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1-(4-Hydroxyphenyl)propan-1-one
ChemFaces products have been cited in many studies from excellent and top scientific journals
Product Name 1-(4-Hydroxyphenyl)propan-1-one
Price: $30 / 20mg
CAS No.: 70-70-2
Catalog No.: CFN97700
Molecular Formula: C9H10O2
Molecular Weight: 150.17 g/mol
Purity: >=98%
Type of Compound: Phenylpropanoids
Physical Desc.: Powder
Source: The herbs of Cedrus deodara
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Download: COA    MSDS    SDF
Similar structural: Comparison (Web)  (SDF)
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According to end customer requirements, ChemFaces provide solvent format. This solvent format of product intended use: Signaling Inhibitors, Biological activities or Pharmacological activities.
Size /Price /Stock 10 mM * 1 mL in DMSO / $7.0 / In-stock
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Related Screening Libraries
Size /Price /Stock 10 mM * 100 uL in DMSO / Inquiry / In-stock
10 mM * 1 mL in DMSO / Inquiry / In-stock
Related Libraries
Biological Activity
Description: Paroxypropione(1-(4-Hydroxyphenyl)propan-1-one) is a manufactured, nonsteroidal estrogen which has been used medically as an antigonadotropin.
Targets: Estrogen receptor
1-(4-Hydroxyphenyl)propan-1-one Description
Source: The herbs of Cedrus deodara
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Storage: Providing storage is as stated on the product vial and the vial is kept tightly sealed, the product can be stored for up to 24 months(2-8C).

Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20C. Generally, these will be useable for up to two weeks. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour.

Need more advice on solubility, usage and handling? Please email to: service@chemfaces.com

After receiving: The packaging of the product may have turned upside down during transportation, resulting in the natural compounds adhering to the neck or cap of the vial. take the vial out of its packaging and gently shake to let the compounds fall to the bottom of the vial. for liquid products, centrifuge at 200-500 RPM to gather the liquid at the bottom of the vial. try to avoid loss or contamination during handling.
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Recently, ChemFaces products have been cited in many studies from excellent and top scientific journals

Cell. 2018 Jan 11;172(1-2):249-261.e12.
doi: 10.1016/j.cell.2017.12.019.
IF=36.216(2019)

PMID: 29328914

Cell Metab. 2020 Mar 3;31(3):534-548.e5.
doi: 10.1016/j.cmet.2020.01.002.
IF=22.415(2019)

PMID: 32004475

Mol Cell. 2017 Nov 16;68(4):673-685.e6.
doi: 10.1016/j.molcel.2017.10.022.
IF=14.548(2019)

PMID: 29149595

ACS Nano. 2018 Apr 24;12(4): 3385-3396.
doi: 10.1021/acsnano.7b08969.
IF=13.903(2019)

PMID: 29553709

Nature Plants. 2016 Dec 22;3: 16206.
doi: 10.1038/nplants.2016.205.
IF=13.297(2019)

PMID: 28005066

Sci Adv. 2018 Oct 24;4(10): eaat6994.
doi: 10.1126/sciadv.aat6994.
IF=12.804(2019)

PMID: 30417089
Calculate Dilution Ratios(Only for Reference)
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 need to make the dilution ratios of the samples. The dilution data of the sheet for your reference. Normally, it's can get a better solubility within lower of Concentrations.
Protocol
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.
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Protopine

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3,7-Di-O-methylquercetin

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CAS No: 2068-02-2
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Acetyleugenol

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Aloenin A

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Cucurbitacin B

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