{"id":71409,"date":"2026-05-20T09:18:16","date_gmt":"2026-05-20T09:18:16","guid":{"rendered":"https:\/\/medsbase.com\/l-carnitine\/"},"modified":"2026-05-21T07:14:09","modified_gmt":"2026-05-21T07:14:09","slug":"l-carnitine","status":"publish","type":"product","link":"https:\/\/medsbase.com\/nl\/l-carnitine\/","title":{"rendered":"L-Carnitine (Levocarnitine)"},"content":{"rendered":"<p><!-- medsbase-tldr-answer --><\/p>\n<div style=\"background: #fff8e1; border-left: 4px solid #f5a623; padding: 18px 22px; margin: 18px 0; border-radius: 4px;\">\n<h3 style=\"margin: 0 0 8px 0; font-size: 16px; color: #1a4a6b;\">Quick Answer \u2014 What is L-Carnitine?<\/h3>\n<p style=\"margin: 0;\"><strong>L-Carnitine<\/strong> (levocarnitine; (3R)-3-hydroxy-4-(trimethylammonio)butanoate) is a small quaternary-ammonium amino-acid derivative \u2014 <em>not a peptide<\/em> \u2014 that functions as the essential carrier molecule for transporting long-chain fatty acids across the mitochondrial inner membrane for \u03b2-oxidation. It is endogenously biosynthesised from L-lysine and L-methionine and is concentrated in skeletal muscle, heart, and liver. L-Carnitine is studied across mitochondrial-function research, fat-oxidation physiology, insulin-sensitivity models, cardiovascular research, neuroprotection (Alzheimer \/ autism in-vitro work), exercise physiology, and sperm-motility research. Supplied in 600 mg and 1200 mg vials as levocarnitine USP-grade zwitterion for laboratory research use only. Stocked in our peptide catalogue alongside <a href=\"https:\/\/medsbase.com\/nl\/nad\/\">NAD\u207a<\/a> as a complementary mitochondrial \/ metabolic research-injectable.<\/p>\n<\/div>\n<div class=\"medsbase-trust-strip\" style=\"background: #f4f8fb; border: 1px solid #d8e3eb; padding: 12px 16px; margin: 16px 0; border-radius: 4px; font-size: 14px;\"><strong>Wat u krijgt bij MedsBase:<\/strong> Research-grade lyophilized compounds \u00b7 HPLC \u226599% purity (COA on request) \u00b7 Discreet temperature-stable packaging \u00b7 Worldwide research-supply courier \u00b7 1,400+ verified <a href=\"https:\/\/medsbase.com\/nl\/reviews\/\">klantbeoordelingen<\/a><\/div>\n<p class=\"medsbase-reship-line\" style=\"font-size: 14px; color: #444; margin: 8px 0 18px;\">\ud83d\udce6 Elke bestelling is gedekt door onze <a href=\"https:\/\/medsbase.com\/nl\/medsbase-re-shipment-assurance-policy\/\"><strong>Reshipment Assurance Policy<\/strong><\/a> \u2014 als uw pakket niet binnen 20 werkdagen arriveert, sturen wij het opnieuw.<\/p>\n<table class=\"medsbase-spec-table\" style=\"width: 100%; border-collapse: collapse; margin: 18px 0; font-size: 14px;\">\n<thead>\n<tr style=\"background: #2c7cb0; color: #fff;\">\n<th style=\"padding: 8px 12px; text-align: left; width: 30%;\">Specificatie<\/th>\n<th style=\"padding: 8px 12px; text-align: left;\">Detail<\/th>\n<\/tr>\n<\/thead>\n<tbody>\n<tr style=\"background: #f9f9f9;\">\n<td style=\"padding: 8px 12px; border-bottom: 1px solid #e0e0e0; width: 30%;\"><strong>CAS-nummer<\/strong><\/td>\n<td style=\"padding: 8px 12px; border-bottom: 1px solid #e0e0e0;\">541-15-1 (L-carnitine inner salt \/ zwitterion)<\/td>\n<\/tr>\n<tr style=\"background: #fff;\">\n<td style=\"padding: 8px 12px; border-bottom: 1px solid #e0e0e0; width: 30%;\"><strong>Type<\/strong><\/td>\n<td style=\"padding: 8px 12px; border-bottom: 1px solid #e0e0e0;\">Quaternary-ammonium amino-acid derivative (<em>not a peptide<\/em>); the levo-rotatory (3R) enantiomer is the biologically active form responsible for mitochondrial long-chain fatty-acid transport via the carnitine palmitoyltransferase (CPT-I \/ CPT-II) system; endogenously biosynthesised from L-lysine and L-methionine; also called levocarnitine (INN) or Vitamin B<sub>T<\/sub> in older literature<\/td>\n<\/tr>\n<tr style=\"background: #f9f9f9;\">\n<td style=\"padding: 8px 12px; border-bottom: 1px solid #e0e0e0; width: 30%;\"><strong>Molecuulformule<\/strong><\/td>\n<td style=\"padding: 8px 12px; border-bottom: 1px