504-63-2
504-63-2
Chemical Structure
1,3-Propanediol
- CAS No.: 504-63-2
- Formula:C3H8O2
- Molecular Weight:76.09
IUPAC Name: propane-1,3-diol
InChIKey: YPFDHNVEDLHUCE-UHFFFAOYSA-N
SMILES: OCCCO
Biological Activity: 1,3-Propanediol is a versatile plant-derived humectant and solvent. 1,3-Propanediol can be produced by Klebsiella pneumoniae via glycerol fermentation, with the highest yield under anaerobic conditions. 1,3-Propanediol serves as a solvent and stabilizer in film preparation processes[1][2].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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1,3-Propanediol | 98.82% | 1,3-Propanediol is a versatile plant-derived humectant and solvent. 1,3-Propanediol can be produced by Klebsiella pneumoniae via glycerol fermentation, with the highest yield under anaerobic conditions. 1,3-Propanediol serves as a solvent and stabilizer in film preparation processes. | ||||||||||||||||||||
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1,3-Propanediol (Standard) | 99.92% | 1,3-Propanediol (Standard) is the analytical standard of 1,3-Propanediol. This product is intended for research and analytical applications. 1,3-Propanediol is produced in nature by the fermentation of glycerol in microorganism, which has orally active. | ||||||||||||||||||||
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1,3-Propanediol-d6 | 99.62% | 1,3-Propanediol-d6 is the deuterium labeled 1,3-Propanediol. 1,3-Propanediol is produced in nature by the fermentation of glycerol in microorganism. | ||||||||||||||||||||
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1,3-Propanediol-d8 | 98.9% | 1,3-Propanediol-d8 is the deuterium labeled 1,3-Propanediol. 1,3-Propanediol is produced in nature by the fermentation of glycerol in microorganism. | ||||||||||||||||||||
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Diethylene glycol (Standard) | 99.94% | Diethylene glycol (Standard) is the analytical standard of Diethylene glycol. This product is intended for research and analytical applications. 2,2'-Oxybis(ethan-1-ol) (DIETHYLENE GLYCOL) has excellent solubility and reactivity in certain chemical reactions and can help accelerate the activation of certain reactants. In addition, it is widely used in the production process of pigments, resins and other chemicals. Although the compound has no direct medical application, it has wide applications in chemical research and industrial production. | ||||||||||||||||||||
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3-Bromopropan-1-ol | 98.60% | 3-Bromopropan-1-ol is an endogenous metabolite. 3-Bromopropan-1-ol is significantly up-regulated during the estrous period of buffaloes. 3-Bromopropan-1-ol acts as an alkylating agent. 3-Bromopropan-1-ol participates in the enantioselective synthesis of nornicotine enantiomers. 3-Bromopropan-1-ol can be used in studies related to estrus detection in buffaloes. | ||||||||||||||||||||
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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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3-Iodopropan-1-ol | 98.64% | 3-Iodopropan-1-ol (3-Iodopropan-1-ol) is a PROTAC linker that can be used in the synthesis of PROTACs. | ||||||||||||||||||||
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3-Mercapto-1-propanol | 99.72% | 3-Mercapto-1-propanol can be used for the preparation of hydrophilic self-assembled monolayers and as a non-marking linker molecule for chemical and enzymatic synthesis of oligosaccharides. | ||||||||||||||||||||
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3-Aminopropan-1-ol | 99.76% | 3-Aminopropan-1-ol is both a primary amine and a primary alcohol, and it is widely used as a versatile chemical building block and molecular linker. | ||||||||||||||||||||
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Ethylene glycol,98% | 99.90% | Ethylene glycol is an organic compound that is often used as an antifreeze agent and coolant. Ethylene glycol lowers the freezing point by forming hydrogen bonds with water molecules, exerting antifreeze activity. Ethylene glycol is also used as a raw material in the synthesis of polymers such as polyester fibers and polyurethanes. | ||||||||||||||||||||
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Ethylene glycol-13C2 | 99.9% | Ethylene glycol-13C2 is the 13C labeled Ethylene glycol. | ||||||||||||||||||||
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References
- [1]. Gingell R, et al. Subchronic Toxicity Study of 1,3-Propanediol Administered Orally to Rats. International Journal of Toxicology. 2000;19(1):27-32.
- [2]. Dong, J., et al. Untargeted Metabolomics Analysis on the Effect of Ventilation on the Production of 1,3-Propanediol by Klebsiella pneumoniae. Appl Biochem Microbiol 61, 266-276 (2025).
