Informations sur le produit
- 2-({[2-(Acetyloxy)Phenyl]Carbonyl}Oxy)Benzoate
- 2-Carboxyphenyl 2-(acetyloxy)benzoate
- 2-[(2-Acetoxybenzoyl)oxy]benzoic acid
- 2-{[2-(Acetyloxy)Benzoyl]Oxy}Benzoic Acid
- Acesalum
- Acetylsalicylsalicylic acid
- Benzoic acid, 2-(acetyloxy)-, 2-carboxyphenyl ester
- Ccris 1740
- Diplosal acetate
- Diplosalacetat
- Voir d'autres synonymes
- Salicylacetylsalicylic acid
- Salicylic acid, salicylate, acetate
Aspirin Impurity D is an impurity that occurs in the synthesis of aspirin. It is a by-product of the acid catalyzed esterification reaction between acetylsalicylic acid and acetic anhydride. This impurity is characterized by its solubility in organic solvents, high UV absorption at 230 nm, and chemical stability to acids. Aspirin Impurity D has been shown to cause autoimmune diseases in rats and cancer in mice when injected intraperitoneally with a dose of 0.5 mg/kg. The target tissue for this impurity is unknown, but it may be due to its lipophilic nature. Aspirin Impurity D can be detected by chromatography with a column of silica gel or alumina as stationary phase and a mobile phase consisting of methanol/chloroform/water (4:4:6).
Propriétés chimiques
Question d’ordre technique sur : 3D-AAA53075 Aspirin Impurity D
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