Bicinchoninic acid disodium salt(BCA) - Moligand™, ≥98% , CAS No.979-88-4

CAS: 979-88-4 Cat. No.: B107658 Peso molecular: 388.28 (anhydrous basis) Número EC: 629-761-2 PubChem CID: 164763

GRADE & PURITY Moligand™, ≥98%

Synonyms

BCA | B5838 | BCADisodium | B4509 | AKOS015951447 | Bicinchoninic Acid Disodium Salt [for Protein Research] | DISODIUM [2,2'-BIQUINOLINE]-4,4'-DICARBOXYLATE | disodium;2-(4-carboxylatoquinolin-2-yl)quinoline-4-carboxylate | (2,2'-Biquinoline)-4,4'-dicarbo

Storage

Store at 2-8°C

Shipped In

Wet ice

Descripción general

For the determination of protein concentration. 

• Bicinchoninic acid disodium salt hydrate has been used to monitor the levels of reducing sugars, thereby helping in the detection of chitinases.

• It has also been used to determine the amount of cellulose reducing ends (micromoles/g cellulose). 

• It has been used for determining protein concentration.

Specifications

Sinónimos

BCA | B5838 | BCADisodium | B4509 | AKOS015951447 | Bicinchoninic Acid Disodium Salt [for Protein Research] | DISODIUM [2, 2'-BIQUINOLINE]-4, 4'-DICARBOXYLATE | disodium;2-(4-carboxylatoquinolin-2-yl)quinoline-4-carboxylate | (2, 2'-Biquinoline)-4, 4'-dicarbo

Especificaciones y pureza

Moligand™, ≥98%

Mecanismos bioquímicos y fisiológicos

Bicinchoninic acid is used for the determination of protein concentration. It is responsible for the making of intense purple complex with cuprous ion (Cu+), in presence of alkaline conditions. The amount of Cu+ is in relation with the protein concentrati

Condiciones de almacenamiento de almacenamiento

Store at 2-8°C

Enviado en

Wet ice

Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.

Grado

Moligand™

Tipo de acción

INHIBITOR

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.

Pureza

≥98%

Nombres e identificadores

• Pubchem Sid: 488188374
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488188374
• Sonrisas canónicas: O.[Na+].[Na+].[O-]C(=O)c1cc(nc2ccccc12)-c3cc(C([O-])=O)c4ccccc4n3
• IUPAC Name: disodium;2-(4-carboxylatoquinolin-2-yl)quinoline-4-carboxylate
• InChIKey: AUPXFICLXPLHBB-UHFFFAOYSA-L
• INCHI: 1S/C20H12N2O4.2Na/c23-19(24)13-9-17(21-15-7-3-1-5-11(13)15)18-10-14(20(25)26)12-6-2-4-8-16(12)22-18;;/h1-10H,(H,23,24)(H,25,26);;/q;2*+1/p-2
• Isómeros SMILES: C1=CC=C2C(=C1)C(=CC(=N2)C3=NC4=CC=CC=C4C(=C3)C(=O)[O-])C(=O)[O-].[Na+].[Na+]
• PubChem CID: 164763
• Peso molecular: 388.28 (anhydrous basis)

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Clase Quinolines and derivatives
      • Subclass Quinoline carboxylic acids

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Clase: Quinolines and derivatives
• Subclass: Quinoline carboxylic acids
• Intermediate Tree Nodes: Not available
• Direct Parent: Quinoline carboxylic acids
• Alternative Parents: Bipyridines and oligopyridines Pyridinecarboxylic acids Dicarboxylic acids and derivatives Benzenoids Heteroaromatic compounds Carboxylic acid salts Carboxylic acids Azacyclic compounds Organopnictogen compounds Organooxygen compounds Organonitrogen compounds Organic zwitterions Organic sodium salts Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aromatic heteropolycyclic compounds
• Substituents: Quinoline-4-carboxylic acid - Bipyridine - Pyridine carboxylic acid - Pyridine carboxylic acid or derivatives - Dicarboxylic acid or derivatives - Benzenoid - Pyridine - Heteroaromatic compound - Carboxylic acid salt - Carboxylic acid derivative - Carboxylic acid - Azacycle - Organic alkali metal salt - Organic nitrogen compound - Organic zwitterion - Organic salt - Organic sodium salt - Organooxygen compound - Organonitrogen compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - Aromatic heteropolycyclic compound
• Descripción: This compound belongs to the class of organic compounds known as quinoline carboxylic acids. These are quinolines in which the quinoline ring system is substituted by a carboxyl group at one or more positions.
• 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. 0.5% sodium bicarbonate: 50 mg/mL
• Sensibilidad: heat sensitive
• Peso molecular: 388.300 g/mol
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 1
• Exact Mass: 388.044 Da
• Monoisotopic Mass: 388.044 Da
• Topological Polar Surface Area: 106.000 Ų
• Heavy Atom Count: 28
• Formal Charge: 0
• Complexity: 495.000
• 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: 3

XLogP3

Referencias

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