Acacetin Chemical Identity
Acacetin (5,7-dihydroxy-4′-methoxyflavone, C16H12O5, molecular weight 284.26) is a flavone: the same three-ring skeleton as apigenin, but with a methoxy group in place of the hydroxyl on the B ring. That single methyl ether lowers polarity and changes metabolism and stability compared with apigenin. In wild chrysanthemum flowers acacetin is found mainly bound to sugar as linarin, the 7-O-rutinoside, and the free aglycone is obtained after the sugar is removed. The natural source is the flower of Chrysanthemum indicum L. (Asteraceae), the wild chrysanthemum, which is a different species from the cultivated C. morifolium. The same formula C16H12O5 is shared with biochanin A, an isoflavone, so mass alone cannot identify the compound. Buyers comparing neighboring products can look at wild chrysanthemum flower powder and Linarin 98%. The glycoside and the aglycone are different compounds with their own identifiers and solubility.
Specifications often mix up the compound with its glycoside. Linarin is acacetin carrying a rutinose sugar, so it is heavier, more polar and used as the marker for wild chrysanthemum in pharmacopoeial work. The acacetin 98% grade is the free flavone, and a purchase order should quote the CAS number 480-44-4 and the single-peak HPLC purity so that the two are not exchanged.












