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1,3-Dihydroxynaphthalene

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

Synonyme(s) :

1,3-Naphthalenediol, Naphthoresorcinol

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About This Item

Formule linéaire :
C10H6(OH)2
Numéro CAS:
132-86-5
Poids moléculaire :
160.17
Numéro Beilstein :
2044002
Numéro CE :
205-079-7
Numéro MDL:
MFCD00003965
Code UNSPSC :
12000000
ID de substance PubChem :
329762646
Nomenclature NACRES :
NA.21

Niveau de qualité

100

Pureté

≥97.0% (HPLC)
≥97.0%

Forme

crystals

Qualité

for spectrophotometric det. of glucuronic acid according to Tollens

Technique(s)

UV/Vis spectroscopy: suitable

Pf

122-125 °C
123-125 °C (lit.)

Chaîne SMILES 

Oc1cc(O)c2ccccc2c1

InChI

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

Clé InChI

XOOMNEFVDUTJPP-UHFFFAOYSA-N

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Catégories apparentées

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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Pictogrammes

Health hazard
GHS08

Mention d'avertissement

Warning

Mentions de danger

H341

Classification des risques

Muta. 2

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

dust mask type N95 (US), Eyeshields, Gloves

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Certificats d'analyse (COA)

Lot/Batch Number
BCCJ6270
BCCC4990
BCCB9343
BCCB5822
BCCB5416

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Consulter la Bibliothèque de documents

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
Hikoto Ohta et al.
Journal of forensic sciences, 49(3), 517-522 (2004-06-03)
The chemical compound 5-(4-nitrophenyl)-2,4-pentadien-1-al (NPPD), called "spy dust," was used in the Soviet Union as a shadowing pursuit, the act of following someone secretly, for investigating the activities of diplomatic personnel. It is also useful for counter-terrorism, and some criminal
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)
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