|
HS Code |
704471 |
| Chemical Name | DL-Carnitine |
| Molecular Formula | C7H15NO3 |
| Molecular Weight | 161.20 g/mol |
| Appearance | White crystalline powder |
| Solubility | Highly soluble in water |
| Odor | Odorless |
| Cas Number | 461-06-3 |
| Ph Value | 5.5-7.5 (1% aqueous solution) |
| Stability | Stable under normal temperatures and pressures |
| Melting Point | 197°C (decomposes) |
| Usage | Nutritional supplement |
| Storage Conditions | Store in a cool, dry place |
| Synonyms | 3-Hydroxy-4-(trimethylammonio)butanoate |
| Optical Activity | Racemic mixture (contains D and L isomers) |
| Taste | Slightly bitter |
As an accredited DL-Carnitine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The DL-Carnitine comes in a sealed, white plastic bottle containing 100 grams, labeled with product details, safety warnings, and storage instructions. |
| Shipping | DL-Carnitine is shipped in tightly sealed, moisture-proof containers to maintain product stability and quality. Packaging complies with regulatory guidelines for chemicals, ensuring safe handling and transit. Standard shipping is via ground or air, with temperature control as necessary. All shipments include accurate labeling and documentation for easy identification and compliance. |
| Storage | DL-Carnitine should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from direct sunlight and sources of heat or moisture. It is recommended to keep it at room temperature, typically between 2–8°C (36–46°F). Protect from incompatible substances and avoid contamination to maintain its stability and effectiveness. |
Competitive DL-Carnitine 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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Tel: +8615371019725
Email: admin@sinochem-nanjing.com
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At our production facility, DL-Carnitine doesn’t come from a distant supply chain; it starts as raw material at our door and finishes as a refined, high-purity ingredient ready for market. Our team oversees every step of the synthesis and quality assurance, watching the product grow from early weighing of materials through to careful packaging. We have spent years learning the small quirks that can affect yield, purity, and usability in downstream applications. Each lot reflects adjustments grounded in experience, market needs, and real-world lab feedback.
We synthesize DL-Carnitine through a controlled reaction sequence, using select intermediates and precise temperature control. Lab operators combine beta-hydroxybutyric acid derivatives with trimethylammonium compounds under standardized environments, with our chemists monitoring for undesired byproducts. After careful purification by crystallization and drying, technicians use high-performance liquid chromatography and infrared spectroscopy to confirm purity often surpassing 98%.
Every reaction teaches us more about how minor changes in solvent quality or batch size will impact the stereochemistry. Our experience tells us that keeping process consistency requires not only trained operators but robust monitoring systems connecting data from each run.
We offer DL-Carnitine as a white, crystalline or powdery solid, tailored to end-user needs. Our standard material ranges from food/nutrition grade to technical grade, each batch matching specific moisture content and particle size distributions. Specifications include:
Daily production relies on continuous improvement based on testing and customer feedback. Over time, we noticed certain markets value extra-low residual solvent content, so our in-house finishing uses additional vacuum drying steps. By adapting as fast as we can validate results, we shape product lots to better suit actual demand rather than catalog promises.
Over years of supply into nutrition, animal feed, and even pharmaceutical markets, we have built expertise in how DL-Carnitine behaves in formulations and processes outside the lab. The DL isomer, as a racemic mix, includes both D- and L- forms. In our production, maintaining correct isomer mixture is less about cost-cutting, more about aligning with real manufacturing needs—some customers formulate finished products that undergo further processing or blending, where bioavailability or taste preference plays a role.
In dietary products, our DL-Carnitine aids fatty acid metabolism thanks to its role as a carrier molecule. Feed manufacturers incorporate it to support growth and recovery in animals, monitoring performance in practical conditions, not just theory. We have seen formulation specialists pair our material with vitamins or amino acids, taking advantage of its solubility and stability in premixes and solid blends.
Pharmaceutical formulators require not only high-purity product, but exacting control of contaminants. Regular discussions with QA departments at production plants refine what controls are truly needed at source, not just paper specifications.
