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Merck
모든 사진(1)

문서

32730

Sigma-Aldrich

1,4-Diaminoanthraquinone

technical, ≥90% (HPLC)

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About This Item

실험식(Hill 표기법):
C14H10N2O2
CAS Number:
Molecular Weight:
238.24
Beilstein:
2216556
EC Number:
MDL number:
UNSPSC 코드:
12162002
PubChem Substance ID:

grade

technical

분석

≥90% (HPLC)

mp

~260 °C
265-269 °C (lit.)

SMILES string

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 key

FBMQNRKSAWNXBT-UHFFFAOYSA-N

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픽토그램

Exclamation mark

신호어

Warning

유해 및 위험 성명서

예방조치 성명서

Hazard Classifications

Skin Sens. 1

Storage Class Code

11 - Combustible Solids

WGK

WGK 2

Flash Point (°F)

644.0 °F - closed cup

Flash Point (°C)

340 °C - closed cup

개인 보호 장비

Eyeshields, Gloves, type N95 (US)


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문서 라이브러리 방문

Jonathan P May et al.
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.
I Kvelland
Hereditas, 99(2), 209-213 (1983-01-01)
V Krishnakumar et al.
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
Mohammad Saeid Hosseini et al.
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
Abhishek Mandal et al.
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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