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531340

8-Amino-1-naphthalenesulfonic acid

Name: 8-Amino-1-naphthalenesulfonic acid
Brand: SIAL

Synonym(s):

1-Amino-8-naphthalenesulfonic acid, Peri acid

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About This Item

Linear Formula:

H₂NC₁₀H₆SO₃H

CAS Number:

82-75-7

Molecular Weight:

223.25

UNSPSC Code:

12171500

PubChem Substance ID:

24877813

EC Number:

201-437-1

MDL number:

MFCD00035730

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mp

>350 °C (lit.)

SMILES string

Nc1cccc2cccc(c12)S(O)(=O)=O

pictograms

GHS05

signalword

Danger

hcodes

H314

pcodes

P280 - P305 + P351 + P338 - P310

Hazard Classifications

Skin Corr. 1B

Storage Class

8B - Non-combustible corrosive hazardous materials

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

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

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number

09826MC

08319DI

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Recovery of components of fluorescence spectra of mixtures by intensity- and anisotropy decay-associated analysis: the bacterial luciferase intermediates.

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

Fusion of Sendai virus with model membranes as affected by dehydrating agents and pH: correlation between viral envelope hydrophobicity and fusion activity.

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

Identification of the hydrophobic ligand-binding region in recombinant glutathione S-transferase P and its binding effect on the conformational state of the enzyme.

J Nishihira et al.

Archives of biochemistry and biophysics, 302(1), 128-133 (1993-04-01)

Recombinant glutathione S-transferase P (GST-P) was purified in a homogeneous state. Fatty acid analysis of the enzyme revealed that the final enzyme preparation endogenously bound fatty acids, mostly palmitic acid or stearic acid, which were difficult to dissociate from the

Interaction of Triton X-100 and octyl glucoside with liposomal membranes at sublytic and lytic concentrations. Spectroscopic studies.

J Lasch et al.

Biochimica et biophysica acta, 1022(2), 171-180 (1990-02-28)

The molecular mechanism of the solubilisation of phospholipid bilayers by nonionic detergents was studied by turbidity changes, carboxyfluorescein fluorescence dequenching, steady-state and time-resolved fluorescence anisotropy of DPH, lifetime measurements, ANS binding and 31P-NMR. Particular attention has been paid to the

Characterization of large peptide fragments derived from the N-terminal domain of the ribosomal protein L9: definition of the minimum folding motif and characterization of local electrostatic interactions.

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

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