367834
1,4-Diaminoanthraquinone
technical grade, ≥88.0%
Synonym(s):
1,4-Diamino-9,10-anthracenedione, 1,4-Diamino-9,10-anthraquinone
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About This Item
Empirical Formula (Hill Notation):
C14H10N2O2
CAS Number:
Molecular Weight:
238.24
Beilstein:
2216556
EC Number:
MDL number:
UNSPSC Code:
12162002
PubChem Substance ID:
NACRES:
NA.23
Recommended Products
grade
technical grade
Assay
≥88.0%
mp
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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Signal Word
Warning
Hazard Statements
Precautionary Statements
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
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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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.
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
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
Vsevolod Katritch et al.
Journal of medicinal chemistry, 53(4), 1799-1809 (2010-01-26)
The recent progress in crystallography of G-protein coupled receptors opens an unprecedented venue for structure-based GPCR drug discovery. To test efficiency of the structure-based approach, we performed molecular docking and virtual ligand screening (VLS) of more than 4 million commercially
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)
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