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HS Code |
190606 |
| Chemical Name | N-(2,4-Dinitrophenyl)-L-Alanine |
| Molecular Formula | C9H9N3O6 |
| Molecular Weight | 255.18 g/mol |
| Appearance | Yellow solid |
| Melting Point | 176-178°C |
| Solubility | Slightly soluble in water, soluble in ethanol and methanol |
| Cas Number | 3747-39-3 |
| Purity | Typically ≥98% |
| Storage Temperature | 2-8°C |
| Boiling Point | Decomposes before boiling |
| Iupac Name | (2S)-2-amino-3-(2,4-dinitrophenyl)propanoic acid |
| Smiles | C[C@H](N)C(=O)O.Nc1ccc([N+](=O)[O-])cc1[N+](=O)[O-] |
| Synonyms | DNP-L-Alanine, 2,4-Dinitrophenylalanine |
| Hazard Statements | May cause skin and eye irritation |
As an accredited N-(2,4-Dinitrophenyl)-L-Alanine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | White, sealed glass bottle with yellow hazard label, containing 5 grams of N-(2,4-Dinitrophenyl)-L-Alanine; includes safety and handling instructions. |
| Shipping | **Shipping Description for N-(2,4-Dinitrophenyl)-L-Alanine:** This chemical should be shipped in tightly sealed containers, protected from light and moisture. It must be handled as a hazardous material, compliant with all local and international regulations. Proper labeling, appropriate documentation, and temperature control (if required) should be ensured during transit to maintain product integrity and safety. |
| Storage | Store **N-(2,4-Dinitrophenyl)-L-Alanine** in a tightly sealed container, protected from light, moisture, and incompatible substances such as strong oxidizing or reducing agents. Keep it in a cool, dry, and well-ventilated area, ideally at 2–8°C (refrigerator temperatures). Ensure storage is clearly labeled, and restrict access to trained personnel only. Always follow appropriate safety and regulatory guidelines. |
Applications of N-(2,4-Dinitrophenyl)-L-Alanine in Industrial ManufacturingN-(2,4-Dinitrophenyl)-L-Alanine supports precision synthesis processes in specialty chemical and pharmaceutical sectors. Our in-house production enables strict supply consistency for advanced downstream integration. The material’s unique reactivity makes it essential for peptide mapping, analytical reference standards, and other complex intermediates applications. 1. Peptide Mapping Reagents for BioanalysisBioanalytical laboratories and research-driven pharmaceutical plants regularly use N-(2,4-Dinitrophenyl)-L-Alanine as a derivatizing agent in peptide mapping. It provides selective labeling of amino acid residues, facilitating chromatographic and spectrometric peptide identification. Quality control analysts depend on the unique chromophoric properties to increase detection accuracy during protein sequence verification and structure–activity studies. The compound reacts post-enzymatic hydrolysis, supporting reproducible identification of N-terminal residues. Industry compliance standards
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2. Chiral Selector Intermediate for Enantioselective ChromatographyChiral separation specialists use N-(2,4-Dinitrophenyl)-L-Alanine as a building block to prepare chiral stationary phases (CSPs) for HPLC columns. The dinitrophenyl moiety combines with the amino acid’s stereochemistry to provide strong π–π and hydrogen bonding interactions with a wide range of analytes. CSP manufacturers perform direct covalent attachment of the raw material onto silica or polymer supports under controlled conditions. This ensures selective enantiomeric resolution in the analysis and purification of pharmaceutical intermediates and APIs. Industry compliance standards
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3. Synthesis of Analytical Reference StandardsCertified reference material (CRM) producers rely on N-(2,4-Dinitrophenyl)-L-Alanine to synthesize specific derivatives for analytical calibration. Its predictable reactivity and chromophore facilitate traceable purity testing and quantification in chemical metrology. The compound supports reliable benchmark creation for analytical instruments, including HPLC and mass spectrometers. Factory batch records must document each stage to ensure ISO 17034 compliance for end-users in regulated environments. Industry compliance standards
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4. Pharmaceutical Intermediate in Peptide Drug SynthesisProcess chemistry groups in peptide drug manufacturing introduce N-(2,4-Dinitrophenyl)-L-Alanine as a selective protecting group or as an intermediate in the staged build-up of drug candidates. The compound’s dinitrophenyl protecting group offers stability during multi-step synthesis, resisting side reactions while allowing selective cleavage under mild conditions. Plant chemists monitor each coupling and deprotection step by HPLC to guarantee peptide purity before final API isolation. Industry compliance standards
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Every day, we make choices in our plant that mirror the challenges faced in laboratories and production workshops across the world. Chemists want reagents that do their job well and don’t create headaches later on. Over the years, N-(2,4-Dinitrophenyl)-L-Alanine (DNP-L-Alanine) has earned its place among essential analytical and synthetic building blocks. Behind the scenes, our engineers and technicians have refined each step—from raw material sourcing to the last quality control check—so every lot we prepare matches the reliability researchers expect.
