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Merck
CN

82100

Propylamine

purum, ≥99.0% (GC)

Synonym(s):

1-Aminopropane

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About This Item

Linear Formula:
CH3CH2CH2NH2
CAS Number:
Molecular Weight:
59.11
NACRES:
NA.22
PubChem Substance ID:
eCl@ss:
39030103
UNSPSC Code:
12352100
MDL number:
Beilstein/REAXYS Number:
1098243
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Product Name

Propylamine, purum, ≥99.0% (GC)

InChI

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

SMILES string

CCCN

InChI key

WGYKZJWCGVVSQN-UHFFFAOYSA-N

vapor density

2 (vs air)

vapor pressure

4.79 psi ( 20 °C)

grade

purum

assay

≥99.0% (GC)

form

liquid

autoignition temp.

604 °F

expl. lim.

10.4 %

refractive index

n20/D 1.388 (lit.)
n20/D 1.388

bp

48 °C (lit.)

mp

−83 °C (lit.)

density

0.719 g/mL at 25 °C (lit.)

functional group

amine

Quality Level

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signalword

Danger

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

3 - Flammable liquids

wgk

WGK 1

flash_point_f

<-31.0 °F

flash_point_c

< -35 °C

ppe

Faceshields, Gloves, Goggles

Regulatory Information

危险化学品
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Ryan R Gordon et al.
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Cell reports, 27(10), 2895-2908 (2019-06-06)
Microglia, the brain's immune cells, maintain homeostasis and sense pathological changes by continuously surveying the parenchyma with highly motile large processes. Here, we demonstrate that microglia also use thin actin-dependent filopodia that allow fast nanoscale sensing within discrete regions. Filopodia
Claire Bagnéris et al.
Proceedings of the National Academy of Sciences of the United States of America, 111(23), 8428-8433 (2014-05-23)
Voltage-gated sodium channels are important targets for the development of pharmaceutical drugs, because mutations in different human sodium channel isoforms have causal relationships with a range of neurological and cardiovascular diseases. In this study, functional electrophysiological studies show that the
Sebastian Finger et al.
Biological chemistry, 395(7-8), 769-778 (2014-07-09)
The binding of cationic polyamines to negatively charged lipid membranes is driven by electrostatic interactions and additional hydrophobic contributions. We investigated the effect of polyamines with different number of charges and charge separation on the phase transition behavior of vesicles

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