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N n dimethyl p phenylenediamine

Manufactured by Merck Group
Sourced in Germany, United States

N,N-dimethyl-p-phenylenediamine is a chemical compound used as a reagent in laboratory analysis and testing. It is a colorless to pale yellow crystalline solid with a characteristic odor. The compound is commonly used in various analytical techniques, such as colorimetric determination of certain analytes. Its core function is to serve as a chemical indicator or detection agent in these laboratory applications.

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11 protocols using n n dimethyl p phenylenediamine

1

Anticancer Effects of Djulis Compound

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Djulis was obtained from Sinfong Agritech Co. (Taipei, Taiwan). Iron (III) chloride hexahydrate, methylene blue, and acetic acid were purchased from Nacalai Tesque (Tokyo, Japan), Showa Chemicals (Tokyo, Japan), and Shimakyu Pure Chemicals (Osaka, Japan), respectively. The Bax primary antibody and Bcl-2 primary antibody were purchased from Cell Signaling Technology (Beverly, MA, USA). Glyceraldehyde-3-phosphate dehydrogenase and the caspase-9 primary antibody were purchased from GeneTex (Irvine, CA, USA). The proliferating cell nuclear antigen (PCNA) primary antibody, goat anti-rabbit immunoglobulin G (IgG) secondary antibody, and peroxidase AffiniPure goat anti-mouse IgG were purchased from Abcam (Cambridge, UK), Southern Biotechnology (Birmingham, AL, USA), and Jackson ImmunoResearch (West Grove, PA, USA), respectively. The β-actin primary antibody, 1,2-dimethylhydrazine (DMH), N,N’-dimethyl-p-phenylenediamine, N,N’-dimethyl-m-phenylenediamine, Alcian blue, and the remaining chemicals were purchased from Sigma Chemical (St. Louis, MO, USA).
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2

Antioxidant Capacity Assay Protocol

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Xanthine oxidase 0.39 U·mg−1 and cellulose acetate were supplied by Fluka AG (Buchs, Switzerland). 2,2′-Azobis(2-amidinopropane) dihydrochloride (AAPH) was supplied by Waco Chem (Richmond, VA, USA). Potassium dihydrogenphosphate, sodium acetate and sodium hydrogenphosphate were supplied by Carlo Erba (Milan, Italy). Polyvinylacetate, acid-2-carboxy-6-hydroxy-2,5,7,8-tetramethylchroman (Trolox) was supplied by Aldrich (Steinheim, Germany). Xanthine (2,6-dihydroxypurine) sodium salt, N,N-dimethyl-p-phenylenediamine, ethylenediamine tetraacetic acid (EDTA) sodium salt, superoxide dismutase 4980 U·mg−1, ferric chloride, dialysis membrane (art. D-9777), and β-phycoerythrin were supplied by Sigma (Milan, Italy).
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3

Antioxidant Capacity Evaluation

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Acetylcholinesterase, acetylcholine iodide2,2′-azino-bis 3-ethylbenzthiazoline-6-sulfonic acid (ABTS), 1,1-diphenyl-2-picrylhydrazyl (DPPH), N,N-dimethyl-p-phenylenediamine (DMPD), 2,9-dimethyl-1,10-phenanthroline (Neocuproine), butylated hydroxytoluene (BHT), butylated hydroxyanisole (BHA), α-tocopherol, trolox, and solvents were obtained from Sigma-Aldrich (Sigma-Aldrich GmbH, Steinheim, Germany). They were of analytical grade and used without further purification steps.
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4

UV-Vis Analysis of Antioxidant Compounds

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Shimadzu UV-1800 (Kyoto, Japon) spectrophotometer was used for absorption measurements. Hellma GmbH & Co. KG (Müllheim, Germany) quartz cuvettes with 1 cm optical thickness were used for the UV-Vis measurements.
All reagents were of analytical reagent grade unless otherwise stated. Quercetin (QR), gallic acid (GA), ferulic acid (FA), caffeic acid (CFA), catechin (CAT), epicatechin, trolox (TR), para-coumaric acid (p-CUM), L-ascorbic acid (AA), L-cysteine (CYS), morin (MR), rutin (RT), hydrogen peroxide (30% by mass), and N,N-Dimethyl-p-phenylenediamine (DMPD) were purchased from Sigma-Aldrich Chemie GmbH (Steinheim, Germany), and all other reagents from Merck KGaA (Darmstadt, Germany) and Sigma-Aldrich Chemie GmbH. Commercial orange juice and green tea samples were obtained from local markets.
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5

Antioxidant and Enzyme Inhibition Assays of Propolis

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Acetylcholinesterase, acetylcholine iodide, α-glycosidase, p-nitrophenyl-D-glycopyranoside, 2,2′-azino-bis 3-ethylbenzthiazoline-6-sulfonic acid (ABTS), 1,1-diphenyl-2-picrylhydrazyl (DPPH), N,N-dimethyl-p-phenylenediamine (DMPD), 2,9-dimethyl-1,10-phenanthroline (Neocuproine), butylated hydroxytoluene (BHT), butylated hydroxyanisole (BHA), α-tocopherol, trolox, and standard phenolic compounds of LC-MS/MS were purchased from Sigma (Sigma-Aldrich GmbH, Steinheim, Germany). The other materials were procured from Sigma-Aldrich or Merck (Darmstadt, Germany), appropriately. Propolis was dissolved in ethanol for antioxidant activities, but in DMSO for enzyme inhibition tests due to the potential inhibitory effects of ethanol.
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6

