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70650

1,3-Dihydroxynaphthalene

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

Synonyme(s) :

1,3-Naphthalenediol, Naphthoresorcinol

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A propos de cet article

Formule linéaire :
C10H6(OH)2
Numéro CAS:
Poids moléculaire :
160.17
UNSPSC Code:
12352200
NACRES:
NA.21
PubChem Substance ID:
EC Number:
205-079-7
Beilstein/REAXYS Number:
2044002
MDL number:
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Quality Level

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

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

signalword

Warning

hcodes

Hazard Classifications

Muta. 2

Classe de stockage

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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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



Numéro d'article de commerce international

RéférenceGTIN
70650-1G04061832842905
70650-5G04061832842912