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Dl-Histidine

    • Product Name Dl-Histidine
    • Alias HISDL
    • Einecs 221-441-2
    • 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
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    Specifications

    HS Code

    164099

    Chemical Name DL-Histidine
    Cas Number 499-94-5
    Molecular Formula C6H9N3O2
    Molecular Weight 155.16
    Appearance White crystalline powder
    Solubility In Water Freely soluble
    Melting Point 287°C (dec.)
    Ph Value 5.4–6.1 (1% in water)
    Chirality Racemic mixture (D and L forms)
    Synonyms DL-2-Amino-3-(1H-imidazol-4-yl)propanoic acid
    Storage Conditions Store in a cool, dry place
    Grade Generally available as pharmaceutical or food grade
    Odor Odorless
    Stability Stable under recommended storage conditions
    Category Amino acid

    As an accredited Dl-Histidine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Dl-Histidine is packaged in a sealed, amber glass bottle containing 100 grams, labeled with chemical name, purity, and safety information.
    Shipping DL-Histidine is shipped in tightly sealed containers to prevent contamination and moisture absorption. It is packaged according to safety regulations for non-hazardous chemicals, ensuring safe transit. Standard shipping includes labeling with proper chemical identifiers and handling instructions. Store in a cool, dry place upon arrival, away from incompatible substances.
    Storage DL-Histidine should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from incompatible substances. Protect it from moisture and direct sunlight. Avoid exposure to excessive heat or freezing conditions. Follow all relevant safety data sheet (SDS) guidelines for safe handling and storage of this chemical. Keep out of reach of unauthorized personnel.
    Application of Dl-Histidine

    Applications of Dl-Histidine in Industrial Manufacturing

    As a direct production manufacturer of Dl-Histidine, we supply this amino acid for industrial partners who require controlled quality and clear compliance documentation for various advanced applications. Below are several authentic downstream sectors utilizing Dl-Histidine, each outlined by specific compliance frameworks, technical formulation ranges, integration procedures, and finished product outputs.

    1. Parenteral Nutrition Formulations (IV Solutions)

    Dl-Histidine serves as a critical amino acid component for medical-grade parenteral nutrition admixtures produced by intravenous solution manufacturers. Its use supports stable physiological pH in amino acid infusions and enables formulation of balanced total parenteral nutrition (TPN), especially in clinical and hospital-based nutrition protocols for adult and pediatric patients with restricted enteral intake.

    Industry compliance standards

    • USP 43–NF38: Amino Acid Injection Monographs
    • European Pharmacopoeia 10.0 Monograph 01/2008:0605
    • China Pharmacopoeia (CP2020) injectable amino acid standards
    • cGMP (Current Good Manufacturing Practice) for injectable formulations

    Typical usage ratio

    • 0.1–0.4% (w/v) relative to total amino acids, adjusted to patient-specific protocols and age; clinical formulation teams may tailor the level based on parenteral nutrition reference patterns.

    Downstream process integration

    • Dissolved in sterilized aqueous base during initial amino acid component blending; introduced prior to pH adjustment and microfiltration. Follows filtration and terminal sterilization for aseptic completion.

    Final product types

    • Total Parenteral Nutrition IV Solutions
    • Peripheral Parenteral Nutrition Amino Acid Injections
    • Specialized Pediatric Amino Acid Formulations

    2. Biopharmaceutical Cell Culture Media Manufacturing

    Industrial cell culture media production incorporates Dl-Histidine as an essential amino acid source for growth and maintenance of mammalian cell lines. Biopharmaceutical manufacturers depend on precise amino acid ratios to optimize recombinant protein and monoclonal antibody yields, supporting both upstream research-grade and large-scale current Good Manufacturing Practice (cGMP) manufacturing processes.

    Industry compliance standards

    • ISO 9001:2015 Quality System for Media Production
    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • Ph. Eur. Monograph 1037 for excipients in biotech manufacturing
    • USP Chapter 1043 for ancillary materials in cell, gene, and tissue-engineered products

    Typical usage ratio

    • 5–50 mg/L in standard basal or feed media; concentrations set according to target cell line demand and production phase, with higher levels in high-protein expression protocols.

    Downstream process integration

    • Directly dissolved into deionized water or primary salt blends during basal or feed medium compounding; critical for both liquid and dry powder medium production prior to sterile filtration and filling.

