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Methyl 3-(2,4-dihydroxyphenyl)propionate

CAS# 17422-90-1

Methyl 3-(2,4-dihydroxyphenyl)propionate

Catalog No. BCN1525----Order now to get a substantial discount!

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Methyl 3-(2,4-dihydroxyphenyl)propionate: 5mg Please Inquire In Stock
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Quality Control of Methyl 3-(2,4-dihydroxyphenyl)propionate

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Chemical structure

Methyl 3-(2,4-dihydroxyphenyl)propionate

3D structure

Chemical Properties of Methyl 3-(2,4-dihydroxyphenyl)propionate

Cas No. 17422-90-1 SDF Download SDF
PubChem ID 12112140 Appearance Oil
Formula C10H12O4 M.Wt 196.2
Type of Compound Phenylpropanoids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name methyl 3-(2,4-dihydroxyphenyl)propanoate
SMILES COC(=O)CCC1=C(C=C(C=C1)O)O
Standard InChIKey AGDUPZONPGNRJL-UHFFFAOYSA-N
Standard InChI InChI=1S/C10H12O4/c1-14-10(13)5-3-7-2-4-8(11)6-9(7)12/h2,4,6,11-12H,3,5H2,1H3
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.

Source of Methyl 3-(2,4-dihydroxyphenyl)propionate

The herbs of Juniperus formosana

Biological Activity of Methyl 3-(2,4-dihydroxyphenyl)propionate

Description1. Methyl 3-(2,4-dihydroxyphenyl)propionate has inhibitory effects on tyrosinase, antioxidant ability, and lightening effect of ultraviolet B (UVB)-induced hyperpigmentation.

Methyl 3-(2,4-dihydroxyphenyl)propionate Dilution Calculator

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Methyl 3-(2,4-dihydroxyphenyl)propionate Molarity Calculator

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Preparing Stock Solutions of Methyl 3-(2,4-dihydroxyphenyl)propionate

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 5.0968 mL 25.4842 mL 50.9684 mL 101.9368 mL 127.421 mL
5 mM 1.0194 mL 5.0968 mL 10.1937 mL 20.3874 mL 25.4842 mL
10 mM 0.5097 mL 2.5484 mL 5.0968 mL 10.1937 mL 12.7421 mL
50 mM 0.1019 mL 0.5097 mL 1.0194 mL 2.0387 mL 2.5484 mL
100 mM 0.051 mL 0.2548 mL 0.5097 mL 1.0194 mL 1.2742 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 3-(2,4-dihydroxyphenyl)propionate

Novel vitamin E derivative with 4-substituted resorcinol moiety has both antioxidant and tyrosinase inhibitory properties.[Pubmed:11834083]

Lipids. 2001 Dec;36(12):1321-6.

A novel vitamin E derivative, (6"-hydroxy-2",5",7",8"-tetramethylchroman-2"-yl)methyl 3-(2',4'-dihydroxyphenyl)propionate (TM4R), which has a chromanoxyl ring and 4-substituted resorcinol moieties, was synthesized; and its inhibitory effects on tyrosinase, antioxidant ability, and lightening effect of ultraviolet B (UVB)-induced hyperpigmentation were estimated. TM4R showed potent inhibitory activity on tyrosinase, which is the rate-limiting enzyme in melanogenesis. The scavenging activities of TM4R on 1,1-diphenyl-2-picrylhydrazyl and hydroxyl radicals were found to be nearly the same as those of alpha-tocopherol. Furthermore, an efficient lightening effect was observed following topical application of TM4R to UVB-stimulated hyperpigmented dorsal skin of brownish guinea pigs. These results suggest that TM4R may be a candidate for an efficient whitening agent, possibly by inhibiting tyrosinase activity and biological reactions caused by reactive oxygen species.

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