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1-Amino-4-hydroxyanthraquinone

CAS# 116-85-8

1-Amino-4-hydroxyanthraquinone

Catalog No. BCC8452----Order now to get a substantial discount!

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1-Amino-4-hydroxyanthraquinone: 5mg $17 In Stock
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Chemical structure

1-Amino-4-hydroxyanthraquinone

3D structure

Chemical Properties of 1-Amino-4-hydroxyanthraquinone

Cas No. 116-85-8 SDF Download SDF
PubChem ID 8323 Appearance Powder
Formula C14H9NO3 M.Wt 239
Type of Compound N/A Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name 1-amino-4-hydroxyanthracene-9,10-dione
SMILES C1=CC=C2C(=C1)C(=O)C3=C(C=CC(=C3C2=O)O)N
Standard InChIKey AQXYVFBSOOBBQV-UHFFFAOYSA-N
Standard InChI InChI=1S/C14H9NO3/c15-9-5-6-10(16)12-11(9)13(17)7-3-1-2-4-8(7)14(12)18/h1-6,16H,15H2
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-Amino-4-hydroxyanthraquinone Dilution Calculator

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1-Amino-4-hydroxyanthraquinone Molarity Calculator

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Preparing Stock Solutions of 1-Amino-4-hydroxyanthraquinone

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 4.1841 mL 20.9205 mL 41.841 mL 83.682 mL 104.6025 mL
5 mM 0.8368 mL 4.1841 mL 8.3682 mL 16.7364 mL 20.9205 mL
10 mM 0.4184 mL 2.0921 mL 4.1841 mL 8.3682 mL 10.4603 mL
50 mM 0.0837 mL 0.4184 mL 0.8368 mL 1.6736 mL 2.0921 mL
100 mM 0.0418 mL 0.2092 mL 0.4184 mL 0.8368 mL 1.046 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-Amino-4-hydroxyanthraquinone

Optochemical sensor for an ornidazole assay using 1-amino-4-allyloxyanthraquinone as a fluorescent indicator.[Pubmed:16122170]

Anal Sci. 2005 Aug;21(8):967-71.

To improve the stability of optochemical sensors (optodes), the fluorescence indicator 1-amino-4-allyloxyanthraquinone (AAA), which was synthesized by reacting allyl bromide with 1-Amino-4-hydroxyanthraquinone, was covalently immobilized on surface-modified glass slides. The resulting sensor was used to determine the content of ornidazole based on fluorescence quenching. It showed a linear response toward ornidazole in the concentration range of 9.0 x 10(-6) to 1.0 x 10(-3) mol L(-1) with a detection limit of 8 x 10(-6) mol L(-1) at pH 7.5. This AAA-immobilized sensor has a rapid response, high stability and good selectivity to ornidazole.

Complexation equilibria and spectrophotometric determination of iron(III) with 1-amino-4-hydroxyanthraquinone.[Pubmed:18966119]

Talanta. 1994 Oct;41(10):1669-74.

The complex equilibria of iron(III) with 1-Amino-4-hydroxyanthraquinone (AMHA) were studied spectrophotometrically in 40% (v/v) ethanol and an ionic strength of 0.1M (NaClO(4)). The complexation reactions were demonstrated and characterized using graphical logarithmic analysis of the absorbance-pH graphs. A simple, rapid, selective and sensitive method for the spectrophotometric determination of trace amounts of Fe(III) is developed based on the formation of Fe(AMHA) complex at pH 2.5 (lambda(max) = 640 nm, epsilon approximately = 2.1 x 10(4) L. mol(-1) . cm(-1)) in the presence of a large number of foreign ions. Interferences caused by palladium(II) was masked by the addition of cyanide ions. The method has been applied to the determination of iron in some synthetic samples and polymetallic iron ores.

Complexes of some rare earth metals with 1-amino-4-hydroxyanthraquinone.[Pubmed:18961210]

Talanta. 1972 Nov;19(11):1481-2.

La, Ce(III), Pr, Nd and Sm(III) form very stable reddishviolet 1:1 complexes with 1-Amino-4-hydroxyanthraquinone in methanol. The stability constants are very similar.

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