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2 3 naphthalene dialdehyde nda

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2,3-Naphthalene dialdehyde (NDA) is a chemical compound used as a reagent in various analytical and research applications. It functions as a fluorescent labeling agent, particularly for the detection and quantification of amino compounds, including amino acids, peptides, and proteins. NDA can form highly fluorescent derivatives when reacting with these target analytes, enabling their sensitive analysis using techniques such as high-performance liquid chromatography (HPLC) and capillary electrophoresis.

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3 protocols using 2 3 naphthalene dialdehyde nda

1

Quantitative Analysis of Taurine

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All solvents used were HPLC grade unless otherwise stated. Sodium hydroxide (NaOH), sulfuric acid (H2SO4), sodium cyanide (NaCN), potassium dihydrogen phosphate (KH2PO4), and dibasic potassium phosphate (K2HPO4), were purchased from Fisher Scientific (Hanover Park, IL). 2,3-Naphthalene dialdehyde (NDA) was obtained from TCI America (Portland, OR). 2-aminoethane sulfonic acid (taurine) and sodium metaborate tetrahydrate (NaBO24H2O) were purchased from Alfa Aesar (Ward Hill, MA). Tetra butyl ammonium sulfate (TBAS) and 2,3,4,5,6-pentaflorobenzyl bromide (PFB-Br) were purchased from Sigma-Aldrich (St. Louis, MO) and Alfa Aesar (Haverhill, MA), respectively.
Phosphate borate buffer (0.05 M; pH 8.5) and NaOH (10 and 100 mM) were prepared in deionized water. H2SO4 (2 M) was diluted with 3.89:5 mL v/v DI water and ethanol. PFB-Br (20 mM) was prepared in ethyl acetate while 10 mM TBAS was diluted with a saturated solution of sodium tetraborate decahydrate (pH 9.5). A stock solution of NaCN was obtained by diluting a 1.8 mM solution (in 10 mM NaOH) with 10 mM aqueous NaOH. An NDA (2 mM) stock solution was prepared in 0.05 M phosphate borate buffer and 40% methanol. A taurine (0.1 M) solution was prepared in phosphate borate buffer. Hydroxoaquocobinamide was obtained from Dr. Gerry Boss, MD (Department of Medicine, University of California, San Diego, La Jolla, USA).
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2

Sensitive Cyanide Quantification in Serum

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All materials used were
HPLC grade unless
otherwise indicated. Sodium hydroxide, sulfuric acid, sodium cyanide,
KH2PO4, K2HPO4, and NH4OH were purchased from Fisher Scientific (Hanover Park, IL).
2,3-Naphthalene dialdehyde (NDA) was obtained from TCI America (Portland,
OR). Taurine (2-aminoethane sulfonic acid) and NaBO2·4H2O were purchased from Alfa Aesar (Ward Hill, MA). NaSCN was
purchased from Acros Organics (Morris Plains, NJ). Human serum albumin
(HSA) and NaHS were purchased from Sigma-Aldrich (St. Louis, MO).
Phosphate (0.1 M)/borate (0.05 M) buffer and stock solutions of sodium
hydroxide (1 M), sulfuric acid (1 M), and NaSCN (1 mM) were prepared
in deionized water. sodium cyanide standards and NaHS were obtained
by dilution from 1.8 mM and 1 M stock solutions, respectively, with
10 mM NaOH. NH4OH was prepared by diluting the original
aqueous solution (29% by weight or 14.5 M) to 30 μM in deionized
water. The NDA (2 mM) stock solution was prepared in phosphate/borate
buffer and 40% methanol. A taurine (50 mM) solution was prepared in
phosphate/borate buffer. A standard HSA solution was obtained by dissolving
3.3 mg of HSA per mL of deionized water.
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3

Sensitive Fluorometric Detection of Cyanide

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All materials used were HPLC grade unless otherwise indicated. Sodium hydroxide, sulfuric acid, sodium cyanide, KH2PO4, K2HPO4, and NH4OH were purchased from Fisher Scientific (Hanover Park, IL). 2,3-Naphthalene dialdehyde (NDA) was obtained from TCI America (Portland, OR). Taurine (2-aminoethane sulfonic acid) and NaBO2·4H2O were purchased from Alfa Aesar (Ward Hill, MA). NaSCN was purchased from Acros Organics (Morris Plains, NJ). Human serum albumin (HSA) and NaHS were purchased from Sigma-Aldrich (St. Louis, MO).
Phosphate (0.1 M)/borate (0.05 M) buffer and stock solutions of Sodium hydroxide (1 M), sulfuric acid (1 M), and NaSCN (1 mM) were prepared in deionized water. sodium cyanide standards and NaHS were obtained by dilution from 1.8 mM and 1 M stock solutions, respectively, with 10 mM NaOH. NH4OH was prepared by diluting the original aqueous solution (29% by weight or 14.5 M) to 30 µM in deionized water. The NDA (2 mM) stock solution was prepared in phosphate/borate buffer and 40% methanol. A taurine (50 mM) solution was prepared in phosphate/borate buffer. A standard HSA solution was obtained by dissolving 3.3 mg of HSA per mL of deionized water.
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