1-Aziridinecarboxamide, N,N'-1,6-hexanediylbis-

Base Information

• Chemical Name: 1-Aziridinecarboxamide, N,N'-1,6-hexanediylbis-
• CAS No.: 2271-93-4
• Deprecated CAS: 157948-35-1
• Molecular Formula: C12H22 N4 O2
• Molecular Weight: 254.332
• Hs Code.: 2933990090
• European Community (EC) Number: 218-877-5
• NSC Number: 146970
• UNII: 4KA5B2WTW1
• DSSTox Substance ID: DTXSID7062297
• Nikkaji Number: J64.510I
• Wikidata: Q72482155
• Mol file: 2271-93-4.mol

Synonyms:N,N'-hexamethylenebis(1-aziridinecarboxamide)

Chemical Property of 1-Aziridinecarboxamide, N,N'-1,6-hexanediylbis-

Chemical Property:

• Melting Point: 106℃ (acetone )
• Refractive Index: 1.6120 (estimate)
• Boiling Point: 579.8°Cat760mmHg
• PKA: 13.98±0.20(Predicted)
• Flash Point: 304.4°C
• PSA: 64.22000
• Density: 1.233g/cm³
• LogP: 1.25480
• Storage Temp.: 2-8°C
• XLogP3: -0.1
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 7
• Exact Mass: 254.17427596
• Heavy Atom Count: 18
• Complexity: 271

Purity/Quality:

99% ^*data from raw suppliers

N,N''-1,6-Hexanediylbis-1-aziridinecarboxamide ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1CN1C(=O)NCCCCCCNC(=O)N2CC2
• Uses: N,N'-1,6-Hexanediylbis-1-aziridinecarboxamide was examined for its effects on deoxyribonucleic acid formation. N,N''-1,6-Hexanediylbis-1-aziridinecarboxamide was examined for its effects on deoxyribonucleic acid formation.

Technology Process of 1-Aziridinecarboxamide, N,N'-1,6-hexanediylbis-

There total 1 articles about 1-Aziridinecarboxamide, N,N'-1,6-hexanediylbis- which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

ethyleneimine (151-56-4,9002-98-6) + Hexamethylene diisocyanate (822-06-0,28182-81-2,28574-90-5,88357-62-4) → N,N'-bis-(aziridine-1-carbonyl)-hexanediyldiamine (2271-93-4)

Guidance literature:

With acetone;

upstream raw materials:

ethyleneimine

Hexamethylene diisocyanate