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HS Code |
976265 |
| Product Name | N-(2,4-Dinitrophenyl)-6-Aminohexanoic Acid |
| Cas Number | 102392-33-6 |
| Molecular Formula | C12H15N3O6 |
| Molecular Weight | 297.26 g/mol |
| Appearance | Yellow solid |
| Solubility | Slightly soluble in water |
| Purity | Typically ≥ 98% |
| Storage Temperature | 2-8°C |
| Synonyms | DNP-ε-Aminocaproic acid |
| Chemical Class | Amino acid derivative |
| Functional Groups | Amino, carboxylic acid, nitro |
| Smiles | C1=CC(=C(C=C1[N+](=O)[O-])N(CCCCCC(=O)O))[N+](=O)[O-] |
| Application | Biochemical research, enzyme substrate |
As an accredited N-(2,4-Dinitrophenyl)-6-Aminohexanoic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, screw cap, 5 grams, tamper-evident seal, white printed label with chemical name, weight, and safety warnings. |
| Shipping | **Shipping Description:** N-(2,4-Dinitrophenyl)-6-Aminohexanoic Acid is shipped in tightly sealed containers, protected from moisture, heat, and light. The package is clearly labeled with hazard information, following chemical transport regulations. Handle with care during transit and store in a cool, dry place upon arrival. Safety data sheets are included with each shipment. |
| Storage | N-(2,4-Dinitrophenyl)-6-Aminohexanoic Acid should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from heat and sunlight. Keep it away from incompatible materials such as strong oxidizing and reducing agents. Ensure proper labeling and restrict access to authorized personnel only. Store at room temperature and protect from moisture to maintain stability. |
Applications of N-(2,4-Dinitrophenyl)-6-Aminohexanoic Acid in Industrial ManufacturingN-(2,4-Dinitrophenyl)-6-Aminohexanoic Acid functions as a specialty reagent in various industrial processes where selective reactivity and robust analytical performance are required. As a manufacturer of this advanced compound, we address the specific processing, compliance, and formulation needs of each downstream industry. The following sections present a detailed overview of its real-world integration in key application scenarios, focusing on standards, practical dosage guidance, processing inputs, and end-product outcomes. 1. Chromogenic Substrate Synthesis for Enzymatic AssaysMany in vitro diagnostic kit manufacturers utilize this compound as a chromogenic component in the formulation of enzyme substrate reagents, ensuring high sensitivity in colorimetric assays. The compound’s specific structure allows tailored derivatization, enabling precise kinetic readouts for target enzyme activity, which is critical in routine laboratory and clinical testing platforms. Industry compliance standards
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2. Analytical Standards Production for Amino Acid QuantificationProducers of HPLC and capillary electrophoresis calibration kits incorporate N-(2,4-Dinitrophenyl)-6-Aminohexanoic Acid as a derivatization control standard for amino acid and peptide quantification. Its distinctive absorbance properties provide a benchmark in method calibration, supporting accuracy in high-sensitivity bioanalytical workflows. Industry compliance standards
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3. Synthesis of Enzyme Inhibitor Screening LibrariesPharmaceutical and biotechnology R&D facilities use this compound as a core building block in the library synthesis of enzyme inhibitors, benefiting from its reactivity and functional group diversity. It enables medicinal chemists to systematically develop structure–activity relationships for new lead candidates in metabolic and proteolytic target classes. Industry compliance standards
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4. Derivatization Agent for Protein Structural ProteomicsSpecialist proteomics laboratories utilize the selective reactivity of this compound to derivatize lysine residues in intact proteins and peptides, supporting advanced mass spectrometry-based structural mapping. Its chromophoric groups facilitate robust spectral tagging, allowing for precise identification of cross-linking sites and post-translational modifications during structural proteomics analysis. Industry compliance standards
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5. Custom Conjugate Intermediate for Immunogen DevelopmentAntibody and vaccine research teams employ N-(2,4-Dinitrophenyl)-6-Aminohexanoic Acid as a linkable hapten for generating immunogens with defined antigenic determinants. The compound’s dual functionality supports controlled conjugation to carrier proteins, raising highly specific antibody responses for diagnostic or preclinical therapeutic screening. Industry compliance standards
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In our plant, the journey from raw materials to pure N-(2,4-Dinitrophenyl)-6-Aminohexanoic Acid takes careful attention at every step. This compound, typically known among chemists as DNP-Lysine, draws attention for its unique function as a functionalized amino acid derivative. The heart of its utility lies in its role as a robust building block in peptide synthesis and diagnostic research. Precise functionalization of the hexanoic acid backbone with the dinitrophenyl group gives this molecule strong reactivity and a bold, identifiable chromophore—a crucial property in analytical and diagnostic settings.
