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About This Item
Linear Formula:
C2H5CH(CH3)CHO
CAS Number:
Molecular Weight:
86.13
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
202-485-6
Beilstein/REAXYS Number:
1633540
MDL number:
Assay:
95%
Form:
liquid
Quality Level
assay
95%
form
liquid
refractive index
n20/D 1.3919 (lit.)
bp
90-92 °C (lit.)
density
0.806 g/mL at 20 °C, 0.804 g/mL at 25 °C (lit.)
SMILES string
[H]C(=O)C(C)CC
InChI
1S/C5H10O/c1-3-5(2)4-6/h4-5H,3H2,1-2H3
InChI key
BYGQBDHUGHBGMD-UHFFFAOYSA-N
Application
2-Methylbutyraldehyde can be used as a reactant to synthesize:
- 2-amino-3-cyanopyridine derivatives via multicomponent condensation with various acetophenones and malononitrile in the presence of ammonium acetate.
- N,N-Diethyl-2-methyl-1-butanamine by reacting with diethylamine via Rh-catalyzed reductive amination reaction in the presence of molecular hydrogen.
- α-(2-Methylbutylidene)benzeneacetonitrile by condensation reaction with benzyl cyanide using tricyclic strong nonionic Lewis bases.
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signalword
Danger
hcodes
Hazard Classifications
Aquatic Chronic 2 - Eye Irrit. 2 - Flam. Liq. 2 - Skin Sens. 1 - STOT SE 3
target_organs
Respiratory system
Storage Class
3 - Flammable liquids
wgk
WGK 2
flash_point_f
23.0 °F
flash_point_c
-5 °C
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Regulatory Information
危险化学品
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Rhodium-Catalysed Reductive Amination for the Synthesis of Tertiary Amines
Bianga J, et al.
advanced synthesis and catalysis, 362(20), 4415-4424 (2020)
Rhodium-Catalysed Reductive Amination for the Synthesis of Tertiary Amines
Bianga J, et al.
Advanced Synthesis & Catalysis, 362(20), 4415-4424 (2020)
Direct synthesis of α ,β-unsaturated nitriles catalyzed by nonionic superbases
D'Sa Bosco A, et al.
The Journal of Organic Chemistry, 63(12), 3961-3967 (1998)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| M33476-50G | 04061834050148 |
| M33476-250G | 04061836696610 |


