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110132

Sigma-Aldrich

Valeraldehyde

97%

Sinónimos:

Pentanal

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About This Item

Fórmula lineal:
CH3(CH2)3CHO
Número de CAS:
110-62-3
Peso molecular:
86.13
Beilstein/REAXYS Number:
1616304
EC Number:
203-784-4
MDL number:
MFCD00007026
UNSPSC Code:
12352100
eCl@ss:
39021107
PubChem Substance ID:
24846963
NACRES:
NA.22

Quality Level

100

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

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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.

pictograms

FlameExclamation mark
GHS02,GHS07

signalword

Danger

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_germany

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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Certificados de análisis (COA)

Lot/Batch Number
STBL3363
STBK2804
STBJ1090
STBH7374
STBF2272V

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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
Aldol condensation of cyclopentanone with valeraldehyde over metal oxides
Maki-Arvela et al.
Catalysis Letters, 149, 1383-1395 (2019)
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
Christophe Yrieix et al.
Chemosphere, 79(4), 414-419 (2010-02-23)
Six European laboratories used the emission test chamber method (EN ISO 16000-9) for the determination of VOC and formaldehyde emissions from a wood based panel (particleboard). The tested panel was conditioned without wrapping over 28 d at 23 degrees C
Trine K Dalsgaard et al.
Journal of agricultural and food chemistry, 54(17), 6367-6373 (2006-08-17)
Aldehydes formed as a result of lipid oxidation form fluorophores after binding to proteins. The structure of the fluorophores formed by reaction between saturated aldehydes and lysine has not yet been identified. The reaction products formed in the reaction between
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