Related Experiment Video
Updated: May 16, 2025

Standardized Identification of Compound Structure in Tibetan Medicine Using Ion Trap Mass Spectrometry and Multiple-Stage Fragmentation Analysis
Published on: March 17, 2023
Brominated 3-Acetyl-11-keto-β-boswellic Acid Derivative from Boswellia serrata Extract Characterized by
Masataka Ito1, Keisuke Misao1, Hironori Suzuki1
1Faculty of Pharmaceutical Sciences, Toho University, 2-2-1 Miyama, Funabashi, Chiba 274-8510, Japan.
Frankincense contains 3-acetyl-11-keto-β-boswellic acid. Researchers discovered a brominated derivative of this compound in Boswellia serrata extracts, offering new insights into its chemical properties.
Area of Science:
- Natural Product Chemistry
- Organic Chemistry
- Structural Biology
Background:
- 3-Acetyl-11-keto-β-boswellic acid is a key pentacyclic triterpenoid found in frankincense resin.
- Boswellia species, particularly Boswellia serrata, are known sources of bioactive compounds.
Purpose of the Study:
- To elucidate the crystal structure of 3-acetyl-11-keto-β-boswellic acid solvates.
- To identify and characterize related compounds present in Boswellia serrata extracts.
Main Methods:
- Single crystal X-ray diffraction analysis.
- Mass spectroscopy.
- Extraction from Boswellia serrata.
Main Results:
- Single crystals of 3-acetyl-11-keto-β-boswellic acid methanol and acetonitrile solvates were successfully obtained.
- X-ray analysis revealed the presence of a novel brominated derivative: 3-acetyl-11-keto-12-bromo-β-boswellic acid.
- Mass spectrometry confirmed the existence of this brominated compound in the plant extract.
Conclusions:
- The findings provide a detailed structural understanding of 3-acetyl-11-keto-β-boswellic acid and its derivatives.
- This structural information may offer insights into the chemical reactivity and biosynthesis pathways within Boswellia serrata.
More Related Videos
Related Concept Videos
High-Resolution Mass Spectrometry (HRMS)
NMR and Mass Spectroscopy of Carboxylic Acids
While α protons of carboxylic acids absorb at 2–2.5 ppm, β protons absorb further upfield.
Carboxylic acids are easily identified by dissolving them in deuterium oxide, which results in a rapid exchange of the acidic protons with deuterium. This leads to the...
Spectroscopy of Carboxylic Acid Derivatives
NMR Spectroscopy of Benzene Derivatives
NMR Spectroscopy and Mass Spectrometry of Aldehydes and Ketones
Mass Spectrometry: Aromatic Compound Fragmentation

