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53877

Supelco

2,6-Diméthoxyphénol

analytical standard

Synonyme(s) :

Éther 1,3-diméthylique de pyrogallol

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About This Item

Formule linéaire :
(CH3O)2C6H3OH
Numéro CAS:
91-10-1
Poids moléculaire :
154.16
Numéro Beilstein :
1526871
Numéro CE :
202-041-1
Numéro MDL:
MFCD00064434
Code UNSPSC :
85151701
ID de substance PubChem :
329758011
Nomenclature NACRES :
NA.24

Qualité

analytical standard

Niveau de qualité

100

Pureté

≥98.0% (GC)

Durée de conservation

limited shelf life, expiry date on the label

Technique(s)

HPLC: suitable
gas chromatography (GC): suitable

Point d'ébullition

261 °C (lit.)

Pf

50-57 °C (lit.)
53-57 °C

Application(s)

cleaning products
cosmetics
flavors and fragrances
food and beverages
personal care

Format

neat

Chaîne SMILES 

COc1cccc(OC)c1O

InChI

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

Clé InChI

KLIDCXVFHGNTTM-UHFFFAOYSA-N

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Catégories apparentées

Description générale

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.

Application

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

Conditionnement

Bottomless glass bottle. Contents are inside inserted fused cone.

Pictogrammes

Exclamation mark
GHS07

Mention d'avertissement

Warning

Mentions de danger

H302,H315,H319,H335

Classification des risques

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Organes cibles

Respiratory system

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

284.0 °F - closed cup

Point d'éclair (°C)

140 °C - closed cup

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Certificats d'analyse (COA)

Lot/Batch Number
BCCG8752
BCCB4008
BCBT3695
BCBN0564V
BCBH6254V

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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
Isabel Pardo et al.
Biotechnology and bioengineering, 109(12), 2978-2986 (2012-06-26)
DNA recombination methods are useful tools to generate diversity in directed evolution protein engineering studies. We have designed an array of chimeric laccases with high-redox potential by in vitro and in vivo DNA recombination of two fungal laccases (from Pycnoporus
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