solid #e0e0e0;\">C<sub>7<\/sub>H<sub>15<\/sub>NEE<sub>3<\/sub><\/td>\n<\/tr>\n<tr style=\"background: #fff;\">\n<td style=\"padding: 8px 12px; border-bottom: 1px solid #e0e0e0; width: 30%;\"><strong>Moleculair gewicht<\/strong><\/td>\n<td style=\"padding: 8px 12px; border-bottom: 1px solid #e0e0e0;\">161.20 g\/mol<\/td>\n<\/tr>\n<tr style=\"background: #f9f9f9;\">\n<td style=\"padding: 8px 12px; border-bottom: 1px solid #e0e0e0; width: 30%;\"><strong>IUPAC Name<\/strong><\/td>\n<td style=\"padding: 8px 12px; border-bottom: 1px solid #e0e0e0;\">(3R)-3-Hydroxy-4-(trimethylazaniumyl)butanoate<\/td>\n<\/tr>\n<tr style=\"background: #fff;\">\n<td style=\"padding: 8px 12px; border-bottom: 1px solid #e0e0e0; width: 30%;\"><strong>Sequentie<\/strong><\/td>\n<td style=\"padding: 8px 12px; border-bottom: 1px solid #e0e0e0;\">n\/a (small-molecule amino-acid derivative \u2014 not a peptide)<\/td>\n<\/tr>\n<tr style=\"background: #f9f9f9;\">\n<td style=\"padding: 8px 12px; border-bottom: 1px solid #e0e0e0; width: 30%;\"><strong>Form<\/strong><\/td>\n<td style=\"padding: 8px 12px; border-bottom: 1px solid #e0e0e0;\">Lyophilized powder, white to off-white (zwitterion \/ inner-salt form)<\/td>\n<\/tr>\n<tr style=\"background: #fff;\">\n<td style=\"padding: 8px 12px; border-bottom: 1px solid #e0e0e0; width: 30%;\"><strong>Zuiverheid<\/strong><\/td>\n<td style=\"padding: 8px 12px; border-bottom: 1px solid #e0e0e0;\">\u226599% (HPLC geverifieerd, COA op aanvraag)<\/td>\n<\/tr>\n<tr style=\"background: #f9f9f9;\">\n<td style=\"padding: 8px 12px; border-bottom: 1px solid #e0e0e0; width: 30%;\"><strong>Opslag<\/strong><\/td>\n<td style=\"padding: 8px 12px; border-bottom: 1px solid #e0e0e0;\">Lyophilized: 2\u20138 \u00b0C (refrigerator) for short-term working stock; \u221220 \u00b0C for long-term storage of unopened vials. Reconstituted: 2\u20138 \u00b0C, use within ~30 days. Protect from light. Avoid repeated freeze\u2013thaw cycles of the reconstituted solution. Levocarnitine is hygroscopic \u2014 reseal vials promptly after each withdrawal.<\/td>\n<\/tr>\n<tr style=\"background: #fff;\">\n<td style=\"padding: 8px 12px; border-bottom: 1px solid #e0e0e0; width: 30%;\"><strong>Oplosbaarheid<\/strong><\/td>\n<td style=\"padding: 8px 12px; border-bottom: 1px solid #e0e0e0;\">Very highly water-soluble (zwitterion at physiological pH). Reconstitutes rapidly in bacteriostatic water or sterile water with gentle swirling. No specialised solvents required. Working solutions can be prepared at concentrations up to ~500 mg\/mL without precipitation.<\/td>\n<\/tr>\n<tr style=\"background: #f9f9f9;\">\n<td style=\"padding: 8px 12px; border-bottom: 1px solid #e0e0e0; width: 30%;\"><strong>Onderzoeksgebruik<\/strong><\/td>\n<td style=\"padding: 8px 12px; border-bottom: 1px solid #e0e0e0;\">Alleen voor laboratoriumonderzoek. Niet voor humaan of veterinair diagnostisch of therapeutisch gebruik.<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p><!-- \/medsbase-tldr-answer --><\/p>\n<h2>What Is L-Carnitine?<\/h2>\n<p><strong>L-Carnitine<\/strong> (levocarnitine) is a small, water-soluble, quaternary-ammonium amino-acid derivative with the molecular formula C<sub>7<\/sub>H<sub>15<\/sub>NEE<sub>3<\/sub> and molecular weight 161.20 g\/mol. It is <em>not a peptide<\/em> \u2014 it is a single-residue zwitterionic molecule derived metabolically from the amino acids L-lysine and L-methionine through a multistep biosynthetic pathway distributed across kidney, liver, and brain. Only the (3R) enantiomer (the L-form \/ levo form \/ levocarnitine) is biologically active; the (3S) enantiomer (D-carnitine) is inactive and is now well-documented to interfere with the L-form&#8217;s transport, which is why pharmaceutical-grade material is supplied as the enantiomerically pure L-form rather than as racemic DL-carnitine.