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1-(4-Hydroxyphenyl)propan-1-one

CAS# 70-70-2

1-(4-Hydroxyphenyl)propan-1-one

Catalog No. BCN4597----Order now to get a substantial discount!

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Quality Control of 1-(4-Hydroxyphenyl)propan-1-one

Number of papers citing our products

Chemical structure

1-(4-Hydroxyphenyl)propan-1-one

3D structure

Chemical Properties of 1-(4-Hydroxyphenyl)propan-1-one

Cas No. 70-70-2 SDF Download SDF
PubChem ID 6271 Appearance Powder
Formula C9H10O2 M.Wt 150.17
Type of Compound Phenylpropanoids Storage Desiccate at -20°C
Solubility DMSO : 100 mg/mL (665.91 mM; Need ultrasonic and warming)
Chemical Name 1-(4-hydroxyphenyl)propan-1-one
SMILES CCC(=O)C1=CC=C(C=C1)O
Standard InChIKey RARSHUDCJQSEFJ-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 1-(4-Hydroxyphenyl)propan-1-one

The herbs of Cedrus deodara

Biological Activity of 1-(4-Hydroxyphenyl)propan-1-one

DescriptionParoxypropione(1-(4-Hydroxyphenyl)propan-1-one) is a manufactured, nonsteroidal estrogen which has been used medically as an antigonadotropin.
TargetsEstrogen receptor

Protocol of 1-(4-Hydroxyphenyl)propan-1-one

Structure Identification
Modern Chinese Medicine, 2008,10(11):13-5.

Studies on the Chemical Constituents of Alpinia Calanga Willd.[Reference: WebLink]

To study the chemical constituents of Alpinia galanga Willd.
METHODS AND RESULTS:
The chem- ical constituents were isolated by various column chromatographic methods,and the structures were elucidated on the basis of UV,IR,MS,~1H-NMR,~(13)C-NMR spectral analysis. Eleven compounds were isolated and their structures were elucidated as 4-[(E)-3-hydroxyprop-1-enyl]phenyl acetate(1),trans-p-hydroxylcinnamaldehyde acetate(2),5-hydroxy-7-(4″-hydroxy-3″-methoxyphenyl)-1-phenyl-3-heptanone(3),7-(4″-hydroxy-3″-me- thoxyphenyl)-1-phenylhep-4-en-3-one(4),[1′S]-1′-acetoxyeugenol acetate(5),trans-p-hydroxylcinnamalde- hyde(6),p-hydroxybenzaldehyde(7),1-(4-Hydroxyphenyl)propan-1-one(8),galangin(9),trans-p-coumaryl diacetate(10),β-sitosterol(11).
CONCLUSIONS:
Compound 1 was obtained from nature for the first time,com- pound 2 was obtained from this genus for the first time,and compounds 3 and 4 were obtained from this plant for the first time.

1-(4-Hydroxyphenyl)propan-1-one Dilution Calculator

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1-(4-Hydroxyphenyl)propan-1-one Molarity Calculator

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Preparing Stock Solutions of 1-(4-Hydroxyphenyl)propan-1-one

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 6.6591 mL 33.2956 mL 66.5912 mL 133.1824 mL 166.478 mL
5 mM 1.3318 mL 6.6591 mL 13.3182 mL 26.6365 mL 33.2956 mL
10 mM 0.6659 mL 3.3296 mL 6.6591 mL 13.3182 mL 16.6478 mL
50 mM 0.1332 mL 0.6659 mL 1.3318 mL 2.6636 mL 3.3296 mL
100 mM 0.0666 mL 0.333 mL 0.6659 mL 1.3318 mL 1.6648 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 1-(4-Hydroxyphenyl)propan-1-one

Phenolic compounds from the branches of Eucalyptus maideni.[Pubmed:22253109]

Chem Biodivers. 2012 Jan;9(1):123-30.

Three new phenolic compounds, eucalmaidin F (1), (3S)-5-guaiacyl-3-hydroxypentanoic acid (2), and 8-beta-C-glucopyranosyl-5,7-dihydroxy-2-isobutylchromone (3), were isolated from the branches of E. maideni, together with 30 known compounds, including four phenylpropanoids, three lignans, four phloroglucinol glucosides, five dihydroflavonoids, seven simple phenolic compounds, six terpenoids, and glycerol. The new structures were established by spectroscopic studies (MS, and 1D- and 2D-NMR), chemical degradation, and modified Mosher's method. Compounds 3, guaiacylglycerol, 3-hydroxy-1-(4-Hydroxyphenyl)propan-1-one, caffeic acid, (2E)-3-(4-hydroxyphenyl)prop-2-enoic acid, (7'S,8R,8'R)-lyoniresinol, (+)-lyoresinol 3alpha-O-alpha-L-rhamnopyranoside, garcimangosone, phlorocetophenone 2'-glucopyranoside, (+)-taxifolin 3alpha-O-alpha-L-rhamnopyranoside, (+)-aromadendrin, (+)-taxifolin, resveratrol, piceatannol, 3,4,5-trihydroxyphenol. Tachiaside, gallic acid, macrocapals A und G, and oleuropeic acid were evaluated for their cytotoxicities against five human cancer cell lines. Resveratrol, piceatannol, gallic acid, and macrocapal G exhibited moderate inhibitory effects on human myeloid heukemia HL-60 cell, with IC(50) values of 22.05, 22.05, 7.75, and 31.93 muM, respectively; and only macrocapal G showed inhibitory effect on hepatocellular carcinoma SMMC-7721 cell, with an IC(50) value of 26.75 muM.

Inactivation of GABA transaminase by 3-chloro-1-(4-hydroxyphenyl)propan-1-one.[Pubmed:19138517]

Bioorg Med Chem Lett. 2009 Feb 1;19(3):731-4.

Previously it was found that 4-hydroxybenzaldehyde is a competitive inhibitor of GABA transaminase. Here 3-chloro-1-(4-Hydroxyphenyl)propan-1-one (9), a 4-hydroxybenzaldehyde analogue, was found to inactivate potently the enzyme in a time-dependent manner. alpha-Ketoglutarate prevented the enzyme from inactivation, suggesting that the inactivation occurs in its active site. Several experiments indicated that the inactivation is irreversible. This study provides a novel strategy for the design of more effective inhibitors.

Description

Paroxypropione is a manufactured, nonsteroidal estrogen which has been used medically as an antigonadotropin.

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