Over years of running batch after batch, we have learned the value of consistency at every production stage. The 2,4-dinitrophenyl group is more than a fingerprint: it provides clear analytical signals, which is why researchers and manufacturers look for exactly this structure when developing peptide-based diagnostics, enzyme substrates, and selective inhibitors.
Bringing N-(2,4-Dinitrophenyl)-6-Aminohexanoic Acid from theoretical structure to industrial-grade product takes a seasoned team. Synthesis starts with proper handling of hazardous starting materials, including dinitrophenyl chloride and protected lysine derivatives. Conditions must stay water-free and temperature controlled. Skipping quality checks leads to batch rejection; our quality assurance lab runs HPLC, NMR, melting point, and UV/Vis analysis on every lot. We have seen how even minor impurities can throw off downstream peptide coupling or diagnostic readouts, which is why every shift in our plant stays vigilant for any drift in process control.
Different customers require product across a range of grades. Researchers trust our lab-scale batches for analytical studies, protease substrate design, and method development. Industrial peptide manufacturers count on multi-kilogram production runs, with each drum recorded and tracked for traceability. The higher the purity, the sharper the signal in analysis—this is a rule we’ve learned the hard way.
Total purity number matters, but it never tells the full story alone. Experienced chemists check not only for purity by HPLC, but also for consistent optical properties and structural integrity. We track moisture content, check for residual solvents, and make sure lot-to-lot consistency holds up over months. Our N-(2,4-Dinitrophenyl)-6-Aminohexanoic Acid usually comes as a bright yellow or orange crystalline powder, easily detected by UV absorbance thanks to its nitroaromatic group, which pairs well with common analytical protocols.
We store the product in air-tight, amber containers away from light and moisture, so the dinitrophenyl moiety won't degrade over time. Our facility maintains a controlled environment across production, packaging, and storage, and we recommend the same at a customer's site for maximum shelf life.
Among functionalized amino acid derivatives, the 2,4-dinitrophenyl group provides distinct advantages. Researchers often select this compound for its strong UV-chromophore, needed for tagging, tracking, and quantification in peptide chemistry or enzyme kinetics. We have seen plenty of cases where faint signals from other labeling groups lead to lost data or require more expensive equipment. The DNP group lets scientists measure peptide concentrations, enzyme activities, or cleavage events reliably using only standard laboratory spectrophotometers.
Our teams have worked directly with pharmaceutical, diagnostic, and analytical companies developing enzyme-linked immunosorbent assays (ELISA), protease activity assays, and custom peptide probes using DNP-6-Lys. The robust signal strength and chemical stability reduce variability and troubleshooting time during new method development.
In a typical catalog, a chemist will see a range of amino acid derivatives, each tailored for specific protections or labels. N-(2,4-Dinitrophenyl)-6-Aminohexanoic Acid stands apart once you see it in action. Basic N-protected lysines—CBZ, Boc, Fmoc variants—are staples in peptide synthesis, letting researchers build up sequences while controlling where reactions take place. DNP-6-Lys moves beyond simple protection by supplying a strong chromophore for tracking and analysis.
Other chromophore-tagged amino acids exist—Dansyl, FITC, or rhodamine complexes—but the DNP label offers distinct photostability and strong absorbance without requiring specialty detectors. Dansyl and fluorescein tags can photobleach, and often require more advanced fluorescence detection or reading at lower wavelengths. DNP-labeled lysine stays visible at 360-400 nm under typical conditions and remains chemically stable through most peptide assembly and purification steps. For routine peptide quantitation or enzyme reaction monitoring, DNP-lysine proves itself more robust and cost-effective, and that matches our customers’ real-world needs.
