1,2-Dimethoxybenzene
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.
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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.
Asian Journal of Chemistry2018, 30(12):2699-2703
Biomolecules.2021, 11(10):1537.
Neurochem Int.2023, 167:105537.
J Ethnopharmacol.2019, 244:112074
Molecules.2023, 28(4):1526.
J of l. Chroma.&Related Tech2020, 43(11-12):414-423.
Kor. J. Pharmacogn.2016, 47(1):62-72
Biochem Biophys Res Commun.2018, 505(4):1148-1153
Korean J of Pharmacognosy2020, 51,49-54.
Food Sci Nutr.2023, 00:1-10.
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Ozonolysis of Lignin Models in Aqueous Solution: Anisole, 1,2-Dimethoxybenzene, 1,4-Dimethoxybenzene, and 1,3,5-Trimethoxybenzene.[Reference:
WebLink]
METHODS AND RESULTS:
Selected 2-methoxyphenols,1,2-Dimethoxybenzenes,and 1,3-benzodioxoleswere tested in the field as attractants for the northern corn root worm (NCR), Diabrotica barberi Smith & Lawrence, in comparison with eugenol (4-allyl-2-methoxyphenol), isoeugenol (2- methoxy-4-(1-propenyl)phenol), and 2-methoxy-4-propylphenoI. Of these, 4-ethyl-2-methoxyphenol and 4-butyl-2-methoxyphenol showed relatively high degrees of attraction.
CONCLUSIONS:
Structural comparisons indicated that in a eugenol-type structure (i.e., a 1,2,4-trisubstituted benzene) a 4-alkyl substituent and a I-hydroxyl group are necessary features for attraction of the NCR. The optimal 4-alkyl chain length is a three-carbon chain.
