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70650

Supelco

1,3-Dihydroxynaphthalene

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

Sinónimos:

1,3-Naphthalenediol, Naphthoresorcinol

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About This Item

Fórmula lineal:
C10H6(OH)2
Número de CAS:
132-86-5
Peso molecular:
160.17
Beilstein/REAXYS Number:
2044002
EC Number:
205-079-7
MDL number:
MFCD00003965
UNSPSC Code:
12000000
PubChem Substance ID:
329762646
NACRES:
NA.21

Quality Level

100

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.)

SMILES string

Oc1cc(O)c2ccccc2c1

InChI

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

InChI key

XOOMNEFVDUTJPP-UHFFFAOYSA-N

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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.

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pictograms

Health hazard
GHS08

signalword

Warning

hcodes

H341

Hazard Classifications

Muta. 2

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificados de análisis (COA)

Lot/Batch Number
BCCC4990
BCCB9343
BCCB5822
BCCB5416
BCBV3108

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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, 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
Wilson Terán et al.
The Journal of biological chemistry, 281(11), 7102-7109 (2006-01-13)
The RND family transporter TtgABC and its cognate repressor TtgR from Pseudomonas putida DOT-T1E were both shown to possess multidrug recognition properties. Structurally unrelated molecules such as chloramphenicol, butyl paraben, 1,3-dihydroxynaphthalene, and several flavonoids are substrates of TtgABC and activate
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)
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.
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