<\/p>\n<p>The molecule&#8217;s central physiological function is to serve as the <strong>obligate carrier<\/strong> for transporting long-chain fatty acids (C<sub>12<\/sub>+) across the otherwise-impermeable mitochondrial inner membrane, where they are subsequently broken down by \u03b2-oxidation to acetyl-CoA, the substrate for the citric acid cycle and ATP synthesis. The transport machinery \u2014 carnitine palmitoyltransferase I (CPT-I) on the outer mitochondrial membrane, the carnitine\/acylcarnitine translocase (CACT) across the inner membrane, and carnitine palmitoyltransferase II (CPT-II) on the matrix side \u2014 converts free fatty acids into acylcarnitines, ferries them across the bilayer, and releases them again as acyl-CoAs for oxidation. L-Carnitine is therefore the rate-limiting metabolite for fat oxidation in tissues with high oxidative demand: skeletal muscle, cardiac muscle, and liver.<\/p>\n<p>L-Carnitine is also a high-affinity buffer of the cellular acyl-CoA \/ free-CoA ratio. By accepting acyl groups onto its hydroxyl side chain, L-carnitine maintains the intracellular pool of free CoA that other CoA-dependent enzymes (pyruvate dehydrogenase, \u03b1-ketoglutarate dehydrogenase, fatty-acid \u03b2-oxidation) require to function. Carnitine deficiency therefore produces effects beyond fat oxidation alone \u2014 propagating into pyruvate handling, TCA-cycle flux, and overall mitochondrial bioenergetic balance.<\/p>\n<p>L-Carnitine has FDA approval (under the name <em>levocarnitine<\/em>) for human therapeutic use in <strong>primary and secondary carnitine deficiency<\/strong> (oral and IV formulations) and is widely used in research contexts that examine mitochondrial bioenergetics, fat oxidation, insulin sensitivity, cardiovascular function, neuroprotection, exercise physiology, and sperm motility. The research-grade L-Carnitine sold here is supplied <strong>uitsluitend voor laboratoriumonderzoek<\/strong> and is not intended for human or veterinary administration without appropriate regulatory authorisation.<\/p>\n<h2>Mechanism of Action \u2014 Mitochondrial Long-Chain Fatty-Acid Transport<\/h2>\n<p>L-Carnitine&#8217;s central mechanism is documented across several decades of mitochondrial biochemistry research:<\/p>\n<ul>\n<li><strong>Carnitine palmitoyltransferase I (CPT-I) \u2014 outer mitochondrial membrane<\/strong> \u2014 Long-chain fatty acids first activate to long-chain acyl-CoA in the cytoplasm. CPT-I, embedded in the outer mitochondrial membrane, transfers the acyl group from CoA onto L-carnitine&#8217;s hydroxyl, generating long-chain acylcarnitine. This is the committed and most heavily regulated step of mitochondrial fat oxidation \u2014 CPT-I is allosterically inhibited by malonyl-CoA (the product of acetyl-CoA carboxylase in fed-state lipogenic metabolism), which is how insulin \/ glucagon and the AMPK system gate fat oxidation against fat synthesis.<\/li>\n<li><strong>Carnitine\/acylcarnitine translocase (CACT) \u2014 inner mitochondrial membrane<\/strong> \u2014 Long-chain acylcarnitine generated by CPT-I cannot diffuse across the inner mitochondrial membrane. CACT, an antiporter, exchanges cytosolic acylcarnitine for matrix free carnitine in a 1:1 stoichiometry, delivering acylcarnitine into the matrix and recycling carnitine for further rounds of CPT-I.<\/li>\n<li><strong>Carnitine palmitoyltransferase II (CPT-II) \u2014 inner mitochondrial membrane, matrix-facing<\/strong> \u2014 In the matrix, CPT-II reverses the CPT-I reaction: it transfers the acyl group from carnitine back onto matrix CoA, regenerating long-chain acyl-CoA, which can now enter \u03b2-oxidation. The free carnitine released is returned across the membrane via CACT for another transport cycle.<\/li>\n<li><strong>Acyl-CoA \/ free-CoA ratio buffering and metabolic flexibility<\/strong> \u2014 Beyond the long-chain shuttle, L-carnitine accepts short- and medium-chain acyl groups (acetylcarnitine, propionylcarnitine) and acts as a high-capacity buffer of the intracellular acyl-CoA \/ free-CoA ratio. This maintains free CoA for pyruvate dehydrogenase, \u03b1-ketoglutarate dehydrogenase, and \u03b2-oxidation. Acetylcarnitine generation also serves as the mechanism by which excess acetyl-CoA \u2014 from fasting, ketogenesis, exercise \u2014 can be safely buffered and exported across the mitochondrial membrane.