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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

Key Documents

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Product Name

o-Anisidine, ≥99%

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
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
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
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