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この商品について
化学式:
(CH3O)2C6H3OH
CAS番号:
分子量:
154.16
UNSPSC Code:
85151701
NACRES:
NA.24
PubChem Substance ID:
EC Number:
202-041-1
Beilstein/REAXYS Number:
1526871
MDL number:
grade
analytical standard
Quality Level
assay
≥98.0% (GC)
shelf life
limited shelf life, expiry date on the label
technique(s)
HPLC: suitable, gas chromatography (GC): suitable
bp
261 °C (lit.)
mp
50-57 °C (lit.), 53-57 °C
application(s)
cleaning products
cosmetics
flavors and fragrances
food and beverages
personal care
format
neat
SMILES string
COc1cccc(OC)c1O
InChI
1S/C8H10O3/c1-10-6-4-3-5-7(11-2)8(6)9/h3-5,9H,1-2H3
InChI key
KLIDCXVFHGNTTM-UHFFFAOYSA-N
General description
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.
Packaging
底の開いたガラス瓶内容物は内部に挿入され接着された円錐部に入っています。
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signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
保管分類
11 - Combustible Solids
wgk
WGK 3
flash_point_f
284.0 °F - closed cup
flash_point_c
140 °C - closed cup
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
