CAS 619-60-3: 4-(Dimethylamino)phenol
Formula:C8H11NO
InChI:InChI=1S/C8H11NO/c1-9(2)7-3-5-8(10)6-4-7/h3-6,10H,1-2H3
InChI key:InChIKey=JVVRCYWZTJLJSG-UHFFFAOYSA-N
SMILES:N(C)(C)C1=CC=C(O)C=C1
Synonyms:- 4-(Dimethylamino)Phenol Ethanedioate (1:1)
- 4-Dimethylaminophenol
- DMAP (antidote)
- N,N-Dimethyl-4-aminophenol
- N,N-Dimethyl-p-hydroxyaniline
- Phenol, 4-(dimethylamino)-
- Phenol, p-(dimethylamino)-
- p-(Dimethylamino)phenol
- p-Hydroxy-N,N-dimethylaniline
- 4-(Dimethylamino)phenol
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Found 8 products.
4-(Dimethylamino)phenol
CAS:4-(Dimethylamino)phenolFormula:C8H11NOPurity:97%Color and Shape: off-white solidMolecular weight:137.18g/mol4-(Dimethylamino)phenol
CAS:4-(Dimethylamino)phenol is a reactive molecule that can react with sodium carbonate to form a fluorescent product. The reaction mechanism has been elucidated by fluorescence spectroscopy and linear calibration curves. 4-DMA(OH)P reacts with sodium carbonate in water at physiological levels, producing p-hydroxybenzoic acid and 4-dimethylaminobenzoic acid. These compounds are also found in the matrix of bacterial cells and may serve as markers for the identification of bacterial metabolism. The reaction between 4DMA(OH)P and sodium carbonate was examined by X-ray crystal structures, which revealed that the reactive site is located on the phenolic hydroxyl group of 4DMA(OH)P. This study showed that the reactive site is localized on the phenolic hydroxy group of 4DMA(OH)P, which makes this molecule useful for identification of bacterial metabolism by means of matrix effect.Formula:C8H11NOPurity:Min. 95%Molecular weight:137.18 g/mol4-(Dimethylamino)phenol
CAS:4-(Dimethylamino)phenol increases LDH, doesn't affect gluconeogenesis, and lowers ATP if membranes leak LDH.Formula:C8H11NOPurity:98.54%Color and Shape:SolidMolecular weight:137.18Phenol, 4-(dimethylamino)-
CAS:Formula:C8H11NOPurity:97%Color and Shape:SolidMolecular weight:137.17904000000001
