Alcian blue 8GX - Dye-content ≥50% , CAS No.33864-99-2

CAS: 33864-99-2 Cat. No.: A105505 Peso molecular: 1298.86 Número EC: 251-705-7 PubChem CID: 16211091

GRADE & PURITY Dye-content ≥50%

Synonyms

CI 74240 | Alcian Blue 8GX, powder | Alcian Blue 8GX, certified | HY-D0001 | Alcian Blue 8GX, for microscopy (Bact., Bot., Hist.) | Ingrain Blue 1 | AKOS015902443 | alcian-blue 8gx | Alcian Blue 8GX, BioReagent, suitable for detection of glycoproteins | A

Storage

Room temperature

Shipped In

Normal

Descripción general

Alcian Blue 8GX is used as a heteroglycan stain for neutral, sulfated and phosphated mucopolysaccharides and glycosaminoglycans in tissues such as cartilage and extracellular matrices.

application：

Alcian Blue 8GX is widely utilized as a heteroglycan stain for acidic, neutral, sulfated and phosphate polysaccharides and glycosaminoglycans in tissues. It finds application in both light and electron microscopy. It serves as an adhesive to stick glycol methacrylate sections to glass slides. Due to its large aromatic surface, it is used as a coating agent and modifies the property on the surfaces. It acts as a gelling agent for lubricating fluids and is also used in the modification of carbon paste electrode which promotes redox behavior and stability of electrode.

Specifications

Sinónimos

CI 74240 | Alcian Blue 8GX, powder | Alcian Blue 8GX, certified | HY-D0001 | Alcian Blue 8GX, for microscopy (Bact., Bot., Hist.) | Ingrain Blue 1 | AKOS015902443 | alcian-blue 8gx | Alcian Blue 8GX, BioReagent, suitable for detection of glycoproteins | A

Especificaciones y pureza

Dye-content ≥50%

Mecanismos bioquímicos y fisiológicos

Alcian Blue 8GX is used as a heteroglycan stain for neutral, sulfated and phosphated mucopolysaccharides and glycosaminoglycans in tissues such as cartilage and extracellular matrices

Condiciones de almacenamiento de almacenamiento

Room temperature

Enviado en

Normal

Nombres e identificadores

• Pubchem Sid: 504768089
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504768089
• Sonrisas canónicas: CN(C)C(=[N+](C)C)SCC1=CC2=C(C=C1)C3=NC4=NC(=NC5=C6C=C(C=CC6=C([N-]5)N=C7C8=C(C=CC(=C8)CSC(=[N+](C)C)N(C)C)C(=N7)N=C2[N-]3)CSC(=[N+](C)C)N(C)C)C9=C4C=C(C=C9)CSC(=[N+](C)C)N(C)C.[Cl-].[Cl-].[Cl-].[Cl-].[Cu+2]
• IUPAC Name: copper;[dimethylamino-[[15,24,33-tris[[dimethylamino(dimethylazaniumylidene)methyl]sulfanylmethyl]-2,11,20,29,37,39-hexaza-38,40-diazanidanonacyclo[28.6.1.13,10.112,19.121,28.04,9.013,18.022,27.031,36]tetraconta-1(37),2,4(9),5,7,10,12(39),13(18),14,16,19,21,23,25,27,29,31(36),32,34-nonadecaen-6-yl]methylsulfanyl]methylidene]-dimethylazanium;tetrachloride
• InChIKey: CKLBXIYTBHXJEH-UHFFFAOYSA-J
• INCHI: 1S/C56H68N16S4.4ClH.Cu/c1-65(2)53(66(3)4)73-29-33-17-21-37-41(25-33)49-57-45(37)62-50-43-27-35(31-75-55(69(9)10)70(11)12)19-23-39(43)47(59-50)64-52-44-28-36(32-76-56(71(13)14)72(15)16)20-24-40(44)48(60-52)63-51-42-26-34(18-22-38(42)46(58-51)61-49)30-74-54(67(5)6)68(7)8;;;;;/h17-28H,29-32H2,1-16H3;4*1H;/q+2;;;;;+2/p-4
• Isómeros SMILES: CN(C)C(=[N+](C)C)SCC1=CC2=C(C=C1)C3=NC4=NC(=NC5=C6C=C(C=CC6=C([N-]5)N=C7C8=C(C=CC(=C8)CSC(=[N+](C)C)N(C)C)C(=N7)N=C2[N-]3)CSC(=[N+](C)C)N(C)C)C9=C4C=C(C=C9)CSC(=[N+](C)C)N(C)C.[Cl-].[Cl-].[Cl-].[Cl-].[Cu+2]
• WGK Alemania: 3
• CAS alternativo: 75881-23-1
• PubChem CID: 16211091
• Peso molecular: 1298.86

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Clase Tetrapyrroles and derivatives
      • Subclass Phthalocyanines

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Clase: Tetrapyrroles and derivatives
• Subclass: Phthalocyanines
• Intermediate Tree Nodes: Not available
• Direct Parent: Phthalocyanines
• Alternative Parents: Isoindoles Benzenoids Pyrroles Heteroaromatic compounds Sulfenyl compounds Propargyl-type 1,3-dipolar organic compounds Organic metal halides Carboximidamides Azacyclic compounds Organic copper salts Organic chloride salts Hydrocarbon derivatives Organic cations
• Molecular Framework: Aromatic heteropolycyclic compounds
• Substituents: Phthalocyanine skeleton - Isoindole - Isoindole or derivatives - Benzenoid - Pyrrole - Heteroaromatic compound - Organic metal halide - Carboximidamide - Sulfenyl compound - Azacycle - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Organic transition metal salt - Organonitrogen compound - Organosulfur compound - Hydrocarbon derivative - Organic salt - Organic chloride salt - Organic nitrogen compound - Organic copper salt - Organic cation - Aromatic heteropolycyclic compound
• Descripción: This compound belongs to the class of organic compounds known as phthalocyanines. These are cyclic tetrapyrroles that contain a phthalocyanine skeleton, which consists of four isoindole-type units, with the connecting carbon atoms in the macrocycle replaced by nitrogen.
• 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

Propiedades químicas y físicas

• Solubilidad: Soluble in water, ethanol, ethylene glycol and 2-ethoxyethanol. Insoluble in xylene.
• Punto de fusión (°C): 148°C
• Peso molecular: 1298.900 g/mol
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 12
• Rotatable Bond Count: 16
• Exact Mass: 1297.27 Da
• Monoisotopic Mass: 1295.27 Da
• Topological Polar Surface Area: 202.000 Ų
• Heavy Atom Count: 81
• Formal Charge: 0
• Complexity: 2270.000
• 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: 6

XLogP3

Referencias

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