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(R)-2-Aminohexane

    • Product Name (R)-2-Aminohexane
    • Alias (R)-2-Aminohexan
    • Einecs 629-426-2
    • 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

    574197

    Cas Number 34425-14-4
    Iupac Name (R)-2-aminohexane
    Molecular Formula C6H15N
    Molecular Weight 101.19 g/mol
    Appearance Colorless liquid
    Boiling Point 132-134°C
    Density 0.77 g/mL at 25°C
    Optical Rotation [α]D20 +20° (c=1, CHCl3)
    Refractive Index 1.422
    Purity Typically ≥98%
    Smiles C[C@H](N)CCCC
    Synonyms (R)-hexan-2-amine
    Melting Point -18°C
    Solubility Miscible with water and organic solvents

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

    Packing & Storage
    Packing A 25g amber glass bottle labeled “(R)-2-Aminohexane, 98%” with hazard pictograms, lot number, and tightly sealed cap.
    Shipping (R)-2-Aminohexane is shipped in secure, tightly sealed containers to prevent leakage and contamination. It is packaged according to chemical safety regulations, labeled with hazard information, and accompanied by safety data sheets. During transit, the chemical is protected from extreme temperatures, moisture, and incompatible substances to ensure safe delivery.
    Storage (R)-2-Aminohexane should be stored in a tightly sealed container, in a cool, dry, well-ventilated area away from incompatible substances such as strong oxidizers and acids. Avoid exposure to moisture and direct sunlight. Store at room temperature, ideally between 2–8 °C. Proper labeling and adherence to local chemical safety regulations are essential for safe storage.
    Application of (R)-2-Aminohexane

    Applications of (R)-2-Aminohexane in Industrial Manufacturing

    As a direct manufacturer of (R)-2-Aminohexane, we supply this chiral amine intermediate for precisely defined downstream processes in industrial sectors where its stereochemistry and reactivity are essential for end-product performance and regulatory compliance. Our material integrates into industry-specific processes under established formulation guidelines and regulatory frameworks, supporting customers in high-value chemical synthesis.

    1. Chiral Pharmaceutical Intermediate Synthesis

    (R)-2-Aminohexane functions as a critical chiral building block in the synthesis of APIs for enantiomerically pure pharmaceuticals, particularly in manufacturing certain antihypertensive agents and investigational active ingredients. Process chemists incorporate it within enantioselective synthesis protocols to construct complex molecular scaffolds, leveraging its chirality at scale with batch-to-batch reproducibility and controlled impurity profiles. The intermediate typically enters at the amidation, reductive amination, or coupling stages, where precise enantiomeric excess (ee) is monitored under stringent GMP controls. The ingredient ratio directly impacts yield and downstream purification needs, often determined by stoichiometry relative to acyl or carbonyl counterparts.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for Active Pharmaceutical Ingredients
    • European Pharmacopeia (Ph. Eur.) monographs for chiral intermediates
    • USP General Chapter <823> Stereoisomerism in Pharmaceuticals
    • FDA 21 CFR 210/211 (for API manufacturing)

    Typical usage ratio

    • 0.93 to 1.05 molar equivalents versus acylating or ketone partners, precise ratio set per target reaction and residual starting material removal constraints.

    Downstream process integration

    • Introduced at amide bond formation, reductive amination, or asymmetric coupling stages prior to key cyclization or ring closure steps; followed by purification, salt formation, and crystallization.

    Final product types

    • Single-enantiomer antihypertensive APIs
    • Investigational new drug candidates with chiral centers
    • Intermediates for CNS active pharmaceutical development
    • GMP-compliant fine chemical intermediates for CDMO projects

    2. Asymmetric Catalyst and Ligand Manufacturing

    Industrial manufacturers of chiral catalysts and complex ligands employ (R)-2-Aminohexane as a key precursor for producing enantiopure phosphoramidites, oxazolines, and diamine-based ligands utilized in large-scale asymmetric hydrogenations and additions in agrochemical and pharma ingredient synthesis. Its configuration determines the selectivity and conversion rates achieved in downstream catalytic processes, while high-purity grades are essential to avoid byproduct formation. Integration happens at early-stage condensation or substitution reactions within catalyst precursor assembly, requiring validated chiral QC and analytical verification to conform to process validation standards.

    Industry compliance standards

    • ISO 9001:2015 Quality Management System
    • REACH (EC No. 1907/2006) registration for manufacturing and import in the EU
    • Responsible Care® program guidelines
    • OECD Test Guidelines for purity and traceability

    Typical usage ratio

    • 0.90 to 1.20 molar equivalents per phosphorus or acid chloride functional group, adjusted based on batch scale and ligand architecture design requirements.

