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08800

Sigma-Aldrich

7-Amino-4-hydroxy-2-naphthalenesulfonic acid

technical, ≥90% (T)

Synonym(s):

6-Amino-1-naphthol-3-sulfonic acid, I-Acid

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About This Item

Empirical Formula (Hill Notation):
C10H9NO4S
CAS Number:
Molecular Weight:
239.25
Beilstein/REAXYS Number:
2217192
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

grade

technical

Quality Level

assay

≥90% (T)

form

powder

functional group

sulfonic acid

SMILES string

Nc1ccc2c(O)cc(cc2c1)S(O)(=O)=O

InChI

1S/C10H9NO4S/c11-7-1-2-9-6(3-7)4-8(5-10(9)12)16(13,14)15/h1-5,12H,11H2,(H,13,14,15)

InChI key

KYARBIJYVGJZLB-UHFFFAOYSA-N

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Storage Class

11 - Combustible Solids

wgk_germany

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges


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T Kumasaka et al.
The Journal of clinical investigation, 97(10), 2362-2369 (1996-05-15)
This study examined the effectiveness of antisense oligonucleotides targeted to intercellular adhesion molecule-1 (ICAM-1) to inhibit endotoxin-induced upregulation of ICAM-1 and neutrophil emigration and compared the apparent role of ICAM-1 when examined using antisense oligonucleotides, anti-ICAM-1 antibodies, and ICAM-1 mutant
Idil Arslan-Alaton et al.
Chemosphere, 76(5), 587-594 (2009-06-02)
H2O2/UV-C treatment of four commercially important aryl sulfonates (naphthalene sulfonic acids H-acid, K-acid, J-acid and benzene sulfonic acid Para base) in aqueous solutions was investigated. Photodegradation kinetics was followed in terms of changes brought about in the parent compound concentration
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