T35505
m-Tolualdehyde
97%
Synonym(s):
3-Methylbenzaldehyde
Sign Into View Organizational & Contract Pricing
All Photos(1)
About This Item
Linear Formula:
CH3C6H4CHO
CAS Number:
Molecular Weight:
120.15
Beilstein:
741964
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Pricing and availability is not currently available.
Recommended Products
Quality Level
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
Looking for similar products? Visit Product Comparison Guide
Storage Class Code
10 - Combustible liquids
WGK
WGK 3
Flash Point(F)
181.4 °F - closed cup
Flash Point(C)
83 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Customers Also Viewed
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)
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
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
Protocols
-Tolualdehyde; Valeraldehyde; Isovaleraldehyde
Active Filters
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service
