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538205

Isobutyraldehyde

dry, 98%

Synonym(s):

2-Methylpropanal, 2-Methylpropionaldehyde

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About This Item

Linear Formula:
(CH3)2CHCHO
CAS Number:
78-84-2
Molecular Weight:
72.11
Beilstein/REAXYS Number:
605330
EC Number:
201-149-6
MDL number:
MFCD00006980
UNSPSC Code:
12352100
PubChem Substance ID:
24878311
NACRES:
NA.22

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vapor density

2.5 (vs air)

vapor pressure

66 mmHg ( 4.4 °C)

assay

98%

autoignition temp.

384 °F

expl. lim.

10 %, 25 °F
2 %, 32 °F

refractive index

n20/D 1.374 (lit.)

bp

63 °C (lit.)

mp

−65 °C (lit.)

solubility

60 g/L at 25 °C

density

0.79 g/mL at 25 °C (lit.)

functional group

aldehyde

storage temp.

2-8°C

SMILES string

[H]C(=O)C(C)C

InChI

1S/C4H8O/c1-4(2)3-5/h3-4H,1-2H3

InChI key

AMIMRNSIRUDHCM-UHFFFAOYSA-N

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1 of 4

This Item
W222003240788W222011
Isobutyraldehyde dry, 98%

Sigma-Aldrich

538205

Isobutyraldehyde

Isobutyraldehyde ≥98%, FG

Sigma-Aldrich

W222003

Isobutyraldehyde

Isobutyraldehyde ≥99%

Sigma-Aldrich

240788

Isobutyraldehyde

Isobutyraldehyde natural, 96%, FG

Sigma-Aldrich

W222011

Isobutyraldehyde

assay

98%

assay

≥98%

assay

≥99%

assay

96%

Quality Level

200

Quality Level

400

Quality Level

200

Quality Level

400

solubility

60 g/L at 25 °C

solubility

60 g/L at 25 °C

solubility

water: soluble 11g/100mL at 20 °C(lit.), acetone: miscible(lit.), benzene: miscible(lit.), carbon disulfide: miscible(lit.), chloroform: miscible(lit.), diethyl ether: miscible(lit.), ethanol: miscible(lit.), toluene: miscible(lit.)

solubility

60 g/L at 25 °C

refractive index

n20/D 1.374 (lit.)

refractive index

n20/D 1.374 (lit.)

refractive index

n20/D 1.374 (lit.)

refractive index

n20/D 1.374 (lit.)

density

0.79 g/mL at 25 °C (lit.)

density

0.79 g/mL at 25 °C (lit.)

density

0.79 g/mL at 25 °C (lit.)

density

0.79 g/mL at 25 °C (lit.)

mp

−65 °C (lit.)

mp

−65 °C (lit.)

mp

−65 °C (lit.)

mp

−65 °C (lit.)

General description

Isobutyraldehyde is an α,α-disubstituted aldehyde.[1] It is an important raw material for the manufacture of various industrially important chemicals. It may be produced from CO2 and overexpression of ribulose 1,5-bisphosphate carboxylase/oxygenase employing genetically engineered strain of Synechococcus elongatus PCC7942.[2] Enantioenriched γ-nitroaldehydes are obtained from the conjugate addition reaction between isobutyraldehyde with nitroalkenes in the presence of chiral organocatalysts.[3]

Application

Isobutyraldehyde may be used in the synthesis of the following compounds:
  • N-cyclohrxyl-α-dimethylaminoisovalerarnide[1]
  • N′-cyclohexyl-N,N-dimethyl-α-dimethylaminoisovaleramidine[1]
  • α-acetoxy-N-cyclohexylisovaleramide[1]
  • acetic anhydride[1]
  • N-cyclohexyl-a-formyloxyisovaleramide[1]
  • cyclic carbonates[4]
  • hydroxypivaldehyde, which is useful for the preparation of neopentyl glycol (NPG)[5]
It may also be employed for the microbial synthesis of isobutanol.[6]

pictograms

FlameExclamation mark
GHS02,GHS07

signalword

Danger

hcodes

H225,H319

Hazard Classifications

Eye Irrit. 2 - Flam. Liq. 2

Storage Class

3 - Flammable liquids

wgk_germany

WGK 1

flash_point_f

-11.2 °F - closed cup

flash_point_c

-24 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
SHBT1733
SHBS4556
SHBS3175
SHBR6547
SHBL4404

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Cross-Aldol condensation of isobutyraldehyde and formaldehyde using phase transfer catalyst.
Hashmi A.
Journal of Saudi Chemical Society (2013)
Reactions of cyclohexylisonitrile and isobutyraldehyde with various nucleophiles and catalysts.
McFarland JW.
The Journal of Organic Chemistry, 28(9), 2179-2181 (1963)
Xiang Liu et al.
Journal of biotechnology, 164(2), 188-195 (2012-09-15)
We have determined the X-ray crystal structures of the NADH-dependent alcohol dehydrogenase LlAdhA from Lactococcus lactis and its laboratory-evolved variant LlAdhA(RE1) at 1.9Å and 2.5Å resolution, respectively. LlAdhA(RE1), which contains three amino acid mutations (Y50F, I212T, and L264V), was engineered
Enantioselective Michael addition of isobutyraldehyde to nitroalkenes organocatalyzed by chiral primary amine-guanidines.
Avila A, et al.
Tetrahedron Asymmetry, 25(5), 462-467 (2014)
Bart A Smit et al.
Journal of agricultural and food chemistry, 52(5), 1263-1268 (2004-03-05)
Formation of flavor compounds from branched-chain alpha-keto acids in fermented foods such as cheese is believed to be mainly an enzymatic process, while the conversion of phenyl pyruvic acid, which is derived from phenylalanine, also proceeds chemically. In this research
View All Related Papers

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