailed chromatograms maintained for both customer view and internal audits. Rather than only meeting the minimum, we listen to end-user requests for extra data—sometimes running custom impurity profiles or stability studies based on project needs. The value here comes from flexibly supporting regulatory filings, rather than hiding behind boilerplate lab results that ignore specialized needs.
Quality team members maintain strong working relationships with national and international standards committees, so that when specifications change or new guidance emerges, we make process changes without delay. We see regulatory challenges not as burdens but as checkpoints for building trust. Years of inspection experience taught us that open documentation and clarity reduce headaches, both for customers stuck in the audit cycle and for our own process improvements. Instead of templated responses, our technical team answers every data request with direct access to lab and production records. Customers with urgent documentation needs get real, up-to-date information, not generic files pulled from an archive. This transparency matters in life science manufacturing, where every source line counts for both safety and scientific reproducibility.
Not all supply chains for 1-Chloro-4-Phenylbutane deliver the same results. Traders and resellers sit many steps removed from hands-on chemistry and in-plant troubleshooting. Problems often circulate for months before reaching someone capable of fixing them. By maintaining end-to-end control, from raw input purchasing to final loading dock operations, we cut through communication gaps and supply uncertainty. Each process failure, user complaint, or deviation in specification runs straight back to a technical team who can take immediate corrective action. That approach—grounded in the outcomes delivered to pilot plants and production lines—makes manufacturer-direct supply more than just a phrase. It means reliable chemistry, support built on real experience, and supply assurance borne out by decades of making and shipping this exact molecule.
This depth of experience and commitment matters most in upstream processes that affect everything downstream: crop protection product launches, new fragrance approvals, or pharma regulatory filings. Every client benefits from faster technical troubleshooting, improved repeatability, and lower risk of cross-contamination. Traders ship labels; real manufacturers ship confidence, traceability, and accountability in every drum. That’s why so many leading R&D labs, fine chemical plants, and specialty formulation houses have stayed with us over cycles of market volatility. Their feedback shapes the process improvements, packaging tweaks, and real-world training delivered to each new batch. With 1-Chloro-4-Phenylbutane, hands-on experience, user-driven evolution, and transparency always outweigh abstract claims of “grade” or “quality.”