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473316

Sigma-Aldrich

Amylamines, mixture of isomers

≥98%

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About This Item

Linear Formula:
C5H11NH2
Molecular Weight:
87.16
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

≥98%

refractive index

n20/D 1.411 (lit.)

bp

104 °C (lit.)

mp

−55 °C (lit.)

density

0.752 g/mL at 25 °C (lit.)

functional group

amine

SMILES string

CCCCCN

InChI

1S/C5H13N/c1-2-3-4-5-6/h2-6H2,1H3

InChI key

DPBLXKKOBLCELK-UHFFFAOYSA-N

General description

The product is a mixture of isomeric amylamines. Amylamine is a simple primary amine. Neopentylamine and tert-amylamine are its isomeric forms. The mechanism of the hydrodenitrogenation of these isomeric amylamines has been studied in the presence of sulfided NiMo/A12O3 catalyst. Kinetics and thermodynamic parameters of the ultrasonic absorptions of its aqueous solutions have been evaluated.

Signal Word

Danger

Hazard Classifications

Acute Tox. 3 Inhalation - Acute Tox. 4 Dermal - Acute Tox. 4 Oral - Aquatic Chronic 3 - Flam. Liq. 2 - Skin Corr. 1B

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

42.8 °F

Flash Point(C)

6 °C


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Mechanism of carbon-nitrogen bond cleavage during amylamine hydrodenitrogenation over a sulphided NiMo/Al2O3 catalyst.
Portefaix JL, et al.
Catalysis Letters, 9(1-2), 127-132 (1991)
Kinetic Studies of Fast Reactions in Aqueous Solutions of Amylamine by Means of Ultrasonic Absorption.
Nishikawa S, et al.
Bulletin of the Chemical Society of Japan, 46(10), 2992-2997 (1973)
Jun Kobayashi et al.
Journal of biomedical materials research. Part A, 102(11), 3883-3893 (2013-12-18)
Antibody-immobilized thermoresponsive poly(N-isopropylacrylamide-co-2-carboxyisopropylacrylamide) [poly(IPAAm-co-CIPAAm)]-grafted cell culture surfaces were designed to enhance both the initial adhesion of weakly adhering cells and the ability of cells to detach in response to low temperature through the regulation of affinity binding between immobilized antibodies
Cui Cui et al.
Bone, 72, 43-52 (2014-12-03)
Serotonin (5-HT)--a monoamine with a variety of physiological functions--has recently emerged as a major regulator of bone mass. 5-HT is synthesized in the brain and the gut, and gut-derived 5-HT contributes to circulating 5-HT levels and is a negative modulator
Lucas H Hofmeister et al.
ACS nano, 9(4), 4435-4446 (2015-03-15)
In regions of the circulation where vessels are straight and unbranched, blood flow is laminar and unidirectional. In contrast, at sites of curvature, branch points, and regions distal to stenoses, blood flow becomes disturbed. Atherosclerosis preferentially develops in these regions

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