| Bioactivity | 10-Undecen-1-ol, converted from ricinoleic acid, can be used as a comonomer for the introduction of functional groups[1][2]. |
| Invitro | Cobalt-catalyzed step growth polymerization of undec-10-en-1-ol and CO affords aliphatic polyesters (Mn 104 g/mol) based entirely on renewable resources[1]. |
| Name | 10-Undecen-1-ol |
| CAS | 112-43-6 |
| Formula | C11H22O |
| Molar Mass | 170.29 |
| Appearance | Liquid |
| Transport | Room temperature in continental US; may vary elsewhere. |
| Storage | 4°C, stored under nitrogen *In solvent : -80°C, 6 months; -20°C, 1 month (stored under nitrogen) |
| Reference | [1]. Quinzler D, et al. Renewable resource-based poly(dodecyloate) by carbonylation polymerization. Chem Commun (Camb). 2009;(36):5400-5402. [2]. Jonas U. A, et al. Functional Beads of Polyvinylpyrrolidone: Promising Support Materials for Solid‐Phase Synthesis. |