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L-CARNITINE (Levocarnitine) - Research Grade Peptide

L-CARNITINE (Levocarnitine) - Research Grade Peptide

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L-CARNITINE (Levocarnitine) – Research-Grade Biochemical Compound

For research purposes only. This product is supplied exclusively for scientific laboratory research and analytical purposes. It is not intended for human or animal use, consumption, clinical use or therapeutic application. It must not be used in any way that contravenes applicable laws or the requirements of the Medicines and Healthcare products Regulatory Agency.

  • Research-grade L-carnitine biochemical compound with batch documentation available where supplied
  • Defined L-enantiomer of carnitine with the specified R stereochemical configuration
  • Supplied as measured dry laboratory material in sealed flip-top headspace vials
  • Batch identity, assay, chromatographic purity and analytical specifications stated in the applicable Certificate of Analysis
  • Handled and supplied exclusively as a research-use laboratory material

L-carnitine, also known as levocarnitine, is a defined chiral biochemical compound rather than a peptide. Each vial contains measured dry laboratory material prepared to support consistent scientific handling, storage and analytical investigation. The stated nominal amount refers to the declared L-carnitine content of a single vial, subject to the applicable batch documentation. Where dissolution is required, the solvent, concentration, handling procedure and storage conditions stated in the applicable Certificate of Analysis, Safety Data Sheet or validated laboratory method should be followed. We do not provide advice or recommendations concerning dosage, administration or use in humans or animals.

Premium ULTIMATE Laboratory Specification

ULTIMATE L-CARNITINE

Enhanced HPLC Purification and More Stringent LPS Testing

Additional preparative high-performance liquid chromatography purification and a more stringent bacterial endotoxin and lipopolysaccharide testing specification for demanding scientific laboratory workflows.

The ULTIMATE L-Carnitine range is our premium research specification for laboratories requiring an enhanced level of purification and quality control. Following the standard production and purification process, the finished L-carnitine research material undergoes an additional preparative high-performance liquid chromatography purification stage designed to reduce residual structurally related and process-related impurities further. ULTIMATE batches are also assessed under a more stringent bacterial endotoxin and lipopolysaccharide testing specification, with the applicable analytical and batch documentation provided where supplied.

Additional HPLC Purification
A further preparative high-performance liquid chromatography purification stage is completed after the standard production and purification workflow.
More Stringent LPS Testing
Assessed under the enhanced ULTIMATE bacterial endotoxin and lipopolysaccharide testing specification.
Premium Research Specification
Intended for laboratory projects requiring additional chromatographic purification and enhanced batch-specific quality-control parameters.
Regular or ULTIMATE?
For the majority of routine analytical, biochemical, formulation and general laboratory work, our Regular research-grade L-Carnitine product remains highly suitable and provides an appropriate balance of material quality, batch documentation and value. The ULTIMATE option is intended for scientific projects where the additional preparative high-performance liquid chromatography purification stage and more stringent bacterial endotoxin and lipopolysaccharide testing specification are specifically required.

ULTIMATE L-Carnitine remains strictly for scientific laboratory research and analytical use only. It is not intended for human or animal use, clinical use, diagnostic use or therapeutic application. Identity, stereochemistry, assay, chromatographic purity, material content, molecular form, water content, residual solvents, bacterial endotoxin results and other analytical specifications are batch-specific and should be confirmed using the applicable Certificate of Analysis. Bacterial endotoxin or LPS testing does not constitute sterility testing.

Chemical Information:

