The crystal structure and physicochemical properties of l-ascorbic acid 2-glucoside
β Scribed by Takahiko Mandai; Masaru Yoneyama; Shuzo Sakai; Norio Muto; Itaru Yamamoto
- Publisher
- Elsevier Science
- Year
- 1992
- Tongue
- English
- Weight
- 497 KB
- Volume
- 232
- Category
- Article
- ISSN
- 0008-6215
No coin nor oath required. For personal study only.
β¦ Synopsis
The stable L-ascorbic acid glucoside produced by the action of the cyclomaltodextrin glucanotransferase (CGTase, EC 2.4.1.19) from Bacillus stearothermophilus was crystallized from an aqueous solution. Determination of the molecular structure by single crystal X-ray analysis showed the compound to be 2-O-alpha-D-glucopyranosyl-L-ascorbic acid (AA-2G). The crystals are orthorhombic, space group P2(1)2(1)2(1), with unit-cell dimensions a = 11.929 A, b = 24.351 A, and c = 4.864 A. The D-glucopyranose residue has the 4C1 conformation. These conclusions are in good agreement with those based on the 13C-NMR spectrum. The general physicochemical properties of crystalline AA-2G are reported.
π SIMILAR VOLUMES
Chemistry of L-Ascorbic Acid. Part 2. The Paterno-Buechi Reaction of L-Ascorbic Acid. -The Paterno-Buechi reaction of protected ascorbic acid is investigated and applied to the synthesis of ketohexose derivatives like (VI). -(THOPATE,
## Abstract In this study, the process of manufacturing and sterilizing an orthopedic implant constructed from poly(Lβlactic acid) (PLLA) was closely simulated. The hydrogen peroxide gas plasma (HPGP) sterilization process was comparatively investigated against ethylene oxide (EtO). Characterizatio