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T81000

Sigma-Aldrich

Trioctylamine

98%

Synonym(s):

TOA

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About This Item

Linear Formula:
[CH3(CH2)7]3N
CAS Number:
1116-76-3
Molecular Weight:
353.67
Beilstein:
1210618
EC Number:
214-242-1
MDL number:
MFCD00009560
UNSPSC Code:
12352100
PubChem Substance ID:
24900500
NACRES:
NA.22

Quality Level

200

Assay

98%

refractive index

n20/D 1.449 (lit.)

bp

164-168 °C/0.7 mmHg (lit.)
365-367 °C (lit.)

density

0.809 g/mL at 25 °C (lit.)

SMILES string

CCCCCCCCN(CCCCCCCC)CCCCCCCC

InChI

1S/C24H51N/c1-4-7-10-13-16-19-22-25(23-20-17-14-11-8-5-2)24-21-18-15-12-9-6-3/h4-24H2,1-3H3

InChI key

XTAZYLNFDRKIHJ-UHFFFAOYSA-N

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Application

Trioctylamine is used as an extractant for organic acids (such as TCA, succinic acid, and acetic acid), and precious metals.

Signal Word

Danger

Hazard Classifications

Aquatic Chronic 2 - Eye Irrit. 2 - Repr. 1B - Skin Irrit. 2 - STOT RE 1 Oral

Target Organs

Heart

Storage Class Code

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3

Flash Point(F)

334.4 °F - closed cup

Flash Point(C)

168 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Yongshuang Zhu et al.
Dalton transactions (Cambridge, England : 2003), 41(10), 2935-2940 (2012-01-24)
Cobalt phosphate-based organic-inorganic hybrid nanobelts were successfully synthesized in the presence of trioctylamine (TOA) via a solvothermal system. The inorganic cobalt phosphate layers and organic n-octylamine layers in this structure arranged alternately, both of which were parallel to the axial
High pressure liquid chromatographic determination of tartrazine in rice milk following ion-pair extraction with tri-n-octylamine.
M L Puttemans et al.
Journal - Association of Official Analytical Chemists, 66(3), 670-672 (1983-05-01)
Young-Si Jun et al.
Biotechnology progress, 21(6), 1673-1679 (2005-12-03)
Kinetic studies for the extraction of succinic acid from aqueous solution with 1-octanol solutions of tri-n-octylamine (TOA) were carried out using a stirred cell with a microporous hydrophobic membrane. The interfacial concentrations of species were correlated and thus the intrinsic
Evgenii S Stoyanov et al.
Journal of the American Chemical Society, 128(26), 8500-8508 (2006-06-29)
The N-H stretching frequencies of tri-n-octylammonium salts are reported for a series of weakly basic anions (A(-)), many of which are the conjugate bases of known strong acids and superacids. Data have been collected primarily in carbon tetrachloride, where Oct(3)N(+)-H...A(-)
M L Puttemans et al.
Journal - Association of Official Analytical Chemists, 67(5), 880-885 (1984-09-01)
Synthetic dyes, benzoic acid, sorbic acid, and saccharin are extracted simultaneously from soft drinks with 0.01M tri-n-octylamine at pH = 5.5 and are back-extracted to an aqueous phase with 0.1M sodium perchlorate. The perchlorate solution is injected directly into the
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