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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Undecane-1,11-diol | 99.72% | Undecane-1,11-diol (1,11-Undecanediol) is a PROTAC linker that can be used in the synthesis of PROTACs. | ||||||||||||||||||||
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Nonanol (Standard) | ≥98% | Nonanol (Standard) is the analytical standard of Nonanol (HY-W008816). This product is intended for research and analytical applications. Nonan-1-ol is an organic compound commonly used in the manufacture of surfactants and lubricants, among others. It can be used as a detergent, emulsifier and stabilizer, and is widely used in some cosmetics, personal care products and printing inks. In addition, the compound has important applications in certain industrial fields, for example in the production of plastics and rubber. | ||||||||||||||||||||
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Hexane-1,6-diol | 99.86% | Hexane-1,6-diol is a 6-carbon straight-chain diol with hydroxyl groups at both ends. Hexane-1,6-diol can be used as an additive for drilling fluids. Hexane-1,6-diol can also be used as a substrate in life science-related research. | ||||||||||||||||||||
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1,7-Heptanediol | 99.53% | 1,7-Heptanediol is a PROTAC linker that can be used in the synthesis of PROTACs. | ||||||||||||||||||||
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8-Chlorooctan-1-ol | 8-Chlorooctan-1-ol is a PROTAC linker that can be used in the synthesis of PROTACs. | |||||||||||||||||||||
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1,10-Decanediol | 99.95% | 1,10-Decanediol is a diol compound that can react with α-ketoglutarate (aKG) to generate polymeric microparticles (termed paKG MPs) for the sustained release of aKG, thereby promoting immunosuppressive regulation. Additionally, paKG MPs can bind to dendritic cells (DCs), reducing their glycolysis and mitochondrial respiration in vitro. These metabolic changes lead to the modulation of MHC-II and CD86 expression in DCs and alter the frequency of regulatory T cells (Tregs) as well as T-helper type 1/2/17 cells in vitro. 1,10-Decanediol can be used in research within the field of immunometabolism. can be used as a surfactant/stabilizer in the synthesis of nanomaterials. | ||||||||||||||||||||
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8-Amino-1-octanol | 99.97% | 8-Amino-1-octanol (NH2-(CH2)7-COOH) is a PROTAC linker that can be used in the synthesis of PROTACs. | ||||||||||||||||||||
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4,4'-Oxybis(butan-1-ol) | 4,4'-Oxybis(butan-1-ol) (Oxybisbutanol) is a PROTAC linker that can be used in the synthesis of PROTACs. | |||||||||||||||||||||
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Nonane-1,9-diol | 99.57% | Nonane-1,9-diol is a straight-chain aliphatic diol and can be used as a drug intermediate. | ||||||||||||||||||||
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8-Bromooctan-1-ol | 98.36% | 8-Bromooctan-1-ol (8-Bromo-1-octanol) is a PROTAC linker that can be used in the synthesis of PROTACs. | ||||||||||||||||||||
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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.