DL-Carnitine stands apart from L-Carnitine due to its stereoisomer content. The L-isomer occurs naturally in animal tissues and is biologically active, supporting fat metabolism and energy production. The D-isomer, though structurally similar, does not participate directly in metabolic pathways in most higher organisms. In practice, DL-Carnitine serves where product function depends more on carnitine presence than stereochemistry.
When compared with pure L-Carnitine, DL-Carnitine is less expensive to produce—racemization reduces the complexity of the synthesis route. The tradeoff involves some loss of specific activity, which matters in regulated pharmaceuticals but less so in broader feed or food applications. Our process allows us to shift production over to the pure L-form for contracts demanding regulatory compliance, but we always communicate these differences rather than relying on technical jargon to obscure them.
We have heard requests for more “natural” profiles from food manufacturers, which requires a switch to L-Carnitine and documented non-synthetic processes. In such cases, we run side-by-side validation to show customers the real impact in their recipes, not just on a spec sheet.
Quality control starts with our own sourcing of base chemicals. Having direct contracts with chemical plants has curbed variability, especially for trimethylamine and related intermediates. In earlier years, gaps in traceability caused some returns and deep investigations. Now, each lot is barcoded from synthesis through packaging, enabling trace-back to date, operator, and raw material batch. Retention samples from each run are logged so any long-term concerns over shelf life or stability can get tested against original output, not a rebuilt sample.
Our analytical lab runs stability testing in accelerated and ambient conditions, exposing DL-Carnitine to everything from temperature swings to humidity spikes. Shelf life typically exceeds two years if sealed and stored below 25°C, but we encourage customers to monitor unopened stock. This habit came from experience facing stockpiles held in less-than-ideal warehouses across different climates.
Quality certifications include ISO9001 and food safety registration, with site audits welcomed by key clients. These can be tedious to prepare for, but always push us to keep clear records and root cause analysis for every deviation. Long-term customers have often learned alongside us, shifting their specs and expectations as our own systems became more transparent.
Manufacturing on a commercial scale brings real-world constraints. Global price swings in base chemicals, resource shortages, and tighter energy policies all change our input costs and lead times. Shipping delays impact production scheduling for customers on JIT inventory strategies. We respond by holding higher inventories for certain buffer stocks, learning over the years where bottlenecks hit hardest.
Another challenge involves avoiding cross-contamination with other choline-based products, since some intermediates overlap. Dedicated lines and frequent equipment cleaning form daily routines, while ongoing operator training prevents people from cutting corners. We replaced several high-touch process steps with semi-automation to capitalize on in-house engineering know-how. Downtime dropped, and we had fewer batch failures resulting from operator error, though training needs shifted from manual technique to PLC troubleshooting.
Increasingly, producers in China and Europe face pressure to reduce volatile organic emissions and hazardous effluent. Over the last five years, environmental upgrades in our facility have included solvent recovery systems, more effective air scrubbing, and closed-loop cooling systems. What once seemed like red tape has become central to our license to operate. Cost outlays for these systems are significant, but regulatory shutdowns are worse.
Operators handle raw materials with full chemical-resistant PPE, and waste handling is monitored by outside auditors. Training for hazardous material handling runs year-round so even temporary or new staff understand risks before their first shift. If any incident happens—a spill or equipment problem—root cause analysis and corrective steps are logged, since customer audits drill into even near-misses.
Market feedback cycles have shortened as brands launch more custom supplements and functional foods. Feed producers want smaller, more frequent lots to minimize warehouse space, while dietary supplement manufacturers ask for traceable, low-contaminant lots to meet auditing demands. We work closely with both, refining our offering over time based on their results, complaints, or evolving regulation.
Shifts in trade policy and pricing have pushed us to balance cost control with innovation. In some years, excess DL-Carnitine on the market led us to sell at lower-than-cost to clear inventory; in others, shortages all over Asia created premium pricing for available stocks. We have survived by staying flexible and transparent with customers about lead times, stock outs, and product origin.
