等級
technical
化驗
≥90% (HPLC)
mp
~260 °C
265-269 °C (lit.)
SMILES 字串
Nc1ccc(N)c2C(=O)c3ccccc3C(=O)c12
InChI
1S/C14H10N2O2/c15-9-5-6-10(16)12-11(9)13(17)7-3-1-2-4-8(7)14(12)18/h1-6H,15-16H2
InChI 密鑰
FBMQNRKSAWNXBT-UHFFFAOYSA-N
尋找類似的產品? 前往 產品比較指南
訊號詞
Warning
危險聲明
危險分類
Skin Sens. 1
儲存類別代碼
11 - Combustible Solids
水污染物質分類(WGK)
WGK 2
閃點(°F)
644.0 °F - closed cup
閃點(°C)
340 °C - closed cup
個人防護裝備
Eyeshields, Gloves, type N95 (US)
Chemical communications (Cambridge, England), (8)(8), 970-971 (2003-05-15)
A novel, long-wavelength, non-fluorescent quencher (LQ), based on 1,4-diaminoanthraquinone, has been incorporated at the 3' and 5'-termini of oligonucleotides. The quencher has been used in Molecular beacons, efficiently quenching the long wavelength fluorophore, Cy5.
The mutagenic effect in bacteriophage T4D of a hair dye, 1,4 diaminoanthraquinone, and of two solvents, dimethylsulfoxide and ethanol.
Hereditas, 99(2), 209-213 (1983-01-01)
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 61(8), 1799-1809 (2005-05-03)
This work deals with the vibrational spectroscopy of 1,4-diaminoanthraquinone (1,4-DAAQ) and 1,5-dichloroanthraquinone (1,5-DCAQ). The mid and far FTIR and FT-Raman spectra were measured in the condensed state. The fundamental vibrational frequencies and intensity of the vibrational bands were evaluated using
Analytical sciences : the international journal of the Japan Society for Analytical Chemistry, 25(6), 807-812 (2009-06-18)
A highly sensitive and selective method has been proposed for speciation determination of trace amounts of Cr(III) and Cr(VI) in water samples using 1,4-diaminoanthraquinone (1,4-DAAQ). The method is based on mixing an organic phase containing 1,4-DAAQ with an acidic solution
Inorganic chemistry, 53(12), 6082-6093 (2014-06-05)
The compounds [(acac)2Ru(III)(μ-H2L(2-))Ru(III)(acac)2] (rac, 1, and meso, 1') and [(bpy)2Ru(II)(μ-H2L(•-))Ru(II)(bpy)2](ClO4)3 (meso, [2](ClO4)3) have been structurally, magnetically, spectroelectrochemically, and computationally characterized (acac(-) = acetylacetonate, bpy = 2,2'-bipyridine, and H4L = 1,4-diamino-9,10-anthraquinone). The N,O;N',O'-coordinated μ-H2L(n-) forms two β-ketiminato-type chelate rings, and 1
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