Safranine T - indicator , CAS No.477-73-6

CAS: 477-73-6 Cat. No.: S104171 Peso molecular: 350.85 Beilstein Registry Number: 3924099 Número EC: 207-518-8

GRADE & PURITY Indicator

Synonyms

A872074 | BASIC RED 2 [INCI] | Mitsui safranine | Phenazinium, 3,7-diamino-2,8-dimethyl-5-phenyl-, chloride (1:1) | Safranine TH | Safranine A | Safranine Zh | Brilliant safranine G | S-0700 | Basic Red 2 (Safranine O) | Phenazinium,7-diamino-2,8-dimethyl

Storage

Room temperature

Shipped In

Normal

Descripción general

Safranin T is a biological stain commonly used as a counter stain for gram-negative bacteria in the Gram stain procedure. Safranin T has been observed to bind to DNA at a pH 2.21. In the Flemming triple stain procedure Safranin T is used to stain for chromosomes. In late Palaeozoic pteridosperm cuticles Safranin T has shown increased contrast, emphasized cutinization differences, and enhanced the three-dimensional morphology of complex epidermal features when compared with other dyes. The compound has also been used with alcian blue in the histochemical study of the distribution and morphometric characteristics of mast cells. Safranin T has also been used to detect mucin and cartilage.
A biological stain used to stain Gram negative bacteria, chormosomes, mucin, cartilage and mast cells.

Specifications

Sinónimos

A872074 | BASIC RED 2 [INCI] | Mitsui safranine | Phenazinium, 3, 7-diamino-2, 8-dimethyl-5-phenyl-, chloride (1:1) | Safranine TH | Safranine A | Safranine Zh | Brilliant safranine G | S-0700 | Basic Red 2 (Safranine O) | Phenazinium, 7-diamino-2, 8-dimethyl

Especificaciones y pureza

indicator

Mecanismos bioquímicos y fisiológicos

Biological stain used to stain Gram negative bacteria, chromosomes, mucin, cartilage and mast cells. Commonly used as a counter stain for gram-negative bacteria in the Gram stain procedure.

Condiciones de almacenamiento de almacenamiento

Room temperature

Enviado en

Normal

Grado

Indicator

Nota

Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.

Nombres e identificadores

• Pubchem Sid: 504760812
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504760812
• Sonrisas canónicas: CC1=CC2=C(C=C1N)[N+](=C3C=C(C(=CC3=N2)C)N)C4=CC=CC=C4.[Cl-]
• IUPAC Name: 3,7-dimethyl-10-phenylphenazin-10-ium-2,8-diamine;chloride
• InChIKey: OARRHUQTFTUEOS-UHFFFAOYSA-N
• INCHI: 1S/C20H18N4.ClH/c1-12-8-17-19(10-15(12)21)24(14-6-4-3-5-7-14)20-11-16(22)13(2)9-18(20)23-17;/h3-11H,1-2H3,(H3,21,22);1H
• Isómeros SMILES: CC1=CC2=C(C=C1N)[N+](=C3C=C(C(=CC3=N2)C)N)C4=CC=CC=C4.[Cl-]
• RTECS: SG1623000
• CAS alternativo: 7006-08-8
• Peso molecular: 350.85
• Beilstein: 3924099
• Reaxy-Rn: 3924099

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Clase Diazanaphthalenes
      • Subclass Benzodiazines
        • Level5 Quinoxalines
          • Level6 Phenazines and derivatives

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Clase: Diazanaphthalenes
• Subclass: Benzodiazines
• Intermediate Tree Nodes: Quinoxalines
• Direct Parent: Phenazines and derivatives
• Alternative Parents: Pyrazinium compounds Pyrazines Benzene and substituted derivatives Heteroaromatic compounds Azacyclic compounds Primary amines Organopnictogen compounds Organic chloride salts Hydrocarbon derivatives
• Molecular Framework: Aromatic heteropolycyclic compounds
• Substituents: Phenazine - Monocyclic benzene moiety - Pyrazine - Pyrazinium - Benzenoid - Heteroaromatic compound - Azacycle - Organic chloride salt - Organic salt - Organonitrogen compound - Amine - Primary amine - Organic nitrogen compound - Hydrocarbon derivative - Organopnictogen compound - Aromatic heteropolycyclic compound
• Descripción: This compound belongs to the class of organic compounds known as phenazines and derivatives. These are polycyclic aromatic compounds containing a phenazine moiety, which is a linear tricyclic system that consists of a two benzene rings joined by a pyrazine ring.
• 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

Mecanismos de acción

Propiedades químicas y físicas

• Solubilidad: Soluble in water (50 mg/ml at 20 °C), and alcohol
• Sensibilidad: Moisture sensitive.
• Punto de ebullición (°C): 507.14°C
• Punto de fusión (°C): >240°C (dec.)
• Peso molecular: 350.800 g/mol
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 1
• Exact Mass: 350.13 Da
• Monoisotopic Mass: 350.13 Da
• Topological Polar Surface Area: 68.800 Ų
• Heavy Atom Count: 25
• Formal Charge: 0
• Complexity: 405.000
• 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: 2

XLogP3

Referencias

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