Ethyl Acetate

Ethyl Acetate

தோற்றம்
: China
CAS எண்
: 141-78-6
HS குறியீடு
: 29153100
அடிப்படை தகவல்
IUPAC Name
: ethyl acetate
Molecular Formula
: C4H8O2
Molecular Weight (g/mol)
: 88.1100
Synonyms & Trade Names
: Ethyl acetate; Acetic acid ethyl ester; EtOAc
Purity / Assay (%)
: 99.5% min
Grade / Quality Level
: Industrial Grade
Physical Form
: Liquid
Concentration
: Pure substance
Appearance / Color
: Clear to slightly colored liquid
Odor
: Fruity, sweet
Melting Point (°C)
: -84.0000
Boiling Point (°C)
: 77
Density (g/cm³)
: 0.9020
Solubility in Water
: Miscible
Signal Word
: Danger
UN Number
: 1173
GHS Hazard Class
: Flammable; Eye irritant
H-Statements
: H225|H319|H336
P-Statements
: P210|P233|P240|P241|P242|P243|P264|P271
REACH Status
: Registered
Drug Precursor Status
: Non-precursor
Storage Class (GHS)
: 3
Storage Conditions
: Cool, dry, ventilated; away from ignition
வகைகள்
இந்த தயாரிப்பை பகிரவும் :
இந்த தயாரிப்பில் ஆர்வமா?

விலை, தனிப்பயனாக்கல் மற்றும் கப்பல் போக்குவரத்து உட்பட விரிவான தகவலுக்கு:

தொழில்நுட்ப ஆவணம்

What is Ethyl Acetate?
Ethyl acetate is a clear colorless liquid with a fruity odor. It is found in alcoholic beverages. It is also found in cereal crops, radishes, fruit juices, beer, wine, spirits, etc. It is produced by Anthemis nobilis (Roman chamomile) and the Rubus species. Ethyl Acetate is an organic ester compound with a molecular formula of CH3COOCH2CH3, commonly abbreviated as EtOAc or EA. It is highly miscible with all common organic solvents (alcohols, ketones, glycols, esters), which make it a common solvent for cleaning, paint removal, and coatings. Due to its agreeable aroma and low cost, ethyl acetate is commonly used and manufactured on a large scale worldwide. Ethyl acetate density is 902 / kg/m³.
Manufacturing Process
Ethyl acetate is synthesized in the industry mainly via the Fischer esterification reaction with ethanol and acetic acid. This mixture converts to the ester in about 65% yield at room temperature:
CH3CH2OH + CH3COOH → CH3COOCH2CH3 + H2O.
The reaction can be accelerated by acid catalysis and the equilibrium can be shifted to the right by the removal of water. It can also be prepared using the Tishchenko reaction by combining two equivalents of acetaldehyde in the presence of an alkoxide catalyst:
2CH3CHO → CH3COOCH2CH3