531340
8-Amino-1-naphthalenesulfonic acid
Synonym(s):
1-Amino-8-naphthalenesulfonic acid, Peri acid
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About This Item
Linear Formula:
H2NC10H6SO3H
CAS Number:
Molecular Weight:
223.25
EC Number:
MDL number:
UNSPSC Code:
12171500
PubChem Substance ID:
mp
>350 °C (lit.)
SMILES string
Nc1cccc2cccc(c12)S(O)(=O)=O
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Skin Corr. 1B
Storage Class Code
8B - Non-combustible corrosive hazardous materials
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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Jia-Cherng Horng et al.
Biochemistry, 41(45), 13360-13369 (2002-11-06)
A set of peptides derived from the N-terminal domain of the ribosomal protein L9 (NTL9) have been characterized in an effort to define the minimum unit of this domain required to fold and to provide model peptides for the analysis
M Cardamone et al.
The Biochemical journal, 282 ( Pt 2), 589-593 (1992-03-01)
The equilibrium binding of the apolar fluorescent dye 1-anilinonaphthalene-8-sulphonate (ANS) to bacteriorhodopsin, BSA, chicken egg lysozyme, ovalbumin, porcine somatotrophin (PST) and bovine pancreatic ribonuclease (RNAase) was quantitatively evaluated using Scatchard- and Klotz-plot analyses. On the basis of the average association
Cécile Cléry-Barraud et al.
European journal of biochemistry, 269(17), 4297-4307 (2002-08-30)
The effects of pressure on structure and activity of recombinant human acetylcholinesterase (rHuAChE) were investigated up to a pressure of 300 MPa using gel electrophoresis under elevated hydrostatic pressure, fluorescence of bound 8-anilinonaphthalene-1-sulfonate (ANS) and activity measurements following exposure to
J Lee et al.
Analytical biochemistry, 185(2), 220-229 (1990-03-01)
Reaction of FMNH2 and O2 with bacterial luciferase followed by blue light irradiation results in a product previously claimed to have the same fluorescence spectral distribution as the bioluminescence. Preparations of this "high fluorescence" intermediate, however, contain two fluorescent components
J Ramalho-Santos et al.
Biochemistry and molecular biology international, 32(6), 1121-1127 (1994-04-01)
We have studied the importance of hydrophobic interactions in the fusion activity of Sendai virus. Viral fusion activity towards model lipid membranes was monitored using a fluorescence dequenching assay. Fusion was dependent on the composition of the target membrane and
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