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[(1R,4S)-4-Aminocyclopent-2-Enyl]Methanol Hydrochloride

    • Product Name [(1R,4S)-4-Aminocyclopent-2-Enyl]Methanol Hydrochloride
    • Alias CYCLOPENT-2-ENYLAMINOMETHANOL HYDROCHLORIDE
    • Einecs 603-246-7
    • 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

    643202

    Product Name [(1R,4S)-4-Aminocyclopent-2-enyl]methanol hydrochloride
    Chemical Formula C6H12ClNO
    Molecular Weight 149.62 g/mol
    Cas Number 1353894-94-0
    Appearance White to off-white solid
    Purity Typically ≥98%
    Solubility Soluble in water
    Storage Temperature 2-8°C (refrigerated)
    Synonyms (1R,4S)-4-Aminocyclopent-2-enylmethanol hydrochloride
    Iupac Name (1R,4S)-4-aminocyclopent-2-en-1-ylmethanol hydrochloride
    Smiles C1C(C=CC1N)CO.Cl
    Usage For research and development use only

    As an accredited [(1R,4S)-4-Aminocyclopent-2-Enyl]Methanol Hydrochloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 10g package features a sealed amber glass bottle, labeled "[(1R,4S)-4-Aminocyclopent-2-enyl]methanol hydrochloride," with safety and handling instructions.
    Shipping `[(1R,4S)-4-Aminocyclopent-2-Enyl]Methanol Hydrochloride` is shipped in secure, chemically resistant containers under ambient conditions. Proper labeling in accordance with chemical safety regulations ensures compliance and safe handling. The package includes necessary documentation and is suitable for standard courier or freight services unless otherwise specified by specific storage or hazard requirements.
    Storage Store **[(1R,4S)-4-Aminocyclopent-2-enyl]methanol hydrochloride** in a tightly sealed container, protected from light and moisture. Keep at 2–8 °C (refrigerated), away from incompatible substances such as strong oxidizers. Ensure the storage area is well-ventilated and clearly labeled. Follow standard laboratory safety measures and local regulations for chemical storage and handling.
    Application of [(1R,4S)-4-Aminocyclopent-2-Enyl]Methanol Hydrochloride

    Applications of [(1R,4S)-4-Aminocyclopent-2-Enyl]Methanol Hydrochloride in Industrial Manufacturing

    [(1R,4S)-4-Aminocyclopent-2-Enyl]Methanol Hydrochloride supports various specialized chemical synthesis workflows in pharmaceutical intermediate production, advanced material development, and precision fine chemical manufacturing. Below we detail key downstream application scenarios, highlighting regulations, formulation ranges, exact process roles, and types of final goods.

    1. Chiral Pharmaceutical Intermediate Synthesis

    Many API manufacturers deploy this hydrochloride compound as a chiral building block in the synthesis of aminocyclopentene-containing actives. The molecular configuration enables selective reactions in the construction of biologically active scaffolds, essential for certain antiviral and CNS drug classes. Our material integrates at the earliest stages of multi-step API synthesis for high-yield, enantioselective transformation.

    Industry compliance standards

    • Current Good Manufacturing Practice (cGMP, ICH Q7)
    • European Pharmacopoeia (EP)
    • United States Pharmacopeia (USP) where relevant to intermediate registration
    • ICH Q3A/B for impurity and residual solvent controls

    Typical usage ratio

    • 0.95 – 1.10 molar equivalents relative to partner reactant in asymmetric addition
    • Adjustable based on downstream chiral purity requirements; typically measured by HPLC

    Downstream process integration

    • Charged during initial coupling or cyclization stages
    • Reacts under inert or controlled-atmosphere batch conditions
    • Strict temperature and pH control to maintain chiral integrity
    • Processed through standard workup and purification, e.g., preparative chromatography

    Final product types

    • Chiral API intermediates for small-molecule antivirals
    • Stereochemically-defined CNS candidate compounds
    • Precursor blocks for anti-inflammatory actives
    • Advanced protected amino alcohol intermediates

    2. Custom Fine Chemical Synthesis for Research Use

    Specialty contract research organizations and lab-scale production units utilize this material when designing new heterocyclic frameworks. Its unique aminocyclopentene moiety provides rare structural motifs valuable for lead optimization and structure-activity relationship studies. Researchers often leverage our batch documentation and traceability for synthesis under controlled laboratory environments.

