23526-45-6 P86438KC5J Vomifoliol, (+-)- UNII-P86438KC5J (+-)-Blumenol A (+-)-Vomifoliol (6S,7E,9R)-6,9-dihydroxy-4,7-megastigmadien-3-one (6S,9R)-6-Hydroxy-3-oxo-alpha-ionol (6S,9R)-Vomifoliol 2-Cyclohexen-1-one, 4-hydroxy-4-((1E,3R)-3-hydroxy-1-buten-1-yl)-3,5,5-trimethyl-, (4S)- 2-Cyclohexen-1-one, 4-hydroxy-4-((1E,3R)-3-hydroxy-1-butenyl)-3,5,5-trimethyl-, (4S)- 2-Cyclohexen-1-one, 4-hydroxy-4-(3-hydroxy-1-butenyl)-3,5,5-trimethyl-, (+-)- 2-Cyclohexen-1-one, 4-hydroxy-4-(3-hydroxy-1-butenyl)-3,5,5-trimethyl-, (S-(R*,S*-(E)))- Roseoside aglycon Vomifoliol CAS 23526-45-6

Purity 97%+In StockPharmaceutical Standards
CAS No.23526-45-6
Molecular FormulaC13H20O3
Molecular Weight224.30 g/mol
CategoryPharmaceutical Standards / API Standards
AvailabilityIn Stock

Chemical Structure

23526-45-6
P86438KC5J
Vomifoliol, (+-)-
UNII-P86438KC5J
(+-)-Blumenol A
(+-)-Vomifoliol
(6S,7E,9R)-6,9-dihydroxy-4,7-megastigmadien-3-one
(6S,9R)-6-Hydroxy-3-oxo-alpha-ionol
(6S,9R)-Vomifoliol
2-Cyclohexen-1-one, 4-hydroxy-4-((1E,3R)-3-hydroxy-1-buten-1-yl)-3,5,5-trimethyl-, (4S)-
2-Cyclohexen-1-one, 4-hydroxy-4-((1E,3R)-3-hydroxy-1-butenyl)-3,5,5-trimethyl-, (4S)-
2-Cyclohexen-1-one, 4-hydroxy-4-(3-hydroxy-1-butenyl)-3,5,5-trimethyl-, (+-)-
2-Cyclohexen-1-one, 4-hydroxy-4-(3-hydroxy-1-butenyl)-3,5,5-trimethyl-, (S-(R*,S*-(E)))-
Roseoside aglycon
Vomifoliol CAS 23526-45-6 chemical structure

Description

Based on its molecular formula C13H20O3, 23526-45-6 P86438KC5J Vomifoliol, (+-)- UNII-P86438KC5J (+-)-Blumenol A (+-)-Vomifoliol (6S,7E,9R)-6,9-dihydroxy-4,7-megastigmadien-3-one (6S,9R)-6-Hydroxy-3-oxo-alpha-ionol (6S,9R)-Vomifoliol 2-Cyclohexen-1-one, 4-hydroxy-4-((1E,3R)-3-hydroxy-1-buten-1-yl)-3,5,5-trimethyl-, (4S)- 2-Cyclohexen-1-one, 4-hydroxy-4-((1E,3R)-3-hydroxy-1-butenyl)-3,5,5-trimethyl-, (4S)- 2-Cyclohexen-1-one, 4-hydroxy-4-(3-hydroxy-1-butenyl)-3,5,5-trimethyl-, (+-)- 2-Cyclohexen-1-one, 4-hydroxy-4-(3-hydroxy-1-butenyl)-3,5,5-trimethyl-, (S-(R*,S*-(E)))- Roseoside aglycon Vomifoliol contains a carboxylic acid group, a hydroxyl group, an ether linkage, an aromatic ring system; these features give the compound characteristic absorption bands in UV spectroscopy. The molecular weight of 224.30 g/mol is directly relevant to the identification of the molecular ion in mass spectrometry. The aromatic system may exhibit native fluorescence, enabling detection with a fluorescence detector (FLD).

CATO supplies 23526-45-6 P86438KC5J Vomifoliol, (+-)- UNII-P86438KC5J (+-)-Blumenol A (+-)-Vomifoliol (6S,7E,9R)-6,9-dihydroxy-4,7-megastigmadien-3-one (6S,9R)-6-Hydroxy-3-oxo-alpha-ionol (6S,9R)-Vomifoliol 2-Cyclohexen-1-one, 4-hydroxy-4-((1E,3R)-3-hydroxy-1-buten-1-yl)-3,5,5-trimethyl-, (4S)- 2-Cyclohexen-1-one, 4-hydroxy-4-((1E,3R)-3-hydroxy-1-butenyl)-3,5,5-trimethyl-, (4S)- 2-Cyclohexen-1-one, 4-hydroxy-4-(3-hydroxy-1-butenyl)-3,5,5-trimethyl-, (+-)- 2-Cyclohexen-1-one, 4-hydroxy-4-(3-hydroxy-1-butenyl)-3,5,5-trimethyl-, (S-(R*,S*-(E)))- Roseoside aglycon Vomifoliol (CAS 23526-45-6), a certified reference material (molecular formula C13H20O3, MW 224.30 g/mol) for analytical method development and quality control.

This reference standard is suitable for quantitative analysis on major chromatographic platforms including HPLC, GC, LC-MS/MS, and GC-MS, serving as an external calibration standard or a system suitability test reference material.

The assigned purity is verified by mass-balance and quantitative NMR (qNMR) approaches, with the expanded uncertainty reported at a 95% confidence level (k=2). Batch homogeneity and stability are independently assessed for every lot.

Physical & Chemical Properties

Molecular FormulaC13H20O3
Molecular Weight224.30 g/mol
AppearanceOff-white to pale yellow crystalline powder
Purity97%+
StorageStore in a cool place (≤25°C), keep sealed and dry
Solubility (reference)Soluble in chloroform, dichloromethane, ethyl acetate, DMSO
StabilityMay oxidize slowly on prolonged air exposure; Hygroscopic; reseal immediately after opening
Degree of Unsaturation (DBE)4.0
UV AbsorptionUV-absorbing
Structural FeaturesAromatic ring present
CAS Registry Year (est.)1963

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