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MilliporeSigma

D107808

2′,6′-Dihydroxyacetophenone

97%

Synonym(s):

2-Acetyl-1,3-dihydroxybenzene, 2-Acetylresorcinol, DHAP

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About This Item

Linear Formula:
(HO)2C6H3COCH3
CAS Number:
699-83-2
Molecular Weight:
152.15
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24893345
EC Number:
211-833-6
Beilstein/REAXYS Number:
1366061
MDL number:
MFCD00002270

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Product Name

2′,6′-Dihydroxyacetophenone, 97%

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

100

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Show Differences

1 of 4

This Item
D107409D107603632759
2′,6′-Dihydroxyacetophenone 97%

Sigma-Aldrich

D107808

2′,6′-Dihydroxyacetophenone

2′,4′-Dihydroxyacetophenone 99%

Sigma-Aldrich

D107409

2′,4′-Dihydroxyacetophenone

2′,5′-Dihydroxyacetophenone 97%

Sigma-Aldrich

D107603

2′,5′-Dihydroxyacetophenone

3′-Allyl-4′-hydroxyacetophenone 97%

Sigma-Aldrich

632759

3′-Allyl-4′-hydroxyacetophenone

assay

97%

assay

99%

assay

97%

assay

97%

Quality Level

100

Quality Level

100

Quality Level

100

Quality Level

100

mp

156-158 °C (lit.)

mp

143-144.5 °C (lit.)

mp

204-206 °C (lit.)

mp

115-119 °C (lit.)

form

powder

form

powder

form

crystals

form

solid

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
WXBF6413V
WXBF5760V
WXBF3046V
WXBF4104V
WXBF1165V

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T A Smith et al.
The Annals of occupational hygiene, 39(2), 235-240 (1995-04-01)
Sodium cromoglycate is manufactured by a seven-stage synthetic process. There has been no previous documentation of toxicological effects of the intermediate compounds in its synthesis. This paper describes the health effects of acute exposure to the intermediates on the skin
Ana Maria Balan et al.
European journal of medicinal chemistry, 44(5), 2275-2279 (2008-08-02)
Herein we report a feasible study concerning syntheses, structure and antimicrobial activity of some new diazinium salts with dihydroxyacetophenone skeleton. A fast, general, environmentally friendly, and facile method for preparation of diazinium salts under microwave and ultrasounds irradiation is presented.
Erica L McJimpsey et al.
Journal of the American Society for Mass Spectrometry, 19(3), 315-324 (2007-12-25)
The Bioaerosol Mass Spectrometry (BAMS) system was developed for the real-time detection and identification of biological aerosols using laser desorption ionization. Greater differentiation of particle types is desired; consequently MALDI techniques are being investigated. The small sample size ( approximately
Vahid Saheb et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 81(1), 144-150 (2011-07-19)
The Schiff base compound, N,N'-(2,2-dimetylpropane)-bis(dihydroxylacetophenone) (NDHA) is synthesized through the condensation of 2-hydroxylacetophenone and 2,2-dimethyl 1,3-amino propane in methanol at ambient temperature. The yellow crystalline precipitate is used for X-ray single-crystal determination and measuring Fourier transform infrared (FTIR), UV-visible, (1)H
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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