| Bioactivity | 1,4-Benzenediacetic acid (Compound 13, p-Phenylenediacetic acid) is an eluent, which is produced by the direct carbonylation of difunctional alcohols 1,2- and 1, 4-benzenediethanol and 2-hydroxybenzenemethanol[1][2]. | ||||||||||||
| CAS | 7325-46-4 | ||||||||||||
| Formula | C10H10O4 | ||||||||||||
| Molar Mass | 194.19 | ||||||||||||
| Appearance | 固体 | ||||||||||||
| Transport | Room temperature in continental US; may vary elsewhere. | ||||||||||||
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| Reference | [1]. Tamaya K, et al. Interpretation of solute retention of some monovalent inorganic anions in anion-exchange chromatography using a dicarboxylic Acid as an eluent. Anal Sci. 2006 May;22(5):715-9. [2]. Lin Y S, et al. Palladium-catalyzed carbonylation of benzyl alcohol and its analogs promoted by HI in aqueous systems[J]. Tetrahedron letters, 1997, 38(21): 3747-3750. |
1,4-Benzenediacetic acid
CAS: 7325-46-4 F: C10H10O4 W: 194.19
1,4-Benzenediacetic acid (Compound 13, p-Phenylenediacetic acid) is an eluent, which is produced by the direct carbonyla
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