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Dl-Carnitine CAS NO 406-76-8


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CAS No.:406-76-8

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

Dl-Carnitine CAS NO 406-76-8 is a synthetic, racemic mixture of the essential nutrient L-carnitine and its enantiomer D-carnitine. This compound is critical for the transport of long-chain fatty acids into the mitochondria for energy production via β-oxidation. It is widely utilized in the pharmaceutical, nutraceutical, and animal feed industries as a key ingredient for metabolic support, energy enhancement, and weight management formulations.

Application

  • Pharmaceutical Intermediates: Serves as a key starting material or intermediate in the synthesis of specialized pharmaceutical actives targeting metabolic disorders.
  • Dietary Supplements & Nutraceuticals: Incorporated into capsules, tablets, and powders aimed at improving exercise performance, supporting fat metabolism, and enhancing energy levels.
  • Functional Food & Beverage Fortification: Used to enrich health-focused drinks, meal replacements, and food products with carnitine's metabolic benefits.
  • Animal Nutrition & Feed Additives: Added to livestock, poultry, and aquaculture feed to improve growth performance, feed efficiency, and overall animal health.
  • Cosmetic & Personal Care: Employed in topical formulations for its potential anti-aging and skin-conditioning properties.
  • Research & Development: Used as a standard or reagent in biochemical, nutritional, and metabolic research studies.

Basic Information

Product Name Dl-Carnitine
CAS No. 406-76-8
Molecular Formula C7H15NO3
Molecular Weight 161.20 g/mol
Synonyms DL-Carnitine; (±)-Carnitine; rac-Carnitine; Vitamin BT; 3-Carboxy-2-hydroxy-N,N,N-trimethyl-1-propanaminium hydroxide, inner salt; (±)-3-Hydroxy-4-(trimethylammonio)butyrate; Bicarnesine; Carnitine (DL-Form); Levocarnitine (racemic mixture)
EINECS 206-976-6

Quality Control

Our Dl-Carnitine is manufactured under a strict quality management system. Production adheres to current Good Manufacturing Practices (cGMP) and is supported by a comprehensive analytical control strategy. Each batch is tested to meet stringent specifications for identity, purity, and potency. Certificates of Analysis (COA) documenting all test results are provided and can be tailored to meet specific customer or regulatory requirements, including those for pharmaceutical (USP/EP), food (FCC), and feed grade applications.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at controlled room temperature (15-25°C). This product is hygroscopic (moisture-sensitive). Keep the container tightly sealed to minimize exposure to atmospheric humidity.

Specification

Item Specification
Appearance White to off-white crystalline powder
Identification (IR) Conforms to standard
Assay (HPLC) 98.0% - 102.0% (on dried basis)
Specific Rotation -0.10° to +0.10° (c=10 in H2O)
Loss on Drying ≤ 1.0%
Residue on Ignition (Sulfated Ash) ≤ 0.1%
Heavy Metals (as Pb) ≤ 10 ppm
Related Substances (HPLC) Total impurities ≤ 2.0%
Microbiological Control Meets standard for intended use

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

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