Skip to Content
Merck
CN

473316

Amylamines, mixture of isomers

≥98%

Sign In to View Organizational & Contract Pricing.

Select a Size

Change View

About This Item

Linear Formula:
C5H11NH2
Molecular Weight:
87.16
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
≥98%
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist


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.


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

Storage Class

3 - Flammable liquids

wgk

WGK 3

flash_point_f

42.8 °F

flash_point_c

6 °C

Regulatory Information

危险化学品

This item has



Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library



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



Global Trade Item Number

SKUGTIN
473316-100ML04061836827090
473316-500ML04061832360867