Chemodex

8-Anilino-1-naphthalenesulfonic acid

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Product Details
Synonyms N-Phenyl peri acid; 1,8-ANS; ANS; ANSA; 8-Anilino-1-naphthalenesulfonate; 1-Anilino-8-naphthalenesulfonic acid; NSC 1746
Product Type Chemical
Properties
Formula C16H13NO3S
MW 299.34
CAS 82-76-8
Source/Host Chemicals Synthetic
Purity Chemicals ≥97% (HPLC)
Appearance Gray to dark green to black powder.
Solubility Soluble in DMSO (20mg/ml), DMF (50 mg/ml) or methanol (20mg/ml). Slightly soluble in water (<1mg/ml).
Identity Determined by 1H-NMR.
Declaration Manufactured by Chemodex.
Other Product Data

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Our product description may differ slightly from the original manufacturers product datasheet.

InChi Key FWEOQOXTVHGIFQ-UHFFFAOYSA-N
Smiles O=S(=O)(O)C1=CC=CC2=CC=CC(NC=3C=CC=CC3)=C21
Shipping and Handling
Shipping AMBIENT
Short Term Storage +20°C
Long Term Storage +20°C
Handling Advice Protect from light and moisture.
Use/Stability Stable for at least 2 years after receipt when stored at RT.
Documents
Product Specification Sheet
Datasheet Download PDF
Description
8-Anilino-1-naphthalenesulfonic acid (ANS) is a widely used environment-sensitive fluorescent probe for studying protein structure, conformational changes, and hydrophobic surface exposure. ANS exhibits weak fluorescence in aqueous solutions but shows a strong increase in fluorescence intensity and a blue shift in emission upon binding to hydrophobic regions of proteins, membranes, or macromolecular complexes. This property makes ANS an essential tool for protein folding/unfolding studies, ligand-binding assays, and investigations of protein–protein interactions. It is commonly applied in biochemical and biophysical research to monitor changes in protein conformation under varying conditions such as pH, temperature, or denaturant concentration. Spectral data: λex 371 nm, λem 480 nm in methanol.
Product References
[1] N. Gains & A.P. Dawson AP; Biochem. J. 148, 157 (1975) | [2] V. Cody & J. Hazel; BBRC 68, 425 (1976) | [3] X.C. Yu & H.W. Strobel; Mol. Cell Biochem. 162, 89 (1996) | [4] J. Ishida, et al.; Biol. Pharm. Bull. 19, 1391 (1996) | [5] J. Malecki & Z. Wasylewski; J. Protein Chem. 17, 745 (1998) | [6] M. Andujar-Sanchez, et al.; J. Mol. Recognit. 24, 548 (2011) | [7] H.K. Vivek, et al.; Anal. Biochem. 461, 27 (2014) | [8] C. Ota & K. Takano; Chemphyschem. 20, 1456 (2019) | [9] E.B. Faber, et al.; ACS Chem. Biol. 15, 1759 (2020)
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