    Final product types

    • Powdered and Liquid Cell Culture Media
    • Custom Feed Supplements for Bioprocessing
    • cGMP-grade Media for Recombinant Protein Production

    3. Food Fortification Additives for Infant Formula

    Food and nutritional manufacturers incorporate Dl-Histidine as a fortification additive to enhance the amino acid profile of infant formula products, compensating for limiting nutrients in cow’s milk-based substrates and meeting regulatory minimums for essential amino acids required during early development stages.

    Industry compliance standards

    • CAC/GL 10-1979 and Codex Alimentarius Standard 72-1981 for Infant Formula
    • GB 10765 (China Standard for Infant Formula)
    • Regulation (EU) 2016/127 for infant formula and follow-on formula
    • US FDA 21 CFR 107.100 for nutrient specifications in infant formula

    Typical usage ratio

    • 0.02–0.08 g/100 g protein in powder blends; formulation teams balance histidine contribution based on total amino acid content to meet Codex minimum specifications.

    Downstream process integration

    • Added during the dry blending stage together with other free amino acids or during liquid pre-mix phase preceding homogenization and spray drying in infant formula production lines.

    Final product types

    • Standard and Specialty Infant Formula Powders
    • Follow-On Milk-Based Nutritional Powders
    • Ready-to-Feed Infant Nutritional Liquids

    4. Diagnostic Reagent Manufacturing (Clinical Chemistry Kits)

    Clinical diagnostics companies use Dl-Histidine as a critical component in composition of reagent buffers designed for enzyme activity assays and calibration solutions. Its buffering capacity ensures stable pH and minimizes interference in substrate-enzyme reactions for reliable quantitative results in automated and bench-top analyzers.

    Industry compliance standards

    • ISO 13485:2016 Quality Management Systems for Medical Devices
    • IVDR (EU) 2017/746 for in vitro diagnostic regulation
    • US FDA 21 CFR Part 820 Quality System Regulation
    • CLSI EP5-A2 precision standards for clinical chemistry

    Typical usage ratio

    • 1–10 mmol/L in buffer solutions; precise levels defined by enzymatic activity measurement protocol or commercial reagent kit formulation needs.

    Downstream process integration

    • Blended in aqueous buffer preparations prior to addition of diagnostic enzymes and substrates; introduced during primary reagent batch mixing, followed by sterile filtration and aliquoting for kit assembly.

    Final product types

    • Clinical Biochemistry Analyzer Reagent Kits
    • Standard Buffer Solutions for Laboratory Testing
    • Calibrators for Enzyme Activity Measurement

    5. Veterinary Amino Acid Supplements

    Dl-Histidine features in veterinary premixes and amino acid supplements intended for companion animal and livestock diets where natural feed sources are inadequate or where balanced amino acid profiles are required for special growth, recovery, or metabolic situations. Its controlled addition supports muscle development and overall protein nutrition in formulated feeds.

    Industry compliance standards

    • AAFCO Official Publication for Feed Ingredient Definitions (US)
    • EU Feed Additive Register (Regulation No 1831/2003)
    • GB/T 17810-2017 Quality Standard for Feed Additives
    • FAMI-QS (European Feed Additives and Premixtures Quality System)

    Typical usage ratio

    • 0.01–0.2% in supplement premixes, titrated by species type, formulas, and nutritional balance targets; veterinary formulators adjust the inclusion levels based on target intake and feed intake patterns.

    Downstream process integration

    • Dry-mixed in powdered supplement blends or incorporated in liquid vitamin-mineral admixtures prior to tablet compression, pelleting, or sachet packaging in feed additive production.

    Final product types

    • Veterinary Nutritional Premixes (powder, granule, liquid)
    • Amino Acid Boluses for Cattle and Horses
    • Companion Animal Oral Nutrient Solutions
    Free Quote

    Competitive Dl-Histidine prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    Dl-Histidine: A Closer Look from a Chemical Manufacturer’s Lens

    Understanding Dl-Histidine Production and Quality Standards

    Working with Dl-Histidine every day, our chemists and engineers see firsthand the effort that goes into producing reliable amino acids for industries ranging from research to food and pharmaceuticals. The model we offer—DL-Histidine, CAS 4998-57-6—has no shortcuts or guesswork. Each lot is manufactured from pharmaceutical-grade starting materials in our automated reactors. We keep tight control over stereochemical integrity and residual solvent levels at every stage. With HPLC analysis and NMR confirmation, we deliver Dl-Histidine with purity typically above 98%, well above the minimum requirements set by several pharmacopoeias.

