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Safety Information

249548

Sigma-Aldrich

2-Naphthalenesulfonic acid

technical grade, 70%

Synonym(s):

β-Naphthalenesulfonic acid, 2-Naphthylsulfonic acid, 2-Sulfonaphthalene

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About This Item

Linear Formula:
C10H7SO3H
CAS Number:
Molecular Weight:
208.23
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

grade

technical grade

Quality Level

Assay

70%

form

solid

solubility

water: freely soluble(lit.)

SMILES string

OS(=O)(=O)c1ccc2ccccc2c1

InChI

1S/C10H8O3S/c11-14(12,13)10-6-5-8-3-1-2-4-9(8)7-10/h1-7H,(H,11,12,13)

InChI key

KVBGVZZKJNLNJU-UHFFFAOYSA-N

Gene Information

Related Categories

General description

The fluorescence of 2-naphthalenesulfonic acid (NSA) is effectively quenched by colloidal silver via photoinduced interfacial electron transfer from the excited singlet of NSA to silver. Adsorption behavior of NSA on a conventional macroporous resin Amberlite XAD4 and hypercrosslinked resins NDA101 and NDA100 has been investigated.

Physical properties

Contains up to 15% sulfuric acid

Pictograms

Corrosion

Signal Word

Danger

Hazard Statements

Hazard Classifications

Eye Dam. 1 - Met. Corr. 1 - Skin Corr. 1A

Storage Class Code

8A - Combustible, corrosive hazardous materials

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


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.

PDSCL

Deleterious substance

ISHL Indicated Name

Substances Subject to be Indicated Names

ISHL Notified Names

Substances Subject to be Notified Names

JAN Code

249548-5G:4.548174004845E12
249548-100G:4.548174004838E12


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Binary competitive and cooperative adsorption of aromatic compounds on polymeric resins.
Zhang W-M, et al.
Chinese Journal of Polymer Science, 23(05), 503-511 (2005)
Sabine Neuberger et al.
Analytical and bioanalytical chemistry, 408(30), 8701-8712 (2016-07-14)
Capillary electrophoresis is commonly applied for the analysis of pharmaceutical products due to its high separation efficiency and selectivity. For this purpose, electrospray-ionization-(ESI)-interfering additives or electrolytes are often required, which complicates the identification of impurities and degradation products by mass
Sabine Neuberger et al.
Journal of pharmaceutical and biomedical analysis, 134, 122-129 (2016-12-03)
In order to ensure the stability of pharmaceutical products appropriate manufacturing and storage conditions are required. In general, the degradation of active pharmaceutical ingredients (APIs) and subsequent formation of degradation products affect the pharmaceutical quality. Thus, a fast and effective
Doyeon Lee et al.
Sensors (Basel, Switzerland), 18(6) (2018-06-09)
Detection of salivary pepsin has been given attention as a new diagnostic tool for laryngopharyngeal reflux (LPR) disease, because saliva collection is non-invasive and relatively comfortable. In this study, we prepared polypyrrole nanocorals (PPNCs) on a screen-printed carbon electrode (SPCE)
Colloidal silver as a quencher for the fluorescence of 2-naphthalenesulfonic acid.
Zang L, et al.
Journal of the Chemical Society. Chemical Communications, 4, 447-448 (1995)

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