share

Valeryl-L-Carnitine Chloride CAS NO 162040-64-4


Unit Price:

CAS No.:162040-64-4

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

Valeryl-L-Carnitine Chloride is a high-purity, specialized carnitine derivative used as a key pharmaceutical intermediate and research biochemical. This compound is valued for its role in the synthesis of more complex molecules targeting metabolic pathways and cellular energy regulation. It is primarily required by manufacturers in the pharmaceutical, nutraceutical, and advanced life science research sectors for developing novel therapeutic agents and diagnostic tools.

Application

  • Pharmaceutical Intermediate: Critical building block in the synthesis of proprietary drug candidates, particularly those targeting metabolic disorders.
  • Biochemical Research: Used as a reference standard and reagent in studies of fatty acid metabolism, mitochondrial function, and carnitine-related pathways.
  • Nutraceutical Development: Serves as a precursor for advanced dietary supplements designed to support energy production and cellular health.
  • Diagnostic Agent Synthesis: Employed in the production of labeled compounds and tracers for metabolic imaging and diagnostic assays.
  • Cosmeceutical Actives: Potential ingredient in high-end skincare formulations aimed at improving cellular energy and vitality.

Basic Information

Item Detail
Product Name Valeryl-L-Carnitine Chloride
CAS No. 162040-64-4
Molecular Formula C12H24ClNO4
Molecular Weight 281.78 g/mol
Synonyms L-Valerylcarnitine Chloride; (R)-3-Carboxy-2-hydroxy-N,N,N-trimethyl-1-propanaminium, 5-oxopentanoate, chloride; Valeryl Carnitine Chloride; Pentanoyl-L-carnitine Chloride; 5-Oxopentanoic acid compound with (R)-3-carboxy-2-hydroxy-N,N,N-trimethyl-1-propanaminium chloride; Valproylcarnitine Chloride (related); Carnitine Valerate Ester Chloride
EINECS Contact for details

Quality Control

Our Valeryl-L-Carnitine Chloride is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including HPLC for purity, chiral analysis, and residual solvent screening, to ensure it meets the stringent requirements for pharmaceutical and research use. A Certificate of Analysis (COA) detailing identity, purity, and impurity profiles is provided with every shipment.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (15-25°C). This material is hygroscopic (moisture-sensitive) and must be kept under anhydrous conditions. For long-term storage, consider desiccants or an inert atmosphere.

Specification

Item Specification
Appearance White to off-white crystalline powder
Identification (IR) Conforms to structure
Identification (HPLC) Retention time matches reference standard
Assay (HPLC) ≥ 98.0%
Optical Rotation [α]20/D -20° to -24° (c=1 in H2O)
Water Content (KF) ≤ 1.0%
Residual Solvents (GC) Meets ICH Q3C guidelines
Heavy Metals ≤ 10 ppm

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

Complete Your RFQ

0/ 2000

Why choose US

Trusted Manufacturer

With our own production facilities, we ensure consistent quality, reliable supply, and full traceability.

Rigorous Quality Assurance

Each batch undergoes strict QC, accompanied by COA, MSDS, and full compliance with international standards.

Advanced R&D Expertise

Our in-house lab drives process innovation, new product development, and tailored synthesis solutions.