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531340

8-Amino-1-naphthalenesulfonic acid

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

Synonyme(s) :

1-Amino-8-naphthalenesulfonic acid, Peri acid

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About This Item

Formule linéaire :

H₂NC₁₀H₆SO₃H

Numéro CAS:

82-75-7

Poids moléculaire :

223.25

Numéro CE :

201-437-1

Numéro MDL:

MFCD00035730

Code UNSPSC :

12171500

ID de substance PubChem :

24877813

Pf

>350 °C (lit.)

Chaîne SMILES

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

Pictogrammes

GHS05

Mention d'avertissement

Danger

Mentions de danger

H314

Conseils de prudence

P280 - P305 + P351 + P338 - P310

Classification des risques

Skin Corr. 1B

Code de la classe de stockage

8B - Non-combustible corrosive hazardous materials

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

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

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Certificats d'analyse (COA)

Lot/Batch Number

09826MC

08319DI

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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

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

The design, synthesis, and characterization of the first cavitand-based de novo hetero-template-assembled synthetic proteins (Hetero-TASPs).

Heidi E K Huttunen-Hennelly et al.

Organic & biomolecular chemistry, 5(22), 3637-3650 (2007-11-01)

The design, synthesis, and characterization of novel cavitand-based hetero-TASPs, TASPs having different peptide sequences within one bundle, are described. Three families of hetero-TASPs were designed: the LG3/LG2 family (different linker lengths), LG3/AG3 family (altering helix hydrophobicity), and the LG3/LG2C family

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