629-41-4
629-41-4
Chemical Structure
1,8-Octanediol
- CAS No.: 629-41-4
- Formula:C8H18O2
- Molecular Weight:146.23
IUPAC Name: octane-1,8-diol
InChIKey: OEIJHBUUFURJLI-UHFFFAOYSA-N
SMILES: OCCCCCCCCO
Biological Activity: 1,8-Octanediol is an aliphatic diol and also a monomer used in the synthesis of polyesters and polyurethanes. As a monomer, 1,8-Octanediol participates in the lipase-catalyzed bulk polycondensation with adipic acid for the synthesis of aliphatic polyesters. 1,8-Octanediol can be applied in relevant studies in fields such as material synthesis[1][2][3].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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1,8-Octanediol | 99.96% | 1,8-Octanediol is an aliphatic diol and also a monomer used in the synthesis of polyesters and polyurethanes. As a monomer, 1,8-Octanediol participates in the lipase-catalyzed bulk polycondensation with adipic acid for the synthesis of aliphatic polyesters. 1,8-Octanediol can be applied in relevant studies in fields such as material synthesis. | ||||||||||||||||||||
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1,8-Octanediol-d12 | 99.67% | 1,8-Octanediol-d12 is the deuterated-labeled 1,8-Octanediol (HY-W017508). 1,8-Octanediol is an aliphatic diol and also a monomer used in the synthesis of polyesters and polyurethanes. As a monomer, 1,8-Octanediol participates in the lipase-catalyzed bulk polycondensation with adipic acid for the synthesis of aliphatic polyesters. 1,8-Octanediol can be applied in relevant studies in fields such as material synthesis. | ||||||||||||||||||||
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References
- [1]. Shou Y F, et al. Toward Renewable and Functional Biomedical Polymers with Tunable Degradation Rates Based on Itaconic Acid and 1,8-Octanediol. ACS Applied Polymer Materials, 2021, 3(4): 1943-1955.
- [2]. Mahapatro A, et al. Solvent-Free Adipic Acid/1,8-Octanediol Condensation Polymerizations Catalyzed by Candida antarctica Lipase B. Macromolecules, 2004, 37(1): 35-40.
- [3]. García-Argüelles S, et al. Deep Eutectic Solvent-Assisted Synthesis of Biodegradable Polyesters with Antibacterial Properties. Langmuir, 2013, 29(30): 9525-9534.
