3,4-Dimethoxybenzyl Alcohol
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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.
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Cell Rep.2020, 32(11):108158.
Plant Physiol Biochem.2023, 202:107913.
Microchemical Journal2024: 196:109676.
Malaysian Journal of Analytical Sciences2022, 26(2):360-369.
J Biochem Mol Toxicol.2021, 35(5):e22731.
Molecules.2021, 26(4):817.
Enzyme Microb Technol.2019, 122:64-73
Phytochemistry.2024, 222:114102.
Wageningen University & Research2018, January 2018
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FEBS Lett. 1987 Sep 14;221(2):327-31.
Regiospecific oxygenations during ring cleavage of a secondary metabolite, 3,4-dimethoxybenzyl alcohol catalyzed by lignin peroxidase.[Pubmed:
3622773]
METHODS AND RESULTS:
Enzymatic oxidation of veratryl alcohol yielded a new ring cleavage product (delta-lactone) in addition to the two known gamma-lactone products. The experiment with 18O-enriched water and dioxygen clearly showed that one oxygen atom each from water and dioxygen is specifically incorporated into the cleavage product at the original C3 or C4 position of 3,4-Dimethoxybenzyl Alcohol.
CONCLUSIONS:
A new type of reaction mechanism proposed for the ring cleavage of this compound is rationally explained in good accord with the one-electron transfer mechanism.