    Industry compliance standards

    • ISO 9001:2015 quality management system
    • Organization for Economic Cooperation and Development (OECD) Good Laboratory Practice (GLP) guidelines
    • REACH (EC 1907/2006) registration for laboratory-scale chemicals in Europe
    • Local chemical safety and traceability regulations (e.g., U.S. Chemical Facility Anti-Terrorism Standards for listed chemicals)

    Typical usage ratio

    • 0.2 – 1.0 mmol per reaction batch in screening syntheses
    • Scale and concentration determined by desired yield of novel compounds

    Downstream process integration

    • Directly charged into reaction vessels for ring functionalization or amine derivatization
    • Participates in library synthesis or SAR workflows for rapid analog development
    • Purification via flash chromatography or preparative HPLC
    • Integrated documentation for compound registration and patent support

    Final product types

    • Heterocyclic analog screening sets
    • Novel candidate molecules for medicinal chemistry
    • Reference materials for analytical method development
    • Small-quantity research intermediates

    3. Precursor for Synthesis of Modified Nucleosides

    Chemical manufacturers focused on advanced nucleotide analogs use this compound to construct cyclopentene-backbone nucleoside intermediates. These intermediates serve as crucial raw materials for synthetic RNA and DNA oligonucleotide products, with applications ranging from research reagents to gene therapy vectors. Purity and enantiomeric excess remain critical, and manufacturing follows stringent biopharmaceutical guidelines.

    Industry compliance standards

    • ICH Q11 (Development and Manufacture of Drug Substances)
    • GMP for oligonucleotide API intermediates
    • USP General Chapter <797> for compounding nucleoside solutions (as applies to end use)
    • ISO 13408 Part 1 (Aseptic Processing), if used in parenteral nucleoside synthesis

    Typical usage ratio

    • 1.00 – 1.25 molar equivalents in ring construction and nucleobase attachment reactions
    • Adjusted to offset competing side reactions during glycosylation steps

    Downstream process integration

    • Feeds at the initial cyclopentene ring opening or amino group protection stage
    • Involved in coupling with protected nucleobases under anhydrous conditions
    • Purification by crystallization or ion-exchange chromatography
    • Process batch records maintained for traceability through to final oligo product

    Final product types

    • Modified nucleoside monomers (RNA/DNA analogs)
    • Precursors for antisense oligonucleotide APIs
    • Raw materials for mRNA synthesis kits
    • Synthetic gene therapy intermediates

    4. Intermediate in Synthesis of Cyclopentene-Based Agrochemical Compounds

    Leading agrochemical synthesis operations apply this compound in the development of cyclopentene-based pesticides and growth regulators. Chemical incorporation occurs during assembling functionalized rings required for target molecule activity. All steps adhere to agricultural chemical safety and performance standards, with in-process controls prioritized for batch reproducibility and environmental compliance.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • OECD Guidelines for Testing of Chemicals (e.g., ENV/JM/MONO protocols)
    • ISO 17025 for accredited agrochemical QA/QC labs
    • REACH substance evaluation for non-pharmaceutical applications in EU markets

    Typical usage ratio

    • 1.05 – 1.15 equivalents in key cyclization or functionalization steps
    • Adjusted as needed for final compound yield optimization through iterative trials

    Downstream process integration

    • Dosed in pre-functionalization stages prior to halogenation, acylation, or other group additions
    • Maintains chemical structure throughout ring modification and bioactivity calibration
    • QC samples drawn at intermediate and final stages for agrochemical performance analysis
    • Byproduct handling follows regional hazardous waste guidelines

    Final product types

    • Cyclopentene-derivative insecticides
    • Plant growth regulation compounds
    • Precursor ingredients for herbicide formulation
    • Advanced intermediates for targeted crop protection solutions
    Free Quote

    Competitive [(1R,4S)-4-Aminocyclopent-2-Enyl]Methanol Hydrochloride prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.

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    Certification & Compliance
    More Introduction

    Introducing [(1R,4S)-4-Aminocyclopent-2-Enyl]Methanol Hydrochloride: Our Journey from Lab Bench to Production Barrel

    Ask anyone with years on the chemical manufacturing floor, and you’ll hear stories about how some molecules are just stubborn. By the time we reached what matters with [(1R,4S)-4-Aminocyclopent-2-Enyl]Methanol Hydrochloride, many hands had already guided its route. This isn’t about showy innovation or chasing something flavor-of-the-month. We’re looking at a molecule that earned its place because of what it does and, maybe more importantly, how consistently it does it. Bringing this hydrochloride to your bench or pilot line took more sweat and know-how than most end-users ever realize.

    What We’ve Learned on the Floor

    We started synthesizing cyclopentene derivatives because our partners in pharmaceutical R&D couldn’t find reliable supply. Variations in chirality, yield, and impurity profiles frustrated their process, stalling projects for weeks. So, we got involved from precursor sourcing to every check between each batch, running analytics that told us how much of the desired (1R,4S)-enantiomer we really pulled. In this hydrochloride, small changes in raw material quality or temperature curve during hydrogenation made all the difference between a premium product and a problem batch. Mastery came from repetition and painful root-cause sessions – not so much from trick instrumentation or theory alone.

