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37468

Supelco

2′,6′-Dihydroxyacetophenone

matrix substance for MALDI-MS, ≥99.5%

Sinonimo/i:

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

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About This Item

Formula condensata:
(HO)2C6H3COCH3
Numero CAS:
699-83-2
Peso molecolare:
152.15
Beilstein:
1366061
Numero CE:
211-833-6
Numero MDL:
MFCD00002270
Codice UNSPSC:
41116105
ID PubChem:
329755650
NACRES:
NA.21

Grado

matrix substance for MALDI-MS

Livello qualitativo

100

Saggio

≥99.5% (HPLC)
≥99.5%

Stato

powder

Classi chimiche degli analiti

glycans, lipids, peptides, proteins

tecniche

MALDI-MS: suitable

Punto di fusione

156-158 °C (lit.)

Solubilità

dioxane: 50 mg/mL, clear

Cationi in tracce

Ca: ≤10 mg/kg
Cd: ≤5 mg/kg
Co: ≤5 mg/kg
Cr: ≤5 mg/kg
Cu: ≤5 mg/kg
Fe: ≤5 mg/kg
K: ≤50 mg/kg
Mg: ≤5 mg/kg
Mn: ≤5 mg/kg
Na: ≤50 mg/kg
Ni: ≤5 mg/kg
Pb: ≤5 mg/kg
Zn: ≤5 mg/kg

Compatibilità

suitable for matrix substance for MALDI-MS

Stringa SMILE

CC(=O)c1c(O)cccc1O

InChI

1S/C8H8O3/c1-5(9)8-6(10)3-2-4-7(8)11/h2-4,10-11H,1H3
YPTJKHVBDCRKNF-UHFFFAOYSA-N

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Applicazioni

Used with diammonium hydrogen citrate for MALDI-MS of PMP-labeled acidic and neutral glycans.

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Pittogrammi

Exclamation mark
GHS07

Avvertenze

Warning

Indicazioni di pericolo

H315,H319,H335

Classi di pericolo

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

Organi bersaglio

Respiratory system

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

dust mask type N95 (US), Eyeshields, Gloves

Scegli una delle versioni più recenti:

Certificati d'analisi (COA)

Lot/Batch Number
BCCJ0565
BCCF4882
BCCB5520
BCBX3910
BCBW9144

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Super-DHB suitable for matrix substance for MALDI-MS, ≥99.0%

Supelco

50862

Super-DHB

Dihydroxyacetone phosphate dilithium salt ≥93% dry basis (enzymatic)

Sigma-Aldrich

D7137

Dihydroxyacetone phosphate dilithium salt

J J Pitt et al.
Analytical biochemistry, 248(1), 63-75 (1997-05-15)
The 1-phenyl-3-methyl-5-pyrazolone (PMP) derivatives of monosaccharides, maltooligosaccharides, and oligosaccharides enzymatically released from asparagine-linked sites in ribonuclease B and fetuin have been investigated using matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF-MS). Use of the matrix 2,6-dihydroxyacetophenone containing diammonium hydrogen citrate (DHAP/DAHC)
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.
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
Johan Jacksén et al.
Analytical biochemistry, 425(1), 18-20 (2012-03-13)
Matrix-assisted laser desorption/ionization mass spectrometry (MALDI-MS) is widely used for analysis of macromolecules like peptides and proteins. The analysis procedure is generally simple but must be adapted to the characteristics of the analytes. Therefore, specific matrices suitable for, e.g., hydrophobic
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
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Mass Spectrometry of Glycans

Explore mass spectrometry analysis of glycans for glycomic & glycoproteomic neutral & acidic glycan analysis. See a general mass spec glycan analysis procedure.

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