Company Name: |
ChemStrong Scientific Co.,Ltd
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Tel: |
0755-0755-66853366 13670046396 |
Email: |
sales@chem-strong.com |
Products Intro: |
Product Name:Butyryl-L-carnitine CAS:25576-40-3 Purity:95% HPLC Package:10mg;25mg;50mg;100mg
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Company Name: |
Sigma-Aldrich
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Tel: |
021-61415566 800-8193336 |
Email: |
orderCN@merckgroup.com |
Products Intro: |
Product Name:Butyryl-L-carnitine CAS:25576-40-3 Purity:>=97.0% (TLC) Package:50MG Remarks:42623-50MG
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| 3-butanoyloxy-4-trimethylammonio-butanoate Basic information |
| 3-butanoyloxy-4-trimethylammonio-butanoate Chemical Properties |
storage temp. | 2-8°C | solubility | soluble in Methanol, Water | form | Solid | color | White | optical activity | [α]/D -23±2°, c = 1 in H2O |
| 3-butanoyloxy-4-trimethylammonio-butanoate Usage And Synthesis |
Uses | A potential prodrug, via the carnitine transporter OCTN2 and the amino acid transporter ATB0,+ | Uses | Butyryl-L-carnitine may be used as an analytical reference standard for the separation and identification of underivatized butyryl-L-carnitine in human plasma samples using high-performance liquid chromatography coupled to tandem mass spectrometry (HPLC-MS/MS). It may also be used as an analytical reference standard for the quantification of the analyte in biological samples using chromatography-based techniques. | Definition | ChEBI: An optically active form of O-butanoylcarnitine having L-configuration. | General Description | Butyryl-L-carnitine is a naturally occurring compound belonging to the acylcarnitine class of compounds as listed in the human metabolome database (HMBD). These compounds are reported to be used as biomarkers in the diagnosis of carnitine deficiency. It acts as a carrier of long chain acyl groups from activated fatty acids across the inner mitochondrial membrane into the mitochondrial matrix where they undergo β-oxidation to acetyl CoA to obtain usable energy via the citric acid cycle. | Biochem/physiol Actions | Butyrylcarnitine is elevated in patients with Acyl-CoA dehydrogenase, short-chain (SCAD) deficiency, in infants with acute acidosis and generalized muscle weakness and in middle-aged patients with chronic myopathy localized in muscle; very long chain Acyl-CoA dehydrogenase deficiency, and celiac disease. |
| 3-butanoyloxy-4-trimethylammonio-butanoate Preparation Products And Raw materials |
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