Benzoyl peroxide
Benzoyl peroxide is a chemical compound commonly used as a lab reagent. It is a white crystalline solid with the chemical formula C6H5COO)2. Benzoyl peroxide has oxidizing properties and is commonly used as a bleaching agent and disinfectant in various laboratory applications.
Lab products found in correlation
89 protocols using benzoyl peroxide
Fibrinogen-Conjugated Nanoparticle Synthesis
Kaempferia galanga Rhizome Extract Characterization
Comprehensive Bone Histomorphometry Analysis
For static analysis, femurs or tibias were fixed in 4% paraformaldehyde (Merck) for 3 days, washed for 2 hours with water, and decalcified in the presence of 15% EDTA for 10 days with mild shaking at 37°C. The bones were embedded in paraffin. Osteoclast number/bone perimeter and osteoclast surface/bone surface were quantified on decalcified sections of either tibia or femur stained for tartrate‐resistant acid phosphatase (TRAP).
Undecalcified femurs were first dehydrated and infiltrated with destabilized methylmetacrylate (Merck), benzoylperoxide (Merck), and nonylphenyl‐polyethyleneglycol acetate (Sigma‐Aldrich, St. Louis, MO, USA) for 14 days. Embedding in methylmetracrylate was done overnight at 4°C, and the femurs were used for dynamic analysis. Osteoblast number/bone perimeter, osteoblast surface/bone surface, and osteocyte number were quantified on toluidine blue‐stained undecalcified femoral sections. Two sections were analyzed for each mouse. Bone formation rate (BFR)/bone surface was measured on undecalcified bone sections by means of fluorochrome labeling. Osteomeasure software was used for the analysis (Osteometrics, Decatur, GA, USA)
Wood Modification with Chemicals
Dimerization of Hex-1-ene using Zirconium Complex
Zirconium complex
Synthesis of D-mannose Oligomers
Synthesis and Functionalization of PS/DVB Particles
Ultrapure water was used as received from a MilliQ-system (Merck-Millipore Billerica, MA, USA). The monomer was synthesized using 4-vinylbenzyl chloride (90%, Sigma-Aldrich, Steinheim, Germany) and N-methyl diethanolamine (≥99% Sigma-Aldrich, Steinheim, Germany) without further treatment. The detailed procedure is given in Ref. [46 (link)]. DMSO (99.5%, Grüssing GmbH, Grüssing, Germany) and benzoyl peroxide (for synthesis, 25% water, Merck, Darmstadt, Germany) as well as the organic solvents for the synthesis were used as received.
For preparation of the eluents sodium carbonate (p.a., VWR chemicals, Leuven, Belgium) and sodium hydroxide solution (50%, p.a., Merck, Darmstadt, Germany) were used. The IC standards were prepared from the sodium salts (p.a.) of the anions.
Synthesis of Nanocomposite Dental Materials
Comprehensive Chemical Reagents Procurement
Synthesis of Organic Compounds: A Comprehensive Approach
nitrate trihydrate
(Merck-AR), sodium hydroxide (Merck-LR), poly(acrylic acid) (weight
average molecular weight MW ∼240000
by GPC, 25 wt % in H2O) (Sigma-Aldrich-AR),
acid (S.D. Fine Chemicals-LR), sodium ascorbate (Merck-LR), propargyl
bromide (Merck-LR), 2-aminophenol (Merck-LR), 2-aminothiophenol (Merck-LR),
4-methylcinnamic acid (Merck-LR), 4-methyl benzaldehyde (Merck-LR),
phosphorus oxychloride (Merck-LR), pyrocatechol (Merck-LR), acetylene
(National Oxygen Limited), N-bromosuccinimide (NBS)
(S.D. Fine Chemicals-LR), benzoyl peroxide (Merck-LR), potassium carbonate
(Merck-LR), sodium bicarbonate (Merck-LR), sodium sulfate (Merck-LR),
dimethyl sulfoxide (DMSO( (Merck-AR), dimethylformamide (DMF) (Merck-AR),
tetrahydrofuran (THF) (Merck-LR), hexane (Merck-LR), acetone (S.D.
Fine Chemicals-AR), chloroform (CHCl3) (S.D. Fine Chemicals-AR),
tetrachloromethane (S.D. Fine Chemicals-AR), methanol (S.D. Fine Chemicals-AR),
ethanol (S.D. Fine Chemicals-AR), and double distilled water were
used.
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