1,2-Diaminoanthraquinone

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1,2-Diaminoanthraquinone

1,2-Diaminoanthraquinone | 1758-68-5

Catalog Number A03-0001
Category Nitric Oxide (NO) & Reactive Oxygen Species (ROS)
Molecular Formula C14H10N2O2
Molecular Weight 238.24
Catalog Number Size Price Quantity
A03-0001 -- $--

Product Introduction

1,2-Diaminoanthraquinone (CAS# 1758-68-5) is for the direct detection of nitric oxide.

Chemical Information

Synonyms DAA;1,2-diaminoanthracene-9,10-dione
Purity 96 %
IUPAC Name 1,2-diaminoanthracene-9,10-dione
Canonical SMILES C1=CC=C2C(=C1)C(=O)C3=C(C2=O)C(=C(C=C3)N)N
InChI InChI=1S/C14H10N2O2/c15-10-6-5-9-11(12(10)16)14(18)8-4-2-1-3-7(8)13(9)17/h1-6H,15-16H2
InChI Key LRMDXTVKVHKWEK-UHFFFAOYSA-N
Density 1.456 g/cm3
Appearance Brown powder
Boiling Point 548.8 °C at 760 mmHg
LogP 2.78880
  • Product Specification
  • Application
Excitation 488(After reaction with NO)
Emission 580 (After reaction with NO)
Storage Store at-10 to-35 °C, Protect from light, Desiccate
Signal Warning
GHS Hazard Statements H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation] H319 (100%): Causes serious eye irritation [Warning Serious eye damage/eye irritation] H335 (100%): May cause respiratory irritation [Warning Specific target organ toxicity, single exposure; Respiratory tract irritation]
Precautionary Statement Codes P261, P264, P264+P265, P271, P280, P302+P352, P304+P340, P305+P351+P338, P319, P321, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501 (The corresponding statement to each P-code can be found at the GHS Classification page.)

1,2-Diaminoanthraquinone, a versatile organic compound, finds widespread use in scientific research and industrial applications. Explore its diverse applications with a narrative characterized by high perplexity and burstiness.

Fluorescent Probes: Delving into the realm of analytical chemistry, 1,2-Diaminoanthraquinone serves as a radiant fluorescent probe, emitting light upon excitation. Researchers harness its fluorescence prowess to detect and quantify ions and molecules in biological and environmental samples, enabling applications in high-sensitivity detection and advanced imaging techniques.

Dye Synthesis: Within the intricate tapestry of the textile and dye industries, 1,2-Diaminoanthraquinone emerges as a pivotal precursor in the synthesis of anthraquinone-based dyes. These dyes boast vibrant hues, exceptional colorfastness, and remarkable compatibility with diverse fibers. By leveraging this compound, manufacturers craft premium-quality dyes for fabrics and assorted materials, enriching the landscape of textile design.

Biochemistry Research: Embarking on a journey through biochemistry, 1,2-Diaminoanthraquinone unlocks new possibilities for studying enzyme kinetics and protein interactions. Acting as both a substrate and inhibitor in biochemical assays, it aids scientists in unraveling the intricate mechanisms of enzyme-catalyzed reactions. This exploration enhances our understanding of metabolic pathways and sheds light on the complexities of protein functionalities.

Environmental Analysis: Navigating the realms of environmental stewardship, 1,2-Diaminoanthraquinone plays a crucial role in monitoring and controlling pollution. Employed in the development of sensors and detection systems, it facilitates the tracking of pollutants, heavy metals, and hazardous substances in water, soil, and air. This application reinforces environmental protection initiatives, bolstering efforts to uphold regulatory standards and safeguard the planet.

Computed Properties

XLogP3 2.1
Hydrogen Bond Donor Count 2
Hydrogen Bond Acceptor Count 4
Rotatable Bond Count 0
Exact Mass 238.074227566 g/mol
Monoisotopic Mass 238.074227566 g/mol
Topological Polar Surface Area 86.2Ų
Heavy Atom Count 18
Formal Charge 0
Complexity 382
Isotope Atom Count 0
Defined Atom Stereocenter Count 0
Undefined Atom Stereocenter Count 0
Defined Bond Stereocenter Count 0
Undefined Bond Stereocenter Count 0
Covalently-Bonded Unit Count 1
Compound Is Canonicalized Yes

Literatures

PMIDPublication DateTitleJournal
29501861 2018-05-02 Synthesis of novel sugar or azasugar modified anthra[1,2-d] imidazole-6,11-dione derivatives and biological evaluation Carbohydrate research
21953703 2011-11-04 Fluorescence of 1,2-diaminoanthraquinone and its nitric oxide reaction product within macrophage cells Chembiochem : a European journal of chemical biology
19571147 2009-07-01 Endogenous nitric oxide is a key promoting factor for initiation of seizure-like events in hippocampal and entorhinal cortex slices The Journal of neuroscience : the official journal of the Society for Neuroscience
21583879 2009-04-18 2-(4-Methyl-phen-yl)-1H-anthraceno[1,2-d]imidazole-6,11-dione: a fluorescent chemosensor Acta crystallographica. Section E, Structure reports online
19384274 2009-04-02 Synthesis of new naphtho[2,3-f]quinoxaline-2,7,12(1H)-trione and anthra-9,10-quinone dyes from furan-2,3-diones Molecules (Basel, Switzerland)

Patents

Publication NumberTitlePriority Date
CN-217929617-U 1.4 High-efficiency drying device for the finished product of hydroxyleuco for the production of di-aminoanthraquinone 2022-08-15
CN-217910308-U A kind of 1.4 di-aminoanthraquinone production with aminoxidant reaction kettle 2022-08-11
CN-114990734-A A kind of graphene assembly fiber and its preparation method and application 2022-06-07
CN-114950492-A A 1,2-diaminoanthraquinone-molybdenum disulfide composite antibacterial material for photoelectric catalytic killing of bacteria 2022-05-31
CN-114377556-B A kind of temperature-resistant composite water treatment membrane and preparation method thereof 2022-01-19
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