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112984

Sigma-Aldrich

2,5-Dimethoxyaniline

98%

Synonym(s):

Aminohydroquinone dimethyl ether

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About This Item

Linear Formula:
(CH3O)2C6H3NH2
CAS Number:
102-56-7
Molecular Weight:
153.18
Beilstein:
776823
EC Number:
203-040-9
MDL number:
MFCD00008368
UNSPSC Code:
12352100
PubChem Substance ID:
24847125
NACRES:
NA.22

Assay

98%

mp

78-80 °C (lit.)

SMILES string

COc1ccc(OC)c(N)c1

InChI

1S/C8H11NO2/c1-10-6-3-4-8(11-2)7(9)5-6/h3-5H,9H2,1-2H3

InChI key

NAZDVUBIEPVUKE-UHFFFAOYSA-N

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Application

2,5-Dimethoxyaniline is used as a laccase inducer which immobilizes the enzyme laccase from Trumetes versicolor.
2,5-Dimethoxyaniline is used for the electrochemical copolymerization of diphenylamine in 4M sulfuric acid.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H302

Precautionary Statements

P301 + P312 + P330

Hazard Classifications

Acute Tox. 4 Oral

Storage Class Code

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 1

Flash Point(F)

266.0 °F - closed cup

Flash Point(C)

130 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Louis Sieuw et al.
Scientific reports, 7(1), 4847-4847 (2017-07-09)
The electrochemistry of poly(2,5-dihydroxyaniline) (PDHA), a novel hybrid molecular configuration with redox active sites and electrical charge conduction along the polymer chain, has been recently reported. The theoretical capacity of this material is estimated at 443 mAh g
C Crecchio et al.
Biotechnology and bioengineering, 48(6), 585-591 (1995-12-20)
Gelatine gels originate from water in oil microemulsions in which the ternary system consists of isooctane/ sulfosuccinic acid bis [2-ethyl hexyl] ester/water; the solubilization of gelatin in the water pool of these microemulsions transforms them into viscous gels in which
Yang CH, et al.
Journal of the Electrochemical Society, 153(5), E85-E93 (2006)

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