N-Succinimidyl N-(2,4-dinitrophenyl)-6-aminocaproate - ≥97% , CAS No.82321-04-8

CAS: 82321-04-8 Cat. No.: N137850 Peso molecular: 394.34 Número EC: 679-788-9

GRADE & PURITY ≥97%

Synonyms

IYBNUJCDIAGXNX-UHFFFAOYSA-N | HY-D1050 | 2,5-Dioxopyrrolidin-1-yl 6-((2,4-dinitrophenyl)amino)hexanoate | AKOS015894369 | 2,5-Dioxopyrrolidin-1-yl6-((2,4-dinitrophenyl)amino)hexanoate | N-Succinimidyl N-(2,4-dinitrophenyl)-6-aminocaproate, >=95% (HPLC) |

Storage

Store at -20°C,Argon charged

Shipped In

Ice chest + Ice pads

Descripción general

application：

N-(2,4-Dinitrophenyl)-6-aminocaproic acid N-succinimidyl ester is an amine-reactive DNP-X succinimidyl ester that may be used to create bioconjugates that may be detected with anti-dinitrophenyl (anti-DNP) antibodies.

Specifications

Sinónimos

IYBNUJCDIAGXNX-UHFFFAOYSA-N | HY-D1050 | 2, 5-Dioxopyrrolidin-1-yl 6-((2, 4-dinitrophenyl)amino)hexanoate | AKOS015894369 | 2, 5-Dioxopyrrolidin-1-yl6-((2, 4-dinitrophenyl)amino)hexanoate | N-Succinimidyl N-(2, 4-dinitrophenyl)-6-aminocaproate, >=95% (HPLC) |

Especificaciones y pureza

≥97%

Condiciones de almacenamiento de almacenamiento

Store at -20°C, Argon charged

Enviado en

Ice chest + Ice pads

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

Pureza

≥97%

Nombres e identificadores

• Pubchem Sid: 504768250
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504768250
• Sonrisas canónicas: C1CC(=O)N(C1=O)OC(=O)CCCCCNC2=C(C=C(C=C2)[N+](=O)[O-])[N+](=O)[O-]
• IUPAC Name: (2,5-dioxopyrrolidin-1-yl) 6-(2,4-dinitroanilino)hexanoate
• InChIKey: IYBNUJCDIAGXNX-UHFFFAOYSA-N
• INCHI: 1S/C16H18N4O8/c21-14-7-8-15(22)18(14)28-16(23)4-2-1-3-9-17-12-6-5-11(19(24)25)10-13(12)20(26)27/h5-6,10,17H,1-4,7-9H2
• Isómeros SMILES: C1CC(=O)N(C1=O)OC(=O)CCCCCNC2=C(C=C(C=C2)[N+](=O)[O-])[N+](=O)[O-]
• Peso molecular: 394.34
• Reaxy-Rn: 9661832
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=9661832&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Clase Benzene and substituted derivatives
      • Subclass Aniline and substituted anilines

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Clase: Benzene and substituted derivatives
• Subclass: Aniline and substituted anilines
• Intermediate Tree Nodes: Not available
• Direct Parent: Dinitroanilines
• Alternative Parents: Nitrobenzenes Nitroaromatic compounds Phenylalkylamines Secondary alkylarylamines Pyrrolidine-2-ones Dicarboximides Lactams Amino acids and derivatives Carboxylic acid salts Organic oxoazanium compounds Propargyl-type 1,3-dipolar organic compounds Monocarboxylic acids and derivatives Azacyclic compounds Organic oxides Organopnictogen compounds Hydrocarbon derivatives Carbonyl compounds Organic salts
• Molecular Framework: Aromatic heteromonocyclic compounds
• Substituents: Dinitroaniline - Nitrobenzene - Nitroaromatic compound - Phenylalkylamine - Secondary aliphatic/aromatic amine - Pyrrolidone - 2-pyrrolidone - Dicarboximide - Pyrrolidine - Amino acid or derivatives - Carboxylic acid salt - Lactam - C-nitro compound - Organic nitro compound - Allyl-type 1,3-dipolar organic compound - Secondary amine - Organoheterocyclic compound - Organic 1,3-dipolar compound - Carboxylic acid derivative - Azacycle - Propargyl-type 1,3-dipolar organic compound - Monocarboxylic acid or derivatives - Organic oxoazanium - Organic oxygen compound - Organic nitrogen compound - Carbonyl group - Organonitrogen compound - Hydrocarbon derivative - Organic oxide - Organooxygen compound - Organopnictogen compound - Organic salt - Amine - Aromatic heteromonocyclic compound
• Descripción: This compound belongs to the class of organic compounds known as dinitroanilines. These are organic compounds containing an aniline moiety, which is substituted at 2 positions by a nitro 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

Propiedades químicas y físicas

• Sensibilidad: Moisture sensitive.
• Peso molecular: 394.340 g/mol
• XLogP3: 2.100
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 9
• Rotatable Bond Count: 9
• Exact Mass: 394.112 Da
• Monoisotopic Mass: 394.112 Da
• Topological Polar Surface Area: 167.000 Ų
• Heavy Atom Count: 28
• Formal Charge: 0
• Complexity: 613.000
• 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