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Sigma-Aldrich

5-Amino-1-naphthalenesulfonic acid

technical, ≥60.0% (T)

Synonym(s):

1-Naphthylamine-5-sulfonic acid, Laurent’s acid

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About This Item

Empirical Formula (Hill Notation):
C10H9NO3S
CAS Number:
84-89-9
Molecular Weight:
223.25
Beilstein:
2214149
EC Number:
201-571-0
MDL number:
MFCD00014315
UNSPSC Code:
12352100
PubChem Substance ID:
57652262
NACRES:
NA.22

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

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Pictograms

CorrosionExclamation mark
GHS05,GHS07

Signal Word

Danger

Hazard Statements

H312 + H332,H314

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

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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S C Tyagi et al.
The Journal of biological chemistry, 262(22), 10684-10688 (1987-08-05)
New fluorescent derivatives of dinucleoside monophosphates, (5'-AmNS)UpA/ApU/GpU/CpA, with a fluorophore, 1-aminonaphthalene-5-sulfonic acid (AmNS), attached to the first nucleotide of the dinucleoside monophosphates via a 5'-secondary amine linkage were synthesized in good yield. The chemical structure of (5'-AmNS)ApU was proved by
V Gianotti et al.
Chemosphere, 67(10), 1993-1999 (2007-01-26)
HPLC-DAD, HPLC-MS/MS, GC-MS and spectrophotometric methods are employed to investigate the degradation process of sodium 1-amino-5-naphthalene sulfonate (1A5NS) aqueous solutions, when exposed to sunlight and UV-lamp (254 nm) irradiations. Experimental results show that both sunlight and 254 nm UV-lamp irradiations
Astria D Ferrão-Gonzales et al.
The Journal of biological chemistry, 280(41), 34747-34754 (2005-07-26)
Aggregation of proteins and peptides has been shown to be responsible for several diseases known as amyloidoses, which include Alzheimer disease (AD), prion diseases, among several others. AD is a neurodegenerative disorder caused primarily by the aggregation of beta-amyloid peptide
Yuta Takigawa et al.
Chemical & pharmaceutical bulletin, 68(3), 258-264 (2020-03-03)
Oxo-octadecadienoic acids (OxoODEs) act as peroxisome proliferator-activated receptor (PPAR) agonists biologically, and are known to be produced in the lipoxygenase/linoleate system. OxoODEs seem to originate from the linoleate alkoxyl radicals that are generated from (E/Z)-hydroperoxy octadecadienoic acids ((E/Z)-HpODEs) by a
Fluorescent nucleotide triphosphate substrates for snake venom phosphodiesterase.
S E Pollack et al.
Analytical biochemistry, 127(1), 81-88 (1982-11-15)
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