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Merck
CN

A88182

o-Anisidine

≥99%

Synonym(s):

2-Aminoanisole, 2-Methoxyaniline

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About This Item

Linear Formula:
CH3OC6H4NH2
CAS Number:
90-04-0
Molecular Weight:
123.15
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24891370
EC Number:
201-963-1
Beilstein/REAXYS Number:
386210
MDL number:
MFCD00007688
Assay:
≥99%
Form:
liquid

Key Documents

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InChI

1S/C7H9NO/c1-9-7-5-3-2-4-6(7)8/h2-5H,8H2,1H3

InChI key

VMPITZXILSNTON-UHFFFAOYSA-N

SMILES string

COc1ccccc1N

assay

≥99%

form

liquid

refractive index

n20/D 1.574 (lit.)

bp

225 °C (lit.)

mp

3-6 °C (lit.)

density

1.092 g/mL at 25 °C (lit.)

Quality Level

200

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General description

o-Anisidine is an aromatic amine used as a building block for the production of dyes, pigments, and pharmaceuticals.

pictograms

Skull and crossbonesHealth hazard
GHS06,GHS08

signalword

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Carc. 1B - Muta. 2

Storage Class

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

wgk

WGK 3

flash_point_f

212.0 °F - closed cup

flash_point_c

100 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

Regulatory Information

危险化学品
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Certificates of Analysis (COA)

Lot/Batch Number
BCCN6515
BCCN1569
BCCG3868
BCBN7484V
1437508V

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D Sangamithirai et al.
Materials science & engineering. C, Materials for biological applications, 91, 512-523 (2018-07-24)
Dopamine (DA) and Folic acid (FA) are co-existing compounds in biological fluids that plays a vital role in central nervous system and human metabolism. DA is an important neurotransmitter in the brain's neural circuits and its diminution often results in
Paulo A Ribeiro et al.
Journal of nanoscience and nanotechnology, 6(5), 1396-1404 (2006-06-24)
Neutron reflectivity measurements were used to investigate the thermal stability of layer-by-layer (LBL) films of poly(o-methoxyaniline) (POMA), which was probed by increasing the temperature up to 80 degrees C of a D2O solution in contact with the LBL films. The
Parimal Routh et al.
Biophysical chemistry, 143(3), 145-153 (2009-06-02)
Biomolecular hybrids of a conducting polymer [poly(o-methoxy aniline) (POMA)] and RNA are prepared at the three different compositions by mixing aqueous solutions of diethyl, 2-hydroxy ethyl, ammonium salt of RNA (type IX from Torula Yeast) and POMA (ES, emeraldine salt;
Marie Stiborová et al.
Mutation research, 500(1-2), 49-66 (2002-03-14)
2-Methoxyaniline (o-anisidine) is a urinary bladder carcinogen in both mice and rats. Since the urinary bladder contains substantial peroxidase activity, we investigated the metabolism of this carcinogen by prostaglandin H synthase (PHS), a prominent enzyme in the urinary bladder, and
M Mazur
The European physical journal. E, Soft matter, 22(1), 67-75 (2007-03-06)
We report on chemical polymerization of two aniline derivatives - 2-methylaniline and 2-methoxyaniline -- in a two-phase water/pentane system. We have found that poly(2-methylaniline) is produced in form of an amorphous material regardless of the fact whether the monomer is
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