For laboratory research use only. Not for human consumption.

Aminos

L-Carnitine (20ML)

L-Carnitine (4-trimethylammonio-3-hydroxybutyrate) is an essential zwitterionic quaternary ammonium compound and obligate cofactor for mitochondrial fatty acid beta-oxidation. Functioning as a primary substrate for carnitine palmitoyltransferase enzymes (CPT-1 and CPT-2), L-Carnitine translocates long-chain fatty acyl-CoA esters across the inner mitochondrial membrane into the matrix for Krebs cycle ATP generation while buffering intracellular acetyl-CoA/free CoA ratios.

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What is L-Carnitine?

L-Carnitine (known chemically as 4-trimethylammonio-3-hydroxybutyrate or (R)-(3-carboxy-2-hydroxypropyl)trimethylammonium hydroxide) is an endogenous amino acid derivative synthesized from L-lysine and L-methionine. Operating as an indispensable metabolic cofactor, L-Carnitine regulates mitochondrial energy production by mediating the transport of activated long-chain fatty acids across the impermeable inner mitochondrial membrane.

By forming transient acylcarnitine esters via carnitine palmitoyltransferase 1 (CPT-1) and carnitine palmitoyltransferase 2 (CPT-2), L-Carnitine supplies long-chain fatty acyl-CoA molecules directly to the mitochondrial matrix for mitochondrial beta-oxidation. Concurrently, it buffers excess matrix acetyl-CoA via carnitine acetyltransferase (CRAT), preventing metabolic feedback inhibition of the Pyruvate Dehydrogenase (PDH) complex.

Batch-verified for high analytical purity at NobleChems, L-Carnitine is supplied in a high-concentration 600mg/mL pre-mixed liquid solution packaged in a 20mL sterile glass vial. Researchers evaluating mitochondrial respiratory capacity, fatty acid oxidation flux, and cellular energy expenditure utilize L-Carnitine alongside complementary metabolic reference standards available on the site, such as SLU-PP-332, BAM15, AICAR, and MOTS-C.

Chemical and Molecular Data

Compound Name L-Carnitine (Levocarnitine)
Quantity / Formats Offered 600mg/mL Liquid Solution in 20mL Glass Vial (12,000mg Total Mass)
Synonyms / Alt Names Levocarnitine, (R)-Carnitine, 4-trimethylammonio-3-hydroxybutyrate, L-Carnitine Base
CAS Number 541-15-1
Chemical Formula C7H15NO3
Molecular Weight 161.20 g/mol
IUPAC Name (3R)-3-hydroxy-4-(trimethylazaniumyl)butanoate
InChIKey InChIKey=XEEIOWLUKPNEGL-LURJTMSTSA-N
SMILES Code CN+(C)CC@@HO

What are the Mechanisms of Action?

The biochemical pathways and cellular targets include:

  • CPT-1 & CPT-2 Mitochondrial Fatty Acid Shuttle: Long-chain fatty acids cannot cross the inner mitochondrial membrane independently. On the outer membrane, CPT-1 transfers the acyl group from fatty acyl-CoA to L-Carnitine, forming acylcarnitine. After translocating across the membrane via carnitine-acylcarnitine translocase (CACT), CPT-2 regenerates fatty acyl-CoA inside the mitochondrial matrix for immediate beta-oxidation.

  • Acetyl-CoA / Free CoA Ratio Buffering (CRAT Pathway): During high metabolic rates, rapid glycolysis generates excess mitochondrial acetyl-CoA. It reacts with acetyl-CoA via carnitine acetyltransferase (CRAT) to form acetyl-L-carnitine and free Coenzyme A (CoA). This liberates free CoA to sustain Pyruvate Dehydrogenase (PDH) activity and Krebs cycle turnover.

  • Mitochondrial Membrane Protection & Lipid Redox Defense: By facilitating the removal of toxic short- and medium-chain acyl groups from cells, L-Carnitine prevents intracellular accumulation of amphiphilic fatty acid intermediates, preserving mitochondrial inner membrane potential (ΔΨm) and reducing reactive oxygen species (ROS) production.

What do Preclinical & Academic Studies Show?

When evaluating research efficacy and published scientific literature:

  • Carnitine Shuttle Kinetics & Beta-Oxidation (PubMed): Landmark bioenergetic studies cataloged on PubMed (PMID: 21521252) confirm that increasing L-Carnitine cell density upregulates CPT-1 enzyme activity, boosting long-chain fatty acid oxidation rates and ATP production in muscle and hepatic cell models.

  • Mitochondrial Energetics & PDH Complex Flux (PMC): Comprehensive biomedical reviews archived in PMC (PMC3099008) document its ability to buffer intramitochondrial acetyl-CoA pools, maintaining glucose and pyruvate oxidation capacity during elevated metabolic stress.

  • Chemical Profiling & Identification (PubChem): Official structural characterization maintained on PubChem verifies the molecular mass (161.20 g/mol), zwitterionic quaternary ammonium structure, and HPLC mass spectrometry profile of CAS 541-15-1.

How does L-Carnitine compare to other compounds?

