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Research PeptidesMETABOLIC
Evidence grade A

L-Carnitine

Grade A applies only to the FDA-approved levocarnitine products (Carnitor and generics) for carnitine deficiency, not research material; weight and exercise research shows only small effects.

Strengths
5,000 mg
Also known as
Levocarnitine, L-(−)-carnitine, Carnitor
Molecule
Quaternary ammonium compound (not a peptide)
Formula
C7H15NO3
Mol. weight
161.20 g/mol
CAS
541-15-1

Origin

A small nutrient-like molecule the body makes from lysine and methionine. Prescription levocarnitine (Carnitor) was first FDA-approved in 1985. Despite the catalog's category, it is not a peptide.

How it works

Carnitine carries long-chain fatty acids across the inner mitochondrial membrane so they can be burned for energy, and helps clear excess acyl groups from cells. Healthy adults make enough, so deficiency mainly occurs with genetic disorders, dialysis and certain drugs. Unabsorbed oral carnitine is converted by gut bacteria into TMAO.

What the research shows

Placebo-controlled trials in dialysis patients supported the approved IV use for deficiency. For weight, pooled oral trials show about 1.2–1.3 kg more loss than placebo, and no weight-loss trials of injectable forms were found. Exercise research suggests a possible benefit only for high-intensity exercise, and the overall evidence is mixed. A 2013 study found gut bacteria convert carnitine to TMAO, which predicted heart events in cardiac patients and increased atherosclerosis in mice.

Key studies

  • Pooyandjoo et al., Obesity Reviews 2016 9 RCTs: about 1.33 kg more weight loss than control, shrinking over time.
  • Talenezhad et al., Clin Nutr ESPEN 2020 37 RCTs: about 1.21 kg less weight; no change in waist or body-fat percentage.
  • Mielgo-Ayuso et al., Nutrients 2021 Possible benefit for high-intensity exercise only.
  • Koeth et al., Nature Medicine 2013 Gut microbes convert carnitine to TMAO, linked to heart risk and atherosclerosis in mice.

Safety findings

The approved label lists nausea, vomiting, body odor and gastritis. Serious risks include seizures (even without a seizure history), anaphylaxis and bronchospasm with IV use, and raised INR with warfarin. A 2022 trial linked L-carnitine to higher total and LDL cholesterol.

Regulatory status

FDA-approved prescription drug (Carnitor injection, oral solution and tablets) for carnitine deficiency; also sold as an oral supplement. As the active ingredient of approved drugs, 503A pharmacies may compound it. Not on the WADA list, though WADA's method rules (M2.2) restrict large-volume IV infusions outside hospital settings. Status as of October 2026.

Catalog notes

Offered as 5,000 mg. No certificate is published yet, and no endotoxin or sterility data are listed. It is listed both as a lyophilized powder and as a 10 mL liquid vial; follow the storage stated on the label. The approved Carnitor is stored at room temperature.