GSP Chemical Industries

Hydroxy Naphthol Blue Acs Grade

Hydroxy Naphthol Blue Acs Grade
Business Type Manufacturer, Supplier
C.A.S. No. 165660-27-5
M.F. C20H12N2O11Na2S3
M.W. 598.50gm
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Preferred Buyer From

Location Anywhere in India

Product Details

Solubility 0.1 % (Dist. Water)
Clear solution
Suitability for Calcium Determination
Passes Test
Absorption maximum (Ammonia buffer pH 12.0+2ml 0.05M E.D.T.A.) ?max
Absorptivity (A1% 1cm at ?max, in Ammonia buffer pH 12.0+2ml 0.05M E.D.T.A.)
Loss On Drying (110°C)

Chemical Name

Sodium (E)-3-hydroxy-4-((2-hydroxy-6-sulfo-3-sulfonatonaphthalen-1-yl)diazenyl)naphthalene-1-sulfonate


InChI Key




Soluble in water (340g/l)


Hydroxy naphthol blue disodium salt is a synthetic dye that has been used as a calcium indicator, which has a ?max = 650 nm. In the pH range between 12 and 13, the solution of the indicator is reddish pink in the presence of calcium ion and deep blue in the presence of excess (Ethylenedinitrilo)tetraacetate. It is used as Laboratory reagent as approx. 3% dispersion in NaCl solution for determination of calcium.



When hydroxynaphthol blue dye (HNB) was added prior to amplification, samples with DNA of the F167Y mutation developed a characteristic sky blue color after the reaction but those without DNA or with different DNA did not. Results of HNB staining method were reconfirmed by gel electrophoresis. The traditional diagnostic method for Pseudorabies virus (PRV) has the defect of cumbersome procedures, long period, high cost and poor specificity. Thus we built a sensitive and specific loop-mediated isothermal amplification (LAMP) method for the detection of PRV, and used hydroxy naphthol blue (HNB) as indicator to judge the reaction result. The highly conserved gB (glycoprotein B) gene was selected to design primers. The detection could be finished within 45 min after the reaction system was established. Both LAMP and PCR were highly specific to PRV,but he LAMP-based assay, whose detection limit was 102 copies of the target sequence,was 10 times more sensitive than that of the PCR assay. In HNB test, when the ultimate concentration of HNB was 150 µmol/L, the color contrast of the LAMP products between positive samples and negative control was obvious and the sensisity of LAMP reaction was the best.The detection of clinical samples showed that the LAMP reaction had the similar detection rate with the PCR assay. In this experiment, the LAMP method is a highly specific and sensitive detection technology, which can be used instead of traditional PCR method.

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