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PureAmino Research
L-Carnitine
99%+ Purity
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COA Included
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U.S. Shipped
Metabolic PeptidesNew

L-Carnitine

LevocarnitineL-Carnitine 6000mgβ-Hydroxy-γ-trimethylaminobutyric acidCarnitor
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Injectable L-Carnitine 6000mg for metabolic research. L-Carnitine facilitates fatty acid transport into mitochondria for beta-oxidation and is studied for fat metabolism, exercise performance, and cellular energy production.

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Compound Profile

Pharmaceutical Data Sheet

PureAmino ResearchResearch Grade · 99%+ Purity

Metabolic Peptides

L-Carnitine

Levocarnitine (Injectable)

CAS Number

541-15-1

Molecular Formula

C₇H₁₅NO₃

Molecular Weight

161.20 g/mol

Purity

> 99% HPLC

Designation

RUO · Research Use Only

Not for human or veterinary consumption. For in vitro laboratory research only.

L-Carnitine

Third-Party Tested · Certificate of Analysis Included · Ships from Tampa, FL USA

Batch VerifiedLyophilized
CPT-1
Carnitine Palmitoyltransferase System
6000mg
High-Dose Injectable Formulation
β-Ox
Mitochondrial Beta-Oxidation Cofactor
FDA
Levocarnitine — FDA-Approved (Carnitor®)

Mechanism of Action

How L-Carnitine Works

L-Carnitine (levocarnitine) is an endogenous quaternary ammonium compound essential for the transport of long-chain fatty acids across the inner mitochondrial membrane via the carnitine palmitoyltransferase (CPT) system. Without carnitine, long-chain fatty acyl-CoA molecules cannot enter the mitochondrial matrix for β-oxidation — making carnitine the rate-limiting cofactor for fat-derived energy production. Injectable L-Carnitine bypasses first-pass metabolism and oral bioavailability limitations (~15%), achieving higher plasma levels for metabolic research.

CPT
Carnitine Palmitoyltransferase System
Primary — Fatty Acid Transport
  • CPT-1 on outer mitochondrial membrane conjugates carnitine to long-chain acyl-CoA
  • CACT translocase shuttles acylcarnitine across inner membrane
  • CPT-2 regenerates acyl-CoA in the matrix for β-oxidation
FAO
Fatty Acid Oxidation
Downstream — Energy Production
  • Enables β-oxidation of C14-C20 long-chain fatty acids
  • Each β-oxidation cycle produces FADH₂, NADH, and acetyl-CoA
  • Acetyl-CoA enters TCA cycle for ATP generation via oxidative phosphorylation
BUF
Acyl-CoA / CoA Buffering
Homeostatic — Metabolic Regulation
  • Maintains free CoA/acyl-CoA ratio in mitochondria
  • Prevents toxic acyl-CoA accumulation during metabolic stress
  • Exports excess acyl groups as acylcarnitine for renal clearance
Key Mechanism
Carnitine Shuttle: CoA → Acylcarnitine → Mitochondrial Matrix → β-Oxidation

At the outer mitochondrial membrane, CPT-1 converts long-chain acyl-CoA to acylcarnitine. Carnitine-acylcarnitine translocase (CACT) shuttles acylcarnitine across the inner membrane. CPT-2 reconverts acylcarnitine to acyl-CoA inside the matrix, releasing free carnitine for recycling. This cycle is the sole mechanism for mitochondrial import of C14-C20 fatty acids.

Primary Source

Bremer J., Physiol Rev (1983): Carnitine — Metabolism and Functions.

Preclinical Findings

Research Models

Mitochondrial Long-Chain FA Import (CPT System)95%
Fat Oxidation Enhancement During Exercise78%
Exercise Recovery & Muscle Damage Reduction72%
Acyl-CoA Buffering & Metabolic Detoxification85%

Clinical Data

Clinical: Enhanced Fat Oxidation, Exercise Performance & Recovery

Clinical — Human Studies

Multiple randomized controlled trials demonstrate that L-Carnitine supplementation increases fat oxidation during submaximal exercise, reduces markers of exercise-induced muscle damage (CK, LDH, DOMS), and improves recovery kinetics. A meta-analysis (Pooyandjoo et al., 2016) of 9 RCTs found significant weight loss in supplemented groups. Injectable routes achieve 100% bioavailability vs. ~15% oral.

Fat Oxidation Increase (2g/day, exercising subjects)21%
Muscle Damage Markers Reduction (Post-Exercise CK)44%
VO₂max-Linked Performance Improvement11%
Source

Pooyandjoo M et al., Obes Rev (2016); Volek JS et al., Am J Clin Nutr (2002); Spiering BA et al., J Strength Cond Res (2007).

Meta-analysis of 9 RCTs; multiple controlled human exercise studies

Research Outcomes

Key Research Success Metrics

21%
fat oxidation increase
2g/day during submaximal exercise
Volek et al., Am J Clin Nutr 2002
44%
muscle damage reduction
Post-exercise CK marker decrease
Spiering et al., JSCR 2007
100%
bioavailability (injectable)
vs. ~15% oral bioavailability
Bypasses first-pass hepatic metabolism

Safety Profile

Research Safety Notes

  • FDA-approved as Carnitor® for primary and secondary carnitine deficiency
  • Generally well-tolerated at doses up to 6g/day in clinical studies
  • Injectable formulations avoid GI side effects (nausea, diarrhea) seen with high-dose oral
  • Rare: transient injection site discomfort at high concentrations
  • Does not affect cardiac QT interval at therapeutic doses (Rebouche, Am J Clin Nutr 2004)
Research Disclaimer

L-Carnitine (levocarnitine) is FDA-approved for carnitine deficiency. Metabolic and performance data is from controlled studies but individual responses vary. This injectable formulation is for research use only.

About L-Carnitine

Injectable L-Carnitine 6000mg for metabolic research. L-Carnitine facilitates fatty acid transport into mitochondria for beta-oxidation and is studied for fat metabolism, exercise performance, and cellular energy production.

All PureAmino Research compounds are manufactured to research-grade standards and independently tested by Janoshik Analytical & Kovera Labs. The Certificate of Analysis for this compound includes full HPLC chromatography data, mass spectrometry confirmation, net purity percentage, and net content verification.

⚠️

Research Use Only

This product is strictly for in vitro research and laboratory use only. Not for human or veterinary consumption. By purchasing, you confirm use in a controlled research setting.

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