<\/li>\n<\/ul>\n<p>The pharmacokinetic profile of orally-administered L-carnitine is unusual: oral bioavailability is low (~15%) due to active intestinal saturation, with the remaining 85% subject to extensive bacterial degradation in the colon (yielding TMA and TMAO \u2014 a finding that has attracted attention in cardiovascular research). Intravenous and intramuscular research routes achieve much higher plasma levels and bypass the gut-microbial degradation pathway entirely, which is why pharmacological research protocols commonly use parenteral administration despite the convenience of oral dosing.<\/p>\n<h2>Gepubliceerde onderzoeksapplicaties<\/h2>\n<p>L-Carnitine is used in laboratory research contexts that investigate:<\/p>\n<ul>\n<li><strong>Mitochondrial function and bioenergetics<\/strong> \u2014 Seahorse \/ Oroboros respirometry, mitochondrial membrane potential, ATP generation rate, fatty-acid-oxidation rate in primary hepatocyte, skeletal-muscle, and cardiomyocyte cultures<\/li>\n<li><strong>Fat oxidation and metabolic flexibility<\/strong> \u2014 switching between glucose and fat oxidation in skeletal muscle and liver; insulin-resistance reversal models; obese-rodent and DIO study cohorts<\/li>\n<li><strong>Insulin sensitivity research<\/strong> \u2014 improvement in skeletal-muscle insulin sensitivity in models of metabolic syndrome and type 2 diabetes preclinical research; mechanistic dissection of the L-carnitine \/ acyl-CoA buffering \/ pyruvate handling axis<\/li>\n<li><strong>Cardiovasculair onderzoek<\/strong> \u2014 angina, heart failure, ischemia-reperfusion injury, cardiomyopathy (in particular doxorubicin-induced cardiotoxicity and primary carnitine-deficiency cardiomyopathy); TMA\/TMAO microbiome-axis cardiovascular research<\/li>\n<li><strong>Onderzoek naar neuroprotectie<\/strong> \u2014 Alzheimer-disease in-vitro models (acetylcarnitine specifically), Parkinson-disease models, peripheral diabetic neuropathy preclinical models, autism-spectrum research where carnitine deficiency has been implicated<\/li>\n<li><strong>Sperm motility and male fertility research<\/strong> \u2014 epididymal acquisition of motility, mitochondrial energetics of sperm flagellar beat, antioxidant protection of spermatozoa; one of the most-studied compounds in male-fertility research<\/li>\n<li><strong>Exercise physiology and endurance research<\/strong> \u2014 substrate utilisation during prolonged exercise, glycogen sparing, post-exercise recovery; research interest in carnitine loading protocols and insulin co-administration to overcome muscle-uptake saturation<\/li>\n<li><strong>Chronic kidney disease \/ haemodialysis research<\/strong> \u2014 carnitine deficiency is common in dialysis-dependent end-stage renal disease patients and L-carnitine has FDA approval for this indication; preclinical research continues on dialysis-related cardiomyopathy and muscle weakness<\/li>\n<\/ul>\n<p>For broader context on mitochondrial and metabolic-axis research compounds in this catalogue, see <a href=\"https:\/\/medsbase.com\/nl\/nad\/\">NAD\u207a<\/a> (oxidised dinucleotide coenzyme, central electron-transport substrate), <a href=\"https:\/\/medsbase.com\/nl\/ss-31-elamipretide\/\">SS-31 (Elamipretide)<\/a> (mitochondrial-targeted cardiolipin-binding peptide), and <a href=\"https:\/\/medsbase.com\/nl\/mots-c\/\">MOTS-c<\/a> (mitochondrial-derived metabolic-regulator peptide). Browse the full <a href=\"https:\/\/medsbase.com\/nl\/peptides\/\">research peptides &amp; compounds catalog<\/a> voor gerelateerde verbindingen.