5-Hydroxy-1-tetraloneCAS# 28315-93-7 |
Quality Control & MSDS
3D structure
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Number of papers citing our products
| Cas No. | 28315-93-7 | SDF | Download SDF |
| PubChem ID | 119921 | Appearance | White crystalline powder |
| Formula | C10H10O2 | M.Wt | 162.19 |
| Type of Compound | N/A | Storage | Desiccate at -20°C |
| Solubility | Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc. | ||
| Chemical Name | 5-hydroxy-3,4-dihydro-2H-naphthalen-1-one | ||
| SMILES | C1CC2=C(C=CC=C2O)C(=O)C1 | ||
| Standard InChIKey | YPPZCRZRQHFRBH-UHFFFAOYSA-N | ||
| Standard InChI | InChI=1S/C10H10O2/c11-9-5-1-3-7-8(9)4-2-6-10(7)12/h1,3,5,11H,2,4,6H2 | ||
| 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. | ||
5-Hydroxy-1-tetralone Dilution Calculator
5-Hydroxy-1-tetralone Molarity Calculator
| 1 mg | 5 mg | 10 mg | 20 mg | 25 mg | |
| 1 mM | 6.1656 mL | 30.828 mL | 61.6561 mL | 123.3122 mL | 154.1402 mL |
| 5 mM | 1.2331 mL | 6.1656 mL | 12.3312 mL | 24.6624 mL | 30.828 mL |
| 10 mM | 0.6166 mL | 3.0828 mL | 6.1656 mL | 12.3312 mL | 15.414 mL |
| 50 mM | 0.1233 mL | 0.6166 mL | 1.2331 mL | 2.4662 mL | 3.0828 mL |
| 100 mM | 0.0617 mL | 0.3083 mL | 0.6166 mL | 1.2331 mL | 1.5414 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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Fluorometric detection of glycosphingolipids on thin-layer chromatographic plates.[Pubmed:7595105]
J Lipid Res. 1995 Aug;36(8):1848-55.
A microdetection system for glycosphingolipid analysis has been developed using 5-Hydroxy-1-tetralone as the fluorescent labeling reagent. The reagents in H2SO4 permit the fluorometric detection of acidic and neutral glycosphingolipids both in test tube and on thin-layer chromatographic plates. Glycosphingolipids can be detected at concentrations as low as 5 pmol on the thin-layer chromatographic plate. The method is a rapid and simple, and feasible for determination of glycosphingolipid from small amounts of biological samples.
Simple and selective assay of 4-hydroxymephenytoin in human urine using solid-phase extraction and high-performance liquid chromatography with electrochemical detection and its preliminary application to phenotyping test.[Pubmed:8852048]
J Chromatogr B Biomed Appl. 1996 Feb 9;676(1):87-94.
A simple and selective HPLC method for the determination of 4-hydroxymephenytoin (4-OH-M) in human urine, using a controlled potential coulometric detector equipped with a dual working electrode cell of fully porous graphite, has been developed. After acid hydrolysis of urine, 4-OH-M and the internal standard (I.S.), 5-Hydroxy-1-tetralone, were extracted from urine by means of a Bond Elut Certify LRC column. The extracts were chromatographed on a reversed-phase mu Bondapak C18 column using methanol-50 mM KH2PO4 (pH 4.0) (30:70, v/v) as the mobile phase at a flow-rate of 1.0 ml/min. Electrochemical detection at applied potential of 800 mV resulted in a limit of quantitation of 0.76 micrograms/ml. The method showed a satisfactory sensitivity, precision, accuracy, recovery and selectivity. The present method was applied to the phenotyping test in thirteen Japanese healthy volunteers who received an oral 100-mg racemic mephenytoin. The phenotypes determined by the present method were found to be in agreement with those obtained with the reported customary assay based on gas chromatography.