In our operation, every drum, bottle, and vial tells a story about precision and hands-on experience. N-(2,4-Dinitrophenyl)-L-Alanine, known for its role in peptide sequence analysis and as a valuable substrate for enzymatic studies, comes off our line in a fine, stable crystalline powder. We achieve high purity through carefully controlled synthesis and purification, verified batch by batch using HPLC, melting point checks, specific rotation measurements, and elemental analysis.
Rather than delivering vague figures, we can point to consistent minimum purity specifications we’ve held ourselves to—greater than 99% by HPLC, with single-digit ppm residual solvents. Routine checks for optical rotation help confirm correct chiral configuration, important in peptide and chiral derivatization work. We avoid trace contaminants that can distort analysis or interfere with enzyme kinetics, supporting the trust researchers and application chemists place in each gram we sell.
Year after year, the protocols in our lab seek to improve batch consistency and performance in downstream reactions. Temperature control during nitration, rigorous washing to remove mineral acid residues, and moisture-limiting storage are the backbone of our approach. What ends up packaged at the end of the line is ready for usage in preparing DNP-protected peptides, validating amino acid sequences, or running enzyme assays.
We refer to our standard product as DNP-L-Ala-101. Each jar comes with certification detailing spectral (NMR, IR), chromatographic (HPLC trace), and basic physical data (melting point, optical rotation). Real-world clients care most about speed and certainty. Our tech team packs batches with a measured moisture level below 0.5% and routinely surpasses published purity specs. Typical batch sizes serve both large academic labs and scale-up requirements in the peptide synthesis sector.
The physical feel of DNP-L-Ala—slightly yellow, free-flowing, and free of caking—matters just as much as a high HPLC readout. Poorly dried or impure batches can stall peptide synthesis or create inconsistencies in amino acid analysis. Rejecting those problems up front, we target physical and chemical quality as two ends of the same spectrum. Nothing leaves our plant in an unsatisfactory state—our in-house team runs repeated homogeneity checks and packs in airtight, light-resistant containers.
From shelf stability to solubility, experience has shown that attention paid in production saves headaches at the bench. Whether our jars end up in a pharma R&D group, a university chemistry department, or an industrial proteomics facility, users find reproducible results batch after batch.
Laboratory professionals ask for DNP-L-Alanine because it delivers fast, clean reactions in amino acid and peptide chemistry. The dinitrophenyl tag simplifies both visualization and isolation of peptides and amino acid derivatives. In practice, users dissolve the product in suitable solvents (often alcohols, DMSO, or buffers depending on the process), combine with peptide mixtures, and recover protected peptides for sequence analysis. High visibility under UV and distinctive absorbance spectra streamline identification and quantification.
Customers report that our high-purity material shortens workup and minimizes byproduct formation, which matters most in multistep synthesis and analysis. Having heard from researchers using mass spec or HPLC, unpredictable impurities in the standard are often the real bottleneck. Our QA routines focus on minimizing those variables, ensuring the DNP-protected alanine integrates seamlessly with other DNP-amino acid series products.
As with any nitroaromatic derivative, safety in handling matters. DNP tags can sensitize skin and pose inhalation risks, so we emphasize proper PPE and the use of vented hoods. Large-volume customers appreciate our clear, experience-based advice for safe bench-top and scale-up operation.
Time after time, we see strong demand among peptide synthesis researchers, enzymology groups investigating hydrolytic cleavage, and academic labs conducting classic Sanger degradation for N-terminal amino acid identification. Although DNA/RNA analysis pushes the boundaries of life science tools today, DNP-labeled α-amino acid derivatives such as this remain the gold standard for certain protein work that still relies on proven chromophore chemistry.
Producing N-(2,4-Dinitrophenyl)-L-Alanine in-house has taught us to recognize fine details that separate true performance from unfortunate surprises. Most competing materials differ in two main ways—impurity profile and reproducibility between lots. Outsourced or resold batches may advertise “99% purity” yet deliver inconsistent HPLC traces, or mask racemization problems that creep into sensitive peptide syntheses. We never take these shortcuts.
Our process controls each parameter—reaction temperature, pH adjustment, residual solvent removal, and fine filtration—so each lot performs with maximum reliability. While suppliers selling blended or repackaged product often cannot guarantee stereo integrity or reject minor foreign residues, our direct oversight allows us to pinpoint issues early and exclude substandard outputs. Laboratories relying on sequence analysis or enzyme diagnostics see fewer side reactions and less troubleshooting as a result.
Users also tell us that our focus on correct chiral form—ensured by using high-quality L-alanine and validated by optical rotation and NMR—sets our DNP-L-Alanine apart. Racemization or even low-level D- contamination can throw off chiral derivatization, leading to ambiguous data. Quality-conscious synthetic chemists and lab managers know the pitfalls of cutting corners here, so we never source racemic precursors or blend batches to “meet spec,” but instead maintain a single, highly controlled route.
