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3,4-Dimethoxybenzyl Alcohol

CAS# 93-03-8

3,4-Dimethoxybenzyl Alcohol

Catalog No. BCN2721----Order now to get a substantial discount!

Product Name & Size Price Stock
3,4-Dimethoxybenzyl Alcohol:5mg Please Inquire In Stock
3,4-Dimethoxybenzyl Alcohol:10mg Please Inquire In Stock
3,4-Dimethoxybenzyl Alcohol:20mg Please Inquire In Stock
3,4-Dimethoxybenzyl Alcohol:50mg Please Inquire In Stock

Quality Control of 3,4-Dimethoxybenzyl Alcohol

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Chemical structure

3,4-Dimethoxybenzyl Alcohol

3D structure

Chemical Properties of 3,4-Dimethoxybenzyl Alcohol

Cas No. 93-03-8 SDF Download SDF
PubChem ID 7118 Appearance Cryst.
Formula C9H12O3 M.Wt 168.19
Type of Compound Phenols Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name (3,4-dimethoxyphenyl)methanol
SMILES COC1=C(C=C(C=C1)CO)OC
Standard InChIKey OEGPRYNGFWGMMV-UHFFFAOYSA-N
General tips For obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while.Stock solution can be stored below -20℃ for several months.
We recommend that you prepare and use the solution on the same day. However, if the test schedule requires, the stock solutions can be prepared in advance, and the stock solution must be sealed and stored below -20℃. In general, the stock solution can be kept for several months.
Before use, we recommend that you leave the vial at room temperature for at least an hour before opening it.
About Packaging 1. The packaging of the product may be reversed during transportation, cause the high purity compounds to adhere to the neck or cap of the vial.Take the vail out of its packaging and shake gently until the compounds fall to the bottom of the vial.
2. For liquid products, please centrifuge at 500xg to gather the liquid to the bottom of the vial.
3. Try to avoid loss or contamination during the experiment.
Shipping Condition Packaging according to customer requirements(5mg, 10mg, 20mg and more). Ship via FedEx, DHL, UPS, EMS or other couriers with RT, or blue ice upon request.

Source of 3,4-Dimethoxybenzyl Alcohol

The roots of Beta vulgaris

Protocol of 3,4-Dimethoxybenzyl Alcohol

Structure Identification
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.

3,4-Dimethoxybenzyl Alcohol Dilution Calculator

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3,4-Dimethoxybenzyl Alcohol Molarity Calculator

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Preparing Stock Solutions of 3,4-Dimethoxybenzyl Alcohol

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 5.9457 mL 29.7283 mL 59.4566 mL 118.9131 mL 148.6414 mL
5 mM 1.1891 mL 5.9457 mL 11.8913 mL 23.7826 mL 29.7283 mL
10 mM 0.5946 mL 2.9728 mL 5.9457 mL 11.8913 mL 14.8641 mL
50 mM 0.1189 mL 0.5946 mL 1.1891 mL 2.3783 mL 2.9728 mL
100 mM 0.0595 mL 0.2973 mL 0.5946 mL 1.1891 mL 1.4864 mL
* Note: If you are in the process of experiment, it's necessary to make the dilution ratios of the samples. The dilution data above is only for reference. Normally, it's can get a better solubility within lower of Concentrations.

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References on 3,4-Dimethoxybenzyl Alcohol

Regiospecific oxygenations during ring cleavage of a secondary metabolite, 3,4-dimethoxybenzyl alcohol catalyzed by lignin peroxidase.[Pubmed:3622773]

FEBS Lett. 1987 Sep 14;221(2):327-31.

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.

Description

Veratryl alcohol (3,4-Dimethoxybenzenemethanol), a secondary metabolite of some lignin degrading fungi, is commonly used nonphenolic substrate for assaying ligninolytic activity.

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