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70382

Supelco

Sodium 1,2-naphthoquinone-4-sulfonate

for spectrophotometric det. of isonicotic hydrazide, amines and amino acids, ≥97.0% (T)

Synonym(s):

1,2-Naphthoquinone-4-sulfonic acid sodium salt, 3,4-Dihydro-3,4-dioxo-1-naphthalenesulfonic acid sodium salt, Folin’s reagent

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About This Item

Empirical Formula (Hill Notation):
C10H5NaO5S
CAS Number:
521-24-4
Molecular Weight:
260.20
Beilstein:
4169788
EC Number:
208-308-9
MDL number:
MFCD00001700
UNSPSC Code:
12000000
PubChem Substance ID:
329762068
NACRES:
NA.21

Assay

≥97.0% (HPLC)
≥97.0% (T)

form

powder

quality

for spectrophotometric det. of isonicotic hydrazide, amines and amino acids

specific analyte(s)

sodium

technique(s)

UV/Vis spectroscopy: suitable
photometry: suitable

solubility

H2O: 50 mg/mL, clear

SMILES string

[Na+].[O-]S(=O)(=O)C1=CC(=O)C(=O)c2ccccc12

InChI

1S/C10H6O5S.Na/c11-8-5-9(16(13,14)15)6-3-1-2-4-7(6)10(8)12;/h1-5H,(H,13,14,15);/q;+1/p-1

InChI key

UBLXEEBHYISRFM-UHFFFAOYSA-M

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Other Notes

Determination of amines

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
BCCH7872
BCCG1438
BCCB1990
BCBW9424
BCBT6993

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C. Molins Legua et al.
Fresenius Journal of Analytical Chemistry, 349, 311-311 (1994)
Y. Asahi et al.
Chemical & Pharmaceutical Bulletin, 32, 3093-3093 (1984)
Liliam K Harada et al.
Biosensors, 11(4) (2021-05-01)
During the last decennium, it has become widely accepted that ubiquitous bacterial viruses, or bacteriophages, exert enormous influences on our planet's biosphere, killing between 4-50% of the daily produced bacteria and constituting the largest genetic diversity pool on our planet.
L G Martinez et al.
Journal of chromatography. B, Biomedical sciences and applications, 718(1), 143-151 (1998-12-01)
Cefotaxime was derivatised with 1,2-naphthoquinone-4-sulphonate (NQS), extracted into solid-phase cartridges (C18) and detected using a UV-visible detection system. Optimum conditions for this new procedure were: hydrogencarbonate-carbonate buffer, pH 10.5, 5-min reaction time at 25 degrees C and an NQS concentration
Ibrahim A Darwish et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 72(4), 897-902 (2009-01-13)
Spectrophotometric study was carried out, for the first time, to investigate the reaction between the antidepressant fluvoxamine (FXM) and 1,2-naphthoquinone-4-sulphonate (NQS) reagent. In alkaline medium (pH 9), an orange-colored product exhibiting maximum absorption peak (lambda(max)) at 470nm was produced. The
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