1,2-Diaminoantraquinona - ≥90% , CAS No.1758-68-5

CAS: 1758-68-5 Cat. No.: D124352 Peso molecular: 238.24 Número EC: 217-156-2

GRADE & PURITY ≥90%

Synonyms

1,2-diamino-10-anthracenedione | NSC 39934 | BDBM50599586 | BIDD:GT0412 | MFCD00001219 | CCRIS 5602 | 1, 2-Diaminoanthraquinone | UPCMLD0ENAT5883742:001 | ANTHRAQUINONE, 1,2-DIAMINO- | EINECS 217-156-2 | SCHEMBL487001 | 1,2-Diamino-9,10-anthraquinone | 1,

Storage

Argón cargado

Shipped In

Normal

Descripción general

la 1,2-Diaminoantraquinona es un reactivo útil para la detección directa de óxido nítrico (NO) La DAA no es fluorescente; sin embargo, reacciona con el NO, en presencia de oxígeno, para formar triazol DAA, produciendo fluorescencia roja, que es visible con un filtro de rodamina (λ ≥ 580 nm).
Para la detección directa de óxido nítrico.

Specifications

Sinónimos

1, 2-diamino-10-anthracenedione | NSC 39934 | BDBM50599586 | BIDD:GT0412 | MFCD00001219 | CCRIS 5602 | 1, 2-Diaminoanthraquinone | UPCMLD0ENAT5883742:001 | ANTHRAQUINONE, 1, 2-DIAMINO- | EINECS 217-156-2 | SCHEMBL487001 | 1, 2-Diamino-9, 10-anthraquinone | 1,

Especificaciones y pureza

≥90%

Condiciones de almacenamiento de almacenamiento

Argón cargado

Enviado en

Normal

Pureza

≥90%

Nombres e identificadores

• Pubchem Sid: 504752689
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504752689
• Sonrisas canónicas: C1=CC=C2C(=C1)C(=O)C3=C(C2=O)C(=C(C=C3)N)N
• IUPAC Name: 1,2-diaminoanthracene-9,10-dione
• InChIKey: LRMDXTVKVHKWEK-UHFFFAOYSA-N
• 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
• Isómeros SMILES: C1=CC=C2C(=C1)C(=O)C3=C(C2=O)C(=C(C=C3)N)N
• WGK Alemania: 3
• RTECS: CB6200000
• Peso molecular: 238.24
• Reaxy-Rn: 2125604
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2125604&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Clase Anthracenes
      • Subclass Anthraquinones

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Clase: Anthracenes
• Subclass: Anthraquinones
• Intermediate Tree Nodes: Not available
• Direct Parent: 2-aminoanthraquinones
• Alternative Parents: Aryl ketones Vinylogous amides Primary amines Organopnictogen compounds Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aromatic homopolycyclic compounds
• Substituents: 2-aminoanthraquinone - Aryl ketone - Vinylogous amide - Ketone - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Primary amine - Organooxygen compound - Organonitrogen compound - Amine - Aromatic homopolycyclic compound
• Descripción: This compound belongs to the class of organic compounds known as 2-aminoanthraquinones. These are organic compounds containing an anthraquinone ring system, which is substituted at the 2-position by an amino group.
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Objetivos asociados (humanos)

MAOA Tclin Monoamine oxidase A (11911 Activities)

Discover Target: MAOA

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

MAOB Tclin Monoamine oxidase B (8835 Activities)

Discover Target: MAOB

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

TERT Tchem Telomerase reverse transcriptase (2428 Activities)

Discover Target: TERT

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mecanismos de acción

Propiedades químicas y físicas

• Solubilidad: Soluble in DMSO (5 mg/ml). Insoluble in water.
• Sensibilidad: Air sensitive
• Punto de fusión (°C): 289-291°C
• Peso molecular: 238.240 g/mol
• XLogP3: 2.100
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 0
• Exact Mass: 238.074 Da
• Monoisotopic Mass: 238.074 Da
• Topological Polar Surface Area: 86.200 Ų
• Heavy Atom Count: 18
• Formal Charge: 0
• Complexity: 382.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1

Referencias

1. Jinyang Peng, Xinran Zhao, Yuxi Huang, Cuijiao Zhao, Jun Yang, Minjie Shi.  (2025)  Electron-Delocalized Benzimidazole-Linked Organic Electrode with Enhanced Redox Availability for High-Performance Ammonium Capture via Capacitive Deionization.  ADVANCED FUNCTIONAL MATERIALS,      [PMID:] [10.1002/adfm.202506369]

2. Jun Yang, Xinran Zhao, Jinyang Peng, Jiachen Yang, Minjie Shi, Liqiu Zhang, Chao Yan.  (2025)  Redox-enhanced ladder-type organic electrode enabling high-rate aqueous ammonium-ion batteries.  JOURNAL OF COLLOID AND INTERFACE SCIENCE,      [PMID:40639166] [10.1016/j.jcis.2025.138339]