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L-Carnitine Hydrochloride CAS NO 10017-44-4


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CAS No.:10017-44-4

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

L-Carnitine Hydrochloride is the hydrochloride salt form of L-Carnitine, a naturally occurring amino acid derivative essential for fatty acid metabolism. This high-purity compound is critical for ensuring optimal bioavailability and stability in demanding formulations. It serves as a vital ingredient for manufacturers in the pharmaceutical, nutraceutical, and functional food and beverage industries, where consistent quality and reliable supply are paramount.

Application

  • Pharmaceutical Formulations: Used in injectable and oral solutions for the treatment of primary and secondary carnitine deficiencies, and as a supportive metabolic agent.
  • Dietary Supplements & Nutraceuticals: A core ingredient in capsules, tablets, and powders targeting weight management, sports nutrition, and energy enhancement.
  • Functional Food & Beverage Fortification: Incorporated into energy drinks, health bars, and meal replacements to add metabolic and nutritional benefits.
  • Animal Nutrition & Feed Additives: Enhances growth performance, meat quality, and energy utilization in livestock, poultry, and aquaculture feeds.
  • Cosmetic & Personal Care: Utilized in topical formulations for its potential antioxidant and skin-conditioning properties.
  • Research & Biochemical Reagents: Serves as a standard and reagent in clinical diagnostics, metabolic research, and enzymatic studies.

Basic Information

Product Name L-Carnitine Hydrochloride
CAS No. 10017-44-4
Molecular Formula C7H15NO3 • HCl
Molecular Weight 197.66 g/mol
Synonyms L-Carnitine HCl; (R)-Carnitine hydrochloride; Levocarnitine hydrochloride; Vitamin Bt hydrochloride; Carnitine inner salt hydrochloride; 3-Carboxy-2-hydroxy-N,N,N-trimethyl-1-propanaminium chloride; (3-Carboxy-2-hydroxypropyl)trimethylammonium chloride
EINECS 233-000-4

Quality Control

Our L-Carnitine Hydrochloride is manufactured under strict quality management systems. It is typically produced to meet or exceed relevant pharmacopeial standards such as USP, EP, and JP, as well as food-grade specifications like FCC. Every batch undergoes rigorous analytical testing including assay, optical rotation, and impurity profiling. A comprehensive Certificate of Analysis (COA) documenting purity, identity, and safety parameters is provided with each shipment to ensure full traceability and compliance.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at a controlled room temperature (15-25°C). This product is hygroscopic (moisture-sensitive) and must be kept in a low-humidity environment to prevent caking and degradation. Keep away from incompatible materials.

Specification

Item Specification
Appearance White crystalline powder
Identification (IR) Conforms
Assay (HPLC) 98.5% ~ 101.0% (on anhydrous basis)
Specific Rotation -21.0° ~ -23.0°
pH (5% solution) 2.5 ~ 3.5
Loss on Drying ≤ 0.5%
Residue on Ignition ≤ 0.1%
Heavy Metals ≤ 10 ppm
Related Substances (HPLC) Total impurities ≤ 1.0%

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

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