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n.1.(Org. Chem.) A colorless liquid base, C4H9.NH2, of which there are four isomeric varieties.
Webster's Revised Unabridged Dictionary, published 1913 by G. & C. Merriam Co.
References in periodicals archive ?
Cwiklinska, Volumetric behaviour of binary liquid mixtures of 2-methoxyethanol with n-butylamine, sec-butylamine and tert-butylamine, J.
The aim of this study is to examine sensing properties of n-butylamine functionalized multiwall carbon nanotube (MWCNT) networks attached to a supporting polyurethane nonwoven filter to solvent vapors of different polarities defined by total Hildebrand solubility parameter.
n-Butylamine (BuN[H.sub.2]), thionyl chloride (SO[Cl.sub.2]) and dimethylformamide (DMF) were supplied by Sigma Aldrich and triethylamine by Merck.
In our case, the increase in the intensity of the peak at 1580 [cm.sup.-1] could arise from the residue of unreacted n-butylamine in the structure of the MWCNTs because of the observation of two different peaks in the deconvoluted N1s spectra; see Figure 4(d).
Busca, "FTIR spectra of adsorbed n-butylamine," Journal of Molecular Structure, vol.
Materials.--Cytochrome C from equine and bovine heart, normal and sickle cell hemoglobin, sinapinic acid, acetic anhydride, amino acids (serine, cysteine, tyrosine, threonine, asparagine, glutamine, lysine, arginine, histidine, and glycine), urea, pepsin, and n-butylamine were purchased from Sigma (St.
Protein digests: Quenching acetylation.--Acetic anhydride (15 [micro]l) and n-butylamine (30 [micro]l) were combined in a plastic vial and allowed to react for 15 minutes.
Then n-butylamine was added in a 2:1 molar ratio and allowed to react for several minutes to quench any unreacted anhydride.
N-butylamine and dibutylamine, both from Tedia Company, were used as received to prepare the 25% (v/v) aqueous solutions used as ESC agents.
Both tests were performed at first without any ECS agent and then with aqueous solutions of dibutylamine and n-butylamine (18).
In a typical synthesis, 0.5 mmol of Ln[(N[O.sub.3]).sub.3] x 6[H.sub.2]O (Ln = Eu, Nd, Dy) was dissolved in 12 mL of distilled water, and then 3 mL of n-butylamine was added under constant stirring.
The growth of Ln[(OH).sub.3] nanorods can be explained by the 1D growth habit and assistance of n-butylamine [25].