1,1'-Hexamethylenebis(3,3-dimethylurea)

Base Information

• Chemical Name: 1,1'-Hexamethylenebis(3,3-dimethylurea)
• CAS No.: 20575-76-2
• Molecular Formula: C12H26N4O2
• Molecular Weight: 258.36
• Hs Code.: 2933990090
• NSC Number: 255317
• UNII: 5Q7CEJ9UES
• DSSTox Substance ID: DTXSID30942767
• Nikkaji Number: J48.955G
• Wikidata: Q72506869
• Mol file: 20575-76-2.mol

Synonyms:20575-76-2;1,1'-Hexamethylenebis(3,3-dimethylurea);1,1'-(Hexane-1,6-diyl)bis(3,3-dimethylurea);3,3'-HEXAMETHYLENEBIS(1,1-DIMETHYLUREA);3-[6-(dimethylcarbamoylamino)hexyl]-1,1-dimethylurea;Urea, 1,1'-hexamethylenebis(3,3-dimethyl-;NSC-255317;1,1'-Hexamethylenebis[3,3-dimethylurea];1,3-dimethylurea];NSC 255317;BRN 2116874;AI3-51108;1,1'-Hexamethylenebis (3,3-dimethylurea);5Q7CEJ9UES;Urea, N,N''-1,6-hexanediylbis(N',N'-dimethyl-;SCHEMBL3099807;DTXSID30942767;NSC255317;AKOS024334223;Urea,1'-hexamethylenebis[3,3-dimethyl-;Urea,N''-1,6-hexanediylbis[N',N'-dimethyl-;N,N''-1,6-Hexanediylbis[N',N'-dimethylurea];1,1'-(Hexane-1,6-diyl)bis(3,3'-dimethylurea);N',N'''-Hexane-1,6-diylbis(N,N-dimethylcarbamimidic acid);1-{6-[(DIMETHYLCARBAMOYL)AMINO]HEXYL}-3,3-DIMETHYLUREA

Chemical Property of 1,1'-Hexamethylenebis(3,3-dimethylurea)

Chemical Property:

• Boiling Point: 512.323 °C at 760 mmHg
• Flash Point: 263.644 °C
• PSA: 64.68000
• Density: 1.021 g/cm³
• LogP: 1.87100
• XLogP3: 0.3
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 7
• Exact Mass: 258.20557608
• Heavy Atom Count: 18
• Complexity: 229

Purity/Quality:

99% ^*data from raw suppliers

3,3'-HEXAMETHYLENEBIS(1,1-DIMETHYLUREA) Aldrich ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CN(C)C(=O)NCCCCCCNC(=O)N(C)C
• Biological Functions: Rutaecarpine also inhibits accumulation of macrophages and cholesterol in atherosclerotic lesions and increases cholesterol excretion in other animal models. Additionally, rutaecarpine inhibits hypoxia-induced production of ROS and lactate dehydrogenase and suppresses apoptosis in myocardiocytes. In other cellular models, rutaecarpine decreases corticosterone production, potentially through inhibition of cAMP, 3β-hydroxysteroid dehydrogenase, and 11β-hydroxylase activity.