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Methyl 2,4-dihydroxybenzoate

CAS# 2150-47-2

Methyl 2,4-dihydroxybenzoate

Catalog No. BCX0312----Order now to get a substantial discount!

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Chemical structure

Methyl 2,4-dihydroxybenzoate

3D structure

Chemical Properties of Methyl 2,4-dihydroxybenzoate

Cas No. 2150-47-2 SDF Download SDF
PubChem ID 16523 Appearance Powder
Formula C8H8O4 M.Wt 168.15
Type of Compound Phenols Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name methyl 2,4-dihydroxybenzoate
SMILES COC(=O)C1=C(C=C(C=C1)O)O
Standard InChIKey IIFCLXHRIYTHPV-UHFFFAOYSA-N
Standard InChI InChI=1S/C8H8O4/c1-12-8(11)6-3-2-5(9)4-7(6)10/h2-4,9-10H,1H3
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.

Methyl 2,4-dihydroxybenzoate Dilution Calculator

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Methyl 2,4-dihydroxybenzoate Molarity Calculator

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Preparing Stock Solutions of Methyl 2,4-dihydroxybenzoate

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 5.9471 mL 29.7354 mL 59.4707 mL 118.9414 mL 148.6768 mL
5 mM 1.1894 mL 5.9471 mL 11.8941 mL 23.7883 mL 29.7354 mL
10 mM 0.5947 mL 2.9735 mL 5.9471 mL 11.8941 mL 14.8677 mL
50 mM 0.1189 mL 0.5947 mL 1.1894 mL 2.3788 mL 2.9735 mL
100 mM 0.0595 mL 0.2974 mL 0.5947 mL 1.1894 mL 1.4868 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 Methyl 2,4-dihydroxybenzoate

Microwave synthesis of iodine-doped bismuth oxychloride microspheres for the visible light photocatalytic removal of toxic hydroxyl-contained intermediates of parabens: catalyst synthesis, characterization, and mechanism insight.[Pubmed:31385253]

Environ Sci Pollut Res Int. 2019 Oct;26(28):28871-28883.

The iodine-doped bismuth oxychloride (I-doped BiOCl) microspheres are synthesized as the visible light photocatalysts for the photocatalytic removal of three toxic hydroxyl-contained intermediates of parabens. With the aid of the unique heating mode of microwave method, the I-doped BiOCl photocatalysts with tunable iodine contents and dispersed energy bands, instead of a mixture of BiOI and BiOCl or solid solution, are synthesized under the controllable conditions. Due to the stretched architectures, high specific surface area, and effective separation of photogenerated carriers, they exhibit high activity to the photocatalytic degradation of Methyl 2,4-dihydroxybenzoate (MDB), methyl 3,4-dihydroxybenzoate (MDHB), and ethyl 2,4-dihydroxybenzoate (EDB). As a typical result, it is indicated that though MDB as the most difficult intermediate of parabens to be degraded, a 91.2% removal ratio can still be achieved over the I-doped BiOCl with an energy band of 2.79 eV within 60 min. In addition, it is also confirmed that these photocatalysts remain stable throughout the photocatalytic reaction and can be reused, and more importantly, the photogenerated h(+) and *O(2)(-) are the key reactive species, while *OH plays a negligible role in the photocatalytic reaction. Resorcinol was identified as the main photodegraded intermediate. These results demonstrate that this photocatalytic system not only exhibit a high efficiency but also avoid the consequent secondary pollutions due to the no formation of complex hydroxyl derivatives.

Synthesis of organosoluble chitosan derivatives with polyphenolic side chains.[Pubmed:22939339]

Carbohydr Polym. 2012 Oct 15;90(3):1259-64.

A one-pot synthesis was used to produce chitosan derivatives with polyphenolic side chains via a regioselective phenolic coupling reaction. Under Mannich reaction conditions, treatment of chitosan with formaldehyde and Methyl 2,4-dihydroxybenzoate gave N-(2,6-dihydroxy-3-methoxycarbonylphenyl)methylated chitosan in good yield (87%). Formation of a CC bond occurred regioselectively at the C(3) position of Methyl 2,4-dihydroxybenzoate. Chitosan derivatives having various phenolic compounds as a side chain were easily synthesized in a similar manner. The chitosan derivatives showed good biodegradability and improved their solubility in methanol (9.8mg mL(-1)) and 2-methoxyethanol (> 10mg mL(-1)). The UV protection provided by the derivatives with phenolic benzophenone side chain was evaluated using UV spectra of polyethylene terephthalate and poly(vinyl butyral-co-vinyl alcohol-co-vinyl acetate) films coated with the derivatives and the derivatives absorbed effectively in the UV-A region (<60%). Self-aggregation of the chitosan derivatives with the phenolic side chain was observed by using a fluorescent probe in aqueous solution.

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