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Lauroyl-DL-carnitine (chloride)
Cat. No.:
OB0626WX-2538
Appearance:
Crystalline solid
Purity:
≥95%
Identity:
Confirmed by IR.
Size:
Add to basket
Product Overview
Description:
Lauroyl-DL-carnitine is a zwitterionic, long-chain acylcarnitine derivative featuring a twelve-carbon lauroyl core bound to a carnitine scaffold. This amphiphilic lipid compound functions as a specialized permeation enhancer, modulating cell membrane fluidity and tight junction dynamics to significantly improve the absorption and delivery of hydrophilic molecular payloads across mucosal barriers.
Synonyms:
3-carboxy-N,N,N-trimethyl-2-[(1-oxododecyl)oxy]-1-propanaminium, monochloride; CAR 12:0; C12:0 Carnitine; DL-Carnitine lauroyl ester; DL-Lauroylcarnitine; 14919-37-0; Lauroylcarnitine chloride; Lauroylcarnitine (chloride); (+/-)-Lauroylcarnitine chloride; (3-carboxy-2-dodecanoyloxypropyl)-trimethylazanium;chloride; Dodecanoyl-DL-carnitine chloride; Lauroyl-DL-carnitine chloride; 1-Propanaminium, 3-carboxy-N,N,N-trimethyl-2-[(1-oxododecyl)oxy]-, chloride (1:1); lauroyl L-carnitine; (3-Carboxy-2-hydroxypropyl)trimethylammonium Chloride Laurate; 3-Carboxy-N,N,N-trimethyl-2-[(1-oxododecyl)oxy]-1-propanaminium Chloride; (3-Carboxy-2-hydroxypropyl)trimethylammonium Chloride Laurate (Ester); 3-Carboxy-2-(dodecanoyloxy)-N,N,N-trimethylpropan-1-aminium Chloride; DL-Lauroylcarnitinechloride; (C12) Dodecanoylcarnitine; (3-Carboxy-2-hydroxypropyl)trimethylammonium chloride, laurate; Ammonium, (3-carboxy-2-hydroxypropyl)trimethyl-, chloride, laurate (ester); 1-Propanaminium, 3-carboxy-N,N,N-trimethyl-2-((1-oxododecyl)oxy)-, chloride
CAS No.:
14919-37-0
Compound CID:
177509
Formula:
C19H38NO4 • Cl
Formula Weight:
380
Specification
Solubility in DMSO:
10 mg/mL
Solubility in Ethanol:
20 mg/mL
Solubility in DMF:
20 mg/mL
Storage:
Storage at -20°C.
Applications:
Lauroyl-DL-carnitine (chloride) serves as an acylcarnitine reference compound for investigating fatty acid transport and acylcarnitine metabolism. It facilitates metabolomic profiling, LC-MS/MS quantification, analytical method development, and studies of mitochondrial lipid metabolism.
