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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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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Determination of carbohydrates by high-performance capillary electrophoresis with indirect absorbance detection.
Journal of Chromatography. B, Biomedical Sciences and Applications, 681(1), 87- 97 (1996)
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
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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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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
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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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