138475-09-9

Basic information

• Product Name: DEA NONOATE
• Synonyms: DEA NONOate,98%
• CAS NO: 138475-09-9
• Molecular Formula: C₄H₁₀N₃O₂*Na
• Molecular Weight: 155.13087
• Mol File: 138475-09-9.mol
• Article Data: 12

Chemical Properties

• Melting Point: 196-200°C
• Boiling Point: 181.4°C at 760 mmHg
• Flash Point: 63.5°C
• Appearance: /
• Vapor Pressure: 0.25mmHg at 25°C
• Storage Temp.: Freezer (-20°C)
• CAS DataBase Reference: DEA NONOATE(CAS DataBase Reference)
• NIST Chemistry Reference: DEA NONOATE(138475-09-9)
• EPA Substance Registry System: DEA NONOATE(138475-09-9)

Safety Data

• Hazardous Substances Data: 138475-09-9(Hazardous Substances Data)

Usage

Chemical Properties

White to yellow powder

InChI:InChI=1/C4H10N3O2/c1-3-6(4-2)7(9)5-8/h3-4H2,1-2H3/q-1

Upstream product

• 109-89-7 diethylamine 

Downstream Products

• 1070883-64-5 O⁽²⁾-((5-nitro-2-(tetrahydropyran-2-yloxy)phenyl)methyl)-1-( N,N-diethylamino)diazen-1-ium-1,2-diolate 
• 109-89-7 diethylamine 
• 1609067-91-5 1-((4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-4-methyl[1-(N,N-diethylamino)diazen-1-ium-1,2-diol-2-ate] 
• 1412945-43-7 C₂₃H₂₉N₉O₇S 
• 1433997-58-0 C₂₃H₂₉N₉O₇S 
• 1402070-26-1 C₂₈H₃₃N₅O₇S 
• 1412945-39-1 C₂₆H₃₁N₅O₇S₂ 
• 1433997-57-9 C₂₆H₃₁N₅O₇S₂ 
• 55-18-5 N-Nitrosodiethylamine 
• 1093078-06-8 O₂-(2,4-dinitro-5-fluorophenyl) 1-(N,N-diethylamino)diazen-1-ium-1,2-diolate 
• 1093077-91-8 1-[1-(N,N-dimethylamino)diazen-1-ium-1,2-diol-2-ato]-2,4-dinitro-5-[1-(N,N-diethylamino)diazen-1-ium-1,2-diol-2-ato]benzene 
• 694-54-2 tetrahydro-2H-2-pyranol 
• 1037206-77-1 O₂-tetrahydropyran-2-yl 1-(N,N-diethylamino)diazen-1-ium-1,2-diolate 
• 112753-64-7 1-n-Propoxy-2-oxo-3,3-diethyl-1-triazene 

Relevant articles and documents

Synthesis of 1-[(nitroxyalkoxy)methoxy]-1-triazene 2-oxides, new hybrid nitrogen monoxide donors

1-[(Nitroxyalkoxy)methoxy]-3,3-dialkyl-1-triazene 2-oxides were obtained by the reaction of 3,3-dialkyl-1-hydroxy-1-triazene 2-oxide sodium salts with β- or γ-nitroxyalcohol chloromethyl ethers or by the reaction of 3,3-dialkyl-1-(bromoalkoxymethoxy)-1-triazene 2-oxides with silver nitrate. These compounds can be of interest as new hybrid NO donors in living organisms.

Synthesis of methylene-bis(1-oxy-3,3-dialkyl-1-triazene 2-oxides) and their analogs

Synthetic procedures towards methylene-bis(1-oxy-3,3-dialkyl-1-triazene 2-oxides), the first representatives of a new class of promising exogenous nitric oxide (NO) donors, which can release NO in living organisms, were developed. Synthesis involves the reactions of salts of 1-hydroxy-3,3-dialkyl-1-triazene 2-oxides with either dibromomethane or 1-chloromethoxy-3,3-dialkyl-1-triazene 2-oxides.

Design, synthesis and cytotoxic evaluation of nitric oxide-releasing derivatives of isosteviol

Twenty-six novel isosteviol derivatives coupled with two types of nitric oxide (NO) donors (furoxans and NONOates) were synthesized and screened for cytotoxic activities against four human cancer cell lines with sunitinib as the positive control. The results showed that seven furoxan-based derivatives (8a, 8b, 8c, 8d, 8e, 9e, and 9f) exhibited desirable cytotoxic activities, while NONOate-based derivatives displayed poor potency because of unstability. Compared with sunitinib, compounds 8a and 8e were more active on all tested cell lines, especially in HCT116 (8a, IC50?=?0.48?±?0.02?μm; 8e, IC50?=?0.94?±?0.01?μm); compounds 8b and 8d were more potent on HCT116 (IC50?=?3.39?±?0.06 and 3.29?±?0.03?μm), HepG2 (IC50?=?1.05?±?0.03 and 5.37?±?0.08?μm), and SW620 (IC50?=?1.33?±?0.02 and 4.11?±?0.05?μm) cell lines, and 8c exhibited higher activities on HepG2 cells with an IC50?=?4.76?±?0.14?μm. NO-releasing experiment of compounds 8a–e, 17a, 18a, 19a, and 21a reminded us that NO-releasing amount of this series of isosteviol derivatives positively correlates with their cytotoxic activities.