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410659

Sigma-Aldrich

4-Hydroxy-3-methoxyphenylacetone

96%

Sinonimo/i:

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

Formula condensata:
HOC6H3(OCH3)CH2COCH3
Numero CAS:
2503-46-0
Peso molecolare:
180.20
Numero CE:
219-704-6
Numero MDL:
MFCD00130260
Codice UNSPSC:
12352100
ID PubChem:
24865542
NACRES:
NA.22

Livello qualitativo

100

Saggio

96%

Forma fisica

liquid

Indice di rifrazione

n20/D 1.55 (lit.)

P. eboll.

126-127 °C/0.3 mmHg (lit.)

Densità

1.163 g/mL at 25 °C (lit.)

Gruppo funzionale

ketone

Stringa SMILE

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
LFVCJQWZGDLHSD-UHFFFAOYSA-N

Categorie correlate

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

10 - Combustible liquids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

235.4 °F - closed cup

Punto d’infiammabilità (°C)

113 °C - closed cup

Dispositivi di protezione individuale

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

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Certificati d'analisi (COA)

Lot/Batch Number
STBK4127
STBJ5251
STBH6557
STBG9279
STBG6762

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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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