Ethylenediamine dihydrochloride - AR, ≥99%, used for Ethylenediamine dihydrochloride was used in modified ethylenediamine condensation method for fluorimetric determination of catecholamines. It was used to investigate the luminescence properties of compl

CAS: 333-18-6 Cat. No.: E108437 Formula: C₂H₈N₂·2HCl Peso molecolare: 133.02 Beilstein Registry Number: 3665235 Numero EC: 206-369-6 PubChem CID: 9521

GRADE & PURITY AR, ≥99%

Synonyms

Ethylenediamine dihydrochloride | 1,2-Ethanediamine, hydrochloride (1:2) | Ethylenediamine hydrochloride (VAN) | EN300-322669 | ethane-1,2-diamine;dihydrochloride | CCRIS 8579 | ETHYLENEDIAMINE DIHYDROCHLORIDE [II] | Q27124121 | Ethylenediammonium chlorid

Storage

Room temperature,Argon charged,Desiccated

Shipped In

Normal

Specifications

Sinonimi

Ethylenediamine dihydrochloride | 1,2-Ethanediamine, hydrochloride (1:2) | Ethylenediamine hydrochloride (VAN) | EN300-322669 | ethane-1,2-diamine;dihydrochloride | CCRIS 8579 | ETHYLENEDIAMINE DIHYDROCHLORIDE [II] | Q27124121 | Ethylenediammonium chlorid

Specifiche e purezza

AR, ≥99%

Applicazione

Ethylenediamine dihydrochloride was used in modified ethylenediamine condensation method for fluorimetric determination of catecholamines. It was used to investigate the luminescence properties of complexes of EuIII and TbIII with ethylenediamine. It was

Condizioni di conservazione di stoccaggio

Room temperature,Argon charged,Desiccated

Spedito in

Normal

Grado

AR

Purezza

≥99%

Nomi e identificatori

Pubchem Sid

508815034

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/508815034

Sorrisi canonici

C(CN)N.Cl.Cl

IUPAC Name

ethane-1,2-diamine;dihydrochloride

InChIKey

OHHBFEVZJLBKEH-UHFFFAOYSA-N

INCHI

1S/C2H8N2.2ClH/c3-1-2-4;;/h1-4H2;2*1H

Isomeri SMILES

C(CN)N.Cl.Cl

WGK Germania

2

RTECS

KV3850000

PubChem CID

9521

Peso molecolare

133.02

Beilstein

3665235

Reaxy-Rn

3665235

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic nitrogen compounds
    • Classe Organonitrogen compounds
      • Subclass Amines
        • Level5 Primary amines
          • Level6 Monoalkylamines

• Kingdom: Organic compounds
• Superclass: Organic nitrogen compounds
• Classe: Organonitrogen compounds
• Subclass: Amines
• Intermediate Tree Nodes: Primary amines
• Direct Parent: Monoalkylamines
• Alternative Parents: Organopnictogen compounds Hydrochlorides Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Organopnictogen compound - Hydrocarbon derivative - Hydrochloride - Primary aliphatic amine - Aliphatic acyclic compound
• Descrizione: This compound belongs to the class of organic compounds known as monoalkylamines. These are organic compounds containing an primary aliphatic amine group.
• External Descriptors: hydrochloride

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

Proprietà chimiche e fisiche

• Solubilità: Soluble in water 300 g/L (20°C).
• Sensibilità: Moisture sensitive.
• Punto di fusione (°C): >300°C
• Peso molecolare: 133.020 g/mol
• Hydrogen Bond Donor Count: 4
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 1
• Exact Mass: 132.022 Da
• Monoisotopic Mass: 132.022 Da
• Topological Polar Surface Area: 52.000 Ų
• Heavy Atom Count: 6
• Formal Charge: 0
• Complexity: 6.000
• 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

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