<\/p>\n<h2>Beschikbare sterktes en concentraties<\/h2>\n<p>MedsBase stocks L-Carnitine in two lyophilized vial sizes calibrated to typical research protocol lengths. Each strength is available in 10-vial or 20-vial pack formats:<\/p>\n<table style=\"width: 100%; border-collapse: collapse; margin: 16px 0;\">\n<thead>\n<tr style=\"background: #2c7cb0; color: #fff;\">\n<th style=\"padding: 10px; border: 1px solid #ddd; text-align: left;\">Vulsterkte<\/th>\n<th style=\"padding: 10px; border: 1px solid #ddd; text-align: left;\">Typisch Onderzoeksgebruik<\/th>\n<th style=\"padding: 10px; border: 1px solid #ddd; text-align: left;\">Verpakkingsgroottes<\/th>\n<\/tr>\n<\/thead>\n<tbody>\n<tr>\n<td style=\"padding: 10px; border: 1px solid #ddd;\"><strong>600 mg<\/strong><\/td>\n<td style=\"padding: 10px; border: 1px solid #ddd;\">Standard research strength \u2014 dose-titration protocols, in-vitro mitochondrial-function panels, short-cycle in-vivo work, sperm-motility research<\/td>\n<td style=\"padding: 10px; border: 1px solid #ddd;\">10 of 20 flesjes<\/td>\n<\/tr>\n<tr style=\"background: #f9f9f9;\">\n<td style=\"padding: 10px; border: 1px solid #ddd;\"><strong>1200 mg<\/strong><\/td>\n<td style=\"padding: 10px; border: 1px solid #ddd;\">Extended-cycle or higher-dose research protocols \u2014 long-arm metabolic studies, exercise-physiology saturation experiments, multi-cohort work; lowest per-mg cost<\/td>\n<td style=\"padding: 10px; border: 1px solid #ddd;\">10 of 20 flesjes<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p>Both strengths are the same chemical form (lyophilized levocarnitine zwitterion, \u226599% HPLC purity). Vial doses are deliberately much larger than the peptide range (5\u201320 mg) because L-carnitine is a small molecule used at gram-level doses \u2014 a 600 mg or 1200 mg vial corresponds roughly to a single intravenous research dose in rodent or large-animal protocols. Researchers should determine specific dose ranges from peer-reviewed literature appropriate to the protocol.<\/p>\n<h2>How It Compares \u2014 L-Carnitine vs NAD\u207a<\/h2>\n<p>L-Carnitine and <a href=\"https:\/\/medsbase.com\/nl\/nad\/\">NAD\u207a<\/a> are the two non-peptide mitochondrial \/ metabolic research compounds in this catalogue, and they target completely different layers of mitochondrial bioenergetics. L-Carnitine sits on the <em>fuel side<\/em> \u2014 it transports long-chain fatty acids into the matrix for \u03b2-oxidation. NAD\u207a sits on the <em>electron-transport side<\/em> \u2014 it is the obligate electron acceptor for \u03b2-oxidation, glycolysis, and the TCA cycle, regenerated by Complex I of the electron transport chain. The two compounds are mechanistically complementary, and research protocols sometimes combine them to probe upstream-substrate vs downstream-electron-flux contributions to mitochondrial output.<\/p>\n<table style=\"width: 100%; border-collapse: collapse; margin: 16px 0;\">\n<thead>\n<tr style=\"background: #2c7cb0; color: #fff;\">\n<th style=\"padding: 10px; border: 1px solid #ddd; text-align: left;\">Criterium<\/th>\n<th style=\"padding: 10px; border: 1px solid #ddd; text-align: left;\">L-Carnitine<\/th>\n<th style=\"padding: 10px; border: 1px solid #ddd; text-align: left;\">NAD\u207a<\/th>\n<\/tr>\n<\/thead>\n<tbody>\n<tr>\n<td style=\"padding: 10px; border: 1px solid #ddd;\"><strong>Chemische klasse<\/strong><\/td>\n<td style=\"padding: 10px; border: 1px solid #ddd;\">Quaternary-ammonium amino-acid derivative (single zwitterion)<\/td>\n<td style=\"padding: 10px; border: 1px solid #ddd;\">Dinucleotide coenzyme (adenine + nicotinamide nucleotides joined via diphosphate)<\/td>\n<\/tr>\n<tr style=\"background: #f9f9f9;\">\n<td style=\"padding: 10px; border: 1px solid #ddd;\"><strong>Molecular weight<\/strong><\/td>\n<td style=\"padding: 10px; border: 1px solid #ddd;\">161.20 g\/mol<\/td>\n<td style=\"padding: 10px; border: 1px solid #ddd;\">663.43 g\/mol<\/td>\n<\/tr>\n<tr>\n<td style=\"padding: 10px; border: 1px solid #ddd;\"><strong>Role in mitochondria<\/strong><\/td>\n<td style=\"padding: 10px; border: 1px solid #ddd;\">Carrier \u2014 long-chain fatty-acid shuttle across the inner membrane<\/td>\n<td