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Merck

70650

1,3-Dihydroxynaphthalene

for spectrophotometric det. of glucuronic acid according to Tollens, ≥97.0%

Synonym(s):

1,3-Naphthalenediol, Naphthoresorcinol

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About This Item

Linear Formula:
C10H6(OH)2
CAS Number:
132-86-5
Molecular Weight:
160.17
UNSPSC Code:
12352200
NACRES:
NA.21
PubChem Substance ID:
329762646
EC Number:
205-079-7
Beilstein/REAXYS Number:
2044002
MDL number:
MFCD00003965

Key Documents

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Product Name

1,3-Dihydroxynaphthalene, for spectrophotometric det. of glucuronic acid according to Tollens, ≥97.0%

InChI key

XOOMNEFVDUTJPP-UHFFFAOYSA-N

InChI

1S/C10H8O2/c11-8-5-7-3-1-2-4-9(7)10(12)6-8/h1-6,11-12H

SMILES string

Oc1cc(O)c2ccccc2c1

assay

≥97.0% (HPLC)
≥97.0%

form

crystals

quality

for spectrophotometric det. of glucuronic acid according to Tollens

technique(s)

UV/Vis spectroscopy: suitable

mp

122-125 °C
123-125 °C (lit.)

Quality Level

100

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Application

1,3-Dihydroxynaphthalene may be used as a background electrolyte (BGE) for the determination of carbohydrates by high-performance capillary electrophoresis (HPCE) method with indirect absorbance detection.

pictograms

Health hazard
GHS08

signalword

Warning

hcodes

H341

Hazard Classifications

Muta. 2

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCJ6270
BCCC4990
BCCB9343
BCCB5822
BCCB5416

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Determination of carbohydrates by high-performance capillary electrophoresis with indirect absorbance detection.
Lee YH and Lin TI
Journal of Chromatography. B, Biomedical Sciences and Applications, 681(1), 87- 97 (1996)
Y Sayato et al.
Mutation research, 226(3), 151-155 (1989-07-01)
The mutagenicity of products formed by chlorination after ozonation of naphthoresorcinol in aqueous solution was assayed with Salmonella typhimurium strains TA98 and TA100 in the presence and absence of S9 mix from phenobarbital- and 5,6-benzoflavone-induced rat liver. Ozonated and subsequently
Amy L Kieran et al.
Chemical communications (Cambridge, England), (14)(14), 1842-1844 (2005-03-30)
New macrocycles incorporating a porphyrin and a [small pi] electron-rich aromatic were prepared from a dynamic disulfide library. The outcome could be influenced by use of templates.
Y Sayato et al.
Mutation research, 189(3), 217-222 (1987-11-01)
The mutagenicity of products formed by ozonation of naphthoresorcinol in aqueous solution was assayed with Salmonella typhimurium strains TA97, TA98, TA100, TA102 and TA104 in the presence and absence of S9 mix from phenobarbital- and 5,6-benzoflavone-induced rat liver. Ozonated naphthoresorcinol
Determination of glycolaldehyde in the presence of hydroxypyruvate and tartronate semialdehyde.
F E de Windt et al.
Analytical biochemistry, 106(2), 342-343 (1980-08-01)
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