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Merck
CN

126330

2,3-Dimethoxyphenol

98%

Synonym(s):

Pyrogallol 1,2-dimethyl ether

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About This Item

Linear Formula:
(CH3O)2C6H3OH
CAS Number:
5150-42-5
Molecular Weight:
154.16
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24847716
EC Number:
225-922-2
Beilstein/REAXYS Number:
1910045
MDL number:
MFCD00008366
Assay:
98%
Form:
liquid

Key Documents

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Product Name

2,3-Dimethoxyphenol, 98%

InChI key

QSZCGGBDNYTQHH-UHFFFAOYSA-N

InChI

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

SMILES string

COc1cccc(O)c1OC

assay

98%

form

liquid

refractive index

n20/D 1.539 (lit.)

bp

233-234 °C (lit.)

density

1.182 g/mL at 25 °C (lit.)

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General description

2,3-Dimethoxyphenol is a plant-derived phenylpropanoid compound that is glycosidated to form glycoside compound.

Application

2,3-Dimethoxyphenol has been used to study the nitrosative deamination of DNA bases induced by reactive nitrogen species (RNS) while studying the cause of mutagenesis.

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

10 - Combustible liquids

wgk

WGK 3

flash_point_f

228.2 °F - closed cup

flash_point_c

109 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

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Certificates of Analysis (COA)

Lot/Batch Number
STBK2776
STBF7141V
STBD3308V
S90930V
S90930

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Shashi Kant Bhatia et al.
Bioresource technology, 289, 121704-121704 (2019-07-06)
Rhodococcus sp. YHY01 was studied to utilize various lignin derived aromatic compounds. It was able to utilize p-coumaric acid, cresol, and 2,6 dimethoxyphenol and resulted in biomass production i.e. 0.38 g dcw/L, 0.25 g dcw/L and 0.1 g dcw/L, and lipid accumulation i.e.
Qi Luo et al.
Environmental science & technology, 52(18), 10617-10626 (2018-08-28)
Perfluorooctanesulfonate (PFOS) is a compound that has wide applications with extreme persistence in the environment and the potential to bioaccumulate, and could induce adverse effects to ecosystems. We investigated the degradation of PFOS by laccase-induced enzyme catalyzed oxidative humification reactions
K Rybczyńska-Tkaczyk et al.
Ecotoxicology and environmental safety, 191, 110203-110203 (2020-01-24)
The aim of this study was to evaluate of possibility of biotransformation and toxicity effect of monoanthraquinone dyes in cultures of Bjerkandera adusta CCBAS 930. Phenolic compounds, free radicals, phytotoxicity (Lepidium sativum L.), ecotoxicity (Vibrio fischeri) and cytotoxicity effect were
Márcia Pessêgo et al.
Journal of pharmacy & bioallied sciences, 3(1), 128-134 (2011-03-25)
Nitrosative deamination of DNA bases induced by reaction with reactive nitrogen species (RNS) has been pointed out as a probable cause of mutagenesis. (Poly)phenols, present in many food items from the Mediterranean diet, are believed to possess antinitrosating properties due
Anna Jasińska et al.
Environmental science and pollution research international, 26(25), 26313-26323 (2019-07-10)
To identify the enzymes potentially useful for the decolorization of azo dyes, the secretome of the ascomycetous fungus Myrothecium roridum IM6482 was studied by using a bottom-up proteomic approach. Among the identified proteins, the most promising for dye removal was
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