V900583
2,5-Dihydroxybenzaldehyde
Vetec™, reagent grade, 98%
Synonym(s):
Gentisaldehyde
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About This Item
Linear Formula:
(HO)2C6H3CHO
CAS Number:
Molecular Weight:
138.12
EC Number:
214-789-6
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
1363961
MDL number:
grade
reagent grade
product line
Vetec™
assay
98%
mp
97-99 °C (lit.)
SMILES string
Oc1ccc(O)c(C=O)c1
InChI
1S/C7H6O3/c8-4-5-3-6(9)1-2-7(5)10/h1-4,9-10H
InChI key
CLFRCXCBWIQVRN-UHFFFAOYSA-N
Legal Information
Vetec is a trademark of Merck KGaA, Darmstadt, Germany
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3
Storage Class
13 - Non Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
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Gobind S Bisht et al.
Langmuir : the ACS journal of surfaces and colloids, 28(39), 14055-14064 (2012-09-06)
We report on the functionalization of a micropatterned carbon electrode fabricated using the carbon-MEMS process for its use as a miniature diffusion-free glucose oxidase anode. Carbon-MEMS based electrodes offer precise manufacturing control on both the micro- and nanoscale and possess
N A Santagati et al.
Journal of pharmaceutical and biomedical analysis, 29(6), 1105-1111 (2002-07-12)
A method was developed for the analysis of primary aliphatic amines by high performance liquid chromatography coupled with electrochemical detector. The electrochemical oxidation of aliphatic amines derivatized with 2,5-dihydroxybenzaldehyde was investigated at porous graphite electrodes. The derivatization reactions were performed
M Xia et al.
The Journal of biological chemistry, 274(6), 3323-3330 (1999-01-28)
The kinetics of xanthine oxidase has been investigated with the aim of addressing several outstanding questions concerning the reaction mechanism of the enzyme. Steady-state and rapid kinetic studies with the substrate 2,5-dihydroxybenzaldehyde demonstrated that (kcat/Km)app and kred/Kd exhibit comparable bell-shaped
Virginia Delgado et al.
Molecules (Basel, Switzerland), 18(1), 721-734 (2013-01-10)
A variety of phenylaminoisoquinolinequinones were synthesized and tested for their antiproliferative activity against three human-tumor derived cancer cell lines. The new aminoquinones were prepared from 4-methoxycarbonyl-3-methylisoquinoline-5,8-quinone (1) via acid-induced amination and bromination reactions. Remarkable differences in antiproliferative activity were observed
S Rauli et al.
Journal of biochemistry, 123(5), 918-923 (1998-06-19)
Measurement of the concentrations of aldehydes in biological samples has become the object of much effort due to their relevance in relation to the toxic effects of lipid peroxidation, through which a number of aldehydes are derived. We have reconsidered
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