3-Octyl alcohol
Reference standards.
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Providing storage is as stated on the product vial and the vial is kept tightly sealed, the product can be stored for up to
24 months(2-8C).
Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20C. Generally, these will be useable for up to two weeks. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour.
Need more advice on solubility, usage and handling? Please email to: service@chemfaces.com
The packaging of the product may have turned upside down during transportation, resulting in the natural compounds adhering to the neck or cap of the vial. take the vial out of its packaging and gently shake to let the compounds fall to the bottom of the vial. for liquid products, centrifuge at 200-500 RPM to gather the liquid at the bottom of the vial. try to avoid loss or contamination during handling.
Nat Commun.2021, 12(1):681.
Molecules.2015, 20(10):19172-88
Phytomedicine.2019, 59:152785
Vietnam Journal of Science2022, 64(2), 69-75.
LWT2024, v208:116677
Molecules.2020, 25(18),4089.
Foods.2022, 12(1):136.
Industrial Crops and Products2020, 146:112186
J Microbiol Biotechnol.2024, 35:e2408022.
Nat Commun.2023 Dec 20;14(1):8457.
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Chemistry of Heterocyclic Compounds, 1979, 15(5):496-498.
Reaction of 3-methyl-2,3-epoxysulfolane with alcohols.[Reference:
WebLink]
METHODS AND RESULTS:
The corresponding dialkyl ethers of 3-methylsulfolane-2,3-diol are formed by the action of alcohols (methanol, ethanol, n-propyl alcohol, isopropyl alcohol, isobutyl alcohol, and n-octyl alcohol) on 3-methyl-2,3-epoxysulfolane in an acidic medium. The reaction proceeds through the intermediate formation of monoethers with subsequent etherification of the hydroxyl group by a second molecule of alcohol.
