Methyl orange
Methyl orange is a chemical compound that serves as a pH indicator, commonly used in analytical chemistry and laboratories. It is a yellow-orange powder that changes color based on the pH of the solution it is added to, making it a valuable tool for monitoring and measuring acidity or alkalinity.
Lab products found in correlation
14 protocols using methyl orange
Synthesis and Characterization of Metal-Organic Complexes
Synthesis and Characterization of Gold Nanoparticles
Synthesis and Characterization of Dye-Loaded Nanocomposites
were of analytical
reagent grade and used without further purification. FeCl3·6H2O, FeCl2·4H2O, and
urea were purchased from Sigma-Aldrich. Al(NO3)3·6H2O, Mg(NO3)2·6H2O, NaOH, and ethylene glycol were purchased from Merck. Polyethylene
glycols (PEG) with different molecular weights (1.5, 2.0, 4.0, and
6.0 k) were purchased from Loba Chemie. Methyl orange, acid blue 113,
acid blue 147, and Nile blue A were purchased from Alfa Aesar. The
stock solution for all the experiments was prepared using double distilled
(DD) water.
Synthesis and Characterization of Nanomaterials
hydroxide (98%), nickel nitrate (98%), sodium borohydride (98%), rhodamine
B, methyl orange, methylene blue, 4-nitrophenol (99%), 2-nitrophenol
(98%), and 2-nitroaniline (98%) were purchased from Alfa Aesar, and
silver nitrate (>99.5%) was bought from Merck. These materials
were
utilized as precursors without further purification. Deionized water
was used for the preparation of solutions and in all the experiments.
Laser Synthesis of Metal Oxide Nanoparticles
Preparation of Pure Titanium Sheets
Versatile Polymer-Mediated Nanocomposites
N-Isopropylacrylamide (NIPAM, 97% Sigma-Aldrich) and 2-acrylamido-2-methylpropane sulfonic acid (AMPS, 99% Sigma-Aldrich) were used as monomers, N,N′-methylene-bis-acrylamide (MBA, 99% Sigma-Aldrich) was used as a crosslinker. Ammonium per sulfate (APS, 98% Sigma-Aldrich) was used as an initiator and sodium dodecyl sulfate (SDS, ≥98.5% BDH Chemicals) was used as a surfactant. Silver nitrate (AgNO3, 99% Sigma-Aldrich) was used as a metal precursor. Sodium borohydride (NaBH4, 98% Sigma-Aldrich) was employed as a reducing agent. 4-Nitrophenol (4-NP, 99% Sigma-Aldrich), 2-nitrophenol (2-NP, 98% Sigma-Aldrich), 2-nitroaniline (2-NA, 98% Sigma-Aldrich), methyl orange (MO, 85% Alpha Aesar), Methylene Blue (MB 82% Alpha Aesar), Eosin Y (EY, 82% Alpha Aesar) were used for catalytic degradation. Deionized water was prepared in the laboratory and used throughout this work.
Synthesis and Characterization of Metal-Dye Complexes
were used as received and without any further purification. Aluminum
nitrate nonahydrate Al(NO3)3·9H2O was provided by BDH. Nickel nitrate hexahydrate Ni(NO3)2·6H2O and ethanol absolute were purchased
from Sigma-Aldrich. Propylene oxide (noted PO; CH3CHCH2O), orange II (noted OII, C16H11N2NaO4S), methyl orange (noted MO, C14H14N3NaO3S), Congo Red (noted CR,
C32H22N6Na2O6S2), methylene blue (noted MB, C16H18ClN3S·xH2O), rhodamine
B (noted rhB, C28H31ClN2O3), and rhodamine 6G (noted rh6G, C28H31N2O3Cl) were provided by Acros. Acetone was purchased
from Scharlau Chemie S.A. Double distilled water was obtained from
our laboratory.
Photochemical Oxidation of Carvacrol and Thymol
Cyclodextrin complexation of plant phenolics
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