style=\"padding: 10px; border: 1px solid #ddd;\">Electron acceptor for \u03b2-oxidation, glycolysis, TCA cycle; substrate for sirtuins and PARPs<\/td>\n<\/tr>\n<tr style=\"background: #f9f9f9;\">\n<td style=\"padding: 10px; border: 1px solid #ddd;\"><strong>Best-studied research focus<\/strong><\/td>\n<td style=\"padding: 10px; border: 1px solid #ddd;\">Fat oxidation, insulin sensitivity, cardiovascular, sperm motility, exercise physiology<\/td>\n<td style=\"padding: 10px; border: 1px solid #ddd;\">Sirtuin biology, longevity, cellular ageing, NAD-axis redox regulation<\/td>\n<\/tr>\n<tr>\n<td style=\"padding: 10px; border: 1px solid #ddd;\"><strong>FDA approval<\/strong><\/td>\n<td style=\"padding: 10px; border: 1px solid #ddd;\">Yes \u2014 levocarnitine, for primary\/secondary carnitine deficiency (oral and IV)<\/td>\n<td style=\"padding: 10px; border: 1px solid #ddd;\">No \u2014 research compound only<\/td>\n<\/tr>\n<tr style=\"background: #f9f9f9;\">\n<td style=\"padding: 10px; border: 1px solid #ddd;\"><strong>Endogenous biosynthesis<\/strong><\/td>\n<td style=\"padding: 10px; border: 1px solid #ddd;\">From L-lysine and L-methionine, in kidney\/liver\/brain<\/td>\n<td style=\"padding: 10px; border: 1px solid #ddd;\">From tryptophan (de novo) or nicotinamide\/niacin (salvage)<\/td>\n<\/tr>\n<tr>\n<td style=\"padding: 10px; border: 1px solid #ddd;\"><strong>Plasma stability<\/strong><\/td>\n<td style=\"padding: 10px; border: 1px solid #ddd;\">Stable \u2014 hours of half-life<\/td>\n<td style=\"padding: 10px; border: 1px solid #ddd;\">Unstable \u2014 short minutes of half-life in solution; oxidises and degrades rapidly<\/td>\n<\/tr>\n<tr style=\"background: #f9f9f9;\">\n<td style=\"padding: 10px; border: 1px solid #ddd;\"><strong>Typische onderzoeksdosis<\/strong><\/td>\n<td style=\"padding: 10px; border: 1px solid #ddd;\">Hundreds of mg to gram-level (single dose in rodent \/ large-animal protocols)<\/td>\n<td style=\"padding: 10px; border: 1px solid #ddd;\">Tens to hundreds of mg (cell culture: \u00b5M concentrations)<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p>For research focused on long-chain fatty-acid oxidation, cardiovascular metabolic function, insulin sensitivity, or sperm motility, L-Carnitine is the canonical reference compound. For research focused on sirtuin biology, longevity-axis biochemistry, or NAD-dependent redox regulation, <a href=\"https:\/\/medsbase.com\/nl\/nad\/\">NAD\u207a<\/a> is the more targeted tool. See also <a href=\"https:\/\/medsbase.com\/nl\/ss-31-elamipretide\/\">SS-31 (Elamipretide)<\/a> for cardiolipin \/ inner-membrane-targeted mitochondrial research and <a href=\"https:\/\/medsbase.com\/nl\/mots-c\/\">MOTS-c<\/a> for mitochondrial-derived peptide-signalling research.<\/p>\n<div style=\"background: #f4f8fb; border-left: 4px solid #2c7cb0; padding: 14px 18px; margin: 18px 0;\"><strong class=\"mb-bac-water-callout\">\ud83d\udca7 Need BAC water?<\/strong> Reconstituting any lyophilized vial requires sterile bacteriostatic water. Pair this product with our <a href=\"\/nl\/bac-water\/\"><strong>BAC Water (Bacteriostatisch Water)<\/strong><\/a> \u2014 30 mL multi-dose vial, 0.9% benzyl-alcohol-preserved, USP-grade.<\/div>\n<h2>Opslag en Reconstituering<\/h2>\n<p><strong>Voor reconstituering:<\/strong> store lyophilized vials refrigerated at 2\u20138 \u00b0C in original packaging for short-term working stock. For long-term storage, freeze unopened vials at \u221220 \u00b0C. Lyophilized L-Carnitine is stable under refrigeration for up to 36 months and at \u221220 \u00b0C for up to 60 months \u2014 substantially more stable than most lyophilized peptides because the small-molecule structure has no amide bonds or disulfide bridges to hydrolyse. The compound is, however, <strong>hygroscopic<\/strong>, so reseal vials promptly after each withdrawal and avoid prolonged exposure to ambient humidity.