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Sigma-Aldrich

o-Tolualdehyd

97%

Synonym(e):

2-Methyl-benzaldehyd

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About This Item

Lineare Formel:
CH3C6H4CHO
CAS-Nummer:
529-20-4
Molekulargewicht:
120.15
Beilstein:
605841
EG-Nummer:
208-452-2
MDL-Nummer:
MFCD00003338
UNSPSC-Code:
12352100
PubChem Substanz-ID:
24847335
NACRES:
NA.22

Assay

97%

Enthält

0.1% Hydroquinone as stabilizer

Brechungsindex

n20/D 1.546 (lit.)

bp

199-200 °C (lit.)

Dichte

1.039 g/mL at 20 °C
1.039 g/mL at 25 °C (lit.)

SMILES String

[H]C(=O)c1ccccc1C

InChI

1S/C8H8O/c1-7-4-2-3-5-8(7)6-9/h2-6H,1H3

InChIKey

BTFQKIATRPGRBS-UHFFFAOYSA-N

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Allgemeine Beschreibung

o-tolualdehyde undergoes atmospheric degradation by direct photolysis by sunlight.

Anwendung

o-tolualdehyde was used in determination of alkenal-2,4-dinitrophenylhydrazones by HPLC by addition of phosphoric acid.

Piktogramme

Exclamation mark
GHS07

Signalwort

Warning

Gefahreneinstufungen

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Zielorgane

Respiratory system

Lagerklassenschlüssel

10 - Combustible liquids

WGK

WGK 3

Flammpunkt (°F)

170.6 °F

Flammpunkt (°C)

77 °C

Persönliche Schutzausrüstung

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

Analysenzertifikate (COA)

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3-Methoxy-benzaldehyd 97%

Sigma-Aldrich

129658

3-Methoxy-benzaldehyd

Phthalid 98%

Sigma-Aldrich

P39605

Phthalid

Measurement of acid-catalyzed isomerization of unsaturated aldehyde-2, 4-dinitrophenylhydrazone derivatives by high-performance liquid chromatography analysis.
Uchiyama S, et al.
Analytica Chimica Acta, 523(2), 157-163 (2004)
C J Cros et al.
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The health effects associated with exposure to ozone range from respiratory irritation to increased mortality. In this paper, we explore the use of three green building materials and an activated carbon (AC) mat that remove ozone from indoor air. We
Qing-Xi Chen et al.
Journal of enzyme inhibition and medicinal chemistry, 18(6), 491-496 (2004-03-11)
The inhibition kinetics on the diphenolase activity of mushroom tyrosinase by some alkylbenzaldehydes has been investigated. The results show that the alkylbenzaldehydes assayed can lead to reversible inhibition to the enzyme; o-tolualdehyde and m-tolualdehyde are mixed-type inhibitors and p-alkylbenzaldehydes are
Grainne M Clifford et al.
Environmental science & technology, 45(22), 9649-9657 (2011-10-20)
The photolysis of o-tolualdehyde by natural sunlight has been investigated at the large outdoor European Photoreactor (EUPHORE) in Valencia, Spain. The photolysis rate coefficient was measured directly under different solar flux levels, with values in the range j(o-tolualdehyde) = (1.62-2.15)
K Watanabe et al.
Drug metabolism and disposition: the biological fate of chemicals, 23(2), 261-265 (1995-02-01)
Mouse hepatic microsomal enzymes catalyzed the oxidation of o-, m-, and p-tolualdehydes, intermediate metabolites of xylene, to the corresponding toluic acids. Cofactor requirement for the catalytic activity indicates that the microsomes contain NAD- and NADPH-dependent enzymes for this reaction. GC/MS

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