    Dl-Histidine brings an equal mix of D- and L-enantiomers. This matters, since L-Histidine occurs naturally in proteins, but the D-form provides a unique profile for specialized uses, especially in animal nutrition and biochemical research. Unlike products sourced through brokers who cannot trace or guarantee the origins of their raw materials, ours comes straight from our integrated manufacturing lines. This gives us knowledge from the vessel wall to the shrink-wrapped drum.

    Why Dl-Histidine Stands Out in Application and Performance

    We see Dl-Histidine requested for a surprising array of uses. Lab technicians use it as a buffer or precursor in synthetic pathways. Pharmaceutical manufacturers value the compound to calibrate analytical instruments or run process checks against the expected reactivity of both D- and L-isomers. In animal nutrition, feed formulators look to Dl-Histidine to balance essential and non-essential amino acid profiles. Unlike the L-form, using the racemic blend helps achieve targeted outcomes for species that metabolize both isomers differently.

    Our customers often ask about the main difference between Dl- and L-Histidine. On the technical side, both versions provide the imidazole ring, important for enzyme activity and metal ion coordination. L-Histidine serves direct dietary supplementation and cell culture, since only the L-form supports human metabolism effectively. The DL-mixture broadens research applications, particularly where stereochemical effects must be controlled or compared, or when pricing and inventory constraints limit access to pure L-Histidine.

    Product Characteristics and Handling Observations

    Years on the production floor taught us how sensitive histidine can be to moisture uptake and degradation. White to off-white powder, free-flowing if stored right, but it begins to cake when packaging conditions turn less than ideal. That's why our process uses double-layered polyethylene liners, nitrogen-flushed with robust tamper evidence, to protect every shipment from warehouse humidity. Each drum is filled and sealed within minutes after the final drying step, no unnecessary delay or exposure.

    If a formulation will spend weeks in transport or storage, every batch’s stability data gets scrutinized. The analytical team tracks not just total histidine but also breakdown products and oxidized forms with ultraviolet spectroscopy and liquid chromatography. This hands-on quality control makes a bigger difference than any line from a spec sheet or marketing handout. Direct access to manufacturing data helps clients avoid the headaches of unexpected failures in R&D pipelines or pilot plant runs.

    Dl-Histidine’s Role in Scientific Progress

    We’ve followed the evolution of amino acid chemistry for decades. Where L-Histidine dominated clinical trials, Dl-Histidine’s value in comparative studies and non-human applications kept growing. Regulatory requirements continue to shift, but as a manufacturer, we stay ready with documentation to trace every lot number, every raw material shipment, and every instrument calibration that touched the product. Our scientists work closely with users, whether their needs involve cGMP or just basic research. Dl-Histidine remains indispensable for groups studying mechanisms of racemization, enzyme substrate specificity, or even protein crystallography where both isomers need to be surveyed.

    Clients sometimes question why racemic histidine is still requested even as L-form pricing drops. The answer ties to the unique biochemistry of non-mammalian species, as well as emerging research in peptides containing D-amino acids. We supply institutes looking at novel antimicrobial peptides, soil microbiology, and chiral catalysis—all areas where a pure, reproducible source of both enantiomers pays real dividends. Keeping a consistent Dl-mixture allows labs to keep batch-to-batch variation controlled, supporting accurate, repeatable results.

    Challenges in Manufacturing and Solutions from Experience

    Challenges crop up in every manufacturing cycle. Maintaining batch purity against cross-contamination, for example, requires both engineering and procedural discipline. Dl-Histidine retains its quality only if produced in dedicated vessels, run with validated cleanout protocols. Any slip—traces of other amino acids, or remnants of cleaning agents—can throw off downstream processes. We’ve invested steadily in dedicated production trains and automated cleaning systems, because one contaminated lot is all it takes to lose credibility.

