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T35505

Sigma-Aldrich

m-Tolualdehyde

97%

Sinónimos:

3-Methylbenzaldehyde

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About This Item

Fórmula lineal:
CH3C6H4CHO
Número de CAS:
620-23-5
Peso molecular:
120.15
Beilstein/REAXYS Number:
741964
EC Number:
210-632-0
MDL number:
MFCD00003374
UNSPSC Code:
12352100
PubChem Substance ID:
24900148
NACRES:
NA.22

assay

97%

refractive index

n20/D 1.541 (lit.)

bp

199 °C (lit.)
80-82 °C/11 mmHg (lit.)

density

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

SMILES string

[H]C(=O)c1cccc(C)c1

InChI

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

InChI key

OVWYEQOVUDKZNU-UHFFFAOYSA-N

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Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

181.4 °F - closed cup

flash_point_c

83 °C - closed cup

ppe

Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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Sigma-Aldrich

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Sigma-Aldrich

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4-Methylbenzaldehyde for synthesis

Sigma-Aldrich

8.06179

4-Methylbenzaldehyde

Z P Lin et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 56A(1), 111-117 (2000-03-23)
Triplet-state energy values obtained from the gas phase are still scarce. In this study, the triplet-state energies of 58 aroyl compounds, introduced as gas chromatographic peaks at atmospheric pressure and typically 473 K, have been determined from the 0-0 bands
Bi-hong Xiao et al.
Zhong yao cai = Zhongyaocai = Journal of Chinese medicinal materials, 34(4), 544-546 (2011-08-04)
To study the secondary metabolites of coastal seaweed endophytic fungi ZJ27. The compounds were isolated by chromatographic technique. The structures were identified by comprehensive physic-chemical properties and spectral methods. Five compounds were isolated and identified as sclerotiorin (1), ochrephilone (2)
Anu Vaidyanathan et al.
Journal of toxicology and environmental health. Part A, 66(12), 1133-1143 (2003-06-07)
Xylene is used as a solvent in paints, cleaning agents, and gasoline. Exposure occurs primarily by inhalation. The volatility and lipophilicity of the xylenes make the lung and nasal mucosa the primary target organs. m-Xylene (m-XYL) has been shown to
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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