Atomfair Cholest-5-en-3-ol (3beta)-, nonanoate CE 9:0 C36H62O2

Description Cholest-5-en-3-ol (3beta)-, nonanoate (CAS 1182-66-7) is a high-purity sterol ester with the molecular formula C36H62O2. This compound, also known as [10,13-dimethyl-17-(6-methylheptan-2-yl)-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] nonanoate, is a derivative of cholesterol esterified with nonanoic acid. It is a valuable biochemical reagent used in lipid metabolism research, membrane studies, and as a reference standard in analytical applications. The product is rigorously tested for purity and stability, ensuring reproducibility in experimental settings. Available in various quantities, it is ideal for researchers in pharmaceuticals, biochemistry, and material science.

Description

Description

Cholest-5-en-3-ol (3beta)-, nonanoate (CAS 1182-66-7) is a high-purity sterol ester with the molecular formula C36H62O2. This compound, also known as [10,13-dimethyl-17-(6-methylheptan-2-yl)-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] nonanoate, is a derivative of cholesterol esterified with nonanoic acid. It is a valuable biochemical reagent used in lipid metabolism research, membrane studies, and as a reference standard in analytical applications. The product is rigorously tested for purity and stability, ensuring reproducibility in experimental settings. Available in various quantities, it is ideal for researchers in pharmaceuticals, biochemistry, and material science.

  • CAS No: 1182-66-7
  • Molecular Formula: C36H62O2
  • Molecular Weight: 526.9
  • Exact Mass: 526.47498122
  • Monoisotopic Mass: 526.47498122
  • IUPAC Name: [10,13-dimethyl-17-(6-methylheptan-2-yl)-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] nonanoate
  • SMILES: CCCCCCCCC(=O)OC1CCC2(C3CCC4(C(C3CC=C2C1)CCC4C(C)CCCC(C)C)C)C
  • Synonyms: Cholest-5-en-3-ol (3beta)-, nonanoate, Cholest-5-en-3-ol (3.beta.)-, nonanoate, [10,13-dimethyl-17-(6-methylheptan-2-yl)-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] nonanoate, CE 9:0, ChemDiv1_018734

Application

Cholest-5-en-3-ol (3beta)-, nonanoate is widely utilized in lipid research as a model sterol ester for studying enzymatic hydrolysis and lipid metabolism pathways. It serves as a substrate for cholesterol esterase and lipase assays, aiding in the investigation of enzyme kinetics. Additionally, this compound is employed in the formulation of lipid-based drug delivery systems due to its amphiphilic properties. Researchers also use it as a standard in chromatographic analysis to quantify sterol esters in biological samples.

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