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126330

Sigma-Aldrich

2,3-Dimethoxyphenol

98%

Sinonimo/i:

Pyrogallol 1,2-dimethyl ether

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About This Item

Formula condensata:
(CH3O)2C6H3OH
Numero CAS:
5150-42-5
Peso molecolare:
154.16
Beilstein:
1910045
Numero CE:
225-922-2
Numero MDL:
MFCD00008366
Codice UNSPSC:
12352100
ID PubChem:
24847716
NACRES:
NA.22

Saggio

98%

Forma fisica

liquid

Indice di rifrazione

n20/D 1.539 (lit.)

P. eboll.

233-234 °C (lit.)

Densità

1.182 g/mL at 25 °C (lit.)

Stringa SMILE

COc1cccc(O)c1OC

InChI

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

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Descrizione generale

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

Applicazioni

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.

Pittogrammi

Exclamation mark
GHS07

Avvertenze

Warning

Indicazioni di pericolo

H315,H319,H335

Classi di pericolo

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

Organi bersaglio

Respiratory system

Codice della classe di stoccaggio

10 - Combustible liquids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

228.2 °F - closed cup

Punto d’infiammabilità (°C)

109 °C - closed cup

Dispositivi di protezione individuale

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

Certificati d'analisi (COA)

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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.
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
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
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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