Abstract
Aminodeoxycelluloses and 6-amino-6-deoxystarch were sulfated with N,N-dimethylformamide-sulfur trioxide complex in order to obtain heparin-like anticoagulant molecules. Sulfated products obtained had a degree of substitution (DS) by the sulfate group, ca. 1.0. I.r spectra showed that the chemical structures of sodium 6-amino-6-deoxycellulose sulfate, sodium 2-amino-2-deoxycellulose sulfate, and sodium 6-amino-6-deoxystarch sulfate were similar to that of sodium heparinate. © 1980, The Society of Fiber Science and Technology, Japan. All rights reserved.
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CITATION STYLE
Teshirogi, T., Yamamoto, H., Sakamoto, M., & Tonami, H. (1980). Preparation of sulfated aminodeoxycelluloses. Sen’i Gakkaishi, 36(12), T560–T563. https://doi.org/10.2115/fiber.36.12_T560
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