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Data bank of environmental chemicals     |     The Finnish Environment Institute (SYKE)
 


7.12.2025

Data bank of environmental properties of chemicals


Chemical
Vinylacetate
CAS-number :
108-05-4
 
Synonyms :
1-acetoxyethylene
acetic acid ethenyl ester
acetic acid vinyl ester
acetoxyethylene
ethenyl acetate
vinyl A monomer
vinyl acetate
vinyl acetate monomer
Vinyyliasetaatti
 
Sumformula of the chemical :
C4H6O2 C4H6O2
EINECS-number :
2035454
 
Uses :
Solvent. 
 
State and appearance :
Colorless, mobile liquid (HSDB 2001)
 
Odor :
Quality: sour, sharp
Hedonic tone: unpleasant
Threshold odour concentration
absolute: 0.12 ppm
50 % recognition: 0.40 ppm
100 % recognition: 0.55 ppm
Odour index 100 % recognition: 220 000
(Hellman & Small 1974)

Sweet smell in small quatities; pleasant fruity; characteristic 
odor. 
Initially pleasant odor which quickly becomes sharp and 
irritating (HSDB 2001).
 
Molecular weight :
86.09
 
Spesicif gravity (water=1) :
0.93  at 20 °C, HSDB 2001
 
Conversion factor, 1 ppm in air=_mg/m3 :
3.57  OVA 1999
 
Conversion factor, 1 mg/m3 in air=_ppm :
0.28  OVA 1999
 
Vapor pressure, mmHg :
85  at 20 °C, Weber et al. 1981
90.2  at 20 °C, HSDB 2001
 
Water solubility, mg/l :
20000  at 20°C, Merck Index 1983
26000  MITI 1992
  --
20000  20 - 24 g/l, at 20 °C
24000  OVA 1999
 
Melting point, °C :
-93.2  Howard 1989
-84  <-84, MITI 1992
-93  IUCLID 2000
 
Boiling point, °C :
72  72 - 73
73  IUCLID 2000
73  MITI 1992
 
Log octanol/water coefficient, log Pow :
0.73  Hansch & Leo 1985
0.73  Sangster 1989
0.73  IUCLID 2001
0.73  LOGKOW 1994
 
Henry's law constant, Pa x m3/mol :
48.7  at 20°C, calc., Howard 1989
49  OVA 1999
 
Volatilization :
The Henry's Law constant suggests that volatilization from
environmental waters can be significant (Lyman et al. 1982).

The volatilization half-life from a model river (1 m deep
flowing 1 m/sec with a wind speed of 3 m/sec) can be estimated
to be 4.4 hr (Lyman et al. 1982).

The volatilization half-life from an environmental pond can be
estimated to be 2.1 days (USEPA 1987).

The estimated volatilization half-life from a model lake (1 m
deep, flowing 0.05 m/sec, wind velocity of 0.5 m/sec) is
estimated as approx. 4 days (HSDB 2001).

The Henry's Law constant value for vinyl acetate indicates that
volatilization from moist soil surfaces may occur. 
The
potential for volatilization of vinyl acetate from dry soil
surfaces may exist based on a vapor pressure of 90.2 mmHg
(HSDB 2001).
 
Adsorption/desorption :
Based on the water solubility and the log Kow, the Koc of vinyl
acetate can be estimated to range from 19 to 59 from
regression-derived equation (Lyman et al. 1982).
 
Mobility :
The estimated Koc values are indicative of very high to high
soil mobility (Swann et al. 1983).

Estimated Koc value of 19 - 59 indicates that significant
leaching is possible; however, concurrent hdrolysis should
decrease the environmental importance of leaching (IUCLID
2000).

Based on a water solubility of 20000 ppm at 20 °C and log Kow
of 0.73, the Koc of acetic acid ethenyl ester can be estimated
to range from 19 - 59 from regrassion-derived equation. 
These
estimated Koc values are indiacative of very high to high soil
mobility (IUCLID 2000).
 
Other physicochemical properties :
Vinyl acetate readily polymerizes, therefore, if vinyl acetate
is released to the environment in a spill situation,
significant polymerization may occur (Howard 1989).
 
Photochemical degradation in air :
Vapor-phase vinyl acetate is degraded rabidly in the atmosphere
by reaction with photochemically produced hydoxyl radicals,
estimated half-life of 14.6 hours in a average atmosphere
(Atkinson 1987).

