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90780

Sigma-Aldrich

Tributylamine

puriss. p.a., ≥99.0% (GC)

Synonym(s):

Tri-n-butylamine

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About This Item

Linear Formula:
[CH3(CH2)3]3N
CAS Number:
Molecular Weight:
185.35
Beilstein:
1698872
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.21

vapor density

6.38 (vs air)

Quality Level

vapor pressure

0.3 mmHg ( 20 °C)
2.4 mmHg ( 55 °C)

grade

puriss. p.a.

Assay

≥99.0% (GC)

form

liquid

autoignition temp.

410 °F

expl. lim.

6 %

impurities

≤0.2% water

refractive index

n20/D 1.428 (lit.)
n20/D 1.429

bp

216 °C (lit.)

mp

−70 °C (lit.)

density

0.778 g/mL at 25 °C (lit.)

cation traces

Al: ≤0.5 mg/kg
Ba: ≤0.1 mg/kg
Bi: ≤0.1 mg/kg
Ca: ≤0.5 mg/kg
Cd: ≤0.05 mg/kg
Co: ≤0.02 mg/kg
Cr: ≤0.02 mg/kg
Cu: ≤0.02 mg/kg
Fe: ≤0.1 mg/kg
K: ≤0.5 mg/kg
Li: ≤0.1 mg/kg
Mg: ≤0.1 mg/kg
Mn: ≤0.02 mg/kg
Mo: ≤0.1 mg/kg
Na: ≤0.5 mg/kg
Ni: ≤0.02 mg/kg
Pb: ≤0.1 mg/kg
Sr: ≤0.1 mg/kg
Zn: ≤0.1 mg/kg

functional group

amine

SMILES string

CCCCN(CCCC)CCCC

InChI

1S/C12H27N/c1-4-7-10-13(11-8-5-2)12-9-6-3/h4-12H2,1-3H3

InChI key

IMFACGCPASFAPR-UHFFFAOYSA-N

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General description

Tributylamine is a tertiary amine. It has been reported to prevent the corrosion of mild steel in HCl solution.

Application

Tributylamine (n-Bu3N) has been used to compose the mobile phase for the liquid chromatography tandem mass spectrometry (LC-MS/MS) analysis.
It may be used in the preparation of PdCl,N and PdOAc,N (palladium nanoparticles). It may be used as an additive during the synthesis of 3-bromothieno[3,2-c]pyridine-4-(5H)-one.

Pictograms

Skull and crossbones

Signal Word

Danger

Hazard Statements

Hazard Classifications

Acute Tox. 1 Inhalation - Acute Tox. 2 Dermal - Acute Tox. 4 Oral - Skin Irrit. 2

Storage Class Code

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

WGK

WGK 1

Flash Point(F)

145.4 °F - closed cup

Flash Point(C)

63 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Palladium nanoparticles obtained from palladium salts and tributylamine in molten tetrabutylammonium bromide: their use for hydrogenolysis-free hydrogenation of olefins.
Le Bras J, et al.
New. J. Chem., 28(12), 1550-1553 (2004)
Thermal Synthesis of 3-Bromothieno [3, 2-c] pyridin-4-(5H)-one: A Telescoped Procedure with Tributylamine.
Boros EE and Kaldor I.
Journal of Heterocyclic Chemistry, 52(1), 302-305 (2015)
Alexander S Misharin et al.
Analytical chemistry, 77(2), 459-470 (2005-01-15)
The analytical performance of an atmospheric pressure sampling, multiple-channel, high-throughput mass spectrometer was investigated using samples of a variety of types. The instrument, based on an array of cylindrical ion traps, was built with four independent channels and here is
A Touati et al.
Journal of protein chemistry, 11(6), 613-621 (1992-12-01)
The study of the solubility of unstructured proteins (alpha s1-, beta-, and kappa-casein) and well-structured globulin (beta-lactoglobulin) in low water binary solvent systems demonstrated the crucial importance of solvent polarity and neutralization of protein polar functions on the final outcome
I E Flesch et al.
Infection and immunity, 56(6), 1464-1469 (1988-06-01)
Bone marrow-derived murine macrophages are able to inhibit the growth of Mycobacterium bovis and of some strains of M. tuberculosis after stimulation with either recombinant gamma interferon (rIFN-gamma) or lymphokines from antigen-specific T-cell clones. To elucidate the mechanism(s) involved in

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