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110132

Sigma-Aldrich

Valeraldehyde

97%

Synonyma:

Pentanal

Přihlásitk zobrazení cen stanovených pro organizaci a smluvních cen
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About This Item

Lineární vzorec:
CH3(CH2)3CHO
Číslo CAS:
110-62-3
Molekulová hmotnost:
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

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.)

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

Osvědčení o analýze (COA)

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SAFC

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di-Sodium tetraborate decahydrate

Propionaldehyde ≥97%, FG

Sigma-Aldrich

W292303

Propionaldehyde

Heptanal ≥95%, FCC, FG

Sigma-Aldrich

W254002

Heptanal

2-Methylbutyraldehyde ≥95%, FG

Sigma-Aldrich

W269107

2-Methylbutyraldehyde

Valeraldehyde-DNPH solution certified reference material, 100 μg/mL in acetonitrile (as the aldehyde), ampule of 1 mL

Supelco

CRM47185

Valeraldehyde-DNPH solution

Isobutyraldehyde ≥99%

Sigma-Aldrich

240788

Isobutyraldehyde

Isobutyraldehyde redistilled, ≥99.5%

Sigma-Aldrich

418110

Isobutyraldehyde

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)
Masayuki Fujita et al.
Plant & cell physiology, 44(5), 481-490 (2003-05-30)
Induction of pumpkin (Cucurbita maxima Duch.) glutathione S-transferase (GST, EC 2.5.1.18) by aldehydes and related compounds was examined. All of the tested compounds induced pumpkin GST to different degrees, and it was found that (1) aldehydes induce GST directly and
P Scalabrini et al.
International journal of food microbiology, 39(3), 213-219 (1998-04-29)
Soybean milk, which serves as a base for a variety of beverages, contains raffinose, stachyose, pentanal and n-hexanal; the former two may be responsible for flatulence after fermentation, whilst the latter two for a beany flavour. Twenty-seven strains of Bifidobacterium
Kimberly J Grossman et al.
The European journal of neuroscience, 27(10), 2676-2685 (2008-05-01)
Odor mixtures can produce several qualitatively different percepts; it is not known at which stage of processing these are determined. We asked if activity within the first stage of olfactory processing, the glomerular layer of the olfactory bulb, predicts odor
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