    Downstream process integration

    • Intake at the initial condensation or substitution reaction with phosphorus or acyl donor reagents; proceeds under inert conditions to maintain enantiopurity before final ligand or catalyst isolation and QC release.

    Final product types

    • Enantiopure phosphoramidite ligands for asymmetric catalysis
    • Chiral diamine and oxazoline series ligands
    • Homogeneous transition metal catalysts for fine chemical production
    • Agrochemical synthesis auxiliaries

    3. Specialty Polymer and Copolymer Modification

    In specialty polymer and advanced material manufacture, (R)-2-Aminohexane serves as a functionalizing agent for producing optically active polyamides and as a co-monomer modifier in select polyimide and nylon-6,6 derivatives. Its use imparts chiral or surface-active properties to finished resins, which target membrane technology, enantioselective separation, and high-performance engineering plastics. Formulators control the input percentage based on targeted mechanical, thermal, or enantioselective parameters, while integration takes place during melt-polymerization or post-polymerization amination with strict control over byproduct removal for compliance with advanced material standards.

    Industry compliance standards

    • ISO 9001 (certified quality system for polymer compounding)
    • ASTM D4066 (Standard Classification System for Nylon & Polyamide Materials)
    • RoHS 2011/65/EU (for electrical and electronic polymer parts)
    • FDA 21 CFR 177.1500 (for indirect food contact if used in packaging membranes)

    Typical usage ratio

    • 0.5% to 4% by weight in polymer blends; precise ratio depends on end-use application and target chirality, adjusted to maintain thermal resistance and mechanical integrity.

    Downstream process integration

    • Added during polycondensation or melt blending; also functionalized onto polymer chains by post-polymerization amidation or amination under controlled temperature and vacuum processing.

    Final product types

    • Chiral polyamide fibers
    • Modified engineering plastics for technical membranes
    • Polyimide copolymers with optical activity
    • Enantioselective polymeric stationary phases for chromatographic media

    4. Fine Chemical Synthesis for Electronic Liquid Crystal Materials

    Manufacturers specializing in liquid crystal (LC) intermediates leverage (R)-2-Aminohexane as a chiral source in custom-synthesized LC materials, especially in constructing C6-type side-chain chiral amine derivatives. Its specific enantiomeric purity influences the optical rotation, transition temperature, and display performance of terminals such as LCD panels and tunable LC filters. The material typically reacts at the initial amide or imine formation stages, proceeding into multi-step organic syntheses that require tight control of reaction conditions and intermediate purification. The formulation quantity aligns with the desired molecular configuration in the LC mixture, balancing downstream performance with cost considerations.

    Industry compliance standards

    • RoHS 3 Directive (EU) 2015/863 for electronic materials
    • IEC 61249-2-21 for halogen-free organic chemicals in electronics manufacturing
    • ISO 14001 for environmental management in chemical synthesis
    • REACH Annex XVII (restrictions for listed hazardous substances in electronic intermediates)

    Typical usage ratio

    • 0.8 to 1.3 molar equivalents, optimized per target LC intermediate and configuration of the chiral core structure.

    Downstream process integration

    • Reaction with acid/aldehyde derivatives in solvent-controlled amidation or imine formation; advances through purification and thin-film analysis prior to LC blending.

    Final product types

    • Optically active LC intermediates for advanced display materials
    • Chiral amine-based LC mesogens
    • Performance additivates for specialty electronic films
    • High-precision dopant agents for LCD panels
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    Certification & Compliance
    More Introduction

    (R)-2-Aminohexane: Pushing Synthetic Chemistry Forward

    From Reaction Kettles to Real-World Solutions

    Stepping into the lab, nothing beats the sense of possibility you find with a bottle of (R)-2-Aminohexane on the bench. This chiral amine sits in a rare niche. Its structural formula, C6H15N, offers a blend of simplicity and clever molecular architecture, with the (R)-configuration opening doors that other amines just cannot unlock. The purity and enantiomeric excess we achieve make each batch a reliable anchor for chiral syntheses. Over years of refining our process, our technicians have learned the quirks and character of this fine amine, from its solvent compatibility to the way it handles extended storage and transport. Customers tell us that consistent quality—delivered without batch-to-batch surprises—matters just as much as the catalog spec sheet.

