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CS-W001157 4
Total: USD 88.00

C13-112-tri-tail

  • CAS No. 1381861-96-6

  • Cat. No. CS-0435691
  • Purity≥98%
  • MDL No.MFCD22574826

*For research and further manufacturing use only, not for direct human use.

C13-112-tri-tail|CS-0435691

Structure of 1381861-96-6

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General Information

  • CAS No. 1381861-96-6
  • Cat. No. CS-0435691
  • Purity ≥98%
  • MDL No. MFCD22574826
  • Storage Sealed in dry,2-8℃
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₄₅H₉₄N₂O₅
  • Molecular Weight 743.24
  • Synonym(s) None
  • SMILES CCCCCCCCCCCC(O)CN(CC(O)CCCCCCCCCCC)CCOCCOCCNCC(O)CCCCCCCCCCC

Description

Sodium lauroyl sarcosinate, the sodium salt of an acyl derivative of sarcosinea natural amino acid occurring in muscles and body tissuesstands out as a valuable component in molecular biology, biochemical, and cell biology research. Derived from a natural fatty acid and the amino acid derivative sarcosine, N-Lauroylsarcosine is a biodegradable anionic surfactant usually synthesized through acylation and neutralization reactions involving lauric acid and sodium sarcosine.This amino acid-type anionic surfactant, also recognized as a fatty acid amide and detergent, exhibits protein denaturant potency and has been integrated into lysing solutions, such as the cornet assay. Its application extends to lysing protoplasts for chromosomal DNA isolation from Streptococcus mutans. Notably, Lauroylsarcosine Sodium Salt, characterized by its ionic detergent properties, is commonly employed for purifying membrane proteins. Additionally, Sodium Lauroyl Sarcosine also plays a crucial role in concentrated salt solutions, facilitating cell lysis in RNA purification protocols and membrane solubilization. Whether its breaking down cell structures or facilitating membrane protein purification, this mild surfactant proves valuable in various applications within the realms of biology and biochemistry.Suitable forsolubilization and separation of membrane proteinslysis of cells during the isolation of RNA inhibition of hexokinase

Safety Information

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Computational Chemistry Data

  • TPSA   94.42
  • LogP   10.7566
  • H_Acceptors   7
  • H_Donors   4
  • Rotatable_Bonds   45

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