2-(4-Aminophenyl)ethylamine - ≥97% , CAS No.13472-00-9

CAS: 13472-00-9 Cat. No.: A151503 Formula: C₈H₁₂N₂ Peso molecolare: 136.2 Beilstein Registry Number: 1099910 Numero EC: 236-739-2

GRADE & PURITY ≥97%

Synonyms

4-Amino-.beta.-phenylethylamine | 4-AMINOPHENYL ETHYLAMINE | 1-Amino-2-(4-aminophenyl)ethane | AMY31595 | 4-aminoethylaniline | 4-(2-Aminoethyl)aniline | 4-(2-Amino-ethyl)-aniline | 4-(2-Aminoethyl)aniline, 97% | FT-0650483 | 2-(4-Aminophenyl)ethylamine |

Storage

Protected from light,Room temperature,Argon charged

Shipped In

Normal

Panoramica

4-(2-Aminoethyl)aniline undergoes coupling with carbohydrates by reductive amination to yield modified carbohydrates.

4-(2-Aminoethyl)aniline has been used in chemical modification of silk fibroin to tailor the overall hydrophilicity and structure of silk. It has been used as reagent in polycondensation reactions.

Specifications

Sinonimi

4-Amino-.beta.-phenylethylamine | 4-AMINOPHENYL ETHYLAMINE | 1-Amino-2-(4-aminophenyl)ethane | AMY31595 | 4-aminoethylaniline | 4-(2-Aminoethyl)aniline | 4-(2-Amino-ethyl)-aniline | 4-(2-Aminoethyl)aniline, 97% | FT-0650483 | 2-(4-Aminophenyl)ethylamine |

Specifiche e purezza

≥97%

Condizioni di conservazione di stoccaggio

Protected from light,Room temperature,Argon charged

Spedito in

Normal

Purezza

≥97%

Nomi e identificatori

• Pubchem Sid: 504754678
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504754678
• Sorrisi canonici: C1=CC(=CC=C1CCN)N
• IUPAC Name: 4-(2-aminoethyl)aniline
• InChIKey: LNPMZQXEPNWCMG-UHFFFAOYSA-N
• INCHI: 1S/C8H12N2/c9-6-5-7-1-3-8(10)4-2-7/h1-4H,5-6,9-10H2
• Isomeri SMILES: C1=CC(=CC=C1CCN)N
• WGK Germania: 3
• Peso molecolare: 136.2
• Beilstein: 1099910
• Reaxy-Rn: 1099913
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1099913&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Classe Benzene and substituted derivatives
      • Subclass Phenethylamines

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Classe: Benzene and substituted derivatives
• Subclass: Phenethylamines
• Intermediate Tree Nodes: Not available
• Direct Parent: Phenethylamines
• Alternative Parents: Aniline and substituted anilines 2-arylethylamines Aralkylamines Organopnictogen compounds Monoalkylamines Hydrocarbon derivatives
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: Phenethylamine - 2-arylethylamine - Aniline or substituted anilines - Aralkylamine - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Primary amine - Organonitrogen compound - Primary aliphatic amine - Amine - Aromatic homomonocyclic compound
• Descrizione: This compound belongs to the class of organic compounds known as phenethylamines. These are compounds containing a phenethylamine moiety, which consists of a phenyl group substituted at the second position by an ethan-1-amine.
• 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

Meccanismi d'azione

Proprietà chimiche e fisiche

• Solubilità: Insoluble in water.
• Sensibilità: Air sensitive ；Light sensitive
• Indice di rifrazione: 1.59
• Punto di infiammabilità (°F): 235.4 °F
• Punto di infiammabilità (°C): 113 °C
• Punto di ebollizione (°C): 142 °C
• Punto di fusione (°C): 28 °C
• Peso molecolare: 136.190 g/mol
• XLogP3: -0.200
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 2
• Exact Mass: 136.1 Da
• Monoisotopic Mass: 136.1 Da
• Topological Polar Surface Area: 52.000 Ų
• Heavy Atom Count: 10
• Formal Charge: 0
• Complexity: 85.300
• 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

Riferimenti

1. Chanjuan Liu, Luyao Yang, Qingfeng Niu, Guangli Yu, Guoyun Li.  (2022)  Carbohydrate microarrays fabricated on poly(2-methylacrylic acid)-based substrates for analysis of carbohydrate–protein interactions.  NEW JOURNAL OF CHEMISTRY,  46  (9): (4300-4306).  [PMID:] [10.1039/D1NJ05758H]