70800
5-Amino-1-naphthalenesulfonic acid
technical, ≥60.0% (T)
Synonym(s):
1-Naphthylamine-5-sulfonic acid, Laurent’s acid
Sign Into View Organizational & Contract Pricing
All Photos(1)
About This Item
Empirical Formula (Hill Notation):
C10H9NO3S
CAS Number:
Molecular Weight:
223.25
Beilstein:
2214149
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
grade
technical
form
powder
concentration
≥60.0% (T)
SMILES string
Nc1cccc2c(cccc12)S(O)(=O)=O
InChI
1S/C10H9NO3S/c11-9-5-1-4-8-7(9)3-2-6-10(8)15(12,13)14/h1-6H,11H2,(H,12,13,14)
InChI key
DQNAQOYOSRJXFZ-UHFFFAOYSA-N
Looking for similar products? Visit Product Comparison Guide
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Dermal - Skin Corr. 1B
Storage Class Code
8B - Non-combustible corrosive hazardous materials
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Fluorescent nucleotide triphosphate substrates for snake venom phosphodiesterase.
S E Pollack et al.
Analytical biochemistry, 127(1), 81-88 (1982-11-15)
Brent A Mulder et al.
Nucleic acids research, 33(15), 4865-4873 (2005-09-06)
The mechanism by which HIV-1 reverse transcriptase (HIV-RT) discriminates between the correct and incorrect nucleotide is not clearly understood. Chemically modified nucleotides containing 1-aminonaphthalene-5-sulfonate (ANS) attached to their gamma-phosphate were synthesized and used to probe nucleotide selection by this error
Y T Kim et al.
The Journal of biological chemistry, 263(27), 13712-13717 (1988-09-25)
Physical interactions between pyridoxal kinase and aspartate aminotransferase were detected by means of emission anisotropy and affinity chromatography techniques. Binding of aspartate aminotransferase (apoenzymes) to pyridoxal kinase tagged with a fluorescent probe was detected by emission anisotropy measurements at pH
J Fick et al.
European journal of biochemistry, 126(2), 367-372 (1982-08-01)
Fluorescence studies of the intramolecular and intermolecular interactions between aminonaphthylsulfonate and nucleotides of uracil or adenine are described. The fluorescence originates solely from the naphthyl moiety and is intramolecularly quenched by the base, uracil being more effective than adenine. The
U Bhattacharyya et al.
The Journal of biological chemistry, 274(21), 14573-14578 (1999-05-18)
In the previous paper we demonstrated that uridine-5'-beta-1-(5-sulfonic acid) naphthylamidate (UDPAmNS) is a stacked and quenched fluorophore that shows severalfold enhancement of fluorescence in a stretched conformation. UDPAmNS was found to be a powerful competitive inhibitor (Ki = 0.2 mM)
Active Filters
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service