We have had customers switch from other tags after running into signal stability issues, especially for long-term storage of labeled peptides or use in high-throughput screening. The DNP group delivers a crucial combination of affordability, reliable detection, and broad compatibility.
DNP-6-Lys sees use early in its life as an analytical probe in university and industrial labs. Peptide chemists introduce it as a tagged building block during solid-phase synthesis, building fluorescent or UV-detectable peptides for tracking, quantification, or as enzymatic substrates. In biochemistry and protease activity research, its powerful chromophore component becomes invaluable. Researchers develop kinetic assays measuring appearance or disappearance of the DNP absorbance signature—providing a direct link between enzyme action and real-time data collection.
Industrial enzyme manufacturers and diagnostic labs weave DNP-labeled peptides into kits for detecting enzyme deficiencies, pathogen markers, or therapeutic drug monitoring. Years ago, some customers struggled with laborious post-synthesis labeling protocols. With our DNP-6-Lys, labeling happens during standard solid-phase peptide synthesis, shaving days off workflows and decreasing costs by simplifying purification and quantification steps. Consistency, strong UV signal, and direct compatibility make DNP-6-Lys crucial for enzyme-substrate or peptide quantitation assays in any medium to high-throughput laboratory.
We have worked with contract research organizations and diagnostic test kit manufacturers who demand scale as well as reproducibility. For them, process consistency—batch after batch—beats novelty. Over time, we refined our synthetic pathways and analytical controls to meet shifting customer requirements. Some projects called for added analytical certificates—full NMR, mass spectrometry, or UV spectral overlays included—so customers could meet shifting regulatory demands in sensitive applications. We took experience from these collaborations and adjusted our processes, extending lot tracking and expediting documentation workflows.
As more research groups transitioned from academic projects toward clinical applications, demand arose for ever tighter impurity profiles and analytical authentication. Diagnostic assays cannot afford questionable results; our lots undergo additional impurity screening for these end-users. Our fully synthetic approach eliminates any risk of biological contamination and delivers a product free from extraneous proteins or peptides, which can interfere in sensitive assays.
Not every customer approaches us with the same set of needs. Some seek gram-quantities for early discovery work and need detailed spectral data for confirmatory analysis. Others commission orders by the kilogram for diagnostic test kit assembly requiring stable bulk supply. Over the years, our support teams learned to interpret the signals behind requests: When a customer needs higher purity, better solubility, or amended analytical documentation, we respond by tuning our purification and testing protocols.
One recurring issue among peptide manufacturers concerns the solubility profile of functionalized lysine derivatives. High dinitrophenyl substitution can alter water solubility, affecting coupling efficiency if peptide solvent conditions deviate from standard practice. Through process feedback and real-world peptide assembly, we adjusted the counterion form—offering both acid (free base) and hydrochloride variants, depending on coupling step requirements. Providing both options allows chemists to match our compound to their established workflows, minimizing troubleshooting and maximizing yield.
Another practical concern for long-term users centers on the stability of the DNP moiety during prolonged storage. DNP groups can undergo slow degradation if exposed to high humidity and light, especially in poorly sealed containers. By switching container materials, ensuring nitrogen-flush lines, and tightening our moisture controls, we improved product shelf life and reduced customer complaints about coloration or loss of assay signal. We continue to monitor field feedback for further improvements.
Day-to-day operations at our facility place high priority on safe handling procedures. The parent dinitrophenyl groups require strict safety protocols during handling: trained technical staff use fume hoods, wear appropriate PPE, and minimize powder handling through closed transfer systems. Usage of DNP-Lys in downstream labs typically involves dissolved solutions and small quantities, but we still encourage all users to respect good laboratory hygiene. Over the years, we have refined waste disposal protocols and offered customer guidance for both hazardous solid and solvent waste. We maintain rigorous documentation to satisfy both internal standards and regulatory requirements.
Each pack of N-(2,4-Dinitrophenyl)-6-Aminohexanoic Acid leaves our site with not just a specification and lot record, but practical handling advice staff have accrued through long experience. We openly share details on recommended solvents, storage conditions, and preferred dissolution routes, taking feedback from customers to inform future batches.