    Quality That Carries through Every Batch

    Paramount to any chiral intermediate is the tight control over its optical rotation and overall purity. Each drum of our (R)-2-Aminohexane matches narrow release targets for both assay and enantiomeric purity, supported by our in-house chromatography and NMR suites. We keep typical levels of related byproducts and trace enantiomer below detection for most synthetic work. Water content remains controlled below 0.20%, and our GC testing screens for volatiles comprehensively. Each kilogram can be traced to a production record that logs each process change, from hydrogen pressure to crystallization temperature. That oversight helps cut down on headaches for process chemists when scaling bench work to larger reactors, which is no small thing in pharma and fine chemical settings.

    Why the (R)-Enantiomer Matters

    In a world where stereochemistry dictates everything from pharmacology to polymer chirality, the (R)- form can spell the difference between a working process and a costly stall. Many researchers remember the scramble for chiral amines during regulatory reviews, when synthesis of an API needed absolute confidence in every input. Medicinal chemists rely on the (R)-enantiomer of 2-aminohexane—its selectivity proves essential in the asymmetric synthesis of beta-blockers, CNS agents, and in fine-tuning the properties of chiral auxiliaries. Racemic blends and (S)-isomers just do not yield the same downstream outcomes, especially when the biological pathway demands high enantioselectivity.

    Synthesizing (R)-2-Aminohexane: Our Approach

    Many manufacturers try to rush through the reductive amination or asymmetric synthesis, but we treat each step with painstaking attention. Starting with optically pure chiral precursors, our engineers developed a process that consistently returns a product with high optical activity. We carry out hydrogenation over supported precious metal catalysts, precisely monitoring temperature and hydrogen uptake. Our team believes that the difference shows up in scale-up yields; lower byproduct formation means less time and solvent spent in purification. After reaction workup, the material undergoes distillation under vacuum to strip volatiles, followed by specific chiral HPLC tests to confirm the (R)-enantiomer content before final packaging.

    Handling and Storage: Protecting the Integrity

    Despite its stability under typical atmospheric conditions, (R)-2-Aminohexane responds best to care in handling. Our operators use dedicated glass-lined and stainless reactors, avoiding cross-exposure with potential stereochemical contaminants. Since the liquid is hygroscopic, we use molecular sieves and nitrogen sparging for both long-term storage and filling operations. To prevent the introduction of trace acids or oxidizers, all contact lines follow a strict cleaning protocol before each batch. Customers can count on shipment in sealed, argon-flushed containers to preserve quality during air and sea freight. Our logistics crew stays vigilant about temperature swings, especially when shipping during extreme seasons.

    Fundamental for Building Blocks

    The versatility of (R)-2-Aminohexane stems from its amine functional group and elongated aliphatic chain. Our clients synthesize advanced intermediates for everything from agrochemical active ingredients to performance polymers and specialty surfactants. The chiral nitrogen imparts desired stereochemistry into downstream molecules, and acts as a handle for coupling, acylation, or cyclization. Peptide chemists value (R)-2-Aminohexane as a scaffold; in polymer research, it forms part of the backbone in specialty nylons and other condensation products. Specialty surfactants and additives take advantage of the molecule’s chain length, offering hydrophobic-lipophilic balance difficult to achieve with shorter amines.

    Comparisons with Other Amines

    A regular question from chemists is how (R)-2-Aminohexane stacks up against close relatives like (S)-2-Aminohexane, 1,6-hexanediamine, or the racemic mixture. For those running asymmetric syntheses or preparing optically active intermediates, the need for a single enantiomer takes precedence. Our product stands out through its combination of optical purity, minimal byproduct profile, and thorough analytical documentation. Compared with 1,6-hexanediamine, which features additional reactivity from the second amine, (R)-2-Aminohexane offers a milder, more controlled behavior as a nucleophile or catalyst precursor. Clients working in biocatalysis have pointed out that the single chiral center allows fine-tuning of selectivity in enzyme-substrate interactions, giving (R)-2-Aminohexane the edge over non-chiral or mixture-based amines in high-value applications.

    Supporting Customers beyond the Sale

    Having spent years refining not just the purity but also the predictability of our product, we make ourselves available to clients who need advice on scale-up, downstream compatibility, or customized packaging. Each customer’s synthesis may demand slight adjustment to handling, so we share our in-house experiences with different reaction partners, temperatures, and solvents. In a few case studies, we’ve seen start-ups cut weeks off their route development by talking through the subtleties of (R)-2-Aminohexane’s chemistry with our technical folks. Tackling process optimization as a chemist myself, I value manufacturers who step up with real-world troubleshooting instead of just selling a chemical—and that’s the role we aim to fill.

