473316
Amylamines, mixture of isomers
≥98%
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A propos de cet article
Formule linéaire :
C5H11NH2
Poids moléculaire :
87.16
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
≥98%
Service technique
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Laissez-nous vous aiderQuality 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.
signalword
Danger
Hazard Classifications
Acute Tox. 3 Inhalation - Acute Tox. 4 Dermal - Acute Tox. 4 Oral - Aquatic Chronic 3 - Flam. Liq. 2 - Skin Corr. 1B
Classe de stockage
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