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410659

Sigma-Aldrich

4-Hydroxy-3-methoxyphenylaceton

96%

Synonym(e):

1-(4-Hydroxy-3-methoxyphenyl)-2-propanone, 2-Propiovanillone, 4-Hydroxy-3-methoxyphenyl-2-propanone, Guaiacylacetone, Methyl vanillyl ketone, Vanillyl methyl ketone

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About This Item

Lineare Formel:
HOC6H3(OCH3)CH2COCH3
CAS-Nummer:
2503-46-0
Molekulargewicht:
180.20
EG-Nummer:
219-704-6
MDL-Nummer:
MFCD00130260
UNSPSC-Code:
12352100
PubChem Substanz-ID:
24865542
NACRES:
NA.22

Assay

96%

Form

liquid

Brechungsindex

n20/D 1.55 (lit.)

bp

126-127 °C/0.3 mmHg (lit.)

Dichte

1.163 g/mL at 25 °C (lit.)

SMILES String

COc1cc(CC(C)=O)ccc1O

InChI

1S/C10H12O3/c1-7(11)5-8-3-4-9(12)10(6-8)13-2/h3-4,6,12H,5H2,1-2H3

InChIKey

LFVCJQWZGDLHSD-UHFFFAOYSA-N

Verwandte Kategorien

Piktogramme

Exclamation mark
GHS07

Signalwort

Warning

Gefahreneinstufungen

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

Zielorgane

Respiratory system

Lagerklassenschlüssel

10 - Combustible liquids

WGK

WGK 3

Flammpunkt (°F)

235.4 °F - closed cup

Flammpunkt (°C)

113 °C - closed cup

Persönliche Schutzausrüstung

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

Analysenzertifikate (COA)

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J Jodynis-Liebert
Xenobiotica; the fate of foreign compounds in biological systems, 23(6), 693-701 (1993-06-01)
1. Metabolites of 1-(4-hydroxy-3-methoxyphenyl)-2-propanone (HMP-one), a smoke flavour compound, were isolated from rat urine using hydrolysis, ether extraction, t.l.c. and g.l.c. 2. Three metabolites were identified by mass spectrometry and independent synthesis, namely: 1-(3, 4-dihydroxyphenyl)-2-propanone (Met I), 1-(3, 4-dihydroxyphenyl)-2-propanol (Met
Michaela Kolb et al.
Journal of chromatography. A, 1307, 144-157 (2013-08-13)
A headspace solid-phase microextraction method with subsequent GC-MS (HS-SPME/GC-MS) was established for the quantitative analysis of volatile lignin derived phenolic monomers in complex aqueous solutions. Extraction was done using a polyacrylate fiber. The optimization of HS-SPME - parameters was performed
Aqueous-phase hydrodeoxygenation of bio-derived phenols to cycloalkanes.
Zhao C, et al.
J. Catal., 280(1), 8-16 (2011)
Mary L Forsling et al.
British journal of pharmacology, 135(3), 649-656 (2002-02-09)
Methylenedioxymethamphetamine (MDMA, 'ecstasy'), widely used as a recreational drug, can produce hyponatraemia. The possibility that this could result from stimulation of vasopressin by MDMA or one of its metabolites has been investigated in vitro. Release of both oxytocin and vasopressin
H J Helmlin et al.
Journal of analytical toxicology, 20(6), 432-440 (1996-10-01)
In Europe, the compound 3,4-methylenedioxymethamphetamine (MDMA, Ecstasy, Adam), in addition to cannabis, is the most abused illicit drug at all-night "techno" parties. Methods for the determination of MDMA and its metabolites, 4-hydroxy-3-methoxymethamphetamine (HMMA), 3,4-dihydroxy-methamphetamine (HHMA), 3,4-methylenedioxyamphetamine (MDA), 4-hydroxy-3-methoxyamphetamine (HMA), and

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