    By choosing hydrochloride salt over the pure base, we handle not just stability but also dosing control. Chemists downstream don’t have to worry about solution pH swings or inconsistent activity. This isn’t about marketing – it’s about batches that behave the same, day in and out, whether you’re using a 10-gram sample or scaling up to 20 kilos. Our product won’t surprise you with drifting solubility or ghost impurities that sneak in midway through your synthesis campaign.

    The Backbone of Emerging Therapeutics

    Much of the buzz today around functionalized cyclopentenes comes from their role as key intermediates in targeted therapies. We’ve watched how research groups rely on small, chiral amine building blocks like this one. Early on, we fielded requests from a team working on antiviral scaffolds – they needed the (1R,4S) configuration to fit their structure-activity relationship studies. Using racemic or poorly defined mixtures wastes resources and can misdirect whole medicinal chemistry programs. We make sure you get only the required enantiomer, with NMR spectra and HPLC traces to back it up for every lot.

    We’ve also shipped it to groups chasing new central nervous system targets. The methanol arm on this structure opens pathways for nucleophilic substitution, letting chemists build out more complex rings or attach groups that tune bioavailability. We kept volumes flexible, letting startups get a foothold and established producers scale as their projects hit later-stage studies.

    Specifications Grounded in Use, Not Just Certificates

    Through hands-on production, we committed to a purity standard above the common threshold. The number on the assay report doesn’t tell the whole story. Contaminants at just a tenth of a percent can cripple crystallization or skew downstream assays, so we drive content above 98% and routinely show lower residual solvents on GC and headspace. Our drying cycle runs longer than what many contract shops consider “finished,” just to ensure you see powder, not caked solid or a sticky mass.

    Particle size took more tuning than almost anything else. Weird as it sounds, some laboratories want almost fluffy, easily dispersed powder for solution-phase chemistry, while others want just enough weight to minimize static charge and dust. Instead of imposing one form, we listened, ran comparative blending studies, and kept a consistent lot profile. What you get from us at 500 grams should not give you measuring headaches at 5 kilograms.

    On water content, this hydrochloride soaks it up in the wrong conditions. That can corrupt downstream yields fast, especially when customers run organometallic steps. We store and ship in moisture-barrier packaging, in lots big enough to run QC on each before you rip open the seal. As always, transparency runs deep: if a batch ever tips near the upper limit, you hear from us before it’s in your inventory.

    A Manufacturer’s Perspective on Safety and Handling

    There’s been plenty of talk lately about upstream traceability and responsible stewardship. Our teams live this daily. Every vessel and line gets a documented clean-out between runs, cutting cross-contamination right out. If our own teams wouldn’t use a given batch for a crucial step, it never heads to the packing floor. We staff routine hazard audits, not because any regulator asked, but because chemical compatibility isn’t a box-ticking exercise, it’s a habit earned over decades.

    Our practices extend past what you see in the drum or foil pouch. Operators on our lines get thorough hazard training – not just slideshows but hands-in-gloves work, so they recognize when a process drifts or a vessel acts up. Customer feedback shapes our packaging, so you won’t find surprises like brittle seals or flaking liners that dump powders into the air. We remember every near-miss so another crew doesn’t repeat it.

    What Sets this Material Apart

    If you’ve ordered similar amines elsewhere, you know the headaches when a product arrives off-ratio or with an impurity fingerprint that flags a column stall or an irritating repeat purification. Our focus never strays from the intended configuration: (1R,4S) and nothing else. Even minor isomeric drift during synthesis demands rerunning our own starting materials or revising process controls. Reports from end-users let us fine-tune operating windows, so every molecule matches its NMR printout, batch after batch.

    Hydrochlorides can leach chloride ions, or worse, pick up environmental moisture leading to clumping. Our formula and drum choice reflect years’ experience handling fine organics with hygroscopic tendencies. The same applies to odor: a back-of-the-lab fishy tang signals an organic breakdown, so we track degradation markers even after standard shelf-life ends. We learned long ago that a small odor shift often points to a process slip upstream.

    Direct Comparison: Mistakes Others Make

    We’ve trialed competitive samples ourselves on developmental chemistry lines. Too often, irregular melting points show lazy control at the neutralization stage. Fluctuating particle sizes can upset metered dispensing, especially with automated feeders. Some suppliers fall back on uncontrolled solvent removal or blend by hand, leading to low-level contamination traceable by HRMS. Companies outside pharma sometimes skip optical rotation altogether, risking a wrong-handed product that wipes out assay results or in vivo models.

