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

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

Catalog No. BCN4597
Size Price Stock
100mg $70 In stock
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Quality Control of 1-(4-Hydroxyphenyl)propan-1-one

Chemical structure

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

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

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

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

Cas No. 70-70-2 SDF Download SDF
Chemical Name 1-(4-hydroxyphenyl)propan-1-one
SMILES CCC(=O)c1ccc(O)cc1
Standard InChIKey RARSHUDCJQSEFJ-UHFFFAOYSA-N
Standard InChI InChI=1S/C9H10O2/c1-2-9(11)7-3-5-8(10)6-4-7/h3-6,10H,2H2,1H3
Type of Compound Phenylpropanoids Appearance Powder
Formula C9H10O2 M.Wt 150.17
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
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.
Shipping Condition Packaging according to customer requirements(5mg, 10mg, 20mg and more). Ship via FedEx, DHL, UPS, EMS or other courier with RT , or blue ice upon request.

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.

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

This product is isolated and purified from the herbs of Cedrus deodara

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

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


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.

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