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1-Naphthol

CAS# 90-15-3

1-Naphthol

2D Structure

Catalog No. BCC8473----Order now to get a substantial discount!

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3D structure

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1-Naphthol

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Chemical Properties of 1-Naphthol

Cas No. 90-15-3 SDF Download SDF
PubChem ID 7005 Appearance Powder
Formula C10H8O M.Wt 144
Type of Compound N/A Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name naphthalen-1-ol
SMILES C1=CC=C2C(=C1)C=CC=C2O
Standard InChIKey KJCVRFUGPWSIIH-UHFFFAOYSA-N
Standard InChI InChI=1S/C10H8O/c11-10-7-3-5-8-4-1-2-6-9(8)10/h1-7,11H
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.

1-Naphthol Dilution Calculator

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1-Naphthol Molarity Calculator

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Preparing Stock Solutions of 1-Naphthol

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 6.9444 mL 34.7222 mL 69.4444 mL 138.8889 mL 173.6111 mL
5 mM 1.3889 mL 6.9444 mL 13.8889 mL 27.7778 mL 34.7222 mL
10 mM 0.6944 mL 3.4722 mL 6.9444 mL 13.8889 mL 17.3611 mL
50 mM 0.1389 mL 0.6944 mL 1.3889 mL 2.7778 mL 3.4722 mL
100 mM 0.0694 mL 0.3472 mL 0.6944 mL 1.3889 mL 1.7361 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-Naphthol

Enhanced Excited-State Proton Transfer via a Mixed Water-Methanol Molecular Bridge of 1-Naphthol-5-Sulfonate in Methanol-Water Mixtures.[Pubmed:29697261]

J Phys Chem A. 2018 May 24;122(20):4704-4716.

We used steady-state and time-resolved fluorescence techniques to study the excited-state proton transfer (ESPT) and the nonradiative properties of two irreversible photoacids, 1-Naphthol-4-sulfonate (1N4S) and 1-Naphthol-5-sulfonate (1N5S). We found that the ESPT rate constant of 1N4S in water is 2.2 x 10(10) s(-1), whereas in methanol, it is smaller by about 3 orders of magnitude and is not observed. The ESPT process of 1N5S competes with a major nonradiative process of equal rate and kPT of 2.2 x 10(10) s(-1). In methanol-water mixtures of chiH2O = 0.2, the fluorescence lifetime of the ROH form of 1N5S is lower by a factor of 10 than that in pure methanol. In the steady-state fluorescence spectra of 1N5S in methanol-water mixtures, there are two iso-emissive points, one for chiH2O < 0.2 and one for chiH2O > 0.3. This large reduction in fluorescence intensity and the two iso-emissive points are explained by the existence of a mixed water-methanol bridge of about three molecules that connects the proton donor 1-OH with the 5-sulfonate in mixtures of chiH2O < 0.2. The bridge enhances both the ESPT and the nonradiative processes. For 1N4S in methanol-water mixtures at chiH2O approximately 0.2, the reduction in the fluorescence lifetime is only by approximately 30%, and only one iso-emissive point exists in the steady-state fluorescence spectra for 0

Description

1-naphthol is an excited state proton transfer (ESPT) fluorescent molecular probe.

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