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240958

Sigma-Aldrich

Propylamine

≥99%

Sinonimo/i:

1-Aminopropane

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About This Item

Formula condensata:
CH3CH2CH2NH2
Numero CAS:
Peso molecolare:
59.11
Beilstein:
1098243
Numero CE:
Numero MDL:
Codice UNSPSC:
12352100
eCl@ss:
39030103
ID PubChem:
NACRES:
NA.22

Densità del vapore

2 (vs air)

Tensione di vapore

4.79 psi ( 20 °C)

Saggio

≥99%

Forma fisica

liquid

Temp. autoaccensione

604 °F

Limite di esplosione

10.4 %

Indice di rifrazione

n20/D 1.388 (lit.)

P. eboll.

48 °C (lit.)

Punto di fusione

−83 °C (lit.)

Solubilità

water: soluble 0.4 part(lit.)
chloroform: soluble 1.5 part(lit.)

Densità

0.719 g/mL at 25 °C (lit.)

Temperatura di conservazione

2-8°C

Stringa SMILE

CCCN

InChI

1S/C3H9N/c1-2-3-4/h2-4H2,1H3
WGYKZJWCGVVSQN-UHFFFAOYSA-N

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Descrizione generale

Propylamine is a primary amine and an important building block in the chemical synthesis. It is generally used as a petroleum additive and solvent in organic syntheses. It can also be used as a finishing agent for paints, drugs, rubber, pesticides, textile, and resin. It is used in the production of fungicides, antivirals, catalysts, molecular sieves, and corrosion inhibitors.

Applicazioni

Propylamine was used in the synthesis of dendritic polymer-modified silica (DPS) stationary phase by consecutive amine-epoxy reactions with aniline and 1,4-butanedioldiglycidyl ether.

Avvertenze

Danger

Classi di pericolo

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 2 - Met. Corr. 1 - Skin Corr. 1B - STOT SE 3

Organi bersaglio

Respiratory system

Codice della classe di stoccaggio

3 - Flammable liquids

Classe di pericolosità dell'acqua (WGK)

WGK 1

Punto d’infiammabilità (°F)

<-31.0 °F

Punto d’infiammabilità (°C)

< -35 °C

Dispositivi di protezione individuale

Faceshields, Gloves, Goggles


Certificati d'analisi (COA)

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Yun Li et al.
Journal of chromatography. A, 1337, 133-139 (2014-03-19)
A novel dendritic polymer-modified silica (DPS) stationary phase was prepared by a divergent synthesis scheme starting from propylamine on silica by consecutive amine-epoxy reactions with 1,4-butanedioldiglycidyl ether and aniline. Both elemental analysis and infrared spectra data shows the successful growth
Marian Cors et al.
Scientific reports, 9(1), 13812-13812 (2019-09-27)
The peculiar linear temperature-dependent swelling of core-shell microgels has been conjectured to be linked to the core-shell architecture combining materials of different transition temperatures. Here the structure of pNIPMAM-core and pNNPAM-shell microgels in water is studied as a function of
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Efficient intracellular delivery of a therapeutic compound is an important feature of smart drug delivery systems (SDDS). Modification of a carrier structure with a cell-penetrating ligand, ie, cholesterol moiety, is a strategy to improve cellular uptake. Cholesterol end-capped poly(N-isopropylacrylamide)s offer
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Two-dimensional (2D) photocatalysts have been widely studied due to their short charge carrier migration pathways and tunable electronic structures. Herein, a facile one-pot solvothermal process with ethylamine (ea) constructs a novel 2D nanojunction based on ZnSe. The ea molecules coordinate

Protocolli

Separation of Propylamine; Butylamine; Pentylamine; Hexylamine; Heptylamine; Octylamine; Nonylamine; Decylamine

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