    Tracing Back to Raw Materials

    Purity and consistency start long before the amination or hydrogenation stage. Our procurement specialists chase down recent lots of chiral stock, turning over analytical data and collaborative supplier testing reports before signing off on incoming shipments. The raw material chain stays tight: the fewer variables that enter upstream, the more reliable the finished product’s performance in a new synthesis. Each consignment gets logged, sampled, and tested before entering the production floor, which helps ensure that small fluctuations in precursor content do not drift into the finished product. Years of data tracking make it possible to spot trends and correct process issues before they reach the customer.

    Documentation You Can Trust

    Analytical support sits at the foundation of our value proposition. The certificate of analysis traces all quality critical data: optical rotation, GC/MS fingerprinting, chiral HPLC purity, and water content. Detailed production records include batch numbers, dates, and the signatures of the technicians who oversaw each step. Regulatory dossiers that support submissions in regulated industries accompany each new lot, supported by third-party audits. In regulated environments, this documentation makes a world of difference, smoothing approvals and helping customers meet their own QA checks.

    Addressing Industry-Specific Needs

    Applications diverge sharply depending on the end customer. Pharmaceutical firms use (R)-2-Aminohexane in patented synthesis routes and demand validation-ready analytical packages; materials developers expect samples that meet rigid mechanical and thermal performance metrics. In agricultural chemistry, the molecule plays its part in herbicide and pesticide active ingredient synthesis, dictating yield and activity profile. Our team maintains communication with wider industry groups, rides the pulse of changing standards, and adapts process controls to reflect evolving best practices. Several new pharma clients have shared detailed feedback on process impurity profiles, prompting us to reshape portions of the purification cascade to knock out even trace byproducts.

    Solutions to Quality and Supply Challenges

    Several challenges surface in supplying a product like (R)-2-Aminohexane: ramping up capacity to meet a rush of demand, maintaining clean separation of chiral streams, and supporting logistics in distant or hostile climates. By investing in dedicated chiral separation units and continuous monitoring systems, our site rarely faces the last-minute pressure that follows when upstream intermediates go short. We keep a buffer stock on-site, and work closely with trusted logistics partners to avoid shipping delays. Feedback from one multi-site API manufacturer led us to implement improved humidity barriers in packaging, which forestalled clumping and off-odors during maritime shipping. Even modest advances in handling keep downstream production running trouble-free.

    What Sets Our (R)-2-Aminohexane Apart

    It takes more than a standard operating procedure to offer a product that process chemists and formulation scientists willingly build entire synthesis platforms around. Our (R)-2-Aminohexane carries a reputation earned through years of meeting repeated audits, through both consistency in purity and transparency in manufacturing. Both small R&D operations and full-scale producers mention our technical advisory team by name, crediting them with providing clear solution paths to route changes and technical snags. Our process offers resilience against raw material fluctuations and regulatory changes, so our partners keep trusted supply lines open, even as standards shift.

    Looking Ahead in Chiral Chemistry

    The growing list of specialty molecules that draw on (R)-2-Aminohexane components—from specialty polymers through active pharmaceutical intermediates—suggests the chiral market segment will only tighten requirements for purity, traceability, and technical support. AI-driven synthesis planning, automated plants, and greater regulatory scrutiny place new weight on every input. Our approach involves more than optimizing batch yields on paper; it means walking the floor, checking yields, training every operator, and solving each puzzle put forward by customers. As enantioselective chemistry pushes forward, the push for even tighter controls and more robust supply chains will intensify.

    Feedback Drives Evolution

    Direct conversations with clients, partners, and on-site chemists drive real change in the way our (R)-2-Aminohexane is made, handled, tested, and delivered. Process changes trace back to complaints, requests, and questions. Through these collaborations, we have engineered better stability under varying climates, improved ease of transfer for those running kilo-lab campaigns, and cut down on solvent and energy consumption by optimizing distillation protocols. Our team regularly workshops improvements—from automating certain analytical tests to implementing digital tracking of shipments.

    Wrapping up: A Product Built on Practice

    Making and supplying (R)-2-Aminohexane is more than just scaling up a chemical reaction. Over the years, every feedback loop, every tweak in processing, and every technical conversation have shaped what we offer today. Whether the end use is in a pilot pharmaceutical synthesis, a specialty polymer run, or early-stage research, we view each batch of (R)-2-Aminohexane as an invitation to build long-term, reliable, and value-driven partnerships. That focus—pairing technical rigor with a commitment to supporting our customers’ innovation—keeps us motivated, batch after batch.