6287-40-7

Usage

Uses

Used in Chemical Reactions:
DIBUTYLAMINE HYDROCHLORIDE is used as a catalyst for facilitating various chemical reactions, enhancing the efficiency and speed of the processes involved.
Used in Rubber and Plastics Production:
DIBUTYLAMINE HYDROCHLORIDE is used as a catalyst in the production of rubber and plastics, contributing to the formation of these materials and improving their properties.
Used in Pharmaceutical Manufacturing:
DIBUTYLAMINE HYDROCHLORIDE is used as an intermediate in the manufacturing of pharmaceuticals, playing a crucial role in the synthesis of various drugs.
Used in Pesticide Production:
DIBUTYLAMINE HYDROCHLORIDE is used as an intermediate in the production of pesticides, aiding in the development of effective and efficient pest control agents.
Used in Oil and Gas Production:
DIBUTYLAMINE HYDROCHLORIDE is used as a corrosion inhibitor in oil and gas production, helping to protect equipment and infrastructure from corrosion and extending their lifespan.
Used in Dye and Surfactant Synthesis:
DIBUTYLAMINE HYDROCHLORIDE is used in the synthesis of dyes and surfactants, contributing to the development of a wide range of colorants and surface-active agents for various applications.

InChI:InChI=1/C8H19N.ClH/c1-3-5-7-9-8-6-4-2;/h9H,3-8H2,1-2H3;1H

Upstream product

• 999-33-7 N-chloro-N,N-dibutylamine 
• 111-92-2 dibutylamine 
• 27918-31-6 pentafluorobenzenesulfenyl chloride 
• 1066-45-1 trimethyltin(IV)chloride 
• 639-58-7 triphenyltin chloride 
• 406679-89-8 α-isocyanatomethylmethyldimethoxysilane 
• 7647-01-0 hydrogenchloride 
• 67-56-1 methanol 
• 2391-80-2 Di-n-butylammonium di-n-butyldithiocarbamate 
• 64-19-7 acetic acid 

Downstream Products

• 619-37-4 N,N-di-n-butylurea 
• 924-16-3 N-nitrosodibutylamine 
• 4164-31-2 N-nitrodibutylamine 
• 96146-78-0 N,N-dibutyl-N'-cyano-guanidine 
• 111-92-2 dibutylamine 
• 25033-65-2 N,N-dibutylbenzamide 
• 1226878-18-7 C₈H₁₉N*C₃₂H₁₂BF₂₄^(1-)*H⁽¹⁺⁾ 
• 749247-78-7 (Bu(n)2)2NH2[Ph2Sn(Cl)(μ2-mercaptoacetate)] 
• 110272-31-6 2-n-Propoxy-3-methoxy-β-dibutylamino-propiophenon 
• 79489-66-0 N¹,N¹-Dibutyl-N²-(p-tolyl)formamidine 
• 79489-67-1 N¹,N¹-Dibutyl-N²-(p-tolyl)acetamidine 
• 79489-61-5 2-Dibutylamino-6-methylquinoline 
• 3529-09-7 n,n-di-n-butylethylenediamine 

Relevant academic research and scientific papers

Synthesis, spectroscopic characterization and crystal and molecular structures of phenylphosphonato SnR3 (R=Ph, Me) derivatives

Four new phenylphosphonato SnR3 (R=Ph, Me) derivatives have been synthesized and characterized by infrared and Moessbauer spectroscopy. The structure of catena-poly[PhPO3HSnMe3]n has been determined by single-crystal X-ray diffraction analysis. The SnIV atoms are five-coordinated in all compounds, with the SnC3O 2 framework in a trans trigonal bipyramidal arrangement and the PhPO3H- anions being in axial positions. The molecular structure of [PhPO3HSnMe3]n is arranged as a one-dimensional coordination polymer in which planar SnMe3 groups are axially bridged by -O-P-O- linkages of the PhPO3H- ligand. Neighboring chains are linked via O-H...O hydrogen bond interactions, generating a layered structure. In the R2NH 2(PhPO3H)2SnR′3 (R=Cy, Bu; R′=Ph, Me), the SnPh3 or SnMe3 residue is axially coordinated by two monodentate PhPO3H-. The role of the dialkylammonium cation, R2NH2+, is crucial in the lattice building via a hydrogen bond network. These hydrogen bonds contribute to the crystal stability and compactness and result in a three-dimensional arrangement. The aqua complex PhPO3(SnPh 3)2·2H2O has a discrete structure and the anion PhPO32- behaves as a bidentate ligand.

PROCESS FOR PREPARING ISOCYANATOORGANOSILANES

The invention provides a process for preparing silanes which possess an isocyanate function, in which the silanes, after their chemical preparation, are purified and, after the purification, are handled exclusively in an atmosphere with a relative air humidity below 10%.

Thermochemical properties of chelates of di-n-butyldithiocarbamate with phosphorus-group elements

The standard molar enthalpies of formation of crystalline tris(di-n-butyldithiocarbamato)E(III), (E = P, As, Sb, or Bi), determined at 298.15 K by solution-reaction calorimetry, are -(705.5 +/- 7.3), -(443.1 +/- 5.4), -(526.2 +/- 2.5), and -(530.7 +/- 5.5) kJ*mol-1, respectively.The enthalpies of sublimation: (136 +/- 3), (128 +/- 3), (179 +/- 3), and (202 +/- 3) kJ*mol-1, were estimated.From the enthalpies of formation of the gaseous complexes, the homolytic and heterolytic mean standard molar element-sulphur bond enthalpies were calculated.These values are correlated with element-sulphur bond distances, and a larger phosphorus- sulphur bond enthalpy reflects a better overlap of d orbitals in bonding formation.

Process for the preparation of carbamates, thiocarbamates and ureas

The invention relates to a process for preparing carbamic acid derivatives of formula: STR1 in which R1 or R2 denotes a hydrogen atom or a substituted or unsubstituted, saturated or unsaturated aliphatic, cycloaliphatic or heterocyclic radical, or R1 and R2 together form a ring, and Y denotes OR, SR, STR2 groups, R being a substituted or unsubstituted, saturated or unsaturated aliphatic or cycloaliphatic radical, or a substituted or unsubstituted aromatic radical, R3 and R4 denote a hydrogen atom or an aliphatic, cycloaliphatic, araliphatic, aromatic or heterocyclic radical or together form a ring, and R6 and R7 denote a saturated or unsaturated, substituted or unsubstituted aliphatic or cycloaliphatic radical, a hydrogen atom, an alkylthio radical or an alkyloxy radical. According to the process, a compound of formula STR3 is reacted with an α-halogenated derivative of formula STR4 at a temperature of -5° to 150° C. in the presence of an acceptor for hydrohalic acid. The carbamates, thiocarbamates or ureas obtained are very useful, especially as pesticides.

Conversion of 2-dialkylamino-3H-azepines into epsilon caprolactams

This invention relates to a process of catalytically converting nitrobenzene to 2-amino-3H-azepines by the reaction of the nitrobenzene with trisaminophosphine and an amine of the formula HNR'2, where R' is lower alkyl containing 1 to 6 carbon atoms. In addition, this invention concerns the catalytic hydrogenation of 2-amino-3H-azepine to epsilon caprolactam.