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About This Item
Linear Formula:
(CH3O)2C6H3NH2
CAS Number:
Molecular Weight:
153.18
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
203-040-9
Beilstein/REAXYS Number:
776823
MDL number:
Product Name
2,5-Dimethoxyaniline, 98%
InChI key
NAZDVUBIEPVUKE-UHFFFAOYSA-N
InChI
1S/C8H11NO2/c1-10-6-3-4-8(11-2)7(9)5-6/h3-5H,9H2,1-2H3
SMILES string
COc1ccc(OC)c(N)c1
assay
98%
mp
78-80 °C (lit.)
Quality Level
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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.
signalword
Warning
hcodes
pcodes
Hazard Classifications
Acute Tox. 4 Oral
Storage Class
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
ppe
Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges
Regulatory Information
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Yang CH, et al.
Journal of the Electrochemical Society, 153(5), E85-E93 (2006)
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
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
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