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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:
102-82-9
Molecular Weight:
185.35
Beilstein/REAXYS Number:
1698872
EC Number:
203-058-7
MDL number:
MFCD00009431
UNSPSC Code:
12352100
PubChem Substance ID:
57653405
NACRES:
NA.21
assay:
≥99.0% (GC)
technique(s):
GC/GC: suitable
bp:
216 °C (lit.)
vapor pressure:
0.3 mmHg ( 20 °C)
2.4 mmHg ( 55 °C)

vapor density

6.38 (vs air)

Quality Level

200

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 %

technique(s)

GC/GC: suitable

impurities

≤0.2% water

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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
GHS06

signalword

Danger

Hazard Classifications

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

Storage Class

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

wgk_germany

WGK 1

flash_point_f

145.4 °F - closed cup

flash_point_c

63 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

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Certificates of Analysis (COA)

Lot/Batch Number
BCCL9961
BCCK5559
BCCB9883
BCBW1080
BCBS7384V

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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)
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
Christopher J Jones et al.
Journal of chromatography. A, 1217(4), 479-488 (2009-12-17)
Reverse-phase ion-pair high performance liquid chromatography (RPIP-HPLC) and ultra-performance liquid chromatography (RPIP-UPLC) are increasingly popular chromatographic techniques for the separation of organic compounds. However, the fine details of the RPIP separation mechanism are still being debated. Many factors including type
A Helenius et al.
The Journal of general virology, 58 Pt 1, 47-61 (1982-01-01)
The effect of five lysosomotropic weak bases (chloroquine, amantadine, tributylamine, methylamine and NH4C1) on Semliki Forest virus (SFV) infection has been studied in BHK-21 cells. When present at concentrations equal to or greater than 0.1, 0.5, 2, 15 and 15
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
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