2'-Hydroxy-4'-methylacetophenoneCAS# 6921-64-8 |
Quality Control & MSDS
3D structure
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Number of papers citing our products
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Cas No. | 6921-64-8 | SDF | Download SDF |
PubChem ID | 81338 | Appearance | Powder |
Formula | C9H10O2 | M.Wt | 150.17 |
Type of Compound | Phenols | Storage | Desiccate at -20°C |
Solubility | Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc. | ||
Chemical Name | 1-(2-hydroxy-4-methylphenyl)ethanone | ||
SMILES | CC1=CC(=C(C=C1)C(=O)C)O | ||
Standard InChIKey | LYKDOWJROLHYOT-UHFFFAOYSA-N | ||
Standard InChI | InChI=1S/C9H10O2/c1-6-3-4-8(7(2)10)9(11)5-6/h3-5,11H,1-2H3 | ||
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. |
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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. |
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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. |
Description | 1. 2'-Hydroxy-4'-methylacetophenone has acaricidal activity. |
Targets | Antifection |
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2'-Hydroxy-4'-methylacetophenone Dilution Calculator
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2'-Hydroxy-4'-methylacetophenone Molarity Calculator
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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Acaricidal toxicity of 2'-hydroxy-4'-methylacetophenone isolated from Angelicae koreana roots and structure-activity relationships of its derivatives.[Pubmed:22429095]
J Agric Food Chem. 2012 Apr 11;60(14):3606-11.
The acaricidal activities of 2'-hydroxy-4'-methylacetophenone derived from Angelica koreana roots and its derivatives against Dermatophagoides farinae, Dermatophagoides pteronyssinus, and Tyrophagus putrescentiae were examined by vapor phase and contact toxicity bioassays. In the vapor phase toxicity bioassay, 2'-methylacetophenone (1.25 mug/cm(2)) was 8.0 times more toxic against D. farinae than benzyl benzoate (10.00 mug/cm(2)), followed by 3'-methylacetophenone (1.26 mug/cm(2)), 4'-methylacetophenone (1.29 mug/cm(2)), 2'-hydroxy-4'-methylacetophenone (1.75 mug/cm(2)), and 2'-hydroxy-5'-methylacetophenone (1.96 mug/cm(2)). In the contact toxicity bioassay, 3'-methylacetophenone (0.58 mug/cm(2)) was 17.24 times more effective against D. farinae than benzyl benzoate (7.52 mug/cm(2)), followed by 2'-methylacetophenone (0.64 mug/cm(2)), 2'-hydroxy-4'-methylacetophenone (0.76 mug/cm(2)), 4'-methylacetophenone (0.77 mug/cm(2)), and 2'-hydroxy-5'-methylacetophenone (1.16 mug/cm(2)). The acaricidal activities of 2'-hydroxy-4'-methylacetophenone derivatives against D. pteronyssinus and T. putrescentiae were similar to those against D. farinae. In terms of structure-activity relationships, acaricidal activity against the three mite species changed with the introduction of hydroxyl and methyl functional groups onto the acetophenone skeleton. Furthermore, some of 2'-hydroxy-4'-methylacetophenone derivatives could be useful for natural acaricides against three mite species.