4 methylbenzaldehyde
4-methylbenzaldehyde is a colorless to pale yellow liquid organic compound. It has a characteristic sweet, almond-like odor. The chemical formula is C8H8O. This compound is commonly used as a chemical intermediate in the production of various pharmaceutical and fragrance products.
Lab products found in correlation
8 protocols using 4 methylbenzaldehyde
Synthesis of Copper-Based Catalyst
Synthesis and Antimicrobial Evaluation
Benzaldehyde Derivatives Synthesis Protocols
Ethyl acetate (for analysis EMSURE ACS, ISO, Reag. Ph Eur) and acetone (for analysis EMPARTA ACS) were acquired from Merck. Thin-layer chromatography (TLC) was conducted using aluminum plates (F-254) covered with silica gel. The experiment included the use of silica gel (230–400 mesh, Merck) for column chromatography.
Pig Blood Lipid Membrane Analysis
Human serum albumin (lyophilized powder, essentially fatty acid free), 2′-hydroxyacetophenone, 4-methylbenzaldehyde, deuterium oxide (D2O), egg yolk phosphatidylcholine (PC) were purchased from Sigma–Aldrich. The probes1,6-diphenyl-1,3,5-hexatriene (DPH) and Laurdan were purchased from Molecular Probes (Eugene, OR, USA).
Chromium Ion Determination Protocol
Synthesis and Characterization of Nickel(II) Catalyst for A³ Coupling Reaction
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.
Synthesis of Substituted Pyrano[2,3-c]pyrazoles
About PubCompare
Our mission is to provide scientists with the largest repository of trustworthy protocols and intelligent analytical tools, thereby offering them extensive information to design robust protocols aimed at minimizing the risk of failures.
We believe that the most crucial aspect is to grant scientists access to a wide range of reliable sources and new useful tools that surpass human capabilities.
However, we trust in allowing scientists to determine how to construct their own protocols based on this information, as they are the experts in their field.
Ready to get started?
Sign up for free.
Registration takes 20 seconds.
Available from any computer
No download required
Revolutionizing how scientists
search and build protocols!