    Some competitors cut corners by air-drying final salts, protecting profits but boosting water uptake and shelf instability. We rejected these tradeoffs after early customers flagged repeat issues in GC-MS and repeat Karl Fischer titrations. Customers told us bluntly when they burnt through time chasing solvent artifacts or running unplanned columns. Learning from their experience, we pushed for in-line analytical controls and standardized checklists with lot traceability for each container, not just a master batch.

    Real World Demand: Stories from the Field

    It’s easy to overlook why this cyclopentene derivative in particular gained traction with medicinal and process chemists. One team reached out after spending months synthesizing lead structures for a new hepatitis C analog – they saw their yields spike after switching to our grade. Little changes added up: different peak shapes in liquid chromatography, cleaner separation, and less time baby-sitting purification. What looked like a small supply chain tweak freed up weeks for other screening efforts.

    Academic labs, tight on budgets, sometimes think a lower-cost variant might save a few dollars. Experience quickly teaches that off-brand batches, lacking strict isomer specification, derail whole semester-long projects. When a PhD candidate’s project timeline rides on timely delivery, we step up, expediting shipments and supporting their method validation. Genuine partnership, not commoditization, drives both sides forward.

    Control Translates to Consistency

    Nobody in our shop pretends chemical manufacturing is free from risk. Not every batch starts identical, and upstream pressure from the supply chain sometimes throws a wrench in yields or solvent sourcing. Still, our process design weeds out variables early and makes each production run less vulnerable to surprise setbacks. Years ago, a small tank temperature deviation sent a run off-spec – this prompted an overhaul that installed more robust local monitoring and redundant flow gauges. Since then, our standard deviation in assay and impurity levels shrunk by a meaningful margin.

    Too many producers put sales first, process second. For us, consistency is the root: before a container moves from our line, a technician signs off, certifying it matches the working standard developed by hands-on chemists. Analytical snapshots from across the production window map out every stage. Customers see not just results, but the underlying trust built batch after batch.

    Solutions to Industry Friction

    Realistically, the world of fine chemicals can’t avoid every raw material shock or regulatory shift. Still, open communication upstream dampens most shocks. We keep direct links with suppliers who know our tolerance for off-standard materials runs low, rewarding reliability. On the customer side, we collaborate during their early synthesis campaigns, troubleshooting unexpected reactivity or solubility quirks through honest conversation. With this molecule, switching from a competitor’s free-base to our hydrochloride froze out solubility surprises that used to shut down scale-up steps.

    On product lifecycle support, our technical team regularly follows up with formulators and process engineers, reviewing batch records and use-cases. These connections feed back knowledge that guides our process tweaks, not just for one flagship. As expected, best practices slip into every run when customers trust you enough to share stumbles along with wins.

    Supporting Safe Growth Without Compromise

    Too much of today’s talk about chemical supply focuses on speed or price. Quality is not a bullet point on a sales flyer; it’s the reason you come back with your next project or grant. [(1R,4S)-4-Aminocyclopent-2-Enyl]Methanol Hydrochloride drew attention because of the real-world difference in downstream performance. Researchers and process managers recognize the gaps – they move away from unreliable lots after the third or fourth unexplained process hiccup.

    Our experience manufacturing this hydrochloride changed how we approach continuous improvement. Unexpected handling quirks, like static build-up or packaging abrasion, prompted critical adjustments, like revised liner thickness and moisture-protection coatings. We fielded late-night field calls when a European customer flagged a shipment outside their humidity window. Future shipments built on that lesson, lowering product loss during long transits.

    Trust Earned One Drum at a Time

    We don’t expect you to take these claims at face value. The proof plays out every month, shipment by shipment, in the confidence our partners express as they scale programs. Keeping a technical line open and resolving questions as chemists use the product ensures problems don’t snowball. Teams come to us not just for a material, but also for insights from years on the bench and at production scale.

    We never chase volume at the expense of what kept us in business. With resources tight across the industry, attention to detail on every batch cements what separates a reliable manufacturer from a mere supplier. This product stands out because it was built on learning from stumbles and listening to feedback from sharp chemists and engineers who won’t settle for “good enough.”

    Final Thoughts: The Pursuit Never Ends

    Even as demand patterns shift, the foundational need for chemically and enantiomerically pure intermediates holds solid. Our history making [(1R,4S)-4-Aminocyclopent-2-Enyl]Methanol Hydrochloride reads as a lesson in doing the basics exceptionally well and taking every bump in the road as a reason to improve. The result speaks through every batch that lands on a customer’s loading dock ready to go: no fuss, no guessing, just a tool designed to keep new ideas moving forward.

    Whether you’re in the trenches of a crowded process development lab or coordinating shipments for a growing biotech, know this: every molecule we send out started as a problem someone couldn’t solve. It became a solution by listening, adjusting, and refusing to compromise on the details that count. We look forward to showing you how much makes a difference in the right hands.