To evaluate metabolic transport mechanisms, mitochondrial energy pathways, and bioenergetic targets, researchers compare L-Carnitine against alternative reference compounds available at NobleChems:

600mg/mL High-Density Liquid Vial vs. Standard Oral Powder Formats

In laboratory research settings, vehicle density and physical format significantly impact experimental utility:

  • 600mg/mL Pre-Solubilized Liquid Solution (20mL Vial): Provides high active mass density (12,000mg total L-Carnitine per bottle) in a pre-mixed, ultra-pure liquid matrix. This allows precise volumetric micropipetting directly into cell culture media or analytical tissue baths without requiring manual dry-powder mass weighing.

  • Standard Oral / Dry Powder Formats: Require weighing step preparation and exhibit variable solubility rates in polar solvents depending on ambient humidity, increasing preparation time and potential mass measurement variance during high-throughput screening.

Compound / Reference Chemical Structure & Class Core Mechanism of Action Research Focus & Profile
L-Carnitine Zwitterionic Quaternary Ammonium Compound Translocates long-chain fatty acids into mitochondria via CPT-1/CPT-2 and buffers acetyl-CoA via CRAT Focuses on mitochondrial beta-oxidation, carnitine shuttle kinetics, fatty acid transport, and systemic metabolic flux
Acetyl-L-Carnitine (ALCAR) Acetylated L-Carnitine Ester Derivative Crosses blood-brain barrier intact; donates acetyl groups for acetylcholine synthesis and mitochondrial ATP production Focuses on neuro-energetics, central nervous system lipid transport, acetyl donor signaling, and cognitive bioenergetics
SLU-PP-332 Pan-ERR Nuclear Receptor Agonist Binds ERRα/β/γ receptors to recruit PGC-1α and upregulate mitochondrial OXPHOS gene transcription Focuses on nuclear receptor exercise mimetics, oxidative muscle fiber switching, and de novo mitochondrial biogenesis
BAM15 Mitochondrial Protonophore Uncoupler Uncouples oxidative phosphorylation from ATP synthesis by discharging the mitochondrial inner membrane proton gradient Focuses on uncoupled respiration, energy expenditure elevation, and lipid oxidation independent of fatty acid shuttles

Frequently Asked Questions (FAQs)

1. Is NobleChems a reliable place to buy compounds?

Yes, NobleChems is a highly trusted vendor for high-purity research chemicals and reference compounds. Every batch undergoes strict third-party analytical testing (including HPLC and Mass Spectrometry) to verify minimum 98%+ chemical purity, exact 600mg/mL concentration, and complete absence of heavy metals or synthesis impurities.

2. What is L-Carnitine and what is its primary biological role in cellular metabolism?

L-Carnitine (4-trimethylammonio-3-hydroxybutyrate) is a naturally occurring quaternary ammonium compound essential for cellular bioenergetics. It acts as an obligate cofactor for carnitine palmitoyltransferase enzymes, facilitating the transport of long-chain fatty acids across the inner mitochondrial membrane for beta-oxidation and ATP production.

3. How does L-Carnitine function in mitochondrial fatty acid transport?

It binds long-chain fatty acyl-CoA molecules via carnitine palmitoyltransferase 1 (CPT-1) on the outer mitochondrial membrane to form acylcarnitine. Acylcarnitine translocates into the mitochondrial matrix via carnitine-acylcarnitine translocase, where CPT-2 regenerates fatty acyl-CoA for Krebs cycle entry.

4. What available formats does NobleChems offer for research?

NobleChems supplies a high-density 600mg/mL pre-solubilized liquid solution packaged in a 20mL sterile glass vial. This format provides high active compound density for precise volumetric addition in cell culture and biochemical assay preparations.

5. How does L-Carnitine modulate cellular acetyl-CoA to CoA ratios?

By reacting with excess mitochondrial acetyl-CoA via carnitine acetyltransferase (CRAT), L-Carnitine forms acetyl-L-carnitine and releases free Coenzyme A. This buffer mechanism maintains Pyruvate Dehydrogenase (PDH) complex activity and prevents metabolic feedback inhibition during elevated glycolytic or oxidative flux.

6. How does L-Carnitine compare to Acetyl-L-Carnitine (ALCAR) in laboratory models?

It functions primarily as a fatty acid transport shuttle across mitochondrial membranes. Acetyl-L-Carnitine (ALCAR) contains an acetylated ester group that enables enhanced lipophilicity and blood-brain barrier transport, serving as both a carnitine donor and an acetyl substrate for central neurotransmitter synthesis.

7. How does NobleChems verify the chemical purity and mass identity?

NobleChems utilizes High-Performance Liquid Chromatography (HPLC) to confirm active purity exceeding 98% and Mass Spectrometry (MS) to verify exact molecular weight (161.20 g/mol) and active compound concentration prior to batch release.

8. What are the recommended storage and stability parameters?

20mL glass vials should be stored tightly sealed in a cool, dry environment (15°C to 25°C) protected from direct sunlight, light exposure, and heat. Under controlled room temperature conditions, this solution maintains complete solubility and stability throughout its designated shelf life.

Disclaimer: All compounds and research materials provided by NobleChems are strictly for laboratory and research professional use only. They are not approved for human or animal use nor consumption by the Food and Drug Administration (FDA). These products should not be used for any form of in vivo experimentation or for any other non-laboratory purpose. Any violation or indication of human or animal use will result in immediate removal from being able to purchase products in the future. By purchasing these products, you acknowledge that they will be used exclusively within a controlled and qualified research environment.

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