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93240

Tripropylamine

purum, ≥98.0% (GC)

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About This Item

Linear Formula:
(CH3CH2CH2)3N
CAS Number:
102-69-2
Molecular Weight:
143.27
EC Number:
203-047-7
UNSPSC Code:
12352100
PubChem Substance ID:
24889818
Beilstein/REAXYS Number:
1098331
MDL number:
MFCD00009363
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vapor density

4.9 (vs air)

vapor pressure

2.9 mmHg ( 20 °C)

grade

purum

assay

≥98.0% (GC)

autoignition temp.

356 °F

expl. lim.

5.6 %

refractive index

n20/D 1.416 (lit.), n20/D 1.417

bp

155-158 °C (lit.), 40-42 °C/11 mmHg (lit.)

mp

−93.5 °C (lit.)

density

0.753 g/mL at 25 °C (lit.)

SMILES string

CCCN(CCC)CCC

InChI

1S/C9H21N/c1-4-7-10(8-5-2)9-6-3/h4-9H2,1-3H3

InChI key

YFTHZRPMJXBUME-UHFFFAOYSA-N

Other Notes

This product has been replaced by 143979-ALDRICH | Tripropylamine ≥98%

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Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Chronic 3 - Eye Dam. 1 - Flam. Liq. 3 - Skin Corr. 1B - STOT SE 3

target_organs

Respiratory system

Storage Class

3 - Flammable liquids

wgk

WGK 2

flash_point_f

93.2 °F - closed cup

flash_point_c

34 °C - closed cup

ppe

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

Regulatory Information

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Xueshu Li et al.
Langmuir : the ACS journal of surfaces and colloids, 28(9), 4152-4159 (2012-02-07)
The micelles of two tripropargylammonium-functionalized cationic surfactants were cross-linked by a disulfide-containing diazido cross-linker in the presence of Cu(I) catalysts. With multiple residual alkyne groups on the surface, the resulting surface cross-linked micelles (SCMs) were postfunctionalized by reaction with 2-azidoethanol
H C Froede et al.
Archives of biochemistry and biophysics, 247(2), 420-423 (1986-06-01)
The theory of noncompetitive inhibition of acetylcholinesterase based on the binding of inhibitor to the acetylenzyme and the free enzyme was proven correct by demonstrating that tripropylammonium ion increases the steady-state concentration of acetylenzyme, as predicted by the theory. By
István Ilisz et al.
Journal of chromatography. A, 1384, 67-75 (2015-02-11)
The enantiomers of four unusual, rather rigid isoxazoline-fused 2-aminocyclopentanecarboxylic acids were directly separated on a quinine- or a quinidine-based zwitterionic ion-exchanger as chiral selector. The effects of the mobile phase composition, the structures of the analytes and temperature on the