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A88182

Sigma-Aldrich

o-Anisidin

≥99%

Synonym(e):

2-Amino-anisol, 2-Methoxy-anilin

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About This Item

Lineare Formel:
CH3OC6H4NH2
CAS-Nummer:
90-04-0
Molekulargewicht:
123.15
Beilstein:
386210
EG-Nummer:
201-963-1
MDL-Nummer:
MFCD00007688
UNSPSC-Code:
12352100
PubChem Substanz-ID:
24891370
NACRES:
NA.22

Qualitätsniveau

200

Assay

≥99%

Form

liquid

Brechungsindex

n20/D 1.574 (lit.)

bp

225 °C (lit.)

mp (Schmelzpunkt)

3-6 °C (lit.)

Dichte

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

InChIKey

VMPITZXILSNTON-UHFFFAOYSA-N

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Allgemeine Beschreibung

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

Piktogramme

Skull and crossbonesHealth hazard
GHS06,GHS08

Signalwort

Danger

Gefahreneinstufungen

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

Lagerklassenschlüssel

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

WGK

WGK 3

Flammpunkt (°F)

212.0 °F - closed cup

Flammpunkt (°C)

100 °C - closed cup

Persönliche Schutzausrüstung

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

Analysenzertifikate (COA)

Suchen Sie nach Analysenzertifikate (COA), indem Sie die Lot-/Chargennummer des Produkts eingeben. Lot- und Chargennummern sind auf dem Produktetikett hinter den Wörtern ‘Lot’ oder ‘Batch’ (Lot oder Charge) zu finden.

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2-Chloranilin ≥99.5% (GC)

Sigma-Aldrich

23300

2-Chloranilin

p-Anisidine for synthesis

Sigma-Aldrich

8.00458

p-Anisidine

2-Aminophenol 99%

Sigma-Aldrich

A71301

2-Aminophenol

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
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.
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
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
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
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