We have run pilot lots of micronized DL-Carnitine for certain formulators needing smaller particle sizes, though routine production stays focused on proven mesh sizes that blend in typical mixer setups. Collaboration with overseas buyers led us to invest in better packaging: double-lined polyethylene bags inside cardboard drums, with desiccant packs for bulk shipments to humid climates.
Not all challenges in this business come from inside the plant. Risk of product degradation during storage—especially from heat or moisture—requires not just good packaging but clear instructions for the supply chain. We found routine customer visits and product handling demos reduce complaints about “clumping” or loss of flow in bulk lots.
Standardization between lots is another concern. Even small differences in moisture absorption can lead to batch-to-batch variation for downstream users. Our solution includes regular calibration of weighing systems, in-process humidity control, and split-tests between shifts. Raw material pre-testing proved essential once, after a minor lot contamination traced back to a drum sourced during a supplier’s production changeover.
Downstream blending brings its own headaches. Too-fine powders or clumped product will slow blending times and frustrate plant operators. We run regular checks on particle size distribution after mill changes or screen replacements. We ship test lots to strategic customers, letting them flag any process trouble before scaling up shipment.
The global market for carnitines continues to shift, with human nutrition, pet food, and functional beverage applications driving most growth. We watch as each region sets its own requirements for product origin, allergen-free status, or environmentally friendly manufacturing. Some buyers now ask for “green chemistry’’ documentation— an opportunity for us to audit our solvent consumption and waste streams, showing how plant upgrades trimmed total output of hazardous byproducts.
We anticipate changes in international labeling, with stricter country-of-origin requirements and more declarations around artificial vs. natural sources. This motivates us to keep refining our documentation chain, from source-of-origin statements on key raw materials to in-house DNA barcoding.
Clients in the feed industry care most about cost, prompt delivery, and ability to blend DL-Carnitine in large batch runs. Their feedback often drives us to improve flow and consistency, since any issue can affect feed uniformity and animal results. On the other hand, dietary supplement brands focus on trace element levels, low microbial counts, and assurance of consistent taste and color. Their requirements sometimes force additional process controls on our end, even if that means higher costs for extra testing.
Local regulations matter. Countries in Southeast Asia inspect heavy metal and dioxin content closely, leading us to invest in more advanced testing equipment. Western European buyers require kosher or halal certification, pushing us to enable production runs on separate lines. We have navigated registration paperwork for different export markets for years, always adapting our documentation process according to where each shipment will land.
Finished pharmaceutical companies, pharmaceutical-grade supplement brands, and custom formulation labs all require tailored support. They expect direct lines to our technical staff during audits, open access to stability data, and rapid answers to technical queries. Rather than just selling DL-Carnitine on price, we have learned that open communication and personalized problem-solving build stronger supply partnerships.
As environmental standards rise, we keep pushing for better reuse of solvents, improved water treatment, and more closed-loop handling of chemical effluent. Since energy and water usage metrics get scrutinized by large buyers, we disclose summary reports and detail progress in annual corporate sustainability reviews. Installation of solar panels reduced our energy bills, but also attracts business from clients required to reduce carbon footprints in their own supply chains.
Social responsibility shows in our labor policies and site safety statistics. We engage local schools for technical training, offer above-standard benefits packages to workers, and track workplace incidents as leading rather than trailing indicators. Transparent reporting to industry organizations also helps us stay informed about sector developments and benchmark our practices against peers.
DL-Carnitine remains a stable, reliable product line because of its flexibility across industries. From basic feed supplements to cutting-edge sports nutrition products, its consistent quality and established track record make it a dependable choice for formulators producing at scale. Its competitive price point and robust shelf life ensure broad appeal for both established companies and emerging brands.
We keep improving every year, investing in both technology and people, knowing market conditions will keep shifting. Through direct technical support, honest discussions about limits and strengths, and regular product development, we keep DL-Carnitine positioned for success in a changing world. The expertise we built in producing, testing, and refining every lot provides real value to our downstream partners, far beyond what any simple data sheet can offer.