SPATHULENOL CAS#6750-60-3

SPATHULENOL CAS#6750-60-3

Naturally Derived Sesquiterpenoid Compound: Spathulenol is a naturally occurring tricyclic sesquiterpenoid commonly found as a component of volatile oils and plant metabolites.


Multiple Biological Functions: The compound exhibits various biological activities, including anesthetic and vasodilatory properties.

Complex and Stable Chemical Structure: Its tricyclic molecular framework with hydroxyl and olefinic functional groups provides valuable chemical versatility for research applications.


Suitable for Pharmaceutical and Natural Product Research: Due to its diverse bioactive characteristics, Spathulenol is widely studied in phytochemical, pharmaceutical, and natural product research fields.



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Product Description

SPATHULENOL CAS#6750-60-3

Spathulenol is a tricyclic sesquiterpenoid compound identified as 4-methylidenedecahydro-1H-cyclopropa[e]azulene with three methyl substituents at the 1, 1, and 7 positions, along with a hydroxyl group at position 7. It functions as a component of volatile oils and a plant-derived metabolite, and has been reported to possess anesthetic and vasodilatory activities. Chemically, it belongs to the classes of sesquiterpenoids, carbotricyclic compounds, tertiary alcohols, and olefinic compounds.


Product Application of SPATHULENOL CAS#6750-60-3

Spathulenol is extracted from Aristolochia yunnanensis and exhibits multiple biological activities, including antioxidant, anti-inflammatory, antiproliferative, and antimycobacterial effects. It demonstrates strong antioxidant capacity, with an IC50 value of 85.60 μg/mL in the DPPH assay system.


Product Information

Parameters


Boiling point284.7 °C
density1.02±0.1 g/cm3(Predicted)
formLiquid
pka15.10±0.40(Predicted)
colorColorless to light yellow
Odorat 100.00 %. earthy herbal fruity
Odor Typeearthy
InChIInChI=1S/C15H24O/c1-9-5-6-11-13(14(11,2)3)12-10(9)7-8-15(12,4)16/h10-13,16H,1,5-8H2,2-4H3/t10-,11+,12+,13+,15-/m0/s1
InChIKeyFRMCCTDTYSRUBE-BGPZULBFSA-N
SMILESC1[C@]2([H])[C@]([H])([C@]3([H])C(C)(C)[C@]3([H])CCC2=C)[C@@](C)(O)C1
LogP4.406 (est)


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