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Key Documents

45779

Supelco

9,10-二甲基蒽

analytical standard

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About This Item

經驗公式(希爾表示法):
C16H14
CAS號碼:
分子量::
206.28
Beilstein:
1909028
EC號碼:
MDL號碼:
分類程式碼代碼:
41116107
PubChem物質ID:

等級

analytical standard

儲存期限

limited shelf life, expiry date on the label

技術

HPLC: suitable
gas chromatography (GC): suitable

mp

182-184 °C (lit.)

應用

environmental

格式

neat

SMILES 字串

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 密鑰

JTGMTYWYUZDRBK-UHFFFAOYSA-N

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一般說明

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.

應用

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.

象形圖

Health hazardExclamation mark

訊號詞

Danger

危險分類

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

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

dust mask type N95 (US), Eyeshields, Faceshields, 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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