<\/p>\n<p><strong>Reconstitueringsprocedure:<\/strong> inject bacteriostatic water down the side wall of the vial (not directly onto the lyophilized cake). For a 600 mg vial, 3.0 mL of bacteriostatic water yields a 200 mg\/mL working concentration; 1.2 mL yields a 500 mg\/mL stock. For a 1200 mg vial, 6.0 mL yields a 200 mg\/mL working stock; 2.4 mL yields a 500 mg\/mL stock. L-Carnitine dissolves very rapidly with gentle swirling \u2014 typically within 10\u201330 seconds \u2014 because it is a small zwitterion with no folded structure to disturb. Once reconstituted, store the vial at 2\u20138 \u00b0C and use within 30 days. Protect from light. Discard if cloudiness, particulates, or colour change appears.<\/p>\n<h2>Veelgestelde vragen<\/h2>\n<h3>Is L-Carnitine a peptide?<\/h3>\n<p>No. L-Carnitine is a small-molecule quaternary-ammonium amino-acid derivative (MW 161.20 g\/mol), <em>niet<\/em> a peptide. We stock it in our research-peptide catalogue alongside <a href=\"https:\/\/medsbase.com\/nl\/nad\/\">NAD\u207a<\/a> because it serves a complementary role in mitochondrial \/ metabolic research and is supplied in the same injectable vial format. The spec table Sequence row is marked &#8220;n\/a&#8221; for this reason.<\/p>\n<h3>What is the difference between L-Carnitine and acetyl-L-carnitine (ALCAR)?<\/h3>\n<p>Acetyl-L-carnitine is L-carnitine with an acetyl group esterified to the hydroxyl side chain. ALCAR crosses the blood-brain barrier more efficiently and is the form most commonly used in CNS-focused research (Alzheimer-disease, peripheral neuropathy). The base L-carnitine zwitterion that we supply here is the form used in peripheral metabolic research (cardiovascular, skeletal muscle, sperm motility, dialysis-related deficiency). The two compounds interconvert metabolically through carnitine acetyltransferase.<\/p>\n<h3>What is the difference between L-Carnitine and racemic DL-carnitine?<\/h3>\n<p>Only the L (3R) enantiomer is biologically active. The D (3S) enantiomer is inactive and is now well-documented to interfere with L-form transport, accumulating in tissue and producing weakness and other adverse effects in long-term high-dose contexts. Pharmaceutical-grade levocarnitine (what we supply) is the enantiomerically pure L-form. The racemic DL-form is obsolete and is no longer used in either clinical or rigorous research contexts.<\/p>\n<h3>Why is the research dose so much larger than the peptide doses in this catalogue?<\/h3>\n<p>L-Carnitine is a small molecule (MW 161) and is used at gram-level doses \u2014 the body&#8217;s endogenous carnitine pool is approximately 25 g, concentrated in skeletal muscle. Research protocols typically use 100\u2013500 mg\/kg in rodent in-vivo work, which translates to hundreds of milligrams to grams per dose. Compare this to research peptides (BPC-157, semaglutide, etc.) where typical doses are 100 \u00b5g to 5 mg per administration \u2014 three to four orders of magnitude smaller, reflecting the different molecular weights and the different receptor \/ mechanism scales.<\/p>\n<h3>What is the TMA \/ TMAO question I see in cardiovascular research?<\/h3>\n<p>A subset of L-carnitine ingested orally is degraded by gut bacteria to trimethylamine (TMA), which the liver then oxidises to trimethylamine-N-oxide (TMAO). Elevated TMAO levels have been associated in epidemiological research with adverse cardiovascular events, raising a controversy about whether long-term high-dose oral L-carnitine supplementation may be net-beneficial or net-harmful for cardiovascular endpoints. The question is active and unresolved. Parenteral L-carnitine bypasses the gut-microbial degradation pathway and is not subject to this concern.<\/p>\n<h3>What does CPT-I inhibition mean in metabolic research?<\/h3>\n<p>Carnitine palmitoyltransferase I (CPT-I) is the rate-limiting enzyme for mitochondrial long-chain fatty-acid uptake. Etomoxir is a classical CPT-I inhibitor used to block fat oxidation in research models; it is the pharmacological tool counterpart to the L-carnitine substrate. Research protocols sometimes combine L-carnitine supplementation (substrate side) with CPT-I inhibition (enzymatic side) to dissect substrate-limited vs enzyme-limited fat oxidation in different tissues and conditions.