ethyl ethanoate


acetic acid ethyl ester; acetic ester; acetic ether; aether aceticus; ethyl acetate; ethyl ethanoate
In russian:этиловый эфир уксусной кислоты; этилацетат
Links:🌍 Wikipedia, 📏 NIST, 📖 PubMed,
📖Houben-Weyl, 2. Band (Essigester); p. 297, 352, 484, 499, 521, 533, 542, 968,
📖Org. Chem., v. Richter, 1. Vol (Acetic Ether); p. 267
CAS RN:[141-78-6]
Formula:C4H8O2; 88.11 g/mol
InChiKey:XEKOWRVHYACXOJ-UHFFFAOYSA-N
SMILES:O=C(OCC)C
Molecular structure of ethyl acetate
Density:0.901 g/mL
Molar volume:97.8 mL/mol
Refractive index:1.372
Molecular refractive power:22.26 mL/mol
Dielectric constant:6.40
Dipole moment:1.88 D
Melting point:-84 °C
Boiling point:77 °C
Vapour pressure:73 Torr
Antoine equation
P(Torr) vs T(°C)
Vapour pressure vs temperature
Surface tension:23.75 dyn/cm
Viscosity:0.45 cP
Critical temperature:250 °C
Critical pressure:37.9 atm
Critical volume:286.00 ml/mol
Evaporation rate (ether):3.0
Evaporation rate (butyl acetate):4.2
Solubility in water:8 % w/w
Solubility of water:3 % w/w
Log10 partition water / activated carbon:2.31
Log10 partition octanol / water:0.73
Snyder P':4.4
Snyder X:Xe: 0.3    Xd: 0.2    Xn: 0.4
Solvent strength (ε0, silica):0.38
Solvent strength (ε0, alumina):0.58
Dimroth ET:38.1
Hildebrant solubility parameter (δ):9.1
Hansen solubility parameter:δd: 7.7 (cal/mL)½   δp: 2.6 (cal/mL)½   δh: 3.5 (cal/mL)½
100g dissolves:
59g cocaine;    57.2g 4-nitrobenzyl chloride;    41.2g benzoic acid;    38g 2-hydroxybenzoic acid;    36.27g 1,3-dinitrobenzene;    24.7g quinine;    21.3g benzophenone;    12.96g 1,2-dinitrobenzene;    7.94g octadecanoic acid;    4.903g hyoscyamine;    4.45g brucine;    4.22g hydrastinine;    3.77g benzoic acid;    3.75g 3,4,5-trihydroxybenzoic acid;    3.07g water;    2.469g quinine;    1.84g 4-chlorobenzoic acid;    1.761g quinidine;    1.76g quinidine;    1.6g hydroxylamine hydrochloride;    1.34g colchicine;    0.626g 9,10-phenanthraquinone;    0.3003g cinchonidine;    0.197g strychnine;    0.1861g morphine;    0.123g tetra(phenyl)plumbane;    0.0719g cinchonine;    0.03g tetracyclohexyl lead
1g dissolves in:
11.72g water
Specific heat capacity:40.0 cal/molK
Latent heat of fusion:2,494 cal/mol

Isomers

butanoic acid
Molecular structure of butanoic acid
(E)-but-2-ene-1,4-diol
Molecular structure of (E)-but-2-ene-1,4-diol
cis-2-butene-1,4-diol
Molecular structure of cis-2-butene-1,4-diol
3,4-dihydroxy-1-butene
Molecular structure of 3,4-dihydroxy-1-butene
dioxane
Molecular structure of dioxane
1,3-dioxane
Molecular structure of 1,3-dioxane
2-ethenoxyethanol
Molecular structure of 2-ethenoxyethanol
ethyl acetate
Molecular structure of ethyl acetate
3-hydroxybutanal
Molecular structure of 3-hydroxybutanal
(S)-3-hydroxybutan-2-one
Molecular structure of (S)-3-hydroxybutan-2-one
3-hydroxy-2-butanone
Molecular structure of 3-hydroxy-2-butanone
4-hydroxy-2-butanone
Molecular structure of 4-hydroxy-2-butanone
(R)-(-)-3-hydroxytetrahydrofuran
Molecular structure of (R)-(-)-3-hydroxytetrahydrofuran
(S)-(+)-3-hydroxytetrahydrofuran
Molecular structure of (S)-(+)-3-hydroxytetrahydrofuran
3-hydroxytetrahydrofuran
Molecular structure of 3-hydroxytetrahydrofuran
isopropyl formate
Molecular structure of isopropyl formate
(2R)-2-(methoxymethyl)oxirane
Molecular structure of (2R)-2-(methoxymethyl)oxirane
(2S)-2-(methoxymethyl)oxirane
Molecular structure of (2S)-2-(methoxymethyl)oxirane
1-methoxypropan-2-one
Molecular structure of 1-methoxypropan-2-one
2-methyl-1,3-dioxolane
Molecular structure of 2-methyl-1,3-dioxolane
4-methyl-1,3-dioxolane
Molecular structure of 4-methyl-1,3-dioxolane
2-methylene-1,3-propanediol
Molecular structure of 2-methylene-1,3-propanediol
methyl propanoate
Molecular structure of methyl propanoate
2-methylpropanoic acid
Molecular structure of 2-methylpropanoic acid
2-oxetanemethanol
Molecular structure of 2-oxetanemethanol
oxetane-3-methanol
Molecular structure of oxetane-3-methanol
propyl formate
Molecular structure of propyl formate