1-Ethylpiperazine - ≥98% , CAS No.5308-25-8

CAS: 5308-25-8 Cat. No.: E103219 Peso molecular: 114.19 Beilstein Registry Number: 102971 Número EC: 226-166-6

GRADE & PURITY ≥98%

Synonyms

N-Ethyl piperazine(NEP) | W-105771 | N-ethylpiperizine | P17082 | DTXSID8073346 | 2,2'-Azobis(2-amidinopropane)hydrochloride | AM81362 | EC 226-166-6 | EINECS 226-166-6 | STL168346

Storage

Room temperature,Argon charged

Shipped In

Normal

Descripción general

1-Ethylpiperazine may be used in the preparation of 2-(2-methoxy-5-((4-methylpiperazin-1-yl)sulfonyl)phenyl)-1H-benzo[d]imidazole hydrochloride and 2-(5-((4-ethylpiperazin-1-yl)sulfonyl)-2-methoxyphenyl)-1H-benzo[d]imidazole hydrochloride.

Specifications

Sinónimos

N-Ethyl piperazine(NEP) | W-105771 | N-ethylpiperizine | P17082 | DTXSID8073346 | 2, 2'-Azobis(2-amidinopropane)hydrochloride | AM81362 | EC 226-166-6 | EINECS 226-166-6 | STL168346

Especificaciones y pureza

≥98%

Condiciones de almacenamiento de almacenamiento

Room temperature, Argon charged

Enviado en

Normal

Pureza

≥98%

Nombres e identificadores

• Pubchem Sid: 504755353
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504755353
• Sonrisas canónicas: CCN1CCNCC1
• IUPAC Name: 1-ethylpiperazine
• InChIKey: WGCYRFWNGRMRJA-UHFFFAOYSA-N
• INCHI: 1S/C6H14N2/c1-2-8-5-3-7-4-6-8/h7H,2-6H2,1H3
• Isómeros SMILES: CCN1CCNCC1
• WGK Alemania: 1
• RTECS: TM0815500
• Número ONU: 1993
• Peso molecular: 114.19
• Beilstein: 102971
• Reaxy-Rn: 102971
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=102971&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Clase Diazinanes
      • Subclass Piperazines

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Clase: Diazinanes
• Subclass: Piperazines
• Intermediate Tree Nodes: Not available
• Direct Parent: N-alkylpiperazines
• Alternative Parents: Trialkylamines Dialkylamines Azacyclic compounds Organopnictogen compounds Hydrocarbon derivatives
• Molecular Framework: Aliphatic heteromonocyclic compounds
• Substituents: N-alkylpiperazine - Tertiary aliphatic amine - Tertiary amine - Azacycle - Secondary amine - Secondary aliphatic amine - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Organonitrogen compound - Amine - Aliphatic heteromonocyclic compound
• Descripción: This compound belongs to the class of organic compounds known as n-alkylpiperazines. These are organic compounds containing a piperazine ring where the nitrogen ring atom carries an alkyl 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

• Solubilidad: Miscible with water.
• Sensibilidad: Air sensitive.
• Índice de refracción: 1.469
• Punto de inflamación (°F): 109.4 °F
• Punto de inflamación (°C): 43°
• Punto de ebullición (°C): 157°C
• Punto de fusión (°C): -60°C
• Peso molecular: 114.190 g/mol
• XLogP3: 0.000
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 1
• Exact Mass: 114.116 Da
• Monoisotopic Mass: 114.116 Da
• Topological Polar Surface Area: 15.300 Ų
• Heavy Atom Count: 8
• Formal Charge: 0
• Complexity: 57.500
• 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

Referencias

1. Jian-Peng Qin, Chun-Yang Pan.  (2023)  Synthesis, structure and optical properties of (H2DMAPA)BiBr5, (H2DMAPA)BiBr2I3, (H2DMAPA)2AgBiBr8 and (H2EP)2AgBiBr8 lead-free perovskites.  JOURNAL OF SOLID STATE CHEMISTRY,      [PMID:] [10.1016/j.jssc.2023.123938]

2. Mei Wang, Na Rao, Yuqing Liu, Jiale Li, Qunpeng Cheng, Jianfen Li.  (2019)  Enhancement of CO2 capture in the MDEA solution by introducing TETA or TETA-AEP mixtures as an activator.  SEPARATION SCIENCE AND TECHNOLOGY,      [PMID:] [10.1080/01496395.2018.1504797]

3. Wenjun Fang, Dongbei Shao, Xiaoxing Lu, Yongsheng Guo, Li Xu.  (2012)  Extraction of Aromatics from Hydrocarbon Fuels Using N-Alkyl Piperazinium-Based Ionic Liquids.  ENERGY & FUELS,      [PMID:] [10.1021/ef201955n]

4. Dongbei Shao, Xiaoxing Lu, Wenjun Fang, Yongsheng Guo, Li Xu.  (2012)  Densities and Viscosities for Binary Mixtures of the Ionic Liquid N-Ethyl Piperazinium Propionate with n-Alcohols at Several Temperatures.  JOURNAL OF CHEMICAL AND ENGINEERING DATA,      [PMID:] [10.1021/je201116t]

5. Fengting Li, Wentao Qu, Yunchao Peng, Liqiang Yang, Li Wang, Huiling Su, Miantuo Li, Zhikun Wang, Jingyue Wang, Yu Fu, Songqing Hu.  (2025)  Regulating π-π interactions in carbon dots via N-doping & ionic liquid modification for enhanced efficiency in 1 M HCl.  CORROSION SCIENCE,      [PMID:] [10.1016/j.corsci.2025.112798]

6. Heng Wang, Weilu Ding, Zhencai Zhang, Yiwen Zhang, Zhao Yang, Mi Feng, Ming Jiang, Fei Xu.  (2024)  Synthesis of novel sustainable optical poly(isosorbide thioethers) with high refractive indices and good biocompatibility using functional ionic liquid catalysts.  Polymer Chemistry,      [PMID:] [10.1039/D4PY00344F]