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D170801

Sigma-Aldrich

2,3-Dimethylnaphthalene

97%

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About This Item

Linear Formula:
C10H6(CH3)2
CAS Number:
Molecular Weight:
156.22
Beilstein:
1852621
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

97%

form

flakes

bp

269 °C (lit.)

mp

103-104 °C (lit.)

SMILES string

Cc1cc2ccccc2cc1C

InChI

1S/C12H12/c1-9-7-11-5-3-4-6-12(11)8-10(9)2/h3-8H,1-2H3

InChI key

WWGUMAYGTYQSGA-UHFFFAOYSA-N

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Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Precautionary Statements

Hazard Classifications

Acute Tox. 4 Oral

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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T Prabhu et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 78(2), 566-574 (2010-12-28)
A combined experimental and theoretical study on molecular and vibrational structure of 2,3-dimethyl naphthalene (2,3-DMN) has been undertaken in the present work. The FTIR and FT Raman spectra of 2,3-DMN were recorded in the region 4000-100 cm(-1). The optimized geometries
Rongfu Huang et al.
Chemosphere, 266, 129017-129017 (2020-12-03)
This work describes a novel application of atmospheric pressure gas chromatography time-of-flight mass spectrometry (APGC-TOF-MS) combined with solid-phase microextraction (SPME) for the simultaneous analysis of hydrocarbons and naphthenic acids (NAs) species in raw and ozone-treated oil sands process water (OSPW).
J Z Hu et al.
Solid state nuclear magnetic resonance, 3(4), 181-197 (1994-08-01)
The magic-angle turning (MAT) experiment introduced by Gan is developed into a powerful and routine method for measuring the principal values of 13C chemical shift tensors in powdered solids. A large-volume MAT probe with stable rotation frequencies down to 22
Sangwoo Lee et al.
Environmental science. Processes & impacts, 19(9), 1117-1125 (2017-08-08)
Polycyclic aromatic hydrocarbons (PAHs) and alkylated PAHs are known to be major toxic contaminants in spills of petroleum hydrocarbons (oil). Spilled oil undergoes weathering and over time, PAHs go through a series of compositional changes. PAHs can disrupt endocrine functions
A A Toropov et al.
European journal of medicinal chemistry, 43(4), 714-740 (2007-07-17)
Simplified molecular input line entry system (SMILES) has been utilized in constructing quantitative structure-property relationships (QSPR) for octanol/water partition coefficient of vitamins and organic compounds of different classes by optimal descriptors. Statistical characteristics of the best model (vitamins) are the

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