<\/p>\n<h3>Can I combine L-Carnitine with NAD\u207a in the same research protocol?<\/h3>\n<p>Yes \u2014 the two compounds target different layers of mitochondrial bioenergetics (substrate transport vs electron transport), and combination is commonly used in research that aims to probe upstream vs downstream limitations on mitochondrial output. They are chemically stable in solution together. Reconstitute each separately first to establish stability and concentration accuracy, then combine immediately before use rather than co-storing reconstituted vials.<\/p>\n<h3>What route of administration is used in published research?<\/h3>\n<p>Intravenous and intramuscular routes are most common in pharmacological research because they bypass the low (~15%) oral bioavailability and the gut-microbial TMA\/TMAO degradation pathway. Subcutaneous administration is used in some rodent protocols. Oral administration is used in pharmacokinetic and nutritional research where the bioavailability question is itself the research focus.<\/p>\n<div class=\"medsbase-trust-strip\" style=\"background: #f4f8fb; border: 1px solid #d8e3eb; padding: 12px 16px; margin: 20px 0 8px; border-radius: 4px; font-size: 14px;\"><strong>Why order research compounds from MedsBase:<\/strong> Lyophilized HPLC \u226599% peptides &amp; compounds \u00b7 COA available on request \u00b7 Discreet temperature-stable packaging \u00b7 Worldwide courier \u00b7 <a href=\"https:\/\/medsbase.com\/nl\/medsbase-re-shipment-assurance-policy\/\">Reshipment Assurance<\/a> on every order \u00b7 1,400+ verified <a href=\"https:\/\/medsbase.com\/nl\/reviews\/\">klantbeoordelingen<\/a><\/div>\n<p><!-- medsbase-related-alts-v1 --><\/p>","protected":false},"excerpt":{"rendered":"<p>\u2705 Mitochondrial long-chain fatty-acid shuttle (not a peptide)<br \/>\n\u2705 CPT-I \/ CACT \/ CPT-II transport machinery substrate<br \/>\n\u2705 Studied in fat-oxidation, insulin-sensitivity, cardiovascular models<br \/>\n\u2705 Acyl-CoA \/ free-CoA ratio buffer; sperm-motility research<br \/>\n\u2705 Levocarnitine FDA-approved for carnitine deficiency (oral and IV)<\/p>\n<p><strong>L-Carnitine<\/strong> contains synthetic levocarnitine.<\/p>","protected":false},"featured_media":71414,"comment_status":"open","ping_status":"closed","template":"","meta":[],"product_brand":[],"product_cat":[5426],"product_tag":[6472,6469,6470,6471],"class_list":{"0":"post-71409","1":"product","2":"type-product","3":"status-publish","4":"has-post-thumbnail","6":"product_cat-peptides","7":"product_tag-amino-acid-derivative","8":"product_tag-l-carnitine","9":"product_tag-levocarnitine","10":"product_tag-mitochondrial","12":"first","13":"instock","14":"shipping-taxable","15":"purchasable","16":"product-type-variable","17":"has-default-attributes"},"acf":[],"_links":{"self":[{"href":"https:\/\/medsbase.com\/nl\/wp-json\/wp\/v2\/product\/71409","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/medsbase.com\/nl\/wp-json\/wp\/v2\/product"}],"about":[{"href":"https:\/\/medsbase.com\/nl\/wp-json\/wp\/v2\/types\/product"}],"replies":[{"embeddable":true,"href":"https:\/\/medsbase.com\/nl\/wp-json\/wp\/v2\/comments?post=71409"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/medsbase.com\/nl\/wp-json\/wp\/v2\/media\/71414"}],"wp:attachment":[{"href":"https:\/\/medsbase.com\/nl\/wp-json\/wp\/v2\/media?parent=71409"}],"wp:term":[{"taxonomy":"product_brand","embeddable":true,"href":"https:\/\/medsbase.com\/nl\/wp-json\/wp\/v2\/product_brand?post=71409"},{"taxonomy":"product_cat","embeddable":true,"href":"https:\/\/medsbase.com\/nl\/wp-json\/wp\/v2\/product_cat?post=71409"},{"taxonomy":"product_tag","embeddable":true,"href":"https:\/\/medsbase.com\/nl\/wp-json\/wp\/v2\/product_tag?post=71409"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}