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Supelco

9,10-Dimethylanthracene

analytical standard

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About This Item

Empirical Formula (Hill Notation):
C16H14
CAS Number:
Molecular Weight:
206.28
Beilstein:
1909028
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:

grade

analytical standard

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

mp

182-184 °C (lit.)

application(s)

environmental

format

neat

SMILES string

Cc1c2ccccc2c(C)c3ccccc13

InChI

1S/C16H14/c1-11-13-7-3-5-9-15(13)12(2)16-10-6-4-8-14(11)16/h3-10H,1-2H3

InChI key

JTGMTYWYUZDRBK-UHFFFAOYSA-N

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General description

9,10-Dimethylanthracene belongs to the class of polynuclear aromatic hydrocarbons (PAHs), which are generally used as potential starting materials for the synthesis of a variety of industrial chemicals.

Application

9,10-Dimethylanthracene may be used as an analytical standard for the determination of the analyte in coal and petroleum products as well as human biological samples by various chromatography techniques.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Pictograms

Health hazardExclamation mark

Signal Word

Danger

Hazard Statements

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Resp. Sens. 1 - Skin Sens. 1

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

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Characterisation of middle-distillates by comprehensive two-dimensional gas chromatography (GC x GC): A powerful alternative for performing various standard analysis of middle-distillates
Vendeuvre C, et al.
Journal of Chromatography A, 1086(1-2), 21-28 (2005)
Analysis of polynuclear aromatic hydrocarbons in heavy products derived from coal and petroleum by high performance liquid chromatography
Zhang C, et al.
Journal of Chromatography A, 1167(2), 171-177 (2007)
Quantitative high-performance liquid chromatographic determination of retinoids in human serum using on-line solid-phase extraction and column switching determination of 9-cis-retinoic acid, 13-cis-retinoic acid, all-trans-retinoic acid, 4-oxo-all-trans-retinoic acid and 4-oxo-13-cis-retinoic acid
Gundersen, TE, et al.
Journal of Chromatography. B, Biomedical Applications, 691(1), 43-58 (1997)
David Bailey et al.
Chemical communications (Cambridge, England), (20)(20), 2569-2571 (2005-05-19)
Irradiating 2,3,6,7-tetraphenylanthracene in the presence of 9,10-dimethylanthracene leads to exclusive formation of the cross-dimer. No photochemical reaction is observed when either of these chromophores is irradiated in the absence of the other.
E Gross et al.
Photochemistry and photobiology, 57(5), 808-813 (1993-05-01)
Two new sensitizers are introduced for a potential use in photodynamic therapy: Zn(2+)- and MG(2+)-tetrabenzoporphyrin (ZnTBP and MgTBP). A comparative study of the quantum yields of singlet oxygen generation (phi delta) of hematoporphyrin derivative (HpD), Photofrin II (PF-II), Zn(2+)-phthalocyanine tetrahydroxyl

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