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53877

Supelco

2,6-dimetossifenolo

analytical standard

Sinonimo/i:

Pirogallolo 1,3-dimetil etere

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About This Item

Formula condensata:
(CH3O)2C6H3OH
Numero CAS:
91-10-1
Peso molecolare:
154.16
Beilstein:
1526871
Numero CE:
202-041-1
Numero MDL:
MFCD00064434
Codice UNSPSC:
85151701
ID PubChem:
329758011
NACRES:
NA.24

Grado

analytical standard

Livello qualitativo

100

Saggio

≥98.0% (GC)

Durata

limited shelf life, expiry date on the label

tecniche

HPLC: suitable
gas chromatography (GC): suitable

P. eboll.

261 °C (lit.)

Punto di fusione

50-57 °C (lit.)
53-57 °C

applicazioni

cleaning products
cosmetics
flavors and fragrances
food and beverages
personal care

Formato

neat

Stringa SMILE

COc1cccc(OC)c1O

InChI

1S/C8H10O3/c1-10-6-4-3-5-7(11-2)8(6)9/h3-5,9H,1-2H3
KLIDCXVFHGNTTM-UHFFFAOYSA-N

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Categorie correlate

Descrizione generale

2,6-Dimethoxyphenol can find applications mainly as a substrate of laccases catalysis and also determine its activity in aqueous solution. It can also be used as a potential marker compound in particular for emission of smoke in the atmosphere from wood.

Applicazioni

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Confezionamento

Bottomless glass bottle. Contents are inside inserted fused cone.

Pittogrammi

Exclamation mark
GHS07

Avvertenze

Warning

Indicazioni di pericolo

H302,H315,H319,H335

Classi di pericolo

Acute Tox. 4 Oral - 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)

284.0 °F - closed cup

Punto d’infiammabilità (°C)

140 °C - closed cup

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Certificati d'analisi (COA)

Lot/Batch Number
BCCL2271
BCCG8752
BCCB4008
BCBT3695
BCBN0564V

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Rate constant and secondary organic aerosol yields for the gas-phase reaction of hydroxyl radicals with syringol (2, 6-dimethoxyphenol)
Lauraguais A, et al.
Atmospheric Environment, 55, 43-48 (2013)
Enzymatic catalysis of 2, 6-dimethoxyphenol by laccases and products characterization in organic solutions
Yang YW, et al.
Science in China. Series B, Chemistry, Life Sciences & Earth Sciences, 51, 669-676 (2008)
A Miele et al.
Journal of applied microbiology, 108(3), 998-1006 (2009-09-09)
To select better performing laccase variants among the 2300 randomly mutated variants of Pleurotus ostreatus POXA1b laccase to develop improved laccase-based biocatalysts. Screening of collections of 2300 randomly mutated variants of POXA1b was performed by assaying activity towards the phenolic
Yu Huan Liu et al.
Applied microbiology and biotechnology, 91(3), 667-675 (2011-04-28)
To obtain better performing laccases for textile dyes decolorization, random mutagenesis of Lac591, a metagenome-derived alkaline laccase, was carried out. After three rounds of error-prone PCR and high-throughput screening by assaying enzymatic activity toward the phenolic substrate 2,6-dimethoxyphenol (2,6-DMP), a
Joseph Zakzeski et al.
ChemSusChem, 4(3), 369-378 (2011-01-20)
The solubilization and aqueous phase reforming of lignin, including kraft, soda, and alcell lignin along with sugarcane bagasse, at low temperatures (T≤498 K) and pressures (P≤29 bar) is reported for the first time for the production of aromatic chemicals and hydrogen. Analysis
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