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A88182

Sigma-Aldrich

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
Beilstein:
386210
EC Number:
201-963-1
MDL number:
MFCD00007688
UNSPSC Code:
12352100
PubChem Substance ID:
24891370
NACRES:
NA.22

Quality Level

200

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.)

SMILES string

COc1ccccc1N

InChI

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

InChI key

VMPITZXILSNTON-UHFFFAOYSA-N

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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

Signal Word

Danger

Hazard Classifications

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

Storage Class Code

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

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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Karel Naiman et al.
Chemical research in toxicology, 21(8), 1610-1621 (2008-07-16)
We investigated the ability of hepatic microsomes from rat and rabbit to metabolize 2-methoxyaniline (o-anisidine), an industrial and environmental pollutant and a bladder carcinogen for rodents. Using HPLC combined with electrospray tandem mass spectrometry, we determined that o-anisidine is oxidized
Karel Naiman et al.
Toxicological sciences : an official journal of the Society of Toxicology, 127(2), 348-359 (2012-03-10)
2-Methoxyaniline (o-anisidine) is an industrial and environmental pollutant causing tumors of urinary bladder in rodents. Here, we investigated the formation and persistence of DNA adducts in the Wistar rat. Using the (32)P-postlabeling method, three o-anisidine-derived DNA adducts were found in
Xin-Gui Li et al.
Small (Weinheim an der Bergstrasse, Germany), 4(8), 1201-1209 (2008-07-31)
Novel copolymer nanoparticles with inherent self-stability, narrow size distribution, and high electrical conductivity are facilely and productively synthesized by the oxidative precipitation polymerization of 5-sulfonic-2-anisidine and aniline in acidic medium without any external stabilizer. The structures of the copolymer particles
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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