    Another persistent headache is supply chain volatility. Raw materials for synthesizing histidine derivatives see price swings and occasional shortages. Rather than depend on single-source suppliers, we diversified our procurement base and brought some precursor syntheses in-house. This adds complexity, but reduces risk for clients who rely on uninterrupted delivery for their scale-up or finished product manufacturing needs. We maintain safety stock of critical intermediates and routinely audit our supply partners for compliance and transparency. If pricing shifts or local regulations change, we engage clients promptly with advice on forecasted changes and practical steps to avoid disruption.

    Supporting Research, Innovation, and Customer Success

    We regularly work with universities and life science companies, local and global. Our technical support team fields questions from researchers setting up new biosynthetic routes, as well as QA leads troubleshooting unexpected findings in end-use products. The direct feedback loop lets us test subtle variations in drying curves, sieve sizes, or particle morphology. Nothing goes into a spec table until our teams have handled it, tested it, and proven its impact on solubility, blending, or analytical consistency. As a result, clients rarely face surprises after they open a drum.

    Technical details only tell part of the story. Our manufacturing experience comes through for projects as diverse as custom isotopically labeled Dl-Histidine, batches for veterinary injectable solutions, and pilot runs for functional feed additives. We support documentation at every stage, with up-to-date methods and standards for analytical purity, identification, and microbial load. For clients dealing with new regulatory hurdles, our scientists and compliance staff prepare the traceable records and statements needed for smooth submissions, export, or contract manufacturing agreements.

    Safety and Environmental Responsibility Embedded in Production

    As producers, we cannot ignore the environmental footprint. Improving energy efficiency and waste stream handling for a product like Dl-Histidine pays off measurably, both in cost and community trust. We review emissions controls quarterly, collect solvent vapors for recovery, and treat aqueous effluent for biological degradability before anything leaves the plant boundary. Waste minimization and recycling targets are part of every staff member’s annual review. Our labs develop greener synthesis methods, testing biocatalytic approaches or water-reduced reaction paths when possible. This hands-on approach makes our sales pitch more than talk—it’s a daily process embedded in production planning and implementation.

    For worker safety, our protocols focus on dust control and personal protective equipment. Amino acid powders present inhalation risks in high concentrations, so production and packaging stay fully enclosed. Automated feeders, negative air pressure in critical rooms, and comprehensive training for all team members mean we avoid both contamination and exposure risks. Our safety record reflects this approach, but we never relax standards. Each shipped drum carries not just our label but the weight of our ongoing commitment to producing safe, reliable Dl-Histidine batch after batch.

    Outlook: Dl-Histidine in Research and Industry

    Demand for Dl-Histidine fluctuates less than trendy intermediates. Researchers, formulators, and manufacturers find ongoing need for both the D- and L-enantiomers, whether for basic chemistry, metabolic studies, or applications in animal health. We expect growth as peptide synthesis and chiral pharmaceuticals advance, because researchers push boundaries and need consistent building blocks to verify new findings. Our role remains the same: manufacture the highest quality Dl-Histidine, control every variable possible, and make technical support direct and actionable.

    Knowing what happens in the plant, not just in the laboratory, matters. We don’t treat Dl-Histidine as an off-the-shelf commodity. The close, hands-on involvement of skilled production staff and chemists leads to steady improvements—tighter impurity profiles, safer packaging, and more usable product for each client. As a company, we commit every day to producing not just a chemical, but a solution that supports scientific progress, product safety, and practical results in clinics, farms, and research centers worldwide.

    Final Thoughts from the Plant Floor

    Working in the manufacturing environment shapes every perspective we have on Dl-Histidine. Seeing raw materials arrive, tracking each synthesis step, and comparing quality testing batch by batch gives us a unique vantage point. This experience tells us no two lots are identical, but careful management, experienced personnel, thoughtful engineering, and responsive customer engagement make all the difference. Each inquiry gives us a chance to learn and improve, whether that means faster response to a technical challenge or accommodating specific application demands.

    Dl-Histidine may not be the highest-volume amino acid on our production schedule, but it draws interest from innovators across fields. Our long view, supported by consistent investment in equipment, staff knowledge, and process rigor, means customers know who they are working with—not a faceless supply chain, but people dedicated to chemical manufacturing done right. The future for Dl-Histidine, as we see it, stays bright, anchored by real-world evidence and ongoing commitment to delivering a product that meets the realities of both the laboratory and the marketplace.