19490
Butylamine
purum, ≥98.0% (GC)
Synonym(s):
1-Aminobutane, n-Butylamine
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About This Item
Linear Formula:
CH3(CH2)3NH2
CAS Number:
Molecular Weight:
73.14
EC Number:
203-699-2
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
605269
MDL number:
vapor density
2.5 (vs air)
vapor pressure
68 mmHg ( 20 °C)
grade
purum
assay
≥98.0% (GC)
autoignition temp.
594 °F
expl. lim.
9.8 %
refractive index
n20/D 1.401
bp
78 °C (lit.)
mp
−49 °C (lit.)
density
0.74 g/mL at 25 °C (lit.)
SMILES string
CCCCN
InChI
1S/C4H11N/c1-2-3-4-5/h2-5H2,1H3
InChI key
HQABUPZFAYXKJW-UHFFFAOYSA-N
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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. 1A - STOT SE 3
target_organs
Respiratory system
Storage Class
3 - Flammable liquids
wgk
WGK 1
flash_point_f
19.4 °F - closed cup
flash_point_c
-7 °C - closed cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
Regulatory Information
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Wen-Ya Wu et al.
Advanced materials (Deerfield Beach, Fla.), 31(4), e1806164-e1806164 (2018-12-01)
Liquid-based thermochromics can be incorporated into an arbitrarily shaped container and provide a visual map of the temperature changes within its volume. However, photochemical degradation, narrow temperature range of operation, and the need for stringent encapsulation processes are challenges that
Javad Gholami et al.
Luminescence : the journal of biological and chemical luminescence, 31(1), 229-235 (2015-05-29)
An N-butylamine functionalized graphene oxide nanolayer was synthesized and characterized by ultraviolet (UV)-visible spectrometry, Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy, and transmission electron microscopy. Detection of iron(III) based on photoluminescence spectroscopy was investigated. The N-butylamine functionalized graphene oxide was
D M N M Dissanayake et al.
Nanotechnology, 20(19), 195205-195205 (2009-05-08)
Organic-inorganic hybrid heterojunctions have potential as the basis for future photovoltaic devices. Herein, we report the results of investigations exploring the possibility of using pentacene and tetracene as photoelectron donors in conjunction with PbS nanocrystals (PbS-NCs). Photoinduced charge transfer was