43623

β-Sitosterol

analytical standard

• Sinónimos: α-Dihydrofucosterol, 22,23-Dihydrostigmasterol, 24α-Ethylcholesterol, 5-Stigmasten-3β-ol
• Fórmula empírica (notación de Hill): C₂₉H₅₀O
• Número de CAS: 83-46-5
• Peso molecular: 414.71
• Beilstein: 1916165
• Número CE: 201-480-6
• Número MDL: MFCD00003631
• Código UNSPSC: 12352104
• ID de la sustancia en PubChem: 329756360
• NACRES: NA.24

Propiedades

• grado: analytical standard
• Nivel de calidad: 100
• Análisis: ≥90.0% (GC)
• caducidad: limited shelf life, expiry date on the label
• técnicas: HPLC: suitable; gas chromatography (GC): suitable
• impurezas: ≤10.0% water
• mp: 136-140 °C (lit.)
• aplicaciones: food and beverages
• formato: neat
• temp. de almacenamiento: 2-8°C
• cadena SMILES: O[C@H](C1)CC[C@@]2(C)C1=CC[C@]3([H])[C@]2([H])CC[C@@]4(C)[C@@]3([H])CC[C@]4([H])[C@H](C)CC[C@H](C(C)C)CC
• InChI: 1S/C29H50O/c1-7-21(19(2)3)9-8-20(4)25-12-13-26-24-11-10-22-18-23(30)14-16-28(22,5)27(24)15-17-29(25,26)6/h10,19-21,23-27,30H,7-9,11-18H2,1-6H3/t20-,21-,23+,24+,25-,26+,27+,28+,29-/m1/s1
• Clave InChI: KZJWDPNRJALLNS-VJSFXXLFSA-N

Descripción

Descripción general

β-Sitosterol is an abundantly found phytosterol in plants. It is known to show anti-inflammatory, immune-modulating, antipyretic, antineoplastic, and blood sugar-controlling properties. β-Sitosterol also acts as an estrogen and estrogen receptor (ERα and Erβ) agonist.

Aplicación

This analytical standard can also be used as follows:

• Identification and determination of β-sitosterol and stigmasterol in the hydro-alcohol extract, prepared from the leaves of B. bambo by reversed-phase high-performance liquid chromatography (RP-HPLC) coupled to photo-diode array detector (PDA)
• Development and validation of two high-performance thin layer chromatography (HPTLC) methods to quantify four biomarkers— β-sitosterol, β-amyrin, lupeol, and ursolic acid in the ethanol extract of G. senegalensis leaves
• Secondary metabolite profiling of various plant parts collected from 82 plants belonging to 21 different cannabis strains using gas chromatography-mass spectrometry (GC-MS) for sterols and terpenoids (mono-, sesqui-, tri-), and high-performance liquid chromatography (HPLC) with UV and mass spectrometric (MS) detection for flavonoids
• High-performance thin layer chromatographic (HPTLC) method-based quantification of β-sitosterol in a herbal formulation prepared from the roots of Gmelina arborea using silica gel precoated 60 F₂₅₄ aluminum plates
• Determination of free sterols or oxysterols in food matrices, using gas chromatography and ion trap mass spectrometry (GC-MS).

Envase

Bottomless glass bottle. Contents are inside inserted fused cone.

Otras notas

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Información de seguridad

• Código de clase de almacenamiento: 11 - Combustible Solids
• Clase de riesgo para el agua (WGK): WGK 3
• Punto de inflamabilidad (°F): Not applicable
• Punto de inflamabilidad (°C): Not applicable