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418102

Sigma-Aldrich

Butyraldehyde

purified by redistillation, ≥99.5%

Synonym(s):

Butanal

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About This Item

Linear Formula:
CH3CH2CH2CHO
CAS Number:
Molecular Weight:
72.11
Beilstein/REAXYS Number:
506061
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

vapor density

2.5 (vs air)

Quality Level

vapor pressure

90 mmHg ( 20 °C)

assay

≥99.5%

form

liquid

autoignition temp.

390 °F

purified by

redistillation

expl. lim.

12.5 %

refractive index

n20/D 1.380 (lit.)

bp

75 °C (lit.)

mp

−96 °C (lit.)

density

0.8 g/mL at 25 °C (lit.)

functional group

aldehyde

organoleptic

pungent

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, also known as Butanal, is an aliphatic aldehyde, that is commonly used as a versatile building block in various organic reactions, such as in the synthesis of diverse C4–C8 alcohols, esters, amines, and carboxylic acids.

Application

Butyraldehyde can be used as a reactant in the:
  • Reductive amination of various nitroarene derivatives to synthesize mono-N-alkylated aniline derivatives.
  • Ionic liquid-catalyzed Knoevenagel condensation with active methylene compounds to synthesize substituted electrophilic alkenes.
  • NiCl2-catalyzed synthesis of α-aminonitriles by reacting with amines and trimethylsilyl cyanides.

pictograms

FlameExclamation mark

signalword

Danger

hcodes

Hazard Classifications

Eye Irrit. 2 - Flam. Liq. 2

Storage Class

3 - Flammable liquids

wgk_germany

WGK 1

flash_point_f

<50.0 °F - Pensky-Martens closed cup

flash_point_c

< 10 °C - Pensky-Martens closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


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Self-condensation of n-butyraldehyde over solid base catalysts.
Tsuji H, et al.
J. Catal., 148(2), 759-770 (1994)
Aldol addition of butyraldehyde over solid base catalysts.
Zhang G, et al.
Bulletin of the Chemical Society of Japan, 62(6), 2070-2072 (1989)
Heterogeneous photocatalytic oxidation of gas-phase organics for air purification: acetone, 1-butanol, butyraldehyde, formaldehyde, and m-xylene oxidation.
Peral J and Ollis DF.
J. Catal., 1136(2), 554-565 (1992)
The condensation of butyraldehyde and aniline.
Kharasch MS, et al.
Journal of the American Chemical Society, 62(3), 494-497 (1940)
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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