Vapor-phase vinyl acetate may also be degraded in the
atmosphere by reaction with ozone with an estimated half-life
of 3.9 days (HSDB 2001).
 
Photochemical degradation in water :
The half-lifes for olefinic structures in sunlit natural waters
are about 13 and 18 days with respect to reaction via hydroxyl
radicals and singlet oxygen. 
Vinyl avetate does not absorb UV
light significantly above 250 nm in ethanol solvent and,
therefore, it should not be susceptible to direct sunlight
photolysis (Mill & Mabey 1985) (Daniels 1983).
 
Hydrolysis in water :
The aqueous hydrolysis half-life of vinyl acetate at 25°C and pH
7 has been reported to 7.3 days. 
Hydrolysis rates will
increase as the soil becomes more alkaline (Mabey & Mill 1978).

The hydrolysis rate at pH 4.4 has been reported to be minimal
(Daniels 1983).

Vinyl acetate is hydrolyzing to acetic acid and acetaldehyde:
  pH      °C       t1/2
   7      25        7.3 d
   7      20         11 d
   7      14         17 d
   7       4       13.5 d
   7.4    37        4.5 hr
   8      37          3 hr
(IUCLID 2000).
 
Total degradation in water :
Biodegradation:
82-98% by BOD
period 14d
substance: 100 mg/l
sludge: 30 mg/l
(MITI 1992)

Biodegradation:
type: aerobic
inoculum: activated sludge, non-adapted
concentration: 100 mg/l related to test substance
degradation: 82 - 98 % after 14 day
result: readily biodegradable
method: OECD Guide-line 301 C
(IUCLID 2000).
 
Other information of degradation :
A 5-day 42% BODT in marine water and a 5-day 51.3% BODT using a
sewage inocula (Takemoto 1981).

A 62% BODT in 5 days and a 72% BODT in 20 days using an
acclimated sewage inoculum; 51 and 69% BODTs in 5 and 15 days,
respectively, in marine water containing a syntetic sewage
seed (Price et al. 1974).

CO2 evolutions of 27 and 49% over 19 and 38 days incubation,
respectively, using non-acclimated sewage inocula; a 58% CO2
evolution in 22 days using an acclimated sewage inocula
(Pahren & Bloodgood 1961).

CO2 evolution of 42% in 10 days using an acclimated sewage
inocula (Ludzack & Ettinger 1960).

A 100% degradation after a 3-day lag period using the Hungate
Serum Bottle technique (aerobic conditons) and enriched methane
cultures (Chou et al. 1979).
 
Other information of bioaccumulation :
An estimated BCF of 2 was calculated for vinyl acetate using a 
log Kow of 0.73 and a regression-derived equation. 
According to 
a classification scheme, this suggests the potential for 
bioconcentration tin aquatic organisms is low (HSDB 2001).
 
LDLo values to mammals in oral exposure, mg/kg :
500  orl-rat
 
Effects on microorganisms :
Toxicity threshold (cell multiplication inhibition test):
bacteria (Pseudomonas putida): 6 mg/l
(Bringmann & Kühn 1980a)
 
LOEC values to algae, mg/l :
35  rpd, schr, Microcystis aeruginosa
  Bringmann & Kühn 1976
 
LC50 values to crustaceans, mg/l :
10  48 hr, Artemia salina, IUCLID 2000
 
EC50 values to crustaceans, mg/l :
52  24 hr, Daphnia magna
330  24 hr, Daphnia magna
  IUCLID 2000
 
LC50 values to fishes, mg/l :
18  96hr, Lepomis macrochirus
19  96hr, Pimephales promelas
  Pickering & Henderson 1966
  --
18  96 hr, Lepomis macrochirus
42.3  96 hr, Carassius auratus
31.1  96 hr, Lebistes reticulates
26  48 hr, Leuciscus idus melanotus
14  14 - 15 mg/l, 96 hr Pimephales promelas
15 
19  96 hr, Pimephales promelas
23  23 - 26 mg/l, 96 hr, Pimephales promelas
26 
41  41 - 44 mg/l, 96 hr, Pimephales promelas
44  IUCLID 2000
 
Other information of water organisms :
Toxicity threshold (cell multiplication inhibition test):
green algae (Scenedesmus quadricauda): 370 mg/l
protozoa (Entosiphon sulcatum): 81 mg/l
(Bringmann & Kühn 1980a).