The precise color and crystal habit of our product—consistently solid yellow, not greenish or brown from side-products—reassures users that they are handling a carefully prepared chemical. From simple weighing to complicated downstream peptide cleavage, subtle differences pop up if corners are cut. Customers regularly tell us that switching to our material shaves minutes, sometimes hours, off purification and troubleshooting. That sort of feedback supports our focus on getting every step right up front.
Late-stage innovation often builds on the certainty that a reagent behaves as advertised. Years of experience supplying university and R&D groups for advanced proteomics and enzyme profiling confirm that researchers need confidence batch to batch and gram to gram. New entrants to the synthetic market may promise low price or quick delivery, but fall short on total transparency regarding contaminant profiles, proven stability, or chiral assurance.
Making DNP-amino acids well is tougher than it looks. Nitroaromatic chemistry demands tight safety protocols, accurate temperature monitoring, and immediate cleanup of spills to prevent dangerous exposures. Our plant follows well-drilled routines—spill kits always accessible, engineered ventilation robustly maintained, and team members wearing appropriate gear. Training refreshers run on a fixed schedule.
Waste handling matters, since solvents and unreacted nitro reagents can’t go down the drain or in general waste. We use specialized waste drums and work closely with local treatment providers to prevent contamination of groundwater or air. We’re investing in state-of-the-art scrubbers and solvent recovery to reduce environmental impact. Our quality team works to lower solvent use per kilo product, track emissions, and write clear SOPs for the entire team.
Efforts to improve automation and production efficiency focus equally on product quality and reduced batch-to-batch variability. Upgraded controllers now track critical variables in real time, minimizing process “drift.” This upgrades product safety as well as output uniformity. Whenever a plant incident occurs or a near-miss is recorded, the lessons are folded immediately into updated protocols, keeping the workplace safe and the product consistent.
DNP chemistry will always demand skill and attention. Careful storage is needed to prevent degradation by light or moisture. Our packaging lines employ UV-blocking bottles and desiccant packets as standard. Whole-lot retained samplers allow us to investigate any field reports of unexpected issues and adapt in real time.
As manufacturers, we see every project as a two-way street. We actively solicit feedback from academic and industrial users, asking not just if the product works, but if our labels, packaging, documentation, and tech support remove daily friction from the lab. Several users have requested different lot sizes or more robust packaging for long-distance shipping, leading us to trial innovative bottle sealing and improved cushioning in our shipments.
Chemists working on automated synthesis complain about dustiness or flowability, so our plant floor operators switched to anti-stick process aids that are compatible with all downstream analytical work. Mistakes in transportation or handling get traced and corrected in training, while our documentation constantly evolves to match new regulatory and research needs.
New regulations requiring stricter documentation of hazardous materials spurred us to overhaul shipping labels, batch tracebacks, and end-user support materials. We respond directly to requests for calibration data, repeat analyses, or regulatory support for grant and publication submissions.
The real learning comes from long-term relationships with return customers across North America, Europe, and Asia. They push us to raise our standards year by year, and we pass this on by keeping our door open to suggestions, new applications, and constructive criticism.
Even as new sequencing technologies hit the market each year, the fundamentals of Sanger dinitrophenyl chemistry remain needed in both teaching labs and high-end analysis. We’re watching shifts in demand toward higher-purity chiral standards, smaller custom lot sizes, and hybrid applications in biocatalysis or medical diagnostics.
Some customers are now blending classical peptide derivatization with advanced detection (LC-MS, UHPLC, real-time monitoring), meaning even tighter demands on purity and physical property consistency. Continuous investment in our plant and lab infrastructure keeps us ahead of these shifts, rather than chasing market changes belatedly. Our experience suggests that only direct control over every process step supports this level of customer demand.
Peptide synthesis groups moving to automated or miniature batch processing need stable, dust-free DNP derivatives that dissolve predictably and filter cleanly—so our upgrades often spark from real-world lab stories. We are always vigilant about improving lot traceability, contamination tracking, and supply-chain reliability, never assuming today’s process will be good enough for tomorrow’s challenge.
Even as regulations on shipping and storage for dinitrophenyl products tighten in some jurisdictions, we invest upfront to guarantee seamless compliance from first order to final delivery. This includes pre-tested documentation, on-call chemist support, and close coordination with freight and logistics partners.
It often takes years of hands-on history to understand why seemingly small changes in raw materials, purification steps, or analytical checks can make the difference between smooth science and endless troubleshooting. Manufacturing N-(2,4-Dinitrophenyl)-L-Alanine at scale means balancing product quality, environmental responsibility, workplace safety, and long-term relationships built on results rather than sales copy.
We continue to work closely with researchers and production chemists who depend on DNP-amino acids for sequence identification, protein modification studies, standardized assay calibration, and chiral reference standards. Each new requirement or unexpected use case gets recorded, discussed, and brought back into our process improvement meetings—there is no substitute for constant, direct dialogue between floor staff and the people actually running the experiments.
As the landscape for analytical biochemistry and peptide research continues to evolve, our long view as both manufacturers and partners centers on integrity. No shortcuts or half-measures survive long in the world of real users and real results. That is why every batch, every year, starts with a commitment to doing things right, right here.