Synthesis and Characterization of PANI

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Citrate-phosphate buffer was prepared with Na2HPO4 and citric acid purchased from Merck Millipore. N,N’-dimethyl-p-phenylenediamine (DMPD), N-methyl-2-pyrrolidone (NMP), aniline, sodium dodecyl sulfate (SDS), docusate sodium salt (AOT) and sodium dodecylbenzenesulfonate (SDBS) were all from Sigma Aldrich. Sodium lauryl ether sulfate (SLES) (40%) was obtained from Gran Velada. Tetrahidrofuran (THF) and N,N-dimethylformamide (DMF) were obtained from LabsScan. 2,2'-Azinobis (3-ethylbenzothiazoline-6-sulfonic acid) diammonium salt (ABTS) was purchased from Roche. Chemical synthesized emeraldine salt (average Mw>15,000 Da) was purchased from Sigma Aldrich. All chemicals were of reagent-grade purity.
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7

Histochemical Staining with AB + PAS

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As described for AB + PAS staining, sections were dewaxed and rehydrated. Slides were washed in PBS and incubated in the dark for 18 h with HID solution (0.24% N,N,dimethyl-m-phenylenediamine (Sigma 219223), 0.04% N,N,dimethyl-p-phenylenediamine (Sigma 193992), 1.68% Iron (III) chloride (sigma 157740)). Slides were then incubated for 5 min in 1% Alcian blue, washed in PBS, dehydrated through an alcohol gradient, cleared with citroclear and coverslips mounted using DPX38 (link).
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8

Amyloid-beta Aggregation Inhibition

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All reagents were purchased from commercial suppliers and used as received unless otherwise stated. N,N-Dimethyl-p-phenylenediamine was purchased from Sigma-Aldrich (St. Louis, MO, USA). Aβ40 and Aβ42 were purchased from AnaSpec (Fremont, CA, USA) (Aβ42 = DAEFRHDSGYEVHHQKL-VFFAEDVGSNKGAIIGLMVGGVVIA). An Agilent 8453 UV–visible (UV–vis) spectrophotometer (Santa Clara, CA, USA) was used to measure optical spectra. Anaerobic reactions were performed in a N2-filled glovebox (Korea Kiyon, Bucheon-si, Gyeonggi-do, Korea). TEM images were taken using a Philips CM-100 transmission electron microscope (Microscopy and Image Analysis Laboratory, University of Michigan, Ann Arbor, MI, USA) or a JEOL JEM-2100 transmission electron microscope (UNIST Central Research Facilities, Ulsan National Institute of Science and Technology, Ulsan, Republic of Korea). Absorbance values for cell viability assay were measured on a SpectraMax M5 microplate reader (Molecular Devices, Sunnyvale, CA, USA). All IM–MS experiments were carried out on a Synapt G2 (Waters, Milford, MA, USA). NMR studies of DMPD with and without Zn(II) were carried out on a 400 MHz Agilent NMR spectrometer. NMR studies of Aβ with DMPD were conducted on a 900 MHz Bruker spectrometer equipped with a TCI triple-resonance inverse detection cryoprobe (Michigan State University, Lansing, MI, USA).
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9

Antioxidant Compounds Characterization

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Taxifolin, methionine, riboflavin, linoleic acid, butylated hydroxyanisole, butylated hydroxytoluene, N,N-dimethyl-p-phenylenediamine, 2,2 0 -azino-bis(3-ethylbenzthiazoline-6-sulfonic acid), 2,9-dimethyl-1,10-phenanthroline, nitroblue tetrazolium, 1,1diphenyl-2-picryl-hydrazyl, 3-(2-pyridyl)-5,6-bis(4-phenyl-sulfonic acid)-1,2,4-triazine, trichloroacetic acid, and a-tocopherol were purchased commercially from Sigma-Aldrich GmbH, Sternheim, Germany. Ammonium thiocyanate was obtained from Merck. All other chemicals used were of analytical grade and attained from either Sigma-Aldrich (Sternheim, Germany) or Merck (Darmstat, Germany).
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10

Terpene and Lipid Histochemistry of Plant Tissues

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The plant material had been fixed in a solution of 50% ethanol and glycerol in a ratio of 7:3 for 24 h to soften the tissues. Hand-cut transverse and tangential longitudinal sections were made from the stem and leaf of the plant. Terpene histochemistry was examined using NADI reagent (0.5 mL of 0.1% α-naphthol (Merck KGaA, Darmstadt, Germany), 0.5 mL of 1% N,N-dimethyl-p-phenylenediamine (Merck KGaA, Darmstadt, Germany), and 49 mL of 0.1 M sodium phosphate buffer, pH 7.2 (Merck KGaA, Darmstadt, Germany) [77 ]. Cross sections were incubated with NADI reagent for 1 h in the dark, washed in sodium phosphate buffer (0.1 M, pH 7.2) for 2 min, and mounted in the same buffer. Lipid histochemistry was examined using Sudan III (Merck KGaA, Darmstadt, Germany). The sections were treated with Sudan III in 70% ethanol for 30 min, rinsed briefly in 80% ethanol, and mounted in 50% glycerol [77 ]. The sections were observed with a light microscope (Leica DM 2000 LED, Leica Microsystems, Wetzlar, Germany) equipped with a digital camera (Leica DMC 2900) and image processing software (Leica Application Suite, LAS).
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