HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1653660Generated: November 2, 2026
beta-Cyclodextrin → HCID 178473453, compound
https://huagongshe.com/reaction/1653660
Participants
| Role | Name | HCID | Charge |
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| Reactant | beta-Cyclodextrin | HCID 444041 | — |
| Reactant | HCID 178473452 | HCID 178473452 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178473453 | HCID 178473453 | — |
Reaction Steps
6.6 g of β-cyclodextrin (5 mmoles, content 14%) and 0.6 g (2.5 mmoles) of Molsidomin are homogenized in a friction mortar protected from light if possible. 3 ml of a 50% ethyl alcohol are added and the dense suspension is stirred for further 30 minutes after spreading the product of hard lubricity and paste like consistence on a watch-glass, it is dried to constant weight in the presence of phosphoruspentoxide in an exsiccator. The product obtained is pulverized, its active ingredient content is 9±0.5% determined by the spectrophotometric method, which corresponds to a molar ratio of about 1:2. DSC curves of Molsidomin, its mechanical mixture and its complex with β-CD are significantly different. The endothermic peak at 140°-142° C. on the DSC curve completely disappeared in the case of complexes with β-CD prepared by both kneading or liophylization. It indicates that the Molsidomin is complexed, and at 130°-160° C. temperature range not even a 50 fold magnified curve showed endothermic peak of melting in the case of complex prepared by lyophilization.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05403840 |
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| Source dataset | uspto-grants-1995_04 |
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| ORD ID | ord-e45c0fe0e313431b85a3e944093daacc |
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| Source note | uspto-grants-1995_04 |
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