Some of the most exciting developments around DNP-6-Lys have come out of collaborative research and new diagnostic kit rollouts. In the proteomics field, for example, our partners used DNP-labeled peptides to calibrate mass spectrometry and develop more sensitive assays for trace protease activity in clinical samples. In one recent program, our customer required batches prepared under enhanced cGMP practices, with certification and separate analytical batch release. The transition from standard research-grade to clinical-grade demanded close alignment between production, QC, and customer feedback teams; together, we enabled our compound to serve as a diagnostic calibrant in thousands of test runs.
Beyond human diagnostics, research labs developing veterinary pathogen assays and food-testing protocols have built DNP-labeled peptide substrates using our material. These new assays accelerate contamination screening, supporting food safety and animal health surveillance. Direct, robust UV detection simplified standardization across laboratories, providing reproducible results even when methods changed between sites.
In education and training programs, N-(2,4-Dinitrophenyl)-6-Aminohexanoic Acid enters classroom experiments highlighting enzyme-substrate specificity, quantifying proteolysis, or illustrating chromatographic analysis. Reliability and safety matter just as much in these environments as in commercial labs: consistent signals let instructors and trainees build confidence in their methods and analytical interpretations.
Our manufacturing staff never rest on process laurels; even incremental improvements deliver measurable benefits across supply chain, efficiency, and final product performance. Over the past decade, we upgraded reactor capacity, automated pH and temperature monitoring, and implemented in-line HPLC sampling for faster batch release. Our quality teams adopted digital tracking for in-process checklists, cutting lead times and improving traceability from raw material sourcing right through to shipping.
The world of peptide chemical synthesis and analytical reagents keeps evolving. As application scientists look for more selective probes, multiplexed assays, or stable diagnostic markers, our team keeps track of development in adjacent chemical and biomedical fields. Practical experience has shaped our product: discussions with academics exploring novel solid-phase synthesis linkers, or industry partners automating high-throughput peptide synthesis, inspire us to anticipate product modifications. For example, some customers requested custom DNP functionalization at other positions on the lysine backbone, or developed unique solvents to enhance crystallinity for large-scale production.
Every kilogram of N-(2,4-Dinitrophenyl)-6-Aminohexanoic Acid we produce embodies what a chemical manufacturing operation can achieve through focus on quality, open communication, and deep product knowledge. Our team recruits chemists and technicians with hands-on experience in analytical method development, industrial-scale synthesis, and regulatory policy; knowledge exchange is a point of pride. If a customer needs batch-specific analytical overlays, technical troubleshooting, or storage advice personalized to their site, we draw on experience from thousands of production runs and global collaboration.
Working with purity-sensitive applications in diagnostics, pharmaceuticals, or industrial peptide synthesis brings motivation and responsibility. Over our operational history, we have adopted industry best practices to ensure no batch of DNP-6-Lysine leaves our plant without full documentation, analytical confirmation, and user-focused technical support.
Developments in chemical synthesis feed back into everything we do. Our process engineers continuously review literature, participate in industry groups, and visit trade shows to identify new instrumentation, purification techniques, and analytical technologies. Learning from peers and partners keeps our team and facility up to date and gives our customers confidence in a steady, reliable supply.
For many years in this business, being a chemical manufacturer has meant more than just shipping a box of bright yellow crystals. From first inquiry to post-delivery technical support, our staff approach each batch of N-(2,4-Dinitrophenyl)-6-Aminohexanoic Acid as both scientists and craftsmen. The functionality, stability, and traceability of our finished product enable robust peptide synthesis, reliable analytical protocols, and meaningful diagnostic applications across the world.
Customer feedback continues to shape our evolution: faster lead times, higher analytical transparency, and continuous support keep both the product and team at the forefront of this specialty chemical field. This compound, with its unique DNP-tagged lysine backbone, has carved out a vital role in research and industry for good reason. Every order tells its own story—of improved assays, streamlined synthesis, or new discovery—and our role is to deliver on the promise and potential built into every molecule.