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Ethyl p-hydroxyphenyllactate

CAS# 62517-34-4

Ethyl p-hydroxyphenyllactate

Catalog No. BCN6654----Order now to get a substantial discount!

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Ethyl p-hydroxyphenyllactate: 5mg $351 In Stock
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Quality Control of Ethyl p-hydroxyphenyllactate

Number of papers citing our products

Chemical structure

Ethyl p-hydroxyphenyllactate

3D structure

Chemical Properties of Ethyl p-hydroxyphenyllactate

Cas No. 62517-34-4 SDF Download SDF
PubChem ID 21930973 Appearance Oil
Formula C11H14O4 M.Wt 210.2
Type of Compound Phenylpropanoids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name ethyl 2-hydroxy-3-(4-hydroxyphenyl)propanoate
SMILES CCOC(=O)C(CC1=CC=C(C=C1)O)O
Standard InChIKey MPPNCBJETJUYAO-UHFFFAOYSA-N
Standard InChI InChI=1S/C11H14O4/c1-2-15-11(14)10(13)7-8-3-5-9(12)6-4-8/h3-6,10,12-13H,2,7H2,1H3
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 Ethyl p-hydroxyphenyllactate

The herbs of Crepis crocea.

Biological Activity of Ethyl p-hydroxyphenyllactate

DescriptionStandard reference

Protocol of Ethyl p-hydroxyphenyllactate

Structure Identification
Zhongguo Zhong Yao Za Zhi. 2015 Oct;40(19):3800-4.

Chemical constituents from Crepis crocea[Pubmed: 26975105]


METHODS AND RESULTS:
Thirteen compounds were isolated from the ethyl acetate fraction of Crepis crocea by column chromatographies on silica gel, Sephadex LH-20 and semi-preparative HPLC. The structures were elucidated on the basis of spectral analysis as tectorone I (1), 8β- (2-methyl- 2-hydroxy-3-oxobutanoyloxy) -glucozaluzanin C (2), tectoroside (3), luteolin-7-O-glucoside (4), cosmosiin (5), esculetin (6), 3,4-dihydroxybenzaldehyde (7), trans-4-hydroxycinnamic acid (8), Caffeic acid (9), mEthyl p-hydroxyphenyllactate (10), Ethyl p-hydroxyphenyllactate (11), cis-3,4-dihydroxy-β-ionion (12).
CONCLUSIONS:
All the compounds, except for compounds 4 and 9, were isolated from this plant for the first time, and tectorone I (1) is a new natural product.

Ethyl p-hydroxyphenyllactate Dilution Calculator

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Ethyl p-hydroxyphenyllactate Molarity Calculator

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Preparing Stock Solutions of Ethyl p-hydroxyphenyllactate

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 4.7574 mL 23.7869 mL 47.5737 mL 95.1475 mL 118.9343 mL
5 mM 0.9515 mL 4.7574 mL 9.5147 mL 19.0295 mL 23.7869 mL
10 mM 0.4757 mL 2.3787 mL 4.7574 mL 9.5147 mL 11.8934 mL
50 mM 0.0951 mL 0.4757 mL 0.9515 mL 1.9029 mL 2.3787 mL
100 mM 0.0476 mL 0.2379 mL 0.4757 mL 0.9515 mL 1.1893 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 Ethyl p-hydroxyphenyllactate

[Chemical constituents from Crepis crocea].[Pubmed:26975105]

Zhongguo Zhong Yao Za Zhi. 2015 Oct;40(19):3800-4.

Thirteen compounds were isolated from the ethyl acetate fraction of Crepis crocea by column chromatographies on silica gel, Sephadex LH-20 and semi-preparative HPLC. The structures were elucidated on the basis of spectral analysis as tectorone I (1), 8beta- (2-methyl- 2-hydroxy-3-oxobutanoyloxy) -glucozaluzanin C (2), tectoroside (3), luteolin-7-O-glucoside (4), cosmosiin (5), esculetin (6), 3,4-dihydroxybenzaldehyde (7), trans-4-hydroxycinnamic acid (8), Caffeic acid (9), mEthyl p-hydroxyphenyllactate (10), ethylp- hydroxyphenyllactate (11), cis-3,4-dihydroxy-beta-ionion (12). All the compounds, except for compounds 4 and 9, were isolated from this plant for the first time, and tectorone I (1) is a new natural product.

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