3,5-Dimethoxybenzylalcohol
3,5-Dimethoxybenzylalcohol is a natural product from Pinus sylvestris.
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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.
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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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BioResources,2016,11(3):6232-43.
Experimental and Theoretical Studies on the Pyrolysis Mechanism of β-1-Type Lignin Dimer Model Compound[Reference:
WebLink]
A β-1-type lignin dimer, 1,2-bis(3,5-dimethoxyphenyl)propane-1,3-diol was employed as a model compound in this study.
METHODS AND RESULTS:
The pyrolysis mechanisms and formation pathways of the pyrolytic products were investigated by using density functional theory (DFT) calculations and analytical pyrolysis-gas chromatography/mass spectrometry (Py-GC/MS). Four possible initial pyrolysis mechanisms were proposed, including the Cα-Cβ homolysis mechanism and three concerted decomposition mechanisms (1, 2, and 3). Results indicated that the lignin dimer decomposed via two concerted decomposition mechanisms, forming 3,5-dimethoxybenzaldehyde, 1,3-dimethoxy-5-vinylbenzene, 3-hydroxy-5-methoxybenzaldehyde, and 3-methoxybenzaldehyde. 3,5-Dimethoxybenzaldehyde was the major product, accounting for greater than 50% of all pyrolytic products.
CONCLUSIONS:
In addition to the two concerted decomposition mechanisms, Cα-Cβ homolysis was a secondary pyrolysis mechanism during the lignin dimer pyrolysis process, and the pyrolytic products included 3,5-Dimethoxybenzylalcohol, 3,5-dimethoxyphenethyl alcohol, 1,3-dimethoxybenzene, and 1,3-dimethoxy-5-methylbenzene.
A third concerted decomposition mechanism was judged to be the least likely pathway to occur because of the high activation energy requirement.
