D107808
2′,6′-二羟基苯乙酮
97%
别名:
2-乙酰-1,3-二羟基苯, 2-乙酰基间苯二酚, DHAP
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关于此项目
线性分子式:
(HO)2C6H3COCH3
化学文摘社编号:
分子量:
152.15
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
211-833-6
Beilstein/REAXYS Number:
1366061
MDL number:
Assay:
97%
Form:
powder
InChI key
YPTJKHVBDCRKNF-UHFFFAOYSA-N
InChI
1S/C8H8O3/c1-5(9)8-6(10)3-2-4-7(8)11/h2-4,10-11H,1H3
SMILES string
CC(=O)c1c(O)cccc1O
assay
97%
form
powder
mp
156-158 °C (lit.)
Quality Level
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signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Junjie Hou et al.
Journal of biomedicine & biotechnology, 2010, 759690-759690 (2010-03-27)
Selecting an appropriate matrix solution is one of the most effective means of increasing the ionization efficiency of phosphopeptides in matrix-assisted laser-desorption/ionization time-of-flight mass spectrometry (MALDI-TOF-MS). In this study, we systematically assessed matrix combinations of 2, 6-dihydroxyacetophenone (DHAP) and diammonium
Gheorghita Zbancioc et al.
Ultrasonics sonochemistry, 19(3), 399-403 (2011-09-13)
A new, selective, straightforward and general method for preparation of highly functionalized coronands or spiro derivatives bearing 1,2-dihydroxyacetophenone unit, under conventional conditions and ultrasonic irradiation, is reported. The reaction setup involves only one step, acylation of an α-chloro-3,4-dihydroxyacetophenone with phthaloyl
MALDI mass spectrometry in the solution of some forensic problems.
R Seraglia et al.
Forensic science international, 146 Suppl, S83-S85 (2005-01-11)
Thomas Wenzel et al.
Rapid communications in mass spectrometry : RCM, 20(5), 785-789 (2006-02-04)
2,5-Dihydroxyacetophenone (DHAP) is presented as a matrix which enables highly sensitive matrix-assisted laser desorption/ionization time-of-flight (MALDI-TOF) mass spectrometric analysis of peptides, proteins and glycoproteins on AnchorChip targets. Depending on the protein, lower fmol amounts can be detected due to the
Jainuch Kanchanapoo et al.
Life sciences, 78(14), 1630-1636 (2005-10-29)
The effects of the choleretic and cholesterol lowering compound, 2,4,6-trihydroxyacetophenone (THA) and its analog, 2,6-dihydroxyacetophenone (DHA), on ileal bile acid absorption were investigated in rats. THA inhibited taurocholate (TC) uptake into ileal brush-border membrane vesicles (BBMV), showing a maximum inhibition
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