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8-Amino-1-naphthalenesulfonic acid

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

Sinonimo/i:

1-Amino-8-naphthalenesulfonic acid, Peri acid

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About This Item

Formula condensata:

H₂NC₁₀H₆SO₃H

Numero CAS:

82-75-7

Peso molecolare:

223.25

Numero CE:

201-437-1

Numero MDL:

MFCD00035730

Codice UNSPSC:

12171500

ID PubChem:

24877813

Punto di fusione

>350 °C (lit.)

Stringa SMILE

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

Pittogrammi

GHS05

Avvertenze

Danger

Indicazioni di pericolo

H314

Consigli di prudenza

P280 - P305 + P351 + P338 - P310

Classi di pericolo

Skin Corr. 1B

Codice della classe di stoccaggio

8B - Non-combustible corrosive hazardous materials

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

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

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Certificati d'analisi (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.

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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

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

Pressure and heat inactivation of recombinant human acetylcholinesterase. Importance of residue E202 for enzyme stability.

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

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