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D108200

Sigma-Aldrich

2,5-Dihydroxybenzaldehyde

98%

Sinónimos:

Gentisaldehyde

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About This Item

Fórmula lineal:
(HO)2C6H3CHO
Número de CAS:
1194-98-5
Peso molecular:
138.12
Beilstein/REAXYS Number:
1363961
EC Number:
214-789-6
MDL number:
MFCD00003333
UNSPSC Code:
12352100
PubChem Substance ID:
24893347
NACRES:
NA.22

Quality Level

100

assay

98%

form

crystals

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

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Categorías relacionadas

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

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Certificados de análisis (COA)

Lot/Batch Number
MKCP9814
MKCM2348
MKCJ7943
MKCG2323
MKCF4749

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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
Javed Iqbal et al.
Organic letters, 14(2), 552-555 (2012-01-06)
Functionalized β-aryl alanine ester derivatives were found to undergo rapid C-N and C-O bond formation with quinol carbonyl compounds to afford 2H-benzo[b][1,4]oxazines in good to excellent yields. This unprecedented finding reported herein offers a straightforward, highly efficient, and rapid method
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
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
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