Ethylene imine polymer(PEI) - ≥99%, M.W. 600 , CAS No.9002-98-6

CAS: 9002-98-6 Cat. No.: E107077 Formule: H(NHCH₂CH₂)nNH₂ Numéro CE: 618-346-1

QUALITÉ & PURETÉ ≥99%, M.W. 600

Synonyms

PEI | Aziridine | Ethyleneimine, inhibited | NSC124034 | NSC-124034 | PEI 1120 | RCRA waste no. P054 | Dihydroazirene | ETHYLENEIMINE | RCRA waste number P054 | 54P5FEX9FH | EC 205-793-9 | Aziridine (Ethyleneimine), stabilized with 1-2% NaOH | PEI 1000 |

Storage

Room temperature,Desiccated

Shipped In

Normal

Vue d’ensemble

Polyethylene imine is a water-soluble polymer produced through the polymerization of ethylene imine. It is not a completely linear polymer, but a partially branched polymer containing primary, secondary, and tertiary amines. Polyethyleneimine, like other low molecular weight amines, has multiple chemical reactivity and can undergo various chemical modifications.

Feature:

The highest cation density among existing materials. 

Very high activity. 

Water solubility ability.

1. Highly adhesive and adsorptive amino groups can react with carboxyl groups to form hydrogen bonds. Amino groups can react with carboxyl groups to form ionic bonds. Amino groups can react with carbonyl groups to form covalent bonds. Polyethyleneimine can bind with different substances due to its polar (amino) and hydrophobic (vinyl) structures. By utilizing these comprehensive binding forces, they can be widely applied in fields such as adhesives, inks, coatings, and bonding agents. 

2. Highly cationic polyethyleneimine exists as a polymeric cation in water, which can neutralize and adsorb all anionic substances, as well as chelate heavy metal ions. By utilizing its high cationic properties, it can be applied in the fields of papermaking water treatment, electroplating solutions, and dispersants. 

3. Reactive polyethyleneimine, due to its highly reactive primary and secondary amines, can easily react with epoxides, acids, isocyanate compounds, and acidic gases. This characteristic can be used as an epoxy resin reactant, aldehyde adsorbent, and dye fixative.

Application:

Detergents, adhesives, water treatment, inks, dyes, cosmetics and paper industry, adhesion aids, laminated primers, fixing agents, coagulants, cationic dispersants, stability enhancers, surfactants, chelating agents, and aldehyde and oxide scavengers.

Protein precipitant.

Spécifications

Synonymes

PEI | Aziridine | Ethyleneimine, inhibited | NSC124034 | NSC-124034 | PEI 1120 | RCRA waste no. P054 | Dihydroazirene | ETHYLENEIMINE | RCRA waste number P054 | 54P5FEX9FH | EC 205-793-9 | Aziridine (Ethyleneimine), stabilized with 1-2% NaOH | PEI 1000 |

Spécifications et pureté

≥99%, M.W. 600

Conditions de stockage de stockage

Room temperature,Desiccated

Expédié en

Normal

Pureté

≥99%

Noms et identifiants

Pubchem Sid

488180927

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/488180927

Sourires canoniques

C1CN1

IUPAC Name

aziridine

InChIKey

NOWKCMXCCJGMRR-UHFFFAOYSA-N

INCHI

1S/C2H5N/c1-2-3-1/h3H,1-2H2

Isomères SMILES

C1CN1

WGK Allemagne

2

RTECS

TQ7917000

CAS alternatif

106899-94-9

Numéro ONU

3082

Groupe d'emballage

III

Reaxy-Rn

102380

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=102380&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Classe Aziridines

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Classe: Aziridines
• Subclass: Not available
• Intermediate Tree Nodes: Not available
• Direct Parent: Aziridines
• Alternative Parents: Dialkylamines Azacyclic compounds Organopnictogen compounds Hydrocarbon derivatives
• Molecular Framework: Aliphatic heteromonocyclic compounds
• Substituents: Azacycle - Secondary amine - Secondary aliphatic amine - Aziridine - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Organonitrogen compound - Amine - Aliphatic heteromonocyclic compound
• Description: This compound belongs to the class of organic compounds known as aziridines. These are organic compounds containing a saturated three-member heterocycle with one amino group and two methylene groups.
• External Descriptors: azacycloalkane - saturated organic heteromonocyclic parent - aziridines

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

Mécanismes d'action

Propriétés chimiques et physiques

• Solubilité: Soluble in toluene, methanol, ethanol, chloroform and xylene. Insoluble in alcohol, benzene, ethyl ether and acetone.
• Sensibilité: Light sensitive.carbon dioxide Sensitive ；Moisture sensitiv
• Indice de réfraction: 1.5290
• Point d'ébullition (°C): 100 °C
• Point de fusion (°C): -10 °C
• Poids moléculaire: 43.070 g/mol
• XLogP3: -0.400
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 0
• Exact Mass: 43.0422 Da
• Monoisotopic Mass: 43.0422 Da
• Topological Polar Surface Area: 21.900 Ų
• Heavy Atom Count: 3
• Formal Charge: 0
• Complexity: 10.300
• 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