110132
Valeraldehyde
97%
Synonym(s):
Pentanal
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About This Item
Linear Formula:
CH3(CH2)3CHO
CAS Number:
Molecular Weight:
86.13
NACRES:
NA.22
PubChem Substance ID:
eCl@ss:
39021107
UNSPSC Code:
12352100
EC Number:
203-784-4
MDL number:
Beilstein/REAXYS Number:
1616304
Assay:
97%
Quality Level
assay
97%
autoignition temp.
428 °F
refractive index
n20/D 1.394 (lit.)
bp
102-103 °C (lit.)
mp
−92 °C (lit.)
density
0.81 g/mL at 25 °C (lit.)
functional group
aldehyde
SMILES string
[H]C(=O)CCCC
InChI
1S/C5H10O/c1-2-3-4-5-6/h5H,2-4H2,1H3
InChI key
HGBOYTHUEUWSSQ-UHFFFAOYSA-N
General description
Valeraldehyde also known as pentanal, serves as a precursor or intermediate to build more complex organic molecules.
Application
Valeraldehyde has been used to study its time-weighted average sampling using solid-phase microextraction (SPME) device.
Valeraldehyde is used as a gaseous standard in the study of the sorptive loss pattern for volatile compounds.
Valeraldehyde is used in flavoring compounds and as a rubber accelerator.
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signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Inhalation - Eye Irrit. 2 - Flam. Liq. 2 - Skin Sens. 1 - STOT SE 3
target_organs
Respiratory system
Storage Class
3 - Flammable liquids
wgk
WGK 1
flash_point_f
44.6 °F
flash_point_c
7 °C
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
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Aldol condensation of cyclopentanone with valeraldehyde over metal oxides
Maki-Arvela et al.
Catalysis Letters, 149, 1383-1395 (2019)
Yong-Hyun Kim et al.
Journal of separation science, 35(21), 2914-2921 (2012-10-16)
In this study, the sorptive loss patterns for volatile organic compounds were evaluated by gaseous standards containing 13 compounds (benzene, toluene, styrene, p-xylene, methyl ethyl ketone, methyl isobutyl ketone, isobutyl alcohol, butyl acetate, acetaldehyde, propionaldehyde, butyraldehyde, isovaleraldehyde, and valeraldehyde). The
François Fenaille et al.
Rapid communications in mass spectrometry : RCM, 18(1), 67-76 (2003-12-23)
Upon hexanal-modification in the presence of NaCNBH(3), the oxidized B chain of insulin becomes mono- and further dialkylated on both the N-terminal and Lys(29) residues. A pseudo-MS(3) study was performed with a triple-quadrupole mass spectrometer on the different modified lysine-containing