References
187Bringmann, G. & Kühn, R. 1976. Vergleichende Befunde der Schadwirkung wassergefährdender Stoffe gegen Bakterien (Pseudomonas putida) und Blaualgen (Microcystis aeruginosa). Gwf-Wasser-Abwasser 117(9).
188Bringmann, G. & Kühn, R. 1980a. Comparison of the toxicity thresholds of water pollutants to bacteria, algae and protozoa in the cell multiplication inhibition test. Water Res. 14: 231 - 241.
2969Chou W. L. et al. 1979. Biotechnol. Bioeng. Symp. 8: 391 - 414.
3075Daniels, W. 1983. Kirk-Othmer Encycl. Chem. Tech. 3rd ed NY: Wiley 23: 817 - 820.
2958Hansch, C and Leo, A. J. 1985. Medchem Project Issue No 26. Claremont C.A. Pomona College.
1673Hellman, T.M. & Small, F.H. 1974. Characterization of the odour properties of 101 petrochemicals using sensory methods. J. Air Pollut. Control Assoc. 24: 979 - 982.
3047Howard, P. H. 1989. Handbook of Environmental Fate and Exposure Data for Organic Chemicals. Vol. I: Large Production and Priority Pollutants. Lewis Publishers, Inc. Chelsea. pp 574.
3114HSDB Database 1992 -. Hazardous Substances Data Bank. US. National Library of Medicine. TOMES Plus CD-ROM.
3253IUCLID 1995 -. International Uniform Chemical Information Database. European Commission. European Chemicals Bureau. Existing Chemicals. Ispra, Italy.
3182LOG KOW 1994. Octanol-water partition coefficient program. Syracure Research Corporation. Chemical Hazard Assessment Division. Environmental Chemistry Center.
3073Ludzack, F. J. & Ettinger, M. B. 1960. J. Water Pollut. Control Fed. 32: 1173 - 1200.
2960Lyman, W. J. et al. 1982. Handbook of Chemical Property Estimation Methods. Environmental behavior of organic compounds. McGraw-Hill New York.
3069Mabey, W & Mill, T. 1978. J. Phys. Chem. Ref. Data 7: 383 - 415.
3006Merck Index. 1983. An Encyclopedia of Chemicals, Drugs and Biologicals 10th ed. p 853.
3074Mill, T. & Mabey, W. 1985. Environ. Exposure from Chemicals. Vol 1, p 208 - 210; Neely, W. B. & Blau, G. E. eds Boca Raton, F. L.: CRC Press.
3105MITI 1992. Biodegradation and bioaccumulation data of existing chemicals based on the CSCL Japan. Compild under the Safety Division Basic Industries Bureau Ministry of International Trade & Industry, Japan. Edited by Chemicals Inspection & Testing Institute, Japan.
3340OVA 1999. The safety instructions for some hazardous chemicals. (available in Finnish)/Onnettomuuden vaaraa aiheuttavat aineet -turvallisuusohjeet (OVA-ohjeet). Työterveyslaitos (Finnish Institute of Occupational Health),Työsuojelurahasto (The Finnish Work Environment Fund). Helsinki. Finland.
3062Pahren, H. R. & Bloodgood, D. E. 1961. Water Pollut. Contr. Fed. J. 33: 233 - 238.
1129Pickering, Q.H. & Henderson, C. 1966. Acute toxicity of some important petrochemicals to fish. J. Water Pollut. Control Feder. 38: 1419 - 1429.
1667Price, K.S. Waggy, G.T. & Conway, R.A. 1974. Brine shrimp bioassay and seawater BOD of petrochemicals. J. Water Pollut. Control. Fed. 46(1): 63 - 77.
3104Sangster, J. 1989. Octanol-water partition coefficients of simple organic compounds. J. Phys. Chem. Ref. Data, Vol 18, No. 3: 1111 - 1229.
2988Swann, R. L. et al. 1984. Res. Rev. 85: 17 - 28.
2967Takemoto, S. et al. 1981. Suishitsu Okadu Kenkyu 4: 80 - 90.
3012Weber, R. C. et al. 1981. Vabor Pressure Distribution of Selected Organic Chemicals. USEPA-600/2-81-021 p 24.

 
 
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