Maleimida Cy5.5 - Ex:678nm, Em:695nm, ≥95% , CAS No.1593644-50-8

CAS: 1593644-50-8 Cat. No.: C171357 Peso molecular: 741.36

GRADE & PURITY Ex:678nm, Em:695nm, ≥95%

Synonyms

1H-Benz[e]indolium, 2-[5-[3-[6-[[2-(2,5-dihydro-2,5-dioxo-1H-pyrrol-1-yl)ethyl]amino]-6-oxohexyl]-1,3-dihydro-1,1-dimethyl-2H-benz[e]indol-2-ylidene]-1,3-pentadien-1-yl]-1,1,3-trimethyl-

Storage

Conservar a -20°C

Shipped In

Hielera + almohadillas de hielo

Descripción general

La maleimida Cyanine5.5 es un colorante reactivo al tiol capaz de marcar selectivamente los grupos sulfhidrilos de las proteínas, un análogo de la maleimida Cy5.5®. La emisión en el infrarrojo cercano de Cyanine5.5 hace que este colorante sea adecuado para aplicaciones de bioimagen. Cyanine5.5 puede sustituir a Cy5.5®, AF680 y DyLight 680.

Specifications

Sinónimos

1H-Benz[e]indolium, 2-[5-[3-[6-[[2-(2, 5-dihydro-2, 5-dioxo-1H-pyrrol-1-yl)ethyl]amino]-6-oxohexyl]-1, 3-dihydro-1, 1-dimethyl-2H-benz[e]indol-2-ylidene]-1, 3-pentadien-1-yl]-1, 1, 3-trimethyl-

Especificaciones y pureza

Ex:678nm, Em:695nm, ≥95%

Condiciones de almacenamiento de almacenamiento

Conservar a -20°C

Enviado en

Hielera + almohadillas de hielo

Grado

Em:695nm, Ex:678nm

Pureza

≥95%

Nombres e identificadores

• Pubchem Sid: 504773654
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504773654
• Sonrisas canónicas: CC1(C(=[N+](C2=C1C3=CC=CC=C3C=C2)C)C=CC=CC=C4C(C5=C(N4CCCCCC(=O)NCCN6C(=O)C=CC6=O)C=CC7=CC=CC=C75)(C)C)C.[Cl-]
• IUPAC Name: 6-[(2Z)-1,1-dimethyl-2-[(2E,4E)-5-(1,1,3-trimethylbenzo[e]indol-3-ium-2-yl)penta-2,4-dienylidene]benzo[e]indol-3-yl]-N-[2-(2,5-dioxopyrrol-1-yl)ethyl]hexanamide;chloride
• InChIKey: VNFHENZPAYHJJQ-UHFFFAOYSA-N
• INCHI: 1S/C46H48N4O3.ClH/c1-45(2)38(48(5)36-25-23-32-16-11-13-18-34(32)43(36)45)20-8-6-9-21-39-46(3,4)44-35-19-14-12-17-33(35)24-26-37(44)49(39)30-15-7-10-22-40(51)47-29-31-50-41(52)27-28-42(50)53;/h6,8-9,11-14,16-21,23-28H,7,10,15,22,29-31H2,1-5H3;1H
• Peso molecular: 741.36
• Reaxy-Rn: 27049242
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=27049242&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Clase Naphthalenes

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Clase: Naphthalenes
• Subclass: Not available
• Intermediate Tree Nodes: Not available
• Direct Parent: Naphthalenes
• Alternative Parents: 3-alkylindoles Tertiary alkylarylamines Maleimides N-acyl amines N-substituted carboxylic acid imides Dicarboximides Pyrrolines Amino acids and derivatives Secondary carboxylic acid amides Propargyl-type 1,3-dipolar organic compounds Enamines Azacyclic compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds Organic chloride salts Organic cations
• Molecular Framework: Aromatic heteropolycyclic compounds
• Substituents: Naphthalene - 3-alkylindole - Indole or derivatives - Tertiary aliphatic/aromatic amine - Maleimide - Fatty amide - Fatty acyl - N-acyl-amine - Carboxylic acid imide, n-substituted - Carboxylic acid imide - Dicarboximide - Pyrroline - Amino acid or derivatives - Carboxamide group - Secondary carboxylic acid amide - Tertiary amine - Carboxylic acid derivative - Enamine - Azacycle - Organoheterocyclic compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Carbonyl group - Organic chloride salt - Organic nitrogen compound - Hydrocarbon derivative - Organic oxide - Organic salt - Organic oxygen compound - Organonitrogen compound - Organooxygen compound - Amine - Organic cation - Aromatic heteropolycyclic compound
• Descripción: This compound belongs to the class of organic compounds known as naphthalenes. These are compounds containing a naphthalene moiety, which consists of two fused benzene rings.
• 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 organic solvents (DMSO, DMF, dichloromethane), practically insoluble in water (< 1 uM, < 1 mg/L)
• Sensibilidad: light sensitive