Passa al contenuto
Merck
Tutte le immagini(1)

Documenti

54050

Sigma-Aldrich

4-Methoxyphenol

purum, ≥98.0% (HPLC)

Sinonimo/i:

4-Hydroxyanisole, 4-MP, HQMME, Hydroquinone monomethyl ether, MEHQ, p-Guaiacol

Autenticatiper visualizzare i prezzi riservati alla tua organizzazione & contrattuali
Tutte le immagini(1)

About This Item

Formula condensata:
CH3OC6H4OH
Numero CAS:
150-76-5
Peso molecolare:
124.14
Beilstein:
507924
Numero CE:
205-769-8
Numero MDL:
MFCD00002332
Codice UNSPSC:
12352100
ID PubChem:
329758018
NACRES:
NA.22

Densità del vapore

4.3 (vs air)

Livello qualitativo

200

Tensione di vapore

<0.01 mmHg ( 20 °C)

Grado

purum

Saggio

≥98.0% (HPLC)

Temp. autoaccensione

789 °F

Impurezze

≤2% hydroquinone dimethyl ether

P. eboll.

243 °C (lit.)

Punto di fusione

54-56 °C
55-57 °C (lit.)

Stringa SMILE

COc1ccc(O)cc1

InChI

1S/C7H8O2/c1-9-7-4-2-6(8)3-5-7/h2-5,8H,1H3
NWVVVBRKAWDGAB-UHFFFAOYSA-N

Informazioni sul gene

human ... TYR(7299)

Cerchi prodotti simili? Visita Guida al confronto tra prodotti

Categorie correlate

Descrizione generale

4-Methoxyphenol, a 4-alkoxyphenol, can be synthesized from hydroquinone. It undergoes polymerization in the presence of horseradish peroxidase (enzymatic catalyst) and sodium dodecyl sulfate (surfactant) to afford poly(4-methoxyphenol).

Applicazioni

4-Methoxyphenol may be used in to synthesize chiral building blocks such as 1,2-diols. It also has various industrial applications, such as an antioxidant, an inhibitor for the polymerization reactions and a stabilizing agent.

Pittogrammi

Exclamation mark
GHS07

Avvertenze

Warning

Indicazioni di pericolo

H302,H317,H319,H412

Classi di pericolo

Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Irrit. 2 - Skin Sens. 1

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 1

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

Choose from one of the most recent versions:

Certificati d'analisi (COA)

Lot/Batch Number
BCCM0172
BCCK9367
BCCJ3241
BCCG5232
BCCF3545

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Possiedi già questo prodotto?

I documenti relativi ai prodotti acquistati recentemente sono disponibili nell’Archivio dei documenti.

Visita l’Archivio dei documenti

I clienti hanno visto anche

Slide 1 of 5

1 of 5

4-tert-Butylcatechol &#8805;97.0% (HPLC)

Sigma-Aldrich

19670

4-tert-Butylcatechol

N,N-Diethylacetoacetamide Arxada quality, 98.0-100.3&#160;% (w/w) (T)

Sigma-Aldrich

690945

N,N-Diethylacetoacetamide

Rebamipide hydrate &#8805;98% (HPLC), powder

Sigma-Aldrich

R5655

Rebamipide hydrate

4-Ethoxyphenol 99%

Sigma-Aldrich

258598

4-Ethoxyphenol

Methacrylic acid contains 250&#160;ppm MEHQ as inhibitor, 99%

Sigma-Aldrich

155721

Methacrylic acid

Enantioselective ring opening of epoxides with 4-methoxyphenol catalyzed by gallium heterobimetallic complexes: An efficient method for the synthesis of optically active 1, 2-diol monoethers.
Iida T, et al.
Angewandte Chemie (International Edition in English), 37(16), 2223-2226 (1998)
Synthesis of poly (4-methoxyphenol) by enzyme-catalyzed polymerization and evaluation of its antioxidant activity.
Zheng K, et al.
New. J. Chem., 37(12), 4185-4191 (2013)
Paolo Ruzza et al.
Journal of medicinal chemistry, 52(15), 4973-4976 (2009-07-16)
We report the synthesis and preliminary in vitro biological evaluations of 4-[(4-hydroxyphenyl)sulfanyl]but-3-en-2-one, a compound designed as a potential bifunctional antimelanoma agent, bearing both a tyrosinase-activatable phenolic moiety and a GSH-reactive alpha,beta-unsaturated carbonyl group. Both the E (1) and Z (2)
Simple synthesis of non-symmetric 1, 4-dialkoxybenzenes via 4-alkoxyphenols.
Radoslaw M, et al.
Organic Communications, 9(1) (2016)
Lisa M Colosi et al.
Environmental science & technology, 41(3), 891-896 (2007-03-03)
Natural organic matter (NOM) of hydroxylated aromatic character can undergo catalyst-mediated self-coupling reactions to form larger molecular aggregates. Indeed, such reactions are central to natural humification processes. Nonhydroxylated persistent aromatic contaminants such as polychlorinated biphenyls (PCBs) are, conversely, inert with
Visualizza tutti i documenti correlati

Il team dei nostri ricercatori vanta grande esperienza in tutte le aree della ricerca quali Life Science, scienza dei materiali, sintesi chimica, cromatografia, discipline analitiche, ecc..

Contatta l'Assistenza Tecnica.