Description

Pivaloylcarnitine is a specialized carnitine derivative, a high-purity biochemical essential for metabolic research and pharmaceutical development. Its primary value lies in its role as a reference standard and a key intermediate in the synthesis of compounds targeting mitochondrial function and metabolic disorders. This product is critical for research institutions, pharmaceutical R&D laboratories, and manufacturers of high-grade nutraceuticals and active pharmaceutical ingredients (APIs).

Application

• Pharmaceutical Reference Standard: Used as a certified reference material (CRM) for analytical method development, validation, and quality control in drug manufacturing.
• Metabolic Research: Serves as a crucial tool in studying fatty acid oxidation, mitochondrial transport, and energy metabolism pathways in preclinical models.
• API Intermediate: Acts as a key synthetic building block in the production of advanced therapeutic agents for metabolic and cardiovascular diseases.
• Nutraceutical Formulation: Incorporated into high-end dietary supplements targeting cellular energy production and metabolic support.
• Diagnostic Reagent Manufacturing: Utilized in the production of assay kits and reagents for clinical diagnostics related to metabolic panels.
• Biochemical Synthesis: Employed in the synthesis of other carnitine analogs and labeled compounds for tracer studies.

Basic Information

Product Name	Pivaloylcarnitine
CAS No.	98299-38-8
Molecular Formula	C12H23NO4
Molecular Weight	245.32 g/mol
Synonyms	Pivaloyl-L-carnitine; (R)-3-Carboxy-2-hydroxy-N,N,N-trimethyl-1-propanaminium inner salt 3-pivalate; L-Pivaloylcarnitine; 3-Pivaloyloxy-4-(trimethylammonio)butanoate; Pivalic acid carnitine ester; Trimethylammonio-3-pivaloyloxybutyrate; Pivaloyl Carnitine; Pivaloylcarnitine chloride (salt form)
EINECS	Contact for details

Quality Control

Our Pivaloylcarnitine is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including HPLC for purity, chiral analysis for enantiomeric excess, and identity confirmation via IR and MS. We provide full traceability and Certificates of Analysis (COA) detailing all specifications. Production can adhere to cGMP guidelines for pharmaceutical applications upon request.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (15-25°C). Due to its hygroscopic nature, the container must be kept tightly sealed in a dry environment to prevent moisture absorption. For long-term storage, consider desiccants or inert atmosphere.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time matches reference standard
Assay (HPLC)	≥ 98.0%
Enantiomeric Purity (Chiral HPLC)	≥ 99.0% (L-isomer)
Water Content (KF)	≤ 1.0%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 10 ppm
Related Substances (HPLC)	Total impurities ≤ 2.0%
Specific Rotation	Contact for details

Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.