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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

1H-Imidazolium, 1-butyl-3-methyl-, nitrate

[O-][N+](=O)[O-].CCCCN1C=C[NH+](C1)C Request for Quotation
Chemical Name: 1H-Imidazolium, 1-butyl-3-methyl-, nitrate
CAS Number: 179075-88-8
Product Number: AG0026S0(AGN-PC-0O52HD)
Synonyms:
MDL No: MFCD08457696
Molecular Formula: C8H17N3O3
Molecular Weight: 203.2389

Identification/Properties

Properties
MP:
18°C
Storage:
Room Temperature;
Stability:
Hygroscopic
Computed Properties
Molecular Weight:
201.226g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
201.111g/mol
Monoisotopic Mass:
201.111g/mol
Topological Polar Surface Area:
71.7A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
112
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
2
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-Butyl-3-Methylimidazolium nitrate is a versatile ionic liquid that finds wide application in chemical synthesis processes. This unique compound serves as an efficient solvent in various organic reactions due to its excellent solubility for a wide range of organic and inorganic compounds. In addition to its solvating properties, 1-Butyl-3-Methylimidazolium nitrate also acts as a catalyst and stabilizer in numerous reactions, enhancing reaction rates and selectivity. Its high thermal stability and non-volatility make it a preferred choice for high-temperature reactions. Furthermore, this compound has been utilized in the synthesis of nanoparticles, polymers, and organometallic complexes, demonstrating its versatility in modern chemical processes.