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About This Item
Linear Formula:
CH3CH2CH2CHO
CAS Number:
Molecular Weight:
72.11
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
204-646-6
Beilstein/REAXYS Number:
506061
MDL number:
Assay:
≥99.5%
Form:
liquid
InChI key
ZTQSAGDEMFDKMZ-UHFFFAOYSA-N
InChI
1S/C4H8O/c1-2-3-4-5/h4H,2-3H2,1H3
SMILES string
[H]C(=O)CCC
vapor density
2.5 (vs air)
vapor pressure
90 mmHg ( 20 °C)
assay
≥99.5%
form
liquid
autoignition temp.
390 °F
purified by
redistillation
expl. lim.
12.5 %
Quality Level
bp
75 °C (lit.)
mp
−96 °C (lit.)
density
0.8 g/mL at 25 °C (lit.)
functional group
aldehyde
organoleptic
pungent
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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.
signalword
Danger
hcodes
Hazard Classifications
Eye Irrit. 2 - Flam. Liq. 2
Storage Class
3 - Flammable liquids
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
flash_point_f
12.2 °F - closed cup
flash_point_c
-11 °C - closed cup
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Renewable synthesis of n-butyraldehyde from glucose by engineered Escherichia coli
Jason T K, et al.
Biotechnology for Biofuels, 10, 1-10 (2017)
Self-condensation of n-butyraldehyde over solid base catalysts.
Tsuji H, et al.
J. Catal., 148(2), 759-770 (1994)
The condensation of butyraldehyde and aniline.
Kharasch MS, et al.
Journal of the American Chemical Society, 62(3), 494-497 (1940)
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)
Phosphazene base promoted anionic polymerization of n-butyraldehyde
Inge W, et al.
European Polymer Journal, 93, 97-102 (2017)
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