ChemFaces is a professional high-purity natural products manufacturer.
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1. Reference standards
2. Pharmacological research
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More articles cited ChemFaces products.
J Breast Cancer2015 Jun;18(2):112-118.Naunyn Schmiedebergs Arch Pharmacol. 2017 Jul 21. Phytomedicine.2018 Jan 1;Food Research InternationalJan. 2016Tumour Biol.2015 Jun 26
Kor. J. Pharmacogn.47(1):62-72(2016)Evid Based Complement Alternat Med. 2018;Cell Physiol Biochem. 2017;44(4);Mol Cell2017 Nov 16;Acta Pharmaceutica Sinica B2015 Apr.7.
Phytomedicine2015 March 20.Sci Rep. Jan. 2018Molecules 2016, 21(6), 739;2016 Jun 14;21(6). BMC Complement Altern Med.2017 Aug 9;
Our products had been exported to the following research institutions and universities, And still growing.
Wroclaw Medical University (Poland)Institute of Bioorganic Chemistr... (Poland)Florida A&M University (USA)Macau University of Science and ... (China)
Universita' Degli Studi Di Cagli... (Italy)Donald Danforth Plant Science Ce... (USA)Cancer Research Initatives Found... (Malaysia)University of Limpopo (South Africa)
Instituto Politécnico de Bragan?a (Portugal)University of Wollongong (Australia)University of Zurich (Switzerland)
3,4-Dimethoxybenzyl Alcohol Description
||The roots of Beta vulgaris
||Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
||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: email@example.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.
Recent ChemFaces New Products and Compounds
Recently, ChemFaces products have been cited in many studies from excellent and top scientific journals
Cell. 2018 Jan 11;172(1-2):249-261.e12. doi: 10.1016/j.cell.2017.12.019.PMID: 29328914
Mol Cell. 2017 Nov 16;68(4):673-685.e6. doi: 10.1016/j.molcel.2017.10.022.PMID: 29149595
Scientific Reports 2017 Dec 11;7(1):17332.doi: 10.1038/s41598-017-17427-6.PMID: 29230013
Molecules. 2017 Oct 27;22(11). pii: E1829.doi: 10.3390/molecules22111829.PMID: 29077044
J Cell Biochem. 2018 Feb;119(2):2231-2239.doi: 10.1002/jcb.26385. PMID: 28857247
Phytomedicine. 2018 Feb 1;40:37-47. doi: 10.1016/j.phymed.2017.12.030.PMID: 29496173
Calculate Dilution Ratios(Only for Reference)
* Note: If you are in the process of experiment, it's need to make the dilution ratios of the samples. The dilution data of the sheet for your reference. Normally, it's can get a better solubility within lower of Concentrations.
|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.
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.