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:
Molecular Weight:
160.17
Beilstein:
2044002
EC Number:
MDL number:
UNSPSC Code:
12000000
PubChem Substance ID:
NACRES:
NA.21
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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
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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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Product No.
Description
Pricing
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Muta. 2
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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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 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.
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
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