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Naphthoresorcinol

CAT: 0804-HY-D0165-01Size: 1 gDry Ice: NoHazardous: No
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CAT#:0804-HY-D0165-01Size:1 g
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Description
Naphthoresorcinol (1,3-Dihydroxynaphthalene) is a fluorescent dye (λex=330 nm, λem=380 nm) that can react with the NPPD (a tracer) and concentrated HCl and develop a red color. Naphthoresorcinol could be used as a background electrolyte (BGE) to determine the carbohydrates[1][2][3].
CAS Number
132-86-5
Product Name Alternative
1,3-Dihydroxynaphthalene
UNSPSC
12171500
Hazard Statement
H341
Target
Fluorescent Dye
Type
Dye Reagents
Related Pathways
Others
Field of Research
Others
Assay Protocol
https://www.medchemexpress.com/naphthoresorcinol.html
Purity
99.60
Solubility
DMSO : 100 mg/mL (ultrasonic)
Smiles
OC1=C2C=CC=CC2=CC(O)=C1
Molecular Formula
C10H8O2
Molecular Weight
160.17
Precautions
H341
References & Citations
[1]Vyas S, et, al. Fluorescence and light scattering studies on the interaction of 1,3-dihydroxynaphthalene with ionic and non-ionic surfactants. Polymer Photochemistry. 1984; 4 (4) :245-253.|[2]Suzuki S, et, al. Development of a field kit for use by non-scientists for chemical tracking using 5- (4-nitrophenyl) -2,4-pentadien-1-al. Forensic Sci Int. 2013 May 10;228 (1-3) :e25-7.|[3]Lee YH, et, al. Determination of carbohydrates by high-performance capillary electrophoresis with indirect absorbance detection. J Chromatogr B Biomed Appl. 1996 May 31;681 (1) :87-97.|[4]Sinha S, et al. A new cytotoxic quinolone alkaloid and a pentacyclic steroidal glycoside from the stem bark of Crataeva nurvala: study of anti-proliferative and apoptosis inducing property. Eur J Med Chem. 2013 Feb;60:490-6.
Shipping Conditions
Room Temperature
Storage Conditions
4°C (Powder, protect from light)
Scientific Category
Dye Reagents
Clinical Information
No Development Reported

Chemical Information

1,3-Dihydroxynaphthalene

1,3-Naphthalenediol has been reported in Salvia officinalis and Magnolia liliiflora with data available.

CAS Number132-86-5
PubChem CID8601
IUPAC Namenaphthalene-1,3-diol
Molecular FormulaC10H8O2
Molecular Weight160.17
XLogP2
Topological Polar Surface Area40.5
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count2
Rotatable Bond Count0
Heavy Atom Count12
Formal Charge0
Complexity158
SMILES
C1=CC=C2C(=C1)C=C(C=C2O)O
InChI
InChI=1S/C10H8O2/c11-8-5-7-3-1-2-4-9(7)10(12)6-8/h1-6,11-12H
InChIKey
XOOMNEFVDUTJPP-UHFFFAOYSA-N
Chemical Structure
2D Structure
2D structure of 1,3-Dihydroxynaphthalene
CAS: 132-86-5
CID: 8601
Formula: C10H8O2
MW: 160.17
Interactive 3D Structure
Loading 3D structure...
View on PubChemRaw 3D data
Computed Properties
PropertyValue
Molecular Weight160.17
XLogP32
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count2
Rotatable Bond Count0
Exact Mass160.052429494
Monoisotopic Mass160.052429494
Topological Polar Surface Area40.5 Ų
Heavy Atom Count12
Formal Charge0
Complexity158
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
Covalently-Bonded Unit Count1
Compound Is CanonicalizedYes

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