Ethyl isobutyrate

Structural formula

• Numbering system
• Physical property data
• Toxicological data
• Ecological data
• Molecular structure data
• Computing chemical data
• More
  • Properties and Stability
  • Storage method
  • Synthesis method
  • Purpose

Numbering system

CAS number:97-62-1

MDL number:MFCD00009165

EINECS number:202-595-4

RTECS number:NQ4675000

BRN number:773846

PubChem number:24881085

Physical property data

1. Properties: Colorless and volatile liquid with fruity aroma. ^[1]

2. Melting point (℃): -88^[2]

3. Boiling point (℃): 110.1^[3]

4. Relative density (water = 1): 0.87^[4]

5. Relative vapor Density (air=1): 4.01^[5]

6. Saturated vapor pressure (kPa): 5.33 (33.8℃)^[6]

7. Heat of combustion (kJ/mol): -3535.0^[7]

8. Critical temperature (℃): 280^[8]

9. Critical pressure (MPa): 3.04^[9]

10. Octanol/water partition coefficient: 1.77 ^[10]

11. Flash point (℃): 13^[11]

12. Solubility: slightly soluble in water, Soluble in ethanol, ether, etc. ^[12]

13. Refractive index (n20ºC): 1.3869

14. Solubility parameter (J·cm^-3)^0.5: 16.504

15. Critical density (g·cm^-3): 0.28

16. Critical volume (cm³·mol^-1): 415

17. Critical compression factor: 0.279

18. Eccentricity factor: 0.426

19.van der Waals Volume (cm³·mol^-1): 73.200

20.van der Waals Area (cm²·mol^-1): 1.050×10¹⁰

21. Liquid phase standard hot melt ( J·mol^-1·K^-1)：209.8

Toxicological data

1. Acute toxicity^[13] LD50: 800mg/kg (mouse vein); 800mg/kg (mouse abdominal cavity)

2. Irritation ^[14] Rabbit transdermal: 500mg (24h), moderate irritation.

Ecological data

1. Ecotoxicity No data available

2. Biodegradability No data available

3 .Non-biodegradability No data yet

4. Other harmful effects^[15] This substance may be harmful to the environment and is harmful to the environment. Bodies of water should be given special attention.

Molecular structure data

1. Molar refractive index: 31.57

2. Molar volume (cm³/mol): 131.4

3. Isotonic specific volume (90.2K ): 292.9

4. Surface tension (dyne/cm): 24.6

5. Dielectric constant:

6. Dipole moment (10^-24cm³):

7. Polarizability: 12.51

Compute chemical data

1. Hydrophobic parameter calculation parameters�� value (XlogP): 1.5

2. Number of hydrogen bond donors: 0

3. Number of hydrogen bond acceptors: 2

4. Yes Number of rotational chemical bonds: 3

5. Number of tautomers: None

6. Topological molecule polar surface area 26.3

7. Number of heavy atoms: 8

8. Surface charge: 0

9. Complexity: 76.6

10. Number of isotope atoms: 0

11. Determine the number of atomic stereocenters: 0

12. Uncertain number of atomic stereocenters: 0

13. Determine the number of chemical bond stereocenters: 0

14. Number of uncertain chemical bond stereocenters: 0

15. Number of covalent bond units: 1

Properties and stability

1. Stability^[16] Stable

2. Incompatible substances^[17] Strong oxidants, strong bases, strong acids

3. Polymerization hazard^[18] No polymerization

Storage method

Storage Precautions^[19] Stored in a cool, ventilated warehouse. Keep away from fire and heat sources. The storage temperature should not exceed 37℃. Keep container tightly sealed. They should be stored separately from oxidants, acids, and alkalis, and avoid mixed storage. Use explosion-proof lighting and ventilation facilities. It is prohibited to use mechanical equipment and tools that are prone to sparks. The storage area should be equipped with emergency release equipment and suitable containment materials.

Synthesis method

1. Obtained from the esterification of isobutyric acid and absolute ethanol. After mixing isobutyric acid and absolute ethanol, carefully add concentrated sulfuric acid, heat to reflux for 14 hours, wash with water, saturated sodium bicarbonate solution, and water in sequence, dry over anhydrous magnesium sulfate, distill, and collect 109-111°C Fraction, 2-methylpropionic acid ethyl ester was obtained with a yield of 69%.

2. It is obtained by heating esterification of isobutyric acid and ethanol under azeotropic conditions and then distilling it.

Purpose

Used in organic synthesis, essence extraction, etc. ^[20]

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