  • Product Name: L-Carnitine
  • Preferred Substance Name: Levocarnitine
  • Alternative Names: L-Carnitine; Levocarnitine; L-(-)-Carnitine; (-)-Carnitine
  • Chemical Classification: Chiral zwitterionic quaternary ammonium compound and beta-hydroxy betaine derivative
  • IUPAC Name: (3R)-3-hydroxy-4-(trimethylazaniumyl)butanoate
  • Alternative Systematic Description: (L-3-carboxy-2-hydroxypropyl)trimethylammonium inner salt
  • Stereochemical Configuration: R configuration at the single chiral centre
  • Physical Charge Form: Zwitterionic inner salt
  • CAS Number: 541-15-1
  • PubChem Compound Identifier: CID 10917
  • Unique Ingredient Identifier: 0G389FZZ9M
  • Molecular Formula: C7H15NO3
  • Average Molecular Weight: Approximately 161.20 g/mol
  • Exact Mass: Approximately 161.1052 Da
  • InChIKey: PHIQHXFUZVPYII-ZCFIWIBFSA-N
  • Physical Form: Dry laboratory powder or lyophilised material, as stated in the applicable batch Certificate of Analysis
  • Appearance: White to off-white laboratory material, subject to confirmation in the applicable batch Certificate of Analysis
  • Assay Specification: The applicable assay result, analytical method and acceptance criterion are stated in the batch Certificate of Analysis
  • Chromatographic Purity: The applicable chromatographic result and analytical method are stated in the batch Certificate of Analysis
  • Chiral Identity: The supplied material should be confirmed as the L-carnitine or R-configured enantiomer using suitable supplier records or chiral analytical data
  • Chemical-Form Confirmation: The formula C7H15NO3 and molecular weight of approximately 161.20 g/mol apply to the uncountered zwitterionic L-carnitine inner salt
  • Alternative Salt Forms: L-carnitine hydrochloride, L-carnitine tartrate and other salt forms have different molecular formulae and molecular weights and should not be represented using the free-form identity
  • Water and Hydration: Water content, hydration state and loss on drying should be interpreted using the applicable batch analytical results
  • Residual Solvents: Any applicable residual-solvent results and acceptance criteria should be stated in the batch Certificate of Analysis
  • Endotoxin Specification: The applicable bacterial endotoxin or LPS result, analytical method, reporting units and acceptance criterion should be stated in the batch Certificate of Analysis
  • Analytical Interpretation: Molecular identity, stereochemical identity, assay, chromatographic purity, water content, residual solvents, inorganic residues and bacterial endotoxin results are separate analytical measurements and should be interpreted together

✓ Batch documentation – Completed Certificate of Analysis documentation is provided where supplied for review.
✓ Certificate of Analysis – Accessible through the product QR code where provided for the applicable batch.
✓ Safety Data Sheet – Supplied to support appropriate laboratory handling, storage and regulatory compliance.
✓ Identity documentation – Chemical identity, molecular formula and stereochemical configuration should be confirmed using the applicable batch records.
✓ Assay documentation – The reported assay applies only to the analytical method and batch stated in the Certificate of Analysis.
✓ Chromatographic documentation – Chromatographic purity should be interpreted separately from assay, water content and total material content.
✓ Chiral identity documentation – Confirmation of the L-carnitine enantiomer should be supported by suitable supplier or analytical records.
✓ Chemical-form documentation – The zwitterionic free form, hydrochloride, tartrate or another salt form should be identified clearly in the applicable product and batch records.
✓ Bacterial endotoxin documentation – The applicable bacterial endotoxin or LPS result should identify the test method, reporting units and acceptance criterion.
✓ Supplier documentation – Reviewed where supporting production, purification and analytical records are supplied.
✓ Fast, reliable and trackable express delivery – Securely packaged and dispatched using insulated or temperature-managed packaging where required by the applicable transport and storage specification.


For Research Use Only
This product is supplied strictly for scientific research, laboratory analysis and experimental work. It is not intended for human consumption, animal use, clinical use, diagnostic use or any form of therapeutic application.


L-Carnitine Product Overview

Our L-Carnitine research-grade biochemical compound, also known as levocarnitine, is supplied for controlled scientific laboratory investigation, analytical method development, biochemical characterisation, high-performance liquid chromatography assessment, mass-spectrometry workflows, formulation studies and reference-material comparison. The material is the R-configured L-enantiomer of carnitine and exists as a zwitterionic quaternary ammonium inner salt.

The material is handled with a focus on batch traceability, documented quality control and consistent laboratory presentation. Product identity, stereochemical identity, assay, chromatographic purity, molecular form, water content, residual solvents, inorganic residues, bacterial endotoxin results and other analytical specifications should be confirmed using the applicable batch Certificate of Analysis.

The CAS number 541-15-1, molecular formula C7H15NO3 and average molecular weight of approximately 161.20 g/mol describe the uncountered zwitterionic L-carnitine inner salt. Where the supplied material is L-carnitine hydrochloride, L-carnitine tartrate or another salt form, the applicable batch documentation should identify the correct chemical form, molecular formula and formula weight.

For the majority of routine analytical, biochemical, formulation and general laboratory work, the Regular L-Carnitine specification remains highly suitable. The premium black-and-gold ULTIMATE L-Carnitine option provides an additional preparative high-performance liquid chromatography purification stage and a more stringent bacterial endotoxin and lipopolysaccharide testing specification for scientific projects requiring enhanced quality-control parameters.

View Certificate of Analysis

View Safety Data Sheet

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