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70430

Sigma-Aldrich

1,4-Dihydroxynaphthalene

technical, ≥90% (HPLC)

Synonym(s):

1,4-Naphthalenediol, p-Naphthohydroquinone (α)

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About This Item

Empirical Formula (Hill Notation):
C10H8O2
CAS Number:
571-60-8
Molecular Weight:
160.17
Beilstein/REAXYS Number:
1307689
EC Number:
209-336-4
MDL number:
MFCD00003977
UNSPSC Code:
12352100
PubChem Substance ID:
57652247
NACRES:
NA.22

grade

technical

Quality Level

100

assay

≥90% (HPLC)

form

crystals

mp

191-192 °C (dec.)

SMILES string

Oc1ccc(O)c2ccccc12

InChI

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

InChI key

PCILLCXFKWDRMK-UHFFFAOYSA-N

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pictograms

CorrosionExclamation mark
GHS05,GHS07

signalword

Danger

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Dam. 1 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCK4183
BCCB7408
BCBL3934V
1400167
1362382

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L S Tsuruda et al.
Archives of toxicology, 69(6), 362-367 (1995-01-01)
Naphthalene (NA) is metabolically activated to the reactive intermediates, naphthalene oxide (NO) and naphthoquinones. To investigate the role of circulating reactive metabolites in NA toxicity, the half-life of NO was examined. The in vitro half-life of NO in both whole
Aurora Molinari et al.
Archiv der Pharmazie, 342(10), 591-599 (2009-09-16)
Several new 6-(3-pyrazolylpropyl) derivatives of 1,4-naphthohydroquinone-1,4-diacetate (NHQ-DA) have been prepared by chemical modifications of the Diels-Alder adduct of alpha-myrcene and 1,4-benzoquinone. All these new compounds and precursors have been evaluated in vitro for their cytotoxicity against cultured human cancer cells
Kevin W Wellington et al.
Bioorganic & medicinal chemistry, 20(14), 4472-4481 (2012-06-12)
Nuclear monoamination of a 1,4-naphthohydroquinone with primary aromatic amines was catalysed by the commercial laccase, Novozym 51003, from Novozymes to afford aminonaphthoquinones. The synthesis was accomplished by reacting a mixture of the primary amine and 1,4-naphthohydroquinone in succinate-lactate buffer and
María Teresa Molina et al.
The Journal of organic chemistry, 74(24), 9573-9575 (2009-11-27)
The NHC-catalyzed conjugate hydroacylation of 1,4-naphthoquinones allows for the synthesis of monoacylated 1,4-dihydroxynaphthalene derivatives. These targets, difficult to prepare selectively by standard protocols, represent important intermediates in the elaboration of highly substituted 1,4-naphthoquinone derivatives, which constitute relevant pharmaceutical scaffolds. High
M Matsumoto et al.
Biological & pharmaceutical bulletin, 24(3), 236-241 (2001-03-21)
The proteases encoded by herpesviruses including herpes simplex virus type 1 (HSV-1) and human cytomegalovirus (HCMV) are attractive targets for antiviral drug development because of their important roles in viral replication. We randomly screened a chemical compound library for inhibitory
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