2,3,4-Tri-O-acetyl-alpha-D-glucuronic acid methyl ester is a fully acetylated glucuronic acid derivative featuring three acetyl groups at the 2, 3, and 4 positions of the pyranose ring, with the anomeric center in the alpha configuration and a methyl ester substituent at the carboxylic acid terminus. This compound arises as a synthetic byproduct during the acetylation of glucuronic acid derivatives, commonly encountered in the production of glycoside-based APIs. Its distinct regiochemistry and ester functionality enable its use as an HPLC reference standard for impurity profiling in parent drug manufacturing.
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InChI=1S/C15H18Cl3NO10/c1-5(20)25-8-9(26-6(2)21)11(27-7(3)22)13(28-10(8)12(23)24-4)29-14(19)15(16,17)18/h8-11,13,19H,1-4H3/t8-,9-,10-,11+,13+/m0/s1
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