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Ursprungszeugnis (CoO)/Analysenzertifikate (CoA)

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531340

1-Aminonaphthalin-8-sulfonsäure

Name: 1-Aminonaphthalin-8-sulfonsäure
Brand: SIAL

Synonym(e):

Clevesäure-1,8

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About This Item

Lineare Formel:

H₂NC₁₀H₆SO₃H

CAS-Nummer:

82-75-7

Molekulargewicht:

223.25

EG-Nummer:

201-437-1

MDL-Nummer:

MFCD00035730

UNSPSC-Code:

12171500

PubChem Substanz-ID:

24877813

mp (Schmelzpunkt)

>350 °C (lit.)

SMILES String

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

Piktogramme

GHS05

Signalwort

Danger

H-Sätze

H314

P-Sätze

P280 - P305 + P351 + P338 - P310

Gefahreneinstufungen

Skin Corr. 1B

Lagerklassenschlüssel

8B - Non-combustible corrosive hazardous materials

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

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

Hier finden Sie alle aktuellen Versionen:

Analysenzertifikate (COA)

Lot/Batch Number

09826MC

08319DI

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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

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

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

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

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

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