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 |
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A03-0001 | -- | $-- |
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Product Introduction
1,2-Diaminoanthraquinone (CAS# 1758-68-5) is for the direct detection of nitric oxide.
Chemical Information |
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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 | |
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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
PMID | Publication Date | Title | Journal |
---|---|---|---|
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 Number | Title | Priority Date |
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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 |
Applications of Fluorescent Probes & Dyes
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