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538191

Sigma-Aldrich

Butyraldehyde

≥99.0%, dry

Synonym(s):

Butanal

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About This Item

Linear Formula:
CH3CH2CH2CHO
CAS Number:
Molecular Weight:
72.11
Beilstein:
506061
EC Number:
MDL number:
UNSPSC Code:
12352114
PubChem Substance ID:
NACRES:
NA.21

vapor density

2.5 (vs air)

vapor pressure

90 mmHg ( 20 °C)

Assay

≥99.0%

autoignition temp.

390 °F

expl. lim.

12.5 %

impurities

≤0.30% (water)

refractive index

n20/D 1.380 (lit.)

bp

75 °C (lit.)

mp

−96 °C (lit.)

solubility

water: soluble 50 g/L at 20 °C

density

0.8 g/mL at 25 °C (lit.)

SMILES string

[H]C(=O)CCC

InChI

1S/C4H8O/c1-2-3-4-5/h4H,2-3H2,1H3

InChI key

ZTQSAGDEMFDKMZ-UHFFFAOYSA-N

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General description

Butyraldehyde (n-Butyraldehyde), an aliphatic aldehyde, can be synthesized by dehydrogenation of butanol in the presence of zinc catalyst. It is an important precursor for preparing polyvinylbutyral. The mechanism of pyrolysis of butyraldehyde in the gas-phase has been described. The kinetic study of the condensation reaction between butyraldehyde and poly(vinyl alcohol) indicates retardation effect.

Application

Butyraldehyde (n-Butyraldehyde) may be used in the preparation of 2-ethylhexanal (2EH) via hydrogenation in the presence of tetraamine palladium(II) chloride supported on the potassium ion-exchanged zeolite X (Pd/KXW) and on the potassium ion-added zeolite X (Pd/KXU).

Pictograms

FlameExclamation mark

Signal Word

Danger

Hazard Statements

Hazard Classifications

Eye Irrit. 2 - Flam. Liq. 2

Storage Class Code

3 - Flammable liquids

WGK

WGK 1

Flash Point(F)

<50.0 °F - Pensky-Martens closed cup

Flash Point(C)

< 10 °C - Pensky-Martens closed cup


Certificates of Analysis (COA)

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Highly selective Pd/KX catalysts for low-pressure one-step synthesis of 2-ethylhexanal from n-butyraldehyde and hydrogen.
Ko AN, et al.
Catalysis Letters, 54(4), 207-210 (1998)
Retardation effect in acetalization of poly (vinyl alcohol) with butyraldehyde.
Rumyantsev M, et al.
Eur. Polymer J., 49(6), 1698-1706 (2013)
Thermal decomposition products of butyraldehyde.
Hatten CD, et al.
J. Chem. Phys. , 139(21), 214303-214303 (2013)
Kinetic studies on dehydrogenation of butanol to butyraldehyde using zinc oxide as catalyst.
Raizada VK, et al.
Journal of Chemical Technology and Biotechnology, 56(3), 265-270 (1993)
N Gregory et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 44(8), 1223-1227 (2006-03-17)
Bovine soles and shavings from the heel were used in laboratory tests that examined the softening and swelling effects of rainwater, cow slurry (faeces plus urine), urine, silage effluent, and washings from recently laid concrete. Formalin, glutaraldehyde and butyraldehyde were

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