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70650

Supelco

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:
132-86-5
Molecular Weight:
160.17
Beilstein:
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

Signal Word

Warning

Hazard Statements

H341

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

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

70650-BULK:
70650-5G:
70650-1G:
70650-VAR:

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Certificates of Analysis (COA)

Lot/Batch Number
BCCJ6270
BCCC4990
BCCB9343
BCCB5822
BCCB5416

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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
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.
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
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
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